geneid | 341676 |
---|---|
ensemblid | ENSG00000197168.14 |
hgncid | 7748 |
symbol | NEK5 |
name | NIMA related kinase 5 |
refseq_nuc | NM_001365552.1 |
refseq_prot | NP_001352481.1 |
ensembl_nuc | ENST00000684899.1 |
ensembl_prot | ENSP00000509632.1 |
mane_status | MANE Select |
chr | chr13 |
start | 52033611 |
end | 52129073 |
strand | - |
ver | v1.2 |
region | chr13:52033611-52129073 |
region5000 | chr13:52028611-52134073 |
regionname0 | NEK5_chr13_52033611_52129073 |
regionname5000 | NEK5_chr13_52028611_52134073 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 832 | 292 | 63 | 53 | 138 | 6 | 30 | 106 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0002 | 0/0 | 832 | 31 | 1 | 13 | 10 | 4 | 3 | 6 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0003 | 0/0 | 832 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0004 | 0/0 | 832 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0005 | 0/0 | 832 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0006 | 0/0 | 832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0007 | 0/0 | 832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0008 | 0/0 | 832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0009 | 0/0 | 832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0010 | 0/0 | 832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2499 | 276 | 58 | 51 | 133 | 6 | 26 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
c0002 | 0/0 | 2499 | 31 | 1 | 13 | 10 | 4 | 3 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
c0003 | 0/0 | 2499 | 9 | 1 | 1 | 4 | 0 | 3 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
c0004 | 0/0 | 2499 | 3 | 3 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
c0005 | 0/0 | 2499 | 3 | 2 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
c0006 | 0/0 | 2499 | 2 | 1 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
c0007 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
c0008 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
c0009 | 0/0 | 2499 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
c0010 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
c0011 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
c0012 | 0/0 | 2499 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
c0013 | 0/0 | 2499 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
c0014 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
c0015 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
c0016 | 0/0 | 2499 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 3473 | 103 | 22 | 10 | 58 | 1 | 11 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0002 | 0/0 | 3476 | 60 | 6 | 13 | 33 | 3 | 5 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0003 | 0/0 | 3476 | 22 | 0 | 3 | 17 | 0 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0004 | 0/0 | 3473 | 18 | 1 | 6 | 9 | 1 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0005 | 0/0 | 3473 | 10 | 0 | 6 | 0 | 3 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0006 | 0/0 | 3470 | 8 | 0 | 8 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0007 | 0/0 | 3477 | 7 | 1 | 0 | 4 | 0 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0008 | 0/0 | 3474 | 6 | 2 | 3 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0009 | 0/0 | 3474 | 5 | 2 | 0 | 2 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0010 | 0/0 | 3473 | 5 | 1 | 1 | 0 | 0 | 3 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0011 | 0/0 | 3475 | 5 | 0 | 3 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0012 | 0/0 | 3472 | 4 | 4 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0013 | 0/0 | 3472 | 4 | 0 | 0 | 4 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0014 | 0/0 | 3473 | 4 | 0 | 3 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0015 | 0/0 | 3474 | 4 | 1 | 0 | 3 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0016 | 0/0 | 3475 | 4 | 4 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0017 | 0/0 | 3472 | 3 | 0 | 0 | 2 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0018 | 0/1 | 3473 | 3 | 0 | 0 | 0 | 0 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0019 | 0/0 | 3472 | 3 | 3 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0020 | 0/0 | 3477 | 3 | 0 | 1 | 1 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0021 | 0/0 | 3476 | 3 | 0 | 0 | 0 | 1 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0022 | 0/0 | 3473 | 3 | 3 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0023 | 0/0 | 3473 | 2 | 2 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0024 | 0/0 | 3473 | 2 | 2 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0025 | 0/0 | 3476 | 2 | 2 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0026 | 0/0 | 3472 | 2 | 2 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0027 | 0/0 | 3473 | 2 | 1 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0028 | 0/0 | 3475 | 2 | 0 | 2 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0029 | 0/0 | 3477 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0030 | 0/0 | 3473 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0031 | 0/0 | 3474 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0032 | 0/0 | 3474 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0033 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0034 | 0/0 | 3475 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0035 | 0/0 | 3474 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0036 | 0/0 | 3475 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0037 | 0/0 | 3474 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0038 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0039 | 0/0 | 3473 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0040 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0041 | 0/0 | 3471 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0042 | 0/0 | 3463 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0043 | 0/0 | 3471 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0044 | 0/0 | 3473 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0045 | 0/0 | 3473 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0046 | 0/0 | 3474 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0047 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0048 | 0/0 | 3474 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0049 | 0/0 | 3474 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0050 | 0/0 | 3473 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0051 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0052 | 0/0 | 3473 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0053 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0054 | 0/0 | 3474 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0055 | 0/0 | 3476 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0056 | 0/0 | 3476 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0057 | 0/0 | 3475 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0058 | 0/0 | 3476 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0059 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0060 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0061 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
t0062 | 0/0 | 3476 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0015 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2499 | 276 | 58 | 51 | 133 | 6 | 26 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0003 | 0/0 | 2499 | 9 | 1 | 1 | 4 | 0 | 3 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0004 | 0/0 | 2499 | 3 | 3 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0009 | 0/0 | 2499 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0010 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0013 | 0/0 | 2499 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0016 | 0/0 | 2499 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0002c0002 | 0/0 | 2499 | 31 | 1 | 13 | 10 | 4 | 3 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0003c0005 | 0/0 | 2499 | 3 | 2 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0004c0006 | 0/0 | 2499 | 2 | 1 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0005c0012 | 0/0 | 2499 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0006c0011 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0007c0008 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0008c0014 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0009c0007 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0010c0015 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5971 | 97 | 20 | 9 | 57 | 1 | 9 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0002 | 0/0 | 5974 | 59 | 5 | 13 | 33 | 3 | 5 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0003 | 0/0 | 5974 | 22 | 0 | 3 | 17 | 0 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0004 | 0/0 | 5971 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0006 | 0/0 | 5968 | 8 | 0 | 8 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0007 | 0/0 | 5975 | 7 | 1 | 0 | 4 | 0 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0008 | 0/0 | 5972 | 6 | 2 | 3 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0009 | 0/0 | 5972 | 4 | 1 | 0 | 2 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0011 | 0/0 | 5973 | 4 | 0 | 2 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0012 | 0/0 | 5970 | 4 | 4 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0014 | 0/0 | 5971 | 4 | 0 | 3 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0015 | 0/0 | 5972 | 4 | 1 | 0 | 3 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0016 | 0/0 | 5973 | 4 | 4 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0017 | 0/0 | 5970 | 3 | 0 | 0 | 2 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0018 | 0/1 | 5971 | 3 | 0 | 0 | 0 | 0 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0020 | 0/0 | 5975 | 3 | 0 | 1 | 1 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0021 | 0/0 | 5974 | 3 | 0 | 0 | 0 | 1 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0022 | 0/0 | 5971 | 3 | 3 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0023 | 0/0 | 5971 | 2 | 2 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0024 | 0/0 | 5971 | 2 | 2 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0025 | 0/0 | 5974 | 2 | 2 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0026 | 0/0 | 5970 | 2 | 2 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0028 | 0/0 | 5973 | 2 | 0 | 2 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0029 | 0/0 | 5975 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0030 | 0/0 | 5971 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0031 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0034 | 0/0 | 5973 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0035 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0036 | 0/0 | 5973 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0037 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0038 | 0/0 | 5969 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0039 | 0/0 | 5971 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0040 | 0/0 | 5970 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0041 | 0/0 | 5969 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0043 | 0/0 | 5969 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0044 | 0/0 | 5971 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0045 | 0/0 | 5971 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0046 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0047 | 0/0 | 5974 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0052 | 0/0 | 5971 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0053 | 0/0 | 5970 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0055 | 0/0 | 5974 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0056 | 0/0 | 5974 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0057 | 0/0 | 5973 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0058 | 0/0 | 5974 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0059 | 0/0 | 5975 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0060 | 0/0 | 5975 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0061 | 0/0 | 5974 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0001t0062 | 0/0 | 5974 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0003t0010 | 0/0 | 5971 | 5 | 1 | 1 | 0 | 0 | 3 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0003t0013 | 0/0 | 5970 | 4 | 0 | 0 | 4 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0004t0019 | 0/0 | 5970 | 3 | 3 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0009t0001 | 0/0 | 5971 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0010t0048 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0013t0001 | 0/0 | 5971 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0001c0016t0001 | 0/0 | 5971 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0002c0002t0004 | 0/0 | 5971 | 16 | 0 | 5 | 9 | 1 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0002c0002t0005 | 0/0 | 5971 | 10 | 0 | 6 | 0 | 3 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0002c0002t0032 | 0/0 | 5972 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0002c0002t0033 | 0/0 | 5970 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0002c0002t0049 | 0/0 | 5972 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0002c0002t0050 | 0/0 | 5971 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0002c0002t0051 | 0/0 | 5970 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0003c0005t0027 | 0/0 | 5971 | 2 | 1 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0003c0005t0054 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0004c0006t0002 | 0/0 | 5974 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0004c0006t0011 | 0/0 | 5973 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0005c0012t0001 | 0/0 | 5971 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0006c0011t0042 | 0/0 | 5961 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0007c0008t0009 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0008c0014t0004 | 0/0 | 5971 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0009c0007t0001 | 0/0 | 5971 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
a0010c0015t0001 | 0/0 | 5971 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | copy fasta | chr13 | 52028611 | 52134073 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0006g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0006g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0006g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0006g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0006g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0006g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0006g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0007g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0007g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0007g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0007g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0007g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0007g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0008g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0008g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0008g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0008g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0009g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0009g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0009g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0011g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0011g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0011g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0011g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0012g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0012g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0012g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0012g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0014g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0014g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0014g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0014g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0015g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0015g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0015g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0015g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0016g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0016g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0016g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0016g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0017g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0017g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0017g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0018g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0018g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0018g0015 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0020g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0020g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0020g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0021g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0021g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0021g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0022g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0022g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0022g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0023g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0023g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0024g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0024g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0025g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0025g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0026g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0026g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0028g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0028g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0029g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0029g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0030g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0031g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0034g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0035g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0036g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0037g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0038g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0039g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0040g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0041g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0043g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0044g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0045g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0046g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0047g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0052g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0053g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0055g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0056g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0057g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0058g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0059g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0060g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0061g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0001t0062g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0003t0010g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0003t0010g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0003t0010g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0003t0010g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0003t0010g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0003t0013g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0003t0013g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0003t0013g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0003t0013g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0004t0019g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0004t0019g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0004t0019g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0009t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0010t0048g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0013t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0001c0016t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0005g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0005g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0005g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0032g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0033g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0049g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0050g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0002c0002t0051g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0003c0005t0027g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0003c0005t0027g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0003c0005t0054g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0004c0006t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0004c0006t0011g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0005c0012t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0006c0011t0042g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0007c0008t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0008c0014t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0009c0007t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
a0010c0015t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0223 | EUR | GBR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00099 | hp2 | a0002 | c0002 | t0005 | g0067 | EUR | GBR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00323 | hp1 | a0002 | c0002 | t0004 | g0181 | EUR | FIN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00323 | hp2 | a0001 | c0001 | t0021 | g0232 | EUR | FIN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00408 | hp2 | a0002 | c0002 | t0004 | g0185 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00544 | hp1 | a0001 | c0003 | t0013 | g0021 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00621 | hp1 | a0002 | c0002 | t0049 | g0190 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00639 | hp1 | a0004 | c0006 | t0011 | g0208 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0271 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00642 | hp2 | a0002 | c0002 | t0005 | g0066 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00733 | hp1 | a0001 | c0001 | t0014 | g0294 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00733 | hp2 | a0002 | c0002 | t0004 | g0184 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00738 | hp1 | a0002 | c0002 | t0005 | g0073 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01074 | hp2 | a0002 | c0002 | t0050 | g0320 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01081 | hp1 | a0002 | c0002 | t0004 | g0182 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01081 | hp2 | a0001 | c0001 | t0008 | g0063 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01099 | hp1 | a0002 | c0002 | t0005 | g0074 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01099 | hp2 | a0001 | c0003 | t0010 | g0017 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01109 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01109 | hp2 | a0001 | c0001 | t0008 | g0062 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01167 | hp1 | a0002 | c0002 | t0005 | g0064 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01168 | hp1 | a0002 | c0002 | t0005 | g0065 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01169 | hp1 | a0002 | c0002 | t0033 | g0075 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01169 | hp2 | a0001 | c0001 | t0008 | g0095 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01192 | hp1 | a0003 | c0005 | t0027 | g0321 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01243 | hp1 | a0001 | c0001 | t0036 | g0032 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01243 | hp2 | a0001 | c0001 | t0052 | g0317 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01255 | hp1 | a0001 | c0001 | t0006 | g0027 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01255 | hp2 | a0001 | c0009 | t0001 | g0041 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01256 | hp1 | a0001 | c0001 | t0006 | g0025 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01256 | hp2 | a0001 | c0001 | t0028 | g0279 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01257 | hp1 | a0001 | c0001 | t0053 | g0295 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01258 | hp1 | a0001 | c0001 | t0028 | g0205 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01258 | hp2 | a0001 | c0001 | t0014 | g0296 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01261 | hp2 | a0002 | c0002 | t0004 | g0180 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01346 | hp2 | a0001 | c0001 | t0020 | g0309 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01358 | hp1 | a0002 | c0002 | t0004 | g0183 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01361 | hp1 | a0001 | c0001 | t0014 | g0297 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01361 | hp2 | a0001 | c0001 | t0006 | g0024 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01433 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01516 | hp1 | a0002 | c0002 | t0005 | g0071 | EUR | IBS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01516 | hp2 | a0001 | c0001 | t0039 | g0146 | EUR | IBS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0268 | EUR | IBS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01517 | hp2 | a0002 | c0002 | t0005 | g0072 | EUR | IBS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01891 | hp1 | a0001 | c0001 | t0012 | g0036 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01891 | hp2 | a0002 | c0002 | t0051 | g0319 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01934 | hp2 | a0001 | c0001 | t0006 | g0028 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01943 | hp1 | a0001 | c0001 | t0040 | g0090 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01943 | hp2 | a0001 | c0001 | t0011 | g0206 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01952 | hp1 | a0001 | c0001 | t0011 | g0242 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01952 | hp2 | a0001 | c0001 | t0006 | g0026 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0258 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01993 | hp1 | a0001 | c0001 | t0058 | g0285 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0257 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02055 | hp2 | a0004 | c0006 | t0002 | g0209 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02071 | hp2 | a0001 | c0001 | t0007 | g0240 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02074 | hp1 | a0001 | c0001 | t0015 | g0198 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02132 | hp2 | a0002 | c0002 | t0004 | g0191 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02135 | hp1 | a0002 | c0002 | t0004 | g0178 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02135 | hp2 | a0001 | c0001 | t0015 | g0229 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CDX | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | CDX | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02165 | hp1 | a0001 | c0001 | t0062 | g0276 | EAS | CDX | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CDX | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02257 | hp1 | a0001 | c0001 | t0012 | g0039 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02257 | hp2 | a0001 | c0001 | t0016 | g0305 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02258 | hp1 | a0001 | c0004 | t0019 | g0299 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02273 | hp1 | a0001 | c0001 | t0006 | g0029 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0289 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02280 | hp1 | a0008 | c0014 | t0004 | g0298 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02280 | hp2 | a0001 | c0001 | t0047 | g0195 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02293 | hp2 | a0002 | c0002 | t0004 | g0189 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02300 | hp2 | a0001 | c0001 | t0055 | g0250 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02451 | hp1 | a0001 | c0001 | t0022 | g0311 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02451 | hp2 | a0001 | c0001 | t0031 | g0053 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02572 | hp2 | a0003 | c0005 | t0054 | g0323 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02602 | hp1 | a0002 | c0002 | t0032 | g0070 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02602 | hp2 | a0001 | c0001 | t0021 | g0224 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02615 | hp1 | a0001 | c0001 | t0043 | g0034 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02615 | hp2 | a0001 | c0001 | t0023 | g0011 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02622 | hp2 | a0001 | c0001 | t0023 | g0012 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02647 | hp1 | a0001 | c0001 | t0007 | g0194 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02717 | hp1 | a0009 | c0007 | t0001 | g0054 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0310 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02738 | hp1 | a0001 | c0001 | t0009 | g0151 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02738 | hp2 | a0002 | c0002 | t0004 | g0192 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02809 | hp2 | a0001 | c0001 | t0024 | g0077 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02886 | hp1 | a0006 | c0011 | t0042 | g0037 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02895 | hp1 | a0001 | c0001 | t0016 | g0303 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02896 | hp1 | a0001 | c0010 | t0048 | g0291 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02896 | hp2 | a0001 | c0001 | t0025 | g0061 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02897 | hp1 | a0001 | c0001 | t0016 | g0306 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02897 | hp2 | a0001 | c0001 | t0046 | g0059 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02965 | hp2 | a0003 | c0005 | t0027 | g0322 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02970 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02970 | hp2 | a0001 | c0001 | t0012 | g0035 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03017 | hp1 | a0001 | c0001 | t0044 | g0016 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03017 | hp2 | a0001 | c0003 | t0010 | g0020 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03041 | hp2 | a0001 | c0001 | t0025 | g0060 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03130 | hp1 | a0001 | c0004 | t0019 | g0301 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03139 | hp2 | a0001 | c0004 | t0019 | g0300 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03209 | hp1 | a0001 | c0001 | t0041 | g0084 | AFR | MSL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03209 | hp2 | a0001 | c0001 | t0030 | g0044 | AFR | MSL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03225 | hp2 | a0001 | c0001 | t0022 | g0313 | AFR | MSL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03239 | hp2 | a0002 | c0002 | t0005 | g0069 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03486 | hp1 | a0001 | c0001 | t0024 | g0033 | AFR | MSL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03486 | hp2 | a0001 | c0001 | t0037 | g0127 | AFR | MSL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03490 | hp1 | a0001 | c0001 | t0018 | g0013 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03491 | hp1 | a0005 | c0012 | t0001 | g0100 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03654 | hp2 | a0001 | c0001 | t0018 | g0014 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03688 | hp1 | a0001 | c0003 | t0010 | g0019 | SAS | STU | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03704 | hp1 | a0001 | c0001 | t0007 | g0244 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03710 | hp1 | a0001 | c0001 | t0020 | g0230 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03710 | hp2 | a0001 | c0013 | t0001 | g0132 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | BEB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03831 | hp2 | a0001 | c0001 | t0017 | g0103 | SAS | BEB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG04115 | hp1 | a0001 | c0001 | t0021 | g0286 | SAS | STU | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG04228 | hp1 | a0001 | c0001 | t0007 | g0203 | SAS | STU | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | CHB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18906 | hp1 | a0007 | c0008 | t0009 | g0154 | AFR | YRI | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | YRI | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18941 | hp2 | a0002 | c0002 | t0004 | g0186 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18964 | hp2 | a0001 | c0001 | t0017 | g0315 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18965 | hp2 | a0001 | c0001 | t0009 | g0120 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18968 | hp1 | a0001 | c0001 | t0011 | g0307 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18970 | hp1 | a0002 | c0002 | t0004 | g0179 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18972 | hp1 | a0001 | c0001 | t0034 | g0135 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18972 | hp2 | a0001 | c0001 | t0057 | g0280 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18973 | hp1 | a0001 | c0001 | t0007 | g0246 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18974 | hp2 | a0001 | c0016 | t0001 | g0171 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18984 | hp2 | a0002 | c0002 | t0004 | g0188 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18985 | hp2 | a0001 | c0001 | t0060 | g0281 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18991 | hp1 | a0002 | c0002 | t0004 | g0187 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18994 | hp1 | a0001 | c0001 | t0008 | g0105 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18994 | hp2 | a0001 | c0003 | t0013 | g0022 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18999 | hp1 | a0002 | c0002 | t0004 | g0177 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19002 | hp1 | a0001 | c0001 | t0011 | g0231 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19009 | hp1 | a0001 | c0001 | t0029 | g0259 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19009 | hp2 | a0001 | c0001 | t0045 | g0093 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19030 | hp1 | a0010 | c0015 | t0001 | g0055 | AFR | LWK | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19030 | hp2 | a0001 | c0001 | t0009 | g0051 | AFR | LWK | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19055 | hp2 | a0002 | c0002 | t0004 | g0176 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19060 | hp1 | a0001 | c0001 | t0029 | g0253 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19063 | hp1 | a0001 | c0001 | t0007 | g0225 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19065 | hp1 | a0001 | c0001 | t0020 | g0278 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19068 | hp1 | a0001 | c0001 | t0014 | g0287 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19075 | hp1 | a0001 | c0001 | t0056 | g0283 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19075 | hp2 | a0001 | c0001 | t0017 | g0126 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19080 | hp1 | a0001 | c0003 | t0013 | g0023 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19082 | hp1 | a0001 | c0001 | t0007 | g0241 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19082 | hp2 | a0001 | c0003 | t0013 | g0018 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19087 | hp1 | a0001 | c0001 | t0015 | g0275 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19087 | hp2 | a0001 | c0001 | t0009 | g0088 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19089 | hp2 | a0001 | c0001 | t0038 | g0118 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19091 | hp1 | a0001 | c0001 | t0059 | g0262 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19240 | hp1 | a0001 | c0001 | t0026 | g0316 | AFR | YRI | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA19240 | hp2 | a0001 | c0001 | t0022 | g0312 | AFR | YRI | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ASW | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ASW | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0202 | EUR | TSI | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA20905 | hp1 | a0001 | c0003 | t0010 | g0175 | SAS | GIH | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | GIH | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG01123 | hp2 | a0002 | c0002 | t0005 | g0068 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02109 | hp2 | a0001 | c0001 | t0012 | g0038 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG02486 | hp2 | a0001 | c0001 | t0061 | g0302 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG06807 | hp1 | a0001 | c0003 | t0010 | g0174 | AFR | USA | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | USA | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA20300 | hp1 | a0001 | c0001 | t0035 | g0125 | AFR | USA | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA20300 | hp2 | a0001 | c0001 | t0026 | g0318 | AFR | USA | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA21309 | hp1 | a0001 | c0001 | t0016 | g0304 | AFR | LWK | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
NA21309 | hp2 | a0001 | c0001 | t0015 | g0201 | AFR | LWK | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0018 | g0015 | REF | REF | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0081 | REF | REF | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:52050158
|
G | T | 1 | a0008 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.2174C>A | p.Ser725Tyr | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/24 | 2309/5971 | 2174/2499 | 725/832 | chr13 | 52050158 | ||
chr13:52076143
|
C | A | 2 | a0003a0006 | 4 | HG01192.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1573G>T | p.Asp525Tyr | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 18/24 | 1708/5971 | 1573/2499 | 525/832 | chr13 | 52076143 | ||
chr13:52086336
|
G | A | 1 | a0004 | 2 | HG00639.hp1 HG02055.hp2 |
missense_variant | MODERATE | c.1420C>T | p.Arg474Cys | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/24 | 1555/5971 | 1420/2499 | 474/832 | chr13 | 52086336 | ||
chr13:52087340
|
G | C | 1 | a0005 | 1 | HG03491.hp1 | missense_variant&splice_region_variant | MODERATE | c.1390C>G | p.Gln464Glu | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/24 | 1525/5971 | 1390/2499 | 464/832 | chr13 | 52087340 | ||
chr13:52099768
|
G | T | 1 | a0007 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.1001C>A | p.Pro334Gln | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/24 | 1136/5971 | 1001/2499 | 334/832 | chr13 | 52099768 | ||
chr13:52102139
|
T | G | 2 | a0002a0008 | 32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
missense_variant | MODERATE | c.763A>C | p.Lys255Gln | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 10/24 | 898/5971 | 763/2499 | 255/832 | chr13 | 52102139 | ||
chr13:52102204
|
T | C | 1 | a0003 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
missense_variant | MODERATE | c.698A>G | p.His233Arg | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 10/24 | 833/5971 | 698/2499 | 233/832 | chr13 | 52102204 | ||
chr13:52110356
|
C | T | 1 | a0009 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.451G>A | p.Ala151Thr | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/24 | 586/5971 | 451/2499 | 151/832 | chr13 | 52110356 | ||
chr13:52119376
|
T | C | 1 | a0010 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.157A>G | p.Ile53Val | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/24 | 292/5971 | 157/2499 | 53/832 | chr13 | 52119376 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:52065581
|
C | T | 1 | a0001c0010 | 1 | HG02896.hp1 | synonymous_variant | LOW | c.1878G>A | p.Val626Val | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/24 | 2013/5971 | 1878/2499 | 626/832 | chr13 | 52065581 | ||
chr13:52065599
|
C | T | 1 | a0001c0009 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.1860G>A | p.Thr620Thr | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/24 | 1995/5971 | 1860/2499 | 620/832 | chr13 | 52065599 | ||
chr13:52093092
|
G | A | 1 | a0001c0003 | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
synonymous_variant | LOW | c.1170C>T | p.Tyr390Tyr | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/24 | 1305/5971 | 1170/2499 | 390/832 | chr13 | 52093092 | ||
chr13:52099833
|
T | C | 1 | a0001c0013 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.936A>G | p.Pro312Pro | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/24 | 1071/5971 | 936/2499 | 312/832 | chr13 | 52099833 | ||
chr13:52101943
|
C | T | 1 | a0001c0004 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.882G>A | p.Lys294Lys | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/24 | 1017/5971 | 882/2499 | 294/832 | chr13 | 52101943 | ||
chr13:52127450
|
C | A | 1 | a0001c0016 | 1 | NA18974.hp2 | synonymous_variant | LOW | c.33G>T | p.Gly11Gly | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/24 | 168/5971 | 33/2499 | 11/832 | chr13 | 52127450 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:52033618
|
T | C | 1 | a0001c0001t0035 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3330A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 3330 | chr13 | 52033618 | |||||
chr13:52033730
|
A | T | 40 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(37): Show | 176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*3218T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 3218 | chr13 | 52033730 | |||||
chr13:52034169
|
A | T | 2 | a0002c0002t0050a0002c0002t0051 | 2 | HG01074.hp2 HG01891.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2779T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2779 | chr13 | 52034169 | |||||
chr13:52034348
|
A | G | 1 | a0001c0001t0044 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2600T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2600 | chr13 | 52034348 | |||||
chr13:52034436
|
T | C | 1 | a0006c0011t0042 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2512A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2512 | chr13 | 52034436 | |||||
chr13:52034504
|
C | CT | 13 | a0001c0001t0007a0001c0001t0008a0001c0001t0012others(10): Show | 28 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2443dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2443 | chr13 | 52034504 | |||||
chr13:52034504
|
C | T | 1 | a0001c0001t0024 | 2 | HG02809.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2444G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2444 | chr13 | 52034504 | |||||
chr13:52034504
|
CT | C | 5 | a0001c0001t0011a0001c0001t0038a0001c0001t0053others(2): Show | 8 | HG00639.hp1 HG01257.hp1 HG01891.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2443delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2443 | chr13 | 52034504 | |||||
chr13:52034564
|
A | G | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(20): Show | 128 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*2384T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2384 | chr13 | 52034564 | |||||
chr13:52034659
|
T | C | 2 | a0001c0001t0016a0001c0001t0061 | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2289A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2289 | chr13 | 52034659 | |||||
chr13:52034695
|
C | CT | 5 | a0001c0001t0016a0001c0001t0036a0001c0001t0037others(2): Show | 8 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2252dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2252 | chr13 | 52034695 | |||||
chr13:52034695
|
C | CTT | 17 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(14): Show | 112 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*2251_*2252dupAA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2252 | chr13 | 52034695 | |||||
chr13:52034695
|
CT | C | 4 | a0001c0001t0017a0001c0001t0038a0001c0001t0041others(1): Show | 9 | HG00544.hp1 HG03209.hp1 HG03831.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2252delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2252 | chr13 | 52034695 | |||||
chr13:52034799
|
A | T | 1 | a0001c0001t0021 | 3 | HG00323.hp2 HG02602.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2149T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2149 | chr13 | 52034799 | |||||
chr13:52034881
|
C | CT | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(19): Show | 120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*2066dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2066 | chr13 | 52034881 | |||||
chr13:52034881
|
C | CTT | 4 | a0001c0001t0020a0001c0001t0056a0001c0001t0057others(1): Show | 6 | HG01346.hp2 HG03710.hp1 NA18972.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2065_*2066dupAA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2066 | chr13 | 52034881 | |||||
chr13:52034881
|
CT | C | 8 | a0001c0001t0006a0001c0001t0026a0001c0001t0039others(5): Show | 18 | HG01109.hp1 HG01169.hp1 HG01243.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2066delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2066 | chr13 | 52034881 | |||||
chr13:52034881
|
CTTTTTTT others(3): Show |
C | 1 | a0006c0011t0042 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2057_*2066delAAAA others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2057 | chr13 | 52034881 | |||||
chr13:52034993
|
A | G | 1 | a0001c0001t0022 | 3 | HG02451.hp1 HG03225.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1955T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1955 | chr13 | 52034993 | |||||
chr13:52035057
|
G | T | 35 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(32): Show | 165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*1891C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1891 | chr13 | 52035057 | |||||
chr13:52035067
|
AAG | A | 2 | a0001c0001t0012a0001c0001t0043 | 5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1879_*1880delCT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1879 | chr13 | 52035067 | |||||
chr13:52035072
|
T | C | 4 | a0001c0001t0003a0001c0001t0029a0001c0001t0055others(1): Show | 26 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1876A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1876 | chr13 | 52035072 | |||||
chr13:52035142
|
T | C | 2 | a0003c0005t0027a0003c0005t0054 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1806A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1806 | chr13 | 52035142 | |||||
chr13:52035240
|
A | C | 1 | a0001c0001t0031 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1708T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1708 | chr13 | 52035240 | |||||
chr13:52035247
|
AAT | A | 1 | a0001c0001t0006 | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1699_*1700delAT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1699 | chr13 | 52035247 | |||||
chr13:52035268
|
G | A | 1 | a0001c0004t0019 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1680C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1680 | chr13 | 52035268 | |||||
chr13:52035304
|
A | T | 1 | a0001c0001t0055 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1644T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1644 | chr13 | 52035304 | |||||
chr13:52035431
|
C | A | 2 | a0001c0001t0018a0001c0001t0044 | 4 | HG03017.hp1 HG03490.hp1 HG03654.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1517G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1517 | chr13 | 52035431 | |||||
chr13:52035540
|
T | C | 1 | a0001c0001t0045 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1408A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1408 | chr13 | 52035540 | |||||
chr13:52035579
|
T | A | 1 | a0001c0001t0060 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1369A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1369 | chr13 | 52035579 | |||||
chr13:52035779
|
T | C | 21 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(18): Show | 119 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1169A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1169 | chr13 | 52035779 | |||||
chr13:52036047
|
C | CA | 2 | a0001c0001t0016a0001c0001t0061 | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*900dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 900 | chr13 | 52036047 | |||||
chr13:52036656
|
C | T | 1 | a0001c0001t0047 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*292G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 292 | chr13 | 52036656 | |||||
chr13:52036787
|
T | C | 1 | a0001c0001t0062 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*161A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 161 | chr13 | 52036787 | |||||
chr13:52036792
|
A | G | 1 | a0001c0001t0030 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*156T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 156 | chr13 | 52036792 | |||||
chr13:52127501
|
T | G | 38 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(35): Show | 174 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
5_prime_UTR_variant | MODIFIER | c.-19A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/24 | 19 | chr13 | 52127501 | |||||
chr13:52127646
|
T | C | 38 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(35): Show | 174 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
5_prime_UTR_variant | MODIFIER | c.-74A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 2/24 | 164 | chr13 | 52127646 | |||||
chr13:52127647
|
T | C | 1 | a0001c0001t0022 | 3 | HG02451.hp1 HG03225.hp2 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-75A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 2/24 | 165 | chr13 | 52127647 | |||||
chr13:52129061
|
G | T | 1 | a0001c0001t0023 | 2 | HG02615.hp2 HG02622.hp2 |
5_prime_UTR_variant | MODIFIER | c.-123C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/24 | 1579 | chr13 | 52129061 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:52037550
|
C | G | 4 | a0003c0005t0027g0321a0003c0005t0027g0322a0003c0005t0054g0323others(1): Show | 4 | HG01192.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2229-332G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52037550 | ||||||
chr13:52037671
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0008g0031 | 2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2229-453G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52037671 | ||||||
chr13:52037694
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2229-476G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52037694 | ||||||
chr13:52037705
|
C | T | 1 | a0001c0001t0002g0245 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2229-487G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52037705 | ||||||
chr13:52037816
|
G | A | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2229-598C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52037816 | ||||||
chr13:52037922
|
C | CA | 18 | a0001c0001t0002g0005a0001c0001t0002g0196a0001c0001t0002g0256others(15): Show | 20 | HG01106.hp2 HG01109.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.2229-705dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52037922 | ||||||
chr13:52037922
|
C | CAA | 104 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0172others(101): Show | 109 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.2229-706_2229-705d others(4): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52037922 | ||||||
chr13:52038054
|
A | G | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2229-836T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038054 | ||||||
chr13:52038170
|
C | CAAAAAAT others(1): Show |
36 | a0001c0001t0004g0271a0001c0001t0026g0316a0001c0001t0026g0318others(33): Show | 36 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.2229-960_2229-953d others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038170 | ||||||
chr13:52038488
|
G | T | 1 | a0010c0015t0001g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2229-1270C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038488 | ||||||
chr13:52038531
|
T | C | 1 | a0001c0001t0015g0229 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2229-1313A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038531 | ||||||
chr13:52038592
|
C | T | 1 | a0001c0001t0037g0127 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2229-1374G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038592 | ||||||
chr13:52038823
|
C | T | 36 | a0001c0001t0004g0271a0001c0001t0026g0316a0001c0001t0026g0318others(33): Show | 36 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.2229-1605G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038823 | ||||||
chr13:52038824
|
T | TA | 3 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317 | 3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2229-1607_2229-160 others(5): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038824 | ||||||
chr13:52038825
|
G | A | 36 | a0001c0001t0004g0271a0001c0001t0026g0316a0001c0001t0026g0318others(33): Show | 36 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.2229-1607C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038825 | ||||||
chr13:52038825
|
G | GA | 35 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0087others(32): Show | 36 | HG00544.hp2 HG00609.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.2229-1608dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038825 | ||||||
chr13:52038825
|
G | GAAA | 7 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0174others(4): Show | 7 | HG00544.hp1 HG01099.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2229-1610_2229-160 others(7): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038825 | ||||||
chr13:52038825
|
G | GAAAA | 95 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0172others(92): Show | 100 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.2229-1611_2229-160 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038825 | ||||||
chr13:52038825
|
G | GAAAAA | 18 | a0001c0001t0002g0005a0001c0001t0002g0196a0001c0001t0002g0216others(15): Show | 19 | HG01106.hp2 HG01358.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2229-1612_2229-160 others(9): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038825 | ||||||
chr13:52038826
|
A | G | 2 | a0001c0001t0001g0078a0001c0001t0008g0095 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2229-1608T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038826 | ||||||
chr13:52038839
|
A | C | 33 | a0001c0001t0004g0271a0002c0002t0004g0176a0002c0002t0004g0177others(30): Show | 33 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.2229-1621T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038839 | ||||||
chr13:52039079
|
C | G | 1 | a0001c0001t0001g0157 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2229-1861G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52039079 | ||||||
chr13:52039138
|
G | A | 159 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(156): Show | 165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.2229-1920C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52039138 | ||||||
chr13:52039201
|
G | A | 33 | a0001c0001t0004g0271a0002c0002t0004g0176a0002c0002t0004g0177others(30): Show | 33 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.2229-1983C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52039201 | ||||||
chr13:52039516
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2229-2298A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52039516 | ||||||
chr13:52039823
|
T | TATAATTT others(12): Show |
1 | a0001c0001t0001g0149 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2229-2606_2229-260 others(23): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52039823 | ||||||
chr13:52039879
|
C | T | 2 | a0001c0001t0031g0053a0010c0015t0001g0055 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2229-2661G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52039879 | ||||||
chr13:52039982
|
G | A | 5 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2229-2764C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52039982 | ||||||
chr13:52039996
|
T | A | 1 | a0001c0001t0002g0221 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2229-2778A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52039996 | ||||||
chr13:52040081
|
C | CT | 12 | a0001c0001t0001g0047a0001c0001t0001g0128a0001c0001t0001g0165others(9): Show | 12 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2229-2864dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52040081 | ||||||
chr13:52040081
|
CT | C | 27 | a0001c0001t0001g0042a0001c0001t0001g0050a0001c0001t0001g0080others(24): Show | 28 | HG01069.hp1 HG01081.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.2229-2864delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52040081 | ||||||
chr13:52040081
|
CTT | C | 116 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(113): Show | 122 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.2229-2865_2229-286 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52040081 | ||||||
chr13:52040081
|
CTTT | C | 9 | a0001c0001t0002g0210a0001c0001t0002g0239a0001c0001t0015g0229others(6): Show | 9 | HG00642.hp2 HG01167.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2229-2866_2229-286 others(7): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52040081 | ||||||
chr13:52040081
|
CTTTT | C | 31 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(28): Show | 31 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.2229-2867_2229-286 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52040081 | ||||||
chr13:52040532
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2229-3314A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52040532 | ||||||
chr13:52040662
|
A | G | 114 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(111): Show | 120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2229-3444T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52040662 | ||||||
chr13:52040815
|
G | A | 114 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(111): Show | 120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2229-3597C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52040815 | ||||||
chr13:52041076
|
C | A | 321 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(318): Show | 332 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.2229-3858G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041076 | ||||||
chr13:52041080
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2229-3862T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041080 | ||||||
chr13:52041438
|
A | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0048 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2229-4220T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041438 | ||||||
chr13:52041726
|
C | A | 1 | a0001c0001t0011g0206 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2229-4508G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041726 | ||||||
chr13:52041728
|
C | CA | 55 | a0001c0001t0001g0079a0001c0001t0001g0091a0001c0001t0001g0096others(52): Show | 56 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.2229-4511dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041728 | ||||||
chr13:52041728
|
C | CAA | 14 | a0001c0001t0001g0111a0001c0001t0002g0204a0001c0001t0002g0222others(11): Show | 14 | HG01192.hp2 HG01243.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.2229-4512_2229-451 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041728 | ||||||
chr13:52041728
|
C | CAAA | 91 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(88): Show | 97 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.2229-4513_2229-451 others(7): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041728 | ||||||
chr13:52041728
|
C | CAAAA | 20 | a0001c0001t0002g0216a0001c0001t0002g0223a0001c0001t0002g0227others(17): Show | 20 | HG00099.hp1 HG01261.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.2229-4514_2229-451 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041728 | ||||||
chr13:52041728
|
C | CAAAAAAA others(3): Show |
3 | a0001c0004t0019g0300a0001c0004t0019g0301a0001c0010t0048g0291 | 3 | HG02896.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2229-4520_2229-451 others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041728 | ||||||
chr13:52041728
|
C | CAAAAAAA others(4): Show |
1 | a0001c0004t0019g0299 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2229-4521_2229-451 others(15): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041728 | ||||||
chr13:52041728
|
CA | C | 12 | a0001c0001t0001g0108a0001c0001t0001g0116a0001c0001t0001g0128others(9): Show | 12 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2229-4511delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041728 | ||||||
chr13:52041728
|
CAA | C | 9 | a0001c0001t0001g0156a0001c0001t0061g0302a0001c0003t0010g0019others(6): Show | 9 | HG00544.hp1 HG02486.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2229-4512_2229-451 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041728 | ||||||
chr13:52041771
|
AAAG | A | 5 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2229-4556_2229-455 others(7): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041771 | ||||||
chr13:52041825
|
A | C | 1 | a0001c0001t0006g0027 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2229-4607T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041825 | ||||||
chr13:52041830
|
A | C | 1 | a0001c0001t0001g0167 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2229-4612T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041830 | ||||||
chr13:52041854
|
T | C | 1 | a0001c0001t0038g0118 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2229-4636A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041854 | ||||||
chr13:52041975
|
A | T | 1 | a0001c0001t0003g0218 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2229-4757T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041975 | ||||||
chr13:52041999
|
T | C | 1 | a0007c0008t0009g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2229-4781A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041999 | ||||||
chr13:52042098
|
T | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2229-4880A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042098 | ||||||
chr13:52042292
|
C | T | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2229-5074G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042292 | ||||||
chr13:52042349
|
G | A | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2229-5131C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042349 | ||||||
chr13:52042373
|
T | C | 2 | a0001c0001t0002g0292a0001c0001t0002g0293 | 2 | HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.2229-5155A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042373 | ||||||
chr13:52042440
|
A | G | 1 | a0001c0001t0002g0207 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2229-5222T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042440 | ||||||
chr13:52042470
|
CA | C | 114 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(111): Show | 120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2229-5253delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042470 | ||||||
chr13:52042566
|
T | C | 1 | a0001c0001t0034g0135 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2229-5348A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042566 | ||||||
chr13:52042835
|
G | A | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2229-5617C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042835 | ||||||
chr13:52042921
|
A | C | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2229-5703T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042921 | ||||||
chr13:52043071
|
G | T | 30 | a0002c0002t0004g0176a0002c0002t0004g0177a0002c0002t0004g0178others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.2229-5853C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52043071 | ||||||
chr13:52043261
|
G | A | 3 | a0001c0001t0012g0035a0001c0001t0015g0201a0001c0001t0043g0034 | 3 | HG02615.hp1 HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2229-6043C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52043261 | ||||||
chr13:52043536
|
C | CA | 14 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0002g0256others(11): Show | 14 | HG00544.hp1 HG01099.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2229-6319dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52043536 | ||||||
chr13:52043546
|
AAAAAAGA others(3): Show |
A | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2229-6338_2229-632 others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52043546 | ||||||
chr13:52043548
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2229-6330T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52043548 | ||||||
chr13:52043563
|
A | G | 3 | a0001c0001t0001g0079a0001c0001t0001g0170a0001c0001t0017g0103 | 3 | HG02735.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2229-6345T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52043563 | ||||||
chr13:52043573
|
GA | G | 7 | a0001c0001t0002g0007a0001c0001t0002g0234a0001c0001t0002g0237others(4): Show | 8 | HG02071.hp2 NA18942.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.2229-6356delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52043573 | ||||||
chr13:52043925
|
T | C | 2 | a0001c0003t0010g0174a0001c0003t0010g0175 | 2 | HG06807.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2228+6179A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52043925 | ||||||
chr13:52044054
|
G | A | 35 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.2228+6050C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52044054 | ||||||
chr13:52044075
|
G | A | 166 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(163): Show | 173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.2228+6029C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52044075 | ||||||
chr13:52044274
|
C | A | 4 | a0001c0001t0002g0008a0001c0001t0002g0254a0001c0001t0007g0241others(1): Show | 5 | NA18969.hp1 NA18983.hp1 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.2228+5830G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52044274 | ||||||
chr13:52044366
|
C | T | 2 | a0001c0001t0002g0243a0001c0001t0002g0288 | 2 | HG02083.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.2228+5738G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52044366 | ||||||
chr13:52044440
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2228+5664A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52044440 | ||||||
chr13:52044490
|
G | A | 1 | a0001c0001t0035g0125 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2228+5614C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52044490 | ||||||
chr13:52044661
|
T | C | 123 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(120): Show | 129 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.2228+5443A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52044661 | ||||||
chr13:52044742
|
C | A | 185 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(182): Show | 192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.2228+5362G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52044742 | ||||||
chr13:52045105
|
A | G | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2228+4999T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045105 | ||||||
chr13:52045130
|
C | CT | 160 | a0001c0001t0001g0089a0001c0001t0001g0165a0001c0001t0002g0005others(157): Show | 166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.2228+4973dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045130 | ||||||
chr13:52045130
|
C | CTT | 14 | a0001c0001t0002g0216a0001c0001t0002g0238a0001c0001t0002g0245others(11): Show | 15 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.2228+4972_2228+497 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045130 | ||||||
chr13:52045200
|
G | GCTCACTG others(15): Show |
2 | a0001c0001t0008g0062a0001c0001t0008g0063 | 2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.2228+4882_2228+490 others(26): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045200 | ||||||
chr13:52045291
|
G | A | 2 | a0001c0001t0023g0011a0001c0001t0023g0012 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2228+4813C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045291 | ||||||
chr13:52045332
|
G | T | 8 | a0001c0001t0002g0005a0001c0001t0002g0196a0001c0001t0002g0256others(5): Show | 9 | HG01106.hp2 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2228+4772C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045332 | ||||||
chr13:52045407
|
G | A | 2 | a0001c0001t0012g0038a0001c0001t0012g0039 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.2228+4697C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045407 | ||||||
chr13:52045468
|
A | G | 8 | a0001c0001t0002g0005a0001c0001t0002g0196a0001c0001t0002g0256others(5): Show | 9 | HG01106.hp2 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2228+4636T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045468 | ||||||
chr13:52045500
|
G | T | 1 | a0002c0002t0004g0178 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2228+4604C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045500 | ||||||
chr13:52045581
|
A | C | 166 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(163): Show | 173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.2228+4523T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045581 | ||||||
chr13:52045634
|
C | G | 1 | a0001c0001t0001g0101 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2228+4470G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045634 | ||||||
chr13:52045657
|
C | T | 3 | a0003c0005t0027g0321a0003c0005t0027g0322a0003c0005t0054g0323 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2228+4447G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045657 | ||||||
chr13:52045714
|
A | G | 176 | a0001c0001t0001g0050a0001c0001t0002g0005a0001c0001t0002g0007others(173): Show | 183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.2228+4390T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045714 | ||||||
chr13:52045764
|
C | CA | 12 | a0001c0001t0001g0099a0001c0001t0001g0113a0001c0001t0001g0165others(9): Show | 12 | HG01943.hp1 HG02258.hp1 HG03130.hp1 others(9): Show |
intron_variant | MODIFIER | c.2228+4339dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045764 | ||||||
chr13:52045764
|
CA | C | 113 | a0001c0001t0001g0052a0001c0001t0001g0097a0001c0001t0001g0155others(110): Show | 119 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.2228+4339delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045764 | ||||||
chr13:52045873
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+4231G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045873 | ||||||
chr13:52045933
|
C | T | 174 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(171): Show | 181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.2228+4171G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045933 | ||||||
chr13:52046047
|
GGCAACAG others(1): Show |
G | 5 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2228+4049_2228+405 others(12): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046047 | ||||||
chr13:52046070
|
C | CA | 9 | a0001c0001t0001g0050a0001c0001t0002g0222a0001c0001t0002g0235others(6): Show | 9 | HG00673.hp1 HG01123.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.2228+4033dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046070 | ||||||
chr13:52046295
|
G | A | 3 | a0001c0010t0048g0291a0002c0002t0004g0191a0002c0002t0049g0190 | 3 | HG00621.hp1 HG02132.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2228+3809C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046295 | ||||||
chr13:52046297
|
C | A | 1 | a0006c0011t0042g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2228+3807G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046297 | ||||||
chr13:52046340
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0008g0043 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2228+3764C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046340 | ||||||
chr13:52046349
|
T | C | 6 | a0001c0001t0002g0008a0001c0001t0002g0227a0001c0001t0002g0254others(3): Show | 7 | NA18969.hp1 NA18973.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.2228+3755A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046349 | ||||||
chr13:52046351
|
C | T | 1 | a0001c0001t0007g0244 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2228+3753G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046351 | ||||||
chr13:52046481
|
T | TA | 37 | a0001c0001t0001g0159a0001c0001t0026g0316a0001c0001t0026g0318others(34): Show | 37 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.2228+3622dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046481 | ||||||
chr13:52046481
|
T | TAAAAAAA others(298): Show |
1 | a0001c0001t0031g0053 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2228+3622_2228+362 others(309): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046481 | ||||||
chr13:52046481
|
T | TAAAAAAA others(300): Show |
1 | a0010c0015t0001g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2228+3622_2228+362 others(311): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046481 | ||||||
chr13:52046481
|
TA | T | 10 | a0001c0001t0001g0115a0001c0001t0001g0136a0001c0001t0001g0139others(7): Show | 10 | HG01168.hp2 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.2228+3622delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046481 | ||||||
chr13:52046526
|
C | T | 1 | a0001c0001t0058g0285 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2228+3578G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046526 | ||||||
chr13:52046616
|
G | A | 159 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(156): Show | 165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.2228+3488C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046616 | ||||||
chr13:52046622
|
T | G | 1 | a0001c0001t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+3482A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046622 | ||||||
chr13:52046712
|
T | C | 1 | a0001c0003t0010g0019 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2228+3392A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046712 | ||||||
chr13:52046731
|
A | C | 3 | a0001c0001t0001g0115a0001c0001t0001g0134a0001c0001t0001g0164 | 3 | NA18948.hp1 NA18956.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.2228+3373T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046731 | ||||||
chr13:52047111
|
A | C | 1 | a0001c0001t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+2993T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047111 | ||||||
chr13:52047113
|
G | GACAACAC others(14): Show |
1 | a0001c0001t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+2990_2228+299 others(25): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047113 | ||||||
chr13:52047115
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+2989C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047115 | ||||||
chr13:52047117
|
A | C | 1 | a0001c0001t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+2987T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047117 | ||||||
chr13:52047120
|
T | G | 1 | a0001c0001t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+2984A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047120 | ||||||
chr13:52047124
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+2980G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047124 | ||||||
chr13:52047127
|
T | A | 1 | a0001c0001t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+2977A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047127 | ||||||
chr13:52047208
|
G | A | 1 | a0002c0002t0004g0188 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2228+2896C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047208 | ||||||
chr13:52047296
|
A | T | 1 | a0001c0001t0001g0161 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2228+2808T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047296 | ||||||
chr13:52047697
|
C | A | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+2407G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047697 | ||||||
chr13:52047744
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2228+2360A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047744 | ||||||
chr13:52047995
|
G | A | 35 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.2228+2109C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047995 | ||||||
chr13:52048090
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2228+2014C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048090 | ||||||
chr13:52048290
|
A | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1814T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048290 | ||||||
chr13:52048303
|
G | A | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1801C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048303 | ||||||
chr13:52048304
|
G | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1800C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048304 | ||||||
chr13:52048306
|
T | A | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1798A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048306 | ||||||
chr13:52048317
|
A | G | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1787T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048317 | ||||||
chr13:52048318
|
T | A | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1786A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048318 | ||||||
chr13:52048319
|
C | A | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1785G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048319 | ||||||
chr13:52048320
|
C | G | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1784G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048320 | ||||||
chr13:52048378
|
C | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1726G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048378 | ||||||
chr13:52048379
|
C | A | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1725G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048379 | ||||||
chr13:52048387
|
C | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1717G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048387 | ||||||
chr13:52048414
|
A | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1690T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048414 | ||||||
chr13:52048415
|
A | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1689T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048415 | ||||||
chr13:52048418
|
A | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1686T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048418 | ||||||
chr13:52048419
|
A | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1685T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048419 | ||||||
chr13:52048420
|
T | A | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1684A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048420 | ||||||
chr13:52048424
|
A | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1680T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048424 | ||||||
chr13:52048428
|
A | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1676T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048428 | ||||||
chr13:52048489
|
T | C | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2228+1615A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048489 | ||||||
chr13:52048640
|
G | A | 1 | a0001c0001t0012g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2228+1464C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048640 | ||||||
chr13:52048779
|
C | A | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2228+1325G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048779 | ||||||
chr13:52048945
|
A | ATTGTATA others(6): Show |
1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1158_2228+115 others(17): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048945 | ||||||
chr13:52048967
|
A | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1137T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048967 | ||||||
chr13:52048969
|
A | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1135T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048969 | ||||||
chr13:52048996
|
A | C | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1108T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048996 | ||||||
chr13:52048998
|
A | G | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1106T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048998 | ||||||
chr13:52049000
|
A | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1104T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049000 | ||||||
chr13:52049008
|
C | A | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1096G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049008 | ||||||
chr13:52049015
|
C | G | 184 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(181): Show | 191 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.2228+1089G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049015 | ||||||
chr13:52049155
|
G | C | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+949C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049155 | ||||||
chr13:52049156
|
C | G | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+948G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049156 | ||||||
chr13:52049200
|
A | G | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+904T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049200 | ||||||
chr13:52049267
|
A | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+837T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049267 | ||||||
chr13:52049348
|
C | A | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+756G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049348 | ||||||
chr13:52049349
|
A | G | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+755T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049349 | ||||||
chr13:52049350
|
G | A | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+754C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049350 | ||||||
chr13:52049352
|
A | G | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+752T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049352 | ||||||
chr13:52049385
|
C | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+719G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049385 | ||||||
chr13:52049414
|
G | A | 2 | a0001c0001t0002g0215a0001c0001t0004g0271 | 2 | HG00639.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2228+690C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049414 | ||||||
chr13:52049533
|
C | T | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2228+571G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049533 | ||||||
chr13:52049550
|
A | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+554T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049550 | ||||||
chr13:52049562
|
A | T | 1 | a0001c0001t0056g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+542T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049562 | ||||||
chr13:52050364
|
T | C | 2 | a0001c0001t0036g0032a0001c0001t0037g0127 | 2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2111-143A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52050364 | ||||||
chr13:52050611
|
C | CT | 161 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0162others(158): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.2111-391dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52050611 | ||||||
chr13:52050611
|
C | CTT | 6 | a0001c0001t0002g0200a0001c0001t0012g0035a0001c0001t0020g0230others(3): Show | 6 | HG00642.hp1 HG02280.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2111-392_2111-391d others(4): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52050611 | ||||||
chr13:52050720
|
C | CT | 16 | a0001c0001t0001g0161a0001c0001t0002g0266a0001c0001t0011g0242others(13): Show | 16 | HG00544.hp1 HG01099.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.2111-500dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52050720 | ||||||
chr13:52050720
|
CT | C | 11 | a0001c0001t0001g0040a0001c0001t0001g0082a0001c0001t0001g0155others(8): Show | 11 | HG01074.hp2 HG01243.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2111-500delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52050720 | ||||||
chr13:52050729
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2111-508A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52050729 | ||||||
chr13:52050865
|
A | G | 1 | a0001c0001t0003g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2111-644T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52050865 | ||||||
chr13:52050970
|
G | A | 1 | a0001c0001t0006g0028 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2111-749C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52050970 | ||||||
chr13:52051021
|
G | C | 3 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317 | 3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2111-800C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051021 | ||||||
chr13:52051059
|
G | A | 160 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(157): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.2111-838C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051059 | ||||||
chr13:52051062
|
CT | C | 150 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(147): Show | 156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.2111-842delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051062 | ||||||
chr13:52051105
|
A | G | 2 | a0001c0001t0002g0215a0001c0001t0004g0271 | 2 | HG00639.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2111-884T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051105 | ||||||
chr13:52051131
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2111-910C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051131 | ||||||
chr13:52051227
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2111-1006A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051227 | ||||||
chr13:52051264
|
A | T | 1 | a0001c0001t0011g0206 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2111-1043T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051264 | ||||||
chr13:52051335
|
C | T | 201 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0045others(198): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2111-1114G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051335 | ||||||
chr13:52051508
|
G | A | 5 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2111-1287C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051508 | ||||||
chr13:52051684
|
C | T | 3 | a0001c0001t0021g0224a0001c0001t0021g0232a0001c0001t0021g0286 | 3 | HG00323.hp2 HG02602.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2111-1463G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051684 | ||||||
chr13:52052045
|
C | A | 160 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(157): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.2111-1824G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52052045 | ||||||
chr13:52052201
|
G | T | 29 | a0002c0002t0004g0176a0002c0002t0004g0177a0002c0002t0004g0178others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.2111-1980C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52052201 | ||||||
chr13:52052209
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2111-1988A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52052209 | ||||||
chr13:52052400
|
C | A | 1 | a0001c0001t0001g0144 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2111-2179G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52052400 | ||||||
chr13:52052507
|
C | T | 186 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(183): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.2111-2286G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52052507 | ||||||
chr13:52052811
|
C | A | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2111-2590G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52052811 | ||||||
chr13:52052820
|
T | G | 2 | a0001c0001t0001g0050a0001c0001t0030g0044 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2111-2599A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52052820 | ||||||
chr13:52053039
|
A | G | 175 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(172): Show | 182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.2111-2818T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52053039 | ||||||
chr13:52053099
|
A | G | 160 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(157): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.2111-2878T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52053099 | ||||||
chr13:52053173
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2111-2952G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52053173 | ||||||
chr13:52053260
|
C | T | 4 | a0003c0005t0027g0321a0003c0005t0027g0322a0003c0005t0054g0323others(1): Show | 4 | HG01192.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2111-3039G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52053260 | ||||||
chr13:52053582
|
C | CT | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2111-3362dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52053582 | ||||||
chr13:52053616
|
C | A | 1 | a0001c0001t0002g0269 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2111-3395G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52053616 | ||||||
chr13:52053686
|
C | T | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2111-3465G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52053686 | ||||||
chr13:52053938
|
T | C | 175 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(172): Show | 182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.2111-3717A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52053938 | ||||||
chr13:52054292
|
G | A | 11 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 11 | HG01069.hp2 HG01255.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.2111-4071C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054292 | ||||||
chr13:52054369
|
G | A | 1 | a0001c0001t0020g0309 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2111-4148C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054369 | ||||||
chr13:52054455
|
G | T | 1 | a0001c0004t0019g0301 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2111-4234C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054455 | ||||||
chr13:52054516
|
A | G | 150 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(147): Show | 156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.2111-4295T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054516 | ||||||
chr13:52054587
|
C | T | 6 | a0001c0001t0001g0167a0001c0001t0012g0035a0001c0001t0012g0036others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2111-4366G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054587 | ||||||
chr13:52054608
|
A | G | 1 | a0001c0001t0002g0284 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2111-4387T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054608 | ||||||
chr13:52054613
|
G | C | 1 | a0001c0001t0001g0169 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2111-4392C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054613 | ||||||
chr13:52054669
|
G | A | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2111-4448C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054669 | ||||||
chr13:52054679
|
G | A | 1 | a0006c0011t0042g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2111-4458C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054679 | ||||||
chr13:52054682
|
G | C | 1 | a0006c0011t0042g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2111-4461C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054682 | ||||||
chr13:52054688
|
G | C | 2 | a0001c0001t0003g0010a0001c0001t0017g0315 | 3 | HG03491.hp2 HG03492.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.2111-4467C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054688 | ||||||
chr13:52054707
|
C | A | 1 | a0001c0001t0003g0010 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2111-4486G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054707 | ||||||
chr13:52054713
|
C | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.2111-4492G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054713 | ||||||
chr13:52054791
|
C | T | 3 | a0001c0001t0002g0222a0001c0001t0002g0228a0001c0001t0002g0236 | 3 | HG01192.hp2 HG01433.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.2111-4570G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054791 | ||||||
chr13:52054868
|
T | G | 1 | a0001c0001t0002g0215 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2111-4647A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054868 | ||||||
chr13:52054878
|
A | G | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.2111-4657T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054878 | ||||||
chr13:52054890
|
A | G | 1 | a0001c0001t0007g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2111-4669T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054890 | ||||||
chr13:52054911
|
C | T | 1 | a0008c0014t0004g0298 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2111-4690G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054911 | ||||||
chr13:52054946
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0130a0001c0001t0009g0051 | 3 | HG02109.hp1 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2111-4725C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054946 | ||||||
chr13:52054962
|
A | G | 3 | a0001c0001t0015g0198a0001c0001t0020g0278a0001c0001t0056g0283 | 3 | HG02074.hp1 NA19065.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.2111-4741T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054962 | ||||||
chr13:52054987
|
G | A | 30 | a0002c0002t0004g0176a0002c0002t0004g0177a0002c0002t0004g0178others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.2111-4766C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054987 | ||||||
chr13:52055142
|
C | T | 1 | a0001c0001t0003g0289 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2111-4921G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055142 | ||||||
chr13:52055170
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2111-4949C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055170 | ||||||
chr13:52055188
|
G | A | 1 | a0001c0001t0012g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2111-4967C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055188 | ||||||
chr13:52055287
|
T | C | 1 | a0001c0001t0061g0302 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2111-5066A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055287 | ||||||
chr13:52055292
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0030g0044 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2111-5071C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055292 | ||||||
chr13:52055319
|
C | A | 5 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2111-5098G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055319 | ||||||
chr13:52055344
|
G | T | 1 | a0001c0001t0001g0150 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2111-5123C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055344 | ||||||
chr13:52055419
|
C | A | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2111-5198G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055419 | ||||||
chr13:52055468
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2111-5247C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055468 | ||||||
chr13:52055508
|
A | G | 4 | a0001c0003t0013g0018a0001c0003t0013g0021a0001c0003t0013g0022others(1): Show | 4 | HG00544.hp1 NA18994.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2111-5287T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055508 | ||||||
chr13:52055593
|
T | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0160a0001c0001t0001g0161others(3): Show | 6 | HG02258.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2111-5372A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055593 | ||||||
chr13:52055634
|
G | GGCCAATA others(3178): Show |
2 | a0001c0001t0001g0040a0009c0007t0001g0054 | 2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2111-5414_2111-541 others(3189): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055634 | ||||||
chr13:52055821
|
C | T | 41 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0172others(38): Show | 43 | HG00597.hp1 HG00621.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.2111-5600G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055821 | ||||||
chr13:52055832
|
A | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0091a0001c0001t0001g0092others(16): Show | 21 | HG00408.hp1 HG00597.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.2111-5611T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055832 | ||||||
chr13:52055865
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2111-5644C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055865 | ||||||
chr13:52056068
|
A | G | 2 | a0001c0001t0001g0040a0009c0007t0001g0054 | 2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2110+5751T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056068 | ||||||
chr13:52056123
|
A | G | 2 | a0001c0001t0003g0260a0001c0001t0029g0259 | 2 | NA18956.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2110+5696T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056123 | ||||||
chr13:52056291
|
A | G | 4 | a0001c0001t0016g0303a0001c0001t0016g0305a0001c0001t0016g0306others(1): Show | 4 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2110+5528T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056291 | ||||||
chr13:52056330
|
T | A | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2110+5489A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056330 | ||||||
chr13:52056378
|
G | A | 1 | a0001c0001t0012g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2110+5441C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056378 | ||||||
chr13:52056388
|
C | T | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2110+5431G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056388 | ||||||
chr13:52056389
|
G | A | 3 | a0003c0005t0027g0321a0003c0005t0027g0322a0003c0005t0054g0323 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2110+5430C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056389 | ||||||
chr13:52056399
|
A | G | 2 | a0002c0002t0050g0320a0002c0002t0051g0319 | 2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2110+5420T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056399 | ||||||
chr13:52056560
|
C | A | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2110+5259G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056560 | ||||||
chr13:52056652
|
A | G | 2 | a0003c0005t0027g0321a0003c0005t0027g0322 | 2 | HG01192.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2110+5167T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056652 | ||||||
chr13:52056655
|
G | A | 162 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(159): Show | 168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2110+5164C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056655 | ||||||
chr13:52056668
|
G | A | 1 | a0001c0001t0007g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2110+5151C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056668 | ||||||
chr13:52056677
|
C | A | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2110+5142G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056677 | ||||||
chr13:52056698
|
G | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0104a0001c0001t0001g0106others(2): Show | 7 | HG00408.hp1 HG01192.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2110+5121C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056698 | ||||||
chr13:52056744
|
C | A | 175 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(172): Show | 182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.2110+5075G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056744 | ||||||
chr13:52056783
|
G | A | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2110+5036C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056783 | ||||||
chr13:52056786
|
G | A | 4 | a0001c0001t0011g0242a0003c0005t0027g0321a0003c0005t0027g0322others(1): Show | 4 | HG01192.hp1 HG01952.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2110+5033C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056786 | ||||||
chr13:52056876
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2110+4943A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056876 | ||||||
chr13:52056928
|
C | G | 1 | a0006c0011t0042g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2110+4891G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056928 | ||||||
chr13:52056928
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2110+4891G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056928 | ||||||
chr13:52056929
|
G | A | 2 | a0001c0001t0003g0258a0001c0001t0003g0289 | 2 | HG01981.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2110+4890C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056929 | ||||||
chr13:52057125
|
A | G | 157 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(154): Show | 163 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.2110+4694T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52057125 | ||||||
chr13:52057284
|
T | G | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2110+4535A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52057284 | ||||||
chr13:52057352
|
C | T | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2110+4467G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52057352 | ||||||
chr13:52057446
|
T | G | 2 | a0001c0001t0001g0030a0001c0001t0008g0031 | 2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2110+4373A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52057446 | ||||||
chr13:52057463
|
C | T | 32 | a0002c0002t0004g0176a0002c0002t0004g0177a0002c0002t0004g0178others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.2110+4356G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52057463 | ||||||
chr13:52057783
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2110+4036C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52057783 | ||||||
chr13:52057980
|
A | G | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2110+3839T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52057980 | ||||||
chr13:52058023
|
C | T | 1 | a0001c0001t0043g0034 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2110+3796G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058023 | ||||||
chr13:52058110
|
G | C | 1 | a0001c0001t0002g0265 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2110+3709C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058110 | ||||||
chr13:52058149
|
A | C | 3 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317 | 3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2110+3670T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058149 | ||||||
chr13:52058202
|
A | T | 1 | a0001c0001t0031g0053 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2110+3617T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058202 | ||||||
chr13:52058257
|
A | G | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2110+3562T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058257 | ||||||
chr13:52058329
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2110+3490A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058329 | ||||||
chr13:52058331
|
T | C | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.2110+3488A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058331 | ||||||
chr13:52058484
|
T | C | 1 | a0007c0008t0009g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2110+3335A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058484 | ||||||
chr13:52058591
|
C | G | 1 | a0001c0003t0013g0023 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2110+3228G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058591 | ||||||
chr13:52058659
|
A | G | 3 | a0003c0005t0027g0321a0003c0005t0027g0322a0003c0005t0054g0323 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2110+3160T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058659 | ||||||
chr13:52058720
|
T | C | 1 | a0001c0001t0002g0216 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2110+3099A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058720 | ||||||
chr13:52058768
|
G | A | 1 | a0001c0003t0010g0020 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2110+3051C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058768 | ||||||
chr13:52058782
|
T | C | 2 | a0001c0001t0001g0080a0001c0001t0001g0163 | 2 | HG02155.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2110+3037A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058782 | ||||||
chr13:52058825
|
C | T | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2110+2994G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058825 | ||||||
chr13:52058829
|
A | G | 1 | a0002c0002t0005g0064 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2110+2990T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058829 | ||||||
chr13:52058873
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2110+2946G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058873 | ||||||
chr13:52058933
|
A | G | 160 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(157): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.2110+2886T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058933 | ||||||
chr13:52059161
|
C | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.2110+2658G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059161 | ||||||
chr13:52059162
|
T | G | 1 | a0001c0001t0038g0118 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2110+2657A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059162 | ||||||
chr13:52059248
|
A | T | 1 | a0001c0001t0002g0220 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2110+2571T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059248 | ||||||
chr13:52059496
|
G | C | 322 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(319): Show | 333 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.2110+2323C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059496 | ||||||
chr13:52059809
|
T | TG | 15 | a0001c0001t0001g0046a0001c0001t0001g0123a0001c0001t0001g0136others(12): Show | 15 | HG00438.hp1 HG00621.hp2 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.2110+2009dupC | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059809 | ||||||
chr13:52059822
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2110+1997C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059822 | ||||||
chr13:52059823
|
A | G | 1 | a0001c0001t0003g0289 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2110+1996T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059823 | ||||||
chr13:52059848
|
A | G | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2110+1971T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059848 | ||||||
chr13:52059883
|
A | T | 2 | a0003c0005t0027g0321a0003c0005t0027g0322 | 2 | HG01192.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2110+1936T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059883 | ||||||
chr13:52059942
|
C | T | 1 | a0001c0001t0009g0088 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2110+1877G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059942 | ||||||
chr13:52060004
|
T | C | 3 | a0002c0002t0005g0065a0002c0002t0005g0067a0002c0002t0033g0075 | 3 | HG00099.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2110+1815A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060004 | ||||||
chr13:52060102
|
G | T | 3 | a0001c0001t0001g0080a0001c0001t0001g0163a0001c0001t0017g0126 | 3 | HG02155.hp1 NA18979.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.2110+1717C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060102 | ||||||
chr13:52060158
|
A | T | 1 | a0001c0001t0002g0237 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2110+1661T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060158 | ||||||
chr13:52060363
|
G | T | 2 | a0001c0001t0002g0245a0001c0001t0060g0281 | 2 | NA18985.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.2110+1456C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060363 | ||||||
chr13:52060475
|
C | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.2110+1344G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060475 | ||||||
chr13:52060597
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2110+1222G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060597 | ||||||
chr13:52060668
|
C | T | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2110+1151G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060668 | ||||||
chr13:52060832
|
A | C | 167 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(164): Show | 174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.2110+987T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060832 | ||||||
chr13:52060870
|
T | C | 5 | a0001c0001t0006g0002a0001c0001t0006g0026a0001c0001t0006g0027others(2): Show | 6 | HG01109.hp1 HG01255.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.2110+949A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060870 | ||||||
chr13:52061180
|
C | T | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2110+639G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52061180 | ||||||
chr13:52061197
|
G | A | 3 | a0003c0005t0027g0321a0003c0005t0027g0322a0003c0005t0054g0323 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2110+622C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52061197 | ||||||
chr13:52061198
|
T | C | 4 | a0001c0001t0018g0013a0001c0001t0018g0014a0001c0001t0018g0015others(1): Show | 4 | HG03017.hp1 HG03490.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.2110+621A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52061198 | ||||||
chr13:52061429
|
G | T | 1 | a0001c0001t0006g0024 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2110+390C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52061429 | ||||||
chr13:52061547
|
G | A | 1 | a0001c0001t0009g0151 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2110+272C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52061547 | ||||||
chr13:52061712
|
C | T | 2 | a0001c0001t0001g0040a0009c0007t0001g0054 | 2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2110+107G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52061712 | ||||||
chr13:52062408
|
C | T | 1 | a0001c0001t0003g0010 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1976-455G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52062408 | ||||||
chr13:52062468
|
A | C | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1976-515T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52062468 | ||||||
chr13:52062506
|
C | T | 1 | a0001c0001t0002g0215 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1976-553G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52062506 | ||||||
chr13:52062545
|
C | G | 1 | a0001c0001t0011g0307 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1976-592G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52062545 | ||||||
chr13:52062652
|
C | T | 1 | a0001c0001t0040g0090 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1976-699G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52062652 | ||||||
chr13:52062978
|
T | C | 5 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1976-1025A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52062978 | ||||||
chr13:52062990
|
C | T | 1 | a0001c0001t0002g0245 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1976-1037G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52062990 | ||||||
chr13:52063044
|
C | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1976-1091G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063044 | ||||||
chr13:52063049
|
CCCCTCTC others(27): Show |
C | 1 | a0001c0004t0019g0300 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1976-1130_1976-109 others(38): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063049 | ||||||
chr13:52063108
|
T | C | 4 | a0001c0001t0002g0197a0001c0001t0002g0199a0001c0001t0002g0200others(1): Show | 4 | HG00642.hp1 HG02486.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1976-1155A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063108 | ||||||
chr13:52063209
|
A | T | 6 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0217others(3): Show | 8 | NA18944.hp1 NA18960.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.1976-1256T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063209 | ||||||
chr13:52063219
|
C | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1976-1266G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063219 | ||||||
chr13:52063280
|
G | A | 160 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(157): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1976-1327C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063280 | ||||||
chr13:52063306
|
C | A | 10 | a0001c0001t0004g0271a0001c0003t0010g0017a0001c0003t0010g0019others(7): Show | 10 | HG00544.hp1 HG00639.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.1976-1353G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063306 | ||||||
chr13:52063341
|
C | T | 1 | a0001c0001t0002g0207 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1976-1388G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063341 | ||||||
chr13:52063379
|
A | G | 3 | a0001c0001t0002g0233a0001c0001t0002g0266a0001c0001t0002g0274 | 3 | NA18974.hp1 NA18978.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1976-1426T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063379 | ||||||
chr13:52063397
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1976-1444A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063397 | ||||||
chr13:52063411
|
C | T | 3 | a0001c0001t0001g0097a0001c0001t0002g0196a0001c0001t0047g0195 | 3 | HG01074.hp1 HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1976-1458G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063411 | ||||||
chr13:52063497
|
C | T | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1976-1544G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063497 | ||||||
chr13:52063498
|
G | A | 2 | a0002c0002t0004g0191a0002c0002t0049g0190 | 2 | HG00621.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1976-1545C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063498 | ||||||
chr13:52063525
|
C | T | 2 | a0001c0001t0002g0245a0001c0001t0060g0281 | 2 | NA18985.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1976-1572G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063525 | ||||||
chr13:52063553
|
G | A | 1 | a0001c0001t0003g0219 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1976-1600C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063553 | ||||||
chr13:52063591
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1976-1638G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063591 | ||||||
chr13:52063602
|
A | C | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1976-1649T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063602 | ||||||
chr13:52063641
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1976-1688G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063641 | ||||||
chr13:52063646
|
A | G | 167 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(164): Show | 174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1976-1693T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063646 | ||||||
chr13:52063671
|
A | ACCTCTGC others(30): Show |
35 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1976-1719_1976-171 others(41): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063671 | ||||||
chr13:52063703
|
G | C | 1 | a0005c0012t0001g0100 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1976-1750C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063703 | ||||||
chr13:52063730
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0133a0001c0001t0030g0044 | 3 | HG03209.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1975+1754C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063730 | ||||||
chr13:52063757
|
C | T | 3 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317 | 3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1975+1727G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063757 | ||||||
chr13:52063762
|
A | G | 321 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(318): Show | 332 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.1975+1722T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063762 | ||||||
chr13:52063801
|
C | T | 3 | a0003c0005t0027g0321a0003c0005t0027g0322a0003c0005t0054g0323 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1975+1683G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063801 | ||||||
chr13:52063861
|
G | A | 1 | a0001c0001t0002g0254 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1975+1623C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063861 | ||||||
chr13:52063915
|
T | C | 201 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0045others(198): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1975+1569A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063915 | ||||||
chr13:52063958
|
G | A | 1 | a0001c0001t0004g0271 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1975+1526C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063958 | ||||||
chr13:52063982
|
G | A | 1 | a0006c0011t0042g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1975+1502C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063982 | ||||||
chr13:52063996
|
T | TG | 34 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(31): Show | 34 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1975+1487dupC | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063996 | ||||||
chr13:52063996
|
TG | T | 19 | a0001c0001t0001g0030a0001c0001t0001g0161a0001c0001t0002g0236others(16): Show | 19 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1975+1487delC | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063996 | ||||||
chr13:52063996
|
TGG | T | 163 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(160): Show | 170 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1975+1486_1975+148 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063996 | ||||||
chr13:52064017
|
C | G | 7 | a0001c0001t0001g0123a0001c0001t0001g0130a0001c0001t0001g0153others(4): Show | 7 | HG02109.hp1 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1975+1467G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064017 | ||||||
chr13:52064035
|
A | ATCCGGGA others(120): Show |
5 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1975+1448_1975+144 others(131): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064035 | ||||||
chr13:52064108
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1975+1376C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064108 | ||||||
chr13:52064112
|
G | A | 1 | a0001c0001t0044g0016 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1975+1372C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064112 | ||||||
chr13:52064161
|
TGTCCGGG others(42): Show |
T | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1975+1274_1975+132 others(53): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064161 | ||||||
chr13:52064192
|
C | G | 35 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1975+1292G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064192 | ||||||
chr13:52064194
|
G | A | 1 | a0001c0001t0007g0225 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1975+1290C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064194 | ||||||
chr13:52064206
|
G | A | 5 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1975+1278C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064206 | ||||||
chr13:52064211
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0149a0001c0001t0012g0035 | 3 | HG00438.hp2 HG02970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1975+1273C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064211 | ||||||
chr13:52064242
|
C | T | 5 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1975+1242G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064242 | ||||||
chr13:52064324
|
T | C | 160 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(157): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1975+1160A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064324 | ||||||
chr13:52064365
|
C | A | 5 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1975+1119G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064365 | ||||||
chr13:52064388
|
G | A | 5 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1975+1096C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064388 | ||||||
chr13:52064391
|
C | T | 1 | a0001c0001t0002g0264 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1975+1093G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064391 | ||||||
chr13:52064416
|
G | C | 1 | a0001c0001t0041g0084 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1975+1068C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064416 | ||||||
chr13:52064451
|
G | A | 6 | a0001c0001t0002g0008a0001c0001t0002g0227a0001c0001t0002g0254others(3): Show | 7 | NA18969.hp1 NA18973.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.1975+1033C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064451 | ||||||
chr13:52064486
|
T | C | 160 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(157): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1975+998A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064486 | ||||||
chr13:52064514
|
C | T | 11 | a0001c0001t0036g0032a0001c0001t0037g0127a0001c0003t0010g0017others(8): Show | 11 | HG00544.hp1 HG01099.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1975+970G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064514 | ||||||
chr13:52064527
|
G | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0056others(1): Show | 4 | HG02622.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+957C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064527 | ||||||
chr13:52064535
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0008g0095 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1975+949G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064535 | ||||||
chr13:52064559
|
C | T | 3 | a0003c0005t0027g0321a0003c0005t0027g0322a0003c0005t0054g0323 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1975+925G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064559 | ||||||
chr13:52064606
|
C | T | 30 | a0002c0002t0004g0176a0002c0002t0004g0177a0002c0002t0004g0178others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.1975+878G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064606 | ||||||
chr13:52064618
|
G | T | 1 | a0001c0001t0001g0147 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1975+866C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064618 | ||||||
chr13:52064648
|
G | A | 1 | a0002c0002t0004g0179 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1975+836C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064648 | ||||||
chr13:52064649
|
G | T | 1 | a0002c0002t0004g0179 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1975+835C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064649 | ||||||
chr13:52064683
|
C | T | 1 | a0010c0015t0001g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1975+801G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064683 | ||||||
chr13:52064995
|
A | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1975+489T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064995 | ||||||
chr13:52065042
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1975+442G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52065042 | ||||||
chr13:52065094
|
C | T | 1 | a0006c0011t0042g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1975+390G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52065094 | ||||||
chr13:52065095
|
G | A | 28 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0172others(25): Show | 30 | HG00597.hp1 HG00621.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.1975+389C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52065095 | ||||||
chr13:52065162
|
C | A | 160 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(157): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1975+322G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52065162 | ||||||
chr13:52065326
|
T | C | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1975+158A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52065326 | ||||||
chr13:52065688
|
A | G | 3 | a0001c0001t0022g0311a0001c0001t0022g0312a0001c0001t0022g0313 | 3 | HG02451.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1850-79T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52065688 | ||||||
chr13:52065878
|
A | G | 1 | a0001c0001t0006g0024 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1850-269T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52065878 | ||||||
chr13:52065891
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0128 | 2 | NA18951.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1850-282T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52065891 | ||||||
chr13:52065983
|
A | G | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1850-374T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52065983 | ||||||
chr13:52066013
|
GA | G | 176 | a0001c0001t0001g0076a0001c0001t0001g0080a0001c0001t0001g0119others(173): Show | 182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1850-405delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066013 | ||||||
chr13:52066325
|
T | C | 1 | a0002c0002t0004g0192 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1850-716A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066325 | ||||||
chr13:52066465
|
G | T | 186 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(183): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1850-856C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066465 | ||||||
chr13:52066493
|
T | G | 2 | a0001c0001t0022g0311a0001c0001t0022g0312 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1850-884A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066493 | ||||||
chr13:52066632
|
C | T | 160 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(157): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1850-1023G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066632 | ||||||
chr13:52066736
|
G | A | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1850-1127C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066736 | ||||||
chr13:52066758
|
C | A | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1850-1149G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066758 | ||||||
chr13:52066760
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0145a0001c0001t0008g0031 | 3 | HG02886.hp2 HG02970.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1850-1151G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066760 | ||||||
chr13:52066795
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1850-1186G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066795 | ||||||
chr13:52066796
|
G | A | 4 | a0001c0003t0013g0018a0001c0003t0013g0021a0001c0003t0013g0022others(1): Show | 4 | HG00544.hp1 NA18994.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1850-1187C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066796 | ||||||
chr13:52066803
|
C | CA | 9 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0083others(6): Show | 9 | HG00621.hp1 HG01123.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1850-1195dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066803 | ||||||
chr13:52066917
|
G | A | 8 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0047others(5): Show | 8 | HG01069.hp2 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1850-1308C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066917 | ||||||
chr13:52067002
|
T | C | 3 | a0001c0001t0001g0115a0001c0001t0001g0134a0001c0001t0001g0164 | 3 | NA18948.hp1 NA18956.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1850-1393A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067002 | ||||||
chr13:52067078
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1850-1469T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067078 | ||||||
chr13:52067317
|
T | G | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1850-1708A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067317 | ||||||
chr13:52067444
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1850-1835G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067444 | ||||||
chr13:52067457
|
A | G | 1 | a0001c0001t0002g0213 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1850-1848T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067457 | ||||||
chr13:52067651
|
C | T | 35 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1850-2042G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067651 | ||||||
chr13:52067670
|
C | G | 10 | a0001c0001t0001g0030a0001c0001t0001g0147a0001c0001t0001g0160others(7): Show | 10 | HG02258.hp2 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1850-2061G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067670 | ||||||
chr13:52067676
|
A | AT | 27 | a0001c0001t0001g0113a0001c0001t0001g0131a0001c0001t0001g0161others(24): Show | 28 | HG00099.hp2 HG00408.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1850-2068dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067676 | ||||||
chr13:52067676
|
A | ATT | 125 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(122): Show | 131 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1850-2069_1850-206 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067676 | ||||||
chr13:52067676
|
A | ATTT | 16 | a0001c0001t0002g0234a0001c0001t0002g0308a0001c0001t0007g0203others(13): Show | 16 | HG00323.hp1 HG00733.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1850-2070_1850-206 others(7): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067676 | ||||||
chr13:52067760
|
T | C | 186 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(183): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1850-2151A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067760 | ||||||
chr13:52067770
|
C | A | 1 | a0001c0001t0062g0276 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1850-2161G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067770 | ||||||
chr13:52067977
|
C | T | 1 | a0001c0001t0015g0229 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1850-2368G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067977 | ||||||
chr13:52068089
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1850-2480G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068089 | ||||||
chr13:52068220
|
G | A | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1850-2611C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068220 | ||||||
chr13:52068230
|
C | A | 1 | a0001c0001t0038g0118 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1850-2621G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068230 | ||||||
chr13:52068231
|
A | C | 1 | a0001c0001t0038g0118 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1850-2622T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068231 | ||||||
chr13:52068232
|
C | A | 1 | a0001c0001t0038g0118 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1850-2623G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068232 | ||||||
chr13:52068293
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1850-2684G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068293 | ||||||
chr13:52068338
|
A | G | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1850-2729T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068338 | ||||||
chr13:52068466
|
T | TAC | 14 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0001g0056others(11): Show | 15 | HG01192.hp1 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1850-2859_1850-285 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068466 | ||||||
chr13:52068466
|
T | TACAC | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0030others(100): Show | 106 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.1850-2861_1850-285 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068466 | ||||||
chr13:52068466
|
T | TACACAC | 10 | a0001c0001t0001g0112a0001c0001t0001g0116a0001c0001t0001g0117others(7): Show | 10 | HG00609.hp1 HG01109.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1850-2863_1850-285 others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068466 | ||||||
chr13:52068466
|
TAC | T | 161 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(158): Show | 168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1850-2859_1850-285 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068466 | ||||||
chr13:52068466
|
TACAC | T | 4 | a0001c0001t0016g0303a0001c0001t0016g0306a0002c0002t0004g0191others(1): Show | 4 | HG00621.hp1 HG02132.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1850-2861_1850-285 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068466 | ||||||
chr13:52068466
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0002g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1850-2869_1850-285 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068466 | ||||||
chr13:52068706
|
C | T | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1850-3097G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068706 | ||||||
chr13:52068790
|
T | C | 1 | a0001c0001t0016g0305 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1849+3154A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068790 | ||||||
chr13:52068803
|
C | G | 1 | a0002c0002t0004g0177 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1849+3141G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068803 | ||||||
chr13:52068844
|
G | A | 3 | a0001c0001t0021g0224a0001c0001t0021g0232a0001c0001t0021g0286 | 3 | HG00323.hp2 HG02602.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1849+3100C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068844 | ||||||
chr13:52068864
|
G | A | 4 | a0001c0001t0018g0013a0001c0001t0018g0014a0001c0001t0018g0015others(1): Show | 4 | HG03017.hp1 HG03490.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1849+3080C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068864 | ||||||
chr13:52068879
|
G | A | 1 | a0001c0001t0007g0225 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1849+3065C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068879 | ||||||
chr13:52068938
|
TC | T | 160 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(157): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1849+3005delG | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068938 | ||||||
chr13:52068970
|
CA | C | 174 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(171): Show | 181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.1849+2973delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068970 | ||||||
chr13:52069000
|
A | G | 2 | a0002c0002t0050g0320a0002c0002t0051g0319 | 2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1849+2944T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069000 | ||||||
chr13:52069034
|
C | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1849+2910G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069034 | ||||||
chr13:52069119
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1849+2825A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069119 | ||||||
chr13:52069176
|
G | T | 2 | a0001c0001t0002g0215a0001c0001t0004g0271 | 2 | HG00639.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1849+2768C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069176 | ||||||
chr13:52069321
|
C | A | 2 | a0001c0001t0002g0292a0001c0001t0002g0293 | 2 | HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1849+2623G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069321 | ||||||
chr13:52069466
|
G | A | 2 | a0001c0001t0001g0040a0009c0007t0001g0054 | 2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1849+2478C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069466 | ||||||
chr13:52069621
|
C | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1849+2323G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069621 | ||||||
chr13:52069639
|
T | C | 1 | a0001c0001t0012g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1849+2305A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069639 | ||||||
chr13:52069937
|
T | C | 2 | a0001c0001t0002g0292a0001c0001t0002g0293 | 2 | HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1849+2007A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069937 | ||||||
chr13:52070115
|
A | G | 1 | a0006c0011t0042g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1849+1829T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52070115 | ||||||
chr13:52070328
|
C | CA | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1849+1615dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52070328 | ||||||
chr13:52070769
|
A | T | 1 | a0001c0001t0038g0118 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1849+1175T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52070769 | ||||||
chr13:52070927
|
C | T | 5 | a0002c0002t0005g0065a0002c0002t0005g0067a0002c0002t0005g0071others(2): Show | 5 | HG00099.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1849+1017G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52070927 | ||||||
chr13:52071145
|
A | G | 29 | a0002c0002t0004g0176a0002c0002t0004g0177a0002c0002t0004g0178others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.1849+799T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071145 | ||||||
chr13:52071275
|
C | T | 4 | a0003c0005t0027g0321a0003c0005t0027g0322a0003c0005t0054g0323others(1): Show | 4 | HG01192.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1849+669G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071275 | ||||||
chr13:52071366
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1849+578G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071366 | ||||||
chr13:52071410
|
C | G | 2 | a0001c0001t0031g0053a0010c0015t0001g0055 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1849+534G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071410 | ||||||
chr13:52071466
|
C | T | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1849+478G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071466 | ||||||
chr13:52071542
|
C | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1849+402G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071542 | ||||||
chr13:52071650
|
T | G | 1 | a0001c0001t0001g0114 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1849+294A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071650 | ||||||
chr13:52071789
|
G | T | 1 | a0001c0001t0038g0118 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1849+155C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071789 | ||||||
chr13:52071859
|
C | T | 1 | a0001c0001t0002g0197 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1849+85G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071859 | ||||||
chr13:52071889
|
A | G | 2 | a0002c0002t0004g0181a0002c0002t0004g0182 | 2 | HG00323.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1849+55T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071889 | ||||||
chr13:52072372
|
A | G | 5 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1723-302T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52072372 | ||||||
chr13:52072441
|
T | C | 2 | a0001c0001t0031g0053a0010c0015t0001g0055 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1723-371A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52072441 | ||||||
chr13:52072466
|
C | A | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1723-396G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52072466 | ||||||
chr13:52072558
|
G | A | 10 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(7): Show | 10 | HG00544.hp1 HG01099.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1723-488C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52072558 | ||||||
chr13:52072926
|
A | C | 1 | a0001c0003t0013g0018 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1723-856T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52072926 | ||||||
chr13:52073068
|
A | T | 1 | a0001c0001t0001g0042 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1723-998T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52073068 | ||||||
chr13:52073216
|
A | G | 3 | a0001c0001t0022g0311a0001c0001t0022g0312a0001c0001t0022g0313 | 3 | HG02451.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1723-1146T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52073216 | ||||||
chr13:52073217
|
T | A | 150 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(147): Show | 156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1723-1147A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52073217 | ||||||
chr13:52073378
|
T | C | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1723-1308A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52073378 | ||||||
chr13:52073542
|
C | T | 1 | a0001c0004t0019g0299 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1723-1472G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52073542 | ||||||
chr13:52073859
|
C | T | 160 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(157): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1723-1789G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52073859 | ||||||
chr13:52073866
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1723-1796G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52073866 | ||||||
chr13:52073976
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1722+1782T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52073976 | ||||||
chr13:52074209
|
G | A | 1 | a0010c0015t0001g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1722+1549C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52074209 | ||||||
chr13:52074605
|
T | C | 12 | a0001c0001t0001g0083a0001c0001t0001g0136a0001c0001t0001g0137others(9): Show | 12 | HG02015.hp1 NA18959.hp1 NA18960.hp2 others(9): Show |
intron_variant | MODIFIER | c.1722+1153A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52074605 | ||||||
chr13:52074791
|
C | T | 4 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0155others(1): Show | 4 | HG02083.hp2 NA18942.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1722+967G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52074791 | ||||||
chr13:52074937
|
C | T | 1 | a0001c0001t0058g0285 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1722+821G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52074937 | ||||||
chr13:52074983
|
G | A | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1722+775C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52074983 | ||||||
chr13:52075093
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1722+665G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52075093 | ||||||
chr13:52075106
|
C | A | 1 | a0006c0011t0042g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1722+652G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52075106 | ||||||
chr13:52075444
|
C | A | 1 | a0006c0011t0042g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1722+314G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52075444 | ||||||
chr13:52075645
|
A | T | 1 | a0001c0001t0060g0281 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1722+113T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52075645 | ||||||
chr13:52075976
|
G | A | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1653+87C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 18/23 | chr13 | 52075976 | ||||||
chr13:52075985
|
A | G | 3 | a0001c0001t0002g0233a0001c0001t0002g0266a0001c0001t0002g0274 | 3 | NA18974.hp1 NA18978.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1653+78T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 18/23 | chr13 | 52075985 | ||||||
chr13:52076484
|
T | C | 1 | a0001c0001t0014g0297 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1573-341A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52076484 | ||||||
chr13:52076487
|
C | T | 1 | a0001c0001t0006g0025 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1573-344G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52076487 | ||||||
chr13:52076539
|
A | G | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1573-396T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52076539 | ||||||
chr13:52076653
|
C | T | 1 | a0001c0001t0037g0127 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1573-510G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52076653 | ||||||
chr13:52076886
|
A | C | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1573-743T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52076886 | ||||||
chr13:52076902
|
C | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1573-759G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52076902 | ||||||
chr13:52077329
|
A | G | 1 | a0001c0003t0010g0017 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1573-1186T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52077329 | ||||||
chr13:52077341
|
T | C | 1 | a0002c0002t0004g0191 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1573-1198A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52077341 | ||||||
chr13:52077355
|
T | C | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1573-1212A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52077355 | ||||||
chr13:52077663
|
C | A | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1573-1520G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52077663 | ||||||
chr13:52077671
|
C | T | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1573-1528G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52077671 | ||||||
chr13:52077767
|
T | C | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1573-1624A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52077767 | ||||||
chr13:52077856
|
C | T | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1573-1713G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52077856 | ||||||
chr13:52077943
|
G | A | 32 | a0002c0002t0004g0176a0002c0002t0004g0177a0002c0002t0004g0178others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1573-1800C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52077943 | ||||||
chr13:52078045
|
G | A | 1 | a0006c0011t0042g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1573-1902C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078045 | ||||||
chr13:52078181
|
A | C | 1 | a0001c0001t0060g0281 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1573-2038T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078181 | ||||||
chr13:52078384
|
G | A | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1573-2241C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078384 | ||||||
chr13:52078520
|
C | A | 186 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(183): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1573-2377G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078520 | ||||||
chr13:52078592
|
G | GT | 55 | a0001c0001t0001g0046a0001c0001t0001g0314a0001c0001t0002g0277others(52): Show | 56 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.1573-2450dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078592 | ||||||
chr13:52078592
|
G | GTT | 114 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(111): Show | 120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1573-2451_1573-245 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078592 | ||||||
chr13:52078714
|
C | T | 3 | a0003c0005t0027g0321a0003c0005t0027g0322a0003c0005t0054g0323 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1573-2571G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078714 | ||||||
chr13:52078839
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0048 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1573-2696C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078839 | ||||||
chr13:52078879
|
T | C | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1573-2736A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078879 | ||||||
chr13:52079058
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1573-2915C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079058 | ||||||
chr13:52079203
|
T | G | 1 | a0001c0001t0002g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1573-3060A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079203 | ||||||
chr13:52079251
|
C | A | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1573-3108G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079251 | ||||||
chr13:52079286
|
A | ATCCCTC | 147 | a0001c0001t0001g0076a0001c0001t0001g0080a0001c0001t0001g0101others(144): Show | 154 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.1573-3149_1573-314 others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079286 | ||||||
chr13:52079286
|
A | ATCCCTCT others(5): Show |
120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(117): Show | 124 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.1573-3155_1573-314 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079286 | ||||||
chr13:52079286
|
ATCCCTC | A | 32 | a0002c0002t0004g0176a0002c0002t0004g0177a0002c0002t0004g0178others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1573-3149_1573-314 others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079286 | ||||||
chr13:52079286
|
ATCCCTCT others(5): Show |
A | 2 | a0001c0001t0001g0040a0009c0007t0001g0054 | 2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1573-3155_1573-314 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079286 | ||||||
chr13:52079308
|
C | CTCTCCCC others(11): Show |
3 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317 | 3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1573-3166_1573-316 others(22): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079308 | ||||||
chr13:52079347
|
C | T | 2 | a0001c0001t0003g0260a0001c0001t0029g0259 | 2 | NA18956.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1573-3204G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079347 | ||||||
chr13:52079348
|
G | A | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1573-3205C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079348 | ||||||
chr13:52079348
|
G | T | 1 | a0001c0001t0003g0248 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1573-3205C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079348 | ||||||
chr13:52079437
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1573-3294A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079437 | ||||||
chr13:52079457
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0170a0001c0001t0017g0103 | 3 | HG02735.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1573-3314C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079457 | ||||||
chr13:52079471
|
C | T | 20 | a0001c0001t0002g0251a0001c0001t0003g0006a0001c0001t0003g0009others(17): Show | 22 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1573-3328G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079471 | ||||||
chr13:52079493
|
G | A | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1573-3350C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079493 | ||||||
chr13:52079725
|
G | T | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1572+3535C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079725 | ||||||
chr13:52079752
|
C | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1572+3508G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079752 | ||||||
chr13:52079817
|
G | A | 1 | a0001c0001t0002g0270 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1572+3443C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079817 | ||||||
chr13:52079829
|
C | T | 1 | a0001c0001t0014g0294 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1572+3431G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079829 | ||||||
chr13:52079872
|
C | T | 5 | a0002c0002t0004g0180a0002c0002t0004g0181a0002c0002t0004g0182others(2): Show | 5 | HG00323.hp1 HG00733.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1572+3388G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079872 | ||||||
chr13:52079880
|
G | A | 3 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0043g0034 | 3 | HG01891.hp1 HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1572+3380C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079880 | ||||||
chr13:52079916
|
C | T | 32 | a0002c0002t0004g0176a0002c0002t0004g0177a0002c0002t0004g0178others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1572+3344G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079916 | ||||||
chr13:52079984
|
C | T | 1 | a0001c0001t0041g0084 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1572+3276G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079984 | ||||||
chr13:52080005
|
G | A | 1 | a0002c0002t0004g0179 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1572+3255C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080005 | ||||||
chr13:52080038
|
A | AAGAAGTG others(33): Show |
114 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(111): Show | 120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1572+3221_1572+322 others(44): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080038 | ||||||
chr13:52080060
|
C | G | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 4 | HG01074.hp1 HG01993.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572+3200G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080060 | ||||||
chr13:52080061
|
C | T | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3199G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080061 | ||||||
chr13:52080073
|
G | C | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3187C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080073 | ||||||
chr13:52080093
|
T | C | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3167A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080093 | ||||||
chr13:52080094
|
A | C | 2 | a0001c0001t0002g0193a0001c0001t0020g0230 | 2 | HG01106.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1572+3166T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080094 | ||||||
chr13:52080109
|
A | G | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3151T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080109 | ||||||
chr13:52080113
|
C | G | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3147G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080113 | ||||||
chr13:52080119
|
G | A | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3141C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080119 | ||||||
chr13:52080122
|
G | A | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3138C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080122 | ||||||
chr13:52080132
|
G | C | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3128C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080132 | ||||||
chr13:52080134
|
C | A | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3126G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080134 | ||||||
chr13:52080137
|
C | T | 2 | a0001c0001t0016g0303a0001c0001t0016g0306 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1572+3123G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080137 | ||||||
chr13:52080161
|
A | T | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3099T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080161 | ||||||
chr13:52080170
|
G | A | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3090C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080170 | ||||||
chr13:52080173
|
G | A | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3087C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080173 | ||||||
chr13:52080174
|
T | G | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3086A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080174 | ||||||
chr13:52080178
|
C | T | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3082G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080178 | ||||||
chr13:52080180
|
C | T | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3080G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080180 | ||||||
chr13:52080186
|
A | C | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3074T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080186 | ||||||
chr13:52080195
|
G | A | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3065C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080195 | ||||||
chr13:52080204
|
G | A | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3056C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080204 | ||||||
chr13:52080214
|
TG | T | 32 | a0001c0001t0002g0256a0002c0002t0004g0176a0002c0002t0004g0177others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1572+3045delC | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080214 | ||||||
chr13:52080215
|
GGGGGGGG others(43): Show |
G | 8 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(5): Show | 8 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.1572+2995_1572+304 others(54): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080215 | ||||||
chr13:52080216
|
GGGGGGGG others(42): Show |
G | 1 | a0001c0003t0013g0018 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1572+2995_1572+304 others(53): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080216 | ||||||
chr13:52080237
|
C | A | 1 | a0001c0001t0020g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3023G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080237 | ||||||
chr13:52080251
|
A | G | 6 | a0001c0001t0020g0230a0002c0002t0004g0191a0002c0002t0049g0190others(3): Show | 6 | HG00621.hp1 HG01192.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1572+3009T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080251 | ||||||
chr13:52080259
|
G | C | 5 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1572+3001C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080259 | ||||||
chr13:52080285
|
G | A | 32 | a0002c0002t0004g0176a0002c0002t0004g0177a0002c0002t0004g0178others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1572+2975C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080285 | ||||||
chr13:52080288
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1572+2972G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080288 | ||||||
chr13:52080296
|
C | G | 1 | a0010c0015t0001g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1572+2964G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080296 | ||||||
chr13:52080323
|
T | C | 8 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(5): Show | 8 | HG01192.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1572+2937A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080323 | ||||||
chr13:52080329
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1572+2931G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080329 | ||||||
chr13:52080353
|
A | G | 179 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(176): Show | 186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1572+2907T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080353 | ||||||
chr13:52080356
|
C | A | 1 | a0003c0005t0054g0323 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1572+2904G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080356 | ||||||
chr13:52080376
|
C | T | 3 | a0001c0001t0021g0224a0001c0001t0021g0232a0001c0001t0021g0286 | 3 | HG00323.hp2 HG02602.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1572+2884G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080376 | ||||||
chr13:52080412
|
C | G | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1572+2848G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080412 | ||||||
chr13:52080572
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1572+2688G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080572 | ||||||
chr13:52080695
|
A | G | 1 | a0001c0001t0003g0010 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1572+2565T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080695 | ||||||
chr13:52080700
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0039g0146 | 2 | HG01516.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1572+2560G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080700 | ||||||
chr13:52080718
|
C | A | 2 | a0002c0002t0005g0065a0002c0002t0033g0075 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1572+2542G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080718 | ||||||
chr13:52080723
|
T | C | 19 | a0001c0001t0001g0076a0001c0001t0001g0080a0001c0001t0001g0119others(16): Show | 19 | HG00609.hp1 HG00673.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1572+2537A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080723 | ||||||
chr13:52080770
|
C | G | 1 | a0001c0001t0001g0139 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1572+2490G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080770 | ||||||
chr13:52080771
|
C | T | 1 | a0001c0001t0016g0305 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1572+2489G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080771 | ||||||
chr13:52080781
|
G | A | 1 | a0001c0004t0019g0299 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1572+2479C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080781 | ||||||
chr13:52080785
|
A | G | 1 | a0001c0001t0003g0272 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1572+2475T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080785 | ||||||
chr13:52080810
|
G | A | 2 | a0001c0001t0014g0296a0001c0001t0053g0295 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1572+2450C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080810 | ||||||
chr13:52080832
|
G | A | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1572+2428C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080832 | ||||||
chr13:52080889
|
TA | T | 14 | a0001c0001t0001g0052a0001c0001t0001g0080a0001c0001t0001g0153others(11): Show | 14 | HG01069.hp2 HG01243.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.1572+2370delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080889 | ||||||
chr13:52080889
|
TAA | T | 156 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(153): Show | 162 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1572+2369_1572+237 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080889 | ||||||
chr13:52080892
|
A | T | 1 | a0001c0001t0002g0228 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1572+2368T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080892 | ||||||
chr13:52080988
|
T | A | 1 | a0001c0001t0011g0206 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1572+2272A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080988 | ||||||
chr13:52080988
|
T | TA | 114 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(111): Show | 120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1572+2271dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080988 | ||||||
chr13:52080989
|
A | T | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1572+2271T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080989 | ||||||
chr13:52081187
|
T | A | 1 | a0001c0001t0014g0287 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1572+2073A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52081187 | ||||||
chr13:52081752
|
T | A | 1 | a0001c0001t0002g0207 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1572+1508A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52081752 | ||||||
chr13:52081870
|
C | T | 1 | a0008c0014t0004g0298 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1572+1390G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52081870 | ||||||
chr13:52082141
|
C | A | 1 | a0001c0001t0002g0243 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1572+1119G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52082141 | ||||||
chr13:52082149
|
C | T | 32 | a0002c0002t0004g0176a0002c0002t0004g0177a0002c0002t0004g0178others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1572+1111G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52082149 | ||||||
chr13:52082246
|
C | T | 5 | a0002c0002t0004g0185a0002c0002t0004g0186a0002c0002t0004g0187others(2): Show | 5 | HG00408.hp2 HG00621.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1572+1014G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52082246 | ||||||
chr13:52082255
|
C | T | 5 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1572+1005G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52082255 | ||||||
chr13:52082256
|
G | A | 3 | a0001c0001t0003g0257a0001c0001t0003g0258a0001c0001t0003g0289 | 3 | HG01981.hp2 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1572+1004C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52082256 | ||||||
chr13:52082542
|
T | C | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1572+718A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52082542 | ||||||
chr13:52082771
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1572+489T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52082771 | ||||||
chr13:52083090
|
G | A | 2 | a0001c0001t0012g0038a0001c0001t0012g0039 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1572+170C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52083090 | ||||||
chr13:52083104
|
C | T | 32 | a0002c0002t0004g0176a0002c0002t0004g0177a0002c0002t0004g0178others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1572+156G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52083104 | ||||||
chr13:52083151
|
A | G | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1572+109T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52083151 | ||||||
chr13:52083171
|
G | A | 8 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1572+89C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52083171 | ||||||
chr13:52083237
|
C | T | 1 | a0002c0002t0032g0070 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1572+23G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52083237 | ||||||
chr13:52083373
|
A | G | 2 | a0002c0002t0050g0320a0002c0002t0051g0319 | 2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1480-21T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52083373 | ||||||
chr13:52083553
|
T | G | 114 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(111): Show | 120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1480-201A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52083553 | ||||||
chr13:52083572
|
T | G | 5 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1480-220A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52083572 | ||||||
chr13:52083727
|
A | G | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1480-375T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52083727 | ||||||
chr13:52083784
|
C | T | 1 | a0001c0001t0058g0285 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1480-432G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52083784 | ||||||
chr13:52083932
|
G | C | 2 | a0001c0001t0008g0062a0001c0001t0008g0063 | 2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1480-580C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52083932 | ||||||
chr13:52084293
|
A | G | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1480-941T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084293 | ||||||
chr13:52084324
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1480-972G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084324 | ||||||
chr13:52084361
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1480-1009C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084361 | ||||||
chr13:52084384
|
A | C | 1 | a0001c0001t0004g0271 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1480-1032T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084384 | ||||||
chr13:52084696
|
T | C | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1480-1344A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084696 | ||||||
chr13:52084699
|
G | A | 11 | a0001c0001t0001g0047a0001c0001t0008g0043a0001c0003t0010g0017others(8): Show | 11 | HG00544.hp1 HG01099.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1480-1347C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084699 | ||||||
chr13:52084724
|
A | C | 1 | a0001c0001t0002g0227 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1480-1372T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084724 | ||||||
chr13:52084730
|
A | T | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 4 | HG01074.hp1 HG01993.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480-1378T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084730 | ||||||
chr13:52084732
|
A | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0153 | 3 | HG02622.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1480-1380T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084732 | ||||||
chr13:52084732
|
AGT | A | 3 | a0001c0001t0001g0098a0001c0001t0001g0168a0001c0001t0008g0062 | 3 | HG01109.hp2 HG01993.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1480-1382_1480-138 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084732 | ||||||
chr13:52084732
|
AGTGAGAG others(41): Show |
A | 1 | a0001c0001t0020g0278 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1480-1428_1480-138 others(52): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084732 | ||||||
chr13:52084734
|
T | A | 121 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0096others(118): Show | 127 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.1480-1382A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084734 | ||||||
chr13:52084734
|
T | TGA | 12 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0099others(9): Show | 15 | HG00408.hp1 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1480-1384_1480-138 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084734 | ||||||
chr13:52084734
|
TGA | T | 8 | a0001c0001t0001g0058a0001c0001t0001g0110a0001c0001t0001g0121others(5): Show | 8 | HG00597.hp2 HG01516.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.1480-1384_1480-138 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084734 | ||||||
chr13:52084734
|
TGAGA | T | 7 | a0001c0001t0035g0125a0002c0002t0004g0181a0002c0002t0004g0182others(4): Show | 7 | HG00323.hp1 HG01081.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1480-1386_1480-138 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084734 | ||||||
chr13:52084734
|
TGAGAGA | T | 4 | a0002c0002t0005g0064a0002c0002t0005g0067a0002c0002t0005g0068others(1): Show | 4 | HG00099.hp2 HG00738.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480-1388_1480-138 others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084734 | ||||||
chr13:52084736
|
A | T | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1480-1384T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084736 | ||||||
chr13:52084736
|
AGAGAGAG others(37): Show |
A | 2 | a0001c0001t0002g0226a0001c0001t0002g0264 | 2 | HG02015.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1480-1428_1480-138 others(48): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084736 | ||||||
chr13:52084738
|
A | T | 1 | a0001c0001t0008g0063 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1480-1386T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084738 | ||||||
chr13:52084738
|
AGAGAGAG others(33): Show |
A | 4 | a0001c0001t0002g0222a0001c0001t0003g0217a0001c0001t0003g0257others(1): Show | 4 | HG01433.hp2 HG02004.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480-1426_1480-138 others(44): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084738 | ||||||
chr13:52084738
|
AGAGAGAG others(35): Show |
A | 9 | a0001c0001t0002g0221a0001c0001t0002g0223a0001c0001t0003g0006others(6): Show | 11 | HG00099.hp1 HG02602.hp2 NA18944.hp1 others(8): Show |
intron_variant | MODIFIER | c.1480-1428_1480-138 others(46): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084738 | ||||||
chr13:52084738
|
AGAGAGAG others(37): Show |
A | 90 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(87): Show | 94 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.1480-1430_1480-138 others(48): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084738 | ||||||
chr13:52084740
|
A | T | 1 | a0001c0001t0008g0062 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1480-1388T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084740 | ||||||
chr13:52084740
|
AGAGAGAG others(33): Show |
A | 3 | a0001c0001t0003g0258a0001c0001t0003g0272a0001c0001t0029g0253 | 3 | HG01981.hp2 NA18948.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1480-1428_1480-138 others(44): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084740 | ||||||
chr13:52084740
|
AGAGAGAG others(35): Show |
A | 4 | a0001c0001t0002g0228a0001c0001t0002g0269a0001c0001t0002g0273others(1): Show | 4 | HG01934.hp1 HG02129.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480-1430_1480-138 others(46): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084740 | ||||||
chr13:52084740
|
AGAGAGAG others(37): Show |
A | 2 | a0001c0001t0002g0245a0001c0001t0007g0244 | 2 | HG03704.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1480-1432_1480-138 others(48): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084740 | ||||||
chr13:52084742
|
A | T | 2 | a0002c0002t0004g0180a0002c0002t0004g0184 | 2 | HG00733.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1480-1390T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084742 | ||||||
chr13:52084756
|
A | AGT | 6 | a0001c0001t0026g0316a0002c0002t0004g0185a0002c0002t0004g0186others(3): Show | 6 | HG00408.hp2 HG00621.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1480-1405_1480-140 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084756 | ||||||
chr13:52084756
|
A | T | 3 | a0002c0002t0004g0192a0002c0002t0050g0320a0008c0014t0004g0298 | 3 | HG01074.hp2 HG02280.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1480-1404T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084756 | ||||||
chr13:52084756
|
AGAGAGAG others(1): Show |
A | 5 | a0001c0001t0026g0318a0001c0001t0052g0317a0002c0002t0004g0183others(2): Show | 5 | HG00642.hp2 HG01243.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1480-1412_1480-140 others(12): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084756 | ||||||
chr13:52084756
|
AGAGAGAG others(3): Show |
A | 7 | a0001c0001t0006g0024a0001c0001t0006g0025a0001c0001t0006g0026others(4): Show | 7 | HG01255.hp1 HG01256.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1480-1414_1480-140 others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084756 | ||||||
chr13:52084756
|
AGAGAGAG others(5): Show |
A | 4 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0004t0019g0301others(1): Show | 5 | HG01099.hp1 HG01109.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1480-1416_1480-140 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084756 | ||||||
chr13:52084756
|
AGAGAGAG others(23): Show |
A | 2 | a0001c0001t0001g0047a0001c0001t0008g0043 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1480-1434_1480-140 others(34): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084756 | ||||||
chr13:52084758
|
A | T | 10 | a0001c0001t0026g0316a0002c0002t0004g0179a0002c0002t0004g0185others(7): Show | 10 | HG00408.hp2 HG00621.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1480-1406T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084758 | ||||||
chr13:52084758
|
AGAGAGTG others(3): Show |
A | 3 | a0001c0003t0010g0020a0001c0003t0010g0175a0001c0004t0019g0299 | 3 | HG02258.hp1 HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1480-1416_1480-140 others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084758 | ||||||
chr13:52084758
|
AGAGAGTG others(5): Show |
A | 4 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0013g0018others(1): Show | 4 | HG01099.hp2 HG03688.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480-1418_1480-140 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084758 | ||||||
chr13:52084758
|
AGAGAGTG others(7): Show |
A | 3 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0043g0034 | 3 | HG01891.hp1 HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1480-1420_1480-140 others(18): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084758 | ||||||
chr13:52084758
|
AGAGAGTG others(17): Show |
A | 1 | a0006c0011t0042g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1480-1430_1480-140 others(28): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084758 | ||||||
chr13:52084760
|
A | AGT | 4 | a0001c0001t0001g0076a0001c0001t0001g0156a0001c0001t0001g0158others(1): Show | 4 | HG02074.hp2 HG03831.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480-1409_1480-140 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084760 | ||||||
chr13:52084760
|
A | AGTGTGTG others(3): Show |
1 | a0002c0002t0004g0177 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1480-1409_1480-140 others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084760 | ||||||
chr13:52084760
|
A | T | 15 | a0001c0001t0026g0316a0002c0002t0004g0176a0002c0002t0004g0178others(12): Show | 15 | HG00408.hp2 HG00621.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1480-1408T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084760 | ||||||
chr13:52084760
|
AGAGTGTG others(3): Show |
A | 1 | a0001c0003t0013g0021 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1480-1418_1480-140 others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084760 | ||||||
chr13:52084760
|
AGAGTGTG others(5): Show |
A | 1 | a0001c0003t0013g0022 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1480-1420_1480-140 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084760 | ||||||
chr13:52084760
|
AGAGTGTG others(7): Show |
A | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1480-1422_1480-140 others(18): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084760 | ||||||
chr13:52084762
|
A | AGAGAGAG others(7): Show |
1 | a0001c0001t0009g0088 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1480-1411_1480-141 others(18): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
A | AGAGAGTG others(1): Show |
3 | a0001c0001t0001g0089a0001c0001t0008g0105a0001c0001t0014g0294 | 3 | HG00733.hp1 NA18994.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1480-1411_1480-141 others(12): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
A | AGAGAGTG others(7): Show |
1 | a0001c0001t0001g0087 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1480-1411_1480-141 others(18): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
A | AGAGT | 8 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0086others(5): Show | 8 | HG00558.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1480-1411_1480-141 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
A | AGAGTGT | 4 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0123others(1): Show | 4 | HG02258.hp2 HG02647.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480-1411_1480-141 others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
A | AGAGTGTG others(3): Show |
3 | a0001c0001t0001g0085a0001c0001t0001g0147a0009c0007t0001g0054 | 3 | HG02572.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1480-1411_1480-141 others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
A | AGAGTGTG others(5): Show |
1 | a0001c0001t0008g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1480-1411_1480-141 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
A | AGT | 4 | a0001c0001t0001g0050a0001c0001t0001g0092a0001c0001t0001g0111others(1): Show | 4 | HG01346.hp1 HG03471.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480-1412_1480-141 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
A | AGTGT | 5 | a0001c0001t0001g0091a0001c0001t0012g0038a0001c0001t0022g0311others(2): Show | 5 | HG01943.hp1 HG02004.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480-1414_1480-141 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
A | AGTGTGT | 5 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0133others(2): Show | 5 | HG00438.hp2 HG02622.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1480-1416_1480-141 others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
A | AGTGTGTG others(1): Show |
4 | a0001c0001t0001g0030a0001c0001t0001g0153a0001c0001t0001g0155others(1): Show | 4 | HG02886.hp2 HG06807.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480-1418_1480-141 others(12): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
A | AGTGTGTG others(5): Show |
1 | a0001c0001t0001g0107 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1480-1422_1480-141 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
A | T | 33 | a0001c0001t0001g0076a0001c0001t0001g0110a0001c0001t0001g0119others(30): Show | 33 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1480-1410T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
AGT | A | 19 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0102others(16): Show | 19 | HG01192.hp1 HG01243.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1480-1412_1480-141 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
AGTGT | A | 9 | a0001c0001t0001g0052a0001c0001t0001g0116a0001c0001t0001g0139others(6): Show | 9 | HG01069.hp2 HG02486.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1480-1414_1480-141 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
AGTGTGT | A | 6 | a0001c0001t0001g0097a0001c0001t0016g0303a0001c0001t0016g0305others(3): Show | 6 | HG01074.hp1 HG01516.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1480-1416_1480-141 others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0022g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1480-1420_1480-141 others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084762
|
AGTGTGTG others(9): Show |
A | 1 | a0005c0012t0001g0100 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1480-1426_1480-141 others(20): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | ||||||
chr13:52084764
|
T | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0056a0001c0001t0001g0057others(21): Show | 26 | HG00408.hp1 HG00544.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.1480-1412A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084764 | ||||||
chr13:52084766
|
T | A | 19 | a0001c0001t0001g0083a0001c0001t0001g0102a0001c0001t0001g0104others(16): Show | 19 | HG00544.hp2 HG01081.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1480-1414A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084766 | ||||||
chr13:52084768
|
T | A | 19 | a0001c0001t0001g0083a0001c0001t0001g0104a0001c0001t0001g0116others(16): Show | 19 | HG01109.hp2 HG01192.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1480-1416A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084768 | ||||||
chr13:52084770
|
T | A | 10 | a0001c0001t0001g0137a0001c0001t0001g0141a0001c0001t0016g0303others(7): Show | 10 | HG01192.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1480-1418A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084770 | ||||||
chr13:52084772
|
T | A | 1 | a0001c0001t0031g0053 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1480-1420A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084772 | ||||||
chr13:52084774
|
T | A | 1 | a0001c0001t0031g0053 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1480-1422A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084774 | ||||||
chr13:52084780
|
T | A | 1 | a0005c0012t0001g0100 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1480-1428A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084780 | ||||||
chr13:52084781
|
G | T | 1 | a0001c0001t0001g0040 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1480-1429C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084781 | ||||||
chr13:52084782
|
T | A | 1 | a0001c0001t0020g0278 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1480-1430A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084782 | ||||||
chr13:52084815
|
GT | G | 3 | a0001c0001t0001g0140a0001c0001t0001g0163a0002c0002t0004g0178 | 3 | HG02135.hp1 NA18979.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1479+1461delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084815 | ||||||
chr13:52084817
|
T | G | 1 | a0009c0007t0001g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1479+1460A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084817 | ||||||
chr13:52084818
|
T | G | 1 | a0001c0001t0001g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1479+1459A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084818 | ||||||
chr13:52085137
|
A | C | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1479+1140T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085137 | ||||||
chr13:52085140
|
G | A | 2 | a0001c0001t0024g0033a0001c0001t0024g0077 | 2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1479+1137C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085140 | ||||||
chr13:52085523
|
A | G | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1479+754T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085523 | ||||||
chr13:52085528
|
C | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1479+749G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085528 | ||||||
chr13:52085711
|
A | C | 1 | a0001c0001t0031g0053 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1479+566T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085711 | ||||||
chr13:52085888
|
T | C | 1 | a0001c0001t0002g0214 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1479+389A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085888 | ||||||
chr13:52085920
|
G | A | 1 | a0006c0011t0042g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1479+357C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085920 | ||||||
chr13:52085967
|
G | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1479+310C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085967 | ||||||
chr13:52085993
|
T | C | 1 | a0002c0002t0004g0188 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1479+284A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085993 | ||||||
chr13:52086098
|
A | G | 32 | a0002c0002t0004g0176a0002c0002t0004g0177a0002c0002t0004g0178others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1479+179T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52086098 | ||||||
chr13:52086169
|
T | C | 1 | a0001c0003t0010g0175 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1479+108A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52086169 | ||||||
chr13:52086170
|
G | T | 35 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1479+107C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52086170 | ||||||
chr13:52086171
|
A | C | 35 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1479+106T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52086171 | ||||||
chr13:52086248
|
C | T | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1479+29G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52086248 | ||||||
chr13:52086446
|
A | C | 1 | a0001c0001t0015g0198 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1393-83T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/23 | chr13 | 52086446 | ||||||
chr13:52086459
|
T | C | 30 | a0002c0002t0004g0176a0002c0002t0004g0177a0002c0002t0004g0178others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.1393-96A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/23 | chr13 | 52086459 | ||||||
chr13:52086802
|
CAAG | C | 36 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(33): Show | 36 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.1393-442_1393-440d others(5): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/23 | chr13 | 52086802 | ||||||
chr13:52087168
|
C | T | 5 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1392+170G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/23 | chr13 | 52087168 | ||||||
chr13:52087245
|
A | T | 1 | a0001c0001t0002g0221 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1392+93T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/23 | chr13 | 52087245 | ||||||
chr13:52087275
|
C | T | 8 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1392+63G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/23 | chr13 | 52087275 | ||||||
chr13:52087279
|
A | G | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1392+59T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/23 | chr13 | 52087279 | ||||||
chr13:52087280
|
C | T | 1 | a0001c0001t0001g0004 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1392+58G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/23 | chr13 | 52087280 | ||||||
chr13:52087502
|
A | T | 1 | a0001c0001t0001g0133 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1276-48T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087502 | ||||||
chr13:52087519
|
A | C | 8 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-65T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087519 | ||||||
chr13:52087652
|
G | A | 8 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-198C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087652 | ||||||
chr13:52087679
|
A | ACAGCGGC others(3): Show |
1 | a0001c0001t0007g0246 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1276-235_1276-226d others(12): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087679 | ||||||
chr13:52087771
|
A | G | 2 | a0001c0001t0002g0202a0001c0001t0002g0270 | 2 | HG01069.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1276-317T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087771 | ||||||
chr13:52087786
|
C | T | 1 | a0001c0001t0002g0221 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1276-332G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087786 | ||||||
chr13:52087877
|
G | A | 8 | a0001c0001t0009g0151a0001c0003t0010g0017a0001c0003t0010g0020others(5): Show | 8 | HG00544.hp1 HG01099.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1276-423C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087877 | ||||||
chr13:52087928
|
C | CT | 10 | a0001c0001t0001g0123a0001c0003t0010g0017a0001c0003t0010g0019others(7): Show | 10 | HG00544.hp1 HG01099.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1276-475dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087928 | ||||||
chr13:52087928
|
CT | C | 9 | a0001c0001t0001g0168a0001c0001t0002g0220a0001c0001t0002g0247others(6): Show | 9 | HG01256.hp1 HG01993.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.1276-475delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087928 | ||||||
chr13:52088019
|
C | A | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1276-565G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088019 | ||||||
chr13:52088099
|
T | C | 2 | a0001c0001t0023g0011a0001c0001t0023g0012 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1276-645A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088099 | ||||||
chr13:52088171
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1276-717G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088171 | ||||||
chr13:52088249
|
G | T | 185 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(182): Show | 192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1276-795C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088249 | ||||||
chr13:52088255
|
G | GT | 18 | a0001c0001t0001g0101a0001c0001t0001g0169a0001c0001t0002g0220others(15): Show | 18 | HG00323.hp1 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1276-802dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088255 | ||||||
chr13:52088294
|
G | A | 9 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(6): Show | 9 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1276-840C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088294 | ||||||
chr13:52088362
|
C | G | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1275+885G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088362 | ||||||
chr13:52088443
|
C | T | 2 | a0001c0001t0012g0038a0001c0001t0012g0039 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1275+804G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088443 | ||||||
chr13:52088542
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1275+705G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088542 | ||||||
chr13:52088581
|
A | C | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1275+666T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088581 | ||||||
chr13:52088734
|
A | G | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1275+513T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088734 | ||||||
chr13:52088839
|
C | G | 1 | a0001c0001t0001g0104 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1275+408G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088839 | ||||||
chr13:52088957
|
G | A | 119 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(116): Show | 125 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1275+290C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088957 | ||||||
chr13:52089054
|
G | A | 2 | a0001c0001t0024g0033a0001c0001t0024g0077 | 2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1275+193C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52089054 | ||||||
chr13:52089077
|
G | A | 1 | a0010c0015t0001g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1275+170C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52089077 | ||||||
chr13:52089093
|
A | AAACAACA others(2): Show |
189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 194 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.1275+145_1275+153d others(11): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52089093 | ||||||
chr13:52089093
|
A | AAACAACA others(5): Show |
132 | a0001c0001t0001g0050a0001c0001t0001g0119a0001c0001t0001g0121others(129): Show | 138 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1275+142_1275+153d others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52089093 | ||||||
chr13:52089355
|
A | G | 172 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(169): Show | 179 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.1209-42T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089355 | ||||||
chr13:52089526
|
G | T | 23 | a0001c0001t0002g0251a0001c0001t0003g0006a0001c0001t0003g0009others(20): Show | 25 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1209-213C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089526 | ||||||
chr13:52089557
|
C | T | 3 | a0002c0002t0004g0185a0002c0002t0004g0186a0002c0002t0004g0187 | 3 | HG00408.hp2 NA18941.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1209-244G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089557 | ||||||
chr13:52089559
|
T | C | 35 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1209-246A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089559 | ||||||
chr13:52089704
|
G | A | 1 | a0003c0005t0027g0322 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1209-391C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089704 | ||||||
chr13:52089754
|
G | A | 1 | a0001c0009t0001g0041 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1209-441C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089754 | ||||||
chr13:52089842
|
G | A | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1209-529C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089842 | ||||||
chr13:52089852
|
G | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0166 | 2 | HG02071.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1209-539C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089852 | ||||||
chr13:52089961
|
C | CA | 36 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(33): Show | 36 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.1209-649dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089961 | ||||||
chr13:52090069
|
T | C | 119 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(116): Show | 125 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1209-756A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52090069 | ||||||
chr13:52090081
|
C | T | 2 | a0001c0001t0006g0024a0001c0001t0006g0025 | 2 | HG01256.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1209-768G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52090081 | ||||||
chr13:52090129
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1209-816G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52090129 | ||||||
chr13:52090156
|
C | A | 3 | a0001c0001t0003g0009a0001c0001t0003g0248a0001c0001t0003g0249 | 4 | NA18944.hp1 NA18960.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.1209-843G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52090156 | ||||||
chr13:52090287
|
A | G | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-974T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52090287 | ||||||
chr13:52090638
|
A | G | 3 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0009g0088 | 3 | NA18950.hp2 NA19077.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1209-1325T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52090638 | ||||||
chr13:52090792
|
A | G | 173 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(170): Show | 180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1209-1479T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52090792 | ||||||
chr13:52091106
|
T | C | 2 | a0001c0001t0001g0047a0001c0001t0008g0043 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1209-1793A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52091106 | ||||||
chr13:52091131
|
C | A | 3 | a0001c0001t0002g0251a0001c0001t0003g0252a0001c0001t0055g0250 | 3 | HG02300.hp2 NA19005.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1209-1818G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52091131 | ||||||
chr13:52091250
|
CAA | C | 42 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(39): Show | 43 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.1208+1802_1208+180 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52091250 | ||||||
chr13:52091280
|
T | C | 5 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208+1774A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52091280 | ||||||
chr13:52091773
|
T | G | 1 | a0001c0001t0029g0253 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1208+1281A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52091773 | ||||||
chr13:52092185
|
C | T | 1 | a0001c0001t0002g0269 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1208+869G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52092185 | ||||||
chr13:52092221
|
CTTTA | C | 35 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1208+829_1208+832d others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52092221 | ||||||
chr13:52092335
|
C | A | 1 | a0001c0001t0002g0265 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1208+719G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52092335 | ||||||
chr13:52092336
|
G | A | 1 | a0001c0001t0002g0265 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1208+718C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52092336 | ||||||
chr13:52092424
|
C | CA | 131 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(128): Show | 137 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1208+629dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52092424 | ||||||
chr13:52092469
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1208+585T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52092469 | ||||||
chr13:52092556
|
C | A | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1208+498G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52092556 | ||||||
chr13:52092618
|
G | A | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208+436C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52092618 | ||||||
chr13:52093013
|
T | C | 2 | a0001c0001t0031g0053a0010c0015t0001g0055 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1208+41A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52093013 | ||||||
chr13:52093330
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1027-95G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52093330 | ||||||
chr13:52093403
|
T | C | 2 | a0001c0001t0001g0050a0001c0001t0030g0044 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1027-168A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52093403 | ||||||
chr13:52093428
|
C | T | 4 | a0001c0003t0013g0018a0001c0003t0013g0021a0001c0003t0013g0022others(1): Show | 4 | HG00544.hp1 NA18994.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-193G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52093428 | ||||||
chr13:52093560
|
C | CA | 33 | a0001c0001t0060g0281a0002c0002t0004g0176a0002c0002t0004g0177others(30): Show | 33 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.1027-326dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52093560 | ||||||
chr13:52093904
|
T | G | 1 | a0002c0002t0004g0178 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1027-669A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52093904 | ||||||
chr13:52093922
|
A | G | 3 | a0003c0005t0027g0321a0003c0005t0027g0322a0003c0005t0054g0323 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1027-687T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52093922 | ||||||
chr13:52094602
|
T | C | 1 | a0001c0001t0002g0254 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1027-1367A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52094602 | ||||||
chr13:52094872
|
T | C | 35 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1027-1637A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52094872 | ||||||
chr13:52094994
|
C | T | 157 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(154): Show | 164 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.1027-1759G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52094994 | ||||||
chr13:52095066
|
G | A | 5 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027-1831C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095066 | ||||||
chr13:52095093
|
A | T | 6 | a0001c0001t0001g0076a0001c0001t0001g0156a0001c0001t0001g0157others(3): Show | 6 | HG00673.hp2 HG02074.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.1027-1858T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095093 | ||||||
chr13:52095169
|
G | A | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1027-1934C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095169 | ||||||
chr13:52095204
|
G | A | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1027-1969C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095204 | ||||||
chr13:52095255
|
CAAG | C | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1027-2023_1027-202 others(7): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095255 | ||||||
chr13:52095503
|
A | G | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1027-2268T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095503 | ||||||
chr13:52095626
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1027-2391C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095626 | ||||||
chr13:52095659
|
G | A | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1027-2424C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095659 | ||||||
chr13:52095848
|
C | A | 2 | a0001c0001t0031g0053a0010c0015t0001g0055 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1027-2613G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095848 | ||||||
chr13:52095927
|
C | G | 1 | a0001c0001t0008g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1027-2692G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095927 | ||||||
chr13:52095947
|
G | A | 2 | a0001c0001t0002g0267a0001c0001t0002g0268 | 2 | HG01261.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1027-2712C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095947 | ||||||
chr13:52095957
|
A | T | 2 | a0001c0001t0002g0267a0001c0001t0002g0268 | 2 | HG01261.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1027-2722T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095957 | ||||||
chr13:52095976
|
T | A | 1 | a0010c0015t0001g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1027-2741A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095976 | ||||||
chr13:52096071
|
C | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0104a0001c0001t0001g0106others(2): Show | 7 | HG00408.hp1 HG02071.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.1027-2836G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52096071 | ||||||
chr13:52096293
|
G | A | 35 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1027-3058C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52096293 | ||||||
chr13:52096331
|
A | G | 2 | a0001c0001t0002g0215a0001c0001t0004g0271 | 2 | HG00639.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1027-3096T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52096331 | ||||||
chr13:52096438
|
G | A | 8 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1027-3203C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52096438 | ||||||
chr13:52096881
|
C | T | 1 | a0002c0002t0051g0319 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1026+2862G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52096881 | ||||||
chr13:52096986
|
G | A | 1 | a0001c0001t0044g0016 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1026+2757C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52096986 | ||||||
chr13:52097113
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1026+2630G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52097113 | ||||||
chr13:52097161
|
C | T | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1026+2582G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52097161 | ||||||
chr13:52097408
|
C | T | 3 | a0003c0005t0027g0321a0003c0005t0027g0322a0003c0005t0054g0323 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1026+2335G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52097408 | ||||||
chr13:52098073
|
G | A | 1 | a0001c0001t0003g0255 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1026+1670C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098073 | ||||||
chr13:52098220
|
C | T | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1026+1523G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098220 | ||||||
chr13:52098261
|
C | CAAAT | 93 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0040others(90): Show | 97 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1026+1478_1026+148 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098261 | ||||||
chr13:52098261
|
C | CAAATAAA others(1): Show |
27 | a0001c0001t0001g0003a0001c0001t0001g0087a0001c0001t0001g0097others(24): Show | 28 | HG00408.hp2 HG00621.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1026+1474_1026+148 others(12): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098261 | ||||||
chr13:52098261
|
C | CAAATAAA others(5): Show |
7 | a0001c0001t0009g0051a0002c0002t0004g0177a0002c0002t0005g0064others(4): Show | 7 | HG00099.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026+1470_1026+148 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098261 | ||||||
chr13:52098261
|
C | CAAATAAA others(9): Show |
1 | a0002c0002t0005g0066 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1026+1466_1026+148 others(20): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098261 | ||||||
chr13:52098261
|
CAAAT | C | 7 | a0001c0001t0001g0058a0001c0001t0012g0035a0001c0001t0012g0038others(4): Show | 7 | HG01358.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026+1478_1026+148 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098261 | ||||||
chr13:52098261
|
CAAATAAA others(9): Show |
C | 126 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(123): Show | 132 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1026+1466_1026+148 others(20): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098261 | ||||||
chr13:52098432
|
T | TC | 161 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(158): Show | 167 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1026+1310_1026+131 others(5): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098432 | ||||||
chr13:52098581
|
G | T | 5 | a0001c0001t0002g0172a0001c0001t0002g0173a0001c0001t0002g0210others(2): Show | 5 | HG00621.hp2 NA18612.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026+1162C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098581 | ||||||
chr13:52098698
|
T | C | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1026+1045A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098698 | ||||||
chr13:52098814
|
C | G | 3 | a0003c0005t0027g0321a0003c0005t0027g0322a0003c0005t0054g0323 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1026+929G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098814 | ||||||
chr13:52098868
|
T | G | 186 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(183): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1026+875A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098868 | ||||||
chr13:52099053
|
G | C | 2 | a0001c0001t0031g0053a0010c0015t0001g0055 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1026+690C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52099053 | ||||||
chr13:52099210
|
AT | A | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1026+532delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52099210 | ||||||
chr13:52099292
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1026+451C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52099292 | ||||||
chr13:52099394
|
G | A | 1 | a0005c0012t0001g0100 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1026+349C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52099394 | ||||||
chr13:52099542
|
C | G | 2 | a0002c0002t0050g0320a0002c0002t0051g0319 | 2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1026+201G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52099542 | ||||||
chr13:52099543
|
G | A | 2 | a0001c0001t0001g0131a0002c0002t0004g0176 | 2 | HG01981.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1026+200C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52099543 | ||||||
chr13:52099637
|
T | C | 1 | a0001c0001t0002g0270 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1026+106A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52099637 | ||||||
chr13:52099651
|
A | T | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1026+92T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52099651 | ||||||
chr13:52099918
|
T | C | 1 | a0001c0001t0002g0270 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.893-42A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52099918 | ||||||
chr13:52100103
|
T | C | 168 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(165): Show | 175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.893-227A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100103 | ||||||
chr13:52100108
|
C | A | 1 | a0010c0015t0001g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.893-232G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100108 | ||||||
chr13:52100162
|
T | C | 3 | a0001c0001t0003g0257a0001c0001t0003g0258a0001c0001t0003g0289 | 3 | HG01981.hp2 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.893-286A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100162 | ||||||
chr13:52100305
|
G | A | 3 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317 | 3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.893-429C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100305 | ||||||
chr13:52100312
|
G | C | 1 | a0001c0001t0001g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.893-436C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100312 | ||||||
chr13:52100322
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.893-446G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100322 | ||||||
chr13:52100496
|
C | T | 2 | a0001c0001t0012g0038a0001c0001t0012g0039 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.893-620G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100496 | ||||||
chr13:52100720
|
A | G | 1 | a0001c0001t0006g0026 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.893-844T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100720 | ||||||
chr13:52100772
|
T | G | 1 | a0001c0001t0001g0167 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.893-896A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100772 | ||||||
chr13:52100911
|
G | A | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.892+1022C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100911 | ||||||
chr13:52101097
|
G | C | 3 | a0003c0005t0027g0321a0003c0005t0027g0322a0003c0005t0054g0323 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.892+836C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52101097 | ||||||
chr13:52101139
|
C | G | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.892+794G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52101139 | ||||||
chr13:52101180
|
C | T | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.892+753G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52101180 | ||||||
chr13:52101195
|
G | A | 2 | a0002c0002t0050g0320a0002c0002t0051g0319 | 2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.892+738C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52101195 | ||||||
chr13:52101399
|
C | T | 8 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.892+534G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52101399 | ||||||
chr13:52101792
|
A | G | 1 | a0002c0002t0004g0185 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.892+141T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52101792 | ||||||
chr13:52102023
|
G | A | 1 | a0010c0015t0001g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.811-9C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 10/23 | chr13 | 52102023 | ||||||
chr13:52102392
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.610-100T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52102392 | ||||||
chr13:52102564
|
G | A | 1 | a0001c0001t0044g0016 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.610-272C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52102564 | ||||||
chr13:52102606
|
T | C | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.610-314A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52102606 | ||||||
chr13:52102646
|
T | A | 1 | a0001c0001t0012g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.610-354A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52102646 | ||||||
chr13:52102650
|
G | A | 1 | a0007c0008t0009g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.610-358C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52102650 | ||||||
chr13:52102812
|
ATTTTG | A | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.610-525_610-521del others(5): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52102812 | ||||||
chr13:52102880
|
G | T | 1 | a0001c0001t0001g0314 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.610-588C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52102880 | ||||||
chr13:52103033
|
G | A | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.610-741C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52103033 | ||||||
chr13:52103351
|
T | A | 186 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(183): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.610-1059A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52103351 | ||||||
chr13:52103711
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.609+787T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52103711 | ||||||
chr13:52103745
|
G | C | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.609+753C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52103745 | ||||||
chr13:52103843
|
T | C | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.609+655A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52103843 | ||||||
chr13:52104175
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.609+323A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52104175 | ||||||
chr13:52104221
|
C | T | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.609+277G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52104221 | ||||||
chr13:52104264
|
A | G | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.609+234T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52104264 | ||||||
chr13:52104605
|
A | G | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.555-53T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52104605 | ||||||
chr13:52104831
|
G | A | 35 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.555-279C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52104831 | ||||||
chr13:52104831
|
G | T | 1 | a0001c0001t0002g0211 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.555-279C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52104831 | ||||||
chr13:52104987
|
T | G | 1 | a0001c0001t0001g0004 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.555-435A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52104987 | ||||||
chr13:52105237
|
G | A | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.555-685C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105237 | ||||||
chr13:52105238
|
A | AGT | 14 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(11): Show | 14 | HG00544.hp2 HG01074.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.555-688_555-687dup others(2): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105238 | ||||||
chr13:52105238
|
A | AGTGT | 4 | a0001c0001t0001g0078a0001c0001t0008g0095a0001c0001t0018g0013others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-690_555-687dup others(4): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105238 | ||||||
chr13:52105238
|
A | AGTGTGT | 5 | a0001c0001t0016g0303a0001c0001t0016g0305a0001c0001t0016g0306others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-692_555-687dup others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105238 | ||||||
chr13:52105238
|
AGT | A | 46 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0048others(43): Show | 47 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.555-688_555-687del others(2): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105238 | ||||||
chr13:52105238
|
AGTGT | A | 114 | a0001c0001t0001g0083a0001c0001t0001g0136a0001c0001t0001g0137others(111): Show | 120 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.555-690_555-687del others(4): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105238 | ||||||
chr13:52105238
|
AGTGTGT | A | 7 | a0001c0001t0002g0265a0001c0001t0002g0292a0001c0001t0002g0293others(4): Show | 7 | HG00738.hp2 HG01168.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.555-692_555-687del others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105238 | ||||||
chr13:52105238
|
AGTGTGTG others(3): Show |
A | 4 | a0001c0001t0003g0260a0001c0001t0003g0261a0001c0001t0029g0259others(1): Show | 4 | NA18956.hp2 NA18959.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-696_555-687del others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105238 | ||||||
chr13:52105238
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0002g0277 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.555-698_555-687del others(12): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105238 | ||||||
chr13:52105244
|
T | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | NA19060.hp2 NA19063.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.555-692A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105244 | ||||||
chr13:52105266
|
T | C | 2 | a0001c0001t0002g0263a0001c0001t0002g0264 | 2 | HG00597.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.555-714A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105266 | ||||||
chr13:52105279
|
GAGA | G | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.555-730_555-728del others(3): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105279 | ||||||
chr13:52105284
|
G | C | 2 | a0001c0001t0014g0296a0001c0001t0053g0295 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.555-732C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105284 | ||||||
chr13:52105332
|
G | C | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.555-780C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105332 | ||||||
chr13:52105452
|
C | G | 1 | a0001c0001t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.555-900G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105452 | ||||||
chr13:52105505
|
C | T | 1 | a0001c0001t0041g0084 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.555-953G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105505 | ||||||
chr13:52105626
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0045g0093 | 3 | NA18954.hp2 NA18971.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.555-1074G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105626 | ||||||
chr13:52105669
|
T | C | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.555-1117A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105669 | ||||||
chr13:52105729
|
C | T | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.555-1177G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105729 | ||||||
chr13:52105786
|
C | T | 4 | a0001c0001t0014g0294a0001c0001t0014g0296a0001c0001t0014g0297others(1): Show | 4 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.555-1234G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105786 | ||||||
chr13:52106053
|
T | A | 2 | a0001c0001t0002g0265a0001c0001t0057g0280 | 2 | NA18972.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.555-1501A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52106053 | ||||||
chr13:52106179
|
C | CA | 11 | a0001c0001t0001g0134a0001c0001t0006g0024a0001c0001t0012g0036others(8): Show | 11 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.555-1628dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52106179 | ||||||
chr13:52106179
|
CA | C | 115 | a0001c0001t0001g0045a0001c0001t0002g0005a0001c0001t0002g0007others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.555-1628delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52106179 | ||||||
chr13:52106441
|
C | T | 1 | a0001c0004t0019g0299 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.554+1877G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52106441 | ||||||
chr13:52106660
|
G | T | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.554+1658C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52106660 | ||||||
chr13:52106753
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.554+1565G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52106753 | ||||||
chr13:52106797
|
G | A | 7 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0012g0038others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.554+1521C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52106797 | ||||||
chr13:52107264
|
T | TACTA | 178 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(175): Show | 185 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.554+1053_554+1054i others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107264 | ||||||
chr13:52107295
|
A | T | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.554+1023T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107295 | ||||||
chr13:52107426
|
A | G | 1 | a0001c0001t0002g0210 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.554+892T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107426 | ||||||
chr13:52107463
|
C | G | 168 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(165): Show | 175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.554+855G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107463 | ||||||
chr13:52107508
|
C | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.554+810G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107508 | ||||||
chr13:52107599
|
TA | T | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.554+718delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107599 | ||||||
chr13:52107621
|
C | G | 3 | a0002c0002t0004g0185a0002c0002t0004g0186a0002c0002t0004g0187 | 3 | HG00408.hp2 NA18941.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.554+697G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107621 | ||||||
chr13:52107626
|
A | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.554+692T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107626 | ||||||
chr13:52107882
|
TTAAG | T | 3 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0043g0034 | 3 | HG01891.hp1 HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.554+432_554+435del others(4): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107882 | ||||||
chr13:52108243
|
T | C | 3 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0009g0088 | 3 | NA18950.hp2 NA19077.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.554+75A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52108243 | ||||||
chr13:52108941
|
T | G | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.468-537A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/23 | chr13 | 52108941 | ||||||
chr13:52108953
|
A | C | 2 | a0001c0001t0012g0038a0001c0001t0012g0039 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.468-549T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/23 | chr13 | 52108953 | ||||||
chr13:52109020
|
C | T | 1 | a0006c0011t0042g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.468-616G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/23 | chr13 | 52109020 | ||||||
chr13:52109127
|
A | C | 186 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(183): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.468-723T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/23 | chr13 | 52109127 | ||||||
chr13:52109787
|
T | C | 168 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(165): Show | 175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.467+553A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/23 | chr13 | 52109787 | ||||||
chr13:52109921
|
C | T | 2 | a0001c0001t0002g0199a0001c0001t0002g0200 | 2 | HG00642.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.467+419G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/23 | chr13 | 52109921 | ||||||
chr13:52109938
|
T | C | 1 | a0007c0008t0009g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.467+402A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/23 | chr13 | 52109938 | ||||||
chr13:52110115
|
G | C | 186 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(183): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.467+225C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/23 | chr13 | 52110115 | ||||||
chr13:52110665
|
TAC | T | 123 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(120): Show | 129 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.313-90_313-89delGT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52110665 | ||||||
chr13:52110667
|
C | T | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.313-90G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52110667 | ||||||
chr13:52110675
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0040g0090 | 3 | HG01346.hp1 HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.313-98G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52110675 | ||||||
chr13:52110681
|
C | T | 18 | a0001c0001t0002g0193a0001c0001t0002g0197a0001c0001t0002g0199others(15): Show | 18 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-104G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52110681 | ||||||
chr13:52110685
|
T | C | 2 | a0002c0002t0050g0320a0002c0002t0051g0319 | 2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.313-108A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52110685 | ||||||
chr13:52110878
|
T | A | 165 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(162): Show | 172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.313-301A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52110878 | ||||||
chr13:52110961
|
A | G | 317 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(314): Show | 328 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.313-384T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52110961 | ||||||
chr13:52111569
|
G | A | 1 | a0001c0001t0003g0010 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.312+699C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52111569 | ||||||
chr13:52111710
|
T | C | 1 | a0001c0001t0016g0305 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.312+558A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52111710 | ||||||
chr13:52111897
|
C | A | 2 | a0001c0001t0008g0062a0001c0001t0008g0063 | 2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.312+371G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52111897 | ||||||
chr13:52111936
|
T | C | 1 | a0001c0001t0009g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.312+332A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52111936 | ||||||
chr13:52111985
|
A | G | 1 | a0001c0001t0009g0151 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.312+283T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52111985 | ||||||
chr13:52112104
|
T | C | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.312+164A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52112104 | ||||||
chr13:52112523
|
C | T | 1 | a0001c0001t0002g0269 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.215-158G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52112523 | ||||||
chr13:52112837
|
C | G | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.215-472G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52112837 | ||||||
chr13:52112933
|
C | T | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.215-568G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52112933 | ||||||
chr13:52113107
|
T | A | 35 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.215-742A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52113107 | ||||||
chr13:52113198
|
G | A | 11 | a0001c0001t0001g0083a0001c0001t0001g0136a0001c0001t0001g0137others(8): Show | 11 | NA18959.hp1 NA18960.hp2 NA18963.hp2 others(8): Show |
intron_variant | MODIFIER | c.215-833C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52113198 | ||||||
chr13:52113343
|
G | A | 1 | a0006c0011t0042g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.215-978C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52113343 | ||||||
chr13:52113574
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.215-1209C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52113574 | ||||||
chr13:52113654
|
T | C | 2 | a0001c0001t0001g0152a0001c0001t0039g0146 | 2 | HG01516.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.215-1289A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52113654 | ||||||
chr13:52113716
|
C | T | 123 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(120): Show | 129 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.215-1351G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52113716 | ||||||
chr13:52113747
|
T | G | 10 | a0001c0001t0001g0030a0001c0001t0001g0147a0001c0001t0001g0160others(7): Show | 10 | HG02258.hp2 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-1382A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52113747 | ||||||
chr13:52113955
|
T | G | 1 | a0001c0001t0015g0198 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.215-1590A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52113955 | ||||||
chr13:52114143
|
T | G | 1 | a0001c0001t0001g0148 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.215-1778A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52114143 | ||||||
chr13:52114731
|
A | G | 1 | a0006c0011t0042g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.215-2366T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52114731 | ||||||
chr13:52114833
|
G | T | 186 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(183): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.215-2468C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52114833 | ||||||
chr13:52115159
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.215-2794C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115159 | ||||||
chr13:52115172
|
C | A | 1 | a0001c0001t0002g0266 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.215-2807G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115172 | ||||||
chr13:52115344
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0009g0088 | 3 | NA18950.hp2 NA19077.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.215-2979G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115344 | ||||||
chr13:52115352
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.215-2987G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115352 | ||||||
chr13:52115557
|
T | A | 2 | a0001c0001t0002g0267a0001c0001t0002g0268 | 2 | HG01261.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.215-3192A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115557 | ||||||
chr13:52115598
|
C | T | 2 | a0001c0001t0008g0062a0001c0001t0008g0063 | 2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.215-3233G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115598 | ||||||
chr13:52115601
|
C | CA | 49 | a0001c0001t0001g0052a0001c0001t0001g0150a0001c0001t0001g0152others(46): Show | 50 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.215-3237dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115601 | ||||||
chr13:52115601
|
C | CAA | 9 | a0002c0002t0004g0179a0002c0002t0004g0184a0002c0002t0004g0191others(6): Show | 9 | HG00621.hp1 HG00733.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.215-3238_215-3237d others(4): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115601 | ||||||
chr13:52115601
|
CA | C | 111 | a0001c0001t0001g0042a0001c0001t0001g0085a0001c0001t0001g0155others(108): Show | 117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.215-3237delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115601 | ||||||
chr13:52115656
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.215-3291G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115656 | ||||||
chr13:52115677
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.215-3312A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115677 | ||||||
chr13:52116117
|
G | T | 1 | a0001c0001t0036g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.214+3202C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52116117 | ||||||
chr13:52116178
|
C | CA | 152 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 156 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.214+3140dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52116178 | ||||||
chr13:52116178
|
C | CAA | 117 | a0001c0001t0001g0152a0001c0001t0001g0164a0001c0001t0002g0005others(114): Show | 123 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.214+3139_214+3140d others(4): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52116178 | ||||||
chr13:52116178
|
C | CAAA | 12 | a0001c0001t0003g0282a0001c0001t0006g0002a0001c0001t0006g0025others(9): Show | 13 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.214+3138_214+3140d others(5): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52116178 | ||||||
chr13:52116503
|
A | C | 11 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(8): Show | 11 | HG01192.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.214+2816T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52116503 | ||||||
chr13:52116507
|
G | A | 1 | a0001c0001t0002g0284 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.214+2812C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52116507 | ||||||
chr13:52116848
|
T | A | 186 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(183): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.214+2471A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52116848 | ||||||
chr13:52116980
|
G | A | 1 | a0001c0001t0058g0285 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.214+2339C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52116980 | ||||||
chr13:52117182
|
G | A | 4 | a0001c0001t0018g0013a0001c0001t0018g0014a0001c0001t0018g0015others(1): Show | 4 | HG03017.hp1 HG03490.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+2137C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52117182 | ||||||
chr13:52117215
|
G | C | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.214+2104C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52117215 | ||||||
chr13:52117279
|
C | T | 4 | a0001c0001t0014g0294a0001c0001t0014g0296a0001c0001t0014g0297others(1): Show | 4 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+2040G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52117279 | ||||||
chr13:52117311
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.214+2008A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52117311 | ||||||
chr13:52117859
|
T | G | 1 | a0007c0008t0009g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.214+1460A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52117859 | ||||||
chr13:52117962
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.214+1357C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52117962 | ||||||
chr13:52118384
|
A | G | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.214+935T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118384 | ||||||
chr13:52118477
|
CAT | C | 3 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317 | 3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.214+840_214+841del others(2): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118477 | ||||||
chr13:52118481
|
G | A | 6 | a0001c0001t0001g0076a0001c0001t0001g0156a0001c0001t0001g0157others(3): Show | 6 | HG00673.hp2 HG02074.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+838C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118481 | ||||||
chr13:52118561
|
C | T | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+758G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118561 | ||||||
chr13:52118580
|
G | A | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+739C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118580 | ||||||
chr13:52118580
|
G | T | 1 | a0009c0007t0001g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.214+739C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118580 | ||||||
chr13:52118587
|
C | T | 1 | a0001c0001t0015g0198 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.214+732G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118587 | ||||||
chr13:52118677
|
C | T | 1 | a0001c0001t0002g0197 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.214+642G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118677 | ||||||
chr13:52118713
|
C | G | 1 | a0001c0001t0024g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.214+606G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118713 | ||||||
chr13:52118767
|
C | G | 3 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317 | 3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.214+552G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118767 | ||||||
chr13:52118967
|
C | T | 35 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.214+352G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118967 | ||||||
chr13:52119138
|
G | A | 1 | a0009c0007t0001g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.214+181C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52119138 | ||||||
chr13:52119299
|
C | T | 3 | a0001c0004t0019g0299a0001c0004t0019g0300a0001c0004t0019g0301 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.214+20G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52119299 | ||||||
chr13:52119470
|
A | G | 1 | a0001c0009t0001g0041 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.118-55T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52119470 | ||||||
chr13:52119678
|
C | T | 1 | a0001c0004t0019g0300 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.118-263G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52119678 | ||||||
chr13:52119732
|
C | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.118-317G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52119732 | ||||||
chr13:52119951
|
T | C | 2 | a0001c0004t0019g0300a0001c0004t0019g0301 | 2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.118-536A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52119951 | ||||||
chr13:52120229
|
T | A | 1 | a0001c0001t0001g0159 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.118-814A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52120229 | ||||||
chr13:52120374
|
A | G | 5 | a0002c0002t0004g0180a0002c0002t0004g0181a0002c0002t0004g0182others(2): Show | 5 | HG00323.hp1 HG00733.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-959T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52120374 | ||||||
chr13:52120471
|
T | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.118-1056A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52120471 | ||||||
chr13:52120566
|
G | A | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-1151C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52120566 | ||||||
chr13:52120677
|
A | G | 162 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(159): Show | 168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.118-1262T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52120677 | ||||||
chr13:52120681
|
C | T | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.118-1266G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52120681 | ||||||
chr13:52120728
|
T | C | 1 | a0001c0001t0014g0297 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.118-1313A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52120728 | ||||||
chr13:52120911
|
C | CA | 6 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 6 | HG04115.hp1 NA18978.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-1497dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52120911 | ||||||
chr13:52121003
|
T | C | 177 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.118-1588A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121003 | ||||||
chr13:52121159
|
C | CT | 123 | a0001c0001t0001g0056a0001c0001t0001g0076a0001c0001t0002g0007others(120): Show | 128 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.118-1745dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121159 | ||||||
chr13:52121159
|
C | CTT | 5 | a0001c0001t0002g0005a0001c0001t0002g0193a0001c0001t0002g0196others(2): Show | 6 | HG01106.hp1 HG01106.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-1746_118-1745d others(4): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121159 | ||||||
chr13:52121299
|
C | T | 1 | a0002c0002t0004g0176 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.118-1884G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121299 | ||||||
chr13:52121667
|
T | C | 8 | a0001c0001t0002g0288a0001c0001t0006g0002a0001c0001t0006g0024others(5): Show | 9 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.118-2252A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121667 | ||||||
chr13:52121845
|
C | T | 178 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(175): Show | 185 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.118-2430G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121845 | ||||||
chr13:52121923
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.118-2508C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121923 | ||||||
chr13:52121935
|
C | CT | 13 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(10): Show | 13 | HG01192.hp1 HG01243.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.118-2521dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121935 | ||||||
chr13:52121935
|
CT | C | 8 | a0001c0001t0001g0056a0001c0001t0001g0167a0001c0001t0003g0289others(5): Show | 8 | HG01081.hp2 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-2521delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121935 | ||||||
chr13:52122077
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.118-2662T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52122077 | ||||||
chr13:52122308
|
A | G | 2 | a0001c0001t0012g0038a0001c0001t0012g0039 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.118-2893T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52122308 | ||||||
chr13:52122348
|
G | A | 2 | a0001c0001t0008g0062a0001c0001t0008g0063 | 2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.118-2933C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52122348 | ||||||
chr13:52122476
|
G | C | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.118-3061C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52122476 | ||||||
chr13:52122766
|
C | CA | 8 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(5): Show | 8 | HG01192.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-3352dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52122766 | ||||||
chr13:52123045
|
A | G | 32 | a0002c0002t0004g0176a0002c0002t0004g0177a0002c0002t0004g0178others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.118-3630T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123045 | ||||||
chr13:52123102
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.118-3687C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123102 | ||||||
chr13:52123137
|
G | C | 1 | a0001c0001t0003g0290 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.118-3722C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123137 | ||||||
chr13:52123341
|
A | G | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-3926T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123341 | ||||||
chr13:52123358
|
G | T | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.118-3943C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123358 | ||||||
chr13:52123376
|
A | G | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-3961T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123376 | ||||||
chr13:52123450
|
A | C | 2 | a0001c0001t0008g0062a0001c0001t0008g0063 | 2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.117+3916T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123450 | ||||||
chr13:52123839
|
G | GAACAAGT others(2760): Show |
1 | a0001c0003t0013g0023 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.117+3526_117+3527i others(2769): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123839 | ||||||
chr13:52123839
|
G | GAACAAGT others(2763): Show |
1 | a0001c0003t0010g0017 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.117+3526_117+3527i others(2772): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123839 | ||||||
chr13:52123839
|
G | GAACAAGT others(2762): Show |
1 | a0001c0003t0010g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.117+3526_117+3527i others(2771): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123839 | ||||||
chr13:52123839
|
G | GAACAAGT others(2761): Show |
2 | a0001c0003t0010g0175a0001c0003t0013g0022 | 2 | NA18994.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.117+3526_117+3527i others(2770): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123839 | ||||||
chr13:52123839
|
G | GAACAAGT others(2762): Show |
1 | a0001c0003t0013g0021 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.117+3526_117+3527i others(2771): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123839 | ||||||
chr13:52123839
|
G | GAACAAGT others(2764): Show |
1 | a0001c0003t0010g0020 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.117+3526_117+3527i others(2773): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123839 | ||||||
chr13:52123839
|
G | GAACAAGT others(2767): Show |
1 | a0001c0003t0010g0019 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.117+3526_117+3527i others(2776): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123839 | ||||||
chr13:52123839
|
G | GAACAAGT others(2764): Show |
1 | a0001c0003t0013g0018 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.117+3526_117+3527i others(2773): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123839 | ||||||
chr13:52123957
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.117+3409A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123957 | ||||||
chr13:52124052
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.117+3314C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52124052 | ||||||
chr13:52124263
|
G | A | 1 | a0001c0001t0012g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.117+3103C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52124263 | ||||||
chr13:52124296
|
C | T | 23 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(20): Show | 23 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+3070G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52124296 | ||||||
chr13:52124415
|
ATAT | A | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+2948_117+2950d others(5): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52124415 | ||||||
chr13:52124640
|
C | G | 162 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(159): Show | 169 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.117+2726G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52124640 | ||||||
chr13:52124866
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.117+2500A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52124866 | ||||||
chr13:52124866
|
T | G | 23 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(20): Show | 23 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+2500A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52124866 | ||||||
chr13:52124909
|
G | C | 1 | a0008c0014t0004g0298 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.117+2457C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52124909 | ||||||
chr13:52125005
|
G | A | 1 | a0001c0001t0012g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.117+2361C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125005 | ||||||
chr13:52125269
|
T | C | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+2097A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125269 | ||||||
chr13:52125283
|
G | A | 23 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(20): Show | 23 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+2083C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125283 | ||||||
chr13:52125512
|
G | A | 23 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(20): Show | 23 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+1854C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125512 | ||||||
chr13:52125530
|
T | A | 23 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317others(20): Show | 23 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+1836A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125530 | ||||||
chr13:52125698
|
G | A | 115 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(112): Show | 121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.117+1668C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125698 | ||||||
chr13:52125800
|
T | A | 1 | a0001c0001t0001g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.117+1566A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125800 | ||||||
chr13:52125847
|
C | A | 1 | a0001c0010t0048g0291 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.117+1519G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125847 | ||||||
chr13:52125893
|
C | T | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+1473G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125893 | ||||||
chr13:52126077
|
G | A | 2 | a0001c0001t0002g0292a0001c0001t0002g0293 | 2 | HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.117+1289C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126077 | ||||||
chr13:52126334
|
A | G | 167 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(164): Show | 174 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.117+1032T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126334 | ||||||
chr13:52126372
|
T | C | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+994A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126372 | ||||||
chr13:52126639
|
C | T | 9 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(6): Show | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+727G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126639 | ||||||
chr13:52126704
|
C | T | 2 | a0001c0001t0002g0172a0001c0001t0002g0173 | 2 | NA18971.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.117+662G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126704 | ||||||
chr13:52126705
|
G | A | 1 | a0008c0014t0004g0298 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.117+661C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126705 | ||||||
chr13:52126780
|
AAAAAG | A | 8 | a0001c0001t0016g0303a0001c0001t0016g0304a0001c0001t0016g0305others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+581_117+585del others(5): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126780 | ||||||
chr13:52126884
|
G | A | 1 | a0001c0001t0011g0307 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.117+482C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126884 | ||||||
chr13:52126903
|
G | T | 3 | a0001c0001t0012g0035a0001c0001t0012g0036a0001c0001t0043g0034 | 3 | HG01891.hp1 HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.117+463C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126903 | ||||||
chr13:52126993
|
T | G | 3 | a0001c0001t0002g0308a0001c0001t0002g0310a0001c0001t0020g0309 | 3 | HG01257.hp2 HG01346.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.117+373A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126993 | ||||||
chr13:52127056
|
T | A | 1 | a0001c0001t0001g0057 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.117+310A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52127056 | ||||||
chr13:52127189
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.117+177A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52127189 | ||||||
chr13:52127354
|
A | ACTT | 192 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0045others(189): Show | 199 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.117+9_117+11dupAAG | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52127354 | ||||||
chr13:52127674
|
C | T | 2 | a0001c0001t0024g0033a0001c0001t0036g0032 | 2 | HG01243.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-90-12G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52127674 | ||||||
chr13:52128187
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0017g0315 | 2 | HG00544.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-90-525C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128187 | ||||||
chr13:52128194
|
TC | T | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90-533delG | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128194 | ||||||
chr13:52128209
|
G | A | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90-547C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128209 | ||||||
chr13:52128248
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0008g0031a0001c0001t0023g0011others(1): Show | 4 | HG02615.hp2 HG02622.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90-586G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128248 | ||||||
chr13:52128555
|
T | C | 3 | a0001c0001t0026g0316a0001c0001t0026g0318a0001c0001t0052g0317 | 3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-91+474A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128555 | ||||||
chr13:52128564
|
G | A | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.-91+465C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128564 | ||||||
chr13:52128594
|
G | A | 2 | a0002c0002t0050g0320a0002c0002t0051g0319 | 2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.-91+435C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128594 | ||||||
chr13:52128624
|
G | A | 3 | a0003c0005t0027g0321a0003c0005t0027g0322a0003c0005t0054g0323 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-91+405C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128624 | ||||||
chr13:52128641
|
A | G | 7 | a0001c0001t0006g0002a0001c0001t0006g0024a0001c0001t0006g0025others(4): Show | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.-91+388T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128641 | ||||||
chr13:52128824
|
C | G | 7 | a0001c0003t0010g0017a0001c0003t0010g0019a0001c0003t0010g0020others(4): Show | 7 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-91+205G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128824 | ||||||
chr13:52129023
|
G | T | 4 | a0001c0001t0018g0013a0001c0001t0018g0014a0001c0001t0018g0015others(1): Show | 4 | HG03017.hp1 HG03490.hp1 HG03654.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.-91+6C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52129023 |