geneid | 343070 |
---|---|
ensemblid | ENSG00000204505.5 |
hgncid | 27996 |
symbol | PRAMEF9 |
name | PRAME family member 9 |
refseq_nuc | NM_001010890.3 |
refseq_prot | NP_001010890.2 |
ensembl_nuc | ENST00000415919.3 |
ensembl_prot | ENSP00000485258.1 |
mane_status | MANE Select |
chr | chr1 |
start | 13171848 |
end | 13179459 |
strand | + |
ver | v1.2 |
region | chr1:13171848-13179459 |
region5000 | chr1:13166848-13184459 |
regionname0 | PRAMEF9_chr1_13171848_13179459 |
regionname5000 | PRAMEF9_chr1_13166848_13184459 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 478 | 82 | 3 | 29 | 37 | 4 | 9 | 31 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0002 | 0/0 | 478 | 35 | 1 | 6 | 26 | 0 | 2 | 19 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0003 | 1/0 | 478 | 22 | 0 | 3 | 17 | 0 | 1 | 13 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0004 | 0/1 | 478 | 19 | 2 | 2 | 11 | 1 | 2 | 11 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0005 | 0/0 | 478 | 8 | 2 | 1 | 2 | 1 | 2 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0006 | 0/0 | 478 | 6 | 1 | 1 | 4 | 0 | 0 | 3 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0007 | 0/0 | 478 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0008 | 0/0 | 478 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0009 | 0/0 | 167 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0010 | 0/0 | 478 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0011 | 0/0 | 478 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0012 | 0/0 | 478 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0013 | 0/0 | 478 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0014 | 0/0 | 478 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0015 | 0/0 | 478 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0016 | 0/0 | 478 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0017 | 0/0 | 215 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0018 | 0/0 | 155 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0019 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0020 | 0/0 | 478 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0021 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0022 | 0/0 | 478 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0023 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0024 | 0/0 | 478 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0025 | 0/0 | 478 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0026 | 0/0 | 478 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0027 | 0/0 | 344 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0028 | 0/0 | 478 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0029 | 0/0 | 478 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0030 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1437 | 81 | 3 | 29 | 36 | 4 | 9 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0002 | 0/0 | 1437 | 33 | 1 | 6 | 24 | 0 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0003 | 1/0 | 1437 | 20 | 0 | 3 | 15 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0004 | 0/1 | 1437 | 19 | 2 | 2 | 11 | 1 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0005 | 0/0 | 1437 | 8 | 2 | 1 | 2 | 1 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0006 | 0/0 | 1437 | 6 | 1 | 1 | 4 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0007 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0008 | 0/0 | 1437 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0009 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0010 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0011 | 0/0 | 1437 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0012 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0013 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0014 | 0/0 | 1437 | 2 | 1 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0015 | 0/0 | 1437 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0016 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0017 | 0/0 | 1437 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0018 | 0/0 | 1437 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0019 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0020 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0021 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0022 | 0/0 | 1759 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0023 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0024 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0025 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0026 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0027 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0028 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0029 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0030 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0031 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0032 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0033 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
c0034 | 0/0 | 1437 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1023 | 78 | 6 | 26 | 34 | 4 | 8 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0002 | 0/0 | 1022 | 26 | 0 | 0 | 25 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0003 | 1/0 | 1029 | 23 | 0 | 5 | 17 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0004 | 0/1 | 1028 | 21 | 3 | 4 | 10 | 1 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0005 | 0/0 | 1023 | 10 | 2 | 1 | 2 | 1 | 4 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0006 | 0/0 | 1029 | 7 | 3 | 0 | 4 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0007 | 0/0 | 1022 | 6 | 0 | 4 | 1 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0008 | 0/0 | 1023 | 5 | 2 | 1 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0009 | 0/0 | 1023 | 3 | 3 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0010 | 0/0 | 1029 | 2 | 1 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0011 | 0/0 | 1023 | 2 | 0 | 1 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0012 | 0/0 | 1023 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0013 | 0/0 | 1028 | 2 | 0 | 0 | 1 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0014 | 0/0 | 1029 | 2 | 0 | 0 | 1 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0015 | 0/0 | 1023 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0016 | 0/0 | 1029 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0017 | 0/0 | 1023 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0018 | 0/0 | 1023 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0019 | 0/0 | 1023 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0020 | 0/0 | 1023 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0021 | 0/0 | 1023 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0022 | 0/0 | 1024 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0023 | 0/0 | 1028 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0024 | 0/0 | 1024 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0025 | 0/0 | 1024 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0026 | 0/0 | 1028 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0027 | 0/0 | 1022 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
t0028 | 0/0 | 1023 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 47 | 2 | 19 | 19 | 1 | 6 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0002 | 0/1 | 17 | 0 | 4 | 9 | 0 | 3 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0003 | 0/0 | 15 | 0 | 6 | 8 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0004 | 1/0 | 13 | 0 | 3 | 8 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0005 | 0/0 | 11 | 1 | 0 | 10 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0006 | 0/0 | 8 | 2 | 0 | 2 | 0 | 4 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0007 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0009 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0011 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1437 | 81 | 3 | 29 | 36 | 4 | 9 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0001c0033 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0002c0002 | 0/0 | 1437 | 33 | 1 | 6 | 24 | 0 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0002c0023 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0002c0024 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0003c0003 | 1/0 | 1437 | 20 | 0 | 3 | 15 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0003c0008 | 0/0 | 1437 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0004c0004 | 0/1 | 1437 | 19 | 2 | 2 | 11 | 1 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0005c0005 | 0/0 | 1437 | 8 | 2 | 1 | 2 | 1 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0006c0006 | 0/0 | 1437 | 6 | 1 | 1 | 4 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0007c0013 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0008c0009 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0009c0014 | 0/0 | 1437 | 2 | 1 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0010c0015 | 0/0 | 1437 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0011c0012 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0012c0007 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0013c0010 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0014c0011 | 0/0 | 1437 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0015c0027 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0016c0028 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0017c0034 | 0/0 | 1437 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0018c0029 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0019c0019 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0020c0030 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0021c0020 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0022c0031 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0023c0032 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0024c0018 | 0/0 | 1437 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0025c0017 | 0/0 | 1437 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0026c0016 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0027c0022 | 0/0 | 1759 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0028c0026 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0029c0025 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0030c0021 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2459 | 69 | 3 | 23 | 31 | 4 | 8 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0001c0001t0008 | 0/0 | 2459 | 3 | 0 | 1 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0001c0001t0011 | 0/0 | 2459 | 2 | 0 | 1 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0001c0001t0012 | 0/0 | 2459 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0001c0001t0019 | 0/0 | 2459 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0001c0001t0020 | 0/0 | 2459 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0001c0001t0022 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0001c0001t0025 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0001c0001t0028 | 0/0 | 2459 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0001c0033t0001 | 0/0 | 2459 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0002c0002t0002 | 0/0 | 2458 | 25 | 0 | 0 | 24 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0002c0002t0007 | 0/0 | 2458 | 5 | 0 | 4 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0002c0002t0015 | 0/0 | 2459 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0002c0002t0027 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0002c0023t0002 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0002c0024t0007 | 0/0 | 2458 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0003c0003t0003 | 1/0 | 2465 | 18 | 0 | 3 | 14 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0003c0003t0013 | 0/0 | 2464 | 2 | 0 | 0 | 1 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0003c0008t0003 | 0/0 | 2465 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0004c0004t0004 | 0/1 | 2464 | 16 | 1 | 2 | 10 | 1 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0004c0004t0014 | 0/0 | 2465 | 2 | 0 | 0 | 1 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0004c0004t0026 | 0/0 | 2464 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0005c0005t0005 | 0/0 | 2459 | 8 | 2 | 1 | 2 | 1 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0006c0006t0006 | 0/0 | 2465 | 4 | 0 | 0 | 4 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0006c0006t0010 | 0/0 | 2465 | 2 | 1 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0007c0013t0008 | 0/0 | 2459 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0008c0009t0006 | 0/0 | 2465 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0008c0009t0016 | 0/0 | 2465 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0009c0014t0001 | 0/0 | 2459 | 2 | 1 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0010c0015t0001 | 0/0 | 2459 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0011c0012t0009 | 0/0 | 2459 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0012c0007t0021 | 0/0 | 2459 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0012c0007t0024 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0013c0010t0004 | 0/0 | 2464 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0014c0011t0004 | 0/0 | 2464 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0015c0027t0005 | 0/0 | 2459 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0016c0028t0005 | 0/0 | 2459 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0017c0034t0017 | 0/0 | 2459 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0018c0029t0001 | 0/0 | 2459 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0019c0019t0006 | 0/0 | 2465 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0020c0030t0001 | 0/0 | 2459 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0021c0020t0006 | 0/0 | 2465 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0022c0031t0001 | 0/0 | 2459 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0023c0032t0001 | 0/0 | 2459 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0024c0018t0003 | 0/0 | 2465 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0025c0017t0003 | 0/0 | 2465 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0026c0016t0003 | 0/0 | 2465 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0027c0022t0018 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0028c0026t0004 | 0/0 | 2464 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0029c0025t0023 | 0/0 | 2464 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
a0030c0021t0009 | 0/0 | 2459 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | copy fasta | chr1 | 13166848 | 13184459 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 40 | 1 | 15 | 17 | 1 | 6 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0011 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0008g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0008g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0011g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0011g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0012g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0012g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0019g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0020g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0022g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0025g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0001t0028g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0001c0033t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0002c0002t0002g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0002c0002t0002g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0002c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0002c0002t0007g0003 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0002c0002t0015g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0002c0002t0027g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0002c0023t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0002c0024t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0003c0003t0003g0004 | 1/0 | 9 | 0 | 2 | 6 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0003c0003t0003g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0003c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0003c0003t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0003c0003t0013g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0003c0003t0013g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0003c0008t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0004c0004t0004g0002 | 0/1 | 13 | 0 | 2 | 9 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0004c0004t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0004c0004t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0004c0004t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0004c0004t0014g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0004c0004t0014g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0004c0004t0026g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0005c0005t0005g0006 | 0/0 | 6 | 2 | 0 | 2 | 0 | 2 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0005c0005t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0005c0005t0005g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0006c0006t0006g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0006c0006t0006g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0006c0006t0010g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0007c0013t0008g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0007c0013t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0008c0009t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0008c0009t0016g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0009c0014t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0009c0014t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0010c0015t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0011c0012t0009g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0012c0007t0021g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0012c0007t0024g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0013c0010t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0014c0011t0004g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0015c0027t0005g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0016c0028t0005g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0017c0034t0017g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0018c0029t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0019c0019t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0020c0030t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0021c0020t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0022c0031t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0023c0032t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0024c0018t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0025c0017t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0026c0016t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0027c0022t0018g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0028c0026t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0029c0025t0023g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
a0030c0021t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00140 | hp2 | a0005 | c0005 | t0005 | g0038 | EUR | GBR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00323 | hp1 | a0004 | c0004 | t0004 | g0042 | EUR | FIN | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00438 | hp1 | a0020 | c0030 | t0001 | g0001 | EAS | CHS | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00438 | hp2 | a0001 | c0033 | t0001 | g0001 | EAS | CHS | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00597 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | CHS | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00609 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | CHS | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00642 | hp2 | a0017 | c0034 | t0017 | g0061 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00738 | hp1 | a0001 | c0001 | t0008 | g0068 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01070 | hp1 | a0001 | c0001 | t0019 | g0001 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01109 | hp1 | a0001 | c0001 | t0012 | g0065 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01109 | hp2 | a0001 | c0001 | t0012 | g0064 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01167 | hp1 | a0006 | c0006 | t0010 | g0009 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01167 | hp2 | a0003 | c0003 | t0003 | g0004 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01168 | hp1 | a0005 | c0005 | t0005 | g0037 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01168 | hp2 | a0009 | c0014 | t0001 | g0063 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01175 | hp1 | a0004 | c0004 | t0004 | g0002 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01256 | hp2 | a0014 | c0011 | t0004 | g0002 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01258 | hp1 | a0014 | c0011 | t0004 | g0002 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01346 | hp1 | a0010 | c0015 | t0001 | g0001 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01361 | hp2 | a0001 | c0001 | t0028 | g0001 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01433 | hp1 | a0003 | c0003 | t0003 | g0027 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01433 | hp2 | a0025 | c0017 | t0003 | g0028 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01891 | hp1 | a0007 | c0013 | t0008 | g0001 | AFR | ACB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01891 | hp2 | a0007 | c0013 | t0008 | g0048 | AFR | ACB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01934 | hp1 | a0004 | c0004 | t0004 | g0002 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01934 | hp2 | a0001 | c0001 | t0011 | g0060 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01952 | hp1 | a0024 | c0018 | t0003 | g0004 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01952 | hp2 | a0002 | c0002 | t0007 | g0003 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01975 | hp1 | a0002 | c0002 | t0007 | g0003 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01978 | hp1 | a0002 | c0002 | t0015 | g0003 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01978 | hp2 | a0002 | c0002 | t0015 | g0003 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02004 | hp1 | a0003 | c0003 | t0003 | g0004 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02015 | hp2 | a0026 | c0016 | t0003 | g0029 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02071 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02074 | hp2 | a0003 | c0008 | t0003 | g0004 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02148 | hp1 | a0002 | c0002 | t0007 | g0003 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02155 | hp1 | a0006 | c0006 | t0006 | g0009 | EAS | CDX | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02155 | hp2 | a0001 | c0001 | t0008 | g0017 | EAS | CDX | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02273 | hp1 | a0002 | c0002 | t0007 | g0003 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02451 | hp1 | a0002 | c0002 | t0027 | g0005 | AFR | ACB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02451 | hp2 | a0030 | c0021 | t0009 | g0058 | AFR | ACB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02615 | hp1 | a0023 | c0032 | t0001 | g0057 | AFR | GWD | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02615 | hp2 | a0021 | c0020 | t0006 | g0023 | AFR | GWD | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02717 | hp1 | a0019 | c0019 | t0006 | g0024 | AFR | GWD | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02717 | hp2 | a0018 | c0029 | t0001 | g0066 | AFR | GWD | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02735 | hp2 | a0004 | c0004 | t0014 | g0002 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03139 | hp1 | a0013 | c0010 | t0004 | g0015 | AFR | ESN | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03139 | hp2 | a0004 | c0004 | t0026 | g0045 | AFR | ESN | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03453 | hp1 | a0027 | c0022 | t0018 | g0039 | AFR | MSL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03486 | hp1 | a0008 | c0009 | t0016 | g0021 | AFR | MSL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03486 | hp2 | a0011 | c0012 | t0009 | g0019 | AFR | MSL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03490 | hp1 | a0003 | c0003 | t0013 | g0004 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03490 | hp2 | a0005 | c0005 | t0005 | g0006 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03579 | hp1 | a0012 | c0007 | t0021 | g0016 | AFR | MSL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03579 | hp2 | a0004 | c0004 | t0004 | g0040 | AFR | MSL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03654 | hp2 | a0029 | c0025 | t0023 | g0002 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03704 | hp2 | a0004 | c0004 | t0004 | g0002 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03831 | hp1 | a0028 | c0026 | t0004 | g0041 | SAS | BEB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03831 | hp2 | a0002 | c0002 | t0007 | g0003 | SAS | BEB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0030 | SAS | BEB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG04184 | hp1 | a0015 | c0027 | t0005 | g0006 | SAS | BEB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG04184 | hp2 | a0005 | c0005 | t0005 | g0006 | SAS | BEB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG04199 | hp1 | a0001 | c0001 | t0011 | g0059 | SAS | STU | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG04199 | hp2 | a0016 | c0028 | t0005 | g0006 | SAS | STU | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18942 | hp1 | a0002 | c0024 | t0007 | g0003 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18942 | hp2 | a0001 | c0001 | t0025 | g0010 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18945 | hp1 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18949 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18953 | hp2 | a0006 | c0006 | t0006 | g0013 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18954 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18954 | hp2 | a0003 | c0003 | t0003 | g0026 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18959 | hp1 | a0004 | c0004 | t0014 | g0043 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18960 | hp2 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18962 | hp1 | a0003 | c0003 | t0013 | g0025 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18962 | hp2 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18968 | hp2 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18970 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18975 | hp1 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18975 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18976 | hp1 | a0006 | c0006 | t0006 | g0009 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18976 | hp2 | a0001 | c0001 | t0008 | g0017 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18977 | hp2 | a0006 | c0006 | t0006 | g0013 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18980 | hp2 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18981 | hp2 | a0003 | c0008 | t0003 | g0004 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18983 | hp1 | a0022 | c0031 | t0001 | g0007 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18990 | hp2 | a0002 | c0023 | t0002 | g0005 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18992 | hp2 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18994 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18995 | hp1 | a0001 | c0001 | t0022 | g0062 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18995 | hp2 | a0005 | c0005 | t0005 | g0006 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19000 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19004 | hp1 | a0001 | c0001 | t0020 | g0007 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19004 | hp2 | a0005 | c0005 | t0005 | g0006 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19064 | hp1 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19067 | hp1 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19067 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19070 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19070 | hp2 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19077 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19079 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19082 | hp1 | a0004 | c0004 | t0004 | g0002 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19084 | hp2 | a0004 | c0004 | t0004 | g0044 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19240 | hp1 | a0013 | c0010 | t0004 | g0015 | AFR | YRI | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA19240 | hp2 | a0006 | c0006 | t0010 | g0009 | AFR | YRI | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01123 | hp1 | a0010 | c0015 | t0001 | g0001 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02486 | hp1 | a0008 | c0009 | t0006 | g0022 | AFR | ACB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG02486 | hp2 | a0011 | c0012 | t0009 | g0019 | AFR | ACB | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG06807 | hp1 | a0005 | c0005 | t0005 | g0006 | AFR | USA | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
HG06807 | hp2 | a0012 | c0007 | t0024 | g0016 | AFR | USA | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA18955 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA20300 | hp1 | a0009 | c0014 | t0001 | g0011 | AFR | USA | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
NA20300 | hp2 | a0005 | c0005 | t0005 | g0006 | AFR | USA | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
homoSapiens_chm13v2 | hp1 | a0004 | c0004 | t0004 | g0002 | REF | REF | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
homoSapiens_grch38 | hp1 | a0003 | c0003 | t0003 | g0004 | REF | REF | PRAMEF9_chr1_13166848_13184459 | PRAMEF9 | chr1 | 13166848 | 13184459 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:13175324
|
C | T | 1 | a0030 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.44C>T | p.Ala15Val | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 745/2465 | 44/1437 | 15/478 | chr1 | 13175324 | ||
chr1:13175335
|
C | G | 1 | a0030 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.55C>G | p.Leu19Val | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 756/2465 | 55/1437 | 19/478 | chr1 | 13175335 | ||
chr1:13175357
|
C | T | 5 | a0004a0013a0014others(2): Show | 25 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(22): Show |
missense_variant | MODERATE | c.77C>T | p.Ala26Val | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 778/2465 | 77/1437 | 26/478 | chr1 | 13175357 | ||
chr1:13175471
|
G | A | 3 | a0005a0015a0016 | 10 | HG00140.hp2 HG01168.hp1 HG03490.hp2 others(7): Show |
missense_variant | MODERATE | c.191G>A | p.Arg64His | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 892/2465 | 191/1437 | 64/478 | chr1 | 13175471 | ||
chr1:13175474
|
G | A | 1 | a0015 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.194G>A | p.Arg65His | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 895/2465 | 194/1437 | 65/478 | chr1 | 13175474 | ||
chr1:13175500
|
A | T | 1 | a0017 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.220A>T | p.Met74Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 921/2465 | 220/1437 | 74/478 | chr1 | 13175500 | ||
chr1:13175535
|
T | G | 1 | a0027 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.255T>G | p.Asp85Glu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 956/2465 | 255/1437 | 85/478 | chr1 | 13175535 | ||
chr1:13175555
|
C | A | 1 | a0027 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.275C>A | p.Thr92Asn | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 976/2465 | 275/1437 | 92/478 | chr1 | 13175555 | ||
chr1:13175558
|
A | T | 1 | a0027 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.278A>T | p.Gln93Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 979/2465 | 278/1437 | 93/478 | chr1 | 13175558 | ||
chr1:13175561
|
G | A | 3 | a0005a0015a0016 | 10 | HG00140.hp2 HG01168.hp1 HG03490.hp2 others(7): Show |
missense_variant | MODERATE | c.281G>A | p.Gly94Glu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 982/2465 | 281/1437 | 94/478 | chr1 | 13175561 | ||
chr1:13175566
|
T | C | 3 | a0017a0026a0027 | 3 | HG00642.hp2 HG02015.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.286T>C | p.Cys96Arg | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 987/2465 | 286/1437 | 96/478 | chr1 | 13175566 | ||
chr1:13176318
|
G | A | 1 | a0027 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.371G>A | p.Arg124His | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1072/2465 | 371/1437 | 124/478 | chr1 | 13176318 | ||
chr1:13176324
|
C | G | 16 | a0001a0006a0007others(13): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
missense_variant | MODERATE | c.377C>G | p.Ser126Cys | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1078/2465 | 377/1437 | 126/478 | chr1 | 13176324 | ||
chr1:13176351
|
C | A | 2 | a0007a0027 | 3 | HG01891.hp1 HG01891.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.404C>A | p.Thr135Lys | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1105/2465 | 404/1437 | 135/478 | chr1 | 13176351 | ||
chr1:13176384
|
A | G | 21 | a0001a0002a0005others(18): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
missense_variant | MODERATE | c.437A>G | p.Gln146Arg | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1138/2465 | 437/1437 | 146/478 | chr1 | 13176384 | ||
chr1:13176415
|
G | A | 1 | a0018 | 1 | HG02717.hp2 | stop_gained | HIGH | c.468G>A | p.Trp156* | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1169/2465 | 468/1437 | 156/478 | chr1 | 13176415 | ||
chr1:13176440
|
T | C | 3 | a0008a0012a0019 | 5 | HG02486.hp1 HG02717.hp1 HG03486.hp1 others(2): Show |
missense_variant | MODERATE | c.493T>C | p.Tyr165His | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1194/2465 | 493/1437 | 165/478 | chr1 | 13176440 | ||
chr1:13176450
|
A | G | 3 | a0008a0012a0027 | 5 | HG02486.hp1 HG03453.hp1 HG03486.hp1 others(2): Show |
missense_variant | MODERATE | c.503A>G | p.Tyr168Cys | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1204/2465 | 503/1437 | 168/478 | chr1 | 13176450 | ||
chr1:13176451
|
C | A | 1 | a0009 | 2 | HG01168.hp2 NA20300.hp1 |
stop_gained | HIGH | c.504C>A | p.Tyr168* | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1205/2465 | 504/1437 | 168/478 | chr1 | 13176451 | ||
chr1:13176517
|
G | C | 1 | a0020 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.570G>C | p.Leu190Phe | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1271/2465 | 570/1437 | 190/478 | chr1 | 13176517 | ||
chr1:13176595
|
C | A | 1 | a0017 | 1 | HG00642.hp2 | stop_gained | HIGH | c.648C>A | p.Cys216* | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1349/2465 | 648/1437 | 216/478 | chr1 | 13176595 | ||
chr1:13176728
|
C | A | 4 | a0004a0014a0028others(1): Show | 23 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(20): Show |
missense_variant | MODERATE | c.781C>A | p.Gln261Lys | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1482/2465 | 781/1437 | 261/478 | chr1 | 13176728 | ||
chr1:13176756
|
A | G | 1 | a0027 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.809A>G | p.His270Arg | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1510/2465 | 809/1437 | 270/478 | chr1 | 13176756 | ||
chr1:13176774
|
A | C | 3 | a0002a0013a0027 | 38 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(35): Show |
missense_variant | MODERATE | c.827A>C | p.Tyr276Ser | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1528/2465 | 827/1437 | 276/478 | chr1 | 13176774 | ||
chr1:13176776
|
A | ATGAACTC others(315): Show |
1 | a0027 | 1 | HG03453.hp1 | frameshift_variant&stop_gained | HIGH | c.840_841insCCTTTTTT others(314): Show |
p.Ser281fs | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1542/2465 | 841/1437 | 281/478 | INFO_REALIGN_3_PRIME | chr1 | 13176776 | |
chr1:13176821
|
A | G | 1 | a0017 | 1 | HG00642.hp2 | missense_variant&splice_region_variant | MODERATE | c.874A>G | p.Ser292Gly | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1575/2465 | 874/1437 | 292/478 | chr1 | 13176821 | ||
chr1:13178614
|
G | A | 1 | a0016 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.919G>A | p.Val307Met | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1620/2465 | 919/1437 | 307/478 | chr1 | 13178614 | ||
chr1:13178639
|
A | G | 1 | a0023 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.944A>G | p.His315Arg | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1645/2465 | 944/1437 | 315/478 | chr1 | 13178639 | ||
chr1:13178665
|
C | G | 1 | a0024 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.970C>G | p.Gln324Glu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1671/2465 | 970/1437 | 324/478 | chr1 | 13178665 | ||
chr1:13178750
|
C | T | 11 | a0001a0007a0009others(8): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
missense_variant | MODERATE | c.1055C>T | p.Ala352Val | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1756/2465 | 1055/1437 | 352/478 | chr1 | 13178750 | ||
chr1:13178789
|
T | C | 1 | a0022 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.1094T>C | p.Ile365Thr | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1795/2465 | 1094/1437 | 365/478 | chr1 | 13178789 | ||
chr1:13178833
|
T | A | 1 | a0027 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1138T>A | p.Phe380Ile | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1839/2465 | 1138/1437 | 380/478 | chr1 | 13178833 | ||
chr1:13178835
|
T | G | 12 | a0001a0007a0009others(9): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
missense_variant | MODERATE | c.1140T>G | p.Phe380Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1841/2465 | 1140/1437 | 380/478 | chr1 | 13178835 | ||
chr1:13178845
|
G | A | 1 | a0027 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1150G>A | p.Ala384Thr | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1851/2465 | 1150/1437 | 384/478 | chr1 | 13178845 | ||
chr1:13178873
|
C | G | 2 | a0027a0028 | 2 | HG03453.hp1 HG03831.hp1 |
missense_variant | MODERATE | c.1178C>G | p.Ser393Cys | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1879/2465 | 1178/1437 | 393/478 | chr1 | 13178873 | ||
chr1:13178912
|
T | C | 2 | a0011a0030 | 3 | HG02451.hp2 HG02486.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.1217T>C | p.Ile406Thr | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1918/2465 | 1217/1437 | 406/478 | chr1 | 13178912 | ||
chr1:13178929
|
G | C | 2 | a0010a0029 | 3 | HG01123.hp1 HG01346.hp1 HG03654.hp2 |
missense_variant | MODERATE | c.1234G>C | p.Val412Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1935/2465 | 1234/1437 | 412/478 | chr1 | 13178929 | ||
chr1:13178935
|
G | C | 2 | a0027a0029 | 2 | HG03453.hp1 HG03654.hp2 |
missense_variant | MODERATE | c.1240G>C | p.Val414Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1941/2465 | 1240/1437 | 414/478 | chr1 | 13178935 | ||
chr1:13178951
|
G | A | 14 | a0001a0005a0007others(11): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
missense_variant | MODERATE | c.1256G>A | p.Arg419Gln | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1957/2465 | 1256/1437 | 419/478 | chr1 | 13178951 | ||
chr1:13178963
|
G | A | 4 | a0006a0008a0019others(1): Show | 10 | HG01167.hp1 HG02155.hp1 HG02486.hp1 others(7): Show |
missense_variant | MODERATE | c.1268G>A | p.Gly423Asp | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1969/2465 | 1268/1437 | 423/478 | chr1 | 13178963 | ||
chr1:13179021
|
C | G | 1 | a0025 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1326C>G | p.Asn442Lys | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 2027/2465 | 1326/1437 | 442/478 | chr1 | 13179021 | ||
chr1:13179030
|
G | T | 1 | a0010 | 2 | HG01123.hp1 HG01346.hp1 |
missense_variant | MODERATE | c.1335G>T | p.Arg445Ser | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 2036/2465 | 1335/1437 | 445/478 | chr1 | 13179030 | ||
chr1:13179065
|
T | C | 1 | a0027 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1370T>C | p.Ile457Thr | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 2071/2465 | 1370/1437 | 457/478 | chr1 | 13179065 | ||
chr1:13179070
|
A | T | 1 | a0027 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1375A>T | p.Asn459Tyr | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 2076/2465 | 1375/1437 | 459/478 | chr1 | 13179070 | ||
chr1:13179071
|
A | G | 1 | a0027 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1376A>G | p.Asn459Ser | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 2077/2465 | 1376/1437 | 459/478 | chr1 | 13179071 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:13175322
|
G | T | 25 | a0001c0001a0001c0033a0002c0002others(22): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
synonymous_variant | LOW | c.42G>T | p.Leu14Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 743/2465 | 42/1437 | 14/478 | chr1 | 13175322 | ||
chr1:13175325
|
G | A | 1 | a0027c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.45G>A | p.Ala15Ala | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 746/2465 | 45/1437 | 15/478 | chr1 | 13175325 | ||
chr1:13175352
|
C | T | 15 | a0001c0001a0001c0033a0005c0005others(12): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
synonymous_variant | LOW | c.72C>T | p.Ala24Ala | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 773/2465 | 72/1437 | 24/478 | chr1 | 13175352 | ||
chr1:13175454
|
G | A | 1 | a0011c0012 | 2 | HG02486.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.174G>A | p.Val58Val | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/4 | 875/2465 | 174/1437 | 58/478 | chr1 | 13175454 | ||
chr1:13176367
|
T | C | 1 | a0002c0023 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.420T>C | p.Cys140Cys | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1121/2465 | 420/1437 | 140/478 | chr1 | 13176367 | ||
chr1:13176625
|
T | C | 3 | a0002c0002a0002c0023a0002c0024 | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
synonymous_variant | LOW | c.678T>C | p.Phe226Phe | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1379/2465 | 678/1437 | 226/478 | chr1 | 13176625 | ||
chr1:13176673
|
C | T | 1 | a0001c0033 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.726C>T | p.Ser242Ser | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/4 | 1427/2465 | 726/1437 | 242/478 | chr1 | 13176673 | ||
chr1:13178643
|
A | C | 3 | a0005c0005a0015c0027a0016c0028 | 10 | HG00140.hp2 HG01168.hp1 HG03490.hp2 others(7): Show |
synonymous_variant | LOW | c.948A>C | p.Leu316Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1649/2465 | 948/1437 | 316/478 | chr1 | 13178643 | ||
chr1:13178682
|
C | T | 1 | a0027c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.987C>T | p.Asp329Asp | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1688/2465 | 987/1437 | 329/478 | chr1 | 13178682 | ||
chr1:13178703
|
C | A | 1 | a0027c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1008C>A | p.Thr336Thr | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1709/2465 | 1008/1437 | 336/478 | chr1 | 13178703 | ||
chr1:13178764
|
T | C | 16 | a0001c0001a0001c0033a0005c0005others(13): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
synonymous_variant | LOW | c.1069T>C | p.Leu357Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1770/2465 | 1069/1437 | 357/478 | chr1 | 13178764 | ||
chr1:13178805
|
C | T | 15 | a0001c0001a0001c0033a0005c0005others(12): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
synonymous_variant | LOW | c.1110C>T | p.Asn370Asn | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1811/2465 | 1110/1437 | 370/478 | chr1 | 13178805 | ||
chr1:13178812
|
C | T | 1 | a0027c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1117C>T | p.Leu373Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1818/2465 | 1117/1437 | 373/478 | chr1 | 13178812 | ||
chr1:13178820
|
C | A | 1 | a0002c0023 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.1125C>A | p.Ala375Ala | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1826/2465 | 1125/1437 | 375/478 | chr1 | 13178820 | ||
chr1:13178820
|
C | G | 2 | a0002c0002a0002c0024 | 34 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(31): Show |
synonymous_variant | LOW | c.1125C>G | p.Ala375Ala | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1826/2465 | 1125/1437 | 375/478 | chr1 | 13178820 | ||
chr1:13178823
|
G | C | 1 | a0027c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1128G>C | p.Leu376Leu | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1829/2465 | 1128/1437 | 376/478 | chr1 | 13178823 | ||
chr1:13178844
|
T | C | 3 | a0002c0024a0022c0031a0027c0022 | 3 | HG03453.hp1 NA18942.hp1 NA18983.hp1 |
synonymous_variant | LOW | c.1149T>C | p.Asn383Asn | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1850/2465 | 1149/1437 | 383/478 | chr1 | 13178844 | ||
chr1:13178949
|
G | C | 1 | a0027c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1254G>C | p.Pro418Pro | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 1955/2465 | 1254/1437 | 418/478 | chr1 | 13178949 | ||
chr1:13179030
|
G | A | 1 | a0027c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1335G>A | p.Arg445Arg | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 2036/2465 | 1335/1437 | 445/478 | chr1 | 13179030 | ||
chr1:13179057
|
T | C | 1 | a0027c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1362T>C | p.Phe454Phe | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 2063/2465 | 1362/1437 | 454/478 | chr1 | 13179057 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:13171863
|
C | G | 1 | a0001c0001t0028 | 1 | HG01361.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-686C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | chr1 | 13171863 | ||||||
chr1:13171870
|
T | C | 6 | a0006c0006t0006a0006c0006t0010a0008c0009t0006others(3): Show | 10 | HG01167.hp1 HG02155.hp1 HG02486.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-679T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3411 | chr1 | 13171870 | |||||
chr1:13171876
|
TTC | T | 5 | a0002c0002t0002a0002c0002t0007a0002c0002t0027others(2): Show | 33 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-671_-670delCT | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3402 | INFO_REALIGN_3_PRIME | chr1 | 13171876 | ||||
chr1:13171877
|
TC | T | 1 | a0002c0002t0015 | 2 | HG01978.hp1 HG01978.hp2 |
5_prime_UTR_variant | MODIFIER | c.-671delC | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3403 | chr1 | 13171877 | |||||
chr1:13171878
|
CT | C | 30 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(27): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
5_prime_UTR_variant | MODIFIER | c.-650delT | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3382 | INFO_REALIGN_3_PRIME | chr1 | 13171878 | ||||
chr1:13171879
|
T | G | 1 | a0002c0002t0015 | 2 | HG01978.hp1 HG01978.hp2 |
5_prime_UTR_variant | MODIFIER | c.-670T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3402 | chr1 | 13171879 | |||||
chr1:13171880
|
T | G | 5 | a0002c0002t0002a0002c0002t0007a0002c0002t0027others(2): Show | 33 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(30): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-669T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | chr1 | 13171880 | ||||||
chr1:13171882
|
T | C | 1 | a0001c0001t0022 | 1 | NA18995.hp1 | 5_prime_UTR_variant | MODIFIER | c.-667T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3399 | chr1 | 13171882 | |||||
chr1:13171883
|
T | C | 23 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(20): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
5_prime_UTR_variant | MODIFIER | c.-666T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3398 | chr1 | 13171883 | |||||
chr1:13171884
|
T | C | 2 | a0001c0001t0025a0012c0007t0024 | 2 | HG06807.hp2 NA18942.hp2 |
5_prime_UTR_variant | MODIFIER | c.-665T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3397 | chr1 | 13171884 | |||||
chr1:13171885
|
T | C | 1 | a0029c0025t0023 | 1 | HG03654.hp2 | 5_prime_UTR_variant | MODIFIER | c.-664T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3396 | chr1 | 13171885 | |||||
chr1:13171887
|
T | C | 2 | a0001c0001t0011a0001c0001t0028 | 3 | HG01361.hp2 HG01934.hp2 HG04199.hp1 |
5_prime_UTR_variant | MODIFIER | c.-662T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3394 | chr1 | 13171887 | |||||
chr1:13171898
|
T | G | 6 | a0002c0002t0002a0002c0002t0007a0002c0002t0015others(3): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-651T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | chr1 | 13171898 | ||||||
chr1:13171899
|
T | A | 3 | a0011c0012t0009a0017c0034t0017a0030c0021t0009 | 4 | HG00642.hp2 HG02451.hp2 HG02486.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-650T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3382 | chr1 | 13171899 | |||||
chr1:13171948
|
C | T | 26 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(23): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
5_prime_UTR_variant | MODIFIER | c.-601C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3333 | chr1 | 13171948 | |||||
chr1:13171977
|
G | C | 6 | a0002c0002t0002a0002c0002t0007a0002c0002t0015others(3): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-572G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3304 | chr1 | 13171977 | |||||
chr1:13171978
|
G | C | 6 | a0002c0002t0002a0002c0002t0007a0002c0002t0015others(3): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-571G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3303 | chr1 | 13171978 | |||||
chr1:13172018
|
G | T | 6 | a0002c0002t0002a0002c0002t0007a0002c0002t0015others(3): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-531G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3263 | chr1 | 13172018 | |||||
chr1:13172020
|
G | T | 19 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(16): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
5_prime_UTR_variant | MODIFIER | c.-529G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3261 | chr1 | 13172020 | |||||
chr1:13172068
|
T | A | 6 | a0002c0002t0002a0002c0002t0007a0002c0002t0015others(3): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-481T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3213 | chr1 | 13172068 | |||||
chr1:13172089
|
T | C | 27 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(24): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
5_prime_UTR_variant | MODIFIER | c.-460T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3192 | chr1 | 13172089 | |||||
chr1:13172090
|
G | C | 4 | a0005c0005t0005a0015c0027t0005a0016c0028t0005others(1): Show | 11 | HG00140.hp2 HG01168.hp1 HG03453.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-459G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3191 | chr1 | 13172090 | |||||
chr1:13172161
|
C | G | 26 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(23): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
5_prime_UTR_variant | MODIFIER | c.-388C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3120 | chr1 | 13172161 | |||||
chr1:13172196
|
T | G | 6 | a0002c0002t0002a0002c0002t0007a0002c0002t0015others(3): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-353T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3085 | chr1 | 13172196 | |||||
chr1:13172209
|
C | A | 6 | a0002c0002t0002a0002c0002t0007a0002c0002t0015others(3): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-340C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 3072 | chr1 | 13172209 | |||||
chr1:13172233
|
G | C | 6 | a0002c0002t0002a0002c0002t0007a0002c0002t0015others(3): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-316G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | chr1 | 13172233 | ||||||
chr1:13172305
|
C | G | 6 | a0002c0002t0002a0002c0002t0007a0002c0002t0015others(3): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-244C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 2976 | chr1 | 13172305 | |||||
chr1:13172322
|
GGTGGA | G | 32 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(29): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
5_prime_UTR_variant | MODIFIER | c.-220_-216delTGGAG | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 2948 | INFO_REALIGN_3_PRIME | chr1 | 13172322 | ||||
chr1:13172343
|
T | G | 1 | a0004c0004t0026 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-206T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 2938 | chr1 | 13172343 | |||||
chr1:13172405
|
G | A | 1 | a0001c0001t0019 | 1 | HG01070.hp1 | 5_prime_UTR_variant | MODIFIER | c.-144G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 2876 | chr1 | 13172405 | |||||
chr1:13172410
|
A | G | 45 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(42): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-139A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | chr1 | 13172410 | ||||||
chr1:13172488
|
G | C | 26 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(23): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
5_prime_UTR_variant | MODIFIER | c.-61G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/4 | 2793 | chr1 | 13172488 | |||||
chr1:13179149
|
A | G | 1 | a0017c0034t0017 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*17A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 17 | chr1 | 13179149 | |||||
chr1:13179153
|
G | A | 1 | a0017c0034t0017 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*21G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 21 | chr1 | 13179153 | |||||
chr1:13179194
|
C | T | 1 | a0027c0022t0018 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*62C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 62 | chr1 | 13179194 | |||||
chr1:13179199
|
T | A | 3 | a0001c0001t0008a0001c0001t0012a0007c0013t0008 | 7 | HG00738.hp1 HG01109.hp1 HG01109.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*67T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 67 | chr1 | 13179199 | |||||
chr1:13179235
|
A | G | 1 | a0008c0009t0016 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*103A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 103 | chr1 | 13179235 | |||||
chr1:13179245
|
T | C | 1 | a0001c0001t0020 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 113 | chr1 | 13179245 | |||||
chr1:13179246
|
A | G | 1 | a0008c0009t0016 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*114A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 114 | chr1 | 13179246 | |||||
chr1:13179269
|
A | T | 23 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(20): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*137A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 137 | chr1 | 13179269 | |||||
chr1:13179287
|
A | C | 2 | a0002c0002t0027a0027c0022t0018 | 2 | HG02451.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*155A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 155 | chr1 | 13179287 | |||||
chr1:13179319
|
T | C | 17 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(14): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*187T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 187 | chr1 | 13179319 | |||||
chr1:13179338
|
A | G | 1 | a0002c0002t0027 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*206A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 206 | chr1 | 13179338 | |||||
chr1:13179394
|
A | C | 3 | a0002c0002t0007a0002c0002t0015a0002c0024t0007 | 8 | HG01952.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*262A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 4/4 | 262 | chr1 | 13179394 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:13172570
|
C | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(41): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.-17+38C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172570 | ||||||
chr1:13172574
|
C | G | 11 | a0004c0004t0004g0002a0004c0004t0004g0040a0004c0004t0004g0042others(8): Show | 25 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.-17+42C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172574 | ||||||
chr1:13172583
|
A | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(62): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-17+51A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172583 | ||||||
chr1:13172610
|
A | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(73): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.-17+78A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172610 | ||||||
chr1:13172618
|
G | C | 15 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(12): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+86G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172618 | ||||||
chr1:13172641
|
TATA | T | 15 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(12): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+110_-17+112del others(3): Show |
PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172641 | ||||||
chr1:13172646
|
A | T | 15 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(12): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+114A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172646 | ||||||
chr1:13172648
|
A | T | 15 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(12): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+116A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172648 | ||||||
chr1:13172649
|
T | C | 15 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(12): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+117T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172649 | ||||||
chr1:13172662
|
T | G | 15 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(12): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+130T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172662 | ||||||
chr1:13172665
|
A | G | 15 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(12): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+133A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172665 | ||||||
chr1:13172675
|
G | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(56): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.-17+143G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172675 | ||||||
chr1:13172695
|
C | A | 1 | a0001c0001t0001g0046 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-17+163C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172695 | ||||||
chr1:13172885
|
A | G | 15 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(12): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+353A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172885 | ||||||
chr1:13172935
|
C | T | 11 | a0004c0004t0004g0002a0004c0004t0004g0040a0004c0004t0004g0042others(8): Show | 25 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.-17+403C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172935 | ||||||
chr1:13172943
|
A | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+411A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172943 | ||||||
chr1:13172947
|
C | A | 15 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(12): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+415C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172947 | ||||||
chr1:13172960
|
A | C | 32 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(29): Show | 71 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.-17+428A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172960 | ||||||
chr1:13172965
|
T | C | 6 | a0005c0005t0005g0006a0005c0005t0005g0037a0005c0005t0005g0038others(3): Show | 11 | HG00140.hp2 HG01168.hp1 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17+433T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13172965 | ||||||
chr1:13173014
|
T | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(41): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.-17+482T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173014 | ||||||
chr1:13173044
|
T | G | 1 | a0008c0009t0016g0021 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-17+512T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173044 | ||||||
chr1:13173084
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0020g0007others(1): Show | 11 | HG00558.hp2 HG02004.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17+552C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173084 | ||||||
chr1:13173091
|
G | T | 1 | a0026c0016t0003g0029 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-17+559G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173091 | ||||||
chr1:13173132
|
C | T | 6 | a0005c0005t0005g0006a0005c0005t0005g0037a0005c0005t0005g0038others(3): Show | 11 | HG00140.hp2 HG01168.hp1 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17+600C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173132 | ||||||
chr1:13173155
|
C | T | 1 | a0001c0001t0008g0068 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-17+623C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173155 | ||||||
chr1:13173220
|
T | C | 15 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(12): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+688T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173220 | ||||||
chr1:13173231
|
C | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(84): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.-17+699C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173231 | ||||||
chr1:13173265
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-17+733T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173265 | ||||||
chr1:13173298
|
C | CCAAAAA | 76 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(73): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.-17+772_-17+777dup others(6): Show |
PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 13173298 | |||||
chr1:13173310
|
T | C | 4 | a0008c0009t0006g0022a0008c0009t0016g0021a0019c0019t0006g0024others(1): Show | 4 | HG02486.hp1 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17+778T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173310 | ||||||
chr1:13173344
|
C | T | 15 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(12): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+812C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173344 | ||||||
chr1:13173384
|
G | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(46): Show | 107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.-17+852G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173384 | ||||||
chr1:13173431
|
C | A | 15 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(12): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+899C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173431 | ||||||
chr1:13173453
|
CAATCTT | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(62): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-17+922_-17+927del others(6): Show |
PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173453 | ||||||
chr1:13173460
|
G | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(62): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-17+928G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173460 | ||||||
chr1:13173481
|
T | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+949T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173481 | ||||||
chr1:13173542
|
A | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(46): Show | 107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.-17+1010A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173542 | ||||||
chr1:13173644
|
T | G | 52 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(49): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.-17+1112T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173644 | ||||||
chr1:13173682
|
A | G | 3 | a0006c0006t0006g0009a0006c0006t0006g0013a0006c0006t0010g0009 | 6 | HG01167.hp1 HG02155.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17+1150A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173682 | ||||||
chr1:13173687
|
C | A | 3 | a0006c0006t0006g0009a0006c0006t0006g0013a0006c0006t0010g0009 | 6 | HG01167.hp1 HG02155.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17+1155C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173687 | ||||||
chr1:13173778
|
G | A | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+1246G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173778 | ||||||
chr1:13173779
|
G | A | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+1247G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173779 | ||||||
chr1:13173804
|
G | A | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+1272G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173804 | ||||||
chr1:13173808
|
A | T | 1 | a0001c0001t0001g0067 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-17+1276A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173808 | ||||||
chr1:13173836
|
T | G | 11 | a0004c0004t0004g0002a0004c0004t0004g0040a0004c0004t0004g0042others(8): Show | 25 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.-17+1304T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173836 | ||||||
chr1:13173858
|
T | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+1326T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173858 | ||||||
chr1:13173870
|
C | T | 3 | a0002c0002t0002g0005a0002c0002t0027g0005a0002c0023t0002g0005 | 11 | HG00597.hp2 HG02071.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17+1338C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173870 | ||||||
chr1:13173880
|
T | A | 6 | a0004c0004t0004g0040a0006c0006t0006g0009a0006c0006t0006g0013others(3): Show | 9 | HG01167.hp1 HG01891.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17+1348T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173880 | ||||||
chr1:13173893
|
C | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+1361C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173893 | ||||||
chr1:13173919
|
G | A | 10 | a0004c0004t0004g0002a0004c0004t0004g0042a0004c0004t0004g0044others(7): Show | 24 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.-16-1346G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173919 | ||||||
chr1:13173940
|
C | A | 5 | a0006c0006t0006g0009a0006c0006t0006g0013a0006c0006t0010g0009others(2): Show | 8 | HG01167.hp1 HG02155.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16-1325C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173940 | ||||||
chr1:13173964
|
A | T | 6 | a0005c0005t0005g0006a0005c0005t0005g0037a0005c0005t0005g0038others(3): Show | 11 | HG00140.hp2 HG01168.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16-1301A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173964 | ||||||
chr1:13173982
|
C | T | 10 | a0001c0001t0001g0011a0001c0001t0001g0047a0001c0001t0012g0064others(7): Show | 11 | HG00140.hp1 HG00642.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16-1283C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173982 | ||||||
chr1:13173985
|
C | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-1280C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13173985 | ||||||
chr1:13174001
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(45): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.-16-1264A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174001 | ||||||
chr1:13174024
|
C | A | 1 | a0001c0001t0001g0049 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-16-1241C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174024 | ||||||
chr1:13174139
|
T | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(41): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.-16-1126T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174139 | ||||||
chr1:13174166
|
C | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-1099C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174166 | ||||||
chr1:13174174
|
C | A | 1 | a0001c0001t0001g0050 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-16-1091C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174174 | ||||||
chr1:13174247
|
T | A | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-1018T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174247 | ||||||
chr1:13174255
|
T | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(72): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.-16-1010T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174255 | ||||||
chr1:13174261
|
T | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-1004T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174261 | ||||||
chr1:13174270
|
G | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-995G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174270 | ||||||
chr1:13174272
|
G | A | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-993G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174272 | ||||||
chr1:13174275
|
G | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-990G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174275 | ||||||
chr1:13174280
|
T | C | 1 | a0028c0026t0004g0041 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-16-985T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174280 | ||||||
chr1:13174292
|
A | G | 1 | a0004c0004t0026g0045 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-16-973A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174292 | ||||||
chr1:13174322
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0025g0010 | 4 | HG02132.hp1 NA18942.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16-943T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174322 | ||||||
chr1:13174324
|
G | A | 11 | a0004c0004t0004g0002a0004c0004t0004g0040a0004c0004t0004g0042others(8): Show | 25 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.-16-941G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174324 | ||||||
chr1:13174357
|
C | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-908C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174357 | ||||||
chr1:13174368
|
C | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-897C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174368 | ||||||
chr1:13174369
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(44): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.-16-896A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174369 | ||||||
chr1:13174404
|
G | T | 7 | a0006c0006t0006g0009a0006c0006t0006g0013a0006c0006t0010g0009others(4): Show | 10 | HG01167.hp1 HG02155.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-16-861G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174404 | ||||||
chr1:13174481
|
A | C | 15 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(12): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-16-784A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174481 | ||||||
chr1:13174492
|
C | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(78): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-16-773C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174492 | ||||||
chr1:13174518
|
T | A | 1 | a0017c0034t0017g0061 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-16-747T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174518 | ||||||
chr1:13174543
|
G | C | 1 | a0017c0034t0017g0061 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-16-722G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174543 | ||||||
chr1:13174555
|
G | A | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-710G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174555 | ||||||
chr1:13174586
|
C | G | 1 | a0011c0012t0009g0019 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-16-679C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174586 | ||||||
chr1:13174615
|
C | G | 2 | a0001c0001t0012g0064a0001c0001t0012g0065 | 2 | HG01109.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.-16-650C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174615 | ||||||
chr1:13174632
|
G | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-633G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174632 | ||||||
chr1:13174641
|
C | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-624C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174641 | ||||||
chr1:13174699
|
T | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-566T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174699 | ||||||
chr1:13174743
|
A | G | 1 | a0001c0001t0001g0012 | 3 | HG00558.hp2 NA19083.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-16-522A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174743 | ||||||
chr1:13174855
|
T | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-410T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174855 | ||||||
chr1:13174876
|
A | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-389A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174876 | ||||||
chr1:13174921
|
C | T | 2 | a0023c0032t0001g0057a0027c0022t0018g0039 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-16-344C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174921 | ||||||
chr1:13174955
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(45): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.-16-310C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174955 | ||||||
chr1:13174958
|
T | C | 1 | a0003c0003t0003g0008 | 7 | HG00597.hp1 NA18954.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16-307T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13174958 | ||||||
chr1:13175055
|
A | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-210A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175055 | ||||||
chr1:13175065
|
C | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-200C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175065 | ||||||
chr1:13175076
|
G | A | 1 | a0005c0005t0005g0037 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-16-189G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175076 | ||||||
chr1:13175110
|
G | C | 5 | a0005c0005t0005g0006a0005c0005t0005g0037a0005c0005t0005g0038others(2): Show | 10 | HG00140.hp2 HG01168.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.-16-155G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175110 | ||||||
chr1:13175159
|
G | A | 2 | a0001c0001t0001g0067a0027c0022t0018g0039 | 2 | HG03453.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-16-106G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175159 | ||||||
chr1:13175162
|
G | C | 2 | a0001c0001t0001g0067a0027c0022t0018g0039 | 2 | HG03453.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-16-103G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175162 | ||||||
chr1:13175164
|
T | A | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-101T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175164 | ||||||
chr1:13175186
|
G | C | 6 | a0006c0006t0006g0009a0006c0006t0006g0013a0006c0006t0010g0009others(3): Show | 9 | HG01167.hp1 HG02155.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16-79G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175186 | ||||||
chr1:13175202
|
A | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-63A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175202 | ||||||
chr1:13175223
|
G | T | 6 | a0005c0005t0005g0006a0005c0005t0005g0037a0015c0027t0005g0006others(3): Show | 11 | HG01168.hp1 HG02615.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16-42G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175223 | ||||||
chr1:13175226
|
T | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-39T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175226 | ||||||
chr1:13175232
|
T | A | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-33T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 1/3 | chr1 | 13175232 | ||||||
chr1:13175583
|
C | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(46): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.293+10C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175583 | ||||||
chr1:13175635
|
G | C | 1 | a0001c0001t0001g0051 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.293+62G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175635 | ||||||
chr1:13175641
|
T | A | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.293+68T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175641 | ||||||
chr1:13175683
|
C | T | 1 | a0004c0004t0004g0044 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.293+110C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175683 | ||||||
chr1:13175734
|
G | C | 11 | a0004c0004t0004g0002a0004c0004t0004g0040a0004c0004t0004g0042others(8): Show | 25 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.293+161G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175734 | ||||||
chr1:13175745
|
G | A | 1 | a0021c0020t0006g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.293+172G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175745 | ||||||
chr1:13175766
|
T | C | 2 | a0021c0020t0006g0023a0023c0032t0001g0057 | 2 | HG02615.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.293+193T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175766 | ||||||
chr1:13175783
|
G | C | 3 | a0008c0009t0006g0022a0008c0009t0016g0021a0017c0034t0017g0061 | 3 | HG00642.hp2 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.293+210G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175783 | ||||||
chr1:13175786
|
C | G | 3 | a0008c0009t0006g0022a0008c0009t0016g0021a0017c0034t0017g0061 | 3 | HG00642.hp2 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.293+213C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175786 | ||||||
chr1:13175831
|
A | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.293+258A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175831 | ||||||
chr1:13175906
|
A | C | 1 | a0002c0002t0002g0036 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.293+333A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175906 | ||||||
chr1:13175913
|
T | A | 1 | a0017c0034t0017g0061 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.294-328T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175913 | ||||||
chr1:13175939
|
C | T | 2 | a0002c0002t0002g0036a0017c0034t0017g0061 | 2 | HG00642.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.294-302C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175939 | ||||||
chr1:13175973
|
A | G | 15 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(12): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.294-268A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175973 | ||||||
chr1:13175989
|
C | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.294-252C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175989 | ||||||
chr1:13175992
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(45): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.294-249A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13175992 | ||||||
chr1:13176036
|
T | C | 1 | a0011c0012t0009g0019 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.294-205T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176036 | ||||||
chr1:13176044
|
G | T | 1 | a0004c0004t0014g0043 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.294-197G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176044 | ||||||
chr1:13176050
|
G | A | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.294-191G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176050 | ||||||
chr1:13176050
|
G | C | 1 | a0001c0001t0022g0062 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.294-191G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176050 | ||||||
chr1:13176061
|
G | T | 10 | a0004c0004t0004g0002a0004c0004t0004g0042a0004c0004t0004g0044others(7): Show | 24 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.294-180G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176061 | ||||||
chr1:13176065
|
TC | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(43): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.294-175delC | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176065 | ||||||
chr1:13176066
|
C | G | 1 | a0001c0001t0001g0052 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.294-175C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176066 | ||||||
chr1:13176067
|
A | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(43): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.294-174A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176067 | ||||||
chr1:13176074
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0056 | 3 | HG00323.hp2 HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.294-167A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176074 | ||||||
chr1:13176083
|
A | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.294-158A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176083 | ||||||
chr1:13176098
|
T | C | 1 | a0008c0009t0006g0022 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.294-143T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176098 | ||||||
chr1:13176105
|
C | G | 14 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0030others(11): Show | 33 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(30): Show |
intron_variant | MODIFIER | c.294-136C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176105 | ||||||
chr1:13176113
|
A | G | 4 | a0003c0003t0003g0026a0003c0003t0003g0027a0003c0003t0013g0025others(1): Show | 4 | HG01433.hp1 HG01433.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.294-128A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176113 | ||||||
chr1:13176171
|
A | C | 1 | a0026c0016t0003g0029 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.294-70A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176171 | ||||||
chr1:13176191
|
A | G | 12 | a0002c0002t0002g0003a0002c0002t0002g0014a0002c0002t0002g0031others(9): Show | 24 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.294-50A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176191 | ||||||
chr1:13176208
|
T | G | 7 | a0002c0002t0002g0031a0005c0005t0005g0006a0005c0005t0005g0037others(4): Show | 12 | HG00140.hp2 HG01168.hp1 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.294-33T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176208 | ||||||
chr1:13176222
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(51): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.294-19C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 2/3 | chr1 | 13176222 | ||||||
chr1:13176871
|
T | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(45): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.875+49T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13176871 | ||||||
chr1:13176874
|
C | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(45): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.875+52C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13176874 | ||||||
chr1:13176876
|
A | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(44): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.875+54A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13176876 | ||||||
chr1:13176880
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(44): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.875+58G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13176880 | ||||||
chr1:13176918
|
A | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(67): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.875+96A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13176918 | ||||||
chr1:13176948
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(44): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.875+126A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13176948 | ||||||
chr1:13176988
|
T | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+166T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13176988 | ||||||
chr1:13176995
|
A | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+173A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13176995 | ||||||
chr1:13177011
|
C | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(45): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.875+189C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177011 | ||||||
chr1:13177012
|
G | A | 15 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(12): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.875+190G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177012 | ||||||
chr1:13177013
|
G | C | 1 | a0004c0004t0004g0044 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.875+191G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177013 | ||||||
chr1:13177024
|
G | C | 10 | a0004c0004t0004g0002a0004c0004t0004g0040a0004c0004t0004g0042others(7): Show | 23 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.875+202G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177024 | ||||||
chr1:13177036
|
A | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+214A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177036 | ||||||
chr1:13177043
|
T | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+221T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177043 | ||||||
chr1:13177046
|
T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(45): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.875+224T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177046 | ||||||
chr1:13177050
|
A | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+228A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177050 | ||||||
chr1:13177062
|
G | C | 7 | a0006c0006t0006g0009a0006c0006t0006g0013a0006c0006t0010g0009others(4): Show | 10 | HG01167.hp1 HG02155.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.875+240G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177062 | ||||||
chr1:13177065
|
A | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(44): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.875+243A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177065 | ||||||
chr1:13177116
|
C | T | 1 | a0001c0001t0008g0068 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.875+294C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177116 | ||||||
chr1:13177146
|
G | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+324G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177146 | ||||||
chr1:13177154
|
A | G | 26 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(23): Show | 59 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.875+332A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177154 | ||||||
chr1:13177179
|
T | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(43): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.875+357T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177179 | ||||||
chr1:13177196
|
G | C | 5 | a0005c0005t0005g0006a0005c0005t0005g0037a0005c0005t0005g0038others(2): Show | 10 | HG00140.hp2 HG01168.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.875+374G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177196 | ||||||
chr1:13177206
|
T | C | 5 | a0005c0005t0005g0006a0005c0005t0005g0037a0005c0005t0005g0038others(2): Show | 10 | HG00140.hp2 HG01168.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.875+384T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177206 | ||||||
chr1:13177208
|
G | A | 1 | a0002c0002t0002g0032 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.875+386G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177208 | ||||||
chr1:13177239
|
G | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+417G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177239 | ||||||
chr1:13177246
|
C | A | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+424C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177246 | ||||||
chr1:13177265
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(45): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.875+443G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177265 | ||||||
chr1:13177270
|
G | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(40): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.875+448G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177270 | ||||||
chr1:13177274
|
T | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+452T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177274 | ||||||
chr1:13177318
|
A | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+496A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177318 | ||||||
chr1:13177320
|
T | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+498T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177320 | ||||||
chr1:13177325
|
A | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+503A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177325 | ||||||
chr1:13177334
|
A | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+512A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177334 | ||||||
chr1:13177337
|
C | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+515C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177337 | ||||||
chr1:13177341
|
G | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+519G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177341 | ||||||
chr1:13177344
|
A | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+522A>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177344 | ||||||
chr1:13177344
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(44): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.875+522A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177344 | ||||||
chr1:13177351
|
C | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+529C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177351 | ||||||
chr1:13177358
|
C | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(44): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.875+536C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177358 | ||||||
chr1:13177369
|
G | C | 2 | a0011c0012t0009g0019a0030c0021t0009g0058 | 3 | HG02451.hp2 HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.875+547G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177369 | ||||||
chr1:13177374
|
A | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+552A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177374 | ||||||
chr1:13177390
|
G | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+568G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177390 | ||||||
chr1:13177395
|
A | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+573A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177395 | ||||||
chr1:13177398
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(36): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.875+576G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177398 | ||||||
chr1:13177413
|
G | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+591G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177413 | ||||||
chr1:13177418
|
T | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+596T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177418 | ||||||
chr1:13177440
|
A | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+618A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177440 | ||||||
chr1:13177445
|
T | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+623T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177445 | ||||||
chr1:13177448
|
G | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+626G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177448 | ||||||
chr1:13177507
|
A | T | 8 | a0006c0006t0006g0009a0006c0006t0006g0013a0006c0006t0010g0009others(5): Show | 11 | HG01167.hp1 HG02155.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.875+685A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177507 | ||||||
chr1:13177508
|
T | G | 10 | a0004c0004t0004g0002a0004c0004t0004g0040a0004c0004t0004g0042others(7): Show | 23 | HG00323.hp1 HG01175.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.875+686T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177508 | ||||||
chr1:13177537
|
C | T | 1 | a0006c0006t0006g0013 | 2 | NA18953.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.875+715C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177537 | ||||||
chr1:13177538
|
G | A | 26 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(23): Show | 59 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.875+716G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177538 | ||||||
chr1:13177540
|
C | A | 25 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(22): Show | 58 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.875+718C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177540 | ||||||
chr1:13177545
|
T | A | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+723T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177545 | ||||||
chr1:13177547
|
G | A | 2 | a0003c0003t0003g0026a0003c0003t0013g0025 | 2 | NA18954.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.875+725G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177547 | ||||||
chr1:13177553
|
C | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(43): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.875+731C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177553 | ||||||
chr1:13177574
|
C | T | 15 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(12): Show | 35 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.875+752C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177574 | ||||||
chr1:13177586
|
C | T | 14 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(11): Show | 34 | HG00558.hp1 HG00597.hp2 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.875+764C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177586 | ||||||
chr1:13177610
|
AAGC | A | 2 | a0011c0012t0009g0019a0030c0021t0009g0058 | 3 | HG02451.hp2 HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.875+791_875+793del others(3): Show |
PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 13177610 | |||||
chr1:13177613
|
C | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(43): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.875+791C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177613 | ||||||
chr1:13177614
|
A | G | 2 | a0012c0007t0021g0016a0012c0007t0024g0016 | 2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.875+792A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177614 | ||||||
chr1:13177622
|
T | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(44): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.875+800T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177622 | ||||||
chr1:13177623
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(45): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.875+801A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177623 | ||||||
chr1:13177643
|
G | T | 1 | a0023c0032t0001g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.875+821G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177643 | ||||||
chr1:13177661
|
C | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+839C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177661 | ||||||
chr1:13177692
|
C | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(35): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.875+870C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177692 | ||||||
chr1:13177704
|
T | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-867T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177704 | ||||||
chr1:13177710
|
G | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-861G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177710 | ||||||
chr1:13177754
|
G | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-817G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177754 | ||||||
chr1:13177780
|
C | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-791C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177780 | ||||||
chr1:13177784
|
A | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(70): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.876-787A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177784 | ||||||
chr1:13177872
|
G | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-699G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177872 | ||||||
chr1:13177884
|
A | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-687A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177884 | ||||||
chr1:13177894
|
C | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-677C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177894 | ||||||
chr1:13177944
|
A | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(36): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.876-627A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177944 | ||||||
chr1:13177959
|
T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(45): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.876-612T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177959 | ||||||
chr1:13177963
|
T | C | 1 | a0002c0002t0002g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.876-608T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177963 | ||||||
chr1:13177996
|
G | A | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-575G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13177996 | ||||||
chr1:13178055
|
A | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-516A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178055 | ||||||
chr1:13178067
|
C | G | 1 | a0003c0003t0003g0026 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.876-504C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178067 | ||||||
chr1:13178071
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(44): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.876-500T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178071 | ||||||
chr1:13178078
|
A | AT | 46 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(43): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.876-485dupT | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 13178078 | |||||
chr1:13178085
|
T | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-486T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178085 | ||||||
chr1:13178091
|
C | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-480C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178091 | ||||||
chr1:13178159
|
T | G | 1 | a0004c0004t0004g0040 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.876-412T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178159 | ||||||
chr1:13178184
|
A | G | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-387A>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178184 | ||||||
chr1:13178186
|
G | A | 1 | a0004c0004t0004g0042 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.876-385G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178186 | ||||||
chr1:13178220
|
T | C | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-351T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178220 | ||||||
chr1:13178271
|
C | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(66): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.876-300C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178271 | ||||||
chr1:13178290
|
G | C | 5 | a0005c0005t0005g0006a0005c0005t0005g0037a0005c0005t0005g0038others(2): Show | 10 | HG00140.hp2 HG01168.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.876-281G>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178290 | ||||||
chr1:13178294
|
G | A | 12 | a0002c0002t0002g0003a0002c0002t0002g0014a0002c0002t0002g0030others(9): Show | 24 | HG00558.hp1 HG01952.hp2 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.876-277G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178294 | ||||||
chr1:13178316
|
C | G | 2 | a0011c0012t0009g0019a0030c0021t0009g0058 | 3 | HG02451.hp2 HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.876-255C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178316 | ||||||
chr1:13178328
|
C | A | 3 | a0011c0012t0009g0019a0017c0034t0017g0061a0030c0021t0009g0058 | 4 | HG00642.hp2 HG02451.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.876-243C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178328 | ||||||
chr1:13178348
|
T | G | 16 | a0004c0004t0004g0002a0004c0004t0004g0040a0004c0004t0004g0042others(13): Show | 34 | HG00140.hp2 HG00323.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.876-223T>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178348 | ||||||
chr1:13178380
|
C | G | 3 | a0001c0001t0011g0060a0017c0034t0017g0061a0027c0022t0018g0039 | 3 | HG00642.hp2 HG01934.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.876-191C>G | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178380 | ||||||
chr1:13178381
|
T | C | 1 | a0001c0001t0011g0060 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.876-190T>C | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178381 | ||||||
chr1:13178386
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(45): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.876-185G>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178386 | ||||||
chr1:13178429
|
C | T | 24 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0014others(21): Show | 57 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.876-142C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178429 | ||||||
chr1:13178474
|
C | T | 1 | a0027c0022t0018g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.876-97C>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178474 | ||||||
chr1:13178479
|
T | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(70): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.876-92T>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178479 | ||||||
chr1:13178481
|
G | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(44): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.876-90G>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178481 | ||||||
chr1:13178489
|
C | A | 1 | a0009c0014t0001g0063 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.876-82C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178489 | ||||||
chr1:13178497
|
A | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(77): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.876-74A>T | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178497 | ||||||
chr1:13178567
|
C | A | 12 | a0001c0001t0008g0017a0001c0001t0008g0068a0001c0001t0012g0064others(9): Show | 16 | HG00738.hp1 HG01109.hp1 HG01109.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.876-4C>A | PRAMEF9 | ENSG00000204505.5 | transcript | ENST00000415919.3 | protein_coding | 3/3 | chr1 | 13178567 |