Item | Value |
---|---|
geneid | 26994 |
ensemblid | ENSG00000123091.5 |
hgncid | 10056 |
symbol | RNF11 |
name | ring finger protein 11 |
refseq_nuc | NM_014372.5 |
refseq_prot | NP_055187.1 |
ensembl_nuc | ENST00000242719.4 |
ensembl_prot | ENSP00000242719.3 |
mane_status | MANE Select |
chr | chr1 |
start | 51236273 |
end | 51273447 |
strand | + |
ver | v1.2 |
region | chr1:51236273-51273447 |
region5000 | chr1:51231273-51278447 |
regionname0 | RNF11_chr1_51236273_51273447 |
regionname5000 | RNF11_chr1_51231273_51278447 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 154 | 274 | 80 | 36 | 116 | 12 | 28 | 90 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 465 | 274 | 80 | 36 | 116 | 12 | 28 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2611 | 72 | 11 | 13 | 25 | 7 | 16 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0002 | 1/1 | 2610 | 70 | 11 | 13 | 34 | 3 | 7 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0003 | 0/0 | 2609 | 24 | 12 | 0 | 11 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0004 | 0/0 | 2610 | 23 | 5 | 0 | 18 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0005 | 0/0 | 2611 | 15 | 1 | 2 | 12 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0006 | 0/0 | 2609 | 7 | 7 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0007 | 0/0 | 2608 | 6 | 6 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0008 | 0/0 | 2608 | 5 | 5 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0009 | 0/0 | 2608 | 4 | 4 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0010 | 0/0 | 2610 | 3 | 2 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0011 | 0/0 | 2609 | 3 | 2 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0012 | 0/0 | 2610 | 3 | 0 | 0 | 3 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0013 | 0/0 | 2611 | 3 | 0 | 0 | 3 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0014 | 0/0 | 2609 | 3 | 0 | 0 | 3 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0015 | 0/0 | 2608 | 3 | 3 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0016 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0017 | 0/0 | 2610 | 2 | 1 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0018 | 0/0 | 2610 | 2 | 0 | 1 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0019 | 0/0 | 2611 | 2 | 0 | 0 | 0 | 0 | 2 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0020 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0021 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0022 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0023 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0024 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0025 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0026 | 0/0 | 2609 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0027 | 0/0 | 2609 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0028 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0029 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0030 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0031 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0032 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0033 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0034 | 0/0 | 2611 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0035 | 0/0 | 2611 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0036 | 0/0 | 2611 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0037 | 0/0 | 2611 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0038 | 0/0 | 2609 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0039 | 0/0 | 2610 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
t0040 | 0/0 | 2611 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 465 | 274 | 80 | 36 | 116 | 12 | 28 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3075 | 72 | 11 | 13 | 25 | 7 | 16 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0002 | 1/1 | 3074 | 70 | 11 | 13 | 34 | 3 | 7 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0003 | 0/0 | 3073 | 24 | 12 | 0 | 11 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0004 | 0/0 | 3074 | 23 | 5 | 0 | 18 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0005 | 0/0 | 3075 | 15 | 1 | 2 | 12 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0006 | 0/0 | 3073 | 7 | 7 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0007 | 0/0 | 3072 | 6 | 6 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0008 | 0/0 | 3072 | 5 | 5 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0009 | 0/0 | 3072 | 4 | 4 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0010 | 0/0 | 3074 | 3 | 2 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0011 | 0/0 | 3073 | 3 | 2 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0012 | 0/0 | 3074 | 3 | 0 | 0 | 3 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0013 | 0/0 | 3075 | 3 | 0 | 0 | 3 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0014 | 0/0 | 3073 | 3 | 0 | 0 | 3 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0015 | 0/0 | 3072 | 3 | 3 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0016 | 0/0 | 3072 | 2 | 2 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0017 | 0/0 | 3074 | 2 | 1 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0018 | 0/0 | 3074 | 2 | 0 | 1 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0019 | 0/0 | 3075 | 2 | 0 | 0 | 0 | 0 | 2 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0020 | 0/0 | 3072 | 2 | 2 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0021 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0022 | 0/0 | 3073 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0023 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0024 | 0/0 | 3073 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0025 | 0/0 | 3073 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0026 | 0/0 | 3073 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0027 | 0/0 | 3073 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0028 | 0/0 | 3074 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0029 | 0/0 | 3074 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0030 | 0/0 | 3074 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0031 | 0/0 | 3074 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0032 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0033 | 0/0 | 3074 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0034 | 0/0 | 3075 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0035 | 0/0 | 3075 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0036 | 0/0 | 3075 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0037 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0038 | 0/0 | 3073 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0039 | 0/0 | 3074 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
a0001c0001t0040 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | copy fasta | chr1 | 51231273 | 51278447 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0005g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0005g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0005g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0006g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0007g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0009g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0009g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0009g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0009g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0010g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0010g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0011g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0012g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0012g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0013g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0013g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0014g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0014g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0015g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0015g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0015g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0016g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0016g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0017g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0017g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0018g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0018g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0019g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0020g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0020g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0021g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0022g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0023g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0024g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0025g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0026g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0027g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0028g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0029g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0030g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0031g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0032g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0033g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0034g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0035g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0036g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0037g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0038g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0039g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
a0001c0001t0040g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0124 | EUR | GBR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0084 | EUR | GBR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | GBR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | FIN | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0105 | EUR | FIN | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | CHS | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | CHS | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | CHS | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00639 | hp2 | a0001 | c0001 | t0010 | g0240 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0057 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01109 | hp1 | a0001 | c0001 | t0017 | g0024 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01167 | hp2 | a0001 | c0001 | t0027 | g0004 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01168 | hp1 | a0001 | c0001 | t0039 | g0101 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01169 | hp1 | a0001 | c0001 | t0018 | g0004 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01169 | hp2 | a0001 | c0001 | t0040 | g0102 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01175 | hp2 | a0001 | c0001 | t0011 | g0020 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | CLM | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | IBS | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0046 | EUR | IBS | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | ACB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01943 | hp1 | a0001 | c0001 | t0038 | g0049 | AMR | PEL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02040 | hp1 | a0001 | c0001 | t0030 | g0152 | EAS | KHV | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0056 | AFR | ACB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02055 | hp2 | a0001 | c0001 | t0022 | g0246 | AFR | ACB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02071 | hp2 | a0001 | c0001 | t0014 | g0072 | EAS | KHV | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | KHV | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0091 | AFR | ACB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02257 | hp1 | a0001 | c0001 | t0008 | g0019 | AFR | ACB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0118 | AFR | ACB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0027 | AFR | ACB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0030 | AFR | ACB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02451 | hp2 | a0001 | c0001 | t0015 | g0092 | AFR | ACB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02602 | hp2 | a0001 | c0001 | t0034 | g0245 | SAS | PJL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02622 | hp2 | a0001 | c0001 | t0009 | g0116 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02630 | hp2 | a0001 | c0001 | t0016 | g0054 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02647 | hp1 | a0001 | c0001 | t0010 | g0015 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02717 | hp2 | a0001 | c0001 | t0015 | g0058 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02809 | hp2 | a0001 | c0001 | t0024 | g0031 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0028 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | ESN | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | ESN | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02965 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | ESN | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02976 | hp1 | a0001 | c0001 | t0015 | g0093 | AFR | ESN | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0047 | AFR | ESN | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03041 | hp2 | a0001 | c0001 | t0009 | g0115 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03098 | hp1 | a0001 | c0001 | t0021 | g0052 | AFR | MSL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0029 | AFR | MSL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ESN | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | ESN | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | ESN | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03139 | hp2 | a0001 | c0001 | t0020 | g0048 | AFR | ESN | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | ESN | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | MSL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0173 | AFR | MSL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0039 | AFR | MSL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | MSL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0217 | AFR | MSL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03486 | hp2 | a0001 | c0001 | t0023 | g0053 | AFR | MSL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ESN | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0094 | AFR | ESN | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03540 | hp2 | a0001 | c0001 | t0025 | g0183 | AFR | GWD | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03654 | hp1 | a0001 | c0001 | t0035 | g0216 | SAS | PJL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03834 | hp1 | a0001 | c0001 | t0018 | g0045 | SAS | BEB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | BEB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03927 | hp1 | a0001 | c0001 | t0019 | g0014 | SAS | BEB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03942 | hp2 | a0001 | c0001 | t0019 | g0014 | SAS | BEB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | STU | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | STU | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0036 | AFR | YRI | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | YRI | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | CHB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | CHB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | CHB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18906 | hp1 | a0001 | c0001 | t0011 | g0025 | AFR | YRI | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0117 | AFR | YRI | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18946 | hp2 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18951 | hp1 | a0001 | c0001 | t0014 | g0017 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18954 | hp2 | a0001 | c0001 | t0012 | g0003 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18957 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18959 | hp2 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18962 | hp1 | a0001 | c0001 | t0037 | g0122 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18962 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18973 | hp1 | a0001 | c0001 | t0031 | g0203 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18973 | hp2 | a0001 | c0001 | t0014 | g0017 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18979 | hp2 | a0001 | c0001 | t0005 | g0063 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18985 | hp1 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18986 | hp1 | a0001 | c0001 | t0012 | g0164 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18989 | hp1 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18990 | hp2 | a0001 | c0001 | t0028 | g0002 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18993 | hp2 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18995 | hp1 | a0001 | c0001 | t0026 | g0235 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18997 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA18998 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19002 | hp2 | a0001 | c0001 | t0013 | g0130 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19003 | hp2 | a0001 | c0001 | t0013 | g0165 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19005 | hp1 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19010 | hp1 | a0001 | c0001 | t0029 | g0155 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19012 | hp2 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19030 | hp1 | a0001 | c0001 | t0017 | g0026 | AFR | LWK | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | LWK | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | LWK | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | LWK | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19055 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19065 | hp1 | a0001 | c0001 | t0033 | g0129 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19065 | hp2 | a0001 | c0001 | t0012 | g0003 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19066 | hp2 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19074 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19075 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19077 | hp2 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19090 | hp2 | a0001 | c0001 | t0005 | g0069 | EAS | JPT | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19240 | hp1 | a0001 | c0001 | t0016 | g0051 | AFR | YRI | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | YRI | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ASW | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA20129 | hp2 | a0001 | c0001 | t0009 | g0127 | AFR | ASW | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA20752 | hp2 | a0001 | c0001 | t0036 | g0238 | EUR | TSI | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | TSI | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | GIH | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | GIH | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0038 | AFR | ACB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | ACB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02486 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | ACB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03471 | hp1 | a0001 | c0001 | t0032 | g0044 | AFR | MSL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG06807 | hp1 | a0001 | c0001 | t0010 | g0215 | AFR | USA | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
HG06807 | hp2 | a0001 | c0001 | t0020 | g0050 | AFR | USA | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | LWK | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | LWK | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0244 | REF | REF | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0172 | REF | REF | RNF11_chr1_51231273_51278447 | RNF11 | chr1 | 51231273 | 51278447 |
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 |
---|
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:51236274 | G | C | 4 | a0001c0001t0016a0001c0001t0021a0001c0001t0022others(1): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-483G>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/3 | chr1 | 51236274 | ||||||
chr1:51236284 | C | A | 4 | a0001c0001t0006a0001c0001t0009a0001c0001t0010others(1): Show | 15 | HG00639.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-473C>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/3 | 473 | chr1 | 51236284 | |||||
chr1:51236308 | C | T | 1 | a0001c0001t0015 | 3 | HG02451.hp2 HG02717.hp2 HG02976.hp1 |
5_prime_UTR_variant | MODIFIER | c.-449C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/3 | 449 | chr1 | 51236308 | |||||
chr1:51236414 | C | T | 2 | a0001c0001t0039a0001c0001t0040 | 2 | HG01168.hp1 HG01169.hp2 |
5_prime_UTR_variant | MODIFIER | c.-343C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/3 | 343 | chr1 | 51236414 | |||||
chr1:51236415 | C | G | 6 | a0001c0001t0004a0001c0001t0005a0001c0001t0014others(3): Show | 47 | HG00642.hp1 HG01257.hp1 HG01943.hp1 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-342C>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/3 | 342 | chr1 | 51236415 | |||||
chr1:51236498 | G | GC | 9 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(6): Show | 97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
5_prime_UTR_variant | MODIFIER | c.-246dupC | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/3 | 245 | INFO_REALIGN_3_PRIME | chr1 | 51236498 | ||||
chr1:51236498 | GC | G | 10 | a0001c0001t0003a0001c0001t0006a0001c0001t0011others(7): Show | 43 | HG00438.hp1 HG00438.hp2 HG01167.hp2 others(40): Show |
5_prime_UTR_variant | MODIFIER | c.-246delC | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/3 | 246 | INFO_REALIGN_3_PRIME | chr1 | 51236498 | ||||
chr1:51236498 | GCC | G | 7 | a0001c0001t0007a0001c0001t0008a0001c0001t0009others(4): Show | 23 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-247_-246delCC | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/3 | 246 | INFO_REALIGN_3_PRIME | chr1 | 51236498 | ||||
chr1:51236504 | C | A | 1 | a0001c0001t0025 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-253C>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/3 | 253 | chr1 | 51236504 | |||||
chr1:51236526 | G | A | 2 | a0001c0001t0020a0001c0001t0038 | 3 | HG01943.hp1 HG03139.hp2 HG06807.hp2 |
5_prime_UTR_variant | MODIFIER | c.-231G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/3 | 231 | chr1 | 51236526 | |||||
chr1:51236685 | G | T | 1 | a0001c0001t0033 | 1 | NA19065.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-72G>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/3 | chr1 | 51236685 | ||||||
chr1:51271403 | G | A | 3 | a0001c0001t0008a0001c0001t0011a0001c0001t0017 | 10 | HG01109.hp1 HG01175.hp2 HG02257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*81G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 3/3 | 81 | chr1 | 51271403 | |||||
chr1:51271429 | A | G | 1 | a0001c0001t0032 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*107A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 3/3 | 107 | chr1 | 51271429 | |||||
chr1:51271598 | G | A | 1 | a0001c0001t0034 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*276G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 3/3 | 276 | chr1 | 51271598 | |||||
chr1:51271674 | C | G | 1 | a0001c0001t0021 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*352C>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 3/3 | 352 | chr1 | 51271674 | |||||
chr1:51271774 | A | G | 2 | a0001c0001t0012a0001c0001t0013 | 6 | NA18954.hp2 NA18986.hp1 NA19002.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*452A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 3/3 | 452 | chr1 | 51271774 | |||||
chr1:51272008 | C | T | 1 | a0001c0001t0019 | 2 | HG03927.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*686C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 3/3 | 686 | chr1 | 51272008 | |||||
chr1:51272109 | T | C | 2 | a0001c0001t0026a0001c0001t0028 | 2 | NA18990.hp2 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*787T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 3/3 | 787 | chr1 | 51272109 | |||||
chr1:51272222 | G | A | 1 | a0001c0001t0029 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*900G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 3/3 | 900 | chr1 | 51272222 | |||||
chr1:51272330 | A | G | 2 | a0001c0001t0031a0001c0001t0037 | 2 | NA18962.hp1 NA18973.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1008A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 3/3 | 1008 | chr1 | 51272330 | |||||
chr1:51272484 | C | T | 2 | a0001c0001t0018a0001c0001t0027 | 3 | HG01167.hp2 HG01169.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1162C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 3/3 | 1162 | chr1 | 51272484 | |||||
chr1:51272518 | G | A | 1 | a0001c0001t0030 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1196G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 3/3 | 1196 | chr1 | 51272518 | |||||
chr1:51272934 | T | C | 1 | a0001c0001t0035 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1612T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 3/3 | 1612 | chr1 | 51272934 | |||||
chr1:51273233 | G | A | 1 | a0001c0001t0036 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1911G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 3/3 | 1911 | chr1 | 51273233 | |||||
chr1:51273248 | T | A | 1 | a0001c0001t0024 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1926T>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 3/3 | 1926 | chr1 | 51273248 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:51236900 | G | A | 1 | a0001c0001t0004g0018 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.123+21G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51236900 | ||||||
chr1:51236996 | C | T | 1 | a0001c0001t0003g0254 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.123+117C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51236996 | ||||||
chr1:51237009 | G | T | 1 | a0001c0001t0002g0253 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.123+130G>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237009 | ||||||
chr1:51237073 | G | A | 10 | a0001c0001t0008g0019a0001c0001t0008g0021a0001c0001t0008g0022others(7): Show | 10 | HG01109.hp1 HG01175.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+194G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237073 | ||||||
chr1:51237133 | T | G | 3 | a0001c0001t0006g0029a0001c0001t0006g0030a0001c0001t0024g0031 | 3 | HG02451.hp1 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.123+254T>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237133 | ||||||
chr1:51237290 | A | G | 1 | a0001c0001t0014g0017 | 2 | NA18951.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.123+411A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237290 | ||||||
chr1:51237348 | T | G | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0002g0032 | 3 | HG02015.hp2 HG02040.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.123+469T>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237348 | ||||||
chr1:51237358 | G | A | 10 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(7): Show | 10 | HG02109.hp1 HG02572.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+479G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237358 | ||||||
chr1:51237422 | G | GTA | 6 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0046others(3): Show | 6 | HG01517.hp2 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+544_123+545ins others(2): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51237422 | |||||
chr1:51237422 | GTGTA | G | 4 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(1): Show | 4 | HG02630.hp2 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+545_123+548del others(4): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51237422 | |||||
chr1:51237424 | G | A | 28 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(25): Show | 28 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.123+545G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237424 | ||||||
chr1:51237424 | G | GTATATAT others(17): Show |
1 | a0001c0001t0010g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.123+563_123+586dup others(24): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51237424 | |||||
chr1:51237436 | A | G | 1 | a0001c0001t0020g0050 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.123+557A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237436 | ||||||
chr1:51237438 | A | ATATATG | 3 | a0001c0001t0018g0004a0001c0001t0018g0045a0001c0001t0027g0004 | 3 | HG01167.hp2 HG01169.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.123+560_123+561ins others(6): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51237438 | |||||
chr1:51237438 | A | G | 17 | a0001c0001t0004g0252a0001c0001t0008g0019a0001c0001t0008g0021others(14): Show | 17 | HG01109.hp1 HG01175.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.123+559A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237438 | ||||||
chr1:51237440 | G | A | 5 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0007g0040others(2): Show | 5 | HG02717.hp1 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+561G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237440 | ||||||
chr1:51237442 | G | A | 7 | a0001c0001t0004g0252a0001c0001t0018g0004a0001c0001t0018g0045others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.123+563G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237442 | ||||||
chr1:51237442 | G | GTA | 58 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0001g0081others(55): Show | 63 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.123+583_123+584dup others(2): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51237442 | |||||
chr1:51237442 | G | GTATA | 8 | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0004g0005others(5): Show | 9 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.123+581_123+584dup others(4): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51237442 | |||||
chr1:51237442 | GTA | G | 5 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0002g0242others(2): Show | 5 | HG01243.hp1 HG02602.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+583_123+584del others(2): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51237442 | |||||
chr1:51237444 | A | G | 11 | a0001c0001t0001g0016a0001c0001t0001g0249a0001c0001t0001g0250others(8): Show | 12 | HG01069.hp1 HG01496.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+565A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237444 | ||||||
chr1:51237539 | C | G | 1 | a0001c0001t0001g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.123+660C>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237539 | ||||||
chr1:51237609 | C | T | 5 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0007g0038others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+730C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237609 | ||||||
chr1:51237631 | A | G | 1 | a0001c0001t0002g0251 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.123+752A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237631 | ||||||
chr1:51237651 | G | C | 4 | a0001c0001t0003g0046a0001c0001t0018g0004a0001c0001t0018g0045others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+772G>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237651 | ||||||
chr1:51237941 | C | G | 1 | a0001c0001t0032g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.123+1062C>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237941 | ||||||
chr1:51237971 | T | C | 30 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(27): Show | 33 | HG02071.hp2 HG02132.hp2 NA18940.hp1 others(30): Show |
intron_variant | MODIFIER | c.123+1092T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51237971 | ||||||
chr1:51237999 | TG | T | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0080others(93): Show | 101 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.123+1125delG | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51237999 | |||||
chr1:51238045 | AT | A | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+1168delT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51238045 | |||||
chr1:51238172 | C | A | 11 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(8): Show | 11 | HG02109.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.123+1293C>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51238172 | ||||||
chr1:51238731 | C | CTT | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+1862_123+1863d others(4): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51238731 | |||||
chr1:51238731 | CT | C | 12 | a0001c0001t0002g0114a0001c0001t0003g0035a0001c0001t0003g0037others(9): Show | 12 | HG02015.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.123+1863delT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51238731 | |||||
chr1:51238752 | G | A | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+1873G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51238752 | ||||||
chr1:51238855 | G | T | 1 | a0001c0001t0002g0105 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.123+1976G>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51238855 | ||||||
chr1:51238889 | C | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+2010C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51238889 | ||||||
chr1:51238939 | A | C | 5 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0007g0038others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+2060A>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51238939 | ||||||
chr1:51239029 | A | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+2150A>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51239029 | ||||||
chr1:51239110 | A | G | 1 | a0001c0001t0016g0054 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123+2231A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51239110 | ||||||
chr1:51239317 | T | C | 1 | a0001c0001t0004g0060 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.123+2438T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51239317 | ||||||
chr1:51239468 | T | C | 4 | a0001c0001t0006g0118a0001c0001t0009g0115a0001c0001t0009g0116others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+2589T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51239468 | ||||||
chr1:51239694 | C | T | 3 | a0001c0001t0020g0048a0001c0001t0020g0050a0001c0001t0038g0049 | 3 | HG01943.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.123+2815C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51239694 | ||||||
chr1:51240108 | C | T | 1 | a0001c0001t0036g0238 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.123+3229C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51240108 | ||||||
chr1:51240273 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.123+3394C>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51240273 | ||||||
chr1:51240280 | A | G | 1 | a0001c0001t0020g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.123+3401A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51240280 | ||||||
chr1:51240318 | A | G | 19 | a0001c0001t0002g0224a0001c0001t0002g0225a0001c0001t0002g0226others(16): Show | 19 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(16): Show |
intron_variant | MODIFIER | c.123+3439A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51240318 | ||||||
chr1:51240340 | C | T | 1 | a0001c0001t0007g0047 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.123+3461C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51240340 | ||||||
chr1:51240418 | A | G | 3 | a0001c0001t0001g0219a0001c0001t0002g0218a0001c0001t0002g0220 | 3 | NA18984.hp1 NA18985.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.123+3539A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51240418 | ||||||
chr1:51240447 | G | GT | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+3572dupT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51240447 | |||||
chr1:51240511 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.123+3632C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51240511 | ||||||
chr1:51240547 | AT | A | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+3679delT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51240547 | |||||
chr1:51240741 | G | GT | 9 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(6): Show | 9 | HG02109.hp1 HG02572.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.123+3871dupT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51240741 | |||||
chr1:51240826 | T | G | 1 | a0001c0001t0005g0061 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.123+3947T>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51240826 | ||||||
chr1:51240908 | T | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+4029T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51240908 | ||||||
chr1:51240911 | G | T | 1 | a0001c0001t0002g0113 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.123+4032G>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51240911 | ||||||
chr1:51240982 | G | A | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+4103G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51240982 | ||||||
chr1:51241172 | CA | C | 10 | a0001c0001t0008g0019a0001c0001t0008g0021a0001c0001t0008g0022others(7): Show | 10 | HG01109.hp1 HG01175.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+4296delA | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51241172 | |||||
chr1:51241185 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.123+4306T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51241185 | ||||||
chr1:51241398 | C | T | 1 | a0001c0001t0002g0006 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.123+4519C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51241398 | ||||||
chr1:51241499 | C | A | 4 | a0001c0001t0003g0046a0001c0001t0018g0004a0001c0001t0018g0045others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+4620C>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51241499 | ||||||
chr1:51241827 | G | A | 10 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(7): Show | 10 | HG02109.hp1 HG02572.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+4948G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51241827 | ||||||
chr1:51242227 | ATT | A | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+5350_123+5351d others(4): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51242227 | |||||
chr1:51242304 | A | G | 1 | a0001c0001t0022g0246 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.123+5425A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51242304 | ||||||
chr1:51242324 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.123+5445C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51242324 | ||||||
chr1:51242325 | C | CT | 8 | a0001c0001t0003g0037a0001c0001t0003g0236a0001c0001t0004g0094others(5): Show | 8 | HG00438.hp2 HG03041.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.123+5465dupT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51242325 | |||||
chr1:51242325 | CT | C | 9 | a0001c0001t0002g0120a0001c0001t0008g0019a0001c0001t0008g0021others(6): Show | 9 | HG01109.hp1 HG01175.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.123+5465delT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51242325 | |||||
chr1:51242472 | C | CAAACAA | 3 | a0001c0001t0011g0025a0001c0001t0017g0024a0001c0001t0017g0026 | 3 | HG01109.hp1 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.123+5603_123+5608d others(8): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51242472 | |||||
chr1:51242577 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.123+5698A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51242577 | ||||||
chr1:51242634 | G | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+5755G>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51242634 | ||||||
chr1:51242702 | A | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+5823A>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51242702 | ||||||
chr1:51242823 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.123+5944G>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51242823 | ||||||
chr1:51242854 | A | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+5975A>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51242854 | ||||||
chr1:51242896 | A | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+6017A>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51242896 | ||||||
chr1:51242968 | C | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+6089C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51242968 | ||||||
chr1:51243024 | A | G | 4 | a0001c0001t0003g0046a0001c0001t0018g0004a0001c0001t0018g0045others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+6145A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51243024 | ||||||
chr1:51243111 | A | G | 74 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(71): Show | 78 | HG00642.hp1 HG01109.hp1 HG01167.hp2 others(75): Show |
intron_variant | MODIFIER | c.123+6232A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51243111 | ||||||
chr1:51243159 | T | TCA | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+6281_123+6282d others(4): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51243159 | |||||
chr1:51243262 | T | C | 7 | a0001c0001t0004g0005a0001c0001t0004g0011a0001c0001t0004g0091others(4): Show | 8 | HG00642.hp1 HG01257.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+6383T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51243262 | ||||||
chr1:51243341 | A | G | 3 | a0001c0001t0004g0005a0001c0001t0005g0005a0001c0001t0005g0057 | 3 | HG00642.hp1 HG01257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.123+6462A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51243341 | ||||||
chr1:51243395 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.123+6516C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51243395 | ||||||
chr1:51243589 | C | G | 3 | a0001c0001t0006g0015a0001c0001t0010g0015a0001c0001t0010g0240 | 3 | HG00639.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.123+6710C>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51243589 | ||||||
chr1:51243630 | G | A | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+6751G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51243630 | ||||||
chr1:51243638 | C | T | 1 | a0001c0001t0035g0216 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.123+6759C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51243638 | ||||||
chr1:51243697 | C | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+6818C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51243697 | ||||||
chr1:51243698 | G | A | 1 | a0001c0001t0037g0122 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.123+6819G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51243698 | ||||||
chr1:51243790 | C | G | 1 | a0001c0001t0019g0014 | 2 | HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.123+6911C>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51243790 | ||||||
chr1:51243850 | T | C | 4 | a0001c0001t0003g0046a0001c0001t0018g0004a0001c0001t0018g0045others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+6971T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51243850 | ||||||
chr1:51243965 | C | T | 1 | a0001c0001t0004g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.123+7086C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51243965 | ||||||
chr1:51244165 | A | G | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+7286A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51244165 | ||||||
chr1:51244309 | C | T | 1 | a0001c0001t0032g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.123+7430C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51244309 | ||||||
chr1:51244387 | T | G | 2 | a0001c0001t0015g0058a0001c0001t0015g0092 | 2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.123+7508T>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51244387 | ||||||
chr1:51244388 | T | G | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+7509T>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51244388 | ||||||
chr1:51244447 | C | T | 2 | a0001c0001t0001g0214a0001c0001t0010g0215 | 2 | HG06807.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.123+7568C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51244447 | ||||||
chr1:51244448 | G | C | 1 | a0001c0001t0003g0123 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.123+7569G>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51244448 | ||||||
chr1:51244475 | C | T | 1 | a0001c0001t0003g0213 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.123+7596C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51244475 | ||||||
chr1:51244535 | C | T | 1 | a0001c0001t0023g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123+7656C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51244535 | ||||||
chr1:51244634 | A | G | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+7755A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51244634 | ||||||
chr1:51244665 | C | T | 10 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(7): Show | 10 | HG02109.hp1 HG02572.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+7786C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51244665 | ||||||
chr1:51244763 | T | C | 10 | a0001c0001t0008g0019a0001c0001t0008g0021a0001c0001t0008g0022others(7): Show | 10 | HG01109.hp1 HG01175.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+7884T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51244763 | ||||||
chr1:51244932 | T | C | 1 | a0001c0001t0002g0124 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.123+8053T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51244932 | ||||||
chr1:51244993 | A | ATACT | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+8116_123+8117i others(6): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51244993 | |||||
chr1:51245050 | A | G | 1 | a0001c0001t0006g0118 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.123+8171A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51245050 | ||||||
chr1:51245126 | C | T | 1 | a0001c0001t0002g0006 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.123+8247C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51245126 | ||||||
chr1:51245205 | G | A | 2 | a0001c0001t0004g0062a0001c0001t0005g0063 | 2 | NA18957.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.123+8326G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51245205 | ||||||
chr1:51245491 | G | A | 7 | a0001c0001t0002g0224a0001c0001t0002g0225a0001c0001t0002g0226others(4): Show | 7 | HG00408.hp2 HG00438.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+8612G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51245491 | ||||||
chr1:51245713 | G | A | 2 | a0001c0001t0001g0125a0001c0001t0002g0126 | 2 | HG02735.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.123+8834G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51245713 | ||||||
chr1:51245843 | A | G | 3 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0003g0210 | 3 | HG01109.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.123+8964A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51245843 | ||||||
chr1:51245909 | A | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0241 | 2 | HG01243.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.123+9030A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51245909 | ||||||
chr1:51246041 | G | A | 3 | a0001c0001t0020g0048a0001c0001t0020g0050a0001c0001t0038g0049 | 3 | HG01943.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.123+9162G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51246041 | ||||||
chr1:51246045 | C | T | 1 | a0001c0001t0007g0047 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.123+9166C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51246045 | ||||||
chr1:51246095 | G | A | 7 | a0001c0001t0004g0005a0001c0001t0004g0011a0001c0001t0004g0091others(4): Show | 8 | HG00642.hp1 HG01257.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+9216G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51246095 | ||||||
chr1:51246233 | C | T | 1 | a0001c0001t0020g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.123+9354C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51246233 | ||||||
chr1:51246248 | A | G | 1 | a0001c0001t0003g0112 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.123+9369A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51246248 | ||||||
chr1:51246261 | A | G | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+9382A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51246261 | ||||||
chr1:51246312 | A | G | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+9433A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51246312 | ||||||
chr1:51246368 | A | G | 1 | a0001c0001t0002g0103 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.123+9489A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51246368 | ||||||
chr1:51246373 | G | A | 1 | a0001c0001t0009g0127 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.123+9494G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51246373 | ||||||
chr1:51246420 | A | T | 3 | a0001c0001t0001g0100a0001c0001t0039g0101a0001c0001t0040g0102 | 3 | HG01168.hp1 HG01169.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.123+9541A>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51246420 | ||||||
chr1:51246442 | G | A | 2 | a0001c0001t0002g0228a0001c0001t0003g0229 | 2 | NA18970.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.123+9563G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51246442 | ||||||
chr1:51246610 | G | A | 1 | a0001c0001t0002g0128 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.123+9731G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51246610 | ||||||
chr1:51246735 | T | C | 1 | a0001c0001t0023g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123+9856T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51246735 | ||||||
chr1:51246841 | C | A | 1 | a0001c0001t0033g0129 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.123+9962C>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51246841 | ||||||
chr1:51246976 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.123+10097T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51246976 | ||||||
chr1:51246979 | T | TA | 17 | a0001c0001t0002g0006a0001c0001t0003g0112a0001c0001t0008g0019others(14): Show | 18 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.123+10117dupA | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51246979 | |||||
chr1:51246979 | T | TAA | 11 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(8): Show | 11 | HG02109.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.123+10116_123+1011 others(6): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51246979 | |||||
chr1:51246979 | TA | T | 5 | a0001c0001t0002g0032a0001c0001t0004g0252a0001c0001t0005g0078others(2): Show | 6 | HG02055.hp2 HG02630.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+10117delA | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51246979 | |||||
chr1:51246996 | A | AC | 4 | a0001c0001t0004g0011a0001c0001t0004g0091a0001c0001t0004g0094others(1): Show | 5 | HG02055.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+10117_123+1011 others(5): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51246996 | ||||||
chr1:51247036 | G | T | 1 | a0001c0001t0033g0129 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.123+10157G>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51247036 | ||||||
chr1:51247046 | A | T | 1 | a0001c0001t0033g0129 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.123+10167A>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51247046 | ||||||
chr1:51247074 | T | C | 10 | a0001c0001t0008g0019a0001c0001t0008g0021a0001c0001t0008g0022others(7): Show | 10 | HG01109.hp1 HG01175.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+10195T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51247074 | ||||||
chr1:51247107 | C | T | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.123+10228C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51247107 | ||||||
chr1:51247298 | C | T | 1 | a0001c0001t0003g0046 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.123+10419C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51247298 | ||||||
chr1:51247454 | G | GT | 12 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(9): Show | 12 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.123+10587dupT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51247454 | |||||
chr1:51247454 | GT | G | 28 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(25): Show | 28 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.123+10587delT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51247454 | |||||
chr1:51247454 | GTT | G | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+10586_123+1058 others(6): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51247454 | |||||
chr1:51247684 | CT | C | 7 | a0001c0001t0004g0005a0001c0001t0004g0011a0001c0001t0004g0091others(4): Show | 8 | HG00642.hp1 HG01257.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+10809delT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51247684 | |||||
chr1:51247751 | T | C | 1 | a0001c0001t0003g0046 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.123+10872T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51247751 | ||||||
chr1:51248054 | G | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+11175G>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51248054 | ||||||
chr1:51248056 | C | T | 4 | a0001c0001t0001g0196a0001c0001t0001g0199a0001c0001t0002g0197others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+11177C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51248056 | ||||||
chr1:51248096 | C | CT | 27 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0003g0035others(24): Show | 27 | HG00438.hp2 HG01175.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.123+11239dupT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51248096 | |||||
chr1:51248096 | CT | C | 17 | a0001c0001t0001g0100a0001c0001t0001g0214a0001c0001t0001g0250others(14): Show | 17 | HG00642.hp1 HG01109.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.123+11239delT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51248096 | |||||
chr1:51248096 | CTTTT | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+11236_123+1123 others(8): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51248096 | |||||
chr1:51248096 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0007g0047 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.123+11228_123+1123 others(16): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51248096 | |||||
chr1:51248131 | C | T | 5 | a0001c0001t0001g0193a0001c0001t0001g0249a0001c0001t0002g0133others(2): Show | 5 | HG00621.hp2 HG01993.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+11252C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51248131 | ||||||
chr1:51248205 | C | CT | 5 | a0001c0001t0005g0077a0001c0001t0007g0047a0001c0001t0018g0004others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+11340dupT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51248205 | |||||
chr1:51248205 | C | CTT | 6 | a0001c0001t0003g0046a0001c0001t0016g0051a0001c0001t0016g0054others(3): Show | 6 | HG01517.hp2 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+11339_123+1134 others(6): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51248205 | |||||
chr1:51248373 | ATTTTGTA others(6250): Show |
A | 1 | a0001c0001t0002g0006 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.123+11514_124-1530 others(4): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51248373 | |||||
chr1:51248429 | C | T | 1 | a0001c0001t0021g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.123+11550C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51248429 | ||||||
chr1:51248449 | G | T | 1 | a0001c0001t0001g0192 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.123+11570G>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51248449 | ||||||
chr1:51248456 | C | T | 3 | a0001c0001t0015g0058a0001c0001t0015g0092a0001c0001t0015g0093 | 3 | HG02451.hp2 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.123+11577C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51248456 | ||||||
chr1:51248506 | G | C | 1 | a0001c0001t0007g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.123+11627G>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51248506 | ||||||
chr1:51248598 | T | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+11719T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51248598 | ||||||
chr1:51248757 | A | G | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+11878A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51248757 | ||||||
chr1:51249278 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.123+12399C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51249278 | ||||||
chr1:51249348 | A | C | 1 | a0001c0001t0007g0047 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.123+12469A>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51249348 | ||||||
chr1:51249427 | C | G | 2 | a0001c0001t0002g0191a0001c0001t0003g0132 | 2 | NA18946.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.123+12548C>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51249427 | ||||||
chr1:51249588 | A | G | 1 | a0001c0001t0007g0047 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.123+12709A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51249588 | ||||||
chr1:51249617 | G | A | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+12738G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51249617 | ||||||
chr1:51249624 | T | TAA | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+12746_123+1274 others(6): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51249624 | |||||
chr1:51249735 | A | G | 30 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(27): Show | 33 | HG02071.hp2 HG02132.hp2 NA18940.hp1 others(30): Show |
intron_variant | MODIFIER | c.123+12856A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51249735 | ||||||
chr1:51249949 | C | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+13070C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51249949 | ||||||
chr1:51250050 | T | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+13171T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51250050 | ||||||
chr1:51250466 | A | G | 1 | a0001c0001t0017g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.123+13587A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51250466 | ||||||
chr1:51250480 | C | T | 3 | a0001c0001t0001g0243a0001c0001t0002g0242a0001c0001t0002g0244 | 3 | HG03017.hp1 NA20805.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.123+13601C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51250480 | ||||||
chr1:51250549 | A | AT | 5 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0007g0038others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+13682dupT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51250549 | |||||
chr1:51250630 | G | A | 1 | a0001c0001t0021g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.123+13751G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51250630 | ||||||
chr1:51250645 | TGGCGTGG others(36): Show |
T | 4 | a0001c0001t0003g0046a0001c0001t0018g0004a0001c0001t0018g0045others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+13768_123+1381 others(47): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51250645 | |||||
chr1:51250664 | G | A | 1 | a0001c0001t0003g0112 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.123+13785G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51250664 | ||||||
chr1:51250760 | G | A | 10 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(7): Show | 10 | HG02109.hp1 HG02572.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+13881G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51250760 | ||||||
chr1:51250772 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.123+13893G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51250772 | ||||||
chr1:51251008 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.123+14129C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251008 | ||||||
chr1:51251010 | AGGATGAT others(8): Show |
A | 1 | a0001c0001t0002g0120 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.123+14137_123+1415 others(19): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51251010 | |||||
chr1:51251012 | G | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+14133G>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251012 | ||||||
chr1:51251032 | C | T | 2 | a0001c0001t0001g0016a0001c0001t0002g0251 | 3 | HG01069.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.123+14153C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251032 | ||||||
chr1:51251042 | C | T | 4 | a0001c0001t0003g0046a0001c0001t0018g0004a0001c0001t0018g0045others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+14163C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251042 | ||||||
chr1:51251057 | A | G | 1 | a0001c0001t0007g0047 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.123+14178A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251057 | ||||||
chr1:51251069 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.123+14190G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251069 | ||||||
chr1:51251199 | A | G | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+14320A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251199 | ||||||
chr1:51251244 | T | G | 1 | a0001c0001t0002g0135 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.123+14365T>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251244 | ||||||
chr1:51251294 | G | A | 2 | a0001c0001t0002g0191a0001c0001t0003g0132 | 2 | NA18946.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.123+14415G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251294 | ||||||
chr1:51251355 | C | T | 3 | a0001c0001t0015g0058a0001c0001t0015g0092a0001c0001t0015g0093 | 3 | HG02451.hp2 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.123+14476C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251355 | ||||||
chr1:51251356 | G | A | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+14477G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251356 | ||||||
chr1:51251359 | T | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+14480T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251359 | ||||||
chr1:51251361 | C | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+14482C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251361 | ||||||
chr1:51251373 | C | T | 1 | a0001c0001t0022g0246 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.123+14494C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251373 | ||||||
chr1:51251379 | C | T | 3 | a0001c0001t0003g0035a0001c0001t0007g0036a0001c0001t0007g0040 | 3 | HG02572.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.123+14500C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251379 | ||||||
chr1:51251440 | G | GC | 30 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0193others(27): Show | 31 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.123+14570dupC | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51251440 | |||||
chr1:51251447 | C | G | 2 | a0001c0001t0003g0221a0001c0001t0003g0227 | 2 | HG00438.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.123+14568C>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251447 | ||||||
chr1:51251476 | G | A | 1 | a0001c0001t0021g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.123+14597G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251476 | ||||||
chr1:51251519 | C | T | 1 | a0001c0001t0002g0099 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.123+14640C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251519 | ||||||
chr1:51251556 | A | G | 4 | a0001c0001t0008g0019a0001c0001t0008g0021a0001c0001t0008g0022others(1): Show | 4 | HG02257.hp1 HG02486.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+14677A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251556 | ||||||
chr1:51251618 | G | A | 20 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(17): Show | 20 | HG01167.hp2 HG01169.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.123+14739G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251618 | ||||||
chr1:51251759 | A | C | 1 | a0001c0001t0003g0037 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.123+14880A>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251759 | ||||||
chr1:51251878 | C | A | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+14999C>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51251878 | ||||||
chr1:51252010 | C | CAG | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+15132_123+1513 others(6): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51252010 | |||||
chr1:51252081 | C | CA | 16 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0136others(13): Show | 16 | HG00597.hp1 HG00597.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.123+15223dupA | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51252081 | |||||
chr1:51252081 | CA | C | 12 | a0001c0001t0001g0190a0001c0001t0001g0214a0001c0001t0002g0087others(9): Show | 12 | HG01175.hp2 HG01943.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.123+15223delA | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51252081 | |||||
chr1:51252116 | A | G | 1 | a0001c0001t0007g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.123+15237A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51252116 | ||||||
chr1:51252124 | G | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+15245G>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51252124 | ||||||
chr1:51252242 | A | G | 1 | a0001c0001t0007g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.123+15363A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51252242 | ||||||
chr1:51252326 | A | G | 1 | a0001c0001t0032g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.123+15447A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51252326 | ||||||
chr1:51252340 | C | T | 1 | a0001c0001t0002g0189 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.123+15461C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51252340 | ||||||
chr1:51252695 | G | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+15816G>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51252695 | ||||||
chr1:51252805 | T | TTG | 26 | a0001c0001t0001g0121a0001c0001t0001g0166a0001c0001t0001g0167others(23): Show | 27 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.123+15956_123+1595 others(6): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51252805 | |||||
chr1:51252805 | T | TTGTG | 21 | a0001c0001t0001g0033a0001c0001t0001g0200a0001c0001t0001g0205others(18): Show | 21 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.123+15954_123+1595 others(8): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51252805 | |||||
chr1:51252805 | T | TTGTGTG | 66 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0137others(63): Show | 70 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.123+15952_123+1595 others(10): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51252805 | |||||
chr1:51252805 | T | TTGTGTGT others(1): Show |
11 | a0001c0001t0001g0095a0001c0001t0001g0239a0001c0001t0002g0145others(8): Show | 11 | HG02083.hp1 HG02083.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.123+15950_123+1595 others(12): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51252805 | |||||
chr1:51252805 | T | TTGTGTGT others(3): Show |
4 | a0001c0001t0001g0144a0001c0001t0002g0124a0001c0001t0002g0143others(1): Show | 4 | HG00099.hp1 HG00738.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+15948_123+1595 others(14): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51252805 | |||||
chr1:51252805 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0001g0142 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.123+15944_123+1595 others(18): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51252805 | |||||
chr1:51252805 | T | TTGTGTGT others(13): Show |
1 | a0001c0001t0022g0246 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.123+15938_123+1595 others(24): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51252805 | |||||
chr1:51252805 | TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0001g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.123+15948_123+1595 others(14): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51252805 | |||||
chr1:51252837 | T | G | 2 | a0001c0001t0002g0141a0001c0001t0003g0230 | 2 | NA18956.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.123+15958T>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51252837 | ||||||
chr1:51252884 | T | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+16005T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51252884 | ||||||
chr1:51252949 | C | T | 5 | a0001c0001t0001g0188a0001c0001t0002g0228a0001c0001t0002g0233others(2): Show | 5 | NA18953.hp1 NA18953.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+16070C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51252949 | ||||||
chr1:51252967 | T | C | 73 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(70): Show | 77 | HG00642.hp1 HG01109.hp1 HG01167.hp2 others(74): Show |
intron_variant | MODIFIER | c.123+16088T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51252967 | ||||||
chr1:51253068 | G | A | 23 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(20): Show | 23 | HG01167.hp2 HG01169.hp1 HG01517.hp2 others(20): Show |
intron_variant | MODIFIER | c.123+16189G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51253068 | ||||||
chr1:51253072 | G | A | 7 | a0001c0001t0004g0005a0001c0001t0004g0011a0001c0001t0004g0091others(4): Show | 8 | HG00642.hp1 HG01257.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+16193G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51253072 | ||||||
chr1:51253244 | G | T | 1 | a0001c0001t0002g0237 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.123+16365G>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51253244 | ||||||
chr1:51253473 | T | C | 2 | a0001c0001t0016g0051a0001c0001t0016g0054 | 2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.124-16483T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51253473 | ||||||
chr1:51253554 | C | G | 257 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0033others(254): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.124-16402C>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51253554 | ||||||
chr1:51253567 | A | G | 10 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(7): Show | 10 | HG02109.hp1 HG02572.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.124-16389A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51253567 | ||||||
chr1:51253612 | G | A | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-16344G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51253612 | ||||||
chr1:51253643 | G | A | 73 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(70): Show | 77 | HG00642.hp1 HG01109.hp1 HG01167.hp2 others(74): Show |
intron_variant | MODIFIER | c.124-16313G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51253643 | ||||||
chr1:51253680 | C | T | 1 | a0001c0001t0002g0138 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.124-16276C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51253680 | ||||||
chr1:51253904 | C | T | 5 | a0001c0001t0001g0003a0001c0001t0012g0003a0001c0001t0012g0164others(2): Show | 6 | NA18954.hp2 NA18986.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-16052C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51253904 | ||||||
chr1:51253962 | C | G | 2 | a0001c0001t0004g0009a0001c0001t0005g0009 | 2 | NA18954.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.124-15994C>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51253962 | ||||||
chr1:51254087 | T | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-15869T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51254087 | ||||||
chr1:51254207 | G | GT | 11 | a0001c0001t0002g0218a0001c0001t0008g0019a0001c0001t0008g0021others(8): Show | 11 | HG01109.hp1 HG01175.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.124-15739dupT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51254207 | |||||
chr1:51254217 | TA | T | 3 | a0001c0001t0015g0058a0001c0001t0015g0092a0001c0001t0015g0093 | 3 | HG02451.hp2 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.124-15736delA | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51254217 | |||||
chr1:51254218 | A | T | 1 | a0001c0001t0032g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.124-15738A>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51254218 | ||||||
chr1:51254528 | C | T | 4 | a0001c0001t0001g0136a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG03490.hp1 HG03492.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-15428C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51254528 | ||||||
chr1:51254682 | C | T | 1 | a0001c0001t0010g0215 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.124-15274C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51254682 | ||||||
chr1:51254763 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.124-15193A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51254763 | ||||||
chr1:51254890 | A | G | 2 | a0001c0001t0004g0005a0001c0001t0005g0005 | 2 | HG01257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.124-15066A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51254890 | ||||||
chr1:51254964 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.124-14992T>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51254964 | ||||||
chr1:51255032 | G | A | 2 | a0001c0001t0001g0147a0001c0001t0002g0146 | 2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.124-14924G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51255032 | ||||||
chr1:51255102 | A | G | 4 | a0001c0001t0003g0046a0001c0001t0018g0004a0001c0001t0018g0045others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-14854A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51255102 | ||||||
chr1:51255194 | A | G | 1 | a0001c0001t0002g0113 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.124-14762A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51255194 | ||||||
chr1:51255363 | G | C | 1 | a0001c0001t0031g0203 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.124-14593G>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51255363 | ||||||
chr1:51255394 | G | A | 2 | a0001c0001t0011g0025a0001c0001t0017g0026 | 2 | NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.124-14562G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51255394 | ||||||
chr1:51255457 | A | G | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-14499A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51255457 | ||||||
chr1:51255545 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.124-14411C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51255545 | ||||||
chr1:51255607 | T | C | 10 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(7): Show | 10 | HG02109.hp1 HG02572.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.124-14349T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51255607 | ||||||
chr1:51255757 | T | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-14199T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51255757 | ||||||
chr1:51255767 | A | G | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-14189A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51255767 | ||||||
chr1:51255791 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.124-14165A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51255791 | ||||||
chr1:51255845 | T | G | 1 | a0001c0001t0003g0112 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.124-14111T>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51255845 | ||||||
chr1:51255947 | A | G | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-14009A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51255947 | ||||||
chr1:51256119 | C | A | 10 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(7): Show | 10 | HG02109.hp1 HG02572.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.124-13837C>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51256119 | ||||||
chr1:51256261 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.124-13695C>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51256261 | ||||||
chr1:51256302 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.124-13654T>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51256302 | ||||||
chr1:51256634 | T | C | 1 | a0001c0001t0007g0047 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.124-13322T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51256634 | ||||||
chr1:51256661 | T | TTTG | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-13277_124-1327 others(7): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51256661 | |||||
chr1:51256758 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.124-13198C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51256758 | ||||||
chr1:51256822 | T | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-13134T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51256822 | ||||||
chr1:51256865 | G | C | 4 | a0001c0001t0004g0007a0001c0001t0004g0062a0001c0001t0005g0063others(1): Show | 5 | HG02132.hp2 NA18957.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-13091G>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51256865 | ||||||
chr1:51256953 | C | T | 6 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(3): Show | 6 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-13003C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51256953 | ||||||
chr1:51257049 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.124-12907A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51257049 | ||||||
chr1:51257145 | C | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-12811C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51257145 | ||||||
chr1:51257186 | A | G | 1 | a0001c0001t0007g0047 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.124-12770A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51257186 | ||||||
chr1:51257220 | A | G | 1 | a0001c0001t0023g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124-12736A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51257220 | ||||||
chr1:51257344 | C | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-12612C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51257344 | ||||||
chr1:51257437 | AT | A | 4 | a0001c0001t0004g0007a0001c0001t0004g0062a0001c0001t0005g0063others(1): Show | 5 | HG02132.hp2 NA18957.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-12513delT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51257437 | |||||
chr1:51257450 | A | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-12506A>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51257450 | ||||||
chr1:51257486 | G | A | 1 | a0001c0001t0023g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124-12470G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51257486 | ||||||
chr1:51257575 | C | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-12381C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51257575 | ||||||
chr1:51257606 | C | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-12350C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51257606 | ||||||
chr1:51257613 | A | G | 1 | a0001c0001t0021g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.124-12343A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51257613 | ||||||
chr1:51257848 | C | CT | 52 | a0001c0001t0001g0100a0001c0001t0001g0137a0001c0001t0001g0142others(49): Show | 56 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.124-12104dupT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51257848 | |||||
chr1:51257852 | TC | T | 9 | a0001c0001t0001g0149a0001c0001t0001g0166a0001c0001t0001g0196others(6): Show | 9 | HG01069.hp1 HG01069.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.124-12103delC | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51257852 | ||||||
chr1:51257853 | C | CTTTT | 8 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0046others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.124-12088_124-1208 others(8): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51257853 | |||||
chr1:51257853 | C | CTTTTTT | 11 | a0001c0001t0003g0037a0001c0001t0008g0021a0001c0001t0008g0023others(8): Show | 11 | HG01109.hp1 HG01175.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.124-12090_124-1208 others(10): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51257853 | |||||
chr1:51257853 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0016g0051a0001c0001t0023g0053 | 2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.124-12098_124-1208 others(18): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51257853 | |||||
chr1:51257853 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0016g0054 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.124-12099_124-1208 others(19): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51257853 | |||||
chr1:51257853 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0021g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.124-12100_124-1208 others(20): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51257853 | |||||
chr1:51257853 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0022g0246 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.124-12101_124-1208 others(21): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51257853 | |||||
chr1:51257853 | C | T | 216 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0033others(213): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.124-12103C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51257853 | ||||||
chr1:51257855 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.124-12101T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51257855 | ||||||
chr1:51258096 | C | T | 4 | a0001c0001t0003g0046a0001c0001t0018g0004a0001c0001t0018g0045others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-11860C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51258096 | ||||||
chr1:51258168 | TAGTGATC | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-11781_124-1177 others(11): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51258168 | |||||
chr1:51258279 | T | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-11677T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51258279 | ||||||
chr1:51258560 | G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0241 | 2 | HG01243.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.124-11396G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51258560 | ||||||
chr1:51258769 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.124-11187C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51258769 | ||||||
chr1:51259040 | A | G | 1 | a0001c0001t0002g0105 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.124-10916A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51259040 | ||||||
chr1:51259259 | T | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-10697T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51259259 | ||||||
chr1:51259275 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.124-10681A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51259275 | ||||||
chr1:51259489 | T | A | 33 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(30): Show | 33 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.124-10467T>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51259489 | ||||||
chr1:51259529 | T | C | 1 | a0001c0001t0019g0014 | 2 | HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.124-10427T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51259529 | ||||||
chr1:51259847 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.124-10109G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51259847 | ||||||
chr1:51259893 | T | A | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-10063T>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51259893 | ||||||
chr1:51259940 | C | G | 4 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(1): Show | 4 | HG02630.hp2 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-10016C>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51259940 | ||||||
chr1:51259986 | T | G | 1 | a0001c0001t0002g0189 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.124-9970T>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51259986 | ||||||
chr1:51260009 | T | C | 3 | a0001c0001t0004g0059a0001c0001t0004g0065a0001c0001t0005g0066 | 3 | NA18968.hp1 NA18969.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.124-9947T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51260009 | ||||||
chr1:51260242 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.124-9714A>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51260242 | ||||||
chr1:51260345 | T | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-9611T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51260345 | ||||||
chr1:51260905 | A | G | 1 | a0001c0001t0004g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.124-9051A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51260905 | ||||||
chr1:51260988 | A | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-8968A>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51260988 | ||||||
chr1:51261158 | A | T | 1 | a0001c0001t0002g0006 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.124-8798A>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51261158 | ||||||
chr1:51261267 | T | G | 4 | a0001c0001t0003g0046a0001c0001t0018g0004a0001c0001t0018g0045others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-8689T>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51261267 | ||||||
chr1:51261317 | T | C | 1 | a0001c0001t0006g0173 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.124-8639T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51261317 | ||||||
chr1:51261354 | T | C | 1 | a0001c0001t0020g0050 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.124-8602T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51261354 | ||||||
chr1:51261355 | G | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-8601G>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51261355 | ||||||
chr1:51261521 | C | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-8435C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51261521 | ||||||
chr1:51261541 | T | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-8415T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51261541 | ||||||
chr1:51261687 | A | AT | 12 | a0001c0001t0001g0186a0001c0001t0002g0226a0001c0001t0003g0035others(9): Show | 12 | HG02109.hp1 HG02572.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.124-8254dupT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51261687 | |||||
chr1:51261711 | G | A | 1 | a0001c0001t0003g0046 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.124-8245G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51261711 | ||||||
chr1:51261751 | G | A | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-8205G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51261751 | ||||||
chr1:51261848 | C | T | 1 | a0001c0001t0003g0236 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.124-8108C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51261848 | ||||||
chr1:51261923 | C | T | 7 | a0001c0001t0004g0005a0001c0001t0004g0011a0001c0001t0004g0091others(4): Show | 8 | HG00642.hp1 HG01257.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-8033C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51261923 | ||||||
chr1:51261941 | G | A | 4 | a0001c0001t0003g0046a0001c0001t0018g0004a0001c0001t0018g0045others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-8015G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51261941 | ||||||
chr1:51262015 | C | T | 3 | a0001c0001t0001g0144a0001c0001t0002g0124a0001c0001t0002g0143 | 3 | HG00099.hp1 HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.124-7941C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51262015 | ||||||
chr1:51262173 | G | A | 1 | a0001c0001t0022g0246 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.124-7783G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51262173 | ||||||
chr1:51262634 | C | T | 1 | a0001c0001t0033g0129 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.124-7322C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51262634 | ||||||
chr1:51262715 | C | CT | 60 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0158others(57): Show | 64 | HG00639.hp1 HG01109.hp1 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.124-7217dupT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51262715 | |||||
chr1:51262715 | C | CTT | 10 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0004g0076others(7): Show | 10 | HG02071.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.124-7218_124-7217d others(4): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51262715 | |||||
chr1:51262715 | CT | C | 11 | a0001c0001t0001g0140a0001c0001t0001g0167a0001c0001t0003g0112others(8): Show | 12 | HG00642.hp1 HG01257.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.124-7217delT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51262715 | |||||
chr1:51262984 | A | G | 2 | a0001c0001t0001g0016a0001c0001t0002g0251 | 3 | HG01069.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.124-6972A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51262984 | ||||||
chr1:51263088 | C | T | 3 | a0001c0001t0020g0048a0001c0001t0020g0050a0001c0001t0038g0049 | 3 | HG01943.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.124-6868C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51263088 | ||||||
chr1:51263091 | G | A | 1 | a0001c0001t0005g0055 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.124-6865G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51263091 | ||||||
chr1:51263183 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.124-6773A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51263183 | ||||||
chr1:51263232 | G | A | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-6724G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51263232 | ||||||
chr1:51263389 | A | T | 2 | a0001c0001t0014g0017a0001c0001t0014g0072 | 3 | HG02071.hp2 NA18951.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.124-6567A>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51263389 | ||||||
chr1:51263451 | TTG | T | 4 | a0001c0001t0003g0046a0001c0001t0018g0004a0001c0001t0018g0045others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-6489_124-6488d others(4): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51263451 | |||||
chr1:51263574 | C | A | 2 | a0001c0001t0016g0051a0001c0001t0016g0054 | 2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.124-6382C>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51263574 | ||||||
chr1:51264190 | G | A | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-5766G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264190 | ||||||
chr1:51264259 | C | CA | 10 | a0001c0001t0001g0095a0001c0001t0001g0100a0001c0001t0001g0139others(7): Show | 10 | HG00597.hp2 HG01517.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.124-5668dupA | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264259 | |||||
chr1:51264259 | CA | C | 20 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0148others(17): Show | 21 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.124-5668delA | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264259 | |||||
chr1:51264259 | CAA | C | 11 | a0001c0001t0001g0098a0001c0001t0001g0171a0001c0001t0001g0184others(8): Show | 12 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-5669_124-5668d others(4): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264259 | |||||
chr1:51264259 | CAAA | C | 6 | a0001c0001t0002g0154a0001c0001t0006g0118a0001c0001t0008g0028others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-5670_124-5668d others(5): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264259 | |||||
chr1:51264270 | AAAAAAAA others(24): Show |
A | 1 | a0001c0001t0023g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124-5684_124-5654d others(33): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264270 | |||||
chr1:51264271 | AAAAAAAA others(27): Show |
A | 3 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052 | 3 | HG02630.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.124-5683_124-5650d others(36): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264271 | |||||
chr1:51264273 | AAAAAAAA others(27): Show |
A | 1 | a0001c0001t0022g0246 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.124-5681_124-5648d others(36): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264273 | |||||
chr1:51264277 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0005g0055 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.124-5677_124-5664d others(16): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264277 | |||||
chr1:51264281 | A | AATATATA others(3): Show |
1 | a0001c0001t0025g0183 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.124-5674_124-5673i others(12): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264281 | |||||
chr1:51264281 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0014g0072 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.124-5673_124-5662d others(14): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264281 | |||||
chr1:51264281 | AAAAAAAA others(7): Show |
A | 3 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0005g0009 | 4 | NA18940.hp1 NA18954.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-5673_124-5660d others(16): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264281 | |||||
chr1:51264281 | AAAAAAAA others(9): Show |
A | 3 | a0001c0001t0004g0059a0001c0001t0005g0061a0001c0001t0005g0078 | 3 | NA18946.hp2 NA18969.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.124-5673_124-5658d others(18): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264281 | |||||
chr1:51264282 | AAAAAAAT others(6): Show |
A | 3 | a0001c0001t0002g0231a0001c0001t0005g0066a0001c0001t0014g0017 | 4 | NA18951.hp1 NA18957.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-5672_124-5660d others(15): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264282 | |||||
chr1:51264282 | AAAAAAAT others(8): Show |
A | 16 | a0001c0001t0004g0007a0001c0001t0004g0018a0001c0001t0004g0060others(13): Show | 17 | HG02132.hp2 NA18948.hp1 NA18949.hp2 others(14): Show |
intron_variant | MODIFIER | c.124-5672_124-5658d others(17): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264282 | |||||
chr1:51264282 | AAAAAAAT others(16): Show |
A | 2 | a0001c0001t0001g0016a0001c0001t0002g0251 | 3 | HG01069.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.124-5672_124-5650d others(25): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264282 | |||||
chr1:51264283 | A | AATATATA others(11): Show |
1 | a0001c0001t0001g0157 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.124-5672_124-5671i others(20): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264283 | |||||
chr1:51264283 | A | ATATAT | 3 | a0001c0001t0001g0121a0001c0001t0002g0228a0001c0001t0003g0229 | 3 | HG00140.hp1 NA18970.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.124-5673_124-5672i others(7): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264283 | ||||||
chr1:51264283 | A | T | 5 | a0001c0001t0001g0147a0001c0001t0002g0090a0001c0001t0002g0237others(2): Show | 5 | HG03540.hp2 HG03654.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-5673A>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264283 | ||||||
chr1:51264283 | AAAAAATA others(7): Show |
A | 2 | a0001c0001t0004g0065a0001c0001t0005g0069 | 2 | NA18968.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.124-5671_124-5658d others(16): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264283 | |||||
chr1:51264283 | AAAAAATA others(15): Show |
A | 1 | a0001c0001t0002g0108 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.124-5671_124-5650d others(24): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264283 | |||||
chr1:51264284 | AAAAATAT others(4): Show |
A | 2 | a0001c0001t0004g0091a0001c0001t0038g0049 | 2 | HG01943.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.124-5670_124-5660d others(13): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264284 | |||||
chr1:51264284 | AAAAATAT others(8): Show |
A | 2 | a0001c0001t0004g0068a0001c0001t0005g0067 | 2 | NA18998.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.124-5670_124-5656d others(17): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264284 | |||||
chr1:51264285 | A | AAT | 6 | a0001c0001t0001g0153a0001c0001t0001g0169a0001c0001t0001g0193others(3): Show | 6 | HG00621.hp1 HG00621.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-5670_124-5669i others(4): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264285 | |||||
chr1:51264285 | A | AATATATA others(5): Show |
1 | a0001c0001t0007g0040 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.124-5670_124-5669i others(14): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264285 | |||||
chr1:51264285 | A | AT | 3 | a0001c0001t0001g0168a0001c0001t0006g0013a0001c0001t0029g0155 | 4 | HG00140.hp2 HG02630.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-5671_124-5670i others(3): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264285 | ||||||
chr1:51264285 | A | ATAT | 3 | a0001c0001t0001g0156a0001c0001t0002g0161a0001c0001t0037g0122 | 3 | HG02080.hp2 NA18962.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.124-5671_124-5670i others(5): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264285 | ||||||
chr1:51264285 | A | ATATATAT | 4 | a0001c0001t0001g0086a0001c0001t0002g0084a0001c0001t0018g0004others(1): Show | 4 | HG00099.hp2 HG00639.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-5671_124-5670i others(9): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264285 | ||||||
chr1:51264285 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0080 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.124-5671_124-5670i others(21): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264285 | ||||||
chr1:51264285 | A | T | 25 | a0001c0001t0001g0081a0001c0001t0001g0111a0001c0001t0001g0121others(22): Show | 25 | HG00140.hp1 HG01943.hp2 HG02615.hp1 others(22): Show |
intron_variant | MODIFIER | c.124-5671A>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264285 | ||||||
chr1:51264285 | AAAATATA others(5): Show |
A | 3 | a0001c0001t0004g0011a0001c0001t0004g0094a0001c0001t0005g0056 | 4 | HG02055.hp1 HG02622.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-5669_124-5658d others(14): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264285 | |||||
chr1:51264285 | AAAATATA others(11): Show |
A | 1 | a0001c0001t0009g0127 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.124-5669_124-5652d others(20): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264285 | |||||
chr1:51264286 | A | T | 1 | a0001c0001t0015g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.124-5670A>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264286 | ||||||
chr1:51264286 | AAATATAT others(4): Show |
A | 1 | a0001c0001t0034g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.124-5668_124-5658d others(13): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264286 | |||||
chr1:51264286 | AAATATAT others(6): Show |
A | 1 | a0001c0001t0003g0112 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.124-5668_124-5656d others(15): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264286 | |||||
chr1:51264287 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.124-5668_124-5667i others(12): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264287 | |||||
chr1:51264287 | A | AAAAAATA others(5): Show |
2 | a0001c0001t0001g0082a0001c0001t0003g0035 | 2 | HG02572.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.124-5668_124-5667i others(14): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264287 | |||||
chr1:51264287 | A | AAAAATAT others(6): Show |
1 | a0001c0001t0003g0042 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.124-5668_124-5667i others(15): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264287 | |||||
chr1:51264287 | A | AAAATATA others(7): Show |
1 | a0001c0001t0002g0113 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.124-5668_124-5667i others(16): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264287 | |||||
chr1:51264287 | A | AATATATA others(3): Show |
2 | a0001c0001t0001g0033a0001c0001t0002g0110 | 2 | HG01891.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.124-5647_124-5638d others(12): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264287 | |||||
chr1:51264287 | A | AT | 4 | a0001c0001t0002g0141a0001c0001t0007g0039a0001c0001t0024g0031others(1): Show | 4 | HG02809.hp2 HG03225.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-5669_124-5668i others(3): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264287 | ||||||
chr1:51264287 | A | ATATAT | 3 | a0001c0001t0001g0206a0001c0001t0002g0189a0001c0001t0007g0038 | 3 | HG01243.hp2 HG02109.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.124-5669_124-5668i others(7): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264287 | ||||||
chr1:51264287 | A | ATATATAT others(4): Show |
1 | a0001c0001t0007g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.124-5669_124-5668i others(13): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264287 | ||||||
chr1:51264287 | A | T | 80 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0086others(77): Show | 83 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.124-5669A>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264287 | ||||||
chr1:51264287 | AAT | A | 7 | a0001c0001t0001g0219a0001c0001t0002g0175a0001c0001t0002g0176others(4): Show | 7 | HG01070.hp1 HG01257.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-5639_124-5638d others(4): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264287 | |||||
chr1:51264287 | AATATATA others(3): Show |
A | 1 | a0001c0001t0007g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.124-5647_124-5638d others(12): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264287 | |||||
chr1:51264288 | A | T | 2 | a0001c0001t0015g0058a0001c0001t0015g0093 | 2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.124-5668A>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264288 | ||||||
chr1:51264288 | AT | A | 5 | a0001c0001t0001g0186a0001c0001t0002g0138a0001c0001t0003g0174others(2): Show | 5 | HG02572.hp1 HG03209.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-5667delT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264288 | ||||||
chr1:51264289 | T | A | 14 | a0001c0001t0001g0140a0001c0001t0001g0201a0001c0001t0001g0239others(11): Show | 14 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.124-5667T>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264289 | ||||||
chr1:51264291 | T | A | 6 | a0001c0001t0001g0186a0001c0001t0001g0219a0001c0001t0002g0138others(3): Show | 6 | HG01070.hp1 HG01517.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-5665T>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264291 | ||||||
chr1:51264293 | T | A | 2 | a0001c0001t0003g0174a0001c0001t0020g0050 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.124-5663T>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264293 | ||||||
chr1:51264297 | T | A | 4 | a0001c0001t0001g0136a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG03490.hp1 HG03492.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-5659T>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264297 | ||||||
chr1:51264299 | T | A | 1 | a0001c0001t0007g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.124-5657T>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264299 | ||||||
chr1:51264304 | A | G | 1 | a0001c0001t0003g0123 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.124-5652A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264304 | ||||||
chr1:51264313 | T | C | 2 | a0001c0001t0015g0093a0001c0001t0023g0053 | 2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.124-5643T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264313 | ||||||
chr1:51264315 | T | C | 6 | a0001c0001t0015g0093a0001c0001t0016g0051a0001c0001t0016g0054others(3): Show | 6 | HG02055.hp2 HG02630.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-5641T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264315 | ||||||
chr1:51264317 | T | C | 38 | a0001c0001t0001g0083a0001c0001t0001g0095a0001c0001t0001g0149others(35): Show | 39 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.124-5639T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264317 | ||||||
chr1:51264317 | T | TACAC | 7 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0241others(4): Show | 7 | HG00099.hp2 HG00639.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-5619_124-5616d others(6): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264317 | |||||
chr1:51264317 | T | TATATATA others(7): Show |
1 | a0001c0001t0001g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.124-5638_124-5637i others(16): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264317 | |||||
chr1:51264317 | T | TATATATA others(9): Show |
1 | a0001c0001t0003g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.124-5638_124-5637i others(18): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264317 | |||||
chr1:51264317 | T | TATATATA others(15): Show |
1 | a0001c0001t0007g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.124-5638_124-5637i others(24): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264317 | |||||
chr1:51264317 | TACACAC | T | 5 | a0001c0001t0008g0019a0001c0001t0008g0021a0001c0001t0008g0022others(2): Show | 5 | HG01175.hp2 HG02257.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-5621_124-5616d others(8): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264317 | |||||
chr1:51264317 | TACACACA others(3): Show |
T | 1 | a0001c0001t0002g0105 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.124-5625_124-5616d others(12): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51264317 | |||||
chr1:51264319 | C | T | 45 | a0001c0001t0001g0137a0001c0001t0001g0160a0001c0001t0001g0193others(42): Show | 49 | HG00621.hp2 HG00642.hp1 HG01257.hp1 others(46): Show |
intron_variant | MODIFIER | c.124-5637C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264319 | ||||||
chr1:51264321 | C | T | 1 | a0001c0001t0017g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.124-5635C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264321 | ||||||
chr1:51264323 | C | T | 2 | a0001c0001t0008g0028a0001c0001t0011g0027 | 2 | HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.124-5633C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264323 | ||||||
chr1:51264329 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.124-5627C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264329 | ||||||
chr1:51264382 | C | G | 96 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0080others(93): Show | 101 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.124-5574C>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264382 | ||||||
chr1:51264813 | C | T | 3 | a0001c0001t0015g0058a0001c0001t0015g0092a0001c0001t0015g0093 | 3 | HG02451.hp2 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.124-5143C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264813 | ||||||
chr1:51264967 | G | A | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-4989G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51264967 | ||||||
chr1:51265181 | C | T | 16 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0018others(13): Show | 17 | NA18940.hp1 NA18946.hp2 NA18948.hp1 others(14): Show |
intron_variant | MODIFIER | c.124-4775C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51265181 | ||||||
chr1:51265195 | G | A | 1 | a0001c0001t0003g0223 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-4761G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51265195 | ||||||
chr1:51265197 | G | A | 3 | a0001c0001t0003g0035a0001c0001t0007g0036a0001c0001t0007g0040 | 3 | HG02572.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.124-4759G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51265197 | ||||||
chr1:51265228 | G | A | 30 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(27): Show | 33 | HG02071.hp2 HG02132.hp2 NA18940.hp1 others(30): Show |
intron_variant | MODIFIER | c.124-4728G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51265228 | ||||||
chr1:51265324 | C | CA | 10 | a0001c0001t0001g0136a0001c0001t0001g0151a0001c0001t0002g0089others(7): Show | 10 | HG02080.hp1 HG02976.hp1 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.124-4615dupA | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51265324 | |||||
chr1:51265324 | CA | C | 10 | a0001c0001t0002g0154a0001c0001t0004g0011a0001c0001t0004g0091others(7): Show | 11 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.124-4615delA | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51265324 | |||||
chr1:51265396 | A | G | 1 | a0001c0001t0021g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.124-4560A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51265396 | ||||||
chr1:51265459 | T | C | 1 | a0001c0001t0003g0042 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.124-4497T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51265459 | ||||||
chr1:51265489 | C | T | 1 | a0001c0001t0023g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124-4467C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51265489 | ||||||
chr1:51265575 | T | C | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-4381T>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51265575 | ||||||
chr1:51265681 | A | G | 7 | a0001c0001t0002g0224a0001c0001t0002g0225a0001c0001t0002g0226others(4): Show | 7 | HG00408.hp2 HG00438.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-4275A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51265681 | ||||||
chr1:51265683 | A | G | 1 | a0001c0001t0002g0231 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.124-4273A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51265683 | ||||||
chr1:51265720 | A | G | 30 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(27): Show | 33 | HG02071.hp2 HG02132.hp2 NA18940.hp1 others(30): Show |
intron_variant | MODIFIER | c.124-4236A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51265720 | ||||||
chr1:51265853 | CT | C | 212 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0033others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.124-4085delT | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51265853 | |||||
chr1:51265853 | CTT | C | 14 | a0001c0001t0001g0081a0001c0001t0001g0179a0001c0001t0001g0190others(11): Show | 15 | HG01069.hp1 HG01069.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.124-4086_124-4085d others(4): Show |
RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr1 | 51265853 | |||||
chr1:51265990 | A | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-3966A>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51265990 | ||||||
chr1:51266107 | A | G | 2 | a0001c0001t0001g0098a0001c0001t0002g0097 | 2 | HG03490.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.124-3849A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51266107 | ||||||
chr1:51266261 | A | T | 1 | a0001c0001t0002g0006 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.124-3695A>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51266261 | ||||||
chr1:51266467 | A | G | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-3489A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51266467 | ||||||
chr1:51266517 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.124-3439G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51266517 | ||||||
chr1:51266651 | C | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-3305C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51266651 | ||||||
chr1:51266803 | T | G | 1 | a0001c0001t0002g0110 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.124-3153T>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51266803 | ||||||
chr1:51267335 | G | A | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-2621G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51267335 | ||||||
chr1:51267357 | C | T | 5 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-2599C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51267357 | ||||||
chr1:51267824 | G | A | 2 | a0001c0001t0016g0051a0001c0001t0016g0054 | 2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.124-2132G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51267824 | ||||||
chr1:51267835 | G | A | 74 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(71): Show | 78 | HG00642.hp1 HG01109.hp1 HG01167.hp2 others(75): Show |
intron_variant | MODIFIER | c.124-2121G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51267835 | ||||||
chr1:51267973 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.124-1983C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51267973 | ||||||
chr1:51268299 | C | G | 7 | a0001c0001t0004g0005a0001c0001t0004g0011a0001c0001t0004g0091others(4): Show | 8 | HG00642.hp1 HG01257.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-1657C>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51268299 | ||||||
chr1:51268525 | G | A | 1 | a0001c0001t0007g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.124-1431G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51268525 | ||||||
chr1:51268714 | A | G | 19 | a0001c0001t0001g0098a0001c0001t0001g0136a0001c0001t0001g0167others(16): Show | 20 | HG00280.hp2 HG01070.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.124-1242A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51268714 | ||||||
chr1:51268809 | T | G | 258 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0033others(255): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.124-1147T>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51268809 | ||||||
chr1:51269338 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.124-618G>C | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 1/2 | chr1 | 51269338 | ||||||
chr1:51270384 | C | G | 23 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0042others(20): Show | 23 | HG01167.hp2 HG01169.hp1 HG01517.hp2 others(20): Show |
intron_variant | MODIFIER | c.293+259C>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 2/2 | chr1 | 51270384 | ||||||
chr1:51270411 | G | A | 1 | a0001c0001t0002g0176 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.293+286G>A | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 2/2 | chr1 | 51270411 | ||||||
chr1:51270800 | T | G | 1 | a0001c0001t0002g0105 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.294-351T>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 2/2 | chr1 | 51270800 | ||||||
chr1:51270921 | C | T | 4 | a0001c0001t0001g0136a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG03490.hp1 HG03492.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.294-230C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 2/2 | chr1 | 51270921 | ||||||
chr1:51270933 | C | T | 4 | a0001c0001t0016g0051a0001c0001t0016g0054a0001c0001t0021g0052others(1): Show | 4 | HG02630.hp2 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.294-218C>T | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 2/2 | chr1 | 51270933 | ||||||
chr1:51271048 | A | G | 1 | a0001c0001t0007g0047 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.294-103A>G | RNF11 | ENSG00000123091.5 | transcript | ENST00000242719.4 | protein_coding | 2/2 | chr1 | 51271048 |