geneid | 51444 |
---|---|
ensemblid | ENSG00000134758.14 |
hgncid | 17765 |
symbol | RNF138 |
name | ring finger protein 138 |
refseq_nuc | NM_016271.5 |
refseq_prot | NP_057355.2 |
ensembl_nuc | ENST00000261593.8 |
ensembl_prot | ENSP00000261593.3 |
mane_status | MANE Select |
chr | chr18 |
start | 32091874 |
end | 32131561 |
strand | + |
ver | v1.2 |
region | chr18:32091874-32131561 |
region5000 | chr18:32086874-32136561 |
regionname0 | RNF138_chr18_32091874_32131561 |
regionname5000 | RNF138_chr18_32086874_32136561 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 245 | 351 | 75 | 62 | 160 | 14 | 38 | 120 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0002 | 0/0 | 245 | 9 | 7 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0003 | 0/0 | 245 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 738 | 344 | 75 | 61 | 154 | 14 | 38 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
c0002 | 0/0 | 738 | 9 | 7 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
c0003 | 0/0 | 738 | 6 | 0 | 0 | 6 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
c0004 | 0/0 | 738 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
c0005 | 0/0 | 738 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2767 | 130 | 15 | 27 | 72 | 8 | 8 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0002 | 1/0 | 2814 | 91 | 11 | 17 | 43 | 3 | 16 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0003 | 0/1 | 2770 | 39 | 15 | 6 | 9 | 2 | 6 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0004 | 0/0 | 2768 | 28 | 2 | 5 | 15 | 0 | 6 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0005 | 0/0 | 2770 | 14 | 13 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0006 | 0/0 | 2770 | 9 | 7 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0007 | 0/0 | 2767 | 8 | 0 | 0 | 8 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0008 | 0/0 | 2813 | 7 | 7 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0009 | 0/0 | 2733 | 4 | 0 | 0 | 4 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0010 | 0/0 | 2812 | 3 | 3 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0011 | 0/0 | 2766 | 3 | 2 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0012 | 0/0 | 2770 | 3 | 2 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0013 | 0/0 | 2814 | 2 | 0 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0014 | 0/0 | 2770 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0015 | 0/0 | 2814 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0016 | 0/0 | 2767 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0017 | 0/0 | 2767 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0018 | 0/0 | 2770 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0019 | 0/0 | 2814 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0020 | 0/0 | 2770 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0021 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0022 | 0/0 | 2767 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0023 | 0/0 | 2814 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0024 | 0/0 | 2814 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0025 | 0/0 | 2722 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0026 | 0/0 | 2768 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0027 | 0/0 | 2767 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0028 | 0/0 | 2814 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0029 | 0/0 | 2814 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0030 | 0/0 | 2767 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
t0031 | 0/0 | 2767 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 11 | 0 | 1 | 9 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0004 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0005 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0031 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0279 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 738 | 344 | 75 | 61 | 154 | 14 | 38 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0003 | 0/0 | 738 | 6 | 0 | 0 | 6 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0005 | 0/0 | 738 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0002c0002 | 0/0 | 738 | 9 | 7 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0003c0004 | 0/0 | 738 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3504 | 130 | 15 | 27 | 72 | 8 | 8 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0002 | 1/0 | 3551 | 86 | 11 | 17 | 38 | 3 | 16 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0003 | 0/1 | 3507 | 38 | 15 | 6 | 8 | 2 | 6 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0004 | 0/0 | 3505 | 27 | 2 | 4 | 15 | 0 | 6 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0005 | 0/0 | 3507 | 14 | 13 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0007 | 0/0 | 3504 | 8 | 0 | 0 | 8 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0008 | 0/0 | 3550 | 7 | 7 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0009 | 0/0 | 3470 | 4 | 0 | 0 | 4 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0010 | 0/0 | 3549 | 3 | 3 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0011 | 0/0 | 3503 | 3 | 2 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0012 | 0/0 | 3507 | 3 | 2 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0013 | 0/0 | 3551 | 2 | 0 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0015 | 0/0 | 3551 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0016 | 0/0 | 3504 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0017 | 0/0 | 3504 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0018 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0019 | 0/0 | 3551 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0020 | 0/0 | 3507 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0021 | 0/0 | 3503 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0022 | 0/0 | 3504 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0023 | 0/0 | 3551 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0024 | 0/0 | 3551 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0025 | 0/0 | 3459 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0026 | 0/0 | 3505 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0027 | 0/0 | 3504 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0028 | 0/0 | 3551 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0029 | 0/0 | 3551 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0030 | 0/0 | 3504 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0001t0031 | 0/0 | 3504 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0003t0002 | 0/0 | 3551 | 5 | 0 | 0 | 5 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0003t0003 | 0/0 | 3507 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0001c0005t0004 | 0/0 | 3505 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0002c0002t0006 | 0/0 | 3507 | 9 | 7 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
a0003c0004t0014 | 0/0 | 3507 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | copy fasta | chr18 | 32086874 | 32136561 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 0 | 1 | 8 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0005 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0279 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0004 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0005g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0005g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0007g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0008g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0008g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0009g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0009g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0009g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0010g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0011g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0011g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0012g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0012g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0013g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0013g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0015g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0015g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0016g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0017g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0018g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0019g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0020g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0021g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0022g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0023g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0024g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0025g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0026g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0027g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0028g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0029g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0030g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0001t0031g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0003t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0003t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0001c0005t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0002c0002t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0002c0002t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0002c0002t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0002c0002t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0002c0002t0006g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0002c0002t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0002c0002t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0002c0002t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
a0003c0004t0014g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0281 | EUR | GBR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0282 | EUR | GBR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | GBR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0080 | EUR | FIN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | FIN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | FIN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00423 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0168 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00639 | hp1 | a0001 | c0005 | t0004 | g0173 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | CHS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0178 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00735 | hp2 | a0001 | c0001 | t0013 | g0053 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0174 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0273 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0271 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0190 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01109 | hp2 | a0001 | c0001 | t0031 | g0230 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01167 | hp1 | a0002 | c0002 | t0006 | g0197 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0280 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01169 | hp2 | a0002 | c0002 | t0006 | g0194 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0175 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01243 | hp1 | a0001 | c0001 | t0027 | g0211 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01346 | hp1 | a0001 | c0001 | t0013 | g0056 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0276 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0172 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0296 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01884 | hp2 | a0001 | c0001 | t0010 | g0014 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0041 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01891 | hp2 | a0002 | c0002 | t0006 | g0196 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02027 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0191 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02055 | hp2 | a0001 | c0001 | t0008 | g0010 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0170 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02145 | hp1 | a0001 | c0001 | t0015 | g0088 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02145 | hp2 | a0002 | c0002 | t0006 | g0199 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | CDX | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CDX | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CDX | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CDX | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0294 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0291 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0297 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02451 | hp2 | a0001 | c0001 | t0008 | g0010 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0293 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0275 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02723 | hp1 | a0003 | c0004 | t0014 | g0024 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0184 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02738 | hp2 | a0001 | c0001 | t0029 | g0083 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02818 | hp2 | a0001 | c0001 | t0010 | g0014 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02895 | hp1 | a0003 | c0004 | t0014 | g0024 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0192 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0186 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03041 | hp2 | a0001 | c0001 | t0011 | g0017 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03098 | hp2 | a0002 | c0002 | t0006 | g0198 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0189 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03139 | hp2 | a0002 | c0002 | t0006 | g0195 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0298 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03195 | hp2 | a0001 | c0001 | t0010 | g0044 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03453 | hp1 | a0002 | c0002 | t0006 | g0033 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03453 | hp2 | a0001 | c0001 | t0030 | g0224 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0295 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03486 | hp2 | a0002 | c0002 | t0006 | g0265 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0022 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0022 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03516 | hp1 | a0001 | c0001 | t0008 | g0098 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03540 | hp1 | a0001 | c0001 | t0012 | g0162 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0292 | AFR | GWD | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03579 | hp1 | a0001 | c0001 | t0008 | g0107 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | MSL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0283 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0181 | SAS | STU | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | STU | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0034 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0284 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0185 | SAS | STU | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG04199 | hp2 | a0001 | c0001 | t0023 | g0058 | SAS | STU | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0188 | AFR | YRI | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | CHB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18747 | hp2 | a0001 | c0001 | t0017 | g0249 | EAS | CHB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0285 | AFR | YRI | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | YRI | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18940 | hp1 | a0001 | c0001 | t0020 | g0244 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18948 | hp1 | a0001 | c0001 | t0024 | g0013 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18952 | hp1 | a0001 | c0001 | t0009 | g0112 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18972 | hp2 | a0001 | c0001 | t0007 | g0137 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18974 | hp2 | a0001 | c0003 | t0003 | g0128 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18978 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18984 | hp1 | a0001 | c0003 | t0002 | g0124 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18988 | hp1 | a0001 | c0001 | t0026 | g0165 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18989 | hp2 | a0001 | c0001 | t0016 | g0222 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18991 | hp1 | a0001 | c0001 | t0021 | g0254 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18991 | hp2 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18992 | hp1 | a0001 | c0001 | t0007 | g0153 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18994 | hp1 | a0001 | c0001 | t0007 | g0018 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18997 | hp1 | a0001 | c0001 | t0011 | g0073 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19002 | hp2 | a0001 | c0001 | t0007 | g0150 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19005 | hp1 | a0001 | c0001 | t0007 | g0151 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19012 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | LWK | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19030 | hp2 | a0002 | c0002 | t0006 | g0033 | AFR | LWK | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | LWK | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19043 | hp2 | a0001 | c0001 | t0008 | g0046 | AFR | LWK | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19057 | hp2 | a0001 | c0003 | t0002 | g0016 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19066 | hp2 | a0001 | c0001 | t0007 | g0139 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19074 | hp2 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19076 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19078 | hp2 | a0001 | c0003 | t0002 | g0123 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19082 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19084 | hp1 | a0001 | c0003 | t0002 | g0016 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19084 | hp2 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19089 | hp2 | a0001 | c0001 | t0019 | g0106 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19091 | hp1 | a0001 | c0001 | t0009 | g0042 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA20129 | hp1 | a0001 | c0001 | t0015 | g0089 | AFR | ASW | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0043 | AFR | ASW | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | TSI | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA20752 | hp2 | a0001 | c0001 | t0025 | g0034 | EUR | TSI | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | TSI | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | TSI | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01123 | hp1 | a0001 | c0001 | t0022 | g0234 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG01123 | hp2 | a0001 | c0001 | t0012 | g0161 | AMR | CLM | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02109 | hp1 | a0001 | c0001 | t0011 | g0017 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02486 | hp1 | a0001 | c0001 | t0012 | g0163 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | ACB | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18955 | hp1 | a0001 | c0003 | t0002 | g0127 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0278 | AFR | USA | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | USA | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA21309 | hp1 | a0001 | c0001 | t0018 | g0202 | AFR | LWK | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
NA21309 | hp2 | a0001 | c0001 | t0028 | g0092 | AFR | LWK | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0279 | REF | REF | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0102 | REF | REF | RNF138_chr18_32086874_32136561 | RNF138 | chr18 | 32086874 | 32136561 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:32092785
|
G | C | 1 | a0002 | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
missense_variant | MODERATE | c.9G>C | p.Glu3Asp | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/8 | 448/3551 | 9/738 | 3/245 | chr18 | 32092785 | ||
chr18:32111885
|
A | G | 1 | a0003 | 2 | HG02723.hp1 HG02895.hp1 |
missense_variant | MODERATE | c.242A>G | p.Lys81Arg | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/8 | 681/3551 | 242/738 | 81/245 | chr18 | 32111885 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:32092872
|
G | C | 1 | a0001c0003 | 6 | NA18955.hp1 NA18974.hp2 NA18984.hp1 others(3): Show |
synonymous_variant | LOW | c.96G>C | p.Thr32Thr | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/8 | 535/3551 | 96/738 | 32/245 | chr18 | 32092872 | ||
chr18:32092872
|
G | T | 1 | a0001c0005 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.96G>T | p.Thr32Thr | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/8 | 535/3551 | 96/738 | 32/245 | chr18 | 32092872 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:32091891
|
A | G | 1 | a0001c0001t0031 | 1 | HG01109.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-422A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | chr18 | 32091891 | ||||||
chr18:32091904
|
T | C | 1 | a0001c0001t0017 | 1 | NA18747.hp2 | 5_prime_UTR_variant | MODIFIER | c.-409T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | 873 | chr18 | 32091904 | |||||
chr18:32091910
|
C | T | 1 | a0001c0001t0030 | 1 | HG03453.hp2 | 5_prime_UTR_variant | MODIFIER | c.-403C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | 867 | chr18 | 32091910 | |||||
chr18:32091923
|
C | T | 1 | a0001c0001t0012 | 3 | HG01123.hp2 HG02486.hp1 HG03540.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-390C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | chr18 | 32091923 | ||||||
chr18:32091942
|
G | A | 1 | a0002c0002t0006 | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-371G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | 835 | chr18 | 32091942 | |||||
chr18:32091953
|
CGGCGCTC others(27): Show |
C | 1 | a0001c0001t0009 | 4 | HG00423.hp2 NA18952.hp1 NA19012.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-358_-325delGCGCTC others(28): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | 789 | INFO_REALIGN_3_PRIME | chr18 | 32091953 | ||||
chr18:32091974
|
C | T | 1 | a0001c0001t0016 | 2 | NA18989.hp2 NA19084.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-339C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | chr18 | 32091974 | ||||||
chr18:32092060
|
C | G | 1 | a0001c0001t0029 | 1 | HG02738.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-253C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | chr18 | 32092060 | ||||||
chr18:32092072
|
G | A | 1 | a0001c0001t0013 | 2 | HG00735.hp2 HG01346.hp1 |
5_prime_UTR_variant | MODIFIER | c.-241G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | 705 | chr18 | 32092072 | |||||
chr18:32092154
|
T | C | 1 | a0001c0001t0005 | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-159T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | 623 | chr18 | 32092154 | |||||
chr18:32092155
|
C | T | 1 | a0001c0001t0007 | 8 | NA18972.hp2 NA18991.hp2 NA18992.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-158C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | chr18 | 32092155 | ||||||
chr18:32092206
|
C | A | 1 | a0001c0001t0018 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/8 | 571 | chr18 | 32092206 | |||||
chr18:32092713
|
G | T | 1 | a0001c0001t0015 | 2 | HG02145.hp1 NA20129.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-64G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/8 | chr18 | 32092713 | ||||||
chr18:32092769
|
C | T | 1 | a0001c0001t0028 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-8C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/8 | 8 | chr18 | 32092769 | |||||
chr18:32129197
|
A | G | 1 | a0001c0001t0027 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 10 | chr18 | 32129197 | |||||
chr18:32129212
|
TG | T | 1 | a0001c0001t0008 | 7 | HG01891.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*26delG | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 26 | chr18 | 32129212 | |||||
chr18:32129306
|
T | A | 1 | a0001c0001t0019 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*119T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 119 | chr18 | 32129306 | |||||
chr18:32129307
|
A | G | 1 | a0001c0001t0019 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*120A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 120 | chr18 | 32129307 | |||||
chr18:32129477
|
T | A | 1 | a0001c0001t0020 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*290T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 290 | chr18 | 32129477 | |||||
chr18:32129482
|
CATT | C | 10 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(7): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*301_*303delTAT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 301 | INFO_REALIGN_3_PRIME | chr18 | 32129482 | ||||
chr18:32129485
|
T | C | 1 | a0001c0001t0020 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*298T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 298 | chr18 | 32129485 | |||||
chr18:32129569
|
C | T | 1 | a0001c0001t0022 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*382C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 382 | chr18 | 32129569 | |||||
chr18:32129712
|
T | C | 1 | a0003c0004t0014 | 2 | HG02723.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*525T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 525 | chr18 | 32129712 | |||||
chr18:32129800
|
T | C | 1 | a0001c0001t0023 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*613T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 613 | chr18 | 32129800 | |||||
chr18:32129853
|
A | G | 1 | a0001c0001t0026 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*666A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 666 | chr18 | 32129853 | |||||
chr18:32129875
|
CTT | C | 1 | a0001c0001t0010 | 3 | HG01884.hp2 HG02818.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*690_*691delTT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 690 | INFO_REALIGN_3_PRIME | chr18 | 32129875 | ||||
chr18:32130076
|
A | G | 1 | a0001c0001t0027 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*889A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 889 | chr18 | 32130076 | |||||
chr18:32130917
|
A | AAG | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(19): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*1732_*1733dupGA | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 1734 | INFO_REALIGN_3_PRIME | chr18 | 32130917 | ||||
chr18:32130972
|
TCAAAGTT others(41): Show |
T | 21 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(18): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*1882_*1929delCAAA others(44): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 1882 | INFO_REALIGN_3_PRIME | chr18 | 32130972 | ||||
chr18:32130972
|
TCAAAGTT others(89): Show |
T | 1 | a0001c0001t0025 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1834_*1929delCAAA others(92): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 1834 | INFO_REALIGN_3_PRIME | chr18 | 32130972 | ||||
chr18:32131012
|
TGGGATTT others(42): Show |
T | 1 | a0001c0001t0021 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1828_*1876delGATT others(45): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 1828 | INFO_REALIGN_3_PRIME | chr18 | 32131012 | ||||
chr18:32131039
|
A | G | 1 | a0001c0001t0024 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1852A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 1852 | chr18 | 32131039 | |||||
chr18:32131298
|
A | C | 11 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(8): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*2111A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 2111 | chr18 | 32131298 | |||||
chr18:32131304
|
CCT | C | 3 | a0001c0001t0004a0001c0001t0026a0001c0005t0004 | 29 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2120_*2121delCT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 2120 | INFO_REALIGN_3_PRIME | chr18 | 32131304 | ||||
chr18:32131376
|
G | GTT | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(19): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*2191_*2192dupTT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 8/8 | 2193 | INFO_REALIGN_3_PRIME | chr18 | 32131376 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:32092365
|
A | T | 7 | a0001c0001t0001g0038a0001c0001t0001g0299a0001c0001t0001g0300others(4): Show | 8 | HG01099.hp1 HG01258.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.-78+130A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/7 | chr18 | 32092365 | ||||||
chr18:32092417
|
C | G | 4 | a0001c0001t0005g0295a0001c0001t0005g0296a0001c0001t0005g0297others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-78+182C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/7 | chr18 | 32092417 | ||||||
chr18:32092529
|
C | T | 5 | a0001c0001t0003g0037a0001c0001t0003g0291a0001c0001t0003g0292others(2): Show | 6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-77-171C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/7 | chr18 | 32092529 | ||||||
chr18:32092596
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(203): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.-77-104A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/7 | chr18 | 32092596 | ||||||
chr18:32092629
|
AG | A | 35 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(32): Show | 39 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.-77-68delG | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 32092629 | |||||
chr18:32092904
|
C | A | 1 | a0001c0001t0002g0039 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.110+18C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32092904 | ||||||
chr18:32092944
|
GGCCCGGG others(13): Show |
G | 5 | a0001c0001t0003g0037a0001c0001t0003g0291a0001c0001t0003g0292others(2): Show | 6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+62_110+81delCG others(18): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32092944 | |||||
chr18:32092978
|
C | A | 32 | a0001c0001t0002g0183a0001c0001t0003g0020a0001c0001t0003g0021others(29): Show | 38 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.110+92C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32092978 | ||||||
chr18:32093105
|
G | GCTCCCGC others(1): Show |
19 | a0001c0001t0001g0025a0001c0001t0001g0203a0001c0001t0001g0204others(16): Show | 23 | HG00280.hp2 HG00423.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.110+257_110+264dup others(8): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32093105 | |||||
chr18:32093105
|
G | GCTCCCGC others(9): Show |
7 | a0001c0001t0001g0193a0001c0001t0005g0007a0001c0001t0005g0023others(4): Show | 10 | HG01109.hp1 HG02055.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.110+249_110+264dup others(16): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32093105 | |||||
chr18:32093105
|
G | GCTCCCGC others(17): Show |
1 | a0001c0001t0005g0188 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+241_110+264dup others(24): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32093105 | |||||
chr18:32093105
|
GCTCCCGC others(1): Show |
G | 88 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(85): Show | 100 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.110+257_110+264del others(8): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32093105 | |||||
chr18:32093105
|
GCTCCCGC others(9): Show |
G | 8 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(5): Show | 10 | HG00408.hp2 HG02109.hp1 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.110+249_110+264del others(16): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32093105 | |||||
chr18:32093393
|
C | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.110+507C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32093393 | ||||||
chr18:32093498
|
G | A | 1 | a0001c0001t0005g0295 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.110+612G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32093498 | ||||||
chr18:32093502
|
T | A | 1 | a0001c0001t0004g0160 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.110+616T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32093502 | ||||||
chr18:32093548
|
G | A | 3 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0163 | 3 | HG01123.hp2 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.110+662G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32093548 | ||||||
chr18:32093592
|
C | T | 47 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(44): Show | 54 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.110+706C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32093592 | ||||||
chr18:32093680
|
G | T | 2 | a0001c0001t0009g0011a0001c0001t0009g0042 | 3 | HG00423.hp2 NA19012.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.110+794G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32093680 | ||||||
chr18:32093770
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.110+884C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32093770 | ||||||
chr18:32093989
|
C | T | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+1103C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32093989 | ||||||
chr18:32094043
|
G | A | 1 | a0001c0001t0008g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.110+1157G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094043 | ||||||
chr18:32094208
|
C | CT | 81 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.110+1332dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32094208 | |||||
chr18:32094328
|
C | T | 1 | a0001c0001t0003g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.110+1442C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094328 | ||||||
chr18:32094437
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.110+1551A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094437 | ||||||
chr18:32094458
|
T | A | 1 | a0001c0001t0004g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.110+1572T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094458 | ||||||
chr18:32094559
|
T | C | 1 | a0001c0001t0005g0189 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.110+1673T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094559 | ||||||
chr18:32094606
|
A | G | 55 | a0001c0001t0002g0183a0001c0001t0003g0020a0001c0001t0003g0021others(52): Show | 63 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.110+1720A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094606 | ||||||
chr18:32094609
|
A | G | 34 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(31): Show | 38 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.110+1723A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094609 | ||||||
chr18:32094642
|
A | T | 1 | a0001c0001t0001g0154 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.110+1756A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094642 | ||||||
chr18:32094780
|
C | CTA | 36 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(33): Show | 40 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.110+1909_110+1910d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32094780 | |||||
chr18:32094851
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.110+1965A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094851 | ||||||
chr18:32094879
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(2): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+1993C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094879 | ||||||
chr18:32094965
|
C | G | 1 | a0001c0001t0001g0115 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.110+2079C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32094965 | ||||||
chr18:32095023
|
T | C | 1 | a0001c0001t0010g0044 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.110+2137T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095023 | ||||||
chr18:32095029
|
G | A | 55 | a0001c0001t0002g0183a0001c0001t0003g0020a0001c0001t0003g0021others(52): Show | 63 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.110+2143G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095029 | ||||||
chr18:32095044
|
T | C | 5 | a0001c0001t0003g0037a0001c0001t0003g0291a0001c0001t0003g0292others(2): Show | 6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+2158T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095044 | ||||||
chr18:32095047
|
A | G | 1 | a0001c0001t0001g0264 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.110+2161A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095047 | ||||||
chr18:32095073
|
G | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0210 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.110+2187G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095073 | ||||||
chr18:32095178
|
G | GT | 8 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0105others(5): Show | 8 | HG01891.hp1 HG02132.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.110+2301dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32095178 | |||||
chr18:32095180
|
T | TA | 204 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(201): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.110+2294_110+2295i others(3): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095180 | ||||||
chr18:32095194
|
T | C | 5 | a0001c0001t0003g0037a0001c0001t0003g0291a0001c0001t0003g0292others(2): Show | 6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+2308T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095194 | ||||||
chr18:32095264
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(2): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+2378C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095264 | ||||||
chr18:32095284
|
C | T | 1 | a0001c0001t0007g0153 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.110+2398C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095284 | ||||||
chr18:32095445
|
G | A | 20 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(17): Show | 22 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.110+2559G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095445 | ||||||
chr18:32095706
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.110+2820G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095706 | ||||||
chr18:32095830
|
C | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(121): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.110+2944C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095830 | ||||||
chr18:32095863
|
A | G | 1 | a0003c0004t0014g0024 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.110+2977A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095863 | ||||||
chr18:32095883
|
T | C | 1 | a0001c0001t0026g0165 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.110+2997T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095883 | ||||||
chr18:32095956
|
G | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | NA19057.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.110+3070G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32095956 | ||||||
chr18:32096171
|
T | C | 1 | a0001c0001t0003g0200 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110+3285T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096171 | ||||||
chr18:32096185
|
C | T | 1 | a0001c0001t0004g0179 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.110+3299C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096185 | ||||||
chr18:32096224
|
A | G | 5 | a0001c0001t0003g0037a0001c0001t0003g0291a0001c0001t0003g0292others(2): Show | 6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+3338A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096224 | ||||||
chr18:32096252
|
A | G | 1 | a0001c0001t0004g0187 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.110+3366A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096252 | ||||||
chr18:32096437
|
C | T | 1 | a0001c0001t0005g0189 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.110+3551C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096437 | ||||||
chr18:32096459
|
T | C | 1 | a0001c0001t0008g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.110+3573T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096459 | ||||||
chr18:32096658
|
A | C | 5 | a0001c0001t0003g0037a0001c0001t0003g0291a0001c0001t0003g0292others(2): Show | 6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+3772A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096658 | ||||||
chr18:32096701
|
A | T | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+3815A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096701 | ||||||
chr18:32096853
|
A | G | 27 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(24): Show | 29 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.110+3967A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096853 | ||||||
chr18:32096907
|
T | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(166): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.110+4021T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096907 | ||||||
chr18:32096914
|
G | T | 1 | a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.110+4028G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096914 | ||||||
chr18:32096971
|
G | A | 1 | a0001c0001t0004g0180 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.110+4085G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32096971 | ||||||
chr18:32097064
|
AT | A | 5 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050others(2): Show | 5 | HG00741.hp1 HG01167.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.110+4180delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097064 | |||||
chr18:32097071
|
T | C | 2 | a0001c0001t0001g0203a0001c0001t0001g0210 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.110+4185T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097071 | ||||||
chr18:32097272
|
A | G | 8 | a0001c0001t0003g0036a0001c0001t0003g0278a0001c0001t0003g0279others(5): Show | 9 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.110+4386A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097272 | ||||||
chr18:32097387
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.110+4501A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097387 | ||||||
chr18:32097534
|
A | G | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | NA18978.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.110+4648A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097534 | ||||||
chr18:32097557
|
T | C | 303 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(300): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.110+4671T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097557 | ||||||
chr18:32097559
|
C | T | 1 | a0001c0001t0004g0185 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.110+4673C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097559 | ||||||
chr18:32097600
|
C | T | 2 | a0001c0001t0002g0125a0001c0001t0002g0126 | 2 | HG02155.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.110+4714C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097600 | ||||||
chr18:32097617
|
G | A | 5 | a0001c0001t0003g0037a0001c0001t0003g0291a0001c0001t0003g0292others(2): Show | 6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+4731G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097617 | ||||||
chr18:32097648
|
C | G | 2 | a0001c0001t0008g0098a0001c0001t0008g0107 | 2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.110+4762C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097648 | ||||||
chr18:32097734
|
G | C | 1 | a0001c0001t0001g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.110+4848G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097734 | ||||||
chr18:32097743
|
G | A | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+4857G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097743 | ||||||
chr18:32097781
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.110+4895C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097781 | ||||||
chr18:32097818
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110+4932C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097818 | ||||||
chr18:32097876
|
G | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(2): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+4990G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097876 | ||||||
chr18:32097878
|
ATATATGT others(5): Show |
A | 1 | a0001c0003t0002g0124 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.110+5008_110+5019d others(14): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097878 | |||||
chr18:32097902
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(206): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.110+5016G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097902 | ||||||
chr18:32097944
|
A | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.110+5058A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097944 | ||||||
chr18:32097944
|
ATG | A | 49 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(46): Show | 56 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.110+5090_110+5091d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097944 | |||||
chr18:32097944
|
ATGTG | A | 11 | a0001c0001t0002g0040a0001c0001t0002g0085a0001c0001t0002g0086others(8): Show | 11 | HG00733.hp2 HG01168.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.110+5088_110+5091d others(6): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097944 | |||||
chr18:32097944
|
ATGTGTG | A | 27 | a0001c0001t0002g0006a0001c0001t0002g0093a0001c0001t0002g0094others(24): Show | 33 | HG01106.hp1 HG01243.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.110+5086_110+5091d others(8): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097944 | |||||
chr18:32097946
|
G | A | 1 | a0001c0001t0013g0053 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.110+5060G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097946 | ||||||
chr18:32097966
|
GTGTGTGT others(4): Show |
G | 2 | a0001c0001t0001g0299a0001c0001t0005g0190 | 2 | HG01109.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.110+5082_110+5092d others(13): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097966 | |||||
chr18:32097968
|
GTGTGTGT others(2): Show |
G | 15 | a0001c0001t0001g0155a0001c0001t0001g0217a0001c0001t0001g0264others(12): Show | 18 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.110+5084_110+5092d others(11): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097968 | |||||
chr18:32097970
|
GTGTGTGT | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 106 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.110+5086_110+5092d others(9): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097970 | |||||
chr18:32097972
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.110+5086G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097972 | ||||||
chr18:32097972
|
GTGTGT | G | 15 | a0001c0001t0001g0031a0001c0001t0001g0132a0001c0001t0001g0133others(12): Show | 16 | HG00140.hp2 HG00597.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.110+5088_110+5092d others(7): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097972 | |||||
chr18:32097974
|
GTGT | G | 56 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 66 | HG00423.hp1 HG00621.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.110+5090_110+5092d others(5): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097974 | |||||
chr18:32097976
|
GT | G | 6 | a0001c0001t0001g0152a0001c0001t0001g0210a0001c0001t0003g0200others(3): Show | 6 | HG00558.hp1 HG00733.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.110+5092delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32097976 | |||||
chr18:32097977
|
T | TG | 6 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(3): Show | 8 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.110+5091_110+5092i others(3): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097977 | ||||||
chr18:32097977
|
T | TGTG | 4 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0271others(1): Show | 4 | HG01099.hp2 NA18612.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+5091_110+5092i others(5): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097977 | ||||||
chr18:32097977
|
T | TGTGTG | 8 | a0001c0001t0003g0034a0001c0001t0003g0268a0001c0001t0003g0269others(5): Show | 8 | HG01070.hp1 HG01361.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.110+5091_110+5092i others(7): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097977 | ||||||
chr18:32097977
|
T | TGTGTGTG | 4 | a0001c0001t0003g0035a0001c0001t0003g0277a0001c0001t0003g0279others(1): Show | 5 | HG03490.hp1 HG03492.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.110+5091_110+5092i others(9): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097977 | ||||||
chr18:32097977
|
T | TGTGTGTG others(2): Show |
4 | a0001c0001t0003g0036a0001c0001t0003g0280a0001c0001t0003g0281others(1): Show | 5 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.110+5091_110+5092i others(11): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097977 | ||||||
chr18:32097977
|
T | TGTGTGTG others(4): Show |
2 | a0001c0001t0003g0283a0001c0001t0003g0284 | 2 | HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.110+5091_110+5092i others(13): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097977 | ||||||
chr18:32097979
|
A | G | 1 | a0001c0001t0002g0052 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.110+5093A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097979 | ||||||
chr18:32097979
|
A | T | 2 | a0001c0001t0001g0218a0001c0001t0004g0187 | 2 | HG00408.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.110+5093A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097979 | ||||||
chr18:32097981
|
T | G | 2 | a0001c0001t0001g0218a0001c0001t0004g0187 | 2 | HG00408.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.110+5095T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32097981 | ||||||
chr18:32098008
|
G | A | 1 | a0001c0001t0003g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.110+5122G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32098008 | ||||||
chr18:32098209
|
A | G | 8 | a0002c0002t0006g0033a0002c0002t0006g0194a0002c0002t0006g0195others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.110+5323A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32098209 | ||||||
chr18:32098298
|
G | A | 1 | a0001c0001t0002g0206 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.110+5412G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32098298 | ||||||
chr18:32098488
|
G | A | 1 | a0001c0001t0012g0161 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.110+5602G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32098488 | ||||||
chr18:32098561
|
T | TA | 307 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(304): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.110+5678dupA | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32098561 | |||||
chr18:32098677
|
C | T | 1 | a0001c0001t0002g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.110+5791C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32098677 | ||||||
chr18:32098688
|
T | TA | 2 | a0001c0001t0001g0028a0001c0001t0001g0219 | 3 | HG00099.hp1 HG00642.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.110+5807dupA | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32098688 | |||||
chr18:32098760
|
G | A | 1 | a0003c0004t0014g0024 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.110+5874G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32098760 | ||||||
chr18:32098780
|
G | A | 31 | a0001c0001t0002g0183a0001c0001t0003g0021a0001c0001t0003g0166others(28): Show | 36 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.110+5894G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32098780 | ||||||
chr18:32098827
|
C | T | 6 | a0002c0002t0006g0194a0002c0002t0006g0195a0002c0002t0006g0196others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+5941C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32098827 | ||||||
chr18:32098914
|
A | AT | 8 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 9 | HG00741.hp1 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.110+6042dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32098914 | |||||
chr18:32098914
|
AT | A | 28 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0203others(25): Show | 32 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.110+6042delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32098914 | |||||
chr18:32098914
|
ATT | A | 45 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(42): Show | 52 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.110+6041_110+6042d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32098914 | |||||
chr18:32099034
|
T | C | 1 | a0001c0001t0003g0200 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110+6148T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099034 | ||||||
chr18:32099068
|
A | G | 2 | a0001c0001t0007g0150a0001c0001t0007g0151 | 2 | NA19002.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.110+6182A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099068 | ||||||
chr18:32099096
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(201): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.110+6210T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099096 | ||||||
chr18:32099161
|
T | C | 1 | a0001c0001t0018g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110+6275T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099161 | ||||||
chr18:32099282
|
T | G | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(2): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+6396T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099282 | ||||||
chr18:32099366
|
AG | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(2): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+6482delG | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32099366 | |||||
chr18:32099406
|
A | G | 26 | a0001c0001t0002g0006a0001c0001t0002g0093a0001c0001t0002g0094others(23): Show | 31 | HG00733.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.110+6520A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099406 | ||||||
chr18:32099433
|
C | T | 1 | a0001c0001t0004g0178 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.110+6547C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099433 | ||||||
chr18:32099533
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(31): Show | 38 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.110+6647G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099533 | ||||||
chr18:32099552
|
A | C | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(2): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+6666A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099552 | ||||||
chr18:32099597
|
G | A | 55 | a0001c0001t0002g0183a0001c0001t0003g0020a0001c0001t0003g0021others(52): Show | 63 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.110+6711G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099597 | ||||||
chr18:32099606
|
T | C | 1 | a0001c0001t0003g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.110+6720T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099606 | ||||||
chr18:32099844
|
C | G | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+6958C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099844 | ||||||
chr18:32099853
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0001g0210 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.110+6967C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099853 | ||||||
chr18:32099944
|
C | T | 1 | a0001c0001t0003g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.110+7058C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099944 | ||||||
chr18:32099959
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(250): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.110+7073A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099959 | ||||||
chr18:32099970
|
A | G | 3 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0015g0089 | 3 | HG01168.hp1 HG03710.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.110+7084A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32099970 | ||||||
chr18:32100201
|
G | GAT | 23 | a0001c0001t0001g0026a0001c0001t0001g0114a0001c0001t0001g0212others(20): Show | 26 | HG00280.hp1 HG01106.hp2 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.110+7335_110+7336d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100201 | |||||
chr18:32100201
|
G | GATAT | 2 | a0001c0001t0001g0027a0001c0001t0002g0082 | 3 | HG02602.hp2 HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.110+7333_110+7336d others(6): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100201 | |||||
chr18:32100201
|
G | GATATAT | 2 | a0001c0001t0003g0037a0001c0001t0003g0293 | 3 | HG02572.hp2 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.110+7331_110+7336d others(8): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100201 | |||||
chr18:32100201
|
G | GATATATA others(3): Show |
1 | a0001c0001t0003g0294 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.110+7327_110+7336d others(12): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100201 | |||||
chr18:32100201
|
GAT | G | 54 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(51): Show | 62 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.110+7335_110+7336d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100201 | |||||
chr18:32100331
|
G | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.110+7445G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100331 | ||||||
chr18:32100462
|
A | G | 1 | a0001c0001t0005g0297 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.110+7576A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100462 | ||||||
chr18:32100468
|
C | CT | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(116): Show | 145 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.110+7606dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100468 | |||||
chr18:32100468
|
C | CTT | 29 | a0001c0001t0001g0115a0001c0001t0001g0252a0001c0001t0001g0253others(26): Show | 31 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.110+7605_110+7606d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100468 | |||||
chr18:32100468
|
C | CTTT | 27 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0166others(24): Show | 33 | HG00408.hp2 HG00639.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.110+7604_110+7606d others(5): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100468 | |||||
chr18:32100468
|
CT | C | 6 | a0001c0001t0002g0040a0001c0001t0002g0048a0001c0001t0002g0054others(3): Show | 6 | HG01167.hp2 HG02922.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.110+7606delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32100468 | |||||
chr18:32100498
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.110+7612G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100498 | ||||||
chr18:32100498
|
G | T | 1 | a0001c0001t0003g0269 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.110+7612G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100498 | ||||||
chr18:32100500
|
A | G | 1 | a0001c0001t0001g0304 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.110+7614A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100500 | ||||||
chr18:32100512
|
G | C | 1 | a0001c0001t0027g0211 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.110+7626G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100512 | ||||||
chr18:32100516
|
G | C | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+7630G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100516 | ||||||
chr18:32100538
|
C | T | 1 | a0001c0001t0004g0187 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.110+7652C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100538 | ||||||
chr18:32100561
|
C | T | 5 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0251others(2): Show | 5 | HG01928.hp1 HG01981.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.110+7675C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100561 | ||||||
chr18:32100588
|
G | A | 1 | a0001c0001t0012g0163 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.110+7702G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100588 | ||||||
chr18:32100624
|
C | T | 1 | a0001c0001t0002g0208 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.110+7738C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100624 | ||||||
chr18:32100668
|
G | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0027g0211 | 3 | HG01243.hp1 HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.110+7782G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100668 | ||||||
chr18:32100771
|
C | T | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+7885C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100771 | ||||||
chr18:32100813
|
C | T | 22 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(19): Show | 24 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.110+7927C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100813 | ||||||
chr18:32100843
|
G | A | 7 | a0001c0001t0001g0038a0001c0001t0001g0299a0001c0001t0001g0300others(4): Show | 8 | HG01099.hp1 HG01258.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.110+7957G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100843 | ||||||
chr18:32100862
|
C | G | 1 | a0001c0001t0002g0108 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.110+7976C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100862 | ||||||
chr18:32100921
|
T | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | NA18978.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.110+8035T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100921 | ||||||
chr18:32100930
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(132): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.110+8044T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32100930 | ||||||
chr18:32101090
|
C | T | 1 | a0001c0001t0003g0274 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.110+8204C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101090 | ||||||
chr18:32101214
|
C | CT | 70 | a0001c0001t0001g0018a0001c0001t0001g0131a0001c0001t0001g0132others(67): Show | 80 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.110+8344dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32101214 | |||||
chr18:32101214
|
C | CTT | 9 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0129others(6): Show | 13 | HG00423.hp1 HG00558.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.110+8343_110+8344d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32101214 | |||||
chr18:32101230
|
TC | T | 4 | a0001c0001t0001g0256a0001c0001t0001g0300a0001c0001t0003g0273others(1): Show | 4 | HG01070.hp1 HG01256.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+8345delC | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101230 | ||||||
chr18:32101231
|
C | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(231): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.110+8345C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101231 | ||||||
chr18:32101232
|
A | T | 1 | a0001c0001t0004g0181 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.110+8346A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101232 | ||||||
chr18:32101283
|
G | A | 301 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(298): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.110+8397G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101283 | ||||||
chr18:32101295
|
T | G | 1 | a0001c0001t0002g0060 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.110+8409T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101295 | ||||||
chr18:32101323
|
A | G | 1 | a0001c0001t0003g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.110+8437A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101323 | ||||||
chr18:32101393
|
G | GTA | 6 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0301others(3): Show | 7 | HG01884.hp2 HG02818.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+8519_110+8520d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32101393 | |||||
chr18:32101468
|
A | G | 5 | a0001c0001t0003g0037a0001c0001t0003g0291a0001c0001t0003g0292others(2): Show | 6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+8582A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101468 | ||||||
chr18:32101573
|
T | A | 1 | a0001c0001t0003g0020 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.110+8687T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101573 | ||||||
chr18:32101631
|
C | T | 17 | a0001c0001t0001g0038a0001c0001t0001g0221a0001c0001t0001g0245others(14): Show | 18 | HG01099.hp1 HG01258.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.110+8745C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101631 | ||||||
chr18:32101646
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.110+8760C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101646 | ||||||
chr18:32101745
|
A | T | 1 | a0001c0001t0002g0051 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.110+8859A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101745 | ||||||
chr18:32101804
|
C | T | 1 | a0001c0001t0004g0022 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.110+8918C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101804 | ||||||
chr18:32101812
|
T | G | 1 | a0001c0001t0001g0031 | 2 | HG00140.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.110+8926T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32101812 | ||||||
chr18:32102043
|
A | AT | 42 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(39): Show | 49 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.110+9172dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32102043 | |||||
chr18:32102079
|
C | T | 2 | a0001c0001t0002g0109a0001c0001t0003g0200 | 2 | HG02155.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.110+9193C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102079 | ||||||
chr18:32102097
|
G | T | 2 | a0001c0001t0001g0203a0001c0001t0001g0210 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.110+9211G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102097 | ||||||
chr18:32102195
|
C | CT | 54 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(51): Show | 63 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.110+9333dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32102195 | |||||
chr18:32102195
|
C | CTT | 6 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0005g0190others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+9332_110+9333d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32102195 | |||||
chr18:32102195
|
CT | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0025others(93): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.110+9333delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32102195 | |||||
chr18:32102195
|
CTT | C | 7 | a0001c0001t0001g0110a0001c0001t0001g0215a0001c0001t0001g0220others(4): Show | 7 | HG00639.hp2 HG01169.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+9332_110+9333d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32102195 | |||||
chr18:32102195
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0003g0291a0001c0001t0003g0294 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.110+9321_110+9333d others(15): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32102195 | |||||
chr18:32102307
|
T | C | 5 | a0001c0001t0003g0037a0001c0001t0003g0291a0001c0001t0003g0292others(2): Show | 6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+9421T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102307 | ||||||
chr18:32102350
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.111-9404C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102350 | ||||||
chr18:32102359
|
G | A | 1 | a0001c0001t0003g0273 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.111-9395G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102359 | ||||||
chr18:32102405
|
G | A | 1 | a0001c0001t0004g0178 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.111-9349G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102405 | ||||||
chr18:32102490
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.111-9264T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102490 | ||||||
chr18:32102538
|
A | G | 25 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(22): Show | 27 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.111-9216A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102538 | ||||||
chr18:32102640
|
C | CT | 12 | a0001c0001t0002g0079a0001c0001t0005g0007a0001c0001t0005g0023others(9): Show | 15 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.111-9104dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32102640 | |||||
chr18:32102669
|
G | A | 1 | a0001c0001t0002g0077 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.111-9085G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102669 | ||||||
chr18:32102681
|
G | A | 32 | a0001c0001t0002g0183a0001c0001t0003g0020a0001c0001t0003g0021others(29): Show | 38 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-9073G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102681 | ||||||
chr18:32102709
|
T | A | 1 | a0001c0001t0030g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.111-9045T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102709 | ||||||
chr18:32102746
|
C | T | 1 | a0001c0001t0003g0201 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.111-9008C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102746 | ||||||
chr18:32102789
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.111-8965C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102789 | ||||||
chr18:32102791
|
C | A | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | NA19005.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.111-8963C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102791 | ||||||
chr18:32102861
|
C | T | 1 | a0001c0001t0027g0211 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.111-8893C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32102861 | ||||||
chr18:32103532
|
T | C | 1 | a0001c0001t0002g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.111-8222T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103532 | ||||||
chr18:32103573
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.111-8181A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103573 | ||||||
chr18:32103658
|
T | G | 1 | a0001c0001t0002g0105 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.111-8096T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103658 | ||||||
chr18:32103729
|
C | T | 1 | a0003c0004t0014g0024 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.111-8025C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103729 | ||||||
chr18:32103824
|
G | C | 1 | a0001c0001t0003g0201 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.111-7930G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103824 | ||||||
chr18:32103876
|
G | GA | 307 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(304): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.111-7877dupA | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32103876 | |||||
chr18:32103906
|
A | C | 1 | a0001c0001t0011g0073 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.111-7848A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103906 | ||||||
chr18:32103921
|
C | T | 1 | a0001c0001t0012g0162 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.111-7833C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103921 | ||||||
chr18:32103955
|
A | G | 8 | a0002c0002t0006g0033a0002c0002t0006g0194a0002c0002t0006g0195others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-7799A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103955 | ||||||
chr18:32103977
|
G | A | 1 | a0001c0001t0011g0073 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.111-7777G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103977 | ||||||
chr18:32103978
|
A | G | 1 | a0001c0001t0011g0073 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.111-7776A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103978 | ||||||
chr18:32103985
|
C | G | 32 | a0001c0001t0002g0183a0001c0001t0003g0020a0001c0001t0003g0021others(29): Show | 38 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-7769C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32103985 | ||||||
chr18:32104013
|
C | CT | 18 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0114others(15): Show | 20 | HG00408.hp1 HG02056.hp2 HG02300.hp2 others(17): Show |
intron_variant | MODIFIER | c.111-7724dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32104013 | |||||
chr18:32104013
|
C | CTT | 52 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0034others(49): Show | 60 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.111-7725_111-7724d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32104013 | |||||
chr18:32104013
|
C | CTTT | 8 | a0001c0001t0002g0183a0001c0001t0003g0270a0001c0001t0003g0272others(5): Show | 8 | HG02027.hp1 HG02056.hp1 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.111-7726_111-7724d others(5): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32104013 | |||||
chr18:32104013
|
CT | C | 10 | a0001c0001t0001g0225a0001c0001t0002g0085a0002c0002t0006g0033others(7): Show | 11 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.111-7724delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32104013 | |||||
chr18:32104013
|
CTTT | C | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-7726_111-7724d others(5): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32104013 | |||||
chr18:32104052
|
C | T | 8 | a0002c0002t0006g0033a0002c0002t0006g0194a0002c0002t0006g0195others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-7702C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104052 | ||||||
chr18:32104089
|
C | G | 1 | a0001c0001t0001g0030 | 2 | NA18982.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.111-7665C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104089 | ||||||
chr18:32104252
|
A | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0149 | 2 | HG02135.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.111-7502A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104252 | ||||||
chr18:32104267
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.111-7487C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104267 | ||||||
chr18:32104284
|
A | C | 1 | a0001c0001t0005g0295 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.111-7470A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104284 | ||||||
chr18:32104295
|
A | G | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-7459A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104295 | ||||||
chr18:32104322
|
A | T | 32 | a0001c0001t0002g0183a0001c0001t0003g0020a0001c0001t0003g0021others(29): Show | 38 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-7432A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104322 | ||||||
chr18:32104556
|
GAAAC | G | 3 | a0001c0001t0004g0180a0001c0001t0004g0182a0001c0001t0004g0187 | 3 | HG00408.hp2 HG02056.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.111-7195_111-7192d others(6): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32104556 | |||||
chr18:32104557
|
A | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(2): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-7197A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104557 | ||||||
chr18:32104635
|
A | T | 34 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(31): Show | 38 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-7119A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104635 | ||||||
chr18:32104707
|
A | G | 1 | a0001c0001t0005g0189 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.111-7047A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104707 | ||||||
chr18:32104933
|
A | G | 1 | a0002c0002t0006g0265 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.111-6821A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104933 | ||||||
chr18:32104955
|
C | A | 1 | a0001c0001t0002g0052 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.111-6799C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104955 | ||||||
chr18:32104991
|
A | T | 1 | a0001c0001t0003g0200 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.111-6763A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32104991 | ||||||
chr18:32105283
|
G | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.111-6471G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105283 | ||||||
chr18:32105327
|
T | C | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.111-6427T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105327 | ||||||
chr18:32105394
|
C | G | 1 | a0001c0001t0001g0144 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.111-6360C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105394 | ||||||
chr18:32105480
|
C | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.111-6274C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105480 | ||||||
chr18:32105531
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.111-6223G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105531 | ||||||
chr18:32105592
|
A | C | 1 | a0001c0001t0001g0263 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.111-6162A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105592 | ||||||
chr18:32105751
|
C | A | 5 | a0001c0001t0003g0037a0001c0001t0003g0291a0001c0001t0003g0292others(2): Show | 6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-6003C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105751 | ||||||
chr18:32105840
|
C | T | 1 | a0001c0001t0007g0151 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.111-5914C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105840 | ||||||
chr18:32105853
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.111-5901A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105853 | ||||||
chr18:32105920
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(206): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.111-5834C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32105920 | ||||||
chr18:32106063
|
A | G | 1 | a0003c0004t0014g0024 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.111-5691A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106063 | ||||||
chr18:32106173
|
G | A | 22 | a0001c0001t0002g0006a0001c0001t0002g0093a0001c0001t0002g0094others(19): Show | 27 | HG00733.hp2 HG01106.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.111-5581G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106173 | ||||||
chr18:32106185
|
G | C | 25 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(22): Show | 27 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.111-5569G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106185 | ||||||
chr18:32106215
|
G | A | 1 | a0001c0001t0008g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.111-5539G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106215 | ||||||
chr18:32106235
|
C | T | 1 | a0001c0001t0003g0200 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.111-5519C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106235 | ||||||
chr18:32106356
|
G | A | 1 | a0001c0001t0004g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.111-5398G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106356 | ||||||
chr18:32106523
|
A | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0299a0001c0001t0001g0300 | 4 | HG01099.hp1 HG01258.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-5231A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106523 | ||||||
chr18:32106524
|
G | T | 1 | a0001c0001t0002g0122 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.111-5230G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106524 | ||||||
chr18:32106547
|
AT | A | 8 | a0001c0001t0002g0183a0001c0001t0004g0022a0001c0001t0004g0181others(5): Show | 9 | HG00408.hp2 HG02056.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.111-5203delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32106547 | |||||
chr18:32106548
|
T | TTTTA | 45 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0034others(42): Show | 52 | HG00099.hp2 HG00140.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.111-5182_111-5179d others(6): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32106548 | |||||
chr18:32106548
|
T | TTTTATTT others(1): Show |
6 | a0001c0001t0003g0200a0001c0001t0003g0275a0001c0001t0004g0170others(3): Show | 6 | HG01123.hp2 HG02080.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-5186_111-5179d others(10): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32106548 | |||||
chr18:32106548
|
TTTTA | T | 9 | a0001c0001t0001g0113a0001c0001t0002g0097a0001c0001t0005g0007others(6): Show | 12 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.111-5182_111-5179d others(6): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32106548 | |||||
chr18:32106595
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(2): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-5159C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106595 | ||||||
chr18:32106702
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0213 | 3 | HG02895.hp2 HG02897.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.111-5052C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106702 | ||||||
chr18:32106710
|
G | A | 8 | a0002c0002t0006g0033a0002c0002t0006g0194a0002c0002t0006g0195others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-5044G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106710 | ||||||
chr18:32106713
|
C | T | 1 | a0001c0001t0018g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.111-5041C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106713 | ||||||
chr18:32106747
|
G | C | 32 | a0001c0001t0002g0183a0001c0001t0003g0020a0001c0001t0003g0021others(29): Show | 38 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.111-5007G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106747 | ||||||
chr18:32106808
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.111-4946C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106808 | ||||||
chr18:32106855
|
C | T | 4 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | NA18947.hp2 NA18951.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-4899C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32106855 | ||||||
chr18:32107051
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(132): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.111-4703C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107051 | ||||||
chr18:32107116
|
C | CT | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(131): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.111-4617dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32107116 | |||||
chr18:32107116
|
C | CTT | 24 | a0001c0001t0001g0029a0001c0001t0001g0133a0001c0001t0001g0143others(21): Show | 27 | HG00597.hp1 HG00642.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.111-4618_111-4617d others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32107116 | |||||
chr18:32107116
|
C | CTTT | 6 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0203others(3): Show | 9 | HG02818.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.111-4619_111-4617d others(5): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32107116 | |||||
chr18:32107116
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.111-4638C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107116 | ||||||
chr18:32107116
|
CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0002g0006a0001c0001t0002g0093a0001c0001t0002g0120others(1): Show | 6 | HG00733.hp2 HG01346.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-4627_111-4617d others(13): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32107116 | |||||
chr18:32107176
|
A | G | 1 | a0001c0001t0029g0083 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.111-4578A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107176 | ||||||
chr18:32107349
|
C | CCTG | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(206): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.111-4405_111-4404i others(5): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107349 | ||||||
chr18:32107479
|
A | C | 1 | a0001c0001t0001g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.111-4275A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107479 | ||||||
chr18:32107510
|
TTTTGTTT others(1): Show |
T | 83 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.111-4224_111-4217d others(10): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32107510 | |||||
chr18:32107637
|
C | A | 1 | a0001c0001t0001g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.111-4117C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107637 | ||||||
chr18:32107638
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.111-4116A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107638 | ||||||
chr18:32107719
|
A | G | 1 | a0001c0001t0003g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.111-4035A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107719 | ||||||
chr18:32107738
|
C | T | 1 | a0001c0001t0002g0101 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.111-4016C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107738 | ||||||
chr18:32107768
|
C | G | 4 | a0001c0001t0008g0010a0001c0001t0008g0041a0001c0001t0008g0098others(1): Show | 5 | HG01891.hp1 HG02055.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-3986C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107768 | ||||||
chr18:32107811
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.111-3943C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107811 | ||||||
chr18:32107819
|
TTTAA | T | 8 | a0002c0002t0006g0033a0002c0002t0006g0194a0002c0002t0006g0195others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-3931_111-3928d others(6): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32107819 | |||||
chr18:32107859
|
T | A | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-3895T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107859 | ||||||
chr18:32107918
|
G | A | 1 | a0001c0005t0004g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.111-3836G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107918 | ||||||
chr18:32107941
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.111-3813A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107941 | ||||||
chr18:32107953
|
C | T | 1 | a0001c0001t0005g0188 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-3801C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32107953 | ||||||
chr18:32108107
|
G | A | 1 | a0001c0001t0002g0090 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.111-3647G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108107 | ||||||
chr18:32108134
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.111-3620C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108134 | ||||||
chr18:32108247
|
A | G | 1 | a0001c0001t0004g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.111-3507A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108247 | ||||||
chr18:32108375
|
C | T | 8 | a0002c0002t0006g0033a0002c0002t0006g0194a0002c0002t0006g0195others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-3379C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108375 | ||||||
chr18:32108409
|
T | C | 5 | a0001c0001t0003g0037a0001c0001t0003g0291a0001c0001t0003g0292others(2): Show | 6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-3345T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108409 | ||||||
chr18:32108824
|
G | A | 1 | a0001c0001t0003g0281 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.111-2930G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108824 | ||||||
chr18:32108970
|
A | G | 1 | a0001c0001t0005g0188 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-2784A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108970 | ||||||
chr18:32108986
|
T | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0287a0001c0001t0001g0289 | 4 | HG00099.hp1 HG00642.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-2768T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108986 | ||||||
chr18:32108988
|
G | A | 1 | a0001c0001t0005g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.111-2766G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32108988 | ||||||
chr18:32109023
|
T | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0287a0001c0001t0001g0289 | 4 | HG00099.hp1 HG00642.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-2731T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109023 | ||||||
chr18:32109157
|
C | CT | 87 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(84): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.111-2582dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32109157 | |||||
chr18:32109161
|
T | C | 1 | a0001c0001t0002g0086 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.111-2593T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109161 | ||||||
chr18:32109193
|
G | T | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-2561G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109193 | ||||||
chr18:32109365
|
T | C | 1 | a0001c0001t0002g0040 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.111-2389T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109365 | ||||||
chr18:32109744
|
G | A | 6 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(3): Show | 8 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.111-2010G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109744 | ||||||
chr18:32109872
|
C | T | 1 | a0001c0001t0003g0201 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.111-1882C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109872 | ||||||
chr18:32109879
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.111-1875C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109879 | ||||||
chr18:32109895
|
A | G | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(2): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-1859A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109895 | ||||||
chr18:32109896
|
A | G | 1 | a0001c0001t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.111-1858A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109896 | ||||||
chr18:32109990
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.111-1764T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32109990 | ||||||
chr18:32110197
|
T | G | 1 | a0001c0001t0026g0165 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.111-1557T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110197 | ||||||
chr18:32110230
|
C | G | 1 | a0001c0001t0003g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.111-1524C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110230 | ||||||
chr18:32110369
|
C | T | 1 | a0001c0001t0004g0169 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.111-1385C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110369 | ||||||
chr18:32110398
|
T | G | 1 | a0001c0001t0003g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.111-1356T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110398 | ||||||
chr18:32110463
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(121): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.111-1291A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110463 | ||||||
chr18:32110525
|
A | G | 1 | a0001c0001t0002g0209 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.111-1229A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110525 | ||||||
chr18:32110548
|
TG | T | 3 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096 | 3 | HG02257.hp1 HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.111-1205delG | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110548 | ||||||
chr18:32110623
|
T | A | 5 | a0001c0001t0003g0037a0001c0001t0003g0291a0001c0001t0003g0292others(2): Show | 6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-1131T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110623 | ||||||
chr18:32110655
|
G | C | 1 | a0003c0004t0014g0024 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.111-1099G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110655 | ||||||
chr18:32110659
|
T | C | 33 | a0001c0001t0002g0183a0001c0001t0003g0020a0001c0001t0003g0021others(30): Show | 39 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.111-1095T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110659 | ||||||
chr18:32110785
|
C | CT | 5 | a0001c0001t0003g0037a0001c0001t0003g0291a0001c0001t0003g0292others(2): Show | 6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-956dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32110785 | |||||
chr18:32110803
|
C | T | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-951C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110803 | ||||||
chr18:32110912
|
C | G | 2 | a0001c0001t0001g0203a0001c0001t0001g0210 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.111-842C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110912 | ||||||
chr18:32110926
|
G | A | 1 | a0001c0001t0004g0174 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.111-828G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110926 | ||||||
chr18:32110970
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(2): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-784C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32110970 | ||||||
chr18:32111034
|
C | T | 8 | a0002c0002t0006g0033a0002c0002t0006g0194a0002c0002t0006g0195others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-720C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111034 | ||||||
chr18:32111069
|
C | T | 1 | a0003c0004t0014g0024 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.111-685C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111069 | ||||||
chr18:32111122
|
T | C | 3 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0163 | 3 | HG01123.hp2 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.111-632T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111122 | ||||||
chr18:32111152
|
C | T | 6 | a0001c0001t0003g0037a0001c0001t0003g0291a0001c0001t0003g0292others(3): Show | 7 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-602C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111152 | ||||||
chr18:32111200
|
C | A | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-554C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111200 | ||||||
chr18:32111250
|
C | T | 2 | a0001c0001t0003g0270a0001c0003t0003g0128 | 2 | NA18956.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.111-504C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111250 | ||||||
chr18:32111314
|
C | A | 2 | a0001c0001t0004g0022a0001c0001t0004g0186 | 3 | HG03017.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.111-440C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111314 | ||||||
chr18:32111401
|
A | G | 1 | a0001c0001t0005g0188 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-353A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111401 | ||||||
chr18:32111578
|
A | C | 1 | a0001c0001t0003g0201 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.111-176A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111578 | ||||||
chr18:32111610
|
A | G | 2 | a0001c0001t0004g0174a0001c0001t0004g0175 | 2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.111-144A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111610 | ||||||
chr18:32111644
|
C | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(121): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.111-110C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111644 | ||||||
chr18:32111715
|
AT | A | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-31delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 32111715 | |||||
chr18:32111733
|
G | A | 6 | a0002c0002t0006g0194a0002c0002t0006g0195a0002c0002t0006g0196others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-21G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111733 | ||||||
chr18:32111736
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.111-18T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 2/7 | chr18 | 32111736 | ||||||
chr18:32111999
|
G | GT | 12 | a0001c0001t0001g0141a0001c0001t0005g0007a0001c0001t0005g0023others(9): Show | 16 | HG00735.hp2 HG01109.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.276+94dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 32111999 | |||||
chr18:32112116
|
GA | G | 6 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0189others(3): Show | 9 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.276+206delA | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 32112116 | |||||
chr18:32112358
|
C | G | 1 | a0001c0001t0003g0201 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.276+439C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112358 | ||||||
chr18:32112396
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.276+477T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112396 | ||||||
chr18:32112443
|
T | C | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.276+524T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112443 | ||||||
chr18:32112444
|
G | A | 1 | a0001c0001t0005g0188 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.276+525G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112444 | ||||||
chr18:32112473
|
G | T | 1 | a0001c0001t0001g0237 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.276+554G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112473 | ||||||
chr18:32112488
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.276+569C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112488 | ||||||
chr18:32112519
|
C | G | 1 | a0001c0001t0001g0252 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.276+600C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112519 | ||||||
chr18:32112598
|
T | G | 1 | a0001c0001t0001g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.276+679T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112598 | ||||||
chr18:32112663
|
CAA | C | 5 | a0001c0001t0003g0037a0001c0001t0003g0291a0001c0001t0003g0292others(2): Show | 6 | HG02257.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.276+745_276+746del others(2): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112663 | ||||||
chr18:32112670
|
G | A | 1 | a0003c0004t0014g0024 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.276+751G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112670 | ||||||
chr18:32112688
|
A | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.276+769A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112688 | ||||||
chr18:32112872
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.277-873C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112872 | ||||||
chr18:32112911
|
G | A | 32 | a0001c0001t0002g0183a0001c0001t0003g0020a0001c0001t0003g0021others(29): Show | 38 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.277-834G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32112911 | ||||||
chr18:32113142
|
G | A | 2 | a0001c0001t0003g0272a0001c0001t0003g0274 | 2 | NA18943.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.277-603G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32113142 | ||||||
chr18:32113208
|
A | G | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.277-537A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32113208 | ||||||
chr18:32113267
|
A | G | 5 | a0001c0001t0002g0006a0001c0001t0002g0093a0001c0001t0002g0120others(2): Show | 7 | HG00733.hp2 HG01106.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.277-478A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32113267 | ||||||
chr18:32113367
|
AT | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(201): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.277-369delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 32113367 | |||||
chr18:32113559
|
A | C | 23 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(20): Show | 25 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.277-186A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 3/7 | chr18 | 32113559 | ||||||
chr18:32113961
|
A | T | 1 | a0001c0001t0029g0083 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.392+101A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32113961 | ||||||
chr18:32114155
|
T | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(31): Show | 38 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.392+295T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32114155 | ||||||
chr18:32114180
|
A | G | 1 | a0001c0001t0002g0096 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.392+320A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32114180 | ||||||
chr18:32114461
|
C | T | 8 | a0002c0002t0006g0033a0002c0002t0006g0194a0002c0002t0006g0195others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.392+601C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32114461 | ||||||
chr18:32114627
|
T | C | 1 | a0001c0001t0003g0270 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.392+767T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32114627 | ||||||
chr18:32114666
|
A | G | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(2): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.392+806A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32114666 | ||||||
chr18:32114876
|
T | TG | 33 | a0001c0001t0002g0183a0001c0001t0003g0020a0001c0001t0003g0021others(30): Show | 39 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.392+1018dupG | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32114876 | |||||
chr18:32114966
|
G | T | 34 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(31): Show | 38 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.392+1106G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32114966 | ||||||
chr18:32115013
|
G | GT | 60 | a0001c0001t0002g0183a0001c0001t0003g0020a0001c0001t0003g0021others(57): Show | 68 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.392+1162dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32115013 | |||||
chr18:32115048
|
A | G | 1 | a0001c0001t0003g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.392+1188A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115048 | ||||||
chr18:32115148
|
G | C | 61 | a0001c0001t0002g0183a0001c0001t0003g0020a0001c0001t0003g0021others(58): Show | 69 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.392+1288G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115148 | ||||||
chr18:32115295
|
A | G | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.392+1435A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115295 | ||||||
chr18:32115473
|
G | A | 1 | a0001c0001t0002g0063 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.392+1613G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115473 | ||||||
chr18:32115677
|
G | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(2): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.392+1817G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115677 | ||||||
chr18:32115736
|
C | G | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.392+1876C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115736 | ||||||
chr18:32115769
|
G | A | 1 | a0003c0004t0014g0024 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.392+1909G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115769 | ||||||
chr18:32115782
|
C | T | 1 | a0001c0001t0003g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.392+1922C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115782 | ||||||
chr18:32115793
|
T | G | 2 | a0001c0001t0001g0287a0001c0001t0001g0289 | 2 | HG02300.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.392+1933T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115793 | ||||||
chr18:32115865
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.392+2005C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115865 | ||||||
chr18:32115993
|
C | G | 1 | a0001c0001t0001g0246 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.392+2133C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32115993 | ||||||
chr18:32116034
|
A | G | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.392+2174A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116034 | ||||||
chr18:32116071
|
A | G | 4 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0002g0208others(1): Show | 4 | HG02559.hp2 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.392+2211A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116071 | ||||||
chr18:32116129
|
T | A | 4 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0268others(1): Show | 4 | NA18612.hp1 NA18966.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.392+2269T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116129 | ||||||
chr18:32116515
|
CT | C | 7 | a0001c0001t0001g0111a0001c0001t0001g0231a0001c0001t0002g0061others(4): Show | 7 | HG00323.hp2 HG00558.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.392+2671delT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32116515 | |||||
chr18:32116518
|
T | C | 1 | a0001c0001t0001g0030 | 2 | NA18982.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.392+2658T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116518 | ||||||
chr18:32116531
|
T | A | 1 | a0001c0001t0003g0283 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.392+2671T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116531 | ||||||
chr18:32116613
|
G | A | 1 | a0001c0001t0002g0055 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.392+2753G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116613 | ||||||
chr18:32116696
|
C | T | 8 | a0002c0002t0006g0033a0002c0002t0006g0194a0002c0002t0006g0195others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.392+2836C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116696 | ||||||
chr18:32116732
|
T | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(121): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.392+2872T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116732 | ||||||
chr18:32116737
|
T | TG | 31 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(28): Show | 35 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.392+2884dupG | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32116737 | |||||
chr18:32116762
|
C | T | 1 | a0001c0001t0003g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.392+2902C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116762 | ||||||
chr18:32116851
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.392+2991C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116851 | ||||||
chr18:32116911
|
T | A | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.392+3051T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116911 | ||||||
chr18:32116937
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.392+3077C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116937 | ||||||
chr18:32116987
|
G | A | 3 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0163 | 3 | HG01123.hp2 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.392+3127G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116987 | ||||||
chr18:32116993
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(29): Show | 36 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.392+3133C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32116993 | ||||||
chr18:32117154
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.392+3294G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32117154 | ||||||
chr18:32117172
|
GATTACAG others(2): Show |
G | 6 | a0002c0002t0006g0194a0002c0002t0006g0195a0002c0002t0006g0196others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.392+3315_392+3323d others(11): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32117172 | |||||
chr18:32117194
|
C | A | 5 | a0001c0001t0002g0012a0001c0001t0002g0055a0001c0001t0002g0064others(2): Show | 6 | HG02080.hp1 HG02083.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.392+3334C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32117194 | ||||||
chr18:32117505
|
G | GA | 8 | a0002c0002t0006g0033a0002c0002t0006g0194a0002c0002t0006g0195others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.392+3654dupA | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32117505 | |||||
chr18:32117591
|
C | T | 3 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0163 | 3 | HG01123.hp2 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.392+3731C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32117591 | ||||||
chr18:32117701
|
C | G | 1 | a0001c0001t0005g0188 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.392+3841C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32117701 | ||||||
chr18:32117705
|
T | C | 1 | a0001c0001t0003g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.392+3845T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32117705 | ||||||
chr18:32118230
|
T | C | 59 | a0001c0001t0002g0183a0001c0001t0003g0020a0001c0001t0003g0021others(56): Show | 67 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.392+4370T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118230 | ||||||
chr18:32118248
|
T | C | 2 | a0001c0001t0003g0270a0001c0003t0003g0128 | 2 | NA18956.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.392+4388T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118248 | ||||||
chr18:32118418
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.392+4558C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118418 | ||||||
chr18:32118563
|
G | A | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.392+4703G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118563 | ||||||
chr18:32118564
|
C | T | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.392+4704C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118564 | ||||||
chr18:32118664
|
C | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(121): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.392+4804C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118664 | ||||||
chr18:32118690
|
G | T | 1 | a0001c0001t0021g0254 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.393-4828G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118690 | ||||||
chr18:32118702
|
G | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(121): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.393-4816G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118702 | ||||||
chr18:32118753
|
C | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0031others(10): Show | 18 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.393-4765C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118753 | ||||||
chr18:32118798
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.393-4720C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118798 | ||||||
chr18:32118982
|
A | G | 5 | a0001c0001t0005g0188a0001c0001t0005g0295a0001c0001t0005g0296others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.393-4536A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32118982 | ||||||
chr18:32119129
|
T | TTGAGGAG others(23): Show |
3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0019g0106 | 3 | NA18984.hp2 NA19062.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.393-4387_393-4358d others(32): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32119129 | |||||
chr18:32119192
|
C | A | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.393-4326C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32119192 | ||||||
chr18:32119296
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.393-4222C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32119296 | ||||||
chr18:32119313
|
C | A | 1 | a0001c0001t0002g0049 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.393-4205C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32119313 | ||||||
chr18:32119358
|
C | T | 5 | a0001c0001t0005g0188a0001c0001t0005g0295a0001c0001t0005g0296others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.393-4160C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32119358 | ||||||
chr18:32119378
|
G | C | 1 | a0001c0001t0001g0246 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.393-4140G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32119378 | ||||||
chr18:32119892
|
A | G | 1 | a0001c0001t0002g0125 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.393-3626A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32119892 | ||||||
chr18:32120031
|
T | G | 1 | a0001c0001t0001g0246 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.393-3487T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120031 | ||||||
chr18:32120036
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.393-3482T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120036 | ||||||
chr18:32120162
|
G | A | 1 | a0001c0001t0003g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.393-3356G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120162 | ||||||
chr18:32120296
|
A | G | 1 | a0001c0001t0003g0267 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.393-3222A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120296 | ||||||
chr18:32120323
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.393-3195C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120323 | ||||||
chr18:32120335
|
T | C | 1 | a0001c0001t0002g0064 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.393-3183T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120335 | ||||||
chr18:32120363
|
A | T | 1 | a0001c0001t0017g0249 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.393-3155A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120363 | ||||||
chr18:32120382
|
A | T | 1 | a0001c0001t0001g0213 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.393-3136A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120382 | ||||||
chr18:32120587
|
T | C | 33 | a0001c0001t0002g0006a0001c0001t0002g0040a0001c0001t0002g0093others(30): Show | 39 | HG00733.hp2 HG01106.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.393-2931T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120587 | ||||||
chr18:32120829
|
A | G | 2 | a0001c0001t0002g0065a0001c0001t0002g0066 | 2 | NA18968.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.393-2689A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120829 | ||||||
chr18:32120879
|
C | T | 1 | a0003c0004t0014g0024 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.393-2639C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120879 | ||||||
chr18:32120892
|
C | T | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.393-2626C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120892 | ||||||
chr18:32120981
|
C | G | 1 | a0001c0001t0001g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393-2537C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32120981 | ||||||
chr18:32121033
|
G | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(2): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.393-2485G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121033 | ||||||
chr18:32121090
|
G | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(2): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.393-2428G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121090 | ||||||
chr18:32121095
|
G | A | 1 | a0001c0001t0005g0188 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.393-2423G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121095 | ||||||
chr18:32121133
|
C | CA | 8 | a0001c0001t0001g0159a0001c0001t0007g0137a0002c0002t0006g0194others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.393-2376dupA | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32121133 | |||||
chr18:32121137
|
A | G | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.393-2381A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121137 | ||||||
chr18:32121138
|
A | C | 1 | a0001c0001t0023g0058 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.393-2380A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121138 | ||||||
chr18:32121142
|
AC | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(154): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.393-2375delC | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121142 | ||||||
chr18:32121143
|
C | A | 82 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(79): Show | 94 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.393-2375C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121143 | ||||||
chr18:32121144
|
A | C | 2 | a0002c0002t0006g0033a0002c0002t0006g0265 | 3 | HG03453.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.393-2374A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121144 | ||||||
chr18:32121443
|
C | T | 1 | a0001c0001t0011g0017 | 2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.393-2075C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121443 | ||||||
chr18:32121758
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.393-1760C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121758 | ||||||
chr18:32121899
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(31): Show | 38 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.393-1619G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121899 | ||||||
chr18:32121996
|
G | A | 3 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0163 | 3 | HG01123.hp2 HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.393-1522G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32121996 | ||||||
chr18:32122014
|
G | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(2): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.393-1504G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122014 | ||||||
chr18:32122017
|
C | T | 1 | a0001c0001t0003g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.393-1501C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122017 | ||||||
chr18:32122124
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(206): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.393-1394T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122124 | ||||||
chr18:32122234
|
T | C | 1 | a0001c0001t0003g0200 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.393-1284T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122234 | ||||||
chr18:32122237
|
C | T | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.393-1281C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122237 | ||||||
chr18:32122262
|
T | C | 33 | a0001c0001t0002g0183a0001c0001t0003g0020a0001c0001t0003g0021others(30): Show | 39 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.393-1256T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122262 | ||||||
chr18:32122329
|
A | G | 1 | a0001c0001t0005g0298 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.393-1189A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122329 | ||||||
chr18:32122387
|
A | T | 59 | a0001c0001t0002g0183a0001c0001t0003g0020a0001c0001t0003g0021others(56): Show | 67 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.393-1131A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122387 | ||||||
chr18:32122401
|
T | G | 1 | a0001c0001t0001g0235 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.393-1117T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122401 | ||||||
chr18:32122426
|
A | G | 1 | a0001c0001t0007g0139 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.393-1092A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122426 | ||||||
chr18:32122473
|
ACTTAT | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.393-1039_393-1035d others(7): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 32122473 | |||||
chr18:32122550
|
G | A | 1 | a0001c0001t0003g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.393-968G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122550 | ||||||
chr18:32122606
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(205): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.393-912T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122606 | ||||||
chr18:32122657
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.393-861C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122657 | ||||||
chr18:32122802
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.393-716C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122802 | ||||||
chr18:32122845
|
A | C | 8 | a0002c0002t0006g0033a0002c0002t0006g0194a0002c0002t0006g0195others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.393-673A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122845 | ||||||
chr18:32122864
|
T | C | 3 | a0001c0001t0003g0272a0001c0001t0003g0274a0001c0001t0003g0277 | 3 | NA18943.hp1 NA18964.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.393-654T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122864 | ||||||
chr18:32122982
|
A | T | 8 | a0002c0002t0006g0033a0002c0002t0006g0194a0002c0002t0006g0195others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.393-536A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32122982 | ||||||
chr18:32123112
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.393-406C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32123112 | ||||||
chr18:32123139
|
T | A | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.393-379T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32123139 | ||||||
chr18:32123159
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.393-359C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32123159 | ||||||
chr18:32123390
|
G | T | 20 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(17): Show | 22 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.393-128G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 4/7 | chr18 | 32123390 | ||||||
chr18:32123652
|
C | CT | 18 | a0001c0001t0001g0140a0001c0001t0001g0148a0001c0001t0001g0217others(15): Show | 21 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.449+95dupT | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 32123652 | |||||
chr18:32123694
|
C | T | 1 | a0001c0001t0003g0281 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.449+120C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32123694 | ||||||
chr18:32123776
|
C | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.449+202C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32123776 | ||||||
chr18:32123860
|
C | T | 1 | a0001c0001t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.449+286C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32123860 | ||||||
chr18:32123965
|
T | TA | 142 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.449+407dupA | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 32123965 | |||||
chr18:32123965
|
T | TAA | 44 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(41): Show | 49 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.449+406_449+407dup others(2): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 32123965 | |||||
chr18:32123965
|
TA | T | 7 | a0001c0001t0002g0066a0001c0001t0002g0109a0001c0001t0005g0007others(4): Show | 10 | HG01109.hp1 HG02055.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.449+407delA | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 32123965 | |||||
chr18:32124161
|
T | A | 2 | a0001c0001t0003g0037a0001c0001t0003g0292 | 3 | HG02723.hp2 HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.450-573T>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124161 | ||||||
chr18:32124163
|
C | A | 1 | a0001c0001t0002g0049 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.450-571C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124163 | ||||||
chr18:32124170
|
A | G | 1 | a0003c0004t0014g0024 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.450-564A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124170 | ||||||
chr18:32124296
|
A | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(31): Show | 38 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.450-438A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124296 | ||||||
chr18:32124301
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.450-433C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124301 | ||||||
chr18:32124390
|
A | G | 2 | a0002c0002t0006g0194a0002c0002t0006g0197 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.450-344A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124390 | ||||||
chr18:32124398
|
A | T | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.450-336A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124398 | ||||||
chr18:32124558
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.450-176G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124558 | ||||||
chr18:32124631
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.450-103T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124631 | ||||||
chr18:32124679
|
C | T | 1 | a0001c0001t0009g0112 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.450-55C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124679 | ||||||
chr18:32124689
|
G | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.450-45G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 5/7 | chr18 | 32124689 | ||||||
chr18:32125121
|
A | G | 1 | a0001c0001t0002g0015 | 2 | HG01516.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.561+276A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125121 | ||||||
chr18:32125129
|
G | A | 8 | a0002c0002t0006g0033a0002c0002t0006g0194a0002c0002t0006g0195others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.561+284G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125129 | ||||||
chr18:32125630
|
T | C | 1 | a0001c0001t0005g0188 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.561+785T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125630 | ||||||
chr18:32125688
|
T | G | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.561+843T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125688 | ||||||
chr18:32125722
|
A | G | 1 | a0001c0001t0003g0200 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.561+877A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125722 | ||||||
chr18:32125746
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(121): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.561+901A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125746 | ||||||
chr18:32125761
|
G | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(121): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.561+916G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125761 | ||||||
chr18:32125876
|
G | T | 1 | a0001c0001t0001g0240 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.562-817G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125876 | ||||||
chr18:32125929
|
C | T | 2 | a0001c0001t0002g0117a0001c0001t0002g0119 | 2 | HG02735.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.562-764C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32125929 | ||||||
chr18:32126028
|
T | G | 34 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(31): Show | 38 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.562-665T>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126028 | ||||||
chr18:32126131
|
A | T | 1 | a0001c0001t0003g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.562-562A>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126131 | ||||||
chr18:32126242
|
G | T | 1 | a0001c0001t0003g0200 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.562-451G>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126242 | ||||||
chr18:32126352
|
T | C | 8 | a0002c0002t0006g0033a0002c0002t0006g0194a0002c0002t0006g0195others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.562-341T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126352 | ||||||
chr18:32126387
|
GCCAGTTA others(4): Show |
G | 1 | a0001c0001t0019g0106 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.562-305_562-295del others(11): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126387 | ||||||
chr18:32126500
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0212others(2): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.562-193C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126500 | ||||||
chr18:32126587
|
C | G | 1 | a0001c0001t0003g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.562-106C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126587 | ||||||
chr18:32126589
|
T | C | 1 | a0001c0001t0002g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.562-104T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126589 | ||||||
chr18:32126594
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.562-99A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126594 | ||||||
chr18:32126651
|
T | C | 1 | a0001c0001t0004g0171 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.562-42T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 6/7 | chr18 | 32126651 | ||||||
chr18:32127322
|
A | G | 1 | a0001c0001t0005g0192 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.669+522A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32127322 | ||||||
chr18:32127631
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0146a0001c0001t0001g0152 | 4 | HG00423.hp1 HG00558.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+831G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32127631 | ||||||
chr18:32127904
|
C | G | 1 | a0001c0001t0002g0051 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.669+1104C>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32127904 | ||||||
chr18:32127936
|
C | T | 1 | a0001c0001t0002g0068 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.669+1136C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32127936 | ||||||
chr18:32127985
|
C | A | 8 | a0002c0002t0006g0033a0002c0002t0006g0194a0002c0002t0006g0195others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.670-1134C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32127985 | ||||||
chr18:32128003
|
C | T | 7 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(4): Show | 10 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.670-1116C>T | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128003 | ||||||
chr18:32128005
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.670-1114G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128005 | ||||||
chr18:32128034
|
C | A | 1 | a0001c0001t0002g0095 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.670-1085C>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128034 | ||||||
chr18:32128081
|
A | AAAAAG | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(200): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.670-1032_670-1028d others(7): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 32128081 | |||||
chr18:32128232
|
G | A | 1 | a0001c0001t0003g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.670-887G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128232 | ||||||
chr18:32128311
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.670-808G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128311 | ||||||
chr18:32128336
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(132): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.670-783A>G | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128336 | ||||||
chr18:32128422
|
T | C | 11 | a0001c0001t0005g0007a0001c0001t0005g0023a0001c0001t0005g0188others(8): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.670-697T>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128422 | ||||||
chr18:32128468
|
G | A | 1 | a0001c0001t0003g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.670-651G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128468 | ||||||
chr18:32128479
|
A | C | 21 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(18): Show | 23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.670-640A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128479 | ||||||
chr18:32128663
|
A | C | 1 | a0001c0001t0004g0180 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.670-456A>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128663 | ||||||
chr18:32128885
|
CTGTT | C | 21 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(18): Show | 23 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.670-225_670-222del others(4): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 32128885 | |||||
chr18:32128957
|
G | C | 1 | a0001c0001t0001g0138 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.670-162G>C | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32128957 | ||||||
chr18:32129005
|
GTGTGTAA others(12): Show |
G | 1 | a0003c0004t0014g0024 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.670-101_670-83delG others(18): Show |
RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 32129005 | |||||
chr18:32129018
|
G | A | 300 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(297): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.670-101G>A | RNF138 | ENSG00000134758.14 | transcript | ENST00000261593.8 | protein_coding | 7/7 | chr18 | 32129018 |