Item | Value |
---|---|
geneid | 140545 |
ensemblid | ENSG00000105982.17 |
hgncid | 17118 |
symbol | RNF32 |
name | ring finger protein 32 |
refseq_nuc | NM_030936.4 |
refseq_prot | NP_112198.1 |
ensembl_nuc | ENST00000317955.10 |
ensembl_prot | ENSP00000315950.5 |
mane_status | MANE Select |
chr | chr7 |
start | 156640774 |
end | 156677130 |
strand | + |
ver | v1.2 |
region | chr7:156640774-156677130 |
region5000 | chr7:156635774-156682130 |
regionname0 | RNF32_chr7_156640774_156677130 |
regionname5000 | RNF32_chr7_156635774_156682130 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 362 | 200 | 26 | 41 | 90 | 8 | 33 | 70 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0002 | 0/0 | 362 | 178 | 43 | 26 | 93 | 7 | 9 | 77 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0003 | 0/0 | 362 | 50 | 14 | 2 | 30 | 1 | 3 | 24 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0004 | 0/0 | 362 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0005 | 0/0 | 362 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0006 | 0/0 | 362 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0007 | 0/0 | 362 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0008 | 0/0 | 362 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0009 | 0/0 | 362 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0010 | 0/0 | 362 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0011 | 0/0 | 362 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1089 | 185 | 12 | 41 | 89 | 8 | 33 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
c0002 | 0/0 | 1089 | 178 | 43 | 26 | 93 | 7 | 9 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
c0003 | 0/0 | 1089 | 50 | 14 | 2 | 30 | 1 | 3 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
c0004 | 0/0 | 1089 | 15 | 14 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
c0005 | 0/0 | 1089 | 7 | 7 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
c0006 | 0/0 | 1089 | 3 | 3 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
c0007 | 0/0 | 1089 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
c0008 | 0/0 | 1089 | 2 | 0 | 0 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
c0009 | 0/0 | 1089 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
c0010 | 0/0 | 1089 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
c0011 | 0/0 | 1089 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
c0012 | 0/0 | 1089 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
c0013 | 0/0 | 1089 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 591 | 166 | 42 | 26 | 82 | 7 | 9 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
t0002 | 1/1 | 591 | 156 | 22 | 35 | 56 | 8 | 33 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
t0003 | 0/0 | 591 | 50 | 7 | 6 | 34 | 0 | 3 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
t0004 | 0/0 | 591 | 45 | 9 | 2 | 30 | 1 | 3 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
t0005 | 0/0 | 591 | 19 | 2 | 1 | 16 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
t0006 | 0/0 | 591 | 10 | 10 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
t0007 | 0/0 | 591 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 18 | 1 | 4 | 7 | 1 | 5 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0002 | 0/0 | 14 | 2 | 2 | 9 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0003 | 0/0 | 13 | 0 | 2 | 11 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0004 | 0/0 | 11 | 1 | 3 | 2 | 2 | 3 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0005 | 0/0 | 10 | 0 | 2 | 6 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0008 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0012 | 0/0 | 5 | 1 | 3 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0015 | 1/0 | 4 | 0 | 3 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0019 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0023 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0027 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0030 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0031 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0059 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0060 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0061 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0062 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1089 | 185 | 12 | 41 | 89 | 8 | 33 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0001c0004 | 0/0 | 1089 | 15 | 14 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0002c0002 | 0/0 | 1089 | 178 | 43 | 26 | 93 | 7 | 9 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0003c0003 | 0/0 | 1089 | 50 | 14 | 2 | 30 | 1 | 3 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0004c0005 | 0/0 | 1089 | 7 | 7 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0004c0012 | 0/0 | 1089 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0005c0006 | 0/0 | 1089 | 3 | 3 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0006c0007 | 0/0 | 1089 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0007c0008 | 0/0 | 1089 | 2 | 0 | 0 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0008c0009 | 0/0 | 1089 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0009c0013 | 0/0 | 1089 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0010c0011 | 0/0 | 1089 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0011c0010 | 0/0 | 1089 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 1/1 | 1679 | 136 | 6 | 35 | 55 | 8 | 30 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0001c0001t0003 | 0/0 | 1679 | 49 | 6 | 6 | 34 | 0 | 3 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0001c0004t0002 | 0/0 | 1679 | 3 | 2 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0001c0004t0003 | 0/0 | 1679 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0001c0004t0005 | 0/0 | 1679 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0001c0004t0006 | 0/0 | 1679 | 10 | 10 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0002c0002t0001 | 0/0 | 1679 | 160 | 42 | 25 | 77 | 7 | 9 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0002c0002t0005 | 0/0 | 1679 | 18 | 1 | 1 | 16 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0003c0003t0002 | 0/0 | 1679 | 6 | 6 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0003c0003t0004 | 0/0 | 1679 | 42 | 6 | 2 | 30 | 1 | 3 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0003c0003t0007 | 0/0 | 1679 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0004c0005t0002 | 0/0 | 1679 | 7 | 7 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0004c0012t0002 | 0/0 | 1679 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0005c0006t0004 | 0/0 | 1679 | 3 | 3 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0006c0007t0001 | 0/0 | 1679 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0007c0008t0002 | 0/0 | 1679 | 2 | 0 | 0 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0008c0009t0001 | 0/0 | 1679 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0009c0013t0001 | 0/0 | 1679 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0010c0011t0002 | 0/0 | 1679 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
a0011c0010t0001 | 0/0 | 1679 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | copy fasta | chr7 | 156635774 | 156682130 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 18 | 1 | 4 | 7 | 1 | 5 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0005 | 0/0 | 10 | 0 | 2 | 6 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0015 | 1/0 | 4 | 0 | 3 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0019 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0023 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0061 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0062 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0003 | 0/0 | 13 | 0 | 2 | 11 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0059 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0006g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0002 | 0/0 | 14 | 2 | 2 | 9 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0004 | 0/0 | 11 | 1 | 3 | 2 | 2 | 3 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0008 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0012 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0027 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0030 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0031 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0002g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0007g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0004c0005t0002g0060 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0004c0005t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0004c0005t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0004c0005t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0004c0005t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0004c0005t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0004c0012t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0005c0006t0004g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0006c0007t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0007c0008t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0008c0009t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0009c0013t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0010c0011t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0011c0010t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0110 | EUR | GBR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0165 | EUR | GBR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0126 | EUR | GBR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0218 | EUR | GBR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0166 | EUR | FIN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0154 | EUR | FIN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00438 | hp2 | a0003 | c0003 | t0004 | g0067 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00609 | hp2 | a0003 | c0003 | t0004 | g0083 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00639 | hp1 | a0002 | c0002 | t0005 | g0065 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0207 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0221 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0199 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01168 | hp2 | a0003 | c0003 | t0004 | g0189 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0168 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01256 | hp1 | a0003 | c0003 | t0004 | g0145 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0045 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0045 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0226 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0262 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01433 | hp1 | a0009 | c0013 | t0001 | g0012 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0030 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | IBS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0038 | EUR | IBS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0134 | EUR | IBS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0004 | EUR | IBS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0038 | EUR | IBS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01884 | hp1 | a0004 | c0005 | t0002 | g0060 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01884 | hp2 | a0004 | c0005 | t0002 | g0268 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0182 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0214 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0261 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0274 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02015 | hp1 | a0002 | c0002 | t0005 | g0007 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02027 | hp2 | a0003 | c0003 | t0004 | g0087 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02071 | hp2 | a0002 | c0002 | t0005 | g0007 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02074 | hp2 | a0001 | c0004 | t0002 | g0223 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02132 | hp1 | a0002 | c0002 | t0005 | g0007 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02135 | hp2 | a0003 | c0003 | t0004 | g0010 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0064 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02145 | hp2 | a0003 | c0003 | t0004 | g0075 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02155 | hp1 | a0003 | c0003 | t0004 | g0089 | EAS | CDX | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02155 | hp2 | a0002 | c0002 | t0005 | g0007 | EAS | CDX | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | CDX | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | CDX | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02257 | hp1 | a0002 | c0002 | t0005 | g0250 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02257 | hp2 | a0003 | c0003 | t0002 | g0190 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02258 | hp1 | a0003 | c0003 | t0004 | g0078 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0030 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02280 | hp1 | a0001 | c0004 | t0006 | g0095 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02280 | hp2 | a0004 | c0005 | t0002 | g0267 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0212 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0063 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0225 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0211 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02523 | hp1 | a0003 | c0003 | t0004 | g0071 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02615 | hp1 | a0003 | c0003 | t0002 | g0229 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0077 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02622 | hp2 | a0001 | c0004 | t0002 | g0217 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02630 | hp1 | a0003 | c0003 | t0004 | g0099 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0213 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02683 | hp1 | a0007 | c0008 | t0002 | g0034 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0239 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02698 | hp1 | a0007 | c0008 | t0002 | g0034 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0231 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02717 | hp2 | a0003 | c0003 | t0002 | g0232 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02723 | hp1 | a0004 | c0005 | t0002 | g0270 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0181 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02809 | hp2 | a0004 | c0012 | t0002 | g0265 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0251 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02895 | hp2 | a0003 | c0003 | t0002 | g0233 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02896 | hp1 | a0001 | c0004 | t0006 | g0094 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02896 | hp2 | a0001 | c0004 | t0002 | g0164 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02897 | hp1 | a0001 | c0004 | t0006 | g0097 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0191 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02970 | hp1 | a0003 | c0003 | t0002 | g0053 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0183 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02976 | hp2 | a0004 | c0005 | t0002 | g0269 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03041 | hp2 | a0001 | c0004 | t0006 | g0014 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03098 | hp1 | a0004 | c0005 | t0002 | g0266 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03098 | hp2 | a0001 | c0004 | t0006 | g0096 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0224 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03139 | hp2 | a0005 | c0006 | t0004 | g0022 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03195 | hp1 | a0001 | c0004 | t0003 | g0248 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03195 | hp2 | a0005 | c0006 | t0004 | g0022 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03209 | hp1 | a0001 | c0004 | t0006 | g0014 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0210 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0216 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0066 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0195 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03453 | hp2 | a0001 | c0004 | t0006 | g0014 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0144 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0215 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03490 | hp2 | a0003 | c0003 | t0004 | g0050 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03492 | hp1 | a0003 | c0003 | t0004 | g0050 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03516 | hp1 | a0003 | c0003 | t0004 | g0092 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0209 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0153 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03579 | hp1 | a0003 | c0003 | t0004 | g0098 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0031 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0257 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0167 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03927 | hp2 | a0010 | c0011 | t0002 | g0043 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | STU | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | STU | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0161 | SAS | STU | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | STU | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | STU | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04204 | hp2 | a0003 | c0003 | t0004 | g0230 | SAS | STU | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | STU | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0264 | SAS | STU | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18522 | hp1 | a0004 | c0005 | t0002 | g0060 | AFR | YRI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0228 | AFR | YRI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18747 | hp1 | a0002 | c0002 | t0005 | g0007 | EAS | CHB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | YRI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | YRI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18944 | hp1 | a0002 | c0002 | t0005 | g0255 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18946 | hp2 | a0002 | c0002 | t0005 | g0007 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18952 | hp2 | a0003 | c0003 | t0004 | g0084 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18953 | hp1 | a0003 | c0003 | t0004 | g0069 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18954 | hp1 | a0006 | c0007 | t0001 | g0011 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18956 | hp2 | a0003 | c0003 | t0004 | g0017 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18962 | hp1 | a0003 | c0003 | t0004 | g0035 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18963 | hp1 | a0003 | c0003 | t0004 | g0070 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18964 | hp1 | a0002 | c0002 | t0005 | g0245 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18968 | hp1 | a0002 | c0002 | t0005 | g0242 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18974 | hp2 | a0002 | c0002 | t0005 | g0240 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18975 | hp2 | a0003 | c0003 | t0004 | g0017 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18981 | hp1 | a0003 | c0003 | t0004 | g0073 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18982 | hp1 | a0002 | c0002 | t0005 | g0007 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18985 | hp2 | a0008 | c0009 | t0001 | g0016 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18986 | hp1 | a0003 | c0003 | t0004 | g0035 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18991 | hp1 | a0002 | c0002 | t0005 | g0056 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18991 | hp2 | a0003 | c0003 | t0004 | g0010 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18992 | hp1 | a0003 | c0003 | t0004 | g0068 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18997 | hp1 | a0003 | c0003 | t0004 | g0010 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18998 | hp2 | a0003 | c0003 | t0004 | g0082 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19000 | hp2 | a0003 | c0003 | t0004 | g0079 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19003 | hp2 | a0003 | c0003 | t0004 | g0100 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19007 | hp1 | a0002 | c0002 | t0005 | g0056 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19010 | hp2 | a0003 | c0003 | t0004 | g0088 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19012 | hp2 | a0003 | c0003 | t0004 | g0080 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0162 | AFR | LWK | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19030 | hp2 | a0001 | c0004 | t0005 | g0247 | AFR | LWK | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | LWK | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19043 | hp2 | a0003 | c0003 | t0007 | g0272 | AFR | LWK | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19054 | hp1 | a0003 | c0003 | t0004 | g0085 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19054 | hp2 | a0008 | c0009 | t0001 | g0016 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19055 | hp2 | a0002 | c0002 | t0005 | g0241 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19062 | hp2 | a0003 | c0003 | t0004 | g0010 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19065 | hp1 | a0003 | c0003 | t0004 | g0086 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19066 | hp2 | a0003 | c0003 | t0004 | g0017 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19067 | hp1 | a0002 | c0002 | t0005 | g0243 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19068 | hp2 | a0006 | c0007 | t0001 | g0011 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19072 | hp1 | a0002 | c0002 | t0005 | g0238 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19074 | hp2 | a0003 | c0003 | t0004 | g0072 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19082 | hp2 | a0011 | c0010 | t0001 | g0222 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19085 | hp1 | a0003 | c0003 | t0004 | g0010 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19087 | hp2 | a0003 | c0003 | t0004 | g0090 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19089 | hp1 | a0003 | c0003 | t0004 | g0081 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19089 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0205 | AFR | YRI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | YRI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20129 | hp1 | a0003 | c0003 | t0004 | g0076 | AFR | ASW | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0192 | AFR | ASW | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0102 | EUR | TSI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20752 | hp2 | a0003 | c0003 | t0004 | g0204 | EUR | TSI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0128 | EUR | TSI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0157 | EUR | TSI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | GIH | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | GIH | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0133 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02559 | hp1 | a0001 | c0004 | t0006 | g0014 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02559 | hp2 | a0005 | c0006 | t0004 | g0022 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03471 | hp1 | a0001 | c0004 | t0006 | g0093 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | USA | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG06807 | hp2 | a0003 | c0003 | t0007 | g0271 | AFR | USA | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | USA | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20300 | hp2 | a0003 | c0003 | t0002 | g0053 | AFR | USA | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | LWK | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA21309 | hp2 | a0001 | c0004 | t0006 | g0125 | AFR | LWK | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0149 | REF | REF | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0015 | REF | REF | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:156644527
|
C | A | 1 | a0011 | 1 | NA19082.hp2 | missense_variant | MODERATE | c.44C>A | p.Ala15Glu | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/9 | 159/1679 | 44/1089 | 15/362 | chr7 | 156644527 | ||
chr7:156644606
|
G | C | 1 | a0010 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.123G>C | p.Lys41Asn | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/9 | 238/1679 | 123/1089 | 41/362 | chr7 | 156644606 | ||
chr7:156644608
|
C | A | 1 | a0010 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.125C>A | p.Thr42Lys | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/9 | 240/1679 | 125/1089 | 42/362 | chr7 | 156644608 | ||
chr7:156644611
|
A | T | 1 | a0010 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.128A>T | p.Gln43Leu | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/9 | 243/1679 | 128/1089 | 43/362 | chr7 | 156644611 | ||
chr7:156654631
|
G | C | 1 | a0006 | 2 | NA18954.hp1 NA19068.hp2 |
missense_variant | MODERATE | c.330G>C | p.Trp110Cys | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/9 | 445/1679 | 330/1089 | 110/362 | chr7 | 156654631 | ||
chr7:156675781
|
T | C | 1 | a0005 | 3 | HG02559.hp2 HG03139.hp2 HG03195.hp2 |
missense_variant | MODERATE | c.770T>C | p.Ile257Thr | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/9 | 885/1679 | 770/1089 | 257/362 | chr7 | 156675781 | ||
chr7:156675787
|
G | A | 1 | a0004 | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
missense_variant | MODERATE | c.776G>A | p.Arg259Gln | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/9 | 891/1679 | 776/1089 | 259/362 | chr7 | 156675787 | ||
chr7:156676429
|
G | A | 2 | a0003a0005 | 53 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(50): Show |
missense_variant | MODERATE | c.863G>A | p.Arg288Gln | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 978/1679 | 863/1089 | 288/362 | chr7 | 156676429 | ||
chr7:156676439
|
C | G | 5 | a0002a0006a0008others(2): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
missense_variant | MODERATE | c.873C>G | p.His291Gln | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 988/1679 | 873/1089 | 291/362 | chr7 | 156676439 | ||
chr7:156676485
|
C | T | 4 | a0002a0006a0009others(1): Show | 182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
missense_variant | MODERATE | c.919C>T | p.Arg307Cys | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 1034/1679 | 919/1089 | 307/362 | chr7 | 156676485 | ||
chr7:156676528
|
C | T | 1 | a0007 | 2 | HG02683.hp1 HG02698.hp1 |
missense_variant | MODERATE | c.962C>T | p.Ser321Phe | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 1077/1679 | 962/1089 | 321/362 | chr7 | 156676528 | ||
chr7:156676620
|
C | T | 1 | a0009 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.1054C>T | p.Arg352Cys | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 1169/1679 | 1054/1089 | 352/362 | chr7 | 156676620 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:156644609
|
A | T | 1 | a0010c0011 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.126A>T | p.Thr42Thr | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/9 | 241/1679 | 126/1089 | 42/362 | chr7 | 156644609 | ||
chr7:156676496
|
A | G | 10 | a0001c0004a0002c0002a0003c0003others(7): Show | 260 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(257): Show |
synonymous_variant | LOW | c.930A>G | p.Ala310Ala | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 1045/1679 | 930/1089 | 310/362 | chr7 | 156676496 | ||
chr7:156676589
|
C | T | 1 | a0004c0012 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1023C>T | p.Asp341Asp | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 1138/1679 | 1023/1089 | 341/362 | chr7 | 156676589 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:156640777
|
C | A | 1 | a0003c0003t0007 | 2 | HG06807.hp2 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-112C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/9 | 3101 | chr7 | 156640777 | |||||
chr7:156640803
|
G | A | 4 | a0001c0001t0003a0001c0004t0003a0001c0004t0005others(1): Show | 69 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(66): Show |
5_prime_UTR_variant | MODIFIER | c.-86G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/9 | 3075 | chr7 | 156640803 | |||||
chr7:156640804
|
G | T | 1 | a0003c0003t0007 | 2 | HG06807.hp2 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-85G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/9 | 3074 | chr7 | 156640804 | |||||
chr7:156676707
|
T | C | 1 | a0001c0004t0006 | 10 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*52T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 52 | chr7 | 156676707 | |||||
chr7:156676760
|
C | T | 2 | a0003c0003t0004a0005c0006t0004 | 45 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*105C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 105 | chr7 | 156676760 | |||||
chr7:156676926
|
T | C | 7 | a0001c0004t0005a0002c0002t0001a0002c0002t0005others(4): Show | 185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*271T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 271 | chr7 | 156676926 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:156640814
|
A | C | 4 | a0001c0001t0002g0062a0001c0001t0002g0273a0002c0002t0001g0274others(1): Show | 5 | HG00423.hp1 HG01123.hp1 HG01257.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.-78+3A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156640814 | ||||||
chr7:156640861
|
C | A | 2 | a0002c0002t0001g0063a0002c0002t0001g0064 | 2 | HG02145.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-78+50C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156640861 | ||||||
chr7:156640914
|
T | C | 1 | a0002c0002t0005g0065 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-78+103T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156640914 | ||||||
chr7:156640985
|
T | C | 2 | a0002c0002t0001g0063a0002c0002t0001g0064 | 2 | HG02145.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-78+174T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156640985 | ||||||
chr7:156641027
|
A | C | 2 | a0003c0003t0007g0271a0003c0003t0007g0272 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-78+216A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641027 | ||||||
chr7:156641034
|
G | C | 1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-78+223G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641034 | ||||||
chr7:156641147
|
T | C | 1 | a0002c0002t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-78+336T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641147 | ||||||
chr7:156641353
|
T | G | 1 | a0003c0003t0004g0067 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-78+542T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641353 | ||||||
chr7:156641452
|
C | G | 2 | a0003c0003t0007g0271a0003c0003t0007g0272 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-78+641C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641452 | ||||||
chr7:156641462
|
C | T | 1 | a0001c0001t0002g0061 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-78+651C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641462 | ||||||
chr7:156641475
|
T | G | 39 | a0001c0001t0002g0018a0001c0001t0002g0074a0001c0004t0006g0014others(36): Show | 51 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.-78+664T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641475 | ||||||
chr7:156641490
|
G | T | 1 | a0003c0003t0004g0100 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-78+679G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641490 | ||||||
chr7:156641491
|
G | A | 37 | a0001c0001t0002g0018a0001c0001t0002g0074a0001c0004t0006g0014others(34): Show | 49 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.-78+680G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641491 | ||||||
chr7:156641523
|
A | G | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78+712A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641523 | ||||||
chr7:156641852
|
A | G | 196 | a0001c0001t0002g0018a0001c0001t0002g0074a0001c0001t0002g0187others(193): Show | 307 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-78+1041A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641852 | ||||||
chr7:156641858
|
GAACTTAT others(6): Show |
G | 7 | a0001c0001t0002g0018a0001c0004t0006g0014a0001c0004t0006g0093others(4): Show | 12 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-78+1048_-78+1060d others(15): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641858 | ||||||
chr7:156641981
|
A | G | 42 | a0001c0001t0002g0263a0001c0001t0003g0003a0001c0001t0003g0032others(39): Show | 70 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.-78+1170A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641981 | ||||||
chr7:156642029
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-78+1218G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642029 | ||||||
chr7:156642084
|
A | T | 42 | a0001c0001t0002g0263a0001c0001t0003g0003a0001c0001t0003g0032others(39): Show | 70 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.-78+1273A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642084 | ||||||
chr7:156642181
|
G | A | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78+1370G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642181 | ||||||
chr7:156642222
|
A | G | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78+1411A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642222 | ||||||
chr7:156642308
|
A | G | 4 | a0002c0002t0001g0231a0003c0003t0002g0053a0003c0003t0002g0232others(1): Show | 5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-77-1493A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642308 | ||||||
chr7:156642421
|
A | G | 1 | a0003c0003t0004g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-77-1380A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642421 | ||||||
chr7:156642515
|
C | A | 1 | a0002c0002t0001g0162 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-77-1286C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642515 | ||||||
chr7:156642525
|
C | G | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-77-1276C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642525 | ||||||
chr7:156642673
|
G | A | 1 | a0001c0001t0003g0234 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-77-1128G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642673 | ||||||
chr7:156642703
|
A | G | 1 | a0003c0003t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-77-1098A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642703 | ||||||
chr7:156642746
|
T | G | 1 | a0002c0002t0001g0163 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-77-1055T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642746 | ||||||
chr7:156642750
|
C | G | 1 | a0003c0003t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-77-1051C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642750 | ||||||
chr7:156642756
|
G | A | 1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-77-1045G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642756 | ||||||
chr7:156642850
|
C | T | 1 | a0002c0002t0001g0161 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-77-951C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642850 | ||||||
chr7:156642905
|
G | A | 10 | a0001c0001t0002g0074a0003c0003t0004g0010a0003c0003t0004g0017others(7): Show | 17 | HG00558.hp2 HG02135.hp2 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.-77-896G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642905 | ||||||
chr7:156643086
|
G | A | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-77-715G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156643086 | ||||||
chr7:156643103
|
A | G | 1 | a0002c0002t0001g0228 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-77-698A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156643103 | ||||||
chr7:156643344
|
A | G | 1 | a0003c0003t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-77-457A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156643344 | ||||||
chr7:156643426
|
C | G | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-77-375C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156643426 | ||||||
chr7:156643968
|
A | G | 1 | a0002c0002t0001g0162 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.15+76A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156643968 | ||||||
chr7:156644021
|
G | A | 2 | a0003c0003t0007g0271a0003c0003t0007g0272 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.15+129G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156644021 | ||||||
chr7:156644042
|
C | CA | 3 | a0003c0003t0004g0075a0003c0003t0004g0098a0003c0003t0004g0099 | 3 | HG02145.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.15+151dupA | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 156644042 | |||||
chr7:156644075
|
C | T | 221 | a0001c0001t0002g0005a0001c0001t0002g0018a0001c0001t0002g0023others(218): Show | 349 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.15+183C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156644075 | ||||||
chr7:156644127
|
G | T | 2 | a0002c0002t0001g0052a0002c0002t0001g0227 | 3 | NA18955.hp1 NA19007.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.15+235G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156644127 | ||||||
chr7:156644154
|
C | T | 1 | a0001c0001t0003g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.15+262C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156644154 | ||||||
chr7:156644171
|
G | A | 193 | a0001c0001t0002g0018a0001c0001t0002g0074a0001c0001t0002g0187others(190): Show | 305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.15+279G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156644171 | ||||||
chr7:156644252
|
G | A | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-247G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156644252 | ||||||
chr7:156644300
|
A | C | 102 | a0001c0001t0002g0143a0001c0001t0002g0187a0001c0001t0002g0200others(99): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.16-199A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156644300 | ||||||
chr7:156644356
|
C | T | 1 | a0001c0004t0002g0164 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.16-143C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156644356 | ||||||
chr7:156644777
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.274+20C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156644777 | ||||||
chr7:156644952
|
A | G | 1 | a0003c0003t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.274+195A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156644952 | ||||||
chr7:156645030
|
T | G | 2 | a0002c0002t0001g0077a0003c0003t0004g0076 | 2 | HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.274+273T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645030 | ||||||
chr7:156645146
|
T | C | 40 | a0001c0001t0002g0074a0001c0004t0006g0014a0001c0004t0006g0093others(37): Show | 50 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.274+389T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645146 | ||||||
chr7:156645378
|
A | G | 1 | a0002c0002t0001g0226 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.274+621A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645378 | ||||||
chr7:156645394
|
A | G | 2 | a0002c0002t0001g0224a0002c0002t0001g0225 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.274+637A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645394 | ||||||
chr7:156645524
|
T | G | 1 | a0004c0012t0002g0265 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.274+767T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645524 | ||||||
chr7:156645559
|
A | G | 1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.274+802A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645559 | ||||||
chr7:156645729
|
T | C | 1 | a0001c0001t0002g0146 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.274+972T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645729 | ||||||
chr7:156645768
|
T | C | 102 | a0001c0001t0002g0187a0001c0001t0002g0200a0001c0004t0002g0164others(99): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.274+1011T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645768 | ||||||
chr7:156645821
|
G | A | 101 | a0001c0001t0002g0187a0001c0001t0002g0200a0001c0004t0002g0217others(98): Show | 171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.274+1064G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645821 | ||||||
chr7:156645851
|
A | G | 1 | a0003c0003t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.274+1094A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645851 | ||||||
chr7:156645969
|
C | T | 6 | a0001c0004t0006g0014a0001c0004t0006g0093a0001c0004t0006g0094others(3): Show | 9 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.274+1212C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645969 | ||||||
chr7:156646030
|
G | A | 2 | a0003c0003t0007g0271a0003c0003t0007g0272 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.274+1273G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646030 | ||||||
chr7:156646040
|
T | C | 1 | a0001c0004t0002g0164 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.274+1283T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646040 | ||||||
chr7:156646075
|
G | A | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+1318G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646075 | ||||||
chr7:156646103
|
T | C | 95 | a0001c0001t0002g0187a0001c0001t0002g0200a0001c0004t0002g0217others(92): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.274+1346T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646103 | ||||||
chr7:156646252
|
A | C | 1 | a0003c0003t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.274+1495A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646252 | ||||||
chr7:156646321
|
T | C | 1 | a0002c0002t0001g0221 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.274+1564T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646321 | ||||||
chr7:156646352
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0061a0001c0001t0002g0141 | 6 | HG01167.hp2 HG01255.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+1595C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646352 | ||||||
chr7:156646392
|
C | T | 4 | a0002c0002t0001g0231a0003c0003t0002g0053a0003c0003t0002g0232others(1): Show | 5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+1635C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646392 | ||||||
chr7:156646450
|
T | A | 2 | a0002c0002t0001g0077a0003c0003t0004g0076 | 2 | HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.274+1693T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646450 | ||||||
chr7:156646861
|
G | GT | 9 | a0001c0001t0002g0006a0001c0001t0002g0020a0001c0001t0002g0135others(6): Show | 19 | HG00423.hp1 NA18747.hp2 NA18951.hp1 others(16): Show |
intron_variant | MODIFIER | c.274+2112dupT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156646861 | |||||
chr7:156646914
|
C | T | 1 | a0003c0003t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.274+2157C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646914 | ||||||
chr7:156647043
|
G | A | 4 | a0002c0002t0001g0066a0002c0002t0001g0165a0002c0002t0001g0166others(1): Show | 4 | HG00099.hp2 HG00280.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+2286G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647043 | ||||||
chr7:156647098
|
C | T | 1 | a0002c0002t0001g0161 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.274+2341C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647098 | ||||||
chr7:156647132
|
G | A | 43 | a0001c0001t0002g0018a0001c0001t0003g0003a0001c0001t0003g0032others(40): Show | 73 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.274+2375G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647132 | ||||||
chr7:156647153
|
G | GT | 36 | a0001c0001t0002g0074a0001c0001t0003g0059a0001c0001t0003g0261others(33): Show | 44 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.274+2405dupT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156647153 | |||||
chr7:156647163
|
A | T | 199 | a0001c0001t0002g0018a0001c0001t0002g0074a0001c0001t0002g0187others(196): Show | 312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.274+2406A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647163 | ||||||
chr7:156647167
|
T | TTTTG | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+2418_274+2421d others(6): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156647167 | |||||
chr7:156647195
|
CT | C | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+2444delT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156647195 | |||||
chr7:156647208
|
T | G | 102 | a0001c0001t0002g0187a0001c0001t0002g0200a0001c0004t0002g0217others(99): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.274+2451T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647208 | ||||||
chr7:156647374
|
A | G | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+2617A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647374 | ||||||
chr7:156647541
|
C | T | 1 | a0002c0002t0001g0133 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.274+2784C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647541 | ||||||
chr7:156647654
|
C | T | 1 | a0002c0002t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.274+2897C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647654 | ||||||
chr7:156647862
|
A | T | 1 | a0004c0012t0002g0265 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.274+3105A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647862 | ||||||
chr7:156647996
|
G | C | 1 | a0001c0001t0002g0135 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.274+3239G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647996 | ||||||
chr7:156648028
|
T | A | 1 | a0003c0003t0004g0078 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.274+3271T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648028 | ||||||
chr7:156648028
|
TG | T | 29 | a0001c0001t0002g0074a0003c0003t0004g0010a0003c0003t0004g0017others(26): Show | 37 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.274+3272delG | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648028 | ||||||
chr7:156648029
|
G | GT | 111 | a0001c0001t0002g0187a0001c0001t0002g0200a0001c0004t0002g0164others(108): Show | 183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.274+3284dupT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156648029 | |||||
chr7:156648029
|
G | T | 9 | a0002c0002t0001g0077a0002c0002t0001g0091a0003c0003t0004g0075others(6): Show | 9 | HG02145.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.274+3272G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648029 | ||||||
chr7:156648066
|
G | A | 1 | a0001c0001t0003g0032 | 3 | HG02083.hp1 HG02129.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.274+3309G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648066 | ||||||
chr7:156648167
|
T | C | 102 | a0001c0001t0002g0187a0001c0001t0002g0200a0001c0004t0002g0217others(99): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.274+3410T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648167 | ||||||
chr7:156648209
|
G | A | 4 | a0002c0002t0001g0231a0003c0003t0002g0053a0003c0003t0002g0232others(1): Show | 5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+3452G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648209 | ||||||
chr7:156648411
|
G | A | 1 | a0001c0001t0002g0102 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.274+3654G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648411 | ||||||
chr7:156648536
|
G | A | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+3779G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648536 | ||||||
chr7:156648615
|
T | A | 1 | a0002c0002t0001g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.274+3858T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648615 | ||||||
chr7:156648625
|
G | A | 1 | a0001c0001t0003g0054 | 2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.274+3868G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648625 | ||||||
chr7:156649156
|
C | CT | 8 | a0002c0002t0001g0219a0004c0005t0002g0060a0004c0005t0002g0266others(5): Show | 9 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.274+4410dupT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156649156 | |||||
chr7:156649234
|
C | T | 1 | a0002c0002t0001g0218 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.274+4477C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649234 | ||||||
chr7:156649295
|
C | T | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+4538C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649295 | ||||||
chr7:156649341
|
T | C | 95 | a0001c0001t0002g0187a0001c0001t0002g0200a0002c0002t0001g0002others(92): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.274+4584T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649341 | ||||||
chr7:156649481
|
G | A | 1 | a0002c0002t0001g0169 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.274+4724G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649481 | ||||||
chr7:156649498
|
G | A | 4 | a0002c0002t0001g0231a0003c0003t0002g0053a0003c0003t0002g0232others(1): Show | 5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+4741G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649498 | ||||||
chr7:156649509
|
T | C | 200 | a0001c0001t0002g0018a0001c0001t0002g0074a0001c0001t0002g0187others(197): Show | 313 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.274+4752T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649509 | ||||||
chr7:156649701
|
T | A | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-4875T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649701 | ||||||
chr7:156649711
|
G | A | 6 | a0001c0004t0002g0223a0002c0002t0001g0016a0002c0002t0001g0031others(3): Show | 10 | HG00423.hp2 HG01069.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.275-4865G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649711 | ||||||
chr7:156649747
|
G | A | 4 | a0002c0002t0001g0231a0003c0003t0002g0053a0003c0003t0002g0232others(1): Show | 5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-4829G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649747 | ||||||
chr7:156649747
|
G | T | 1 | a0003c0003t0004g0090 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.275-4829G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649747 | ||||||
chr7:156650025
|
G | GCT | 200 | a0001c0001t0002g0018a0001c0001t0002g0074a0001c0001t0002g0187others(197): Show | 313 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.275-4550_275-4549d others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156650025 | |||||
chr7:156650204
|
G | A | 1 | a0003c0003t0004g0068 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.275-4372G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650204 | ||||||
chr7:156650322
|
C | T | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-4254C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650322 | ||||||
chr7:156650350
|
T | C | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-4226T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650350 | ||||||
chr7:156650445
|
C | T | 1 | a0003c0003t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.275-4131C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650445 | ||||||
chr7:156650447
|
C | T | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-4129C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650447 | ||||||
chr7:156650475
|
T | C | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-4101T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650475 | ||||||
chr7:156650545
|
G | T | 1 | a0001c0004t0002g0164 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.275-4031G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650545 | ||||||
chr7:156650667
|
T | C | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-3909T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650667 | ||||||
chr7:156650678
|
G | A | 1 | a0001c0004t0002g0164 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.275-3898G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650678 | ||||||
chr7:156650768
|
C | T | 4 | a0001c0001t0003g0033a0001c0001t0003g0257a0001c0001t0003g0258others(1): Show | 6 | HG00597.hp2 HG00609.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-3808C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650768 | ||||||
chr7:156650790
|
G | A | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-3786G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650790 | ||||||
chr7:156651000
|
C | T | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-3576C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651000 | ||||||
chr7:156651092
|
A | C | 1 | a0001c0001t0003g0256 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.275-3484A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651092 | ||||||
chr7:156651213
|
T | G | 1 | a0002c0002t0001g0169 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.275-3363T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651213 | ||||||
chr7:156651215
|
C | CT | 9 | a0001c0001t0002g0040a0001c0001t0002g0101a0001c0004t0002g0164others(6): Show | 14 | HG00423.hp2 HG00438.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.275-3345dupT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156651215 | |||||
chr7:156651215
|
C | CTT | 44 | a0001c0001t0002g0018a0001c0001t0002g0263a0001c0001t0003g0003others(41): Show | 74 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.275-3346_275-3345d others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156651215 | |||||
chr7:156651215
|
CT | C | 51 | a0001c0001t0002g0074a0001c0001t0002g0103a0001c0001t0002g0136others(48): Show | 63 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.275-3345delT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156651215 | |||||
chr7:156651288
|
A | G | 40 | a0001c0001t0002g0074a0001c0004t0006g0014a0001c0004t0006g0093others(37): Show | 50 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.275-3288A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651288 | ||||||
chr7:156651296
|
C | T | 6 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(3): Show | 7 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.275-3280C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651296 | ||||||
chr7:156651474
|
A | G | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-3102A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651474 | ||||||
chr7:156651511
|
G | A | 6 | a0001c0004t0006g0014a0001c0004t0006g0093a0001c0004t0006g0094others(3): Show | 9 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.275-3065G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651511 | ||||||
chr7:156651522
|
A | C | 6 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(3): Show | 7 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.275-3054A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651522 | ||||||
chr7:156651545
|
C | T | 29 | a0001c0001t0002g0074a0002c0002t0001g0077a0003c0003t0004g0010others(26): Show | 36 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.275-3031C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651545 | ||||||
chr7:156651651
|
T | C | 44 | a0001c0001t0002g0018a0001c0001t0002g0263a0001c0001t0003g0003others(41): Show | 74 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.275-2925T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651651 | ||||||
chr7:156651671
|
C | T | 2 | a0003c0003t0007g0271a0003c0003t0007g0272 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.275-2905C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651671 | ||||||
chr7:156651753
|
C | A | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-2823C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651753 | ||||||
chr7:156651916
|
C | A | 1 | a0001c0001t0002g0149 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.275-2660C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651916 | ||||||
chr7:156652005
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.275-2571C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652005 | ||||||
chr7:156652120
|
C | T | 3 | a0002c0002t0001g0051a0002c0002t0001g0215a0002c0002t0001g0216 | 4 | HG03041.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-2456C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652120 | ||||||
chr7:156652285
|
C | T | 1 | a0003c0003t0004g0078 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.275-2291C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652285 | ||||||
chr7:156652303
|
G | A | 4 | a0003c0003t0004g0145a0003c0003t0007g0271a0003c0003t0007g0272others(1): Show | 6 | HG01256.hp1 HG02559.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.275-2273G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652303 | ||||||
chr7:156652474
|
CTTGA | C | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-2099_275-2096d others(6): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156652474 | |||||
chr7:156652530
|
C | T | 1 | a0002c0002t0005g0255 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.275-2046C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652530 | ||||||
chr7:156652694
|
A | T | 1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.275-1882A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652694 | ||||||
chr7:156652739
|
T | TATA | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-1836_275-1835i others(5): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156652739 | |||||
chr7:156652793
|
T | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0135 | 4 | NA18967.hp2 NA18975.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.275-1783T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652793 | ||||||
chr7:156652870
|
A | G | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-1706A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652870 | ||||||
chr7:156652870
|
A | T | 1 | a0001c0001t0002g0273 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.275-1706A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652870 | ||||||
chr7:156652929
|
TA | T | 102 | a0001c0001t0002g0187a0001c0001t0002g0200a0001c0004t0002g0164others(99): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.275-1641delA | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156652929 | |||||
chr7:156652948
|
G | T | 1 | a0003c0003t0004g0089 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.275-1628G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652948 | ||||||
chr7:156653001
|
A | G | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-1575A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653001 | ||||||
chr7:156653039
|
T | C | 1 | a0001c0001t0003g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.275-1537T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653039 | ||||||
chr7:156653091
|
GCACT | G | 102 | a0001c0001t0002g0187a0001c0001t0002g0200a0001c0004t0002g0164others(99): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.275-1476_275-1473d others(6): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156653091 | |||||
chr7:156653200
|
A | G | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-1376A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653200 | ||||||
chr7:156653211
|
A | G | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-1365A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653211 | ||||||
chr7:156653220
|
A | T | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-1356A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653220 | ||||||
chr7:156653351
|
A | G | 155 | a0001c0001t0002g0074a0001c0001t0002g0187a0001c0001t0002g0200others(152): Show | 238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.275-1225A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653351 | ||||||
chr7:156653380
|
C | T | 1 | a0003c0003t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.275-1196C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653380 | ||||||
chr7:156653415
|
C | T | 8 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(5): Show | 10 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.275-1161C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653415 | ||||||
chr7:156653444
|
T | C | 1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.275-1132T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653444 | ||||||
chr7:156653476
|
G | A | 1 | a0001c0001t0002g0018 | 3 | HG01243.hp1 HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.275-1100G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653476 | ||||||
chr7:156653556
|
C | T | 2 | a0001c0004t0006g0014a0001c0004t0006g0096 | 5 | HG02559.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-1020C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653556 | ||||||
chr7:156653618
|
T | C | 1 | a0001c0001t0003g0235 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.275-958T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653618 | ||||||
chr7:156653624
|
C | T | 102 | a0001c0001t0002g0187a0001c0001t0002g0200a0001c0004t0002g0164others(99): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.275-952C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653624 | ||||||
chr7:156653706
|
A | G | 102 | a0001c0001t0002g0187a0001c0001t0002g0200a0001c0004t0002g0164others(99): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.275-870A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653706 | ||||||
chr7:156653802
|
T | A | 4 | a0002c0002t0001g0231a0003c0003t0002g0053a0003c0003t0002g0232others(1): Show | 5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-774T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653802 | ||||||
chr7:156653815
|
A | G | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-761A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653815 | ||||||
chr7:156653911
|
G | T | 1 | a0001c0001t0002g0160 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.275-665G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653911 | ||||||
chr7:156654113
|
A | T | 1 | a0001c0001t0002g0074 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.275-463A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156654113 | ||||||
chr7:156654122
|
C | T | 1 | a0003c0003t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.275-454C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156654122 | ||||||
chr7:156654142
|
A | G | 102 | a0001c0001t0002g0187a0001c0001t0002g0200a0001c0004t0002g0164others(99): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.275-434A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156654142 | ||||||
chr7:156654154
|
C | T | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-422C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156654154 | ||||||
chr7:156654166
|
A | G | 1 | a0001c0001t0002g0143 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.275-410A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156654166 | ||||||
chr7:156654211
|
T | TA | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-359dupA | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156654211 | |||||
chr7:156654229
|
CAATAT | C | 3 | a0001c0001t0002g0104a0001c0001t0002g0105a0007c0008t0002g0034 | 4 | HG00738.hp2 HG01175.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.275-342_275-338del others(5): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156654229 | |||||
chr7:156654377
|
A | G | 102 | a0001c0001t0002g0187a0001c0001t0002g0200a0001c0004t0002g0164others(99): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.275-199A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156654377 | ||||||
chr7:156654483
|
A | C | 4 | a0001c0001t0002g0024a0001c0001t0002g0147a0001c0001t0002g0148others(1): Show | 6 | NA18950.hp2 NA18952.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-93A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156654483 | ||||||
chr7:156654731
|
C | T | 1 | a0002c0002t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.417+13C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156654731 | ||||||
chr7:156654858
|
T | A | 2 | a0001c0001t0002g0106a0001c0001t0002g0107 | 2 | HG01081.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.417+140T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156654858 | ||||||
chr7:156655014
|
G | A | 36 | a0001c0001t0002g0187a0002c0002t0001g0004a0002c0002t0001g0025others(33): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.417+296G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655014 | ||||||
chr7:156655232
|
C | CGG | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.417+515_417+516ins others(2): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 156655232 | |||||
chr7:156655237
|
G | A | 1 | a0001c0001t0003g0236 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.417+519G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655237 | ||||||
chr7:156655239
|
G | A | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.417+521G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655239 | ||||||
chr7:156655239
|
G | GCA | 20 | a0001c0001t0002g0005a0001c0001t0002g0023a0001c0001t0002g0024others(17): Show | 34 | HG00280.hp2 HG00642.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.417+544_417+545dup others(2): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 156655239 | |||||
chr7:156655239
|
G | GCACA | 2 | a0001c0001t0002g0041a0001c0001t0002g0150 | 3 | HG03704.hp2 HG03834.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.417+542_417+545dup others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 156655239 | |||||
chr7:156655239
|
GCA | G | 45 | a0001c0001t0002g0074a0001c0001t0002g0131a0001c0004t0006g0014others(42): Show | 57 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.417+544_417+545del others(2): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 156655239 | |||||
chr7:156655262
|
C | CAG | 3 | a0001c0001t0003g0237a0002c0002t0001g0228a0003c0003t0002g0190 | 3 | HG02027.hp1 HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.417+558_417+559dup others(2): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 156655262 | |||||
chr7:156655262
|
C | G | 182 | a0001c0001t0002g0018a0001c0001t0002g0074a0001c0001t0002g0187others(179): Show | 291 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.417+544C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655262 | ||||||
chr7:156655293
|
T | G | 101 | a0001c0001t0002g0102a0001c0001t0002g0106a0001c0001t0002g0109others(98): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.417+575T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655293 | ||||||
chr7:156655295
|
G | T | 51 | a0001c0001t0002g0005a0001c0001t0002g0023a0001c0001t0002g0041others(48): Show | 74 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.417+577G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655295 | ||||||
chr7:156655297
|
G | T | 4 | a0001c0001t0002g0149a0001c0001t0002g0157a0001c0001t0003g0058others(1): Show | 5 | NA18948.hp2 NA18990.hp1 NA19089.hp2 others(2): Show |
intron_variant | MODIFIER | c.417+579G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655297 | ||||||
chr7:156655416
|
G | A | 1 | a0001c0004t0002g0164 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.417+698G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655416 | ||||||
chr7:156655421
|
T | C | 1 | a0001c0001t0002g0018 | 3 | HG01243.hp1 HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.417+703T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655421 | ||||||
chr7:156655424
|
G | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0115 | 3 | HG00408.hp2 HG02056.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.417+706G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655424 | ||||||
chr7:156655449
|
C | T | 148 | a0001c0001t0002g0074a0001c0001t0002g0187a0001c0001t0002g0200others(145): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.417+731C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655449 | ||||||
chr7:156655451
|
T | C | 4 | a0002c0002t0001g0051a0002c0002t0001g0215a0002c0002t0001g0216others(1): Show | 5 | HG03041.hp1 HG03225.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.417+733T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655451 | ||||||
chr7:156655453
|
G | T | 2 | a0003c0003t0004g0145a0005c0006t0004g0022 | 4 | HG01256.hp1 HG02559.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.417+735G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655453 | ||||||
chr7:156655609
|
G | A | 1 | a0001c0001t0002g0116 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.417+891G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655609 | ||||||
chr7:156655747
|
A | G | 1 | a0001c0001t0002g0039 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.417+1029A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655747 | ||||||
chr7:156655787
|
T | TTAGTAAT others(344): Show |
1 | a0001c0001t0003g0258 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.417+1081_417+1082i others(353): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 156655787 | |||||
chr7:156655787
|
T | TTAGTAAT others(345): Show |
1 | a0001c0001t0003g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.417+1081_417+1082i others(354): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 156655787 | |||||
chr7:156655787
|
T | TTAGTAAT others(350): Show |
1 | a0001c0001t0003g0257 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.417+1081_417+1082i others(359): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 156655787 | |||||
chr7:156655998
|
C | T | 155 | a0001c0001t0002g0074a0001c0001t0002g0187a0001c0001t0002g0200others(152): Show | 238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.417+1280C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655998 | ||||||
chr7:156656018
|
C | T | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.417+1300C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156656018 | ||||||
chr7:156656520
|
T | C | 1 | a0002c0002t0001g0191 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.418-1021T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156656520 | ||||||
chr7:156656566
|
G | C | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.418-975G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156656566 | ||||||
chr7:156656762
|
A | C | 199 | a0001c0001t0002g0018a0001c0001t0002g0074a0001c0001t0002g0187others(196): Show | 312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.418-779A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156656762 | ||||||
chr7:156656764
|
C | A | 43 | a0001c0001t0002g0018a0001c0001t0002g0263a0001c0001t0003g0003others(40): Show | 73 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.418-777C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156656764 | ||||||
chr7:156656857
|
T | C | 38 | a0001c0001t0002g0074a0001c0004t0006g0014a0001c0004t0006g0093others(35): Show | 48 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.418-684T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156656857 | ||||||
chr7:156656925
|
T | C | 1 | a0001c0001t0002g0159 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.418-616T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156656925 | ||||||
chr7:156657046
|
A | G | 2 | a0004c0005t0002g0060a0004c0005t0002g0270 | 3 | HG01884.hp1 HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.418-495A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156657046 | ||||||
chr7:156657215
|
C | G | 2 | a0003c0003t0007g0271a0003c0003t0007g0272 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.418-326C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156657215 | ||||||
chr7:156657366
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.418-175G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156657366 | ||||||
chr7:156657384
|
C | T | 1 | a0003c0003t0004g0084 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.418-157C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156657384 | ||||||
chr7:156657866
|
C | T | 1 | a0001c0004t0002g0217 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.451-262C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 5/8 | chr7 | 156657866 | ||||||
chr7:156658269
|
C | T | 1 | a0002c0002t0001g0162 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.575+17C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 6/8 | chr7 | 156658269 | ||||||
chr7:156658276
|
C | T | 1 | a0001c0001t0002g0061 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.575+24C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 6/8 | chr7 | 156658276 | ||||||
chr7:156658652
|
T | C | 1 | a0002c0002t0001g0048 | 2 | NA18971.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.684+82T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156658652 | ||||||
chr7:156658740
|
C | T | 1 | a0002c0002t0001g0211 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.684+170C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156658740 | ||||||
chr7:156658998
|
T | C | 1 | a0011c0010t0001g0222 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.684+428T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156658998 | ||||||
chr7:156659022
|
A | G | 3 | a0002c0002t0001g0091a0003c0003t0004g0078a0003c0003t0004g0092 | 3 | HG02258.hp1 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.684+452A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659022 | ||||||
chr7:156659066
|
A | G | 5 | a0001c0001t0002g0018a0001c0001t0003g0054a0001c0001t0003g0249others(2): Show | 8 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.684+496A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659066 | ||||||
chr7:156659114
|
C | G | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+544C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659114 | ||||||
chr7:156659272
|
A | C | 2 | a0001c0001t0003g0235a0001c0001t0003g0237 | 2 | HG02015.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.684+702A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659272 | ||||||
chr7:156659395
|
G | A | 3 | a0001c0001t0002g0020a0001c0001t0002g0135a0001c0001t0002g0137 | 5 | NA18967.hp2 NA18975.hp1 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+825G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659395 | ||||||
chr7:156659512
|
C | A | 1 | a0001c0001t0002g0129 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.684+942C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659512 | ||||||
chr7:156659534
|
CATA | C | 4 | a0002c0002t0001g0231a0003c0003t0002g0053a0003c0003t0002g0232others(1): Show | 5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.684+965_684+967del others(3): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659534 | ||||||
chr7:156659553
|
A | G | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+983A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659553 | ||||||
chr7:156659584
|
C | A | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+1014C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659584 | ||||||
chr7:156659858
|
T | G | 1 | a0001c0001t0002g0151 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.684+1288T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659858 | ||||||
chr7:156660040
|
A | G | 1 | a0002c0002t0001g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.684+1470A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660040 | ||||||
chr7:156660108
|
C | A | 6 | a0001c0004t0006g0014a0001c0004t0006g0093a0001c0004t0006g0094others(3): Show | 9 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.684+1538C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660108 | ||||||
chr7:156660130
|
G | T | 1 | a0002c0002t0001g0182 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.684+1560G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660130 | ||||||
chr7:156660559
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.684+1989G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660559 | ||||||
chr7:156660642
|
T | C | 1 | a0002c0002t0001g0184 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.684+2072T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660642 | ||||||
chr7:156660695
|
G | A | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+2125G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660695 | ||||||
chr7:156660719
|
T | G | 1 | a0002c0002t0001g0045 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.684+2149T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660719 | ||||||
chr7:156660820
|
T | C | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+2250T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660820 | ||||||
chr7:156660821
|
G | C | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+2251G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660821 | ||||||
chr7:156660828
|
G | A | 1 | a0001c0001t0002g0152 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.684+2258G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660828 | ||||||
chr7:156660960
|
T | G | 3 | a0001c0001t0002g0109a0001c0001t0002g0110a0001c0001t0002g0111 | 3 | HG00099.hp1 HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.684+2390T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660960 | ||||||
chr7:156660966
|
A | G | 1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.684+2396A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660966 | ||||||
chr7:156661066
|
T | C | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+2496T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661066 | ||||||
chr7:156661074
|
G | A | 1 | a0002c0002t0001g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.684+2504G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661074 | ||||||
chr7:156661116
|
G | T | 4 | a0002c0002t0001g0231a0003c0003t0002g0053a0003c0003t0002g0232others(1): Show | 5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.684+2546G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661116 | ||||||
chr7:156661146
|
C | T | 2 | a0003c0003t0007g0271a0003c0003t0007g0272 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.684+2576C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661146 | ||||||
chr7:156661210
|
C | CATA | 161 | a0001c0001t0002g0074a0001c0001t0002g0187a0001c0001t0002g0200others(158): Show | 245 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.684+2642_684+2644d others(5): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156661210 | |||||
chr7:156661240
|
G | A | 1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.684+2670G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661240 | ||||||
chr7:156661298
|
C | T | 1 | a0002c0002t0001g0210 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.684+2728C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661298 | ||||||
chr7:156661299
|
G | A | 2 | a0003c0003t0002g0232a0003c0003t0002g0233 | 2 | HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.684+2729G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661299 | ||||||
chr7:156661302
|
C | A | 1 | a0002c0002t0001g0193 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.684+2732C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661302 | ||||||
chr7:156661322
|
A | AT | 139 | a0001c0001t0002g0074a0001c0001t0002g0105a0001c0001t0002g0110others(136): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.684+2767dupT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156661322 | |||||
chr7:156661322
|
A | ATT | 10 | a0001c0004t0002g0164a0002c0002t0001g0179a0002c0002t0001g0180others(7): Show | 10 | HG02738.hp1 HG02896.hp2 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.684+2766_684+2767d others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156661322 | |||||
chr7:156661479
|
C | T | 1 | a0004c0012t0002g0265 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.684+2909C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661479 | ||||||
chr7:156661617
|
T | C | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+3047T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661617 | ||||||
chr7:156661729
|
T | A | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+3159T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661729 | ||||||
chr7:156661786
|
G | T | 1 | a0002c0002t0001g0128 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.684+3216G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661786 | ||||||
chr7:156662011
|
T | C | 1 | a0002c0002t0001g0195 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.684+3441T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156662011 | ||||||
chr7:156662169
|
G | A | 107 | a0001c0001t0002g0187a0001c0001t0002g0200a0001c0004t0002g0164others(104): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.684+3599G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156662169 | ||||||
chr7:156662367
|
T | C | 1 | a0003c0003t0004g0035 | 2 | NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.684+3797T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156662367 | ||||||
chr7:156662395
|
T | C | 1 | a0002c0002t0001g0212 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.684+3825T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156662395 | ||||||
chr7:156662559
|
C | G | 4 | a0002c0002t0001g0231a0003c0003t0002g0053a0003c0003t0002g0232others(1): Show | 5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.684+3989C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156662559 | ||||||
chr7:156662611
|
G | A | 8 | a0003c0003t0002g0232a0004c0005t0002g0060a0004c0005t0002g0266others(5): Show | 9 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.684+4041G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156662611 | ||||||
chr7:156662631
|
C | T | 33 | a0001c0001t0002g0074a0002c0002t0001g0077a0002c0002t0001g0091others(30): Show | 40 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.684+4061C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156662631 | ||||||
chr7:156662847
|
C | CT | 12 | a0001c0001t0002g0038a0001c0001t0002g0106a0001c0001t0002g0127others(9): Show | 15 | HG00639.hp2 HG01192.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.684+4295dupT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156662847 | |||||
chr7:156662847
|
CT | C | 12 | a0001c0004t0002g0164a0002c0002t0001g0171a0002c0002t0001g0185others(9): Show | 13 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.684+4295delT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156662847 | |||||
chr7:156663061
|
C | A | 9 | a0002c0002t0001g0008a0002c0002t0001g0011a0002c0002t0001g0029others(6): Show | 20 | HG00408.hp1 HG00423.hp1 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.684+4491C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156663061 | ||||||
chr7:156663157
|
A | C | 154 | a0001c0001t0002g0074a0001c0001t0002g0187a0001c0001t0002g0200others(151): Show | 236 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.684+4587A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156663157 | ||||||
chr7:156663585
|
C | T | 146 | a0001c0001t0002g0074a0001c0001t0002g0187a0001c0001t0002g0200others(143): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.684+5015C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156663585 | ||||||
chr7:156663673
|
T | C | 1 | a0002c0002t0001g0197 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.684+5103T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156663673 | ||||||
chr7:156663815
|
AAAATTAT others(3): Show |
A | 1 | a0002c0002t0001g0208 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.684+5247_684+5256d others(12): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156663815 | |||||
chr7:156663913
|
C | G | 1 | a0002c0002t0001g0167 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.684+5343C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156663913 | ||||||
chr7:156663996
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.684+5426T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156663996 | ||||||
chr7:156664021
|
G | A | 1 | a0002c0002t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.684+5451G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664021 | ||||||
chr7:156664043
|
A | G | 194 | a0001c0001t0002g0018a0001c0001t0002g0074a0001c0001t0002g0187others(191): Show | 306 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.684+5473A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664043 | ||||||
chr7:156664059
|
G | A | 12 | a0002c0002t0001g0025a0002c0002t0001g0028a0002c0002t0001g0046others(9): Show | 18 | HG02080.hp2 HG02135.hp1 NA18943.hp2 others(15): Show |
intron_variant | MODIFIER | c.684+5489G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664059 | ||||||
chr7:156664085
|
T | C | 1 | a0001c0001t0002g0115 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.684+5515T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664085 | ||||||
chr7:156664098
|
C | G | 1 | a0003c0003t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.684+5528C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664098 | ||||||
chr7:156664136
|
G | A | 3 | a0002c0002t0001g0047a0002c0002t0001g0176a0002c0002t0001g0186 | 4 | HG00597.hp1 NA18960.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.684+5566G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664136 | ||||||
chr7:156664164
|
A | G | 197 | a0001c0001t0002g0018a0001c0001t0002g0074a0001c0001t0002g0187others(194): Show | 310 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.684+5594A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664164 | ||||||
chr7:156664183
|
C | T | 1 | a0003c0003t0004g0088 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.684+5613C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664183 | ||||||
chr7:156664218
|
T | C | 2 | a0002c0002t0001g0162a0003c0003t0002g0190 | 2 | HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.684+5648T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664218 | ||||||
chr7:156664275
|
A | C | 4 | a0002c0002t0001g0011a0002c0002t0001g0049a0002c0002t0001g0193others(1): Show | 8 | NA18942.hp2 NA18954.hp1 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+5705A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664275 | ||||||
chr7:156664318
|
G | A | 2 | a0001c0001t0002g0038a0001c0001t0002g0118 | 3 | HG01261.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.684+5748G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664318 | ||||||
chr7:156664321
|
C | G | 102 | a0001c0001t0002g0187a0001c0001t0002g0200a0001c0004t0002g0164others(99): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.684+5751C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664321 | ||||||
chr7:156664322
|
G | T | 1 | a0002c0002t0001g0206 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.684+5752G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664322 | ||||||
chr7:156664329
|
C | T | 2 | a0001c0001t0002g0043a0010c0011t0002g0043 | 2 | HG03017.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.684+5759C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664329 | ||||||
chr7:156664330
|
G | A | 44 | a0001c0001t0002g0018a0001c0001t0003g0003a0001c0001t0003g0032others(41): Show | 74 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.684+5760G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664330 | ||||||
chr7:156664333
|
C | T | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+5763C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664333 | ||||||
chr7:156664375
|
A | C | 1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.684+5805A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664375 | ||||||
chr7:156664381
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.684+5811C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664381 | ||||||
chr7:156664385
|
C | T | 1 | a0002c0002t0001g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.684+5815C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664385 | ||||||
chr7:156664484
|
A | T | 2 | a0004c0005t0002g0060a0004c0005t0002g0270 | 3 | HG01884.hp1 HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.684+5914A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664484 | ||||||
chr7:156664583
|
T | C | 12 | a0001c0001t0002g0200a0002c0002t0001g0009a0002c0002t0001g0194others(9): Show | 17 | HG00639.hp2 HG01167.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.684+6013T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664583 | ||||||
chr7:156664739
|
T | C | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+6169T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664739 | ||||||
chr7:156664988
|
G | A | 1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.684+6418G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664988 | ||||||
chr7:156665086
|
CT | C | 4 | a0001c0001t0003g0058a0001c0001t0003g0252a0001c0001t0003g0254others(1): Show | 5 | NA18939.hp2 NA18948.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.684+6519delT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156665086 | |||||
chr7:156665314
|
CT | C | 29 | a0001c0001t0002g0074a0002c0002t0001g0077a0003c0003t0004g0010others(26): Show | 36 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.684+6745delT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156665314 | ||||||
chr7:156665624
|
A | G | 1 | a0003c0003t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.684+7054A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156665624 | ||||||
chr7:156665641
|
A | G | 1 | a0001c0001t0002g0109 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.684+7071A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156665641 | ||||||
chr7:156665670
|
CCT | C | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+7101_684+7102d others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156665670 | ||||||
chr7:156665768
|
T | C | 50 | a0001c0001t0002g0074a0001c0004t0006g0014a0001c0004t0006g0093others(47): Show | 64 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.684+7198T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156665768 | ||||||
chr7:156665852
|
G | T | 38 | a0001c0001t0002g0018a0001c0001t0003g0003a0001c0001t0003g0032others(35): Show | 66 | HG00673.hp1 HG01243.hp1 HG01358.hp2 others(63): Show |
intron_variant | MODIFIER | c.684+7282G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156665852 | ||||||
chr7:156665877
|
G | C | 3 | a0001c0004t0002g0223a0002c0002t0001g0016a0008c0009t0001g0016 | 5 | HG00423.hp2 HG02056.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.684+7307G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156665877 | ||||||
chr7:156666032
|
A | G | 1 | a0003c0003t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.684+7462A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666032 | ||||||
chr7:156666046
|
T | C | 1 | a0001c0001t0003g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.684+7476T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666046 | ||||||
chr7:156666061
|
G | A | 1 | a0001c0004t0002g0164 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.684+7491G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666061 | ||||||
chr7:156666144
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.684+7574G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666144 | ||||||
chr7:156666383
|
C | G | 5 | a0002c0002t0001g0051a0002c0002t0001g0162a0002c0002t0001g0215others(2): Show | 6 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.684+7813C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666383 | ||||||
chr7:156666510
|
T | C | 5 | a0002c0002t0001g0051a0002c0002t0001g0162a0002c0002t0001g0215others(2): Show | 6 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.684+7940T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666510 | ||||||
chr7:156666656
|
G | A | 1 | a0002c0002t0001g0231 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.684+8086G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666656 | ||||||
chr7:156666680
|
G | A | 20 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0041others(17): Show | 33 | HG00280.hp2 HG00642.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.684+8110G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666680 | ||||||
chr7:156666726
|
T | G | 9 | a0001c0004t0002g0223a0002c0002t0001g0016a0002c0002t0001g0031others(6): Show | 13 | HG00423.hp2 HG01069.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.684+8156T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666726 | ||||||
chr7:156666866
|
T | G | 4 | a0002c0002t0001g0144a0003c0003t0002g0053a0003c0003t0002g0232others(1): Show | 5 | HG02717.hp2 HG02895.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+8296T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666866 | ||||||
chr7:156666988
|
G | A | 1 | a0002c0002t0001g0201 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.684+8418G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666988 | ||||||
chr7:156667002
|
C | T | 3 | a0004c0005t0002g0060a0004c0005t0002g0269a0004c0005t0002g0270 | 4 | HG01884.hp1 HG02723.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+8432C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667002 | ||||||
chr7:156667037
|
C | G | 4 | a0001c0001t0002g0019a0001c0001t0002g0106a0001c0001t0002g0107others(1): Show | 6 | HG00140.hp1 HG00741.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.684+8467C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667037 | ||||||
chr7:156667341
|
T | A | 1 | a0003c0003t0004g0070 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.685-8355T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667341 | ||||||
chr7:156667348
|
A | T | 1 | a0003c0003t0004g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.685-8348A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667348 | ||||||
chr7:156667491
|
T | C | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-8205T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667491 | ||||||
chr7:156667510
|
T | C | 3 | a0003c0003t0002g0053a0003c0003t0002g0232a0003c0003t0002g0233 | 4 | HG02717.hp2 HG02895.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-8186T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667510 | ||||||
chr7:156667561
|
A | G | 1 | a0001c0001t0002g0131 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.685-8135A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667561 | ||||||
chr7:156667665
|
ACACGGAA others(9): Show |
A | 1 | a0001c0001t0002g0119 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.685-8030_685-8015d others(18): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667665 | ||||||
chr7:156667737
|
A | G | 7 | a0001c0004t0006g0014a0001c0004t0006g0094a0001c0004t0006g0095others(4): Show | 10 | HG01884.hp2 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.685-7959A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667737 | ||||||
chr7:156667769
|
G | C | 1 | a0002c0002t0001g0202 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.685-7927G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667769 | ||||||
chr7:156667820
|
C | A | 53 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0019others(50): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.685-7876C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667820 | ||||||
chr7:156667866
|
A | C | 6 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(3): Show | 7 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-7830A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667866 | ||||||
chr7:156667920
|
G | A | 1 | a0002c0002t0001g0199 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.685-7776G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667920 | ||||||
chr7:156667925
|
A | G | 10 | a0001c0004t0006g0014a0001c0004t0006g0093a0001c0004t0006g0094others(7): Show | 15 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.685-7771A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667925 | ||||||
chr7:156668051
|
C | G | 8 | a0001c0004t0006g0014a0001c0004t0006g0093a0001c0004t0006g0094others(5): Show | 12 | HG02280.hp1 HG02559.hp1 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.685-7645C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668051 | ||||||
chr7:156668077
|
A | G | 1 | a0003c0003t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.685-7619A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668077 | ||||||
chr7:156668157
|
A | C | 3 | a0001c0001t0003g0032a0001c0001t0003g0235a0001c0004t0002g0223 | 5 | HG02015.hp2 HG02074.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-7539A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668157 | ||||||
chr7:156668174
|
G | A | 1 | a0001c0001t0003g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.685-7522G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668174 | ||||||
chr7:156668360
|
T | C | 1 | a0002c0002t0001g0275 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.685-7336T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668360 | ||||||
chr7:156668488
|
C | A | 103 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(100): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.685-7208C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668488 | ||||||
chr7:156668491
|
C | CAGTGACT others(11): Show |
1 | a0001c0001t0002g0119 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.685-7204_685-7187d others(20): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156668491 | |||||
chr7:156668513
|
T | C | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-7183T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668513 | ||||||
chr7:156668521
|
C | G | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-7175C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668521 | ||||||
chr7:156668535
|
C | T | 3 | a0003c0003t0002g0190a0003c0003t0007g0271a0003c0003t0007g0272 | 3 | HG02257.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.685-7161C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668535 | ||||||
chr7:156668568
|
C | T | 1 | a0002c0002t0001g0133 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.685-7128C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668568 | ||||||
chr7:156668596
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.685-7100G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668596 | ||||||
chr7:156668654
|
G | A | 6 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(3): Show | 7 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-7042G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668654 | ||||||
chr7:156668684
|
A | G | 7 | a0001c0004t0006g0014a0001c0004t0006g0093a0001c0004t0006g0094others(4): Show | 10 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.685-7012A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668684 | ||||||
chr7:156668687
|
G | A | 1 | a0003c0003t0004g0050 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.685-7009G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668687 | ||||||
chr7:156668773
|
T | C | 1 | a0003c0003t0004g0189 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.685-6923T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668773 | ||||||
chr7:156668774
|
G | A | 2 | a0003c0003t0004g0085a0003c0003t0004g0090 | 2 | NA19054.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.685-6922G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668774 | ||||||
chr7:156668928
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.685-6768T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668928 | ||||||
chr7:156669178
|
A | G | 1 | a0002c0002t0001g0091 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.685-6518A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669178 | ||||||
chr7:156669215
|
G | A | 2 | a0003c0003t0004g0081a0007c0008t0002g0034 | 3 | HG02683.hp1 HG02698.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.685-6481G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669215 | ||||||
chr7:156669248
|
G | T | 7 | a0001c0004t0006g0014a0001c0004t0006g0093a0001c0004t0006g0094others(4): Show | 10 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.685-6448G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669248 | ||||||
chr7:156669264
|
G | A | 37 | a0001c0001t0002g0187a0002c0002t0001g0077a0003c0003t0004g0010others(34): Show | 47 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.685-6432G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669264 | ||||||
chr7:156669266
|
A | G | 45 | a0001c0001t0002g0187a0001c0004t0006g0014a0001c0004t0006g0093others(42): Show | 58 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(55): Show |
intron_variant | MODIFIER | c.685-6430A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669266 | ||||||
chr7:156669273
|
G | A | 1 | a0002c0002t0001g0026 | 3 | NA18953.hp2 NA18973.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.685-6423G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669273 | ||||||
chr7:156669409
|
G | A | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-6287G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669409 | ||||||
chr7:156669412
|
G | A | 1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.685-6284G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669412 | ||||||
chr7:156669537
|
G | A | 1 | a0002c0002t0001g0174 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.685-6159G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669537 | ||||||
chr7:156669641
|
C | G | 2 | a0001c0004t0002g0164a0001c0004t0002g0217 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.685-6055C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669641 | ||||||
chr7:156669670
|
A | G | 14 | a0001c0004t0006g0014a0001c0004t0006g0093a0001c0004t0006g0094others(11): Show | 18 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.685-6026A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669670 | ||||||
chr7:156669742
|
G | A | 1 | a0004c0005t0002g0269 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.685-5954G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669742 | ||||||
chr7:156669884
|
C | T | 1 | a0002c0002t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.685-5812C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669884 | ||||||
chr7:156669886
|
G | A | 5 | a0003c0003t0004g0067a0003c0003t0004g0072a0003c0003t0004g0080others(2): Show | 5 | HG00438.hp2 NA18998.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-5810G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669886 | ||||||
chr7:156669888
|
A | G | 1 | a0002c0002t0001g0208 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.685-5808A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669888 | ||||||
chr7:156669934
|
C | T | 6 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(3): Show | 7 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-5762C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669934 | ||||||
chr7:156669968
|
A | T | 3 | a0002c0002t0005g0242a0002c0002t0005g0243a0002c0002t0005g0255 | 3 | NA18944.hp1 NA18968.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.685-5728A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669968 | ||||||
chr7:156670051
|
T | C | 1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.685-5645T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670051 | ||||||
chr7:156670096
|
C | T | 105 | a0001c0004t0002g0223a0002c0002t0001g0002a0002c0002t0001g0004others(102): Show | 179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.685-5600C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670096 | ||||||
chr7:156670163
|
C | T | 1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.685-5533C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670163 | ||||||
chr7:156670255
|
C | T | 3 | a0001c0004t0002g0223a0002c0002t0001g0016a0008c0009t0001g0016 | 5 | HG00423.hp2 HG02056.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-5441C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670255 | ||||||
chr7:156670327
|
G | C | 1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.685-5369G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670327 | ||||||
chr7:156670328
|
G | A | 1 | a0001c0001t0002g0113 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.685-5368G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670328 | ||||||
chr7:156670599
|
C | T | 1 | a0002c0002t0001g0169 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.685-5097C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670599 | ||||||
chr7:156670677
|
G | A | 2 | a0001c0004t0002g0164a0001c0004t0002g0217 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.685-5019G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670677 | ||||||
chr7:156670932
|
C | T | 3 | a0002c0002t0001g0013a0002c0002t0001g0214a0002c0002t0001g0231 | 7 | HG01952.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.685-4764C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670932 | ||||||
chr7:156671064
|
C | A | 1 | a0001c0001t0002g0117 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.685-4632C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671064 | ||||||
chr7:156671134
|
A | G | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-4562A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671134 | ||||||
chr7:156671286
|
T | C | 183 | a0001c0001t0002g0005a0001c0001t0002g0018a0001c0001t0002g0023others(180): Show | 300 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.685-4410T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671286 | ||||||
chr7:156671395
|
G | A | 182 | a0001c0001t0002g0005a0001c0001t0002g0018a0001c0001t0002g0023others(179): Show | 299 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.685-4301G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671395 | ||||||
chr7:156671417
|
G | A | 226 | a0001c0001t0002g0005a0001c0001t0002g0018a0001c0001t0002g0023others(223): Show | 354 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.685-4279G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671417 | ||||||
chr7:156671452
|
A | G | 1 | a0001c0004t0002g0164 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.685-4244A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671452 | ||||||
chr7:156671520
|
T | C | 61 | a0001c0001t0002g0005a0001c0001t0002g0018a0001c0001t0002g0023others(58): Show | 99 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.685-4176T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671520 | ||||||
chr7:156671534
|
A | T | 106 | a0001c0004t0002g0223a0002c0002t0001g0002a0002c0002t0001g0004others(103): Show | 180 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.685-4162A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671534 | ||||||
chr7:156671587
|
A | C | 14 | a0001c0004t0006g0014a0001c0004t0006g0093a0001c0004t0006g0094others(11): Show | 18 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.685-4109A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671587 | ||||||
chr7:156671645
|
A | G | 72 | a0001c0001t0002g0005a0001c0001t0002g0018a0001c0001t0002g0023others(69): Show | 113 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.685-4051A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671645 | ||||||
chr7:156671652
|
T | C | 1 | a0003c0003t0004g0100 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.685-4044T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671652 | ||||||
chr7:156671656
|
T | TGCGGTAC others(53): Show |
1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.685-4031_685-4030i others(62): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156671656 | |||||
chr7:156671666
|
G | A | 1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.685-4030G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671666 | ||||||
chr7:156671698
|
C | G | 1 | a0003c0003t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.685-3998C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671698 | ||||||
chr7:156671720
|
C | T | 2 | a0001c0004t0002g0164a0001c0004t0002g0217 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.685-3976C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671720 | ||||||
chr7:156671756
|
C | T | 1 | a0003c0003t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.685-3940C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671756 | ||||||
chr7:156671765
|
T | G | 9 | a0002c0002t0001g0047a0002c0002t0001g0176a0002c0002t0001g0184others(6): Show | 11 | HG00597.hp1 NA18940.hp1 NA18944.hp1 others(8): Show |
intron_variant | MODIFIER | c.685-3931T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671765 | ||||||
chr7:156671773
|
T | C | 1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.685-3923T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671773 | ||||||
chr7:156671817
|
G | A | 164 | a0001c0001t0002g0187a0001c0004t0006g0014a0001c0004t0006g0093others(161): Show | 254 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.685-3879G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671817 | ||||||
chr7:156671840
|
A | AT | 104 | a0001c0004t0002g0223a0002c0002t0001g0002a0002c0002t0001g0004others(101): Show | 176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.685-3848dupT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156671840 | |||||
chr7:156671848
|
T | A | 3 | a0003c0003t0002g0053a0003c0003t0002g0232a0003c0003t0002g0233 | 4 | HG02717.hp2 HG02895.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-3848T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671848 | ||||||
chr7:156671849
|
A | T | 5 | a0001c0004t0006g0095a0002c0002t0005g0241a0003c0003t0002g0190others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-3847A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671849 | ||||||
chr7:156671884
|
G | A | 185 | a0001c0001t0002g0005a0001c0001t0002g0018a0001c0001t0002g0023others(182): Show | 302 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.685-3812G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671884 | ||||||
chr7:156672045
|
G | C | 1 | a0001c0001t0002g0124 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.685-3651G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156672045 | ||||||
chr7:156672045
|
GA | G | 21 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0041others(18): Show | 34 | HG00280.hp2 HG00642.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.685-3649delA | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156672045 | |||||
chr7:156672488
|
C | G | 1 | a0001c0001t0003g0252 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.685-3208C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156672488 | ||||||
chr7:156672515
|
T | G | 1 | a0001c0001t0002g0138 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.685-3181T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156672515 | ||||||
chr7:156672660
|
A | G | 3 | a0003c0003t0004g0078a0003c0003t0004g0092a0005c0006t0004g0022 | 5 | HG02258.hp1 HG02559.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-3036A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156672660 | ||||||
chr7:156672666
|
G | A | 3 | a0003c0003t0002g0190a0003c0003t0007g0271a0003c0003t0007g0272 | 3 | HG02257.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.685-3030G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156672666 | ||||||
chr7:156672736
|
T | C | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-2960T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156672736 | ||||||
chr7:156672821
|
G | A | 1 | a0002c0002t0001g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.685-2875G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156672821 | ||||||
chr7:156672987
|
C | T | 1 | a0011c0010t0001g0222 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.685-2709C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156672987 | ||||||
chr7:156673002
|
A | G | 226 | a0001c0001t0002g0005a0001c0001t0002g0018a0001c0001t0002g0023others(223): Show | 354 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.685-2694A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673002 | ||||||
chr7:156673528
|
G | T | 1 | a0003c0003t0004g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.685-2168G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673528 | ||||||
chr7:156673543
|
T | C | 1 | a0007c0008t0002g0034 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.685-2153T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673543 | ||||||
chr7:156673548
|
C | T | 1 | a0001c0001t0002g0140 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.685-2148C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673548 | ||||||
chr7:156673631
|
C | G | 1 | a0001c0001t0002g0115 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.685-2065C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673631 | ||||||
chr7:156673684
|
C | T | 31 | a0001c0001t0002g0187a0002c0002t0001g0077a0003c0003t0004g0010others(28): Show | 39 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.685-2012C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673684 | ||||||
chr7:156673906
|
T | TAA | 6 | a0001c0004t0006g0014a0001c0004t0006g0093a0001c0004t0006g0094others(3): Show | 9 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-1775_685-1774d others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156673906 | |||||
chr7:156673906
|
T | TAAAAA | 6 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(3): Show | 7 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-1778_685-1774d others(7): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156673906 | |||||
chr7:156673906
|
TA | T | 61 | a0001c0001t0002g0005a0001c0001t0002g0018a0001c0001t0002g0023others(58): Show | 99 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.685-1774delA | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156673906 | |||||
chr7:156673907
|
A | T | 3 | a0003c0003t0002g0053a0003c0003t0002g0232a0003c0003t0002g0233 | 4 | HG02717.hp2 HG02895.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-1789A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673907 | ||||||
chr7:156673915
|
A | AAG | 5 | a0002c0002t0001g0046a0002c0002t0001g0052a0002c0002t0001g0172others(2): Show | 7 | NA18522.hp2 NA18943.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.685-1780_685-1779i others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156673915 | |||||
chr7:156673918
|
A | G | 60 | a0001c0001t0002g0005a0001c0001t0002g0018a0001c0001t0002g0023others(57): Show | 98 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.685-1778A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673918 | ||||||
chr7:156673919
|
A | AAG | 100 | a0001c0004t0002g0223a0002c0002t0001g0002a0002c0002t0001g0004others(97): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.685-1776_685-1775i others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156673919 | |||||
chr7:156673919
|
A | G | 5 | a0002c0002t0001g0046a0002c0002t0001g0052a0002c0002t0001g0172others(2): Show | 7 | NA18522.hp2 NA18943.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.685-1777A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673919 | ||||||
chr7:156673922
|
AG | A | 37 | a0001c0001t0002g0187a0002c0002t0001g0077a0003c0003t0004g0010others(34): Show | 47 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.685-1773delG | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673922 | ||||||
chr7:156673925
|
A | G | 37 | a0001c0001t0002g0187a0002c0002t0001g0077a0003c0003t0004g0010others(34): Show | 47 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.685-1771A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673925 | ||||||
chr7:156673985
|
A | C | 1 | a0002c0002t0001g0162 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.685-1711A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673985 | ||||||
chr7:156674072
|
C | T | 1 | a0001c0001t0003g0239 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.685-1624C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674072 | ||||||
chr7:156674105
|
G | A | 4 | a0001c0001t0002g0102a0001c0001t0002g0149a0001c0001t0002g0154others(1): Show | 4 | HG00280.hp2 HG02451.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-1591G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674105 | ||||||
chr7:156674166
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.685-1530G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674166 | ||||||
chr7:156674226
|
G | A | 8 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(5): Show | 10 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.685-1470G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674226 | ||||||
chr7:156674518
|
G | A | 3 | a0003c0003t0002g0190a0003c0003t0007g0271a0003c0003t0007g0272 | 3 | HG02257.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.685-1178G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674518 | ||||||
chr7:156674531
|
G | A | 24 | a0001c0001t0002g0074a0001c0001t0002g0131a0001c0001t0003g0003others(21): Show | 43 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.685-1165G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674531 | ||||||
chr7:156674547
|
T | C | 186 | a0001c0001t0002g0005a0001c0001t0002g0018a0001c0001t0002g0023others(183): Show | 303 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.685-1149T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674547 | ||||||
chr7:156674548
|
G | A | 1 | a0002c0002t0001g0228 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.685-1148G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674548 | ||||||
chr7:156674601
|
G | A | 1 | a0002c0002t0001g0049 | 2 | NA18942.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.685-1095G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674601 | ||||||
chr7:156674624
|
T | C | 7 | a0004c0005t0002g0060a0004c0005t0002g0266a0004c0005t0002g0267others(4): Show | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-1072T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674624 | ||||||
chr7:156674660
|
C | T | 2 | a0001c0001t0002g0040a0001c0001t0002g0127 | 3 | HG00438.hp1 HG02080.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.685-1036C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674660 | ||||||
chr7:156674729
|
C | T | 1 | a0001c0001t0002g0037 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.685-967C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674729 | ||||||
chr7:156674730
|
G | A | 1 | a0002c0002t0001g0175 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.685-966G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674730 | ||||||
chr7:156674811
|
T | C | 1 | a0001c0001t0002g0122 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.685-885T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674811 | ||||||
chr7:156675016
|
G | C | 1 | a0002c0002t0001g0176 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.685-680G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675016 | ||||||
chr7:156675032
|
G | A | 1 | a0002c0002t0001g0191 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.685-664G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675032 | ||||||
chr7:156675070
|
G | A | 58 | a0001c0001t0002g0187a0001c0004t0006g0014a0001c0004t0006g0093others(55): Show | 74 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(71): Show |
intron_variant | MODIFIER | c.685-626G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675070 | ||||||
chr7:156675115
|
AGACCCGA others(12): Show |
A | 1 | a0001c0001t0002g0141 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.685-571_685-553del others(19): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156675115 | |||||
chr7:156675134
|
C | A | 205 | a0001c0001t0002g0018a0001c0001t0002g0023a0001c0001t0002g0074others(202): Show | 320 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.685-562C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675134 | ||||||
chr7:156675227
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A | G | 20 | a0001c0004t0002g0164a0001c0004t0003g0248a0001c0004t0006g0014others(17): Show | 25 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.685-469A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675227 | ||||||
chr7:156675379
|
G | A | 1 | a0003c0003t0004g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.685-317G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675379 | ||||||
chr7:156675500
|
G | A | 1 | a0001c0004t0003g0248 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.685-196G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675500 | ||||||
chr7:156675683
|
G | A | 1 | a0002c0002t0005g0242 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.685-13G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675683 | ||||||
chr7:156675683
|
G | C | 162 | a0001c0004t0003g0248a0001c0004t0006g0014a0001c0004t0006g0093others(159): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.685-13G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675683 | ||||||
chr7:156675684
|
C | A | 102 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(99): Show | 176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.685-12C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675684 | ||||||
chr7:156675684
|
C | T | 7 | a0001c0004t0006g0014a0001c0004t0006g0093a0001c0004t0006g0094others(4): Show | 10 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.685-12C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675684 | ||||||
chr7:156675685
|
C | G | 3 | a0003c0003t0002g0190a0003c0003t0007g0271a0003c0003t0007g0272 | 3 | HG02257.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.685-11C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675685 | ||||||
chr7:156675685
|
C | T | 1 | a0002c0002t0005g0242 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.685-11C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675685 | ||||||
chr7:156675865
|
T | C | 44 | a0002c0002t0001g0077a0003c0003t0002g0053a0003c0003t0002g0190others(41): Show | 55 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(52): Show |
splice_donor_variant&intron_variant | HIGH | c.852+2T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | chr7 | 156675865 | ||||||
chr7:156675916
|
G | A | 1 | a0002c0002t0001g0177 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.852+53G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | chr7 | 156675916 | ||||||
chr7:156675962
|
G | A | 116 | a0001c0001t0003g0236a0002c0002t0001g0002a0002c0002t0001g0004others(113): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.852+99G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | chr7 | 156675962 | ||||||
chr7:156675962
|
G | GAGCCTAG others(76): Show |
1 | a0001c0004t0003g0248 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.852+130_852+131ins others(83): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 156675962 | |||||
chr7:156675971
|
A | AGTGTCAG others(61): Show |
1 | a0001c0001t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.852+109_852+176dup others(68): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 156675971 | |||||
chr7:156675994
|
G | A | 8 | a0001c0004t0003g0248a0001c0004t0006g0014a0001c0004t0006g0093others(5): Show | 11 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.852+131G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | chr7 | 156675994 | ||||||
chr7:156676062
|
T | G | 207 | a0001c0001t0002g0018a0001c0001t0002g0023a0001c0001t0002g0074others(204): Show | 322 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.852+199T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | chr7 | 156676062 | ||||||
chr7:156676065
|
C | T | 109 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(106): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.852+202C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | chr7 | 156676065 | ||||||
chr7:156676245
|
G | GTA | 8 | a0001c0004t0003g0248a0001c0004t0006g0014a0001c0004t0006g0093others(5): Show | 11 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.853-164_853-163dup others(2): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 156676245 | |||||
chr7:156676245
|
G | GTGTA | 110 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0008others(107): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.853-173_853-172ins others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 156676245 | |||||
chr7:156676402
|
C | T | 118 | a0001c0001t0002g0019a0001c0001t0002g0038a0001c0001t0002g0101others(115): Show | 195 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.853-17C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | chr7 | 156676402 |