geneid | 27246 |
---|---|
ensemblid | ENSG00000265491.5 |
hgncid | 18154 |
symbol | RNF115 |
name | ring finger protein 115 |
refseq_nuc | NM_014455.4 |
refseq_prot | NP_055270.1 |
ensembl_nuc | ENST00000582693.5 |
ensembl_prot | ENSP00000463650.1 |
mane_status | MANE Select |
chr | chr1 |
start | 145738868 |
end | 145824095 |
strand | - |
ver | v1.2 |
region | chr1:145738868-145824095 |
region5000 | chr1:145733868-145829095 |
regionname0 | RNF115_chr1_145738868_145824095 |
regionname5000 | RNF115_chr1_145733868_145829095 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 304 | 272 | 76 | 54 | 102 | 14 | 24 | 80 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 915 | 270 | 76 | 54 | 101 | 14 | 23 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
c0002 | 0/0 | 915 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
c0003 | 0/0 | 915 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 8216 | 56 | 13 | 15 | 23 | 2 | 3 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0002 | 0/0 | 8218 | 40 | 3 | 9 | 24 | 0 | 4 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0003 | 0/0 | 8219 | 33 | 2 | 14 | 10 | 3 | 4 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0004 | 0/0 | 8217 | 11 | 0 | 0 | 11 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0005 | 0/0 | 8215 | 11 | 0 | 3 | 2 | 3 | 3 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0006 | 0/0 | 8216 | 9 | 8 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0007 | 0/0 | 8221 | 6 | 6 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0008 | 0/1 | 8217 | 4 | 1 | 1 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0009 | 0/0 | 8216 | 4 | 0 | 0 | 4 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0010 | 0/0 | 8219 | 4 | 4 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0011 | 0/0 | 8219 | 4 | 4 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0012 | 0/0 | 8206 | 3 | 3 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0013 | 0/0 | 8217 | 3 | 0 | 1 | 2 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0014 | 0/0 | 8216 | 3 | 3 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0015 | 0/0 | 8219 | 3 | 0 | 0 | 0 | 3 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0016 | 0/0 | 8218 | 3 | 1 | 1 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0017 | 0/0 | 8219 | 3 | 0 | 1 | 1 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0018 | 0/0 | 8222 | 2 | 2 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0019 | 0/0 | 8218 | 2 | 0 | 2 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0020 | 0/0 | 8217 | 2 | 0 | 0 | 1 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0021 | 0/0 | 8218 | 2 | 2 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0022 | 0/0 | 8215 | 2 | 1 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0023 | 0/0 | 8216 | 2 | 0 | 0 | 2 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0024 | 0/0 | 8217 | 2 | 1 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0025 | 0/0 | 8216 | 2 | 2 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0026 | 0/0 | 8216 | 2 | 0 | 0 | 2 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0027 | 0/0 | 8216 | 2 | 2 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0028 | 0/0 | 8218 | 2 | 0 | 0 | 0 | 1 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0029 | 0/0 | 8212 | 2 | 0 | 0 | 2 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0030 | 0/0 | 8219 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0031 | 0/0 | 8221 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0032 | 0/0 | 8221 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0033 | 0/0 | 8219 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0034 | 0/0 | 8221 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0035 | 0/0 | 8217 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0036 | 0/0 | 8218 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0037 | 0/0 | 8213 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0038 | 0/0 | 8220 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0039 | 0/0 | 8221 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0040 | 0/0 | 8220 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0041 | 0/0 | 8220 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0042 | 0/0 | 8222 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0043 | 0/0 | 8218 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0044 | 1/0 | 8221 | 1 | 0 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0045 | 0/0 | 8218 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0046 | 0/0 | 8217 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0047 | 0/0 | 8219 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0048 | 0/0 | 8218 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0049 | 0/0 | 8219 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0050 | 0/0 | 8221 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0051 | 0/0 | 8220 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0052 | 0/0 | 8218 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0053 | 0/0 | 8215 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0054 | 0/0 | 8216 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0055 | 0/0 | 8216 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0056 | 0/0 | 8216 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0057 | 0/0 | 8218 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0058 | 0/0 | 8216 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0059 | 0/0 | 8217 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0060 | 0/0 | 8216 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0061 | 0/0 | 8216 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0062 | 0/0 | 8217 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0063 | 0/0 | 8216 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0064 | 0/0 | 8215 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0065 | 0/0 | 8216 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0066 | 0/0 | 8216 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0067 | 0/0 | 8218 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0068 | 0/0 | 8220 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0069 | 0/0 | 8219 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0070 | 0/0 | 8220 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0071 | 0/0 | 8219 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0072 | 0/0 | 8219 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0073 | 0/0 | 8217 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0074 | 0/0 | 8217 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0075 | 0/0 | 8217 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0076 | 0/0 | 8220 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
t0077 | 0/0 | 8218 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0032 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 915 | 270 | 76 | 54 | 101 | 14 | 23 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0002 | 0/0 | 915 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0003 | 0/0 | 915 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 9130 | 56 | 13 | 15 | 23 | 2 | 3 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0002 | 0/0 | 9132 | 39 | 3 | 9 | 24 | 0 | 3 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0003 | 0/0 | 9133 | 33 | 2 | 14 | 10 | 3 | 4 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0004 | 0/0 | 9131 | 11 | 0 | 0 | 11 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0005 | 0/0 | 9129 | 11 | 0 | 3 | 2 | 3 | 3 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0006 | 0/0 | 9130 | 9 | 8 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0007 | 0/0 | 9135 | 6 | 6 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0008 | 0/1 | 9131 | 4 | 1 | 1 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0009 | 0/0 | 9130 | 4 | 0 | 0 | 4 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0010 | 0/0 | 9133 | 4 | 4 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0011 | 0/0 | 9133 | 4 | 4 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0012 | 0/0 | 9120 | 3 | 3 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0013 | 0/0 | 9131 | 3 | 0 | 1 | 2 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0014 | 0/0 | 9130 | 3 | 3 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0015 | 0/0 | 9133 | 3 | 0 | 0 | 0 | 3 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0016 | 0/0 | 9132 | 3 | 1 | 1 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0017 | 0/0 | 9133 | 3 | 0 | 1 | 1 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0018 | 0/0 | 9136 | 2 | 2 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0019 | 0/0 | 9132 | 2 | 0 | 2 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0020 | 0/0 | 9131 | 2 | 0 | 0 | 1 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0021 | 0/0 | 9132 | 2 | 2 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0022 | 0/0 | 9129 | 2 | 1 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0023 | 0/0 | 9130 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0024 | 0/0 | 9131 | 2 | 1 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0025 | 0/0 | 9130 | 2 | 2 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0026 | 0/0 | 9130 | 2 | 0 | 0 | 2 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0027 | 0/0 | 9130 | 2 | 2 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0028 | 0/0 | 9132 | 2 | 0 | 0 | 0 | 1 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0029 | 0/0 | 9126 | 2 | 0 | 0 | 2 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0030 | 0/0 | 9133 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0031 | 0/0 | 9135 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0032 | 0/0 | 9135 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0033 | 0/0 | 9133 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0034 | 0/0 | 9135 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0035 | 0/0 | 9131 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0036 | 0/0 | 9132 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0037 | 0/0 | 9127 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0038 | 0/0 | 9134 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0039 | 0/0 | 9135 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0040 | 0/0 | 9134 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0041 | 0/0 | 9134 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0042 | 0/0 | 9136 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0043 | 0/0 | 9132 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0044 | 1/0 | 9135 | 1 | 0 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0045 | 0/0 | 9132 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0046 | 0/0 | 9131 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0047 | 0/0 | 9133 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0048 | 0/0 | 9132 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0049 | 0/0 | 9133 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0050 | 0/0 | 9135 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0051 | 0/0 | 9134 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0052 | 0/0 | 9132 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0053 | 0/0 | 9129 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0054 | 0/0 | 9130 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0055 | 0/0 | 9130 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0056 | 0/0 | 9130 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0057 | 0/0 | 9132 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0058 | 0/0 | 9130 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0059 | 0/0 | 9131 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0060 | 0/0 | 9130 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0061 | 0/0 | 9130 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0062 | 0/0 | 9131 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0063 | 0/0 | 9130 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0064 | 0/0 | 9129 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0065 | 0/0 | 9130 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0066 | 0/0 | 9130 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0067 | 0/0 | 9132 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0068 | 0/0 | 9134 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0069 | 0/0 | 9133 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0070 | 0/0 | 9134 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0071 | 0/0 | 9133 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0072 | 0/0 | 9133 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0073 | 0/0 | 9131 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0074 | 0/0 | 9131 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0075 | 0/0 | 9131 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0076 | 0/0 | 9134 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0001t0077 | 0/0 | 9132 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0002t0023 | 0/0 | 9130 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
a0001c0003t0002 | 0/0 | 9132 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | copy fasta | chr1 | 145733868 | 145829095 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0005g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0007g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0008g0032 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0008g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0008g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0009g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0009g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0009g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0009g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0010g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0010g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0010g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0010g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0011g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0011g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0012g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0012g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0013g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0013g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0013g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0014g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0014g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0014g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0015g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0015g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0015g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0016g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0016g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0016g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0017g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0017g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0017g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0018g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0018g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0019g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0019g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0020g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0020g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0021g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0021g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0022g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0022g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0023g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0024g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0024g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0025g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0025g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0026g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0026g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0027g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0027g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0028g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0028g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0029g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0029g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0030g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0031g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0032g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0033g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0034g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0035g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0036g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0037g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0038g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0039g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0040g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0041g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0042g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0043g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0044g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0045g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0046g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0047g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0048g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0049g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0050g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0051g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0052g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0053g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0054g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0055g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0056g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0057g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0058g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0059g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0060g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0061g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0062g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0063g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0064g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0065g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0066g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0067g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0068g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0069g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0070g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0071g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0072g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0073g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0074g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0075g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0076g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0001t0077g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0002t0023g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
a0001c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00099 | hp2 | a0001 | c0001 | t0028 | g0247 | EUR | GBR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0253 | EUR | FIN | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00323 | hp2 | a0001 | c0001 | t0015 | g0218 | EUR | FIN | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00558 | hp2 | a0001 | c0001 | t0035 | g0057 | EAS | CHS | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00639 | hp1 | a0001 | c0001 | t0017 | g0254 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0258 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | CHS | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | CHS | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00733 | hp1 | a0001 | c0001 | t0005 | g0083 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00733 | hp2 | a0001 | c0001 | t0016 | g0236 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00735 | hp1 | a0001 | c0001 | t0071 | g0256 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00735 | hp2 | a0001 | c0001 | t0057 | g0036 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00741 | hp1 | a0001 | c0001 | t0056 | g0002 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01099 | hp2 | a0001 | c0001 | t0019 | g0171 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01106 | hp1 | a0001 | c0001 | t0008 | g0089 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01109 | hp2 | a0001 | c0001 | t0019 | g0173 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01243 | hp1 | a0001 | c0001 | t0053 | g0081 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0216 | AMR | PUR | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01256 | hp1 | a0001 | c0001 | t0076 | g0246 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0226 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01433 | hp2 | a0001 | c0001 | t0031 | g0190 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0244 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01515 | hp1 | a0001 | c0001 | t0017 | g0252 | EUR | IBS | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01515 | hp2 | a0001 | c0001 | t0015 | g0240 | EUR | IBS | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0001 | EUR | IBS | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0227 | EUR | IBS | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0001 | EUR | IBS | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01517 | hp2 | a0001 | c0001 | t0015 | g0239 | EUR | IBS | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01884 | hp1 | a0001 | c0001 | t0032 | g0194 | AFR | ACB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | ACB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | PEL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | PEL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0105 | AMR | PEL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | PEL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02015 | hp1 | a0001 | c0001 | t0077 | g0271 | EAS | KHV | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | KHV | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02055 | hp1 | a0001 | c0001 | t0050 | g0188 | AFR | ACB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | KHV | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02071 | hp2 | a0001 | c0001 | t0065 | g0102 | EAS | KHV | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02074 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | KHV | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02083 | hp1 | a0001 | c0001 | t0060 | g0116 | EAS | KHV | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02083 | hp2 | a0001 | c0001 | t0017 | g0235 | EAS | KHV | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | KHV | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02129 | hp2 | a0001 | c0001 | t0013 | g0068 | EAS | KHV | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02145 | hp1 | a0001 | c0001 | t0059 | g0005 | AFR | ACB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02145 | hp2 | a0001 | c0001 | t0063 | g0264 | AFR | ACB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | CDX | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | CDX | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02257 | hp2 | a0001 | c0001 | t0058 | g0262 | AFR | ACB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0091 | AFR | ACB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02258 | hp2 | a0001 | c0001 | t0073 | g0179 | AFR | ACB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | ACB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02280 | hp2 | a0001 | c0001 | t0075 | g0030 | AFR | ACB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02293 | hp1 | a0001 | c0001 | t0013 | g0097 | AMR | PEL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | PEL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | PEL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02300 | hp2 | a0001 | c0001 | t0036 | g0058 | AMR | PEL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | KHV | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02572 | hp1 | a0001 | c0001 | t0033 | g0198 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02602 | hp1 | a0001 | c0001 | t0005 | g0113 | SAS | PJL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02602 | hp2 | a0001 | c0003 | t0002 | g0270 | SAS | PJL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02615 | hp1 | a0001 | c0001 | t0014 | g0266 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02615 | hp2 | a0001 | c0001 | t0011 | g0213 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02630 | hp1 | a0001 | c0001 | t0010 | g0203 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02630 | hp2 | a0001 | c0001 | t0051 | g0200 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02647 | hp1 | a0001 | c0001 | t0007 | g0189 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0034 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0115 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02723 | hp1 | a0001 | c0001 | t0061 | g0047 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02723 | hp2 | a0001 | c0001 | t0010 | g0204 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02735 | hp2 | a0001 | c0001 | t0064 | g0079 | SAS | PJL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02818 | hp1 | a0001 | c0001 | t0021 | g0178 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02818 | hp2 | a0001 | c0001 | t0039 | g0195 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02886 | hp1 | a0001 | c0001 | t0011 | g0212 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02895 | hp2 | a0001 | c0001 | t0014 | g0265 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0191 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02896 | hp2 | a0001 | c0001 | t0024 | g0012 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0192 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02922 | hp1 | a0001 | c0001 | t0012 | g0130 | AFR | ESN | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02965 | hp1 | a0001 | c0001 | t0016 | g0257 | AFR | ESN | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | ESN | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0064 | AFR | ESN | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02976 | hp2 | a0001 | c0001 | t0014 | g0267 | AFR | ESN | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03041 | hp1 | a0001 | c0001 | t0041 | g0199 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03041 | hp2 | a0001 | c0001 | t0025 | g0029 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03098 | hp2 | a0001 | c0001 | t0012 | g0129 | AFR | MSL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03130 | hp1 | a0001 | c0001 | t0018 | g0185 | AFR | ESN | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03139 | hp1 | a0001 | c0001 | t0010 | g0202 | AFR | ESN | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0055 | AFR | ESN | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03195 | hp2 | a0001 | c0001 | t0038 | g0196 | AFR | ESN | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0193 | AFR | MSL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03225 | hp2 | a0001 | c0001 | t0027 | g0268 | AFR | MSL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03453 | hp1 | a0001 | c0001 | t0011 | g0208 | AFR | MSL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | MSL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03486 | hp1 | a0001 | c0001 | t0040 | g0197 | AFR | MSL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | MSL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0250 | SAS | PJL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0076 | SAS | PJL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0230 | SAS | PJL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03540 | hp1 | a0001 | c0001 | t0010 | g0205 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03540 | hp2 | a0001 | c0001 | t0012 | g0131 | AFR | GWD | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03669 | hp1 | a0001 | c0001 | t0008 | g0039 | SAS | PJL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03669 | hp2 | a0001 | c0001 | t0049 | g0237 | SAS | PJL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03704 | hp2 | a0001 | c0001 | t0020 | g0167 | SAS | PJL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03710 | hp2 | a0001 | c0001 | t0028 | g0238 | SAS | PJL | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03834 | hp1 | a0001 | c0001 | t0054 | g0114 | SAS | BEB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03834 | hp2 | a0001 | c0001 | t0048 | g0164 | SAS | BEB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03927 | hp1 | a0001 | c0001 | t0016 | g0260 | SAS | BEB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | BEB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG04184 | hp1 | a0001 | c0001 | t0052 | g0022 | SAS | BEB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG04184 | hp2 | a0001 | c0001 | t0042 | g0146 | SAS | BEB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | STU | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0229 | SAS | STU | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0259 | SAS | STU | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG04228 | hp2 | a0001 | c0001 | t0005 | g0075 | SAS | STU | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0201 | AFR | YRI | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18747 | hp1 | a0001 | c0001 | t0022 | g0077 | EAS | CHB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | CHB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18939 | hp1 | a0001 | c0001 | t0009 | g0074 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18959 | hp1 | a0001 | c0001 | t0037 | g0007 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18959 | hp2 | a0001 | c0001 | t0030 | g0135 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18961 | hp2 | a0001 | c0001 | t0072 | g0228 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18962 | hp1 | a0001 | c0001 | t0029 | g0088 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18964 | hp1 | a0001 | c0001 | t0009 | g0040 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18964 | hp2 | a0001 | c0001 | t0055 | g0093 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18965 | hp1 | a0001 | c0001 | t0074 | g0050 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18966 | hp2 | a0001 | c0001 | t0006 | g0071 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18969 | hp1 | a0001 | c0001 | t0020 | g0182 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18974 | hp1 | a0001 | c0001 | t0043 | g0158 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18974 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18977 | hp2 | a0001 | c0001 | t0069 | g0206 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18980 | hp1 | a0001 | c0001 | t0026 | g0108 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18983 | hp2 | a0001 | c0001 | t0009 | g0017 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18986 | hp1 | a0001 | c0001 | t0009 | g0016 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18988 | hp1 | a0001 | c0001 | t0045 | g0161 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18988 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19001 | hp2 | a0001 | c0001 | t0026 | g0107 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19005 | hp1 | a0001 | c0001 | t0013 | g0103 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19030 | hp1 | a0001 | c0001 | t0007 | g0184 | AFR | LWK | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19030 | hp2 | a0001 | c0001 | t0066 | g0096 | AFR | LWK | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19043 | hp2 | a0001 | c0001 | t0062 | g0052 | AFR | LWK | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19060 | hp2 | a0001 | c0001 | t0029 | g0084 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0109 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19068 | hp2 | a0001 | c0001 | t0068 | g0209 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19070 | hp2 | a0001 | c0001 | t0023 | g0122 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19075 | hp2 | a0001 | c0001 | t0024 | g0073 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19078 | hp1 | a0001 | c0001 | t0047 | g0151 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19078 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19079 | hp1 | a0001 | c0002 | t0023 | g0124 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19091 | hp2 | a0001 | c0001 | t0046 | g0155 | EAS | JPT | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19240 | hp1 | a0001 | c0001 | t0018 | g0187 | AFR | YRI | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA19240 | hp2 | a0001 | c0001 | t0021 | g0128 | AFR | YRI | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ASW | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA20129 | hp2 | a0001 | c0001 | t0022 | g0027 | AFR | ASW | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0251 | EUR | TSI | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0078 | EUR | TSI | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA20805 | hp2 | a0001 | c0001 | t0070 | g0249 | EUR | TSI | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0217 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | CLM | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02109 | hp1 | a0001 | c0001 | t0067 | g0263 | AFR | ACB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02109 | hp2 | a0001 | c0001 | t0011 | g0207 | AFR | ACB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02486 | hp1 | a0001 | c0001 | t0027 | g0269 | AFR | ACB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0098 | AFR | ACB | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | USA | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
HG06807 | hp2 | a0001 | c0001 | t0025 | g0010 | AFR | USA | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | USA | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
NA20300 | hp2 | a0001 | c0001 | t0034 | g0186 | AFR | USA | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0008 | g0032 | REF | REF | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0044 | g0147 | REF | REF | RNF115_chr1_145733868_145829095 | RNF115 | chr1 | 145733868 | 145829095 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:145750432
|
T | C | 1 | a0001c0002 | 1 | NA19079.hp1 | synonymous_variant | LOW | c.642A>G | p.Thr214Thr | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 7/9 | 864/9135 | 642/915 | 214/304 | chr1 | 145750432 | ||
chr1:145823808
|
G | A | 1 | a0001c0003 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.66C>T | p.Cys22Cys | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/9 | 288/9135 | 66/915 | 22/304 | chr1 | 145823808 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:145739163
|
C | A | 7 | a0001c0001t0007a0001c0001t0018a0001c0001t0031others(4): Show | 13 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7703G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 7703 | chr1 | 145739163 | |||||
chr1:145739376
|
T | C | 4 | a0001c0001t0038a0001c0001t0039a0001c0001t0040others(1): Show | 4 | HG02818.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7490A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 7490 | chr1 | 145739376 | |||||
chr1:145739509
|
T | C | 1 | a0001c0001t0071 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7357A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 7357 | chr1 | 145739509 | |||||
chr1:145739579
|
A | AT | 5 | a0001c0001t0039a0001c0001t0047a0001c0001t0057others(2): Show | 5 | HG00735.hp2 HG02818.hp2 NA19068.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7286dupA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 7286 | chr1 | 145739579 | |||||
chr1:145739579
|
AT | A | 40 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(37): Show | 142 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*7286delA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 7286 | chr1 | 145739579 | |||||
chr1:145739768
|
C | T | 1 | a0001c0001t0052 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7098G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 7098 | chr1 | 145739768 | |||||
chr1:145740000
|
C | T | 2 | a0001c0001t0045a0001c0001t0046 | 2 | NA18988.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6866G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 6866 | chr1 | 145740000 | |||||
chr1:145740072
|
C | A | 1 | a0001c0001t0064 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6794G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 6794 | chr1 | 145740072 | |||||
chr1:145740125
|
C | T | 2 | a0001c0001t0056a0001c0001t0059 | 2 | HG00741.hp1 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6741G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 6741 | chr1 | 145740125 | |||||
chr1:145740240
|
C | A | 1 | a0001c0001t0060 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6626G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 6626 | chr1 | 145740240 | |||||
chr1:145740276
|
T | C | 5 | a0001c0001t0033a0001c0001t0038a0001c0001t0039others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6590A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 6590 | chr1 | 145740276 | |||||
chr1:145740567
|
C | T | 2 | a0001c0001t0023a0001c0002t0023 | 2 | NA19070.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6299G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 6299 | chr1 | 145740567 | |||||
chr1:145740625
|
G | C | 1 | a0001c0001t0031 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6241C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 6241 | chr1 | 145740625 | |||||
chr1:145740671
|
GAATA | G | 1 | a0001c0001t0012 | 3 | HG02922.hp1 HG03098.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6191_*6194delTATT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 6191 | chr1 | 145740671 | |||||
chr1:145741332
|
C | T | 1 | a0001c0001t0061 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5534G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 5534 | chr1 | 145741332 | |||||
chr1:145741453
|
T | A | 1 | a0001c0001t0067 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5413A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 5413 | chr1 | 145741453 | |||||
chr1:145741704
|
T | C | 14 | a0001c0001t0003a0001c0001t0010a0001c0001t0011others(11): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*5162A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 5162 | chr1 | 145741704 | |||||
chr1:145741859
|
C | T | 5 | a0001c0001t0033a0001c0001t0038a0001c0001t0039others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5007G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 5007 | chr1 | 145741859 | |||||
chr1:145742220
|
T | A | 1 | a0001c0001t0061 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4646A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 4646 | chr1 | 145742220 | |||||
chr1:145742338
|
A | G | 1 | a0001c0001t0015 | 3 | HG00323.hp2 HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4528T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 4528 | chr1 | 145742338 | |||||
chr1:145742379
|
T | C | 1 | a0001c0001t0072 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4487A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 4487 | chr1 | 145742379 | |||||
chr1:145742466
|
C | A | 2 | a0001c0001t0012a0001c0001t0021 | 5 | HG02818.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4400G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 4400 | chr1 | 145742466 | |||||
chr1:145742948
|
T | C | 64 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(61): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*3918A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 3918 | chr1 | 145742948 | |||||
chr1:145743010
|
T | C | 4 | a0001c0001t0025a0001c0001t0058a0001c0001t0062others(1): Show | 5 | HG02257.hp2 HG02280.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3856A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 3856 | chr1 | 145743010 | |||||
chr1:145743166
|
G | A | 1 | a0001c0001t0048 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3700C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 3700 | chr1 | 145743166 | |||||
chr1:145743168
|
A | G | 64 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(61): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*3698T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 3698 | chr1 | 145743168 | |||||
chr1:145743263
|
G | A | 1 | a0001c0001t0063 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3603C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 3603 | chr1 | 145743263 | |||||
chr1:145743399
|
A | G | 1 | a0001c0001t0038 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3467T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 3467 | chr1 | 145743399 | |||||
chr1:145743427
|
T | A | 2 | a0001c0001t0068a0001c0001t0069 | 2 | NA18977.hp2 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3439A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 3439 | chr1 | 145743427 | |||||
chr1:145743738
|
A | G | 48 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(45): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*3128T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 3128 | chr1 | 145743738 | |||||
chr1:145743785
|
AAT | A | 5 | a0001c0001t0005a0001c0001t0022a0001c0001t0026others(2): Show | 17 | HG00733.hp1 HG01243.hp1 HG01346.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3079_*3080delAT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 3079 | chr1 | 145743785 | |||||
chr1:145743786
|
AT | A | 30 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(27): Show | 117 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*3079delA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 3079 | chr1 | 145743786 | |||||
chr1:145743787
|
T | A | 22 | a0001c0001t0003a0001c0001t0010a0001c0001t0011others(19): Show | 68 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*3079A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 3079 | chr1 | 145743787 | |||||
chr1:145743791
|
T | A | 36 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(33): Show | 127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*3075A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 3075 | chr1 | 145743791 | |||||
chr1:145743795
|
T | A | 5 | a0001c0001t0005a0001c0001t0026a0001c0001t0053others(2): Show | 16 | HG00733.hp1 HG01243.hp1 HG01346.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3071A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 3071 | chr1 | 145743795 | |||||
chr1:145743804
|
AAATAAAT others(4): Show |
A | 1 | a0001c0001t0012 | 3 | HG02922.hp1 HG03098.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3051_*3061delATTT others(7): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 3051 | chr1 | 145743804 | |||||
chr1:145743812
|
AAAT | A | 69 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(66): Show | 254 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*3051_*3053delATT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 3051 | chr1 | 145743812 | |||||
chr1:145743881
|
C | A | 1 | a0001c0001t0034 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2985G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 2985 | chr1 | 145743881 | |||||
chr1:145743975
|
C | T | 64 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(61): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*2891G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 2891 | chr1 | 145743975 | |||||
chr1:145744088
|
G | C | 64 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(61): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*2778C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 2778 | chr1 | 145744088 | |||||
chr1:145744321
|
C | T | 1 | a0001c0001t0055 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2545G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 2545 | chr1 | 145744321 | |||||
chr1:145744335
|
A | G | 1 | a0001c0001t0043 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2531T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 2531 | chr1 | 145744335 | |||||
chr1:145744545
|
T | C | 1 | a0001c0001t0073 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2321A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 2321 | chr1 | 145744545 | |||||
chr1:145744615
|
G | A | 10 | a0001c0001t0003a0001c0001t0015a0001c0001t0016others(7): Show | 49 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2251C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 2251 | chr1 | 145744615 | |||||
chr1:145744617
|
C | T | 1 | a0001c0001t0054 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2249G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 2249 | chr1 | 145744617 | |||||
chr1:145744739
|
T | C | 1 | a0001c0001t0041 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2127A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 2127 | chr1 | 145744739 | |||||
chr1:145744803
|
T | A | 1 | a0001c0001t0077 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2063A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 2063 | chr1 | 145744803 | |||||
chr1:145744959
|
T | G | 1 | a0001c0001t0073 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1907A>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 1907 | chr1 | 145744959 | |||||
chr1:145745091
|
T | C | 1 | a0001c0001t0009 | 4 | NA18939.hp1 NA18964.hp1 NA18983.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1775A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 1775 | chr1 | 145745091 | |||||
chr1:145745123
|
CACTT | C | 2 | a0001c0001t0029a0001c0001t0037 | 3 | NA18959.hp1 NA18962.hp1 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1739_*1742delAAGT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 1739 | chr1 | 145745123 | |||||
chr1:145745194
|
T | C | 1 | a0001c0001t0066 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1672A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 1672 | chr1 | 145745194 | |||||
chr1:145745242
|
T | C | 1 | a0001c0001t0073 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1624A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 1624 | chr1 | 145745242 | |||||
chr1:145745378
|
C | T | 1 | a0001c0001t0053 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1488G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 1488 | chr1 | 145745378 | |||||
chr1:145745459
|
A | AT | 18 | a0001c0001t0003a0001c0001t0010a0001c0001t0011others(15): Show | 64 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1406dupA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 1406 | chr1 | 145745459 | |||||
chr1:145745614
|
C | G | 12 | a0001c0001t0007a0001c0001t0018a0001c0001t0031others(9): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1252G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 1252 | chr1 | 145745614 | |||||
chr1:145745698
|
G | A | 2 | a0001c0001t0014a0001c0001t0027 | 5 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1168C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 1168 | chr1 | 145745698 | |||||
chr1:145745706
|
C | T | 1 | a0001c0001t0035 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1160G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 1160 | chr1 | 145745706 | |||||
chr1:145745816
|
T | C | 15 | a0001c0001t0003a0001c0001t0010a0001c0001t0011others(12): Show | 60 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1050A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 1050 | chr1 | 145745816 | |||||
chr1:145746017
|
G | A | 1 | a0001c0001t0073 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*849C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 849 | chr1 | 145746017 | |||||
chr1:145746119
|
C | T | 12 | a0001c0001t0007a0001c0001t0018a0001c0001t0031others(9): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*747G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 747 | chr1 | 145746119 | |||||
chr1:145746184
|
C | T | 1 | a0001c0001t0049 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*682G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 682 | chr1 | 145746184 | |||||
chr1:145746194
|
T | C | 64 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(61): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*672A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 672 | chr1 | 145746194 | |||||
chr1:145746209
|
G | C | 1 | a0001c0001t0029 | 2 | NA18962.hp1 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*657C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 657 | chr1 | 145746209 | |||||
chr1:145746212
|
C | T | 1 | a0001c0001t0019 | 2 | HG01099.hp2 HG01109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*654G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 654 | chr1 | 145746212 | |||||
chr1:145746225
|
C | CA | 7 | a0001c0001t0038a0001c0001t0039a0001c0001t0040others(4): Show | 7 | HG01256.hp1 HG02280.hp2 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*640dupT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 640 | chr1 | 145746225 | |||||
chr1:145746404
|
G | GT | 15 | a0001c0001t0004a0001c0001t0007a0001c0001t0018others(12): Show | 31 | HG00558.hp2 HG00673.hp1 HG01433.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*461dupA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 9/9 | 461 | chr1 | 145746404 | |||||
chr1:145823958
|
C | A | 1 | a0001c0001t0077 | 1 | HG02015.hp1 | 5_prime_UTR_variant | MODIFIER | c.-85G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/9 | 85 | chr1 | 145823958 | |||||
chr1:145824013
|
T | G | 1 | a0001c0001t0077 | 1 | HG02015.hp1 | 5_prime_UTR_variant | MODIFIER | c.-140A>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/9 | 140 | chr1 | 145824013 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:145747316
|
A | G | 6 | a0001c0001t0002g0137a0001c0001t0002g0152a0001c0001t0002g0159others(3): Show | 6 | HG01106.hp2 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.784-319T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 8/8 | chr1 | 145747316 | ||||||
chr1:145747553
|
G | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(132): Show | 136 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.783+442C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 8/8 | chr1 | 145747553 | ||||||
chr1:145747557
|
C | T | 60 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.783+438G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 8/8 | chr1 | 145747557 | ||||||
chr1:145747579
|
G | A | 1 | a0001c0001t0007g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.783+416C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 8/8 | chr1 | 145747579 | ||||||
chr1:145747599
|
C | T | 5 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.783+396G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 8/8 | chr1 | 145747599 | ||||||
chr1:145747728
|
C | T | 1 | a0001c0001t0024g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.783+267G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 8/8 | chr1 | 145747728 | ||||||
chr1:145747729
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.783+266C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 8/8 | chr1 | 145747729 | ||||||
chr1:145747968
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.783+27T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 8/8 | chr1 | 145747968 | ||||||
chr1:145748649
|
G | T | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(135): Show | 139 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.668-539C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 7/8 | chr1 | 145748649 | ||||||
chr1:145748838
|
T | G | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0250 | 3 | HG03491.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.668-728A>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 7/8 | chr1 | 145748838 | ||||||
chr1:145748883
|
C | CA | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(150): Show | 154 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.668-774dupT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 7/8 | chr1 | 145748883 | ||||||
chr1:145748898
|
T | A | 3 | a0001c0001t0003g0214a0001c0001t0003g0215a0001c0001t0006g0091 | 3 | HG00673.hp2 HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.668-788A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 7/8 | chr1 | 145748898 | ||||||
chr1:145749009
|
C | G | 13 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(10): Show | 13 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.668-899G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 7/8 | chr1 | 145749009 | ||||||
chr1:145749216
|
TC | T | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.668-1107delG | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 7/8 | chr1 | 145749216 | ||||||
chr1:145749545
|
T | C | 1 | a0001c0001t0002g0136 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.667+862A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 7/8 | chr1 | 145749545 | ||||||
chr1:145749827
|
A | G | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.667+580T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 7/8 | chr1 | 145749827 | ||||||
chr1:145750353
|
G | A | 1 | a0001c0001t0063g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.667+54C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 7/8 | chr1 | 145750353 | ||||||
chr1:145750684
|
A | G | 1 | a0001c0001t0008g0039 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.574-184T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 6/8 | chr1 | 145750684 | ||||||
chr1:145751196
|
G | T | 2 | a0001c0001t0027g0268a0001c0001t0027g0269 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.573+242C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 6/8 | chr1 | 145751196 | ||||||
chr1:145751751
|
C | G | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.501-241G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145751751 | ||||||
chr1:145751762
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0261 | 2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.501-252C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145751762 | ||||||
chr1:145751918
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.501-408G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145751918 | ||||||
chr1:145751965
|
A | T | 2 | a0001c0001t0005g0001a0001c0001t0005g0006 | 3 | HG01346.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.501-455T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145751965 | ||||||
chr1:145752058
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.501-548A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752058 | ||||||
chr1:145752202
|
A | G | 3 | a0001c0001t0001g0045a0001c0001t0004g0031a0001c0001t0004g0099 | 3 | HG02165.hp1 NA18949.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.501-692T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752202 | ||||||
chr1:145752305
|
T | A | 1 | a0001c0001t0006g0048 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.500+673A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752305 | ||||||
chr1:145752382
|
C | T | 1 | a0001c0001t0006g0048 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.500+596G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752382 | ||||||
chr1:145752453
|
A | G | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.500+525T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752453 | ||||||
chr1:145752585
|
C | CTTTTTT | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(110): Show | 114 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.500+387_500+392dup others(6): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752585 | ||||||
chr1:145752585
|
C | CTTTTTTT | 16 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0026others(13): Show | 16 | HG00673.hp1 HG00733.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.500+386_500+392dup others(7): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752585 | ||||||
chr1:145752585
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0007g0192a0001c0001t0041g0199 | 2 | HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.500+382_500+392dup others(11): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752585 | ||||||
chr1:145752585
|
C | CTTTTTTT others(5): Show |
6 | a0001c0001t0007g0189a0001c0001t0007g0191a0001c0001t0018g0185others(3): Show | 6 | HG01433.hp2 HG02109.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.500+381_500+392dup others(12): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752585 | ||||||
chr1:145752585
|
C | CTTTTTTT others(6): Show |
5 | a0001c0001t0007g0184a0001c0001t0007g0193a0001c0001t0033g0198others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.500+380_500+392dup others(13): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752585 | ||||||
chr1:145752585
|
C | CTTTTTTT others(7): Show |
4 | a0001c0001t0018g0187a0001c0001t0038g0196a0001c0001t0039g0195others(1): Show | 4 | HG02630.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.500+379_500+392dup others(14): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752585 | ||||||
chr1:145752585
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0007g0201a0001c0001t0032g0194 | 2 | HG01884.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.500+378_500+392dup others(15): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752585 | ||||||
chr1:145752585
|
CT | C | 58 | a0001c0001t0002g0136a0001c0001t0002g0162a0001c0001t0003g0210others(55): Show | 58 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.500+392delA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752585 | ||||||
chr1:145752628
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.500+350C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752628 | ||||||
chr1:145752637
|
G | A | 1 | a0001c0001t0008g0039 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.500+341C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752637 | ||||||
chr1:145752643
|
C | T | 1 | a0001c0001t0008g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.500+335G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752643 | ||||||
chr1:145752649
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0004g0123 | 2 | NA18973.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.500+329G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752649 | ||||||
chr1:145752744
|
C | T | 1 | a0001c0001t0033g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.500+234G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752744 | ||||||
chr1:145752809
|
G | A | 1 | a0001c0001t0033g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.500+169C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 5/8 | chr1 | 145752809 | ||||||
chr1:145753132
|
T | A | 1 | a0001c0001t0008g0089 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.429-83A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145753132 | ||||||
chr1:145753279
|
T | A | 1 | a0001c0001t0001g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.429-230A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145753279 | ||||||
chr1:145753588
|
A | G | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.429-539T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145753588 | ||||||
chr1:145753828
|
TGCCTTA | T | 3 | a0001c0001t0018g0185a0001c0001t0018g0187a0001c0001t0034g0186 | 3 | HG03130.hp1 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.429-785_429-780del others(6): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145753828 | ||||||
chr1:145753855
|
T | A | 1 | a0001c0001t0048g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.429-806A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145753855 | ||||||
chr1:145753877
|
C | T | 1 | a0001c0001t0002g0177 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.429-828G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145753877 | ||||||
chr1:145754048
|
A | C | 1 | a0001c0001t0033g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.429-999T>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145754048 | ||||||
chr1:145754153
|
T | C | 1 | a0001c0001t0020g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.429-1104A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145754153 | ||||||
chr1:145754231
|
A | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(125): Show | 129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.429-1182T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145754231 | ||||||
chr1:145754351
|
GT | G | 88 | a0001c0001t0002g0141a0001c0001t0002g0183a0001c0001t0003g0210others(85): Show | 88 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.429-1303delA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145754351 | ||||||
chr1:145754351
|
GTTTTT | G | 134 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(131): Show | 135 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.429-1307_429-1303d others(7): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145754351 | ||||||
chr1:145754439
|
C | T | 13 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(10): Show | 13 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.429-1390G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145754439 | ||||||
chr1:145754839
|
T | C | 1 | a0001c0001t0067g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.429-1790A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145754839 | ||||||
chr1:145755002
|
T | C | 1 | a0001c0001t0063g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.429-1953A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145755002 | ||||||
chr1:145755169
|
G | A | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.429-2120C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145755169 | ||||||
chr1:145755357
|
GA | G | 4 | a0001c0001t0010g0202a0001c0001t0010g0203a0001c0001t0010g0204others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.429-2309delT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145755357 | ||||||
chr1:145756024
|
A | G | 2 | a0001c0001t0068g0209a0001c0001t0069g0206 | 2 | NA18977.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.429-2975T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145756024 | ||||||
chr1:145756233
|
G | T | 1 | a0001c0001t0033g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.429-3184C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145756233 | ||||||
chr1:145756276
|
C | G | 18 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.429-3227G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145756276 | ||||||
chr1:145756445
|
G | C | 18 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.429-3396C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145756445 | ||||||
chr1:145756457
|
C | CA | 24 | a0001c0001t0001g0063a0001c0001t0001g0100a0001c0001t0005g0083others(21): Show | 24 | HG00733.hp1 HG00735.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.429-3409dupT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145756457 | ||||||
chr1:145756560
|
A | C | 1 | a0001c0001t0007g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.429-3511T>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145756560 | ||||||
chr1:145756743
|
T | C | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.429-3694A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145756743 | ||||||
chr1:145756759
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.429-3710G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145756759 | ||||||
chr1:145756804
|
C | CTGTGTTC others(1): Show |
213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.429-3763_429-3756d others(10): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145756804 | ||||||
chr1:145756827
|
GCTT | G | 5 | a0001c0001t0002g0137a0001c0001t0002g0159a0001c0001t0002g0160others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.429-3781_429-3779d others(5): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145756827 | ||||||
chr1:145756831
|
C | CT | 44 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0042others(41): Show | 44 | HG01106.hp1 HG01175.hp2 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.429-3783dupA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145756831 | ||||||
chr1:145756831
|
C | CTT | 8 | a0001c0001t0008g0032a0001c0001t0008g0039a0001c0001t0034g0186others(5): Show | 8 | HG00735.hp2 HG02818.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.429-3784_429-3783d others(4): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145756831 | ||||||
chr1:145756831
|
CT | C | 9 | a0001c0001t0001g0021a0001c0001t0001g0080a0001c0001t0002g0134others(6): Show | 9 | HG01257.hp1 HG01261.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.429-3783delA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145756831 | ||||||
chr1:145756952
|
C | T | 1 | a0001c0001t0005g0006 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.429-3903G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145756952 | ||||||
chr1:145757025
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.429-3976C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145757025 | ||||||
chr1:145757256
|
G | A | 2 | a0001c0001t0014g0265a0001c0001t0014g0267 | 2 | HG02895.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.429-4207C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145757256 | ||||||
chr1:145757293
|
T | C | 1 | a0001c0001t0024g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.429-4244A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145757293 | ||||||
chr1:145757312
|
C | A | 1 | a0001c0001t0017g0235 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.429-4263G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145757312 | ||||||
chr1:145757339
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.429-4290G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145757339 | ||||||
chr1:145757803
|
G | GGTGT | 49 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.429-4758_429-4755d others(6): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145757803 | ||||||
chr1:145757865
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.429-4816A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145757865 | ||||||
chr1:145757978
|
T | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.429-4929A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145757978 | ||||||
chr1:145758390
|
G | A | 5 | a0001c0001t0002g0153a0001c0001t0002g0170a0001c0001t0002g0180others(2): Show | 5 | HG01257.hp1 NA18949.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.429-5341C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145758390 | ||||||
chr1:145758797
|
T | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(126): Show | 130 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.429-5748A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145758797 | ||||||
chr1:145758853
|
A | G | 218 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.429-5804T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145758853 | ||||||
chr1:145758959
|
A | G | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.429-5910T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145758959 | ||||||
chr1:145758965
|
T | C | 1 | a0001c0001t0002g0174 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.429-5916A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145758965 | ||||||
chr1:145759113
|
T | C | 1 | a0001c0001t0012g0131 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.429-6064A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145759113 | ||||||
chr1:145759132
|
A | G | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.429-6083T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145759132 | ||||||
chr1:145759142
|
A | G | 4 | a0001c0001t0011g0207a0001c0001t0011g0208a0001c0001t0011g0212others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.429-6093T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145759142 | ||||||
chr1:145759453
|
C | A | 2 | a0001c0001t0003g0253a0001c0001t0015g0218 | 2 | HG00323.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.429-6404G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145759453 | ||||||
chr1:145759485
|
C | T | 1 | a0001c0001t0002g0169 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.429-6436G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145759485 | ||||||
chr1:145759532
|
G | C | 1 | a0001c0001t0077g0271 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.429-6483C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145759532 | ||||||
chr1:145759591
|
A | G | 1 | a0001c0001t0003g0221 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.429-6542T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145759591 | ||||||
chr1:145759665
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.429-6616T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145759665 | ||||||
chr1:145760009
|
A | T | 1 | a0001c0001t0003g0259 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.429-6960T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145760009 | ||||||
chr1:145760054
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.429-7005G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145760054 | ||||||
chr1:145760198
|
G | A | 134 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(131): Show | 135 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.429-7149C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145760198 | ||||||
chr1:145760259
|
A | T | 1 | a0001c0001t0047g0151 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.429-7210T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145760259 | ||||||
chr1:145760332
|
G | A | 1 | a0001c0001t0030g0135 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.429-7283C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145760332 | ||||||
chr1:145760454
|
G | A | 1 | a0001c0001t0059g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.429-7405C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145760454 | ||||||
chr1:145760479
|
T | C | 1 | a0001c0001t0021g0128 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.429-7430A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145760479 | ||||||
chr1:145760593
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0090a0001c0001t0001g0095 | 3 | HG00099.hp1 HG01168.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.429-7544G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145760593 | ||||||
chr1:145760646
|
C | T | 10 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(7): Show | 10 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.429-7597G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145760646 | ||||||
chr1:145760673
|
G | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0056g0002others(1): Show | 4 | HG00741.hp1 HG02145.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.429-7624C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145760673 | ||||||
chr1:145760677
|
T | C | 2 | a0001c0001t0001g0046a0001c0001t0074g0050 | 2 | NA18965.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.429-7628A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145760677 | ||||||
chr1:145760787
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.429-7738A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145760787 | ||||||
chr1:145760914
|
A | T | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.429-7865T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145760914 | ||||||
chr1:145760979
|
C | G | 1 | a0001c0001t0055g0093 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.429-7930G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145760979 | ||||||
chr1:145761132
|
T | C | 17 | a0001c0001t0002g0132a0001c0001t0002g0138a0001c0001t0002g0148others(14): Show | 17 | HG00438.hp2 HG01496.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.429-8083A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145761132 | ||||||
chr1:145761302
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.429-8253T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145761302 | ||||||
chr1:145761357
|
C | T | 1 | a0001c0001t0014g0265 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.429-8308G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145761357 | ||||||
chr1:145761379
|
G | C | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.429-8330C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145761379 | ||||||
chr1:145761682
|
C | T | 1 | a0001c0001t0018g0187 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.429-8633G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145761682 | ||||||
chr1:145761723
|
G | A | 7 | a0001c0001t0006g0115a0001c0001t0025g0010a0001c0001t0025g0029others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.429-8674C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145761723 | ||||||
chr1:145761753
|
G | A | 2 | a0001c0001t0050g0188a0001c0001t0051g0200 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.429-8704C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145761753 | ||||||
chr1:145761807
|
T | C | 1 | a0001c0001t0067g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.429-8758A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145761807 | ||||||
chr1:145762045
|
A | T | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.429-8996T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145762045 | ||||||
chr1:145762076
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.429-9027C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145762076 | ||||||
chr1:145762215
|
T | C | 1 | a0001c0001t0067g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.429-9166A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145762215 | ||||||
chr1:145762473
|
G | GT | 13 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(10): Show | 13 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.428+9237dupA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145762473 | ||||||
chr1:145762760
|
AC | A | 4 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0040others(1): Show | 4 | NA18939.hp1 NA18964.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.428+8950delG | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145762760 | ||||||
chr1:145762898
|
T | A | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.428+8813A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145762898 | ||||||
chr1:145762899
|
T | C | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.428+8812A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145762899 | ||||||
chr1:145763110
|
A | G | 5 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.428+8601T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763110 | ||||||
chr1:145763143
|
G | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0028others(2): Show | 5 | HG02723.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.428+8568C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763143 | ||||||
chr1:145763163
|
T | A | 1 | a0001c0001t0047g0151 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.428+8548A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763163 | ||||||
chr1:145763287
|
C | A | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.428+8424G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763287 | ||||||
chr1:145763346
|
A | G | 1 | a0001c0001t0020g0182 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.428+8365T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763346 | ||||||
chr1:145763423
|
C | A | 2 | a0001c0001t0006g0024a0001c0001t0006g0034 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.428+8288G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763423 | ||||||
chr1:145763428
|
T | A | 5 | a0001c0001t0033g0198a0001c0001t0038g0196a0001c0001t0039g0195others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.428+8283A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763428 | ||||||
chr1:145763481
|
T | C | 1 | a0001c0001t0033g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.428+8230A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763481 | ||||||
chr1:145763563
|
G | T | 1 | a0001c0001t0005g0094 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.428+8148C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763563 | ||||||
chr1:145763564
|
T | G | 1 | a0001c0001t0005g0094 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.428+8147A>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763564 | ||||||
chr1:145763607
|
G | C | 60 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.428+8104C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763607 | ||||||
chr1:145763876
|
T | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.428+7835A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763876 | ||||||
chr1:145763883
|
GCCCTCC | G | 3 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131 | 3 | HG02922.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.428+7822_428+7827d others(8): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763883 | ||||||
chr1:145763884
|
CCCTCCCC others(73): Show |
C | 2 | a0001c0001t0006g0024a0001c0001t0006g0034 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.428+7747_428+7826d others(82): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763884 | ||||||
chr1:145763893
|
T | TC | 5 | a0001c0001t0002g0159a0001c0001t0003g0229a0001c0001t0004g0037others(2): Show | 5 | HG00735.hp2 HG01169.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.428+7817dupG | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763893 | ||||||
chr1:145763901
|
CCCCTCT | C | 28 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0061others(25): Show | 28 | HG00438.hp1 HG00738.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.428+7804_428+7809d others(8): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763901 | ||||||
chr1:145763907
|
T | C | 2 | a0001c0001t0002g0162a0001c0001t0042g0146 | 2 | HG02523.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.428+7804A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763907 | ||||||
chr1:145763940
|
G | T | 211 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.428+7771C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145763940 | ||||||
chr1:145764010
|
C | A | 1 | a0001c0001t0002g0170 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.428+7701G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764010 | ||||||
chr1:145764164
|
C | T | 1 | a0001c0001t0035g0057 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.428+7547G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764164 | ||||||
chr1:145764223
|
T | C | 1 | a0001c0001t0006g0115 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.428+7488A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764223 | ||||||
chr1:145764260
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.428+7451C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764260 | ||||||
chr1:145764357
|
G | A | 1 | a0001c0001t0021g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.428+7354C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764357 | ||||||
chr1:145764370
|
C | T | 1 | a0001c0001t0009g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.428+7341G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764370 | ||||||
chr1:145764396
|
C | T | 1 | a0001c0001t0028g0238 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.428+7315G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764396 | ||||||
chr1:145764404
|
C | T | 2 | a0001c0001t0050g0188a0001c0001t0051g0200 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.428+7307G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764404 | ||||||
chr1:145764449
|
G | C | 1 | a0001c0001t0005g0094 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.428+7262C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764449 | ||||||
chr1:145764467
|
G | A | 1 | a0001c0001t0002g0149 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.428+7244C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764467 | ||||||
chr1:145764494
|
G | T | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.428+7217C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764494 | ||||||
chr1:145764574
|
G | A | 5 | a0001c0001t0002g0132a0001c0001t0002g0138a0001c0001t0002g0175others(2): Show | 5 | HG00438.hp2 HG02486.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.428+7137C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764574 | ||||||
chr1:145764608
|
C | T | 5 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.428+7103G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764608 | ||||||
chr1:145764613
|
C | T | 1 | a0001c0001t0063g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.428+7098G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764613 | ||||||
chr1:145764649
|
G | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0069others(3): Show | 6 | HG00438.hp1 HG02129.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.428+7062C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764649 | ||||||
chr1:145764679
|
C | T | 2 | a0001c0001t0029g0084a0001c0001t0029g0088 | 2 | NA18962.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.428+7032G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764679 | ||||||
chr1:145764697
|
C | T | 1 | a0001c0001t0041g0199 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.428+7014G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764697 | ||||||
chr1:145764728
|
GGCCAGCT others(39): Show |
G | 1 | a0001c0001t0001g0061 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.428+6937_428+6982d others(48): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764728 | ||||||
chr1:145764755
|
T | G | 1 | a0001c0001t0047g0151 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.428+6956A>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764755 | ||||||
chr1:145764756
|
G | T | 1 | a0001c0001t0047g0151 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.428+6955C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764756 | ||||||
chr1:145764757
|
G | T | 1 | a0001c0001t0003g0214 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.428+6954C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764757 | ||||||
chr1:145764760
|
G | A | 1 | a0001c0001t0006g0115 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.428+6951C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764760 | ||||||
chr1:145764774
|
A | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(125): Show | 129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.428+6937T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764774 | ||||||
chr1:145764791
|
G | A | 2 | a0001c0001t0003g0214a0001c0001t0003g0215 | 2 | HG00673.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.428+6920C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764791 | ||||||
chr1:145764819
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.428+6892C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764819 | ||||||
chr1:145764880
|
G | C | 1 | a0001c0001t0002g0183 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.428+6831C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764880 | ||||||
chr1:145764885
|
G | A | 1 | a0001c0001t0071g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.428+6826C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764885 | ||||||
chr1:145764897
|
G | C | 2 | a0001c0001t0002g0153a0001c0001t0002g0170 | 2 | HG01257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.428+6814C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764897 | ||||||
chr1:145764993
|
G | A | 1 | a0001c0001t0032g0194 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.428+6718C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145764993 | ||||||
chr1:145765119
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.428+6592G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145765119 | ||||||
chr1:145765184
|
T | C | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.428+6527A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145765184 | ||||||
chr1:145765197
|
T | G | 1 | a0001c0001t0018g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.428+6514A>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145765197 | ||||||
chr1:145765242
|
A | G | 1 | a0001c0001t0018g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.428+6469T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145765242 | ||||||
chr1:145765255
|
C | T | 1 | a0001c0001t0018g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.428+6456G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145765255 | ||||||
chr1:145765263
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.428+6448G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145765263 | ||||||
chr1:145765282
|
T | C | 1 | a0001c0001t0018g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.428+6429A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145765282 | ||||||
chr1:145765297
|
C | T | 1 | a0001c0001t0018g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.428+6414G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145765297 | ||||||
chr1:145765416
|
T | TA | 56 | a0001c0001t0003g0210a0001c0001t0003g0214a0001c0001t0003g0215others(53): Show | 56 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.428+6294dupT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145765416 | ||||||
chr1:145765416
|
TA | T | 6 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.428+6294delT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145765416 | ||||||
chr1:145765422
|
A | G | 1 | a0001c0001t0060g0116 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.428+6289T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145765422 | ||||||
chr1:145765487
|
C | T | 1 | a0001c0001t0020g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.428+6224G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145765487 | ||||||
chr1:145765539
|
T | C | 5 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0001t0015g0239others(2): Show | 5 | HG01123.hp1 HG01243.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.428+6172A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145765539 | ||||||
chr1:145765647
|
TCA | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(125): Show | 129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.428+6062_428+6063d others(4): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145765647 | ||||||
chr1:145765774
|
C | T | 1 | a0001c0001t0004g0059 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.428+5937G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145765774 | ||||||
chr1:145766002
|
CT | C | 10 | a0001c0001t0001g0028a0001c0001t0001g0080a0001c0001t0002g0134others(7): Show | 10 | HG01168.hp1 HG01943.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.428+5708delA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766002 | ||||||
chr1:145766233
|
A | C | 18 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.428+5478T>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766233 | ||||||
chr1:145766249
|
G | A | 1 | a0001c0001t0003g0225 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.428+5462C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766249 | ||||||
chr1:145766272
|
G | C | 1 | a0001c0001t0001g0045 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.428+5439C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766272 | ||||||
chr1:145766302
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.428+5409C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766302 | ||||||
chr1:145766339
|
G | A | 13 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(10): Show | 13 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.428+5372C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766339 | ||||||
chr1:145766494
|
C | T | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.428+5217G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766494 | ||||||
chr1:145766523
|
C | CG | 4 | a0001c0001t0002g0176a0001c0001t0010g0203a0001c0001t0047g0151others(1): Show | 4 | HG01243.hp1 HG02630.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+5187dupC | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766523 | ||||||
chr1:145766531
|
T | G | 1 | a0001c0001t0047g0151 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.428+5180A>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766531 | ||||||
chr1:145766533
|
GCCGGGCA others(169): Show |
G | 2 | a0001c0001t0002g0133a0001c0001t0002g0142 | 2 | NA18747.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.428+5002_428+5177d others(2): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766533 | ||||||
chr1:145766533
|
GCCGGGCA others(307): Show |
G | 1 | a0001c0001t0002g0143 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.428+4864_428+5177d others(2): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766533 | ||||||
chr1:145766597
|
G | T | 1 | a0001c0001t0004g0099 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.428+5114C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766597 | ||||||
chr1:145766600
|
CGGGGCGG others(42): Show |
C | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0104 | 3 | HG01175.hp2 HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.428+5062_428+5110d others(51): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766600 | ||||||
chr1:145766617
|
C | G | 1 | a0001c0001t0047g0151 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.428+5094G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766617 | ||||||
chr1:145766618
|
G | C | 1 | a0001c0001t0047g0151 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.428+5093C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766618 | ||||||
chr1:145766666
|
CGGGGGGC others(131): Show |
C | 4 | a0001c0001t0002g0172a0001c0001t0002g0174a0001c0001t0003g0229others(1): Show | 4 | HG01361.hp2 HG04199.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.428+4907_428+5044d others(2): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766666 | ||||||
chr1:145766688
|
CCCTCCCG others(209): Show |
C | 3 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131 | 3 | HG02922.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.428+4807_428+5022d others(2): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766688 | ||||||
chr1:145766703
|
C | T | 5 | a0001c0001t0025g0010a0001c0001t0025g0029a0001c0001t0058g0262others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.428+5008G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766703 | ||||||
chr1:145766749
|
G | A | 1 | a0001c0001t0003g0234 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.428+4962C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766749 | ||||||
chr1:145766777
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(122): Show | 126 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.428+4934T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766777 | ||||||
chr1:145766781
|
C | T | 18 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.428+4930G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766781 | ||||||
chr1:145766788
|
C | CCGGGG | 3 | a0001c0001t0011g0207a0001c0001t0011g0208a0001c0001t0016g0236 | 3 | HG00733.hp2 HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.428+4918_428+4922d others(7): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766788 | ||||||
chr1:145766789
|
C | CGGGGGGG others(3): Show |
1 | a0001c0001t0002g0166 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.428+4912_428+4921d others(12): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766789 | ||||||
chr1:145766789
|
C | CGGGGGGG others(4): Show |
3 | a0001c0001t0002g0148a0001c0001t0002g0152a0001c0001t0002g0159 | 3 | HG01106.hp2 HG01169.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.428+4911_428+4921d others(13): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766789 | ||||||
chr1:145766789
|
C | CGGGGGGG others(7): Show |
1 | a0001c0001t0002g0181 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.428+4908_428+4921d others(16): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766789 | ||||||
chr1:145766789
|
C | CGGGGGGG others(8): Show |
2 | a0001c0001t0002g0153a0001c0001t0002g0160 | 2 | HG01257.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.428+4907_428+4921d others(17): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766789 | ||||||
chr1:145766789
|
CGGGGGGG others(4): Show |
C | 1 | a0001c0001t0008g0089 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.428+4911_428+4921d others(13): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766789 | ||||||
chr1:145766789
|
CGGGGGGG others(6): Show |
C | 24 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(21): Show | 24 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.428+4909_428+4921d others(15): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766789 | ||||||
chr1:145766793
|
G | C | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(121): Show | 125 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.428+4918C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766793 | ||||||
chr1:145766793
|
G | GC | 8 | a0001c0001t0003g0210a0001c0001t0003g0227a0001c0001t0003g0242others(5): Show | 8 | HG01255.hp1 HG01516.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.428+4917_428+4918i others(3): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766793 | ||||||
chr1:145766794
|
G | C | 25 | a0001c0001t0003g0211a0001c0001t0003g0214a0001c0001t0003g0215others(22): Show | 25 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.428+4917C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766794 | ||||||
chr1:145766795
|
G | C | 7 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0001t0003g0234others(4): Show | 7 | HG00639.hp1 HG01175.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.428+4916C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766795 | ||||||
chr1:145766796
|
G | C | 1 | a0001c0001t0028g0247 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.428+4915C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766796 | ||||||
chr1:145766797
|
GGGGGGGG others(138): Show |
G | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0104 | 3 | HG01175.hp2 HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.428+4769_428+4913d others(2): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766797 | ||||||
chr1:145766799
|
G | GCTGACCC others(31): Show |
120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(117): Show | 121 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.428+4911_428+4912i others(40): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766799 | ||||||
chr1:145766799
|
G | GCTGACCC others(32): Show |
2 | a0001c0001t0001g0021a0001c0001t0005g0075 | 2 | HG01261.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.428+4911_428+4912i others(41): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766799 | ||||||
chr1:145766800
|
G | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(119): Show | 123 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.428+4911C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766800 | ||||||
chr1:145766800
|
G | GCTGACCC others(32): Show |
2 | a0001c0001t0008g0039a0001c0001t0065g0102 | 2 | HG02071.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.428+4910_428+4911i others(41): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766800 | ||||||
chr1:145766801
|
G | GGGGGGGG others(15): Show |
1 | a0001c0001t0047g0151 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.428+4909_428+4910i others(24): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766801 | ||||||
chr1:145766803
|
G | T | 2 | a0001c0001t0003g0230a0001c0001t0003g0250 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.428+4908C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766803 | ||||||
chr1:145766804
|
G | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(122): Show | 126 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.428+4907C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766804 | ||||||
chr1:145766811
|
C | A | 1 | a0001c0001t0005g0076 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.428+4900G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766811 | ||||||
chr1:145766832
|
C | T | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.428+4879G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766832 | ||||||
chr1:145766850
|
G | A | 5 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.428+4861C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766850 | ||||||
chr1:145766887
|
A | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(124): Show | 128 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.428+4824T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766887 | ||||||
chr1:145766887
|
AGGCAGAG others(125): Show |
A | 1 | a0001c0001t0027g0268 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.428+4692_428+4823d others(2): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766887 | ||||||
chr1:145766911
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.428+4800C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766911 | ||||||
chr1:145766915
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(122): Show | 126 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.428+4796C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766915 | ||||||
chr1:145766931
|
C | G | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(121): Show | 125 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.428+4780G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766931 | ||||||
chr1:145766932
|
G | A | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.428+4779C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766932 | ||||||
chr1:145766932
|
GGGGGGCT others(125): Show |
G | 1 | a0001c0001t0002g0144 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.428+4647_428+4778d others(2): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766932 | ||||||
chr1:145766935
|
GGGCTGAC | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(120): Show | 124 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.428+4769_428+4775d others(9): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766935 | ||||||
chr1:145766942
|
CCTGACCC others(120): Show |
C | 4 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(1): Show | 4 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.428+4642_428+4768d others(2): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766942 | ||||||
chr1:145766965
|
G | A | 1 | a0001c0001t0054g0114 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.428+4746C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145766965 | ||||||
chr1:145767064
|
A | G | 1 | a0001c0001t0027g0268 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.428+4647T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767064 | ||||||
chr1:145767137
|
G | A | 16 | a0001c0001t0003g0258a0001c0001t0007g0184a0001c0001t0007g0189others(13): Show | 16 | HG00639.hp2 HG00735.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.428+4574C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767137 | ||||||
chr1:145767189
|
G | A | 1 | a0001c0001t0018g0187 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.428+4522C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767189 | ||||||
chr1:145767256
|
C | T | 1 | a0001c0001t0061g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.428+4455G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767256 | ||||||
chr1:145767291
|
TCAGA | T | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(126): Show | 130 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.428+4416_428+4419d others(6): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767291 | ||||||
chr1:145767331
|
T | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.428+4380A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767331 | ||||||
chr1:145767373
|
C | CG | 4 | a0001c0001t0002g0152a0001c0001t0004g0037a0001c0001t0019g0171others(1): Show | 4 | HG01099.hp2 HG01106.hp2 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+4337dupC | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767373 | ||||||
chr1:145767473
|
C | T | 2 | a0001c0001t0006g0064a0001c0001t0008g0098 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.428+4238G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767473 | ||||||
chr1:145767544
|
A | T | 1 | a0001c0001t0003g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.428+4167T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767544 | ||||||
chr1:145767622
|
A | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(125): Show | 129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.428+4089T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767622 | ||||||
chr1:145767667
|
C | A | 1 | a0001c0001t0001g0051 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.428+4044G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767667 | ||||||
chr1:145767667
|
C | T | 1 | a0001c0001t0063g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.428+4044G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767667 | ||||||
chr1:145767792
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.428+3919C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767792 | ||||||
chr1:145767819
|
G | A | 1 | a0001c0001t0007g0201 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.428+3892C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767819 | ||||||
chr1:145767919
|
A | G | 1 | a0001c0001t0016g0257 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.428+3792T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767919 | ||||||
chr1:145767947
|
TCAGAGA | T | 218 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.428+3758_428+3763d others(8): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767947 | ||||||
chr1:145767983
|
G | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0028others(2): Show | 5 | HG02723.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.428+3728C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767983 | ||||||
chr1:145767992
|
TGGGGAG | T | 10 | a0001c0001t0003g0211a0001c0001t0003g0220a0001c0001t0003g0223others(7): Show | 10 | HG02015.hp2 HG02071.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.428+3713_428+3718d others(8): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767992 | ||||||
chr1:145767993
|
G | T | 49 | a0001c0001t0003g0210a0001c0001t0003g0214a0001c0001t0003g0215others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.428+3718C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767993 | ||||||
chr1:145767999
|
A | T | 10 | a0001c0001t0003g0211a0001c0001t0003g0220a0001c0001t0003g0223others(7): Show | 10 | HG02015.hp2 HG02071.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.428+3712T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145767999 | ||||||
chr1:145768325
|
C | A | 5 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131others(2): Show | 5 | HG02818.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.428+3386G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145768325 | ||||||
chr1:145768362
|
C | T | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.428+3349G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145768362 | ||||||
chr1:145768451
|
G | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(125): Show | 129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.428+3260C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145768451 | ||||||
chr1:145768706
|
A | G | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.428+3005T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145768706 | ||||||
chr1:145768999
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0074g0050 | 2 | NA18965.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.428+2712G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145768999 | ||||||
chr1:145769068
|
G | A | 1 | a0001c0001t0006g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.428+2643C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145769068 | ||||||
chr1:145769131
|
A | G | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.428+2580T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145769131 | ||||||
chr1:145769170
|
A | T | 269 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.428+2541T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145769170 | ||||||
chr1:145769312
|
G | A | 2 | a0001c0001t0018g0185a0001c0001t0018g0187 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.428+2399C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145769312 | ||||||
chr1:145769601
|
T | G | 2 | a0001c0001t0002g0149a0001c0001t0002g0157 | 2 | NA18941.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.428+2110A>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145769601 | ||||||
chr1:145769760
|
T | TA | 74 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0038others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.428+1950dupT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145769760 | ||||||
chr1:145769760
|
T | TAA | 120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(117): Show | 121 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.428+1949_428+1950d others(4): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145769760 | ||||||
chr1:145769760
|
T | TAAA | 9 | a0001c0001t0001g0045a0001c0001t0006g0015a0001c0001t0006g0024others(6): Show | 9 | HG02258.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.428+1948_428+1950d others(5): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145769760 | ||||||
chr1:145769760
|
TA | T | 7 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0142others(4): Show | 7 | HG01168.hp1 HG01257.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.428+1950delT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145769760 | ||||||
chr1:145769824
|
C | T | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.428+1887G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145769824 | ||||||
chr1:145769872
|
T | G | 1 | a0001c0001t0002g0176 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.428+1839A>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145769872 | ||||||
chr1:145769904
|
G | A | 1 | a0001c0001t0063g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.428+1807C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145769904 | ||||||
chr1:145770643
|
C | T | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.428+1068G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145770643 | ||||||
chr1:145770658
|
T | TTC | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.428+1051_428+1052d others(4): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145770658 | ||||||
chr1:145770702
|
G | A | 4 | a0001c0001t0011g0207a0001c0001t0011g0208a0001c0001t0011g0212others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+1009C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145770702 | ||||||
chr1:145770921
|
C | T | 1 | a0001c0001t0063g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.428+790G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145770921 | ||||||
chr1:145771120
|
T | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(125): Show | 129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.428+591A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145771120 | ||||||
chr1:145771160
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.428+551C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145771160 | ||||||
chr1:145771261
|
G | T | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.428+450C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145771261 | ||||||
chr1:145771531
|
A | G | 1 | a0001c0001t0004g0059 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.428+180T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145771531 | ||||||
chr1:145771541
|
T | C | 7 | a0001c0001t0006g0115a0001c0001t0025g0010a0001c0001t0025g0029others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.428+170A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145771541 | ||||||
chr1:145771579
|
C | T | 5 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.428+132G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145771579 | ||||||
chr1:145771592
|
T | C | 1 | a0001c0001t0077g0271 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.428+119A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 4/8 | chr1 | 145771592 | ||||||
chr1:145772225
|
A | T | 61 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(58): Show | 61 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.220-306T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145772225 | ||||||
chr1:145772412
|
A | G | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.220-493T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145772412 | ||||||
chr1:145773051
|
C | T | 1 | a0001c0001t0022g0077 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.220-1132G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145773051 | ||||||
chr1:145773146
|
T | C | 25 | a0001c0001t0003g0210a0001c0001t0003g0216a0001c0001t0003g0217others(22): Show | 25 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.220-1227A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145773146 | ||||||
chr1:145773147
|
T | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.220-1228A>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145773147 | ||||||
chr1:145773181
|
G | T | 2 | a0001c0001t0004g0110a0001c0001t0004g0117 | 2 | NA18946.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.220-1262C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145773181 | ||||||
chr1:145773290
|
T | A | 2 | a0001c0001t0002g0133a0001c0001t0002g0142 | 2 | NA18747.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.220-1371A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145773290 | ||||||
chr1:145773291
|
A | T | 2 | a0001c0001t0001g0086a0001c0001t0055g0093 | 2 | HG03710.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.220-1372T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145773291 | ||||||
chr1:145773482
|
A | G | 1 | a0001c0001t0033g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.220-1563T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145773482 | ||||||
chr1:145773635
|
C | T | 18 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.220-1716G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145773635 | ||||||
chr1:145773765
|
G | A | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.220-1846C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145773765 | ||||||
chr1:145773791
|
G | GT | 14 | a0001c0001t0002g0133a0001c0001t0007g0184a0001c0001t0007g0189others(11): Show | 14 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-1873dupA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145773791 | ||||||
chr1:145773813
|
G | T | 5 | a0001c0001t0033g0198a0001c0001t0038g0196a0001c0001t0039g0195others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-1894C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145773813 | ||||||
chr1:145774009
|
T | A | 1 | a0001c0001t0002g0143 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.220-2090A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145774009 | ||||||
chr1:145774125
|
G | A | 2 | a0001c0001t0002g0141a0001c0001t0002g0183 | 2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.220-2206C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145774125 | ||||||
chr1:145774147
|
T | A | 1 | a0001c0001t0024g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.220-2228A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145774147 | ||||||
chr1:145774300
|
A | AT | 50 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(47): Show | 50 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.220-2382dupA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145774300 | ||||||
chr1:145774300
|
A | ATT | 12 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.220-2383_220-2382d others(4): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145774300 | ||||||
chr1:145774300
|
AT | A | 76 | a0001c0001t0002g0127a0001c0001t0002g0134a0001c0001t0002g0136others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.220-2382delA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145774300 | ||||||
chr1:145774332
|
G | C | 1 | a0001c0001t0001g0101 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.220-2413C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145774332 | ||||||
chr1:145774406
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.220-2487C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145774406 | ||||||
chr1:145774412
|
C | T | 60 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.220-2493G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145774412 | ||||||
chr1:145774415
|
T | C | 3 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131 | 3 | HG02922.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.220-2496A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145774415 | ||||||
chr1:145774418
|
C | T | 1 | a0001c0001t0003g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.220-2499G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145774418 | ||||||
chr1:145774526
|
T | C | 2 | a0001c0001t0016g0236a0001c0001t0016g0260 | 2 | HG00733.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.220-2607A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145774526 | ||||||
chr1:145774674
|
T | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0090a0001c0001t0001g0095 | 3 | HG00099.hp1 HG01168.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.220-2755A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145774674 | ||||||
chr1:145774922
|
G | A | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.220-3003C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145774922 | ||||||
chr1:145775024
|
A | ATCGCTTG others(47): Show |
1 | a0001c0001t0006g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.220-3159_220-3106d others(56): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145775024 | ||||||
chr1:145775027
|
G | A | 3 | a0001c0001t0008g0032a0001c0001t0008g0039a0001c0001t0057g0036 | 3 | HG00735.hp2 HG03669.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.220-3108C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145775027 | ||||||
chr1:145775396
|
C | CT | 9 | a0001c0001t0001g0063a0001c0001t0002g0176a0001c0001t0003g0241others(6): Show | 9 | HG00673.hp1 NA18949.hp2 NA18974.hp1 others(6): Show |
intron_variant | MODIFIER | c.220-3478dupA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145775396 | ||||||
chr1:145775396
|
CT | C | 14 | a0001c0001t0001g0042a0001c0001t0001g0085a0001c0001t0001g0090others(11): Show | 15 | HG00733.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.220-3478delA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145775396 | ||||||
chr1:145775564
|
TA | T | 21 | a0001c0001t0002g0160a0001c0001t0003g0253a0001c0001t0007g0184others(18): Show | 21 | HG00323.hp1 HG00323.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.220-3646delT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145775564 | ||||||
chr1:145775775
|
T | C | 8 | a0001c0001t0003g0220a0001c0001t0003g0223a0001c0001t0003g0231others(5): Show | 8 | HG02015.hp2 HG02071.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.220-3856A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145775775 | ||||||
chr1:145775999
|
AAAAAAT | A | 18 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.220-4086_220-4081d others(8): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145775999 | ||||||
chr1:145776045
|
T | C | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0104 | 3 | HG01175.hp2 HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.220-4126A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145776045 | ||||||
chr1:145776090
|
A | AG | 26 | a0001c0001t0002g0127a0001c0001t0002g0176a0001c0001t0007g0184others(23): Show | 26 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.220-4172dupC | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145776090 | ||||||
chr1:145776090
|
A | AGG | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(122): Show | 126 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.220-4173_220-4172d others(4): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145776090 | ||||||
chr1:145776164
|
A | ATT | 141 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 142 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.220-4247_220-4246d others(4): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145776164 | ||||||
chr1:145776164
|
A | ATTT | 7 | a0001c0001t0001g0019a0001c0001t0001g0070a0001c0001t0004g0099others(4): Show | 7 | HG00438.hp1 HG02145.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.220-4248_220-4246d others(5): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145776164 | ||||||
chr1:145776241
|
T | C | 18 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.220-4322A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145776241 | ||||||
chr1:145776964
|
A | G | 1 | a0001c0001t0005g0113 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.220-5045T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145776964 | ||||||
chr1:145777029
|
G | A | 1 | a0001c0001t0002g0169 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.220-5110C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145777029 | ||||||
chr1:145777367
|
A | G | 1 | a0001c0001t0002g0145 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.220-5448T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145777367 | ||||||
chr1:145777371
|
T | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(125): Show | 129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.220-5452A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145777371 | ||||||
chr1:145777488
|
T | C | 1 | a0001c0001t0063g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.220-5569A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145777488 | ||||||
chr1:145777505
|
A | C | 1 | a0001c0001t0001g0106 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.220-5586T>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145777505 | ||||||
chr1:145777581
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.220-5662A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145777581 | ||||||
chr1:145778293
|
C | T | 2 | a0001c0001t0002g0153a0001c0001t0002g0170 | 2 | HG01257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.219+6246G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145778293 | ||||||
chr1:145778504
|
T | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.219+6035A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145778504 | ||||||
chr1:145778843
|
A | G | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.219+5696T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145778843 | ||||||
chr1:145779175
|
AT | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(125): Show | 129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.219+5363delA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145779175 | ||||||
chr1:145779332
|
A | C | 1 | a0001c0001t0001g0106 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.219+5207T>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145779332 | ||||||
chr1:145779467
|
C | T | 1 | a0001c0001t0077g0271 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.219+5072G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145779467 | ||||||
chr1:145779468
|
G | C | 1 | a0001c0001t0007g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.219+5071C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145779468 | ||||||
chr1:145779551
|
A | G | 1 | a0001c0001t0033g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.219+4988T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145779551 | ||||||
chr1:145779707
|
G | A | 1 | a0001c0001t0058g0262 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.219+4832C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145779707 | ||||||
chr1:145779766
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0013g0068 | 2 | HG02129.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.219+4773C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145779766 | ||||||
chr1:145779812
|
G | A | 1 | a0001c0001t0055g0093 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.219+4727C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145779812 | ||||||
chr1:145779823
|
T | C | 222 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.219+4716A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145779823 | ||||||
chr1:145779965
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.219+4574T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145779965 | ||||||
chr1:145779967
|
C | A | 1 | a0001c0001t0063g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.219+4572G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145779967 | ||||||
chr1:145780096
|
C | T | 3 | a0001c0001t0005g0001a0001c0001t0005g0078a0001c0001t0005g0105 | 4 | HG01516.hp1 HG01517.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+4443G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145780096 | ||||||
chr1:145780161
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.219+4378C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145780161 | ||||||
chr1:145780339
|
G | A | 1 | a0001c0001t0024g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.219+4200C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145780339 | ||||||
chr1:145780342
|
C | T | 3 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267 | 3 | HG02615.hp1 HG02895.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.219+4197G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145780342 | ||||||
chr1:145780430
|
C | T | 1 | a0001c0001t0074g0050 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.219+4109G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145780430 | ||||||
chr1:145780477
|
A | T | 3 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131 | 3 | HG02922.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.219+4062T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145780477 | ||||||
chr1:145780568
|
C | T | 1 | a0001c0001t0005g0094 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.219+3971G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145780568 | ||||||
chr1:145780618
|
T | TA | 23 | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0001g0065others(20): Show | 23 | HG00735.hp2 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.219+3920dupT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145780618 | ||||||
chr1:145780618
|
TA | T | 8 | a0001c0001t0001g0080a0001c0001t0004g0117a0001c0001t0008g0032others(5): Show | 8 | HG02615.hp1 HG02735.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.219+3920delT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145780618 | ||||||
chr1:145780618
|
TAAAAAAA | T | 9 | a0001c0001t0002g0127a0001c0001t0002g0134a0001c0001t0002g0136others(6): Show | 9 | HG02015.hp1 HG02165.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.219+3914_219+3920d others(9): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145780618 | ||||||
chr1:145780716
|
C | A | 2 | a0001c0001t0001g0072a0001c0001t0006g0071 | 2 | NA18941.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.219+3823G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145780716 | ||||||
chr1:145781097
|
C | A | 2 | a0001c0001t0001g0069a0001c0001t0013g0068 | 2 | HG02129.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.219+3442G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145781097 | ||||||
chr1:145781151
|
AT | A | 3 | a0001c0001t0003g0211a0001c0001t0004g0060a0001c0001t0024g0073 | 3 | NA18989.hp1 NA19075.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.219+3387delA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145781151 | ||||||
chr1:145781555
|
T | C | 3 | a0001c0001t0001g0045a0001c0001t0004g0031a0001c0001t0004g0099 | 3 | HG02165.hp1 NA18949.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.219+2984A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145781555 | ||||||
chr1:145781802
|
T | C | 1 | a0001c0001t0008g0032 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.219+2737A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145781802 | ||||||
chr1:145781900
|
C | CT | 17 | a0001c0001t0001g0065a0001c0001t0001g0120a0001c0001t0008g0032others(14): Show | 17 | HG00735.hp2 HG01175.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.219+2638dupA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145781900 | ||||||
chr1:145782015
|
G | T | 3 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267 | 3 | HG02615.hp1 HG02895.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.219+2524C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145782015 | ||||||
chr1:145782157
|
G | A | 1 | a0001c0001t0020g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.219+2382C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145782157 | ||||||
chr1:145782456
|
A | AAC | 3 | a0001c0001t0001g0035a0001c0001t0001g0261a0001c0001t0037g0007 | 3 | HG02257.hp1 HG02717.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.219+2081_219+2082d others(4): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145782456 | ||||||
chr1:145782938
|
C | T | 212 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(209): Show | 213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.219+1601G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145782938 | ||||||
chr1:145783113
|
T | C | 1 | a0001c0001t0063g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.219+1426A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145783113 | ||||||
chr1:145783115
|
G | A | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(124): Show | 128 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.219+1424C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145783115 | ||||||
chr1:145783203
|
G | T | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.219+1336C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145783203 | ||||||
chr1:145783218
|
C | T | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.219+1321G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145783218 | ||||||
chr1:145783670
|
T | C | 18 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.219+869A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145783670 | ||||||
chr1:145783833
|
A | T | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.219+706T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145783833 | ||||||
chr1:145783834
|
A | T | 2 | a0001c0001t0006g0071a0001c0001t0017g0254 | 2 | HG00639.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.219+705T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145783834 | ||||||
chr1:145783866
|
T | C | 18 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.219+673A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145783866 | ||||||
chr1:145784013
|
A | T | 3 | a0001c0001t0008g0032a0001c0001t0008g0039a0001c0001t0057g0036 | 3 | HG00735.hp2 HG03669.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.219+526T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145784013 | ||||||
chr1:145784061
|
T | C | 2 | a0001c0001t0002g0141a0001c0001t0002g0183 | 2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.219+478A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145784061 | ||||||
chr1:145784465
|
G | C | 1 | a0001c0001t0005g0006 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.219+74C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 3/8 | chr1 | 145784465 | ||||||
chr1:145784644
|
C | A | 1 | a0001c0001t0006g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.162-48G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145784644 | ||||||
chr1:145785024
|
A | G | 1 | a0001c0001t0067g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.162-428T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145785024 | ||||||
chr1:145785157
|
TAA | T | 26 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0041others(23): Show | 26 | HG00438.hp1 HG00738.hp2 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.162-563_162-562del others(2): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145785157 | ||||||
chr1:145785167
|
C | T | 1 | a0001c0001t0054g0114 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.162-571G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145785167 | ||||||
chr1:145785369
|
C | T | 1 | a0001c0001t0003g0255 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.162-773G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145785369 | ||||||
chr1:145785731
|
CTAGT | C | 7 | a0001c0001t0002g0133a0001c0001t0002g0142a0001c0001t0002g0143others(4): Show | 7 | NA18747.hp2 NA18949.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.162-1139_162-1136d others(6): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145785731 | ||||||
chr1:145785992
|
A | G | 1 | a0001c0001t0067g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.162-1396T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145785992 | ||||||
chr1:145786083
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.162-1487A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145786083 | ||||||
chr1:145786241
|
A | G | 1 | a0001c0001t0017g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.162-1645T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145786241 | ||||||
chr1:145786426
|
T | G | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.162-1830A>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145786426 | ||||||
chr1:145786428
|
G | T | 218 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.162-1832C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145786428 | ||||||
chr1:145786443
|
C | T | 2 | a0001c0001t0027g0268a0001c0001t0027g0269 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.162-1847G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145786443 | ||||||
chr1:145786594
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.162-1998A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145786594 | ||||||
chr1:145786679
|
T | G | 1 | a0001c0001t0005g0075 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.162-2083A>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145786679 | ||||||
chr1:145786807
|
C | T | 5 | a0001c0001t0033g0198a0001c0001t0038g0196a0001c0001t0039g0195others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+2101G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145786807 | ||||||
chr1:145786921
|
T | C | 1 | a0001c0001t0021g0128 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.161+1987A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145786921 | ||||||
chr1:145787033
|
T | C | 2 | a0001c0001t0027g0268a0001c0001t0027g0269 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.161+1875A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145787033 | ||||||
chr1:145787312
|
A | G | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.161+1596T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145787312 | ||||||
chr1:145787349
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.161+1559C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145787349 | ||||||
chr1:145787539
|
T | A | 4 | a0001c0001t0005g0094a0001c0001t0005g0109a0001c0001t0026g0107others(1): Show | 4 | NA18980.hp1 NA19001.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+1369A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145787539 | ||||||
chr1:145787571
|
CA | C | 20 | a0001c0001t0001g0021a0001c0001t0001g0041a0001c0001t0001g0042others(17): Show | 21 | HG00558.hp1 HG00558.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.161+1336delT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145787571 | ||||||
chr1:145787571
|
CAA | C | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.161+1335_161+1336d others(4): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145787571 | ||||||
chr1:145787584
|
A | G | 1 | a0001c0001t0003g0259 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.161+1324T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145787584 | ||||||
chr1:145787588
|
A | G | 1 | a0001c0001t0067g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.161+1320T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145787588 | ||||||
chr1:145787593
|
A | G | 1 | a0001c0001t0003g0211 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.161+1315T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145787593 | ||||||
chr1:145787693
|
C | G | 5 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+1215G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145787693 | ||||||
chr1:145787809
|
A | G | 2 | a0001c0001t0029g0084a0001c0001t0029g0088 | 2 | NA18962.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.161+1099T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145787809 | ||||||
chr1:145787904
|
A | C | 1 | a0001c0001t0017g0252 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.161+1004T>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145787904 | ||||||
chr1:145788436
|
T | C | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.161+472A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145788436 | ||||||
chr1:145788542
|
G | C | 1 | a0001c0001t0021g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.161+366C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145788542 | ||||||
chr1:145788674
|
G | GATACATA others(8): Show |
1 | a0001c0001t0001g0125 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.161+233_161+234ins others(15): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145788674 | ||||||
chr1:145788701
|
T | C | 3 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267 | 3 | HG02615.hp1 HG02895.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.161+207A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 2/8 | chr1 | 145788701 | ||||||
chr1:145789102
|
G | GT | 5 | a0001c0001t0003g0225a0001c0001t0005g0094a0001c0001t0007g0189others(2): Show | 5 | HG02055.hp1 HG02293.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-137dupA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145789102 | ||||||
chr1:145789200
|
G | T | 218 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.103-234C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145789200 | ||||||
chr1:145789261
|
C | A | 60 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.103-295G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145789261 | ||||||
chr1:145789475
|
G | A | 60 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.103-509C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145789475 | ||||||
chr1:145789545
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.103-579A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145789545 | ||||||
chr1:145789700
|
C | CT | 24 | a0001c0001t0001g0063a0001c0001t0001g0092a0001c0001t0001g0104others(21): Show | 24 | HG00741.hp2 HG01106.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.103-735dupA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145789700 | ||||||
chr1:145789700
|
CT | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0082a0001c0001t0004g0112others(2): Show | 5 | HG00099.hp1 HG01256.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-735delA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145789700 | ||||||
chr1:145789700
|
CTTTTTTT | C | 56 | a0001c0001t0003g0210a0001c0001t0003g0214a0001c0001t0003g0215others(53): Show | 56 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.103-741_103-735del others(7): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145789700 | ||||||
chr1:145789700
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0044 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.103-746_103-735del others(12): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145789700 | ||||||
chr1:145789798
|
C | T | 1 | a0001c0001t0002g0133 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.103-832G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145789798 | ||||||
chr1:145789995
|
G | C | 1 | a0001c0001t0003g0258 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.103-1029C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145789995 | ||||||
chr1:145790000
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.103-1034C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145790000 | ||||||
chr1:145790097
|
G | A | 60 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.103-1131C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145790097 | ||||||
chr1:145790620
|
C | T | 3 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131 | 3 | HG02922.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.103-1654G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145790620 | ||||||
chr1:145790621
|
G | A | 5 | a0001c0001t0001g0038a0001c0001t0025g0029a0001c0001t0058g0262others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-1655C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145790621 | ||||||
chr1:145790870
|
G | A | 134 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(131): Show | 135 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.103-1904C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145790870 | ||||||
chr1:145790879
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(127): Show | 131 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.103-1913G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145790879 | ||||||
chr1:145790907
|
T | C | 218 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.103-1941A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145790907 | ||||||
chr1:145791121
|
G | A | 1 | a0001c0001t0067g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.103-2155C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145791121 | ||||||
chr1:145791136
|
T | C | 134 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(131): Show | 135 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.103-2170A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145791136 | ||||||
chr1:145791262
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.103-2296G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145791262 | ||||||
chr1:145791350
|
T | TA | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(203): Show | 207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.103-2385dupT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145791350 | ||||||
chr1:145791350
|
T | TAA | 6 | a0001c0001t0003g0233a0001c0001t0033g0198a0001c0001t0038g0196others(3): Show | 6 | HG02071.hp1 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-2386_103-2385d others(4): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145791350 | ||||||
chr1:145791468
|
C | T | 3 | a0001c0001t0007g0184a0001c0001t0007g0193a0001c0001t0007g0201 | 3 | HG03225.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.103-2502G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145791468 | ||||||
chr1:145791469
|
G | GCCATTGC others(4): Show |
1 | a0001c0001t0003g0211 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.103-2514_103-2504d others(13): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145791469 | ||||||
chr1:145791509
|
C | T | 212 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(209): Show | 213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.103-2543G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145791509 | ||||||
chr1:145791512
|
C | CA | 7 | a0001c0001t0001g0125a0001c0001t0033g0198a0001c0001t0034g0186others(4): Show | 7 | HG02572.hp1 HG02818.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-2547dupT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145791512 | ||||||
chr1:145791525
|
A | C | 2 | a0001c0001t0001g0061a0001c0001t0054g0114 | 2 | HG01257.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.103-2559T>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145791525 | ||||||
chr1:145791533
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.103-2567T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145791533 | ||||||
chr1:145791628
|
G | A | 2 | a0001c0001t0004g0110a0001c0001t0004g0117 | 2 | NA18946.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.103-2662C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145791628 | ||||||
chr1:145791699
|
T | C | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.103-2733A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145791699 | ||||||
chr1:145792007
|
C | G | 5 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-3041G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145792007 | ||||||
chr1:145792197
|
C | T | 1 | a0001c0001t0020g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.103-3231G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145792197 | ||||||
chr1:145792297
|
T | C | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.103-3331A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145792297 | ||||||
chr1:145792451
|
G | A | 1 | a0001c0001t0063g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.103-3485C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145792451 | ||||||
chr1:145792686
|
A | G | 1 | a0001c0001t0003g0227 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.103-3720T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145792686 | ||||||
chr1:145792994
|
G | A | 3 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131 | 3 | HG02922.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.103-4028C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145792994 | ||||||
chr1:145793001
|
G | A | 1 | a0001c0001t0005g0075 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.103-4035C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145793001 | ||||||
chr1:145793044
|
C | T | 5 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0040others(2): Show | 5 | NA18939.hp1 NA18964.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-4078G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145793044 | ||||||
chr1:145793195
|
A | G | 212 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(209): Show | 213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.103-4229T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145793195 | ||||||
chr1:145793367
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.103-4401C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145793367 | ||||||
chr1:145793547
|
G | T | 1 | a0001c0001t0001g0080 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.103-4581C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145793547 | ||||||
chr1:145793626
|
T | TCA | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(129): Show | 133 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.103-4662_103-4661d others(4): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145793626 | ||||||
chr1:145793658
|
A | G | 1 | a0001c0001t0002g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.103-4692T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145793658 | ||||||
chr1:145793685
|
G | A | 218 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.103-4719C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145793685 | ||||||
chr1:145793780
|
C | T | 3 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267 | 3 | HG02615.hp1 HG02895.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.103-4814G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145793780 | ||||||
chr1:145793842
|
C | CT | 29 | a0001c0001t0001g0067a0001c0001t0001g0092a0001c0001t0001g0119others(26): Show | 29 | HG01106.hp2 HG01361.hp2 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.103-4877dupA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145793842 | ||||||
chr1:145793842
|
CT | C | 6 | a0001c0001t0001g0082a0001c0001t0002g0136a0001c0001t0003g0222others(3): Show | 6 | HG01256.hp2 HG02965.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-4877delA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145793842 | ||||||
chr1:145793962
|
G | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0011 | 2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.103-4996C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145793962 | ||||||
chr1:145793970
|
A | C | 1 | a0001c0001t0001g0120 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.103-5004T>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145793970 | ||||||
chr1:145794004
|
C | T | 18 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.103-5038G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794004 | ||||||
chr1:145794487
|
G | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(125): Show | 129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.103-5521C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794487 | ||||||
chr1:145794491
|
C | G | 2 | a0001c0001t0002g0133a0001c0001t0002g0142 | 2 | NA18747.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.103-5525G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794491 | ||||||
chr1:145794502
|
C | CT | 42 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0042others(39): Show | 42 | HG00323.hp1 HG00323.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.103-5537dupA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794502 | ||||||
chr1:145794502
|
C | CTT | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0003g0210others(57): Show | 60 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.103-5538_103-5537d others(4): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794502 | ||||||
chr1:145794502
|
C | CTTT | 5 | a0001c0001t0003g0232a0001c0001t0003g0234a0001c0001t0003g0255others(2): Show | 5 | HG01175.hp1 HG01255.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-5539_103-5537d others(5): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794502 | ||||||
chr1:145794502
|
CT | C | 8 | a0001c0001t0001g0082a0001c0001t0001g0120a0001c0001t0005g0076others(5): Show | 8 | HG01256.hp2 HG02896.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.103-5537delA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794502 | ||||||
chr1:145794549
|
G | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.103-5583C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794549 | ||||||
chr1:145794586
|
A | G | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.103-5620T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794586 | ||||||
chr1:145794653
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.103-5687C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794653 | ||||||
chr1:145794701
|
G | C | 5 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-5735C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794701 | ||||||
chr1:145794783
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.103-5817G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794783 | ||||||
chr1:145794831
|
C | T | 2 | a0001c0001t0018g0185a0001c0001t0018g0187 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103-5865G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794831 | ||||||
chr1:145794847
|
C | A | 1 | a0001c0001t0072g0228 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.103-5881G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794847 | ||||||
chr1:145794908
|
T | C | 2 | a0001c0001t0023g0122a0001c0002t0023g0124 | 2 | NA19070.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.103-5942A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794908 | ||||||
chr1:145794920
|
A | G | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.103-5954T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794920 | ||||||
chr1:145794944
|
G | C | 1 | a0001c0001t0006g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.103-5978C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794944 | ||||||
chr1:145794979
|
C | T | 1 | a0001c0001t0066g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.103-6013G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145794979 | ||||||
chr1:145795016
|
C | CAA | 52 | a0001c0001t0003g0210a0001c0001t0003g0215a0001c0001t0003g0216others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.103-6052_103-6051d others(4): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795016 | ||||||
chr1:145795016
|
C | CAAA | 8 | a0001c0001t0003g0214a0001c0001t0003g0234a0001c0001t0003g0241others(5): Show | 8 | HG00673.hp2 HG01175.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.103-6053_103-6051d others(5): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795016 | ||||||
chr1:145795016
|
CA | C | 8 | a0001c0001t0001g0008a0001c0001t0001g0046a0001c0001t0001g0080others(5): Show | 8 | HG01099.hp1 HG01255.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.103-6051delT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795016 | ||||||
chr1:145795038
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103-6072C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795038 | ||||||
chr1:145795040
|
T | G | 1 | a0001c0001t0001g0125 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103-6074A>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795040 | ||||||
chr1:145795042
|
G | T | 1 | a0001c0001t0001g0125 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103-6076C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795042 | ||||||
chr1:145795283
|
G | A | 1 | a0001c0001t0003g0231 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.103-6317C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795283 | ||||||
chr1:145795343
|
A | G | 221 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.103-6377T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795343 | ||||||
chr1:145795346
|
C | T | 3 | a0001c0001t0005g0001a0001c0001t0005g0078a0001c0001t0005g0105 | 4 | HG01516.hp1 HG01517.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-6380G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795346 | ||||||
chr1:145795449
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.103-6483G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795449 | ||||||
chr1:145795480
|
T | C | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.103-6514A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795480 | ||||||
chr1:145795549
|
C | T | 13 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(10): Show | 13 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.103-6583G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795549 | ||||||
chr1:145795555
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.103-6589A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795555 | ||||||
chr1:145795578
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.103-6612T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795578 | ||||||
chr1:145795644
|
G | T | 1 | a0001c0001t0067g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.103-6678C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795644 | ||||||
chr1:145795753
|
C | A | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.103-6787G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795753 | ||||||
chr1:145795829
|
C | T | 4 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131others(1): Show | 4 | HG02922.hp1 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-6863G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145795829 | ||||||
chr1:145796075
|
T | C | 1 | a0001c0001t0002g0141 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.103-7109A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145796075 | ||||||
chr1:145796082
|
C | T | 1 | a0001c0001t0066g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.103-7116G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145796082 | ||||||
chr1:145796428
|
CT | C | 207 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.103-7463delA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145796428 | ||||||
chr1:145796441
|
T | A | 1 | a0001c0001t0001g0125 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103-7475A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145796441 | ||||||
chr1:145796447
|
G | C | 1 | a0001c0001t0001g0125 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103-7481C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145796447 | ||||||
chr1:145796449
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103-7483G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145796449 | ||||||
chr1:145796453
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103-7487C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145796453 | ||||||
chr1:145796455
|
C | G | 1 | a0001c0001t0001g0125 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103-7489G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145796455 | ||||||
chr1:145796457
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.103-7491G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145796457 | ||||||
chr1:145796536
|
C | G | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.103-7570G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145796536 | ||||||
chr1:145796576
|
G | C | 1 | a0001c0001t0001g0018 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.103-7610C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145796576 | ||||||
chr1:145796588
|
T | C | 218 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.103-7622A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145796588 | ||||||
chr1:145796689
|
T | A | 3 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131 | 3 | HG02922.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.103-7723A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145796689 | ||||||
chr1:145797055
|
G | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(125): Show | 129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.103-8089C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145797055 | ||||||
chr1:145797106
|
A | G | 1 | a0001c0001t0020g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.103-8140T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145797106 | ||||||
chr1:145797300
|
T | C | 1 | a0001c0001t0041g0199 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.103-8334A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145797300 | ||||||
chr1:145797314
|
G | A | 2 | a0001c0001t0017g0252a0001c0001t0017g0254 | 2 | HG00639.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.103-8348C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145797314 | ||||||
chr1:145797636
|
T | C | 1 | a0001c0001t0020g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.103-8670A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145797636 | ||||||
chr1:145797836
|
C | T | 2 | a0001c0001t0027g0268a0001c0001t0027g0269 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.103-8870G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145797836 | ||||||
chr1:145797857
|
A | G | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0250 | 3 | HG03491.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.103-8891T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145797857 | ||||||
chr1:145797970
|
C | A | 2 | a0001c0001t0012g0129a0001c0001t0012g0130 | 2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.103-9004G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145797970 | ||||||
chr1:145798021
|
GTTCT | G | 5 | a0001c0001t0033g0198a0001c0001t0038g0196a0001c0001t0039g0195others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-9059_103-9056d others(6): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145798021 | ||||||
chr1:145798110
|
A | G | 5 | a0001c0001t0033g0198a0001c0001t0038g0196a0001c0001t0039g0195others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-9144T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145798110 | ||||||
chr1:145798170
|
G | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.103-9204C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145798170 | ||||||
chr1:145798318
|
C | A | 1 | a0001c0001t0001g0120 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.103-9352G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145798318 | ||||||
chr1:145798570
|
G | C | 1 | a0001c0001t0003g0258 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.103-9604C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145798570 | ||||||
chr1:145798844
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0004g0031a0001c0001t0004g0099 | 3 | HG02165.hp1 NA18949.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.103-9878C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145798844 | ||||||
chr1:145798852
|
C | T | 60 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.103-9886G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145798852 | ||||||
chr1:145799019
|
C | A | 2 | a0001c0001t0018g0185a0001c0001t0018g0187 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103-10053G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145799019 | ||||||
chr1:145799076
|
T | C | 13 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(10): Show | 13 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.103-10110A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145799076 | ||||||
chr1:145799608
|
G | A | 1 | a0001c0001t0026g0107 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.103-10642C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145799608 | ||||||
chr1:145799609
|
A | G | 1 | a0001c0001t0026g0107 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.103-10643T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145799609 | ||||||
chr1:145799669
|
C | T | 5 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-10703G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145799669 | ||||||
chr1:145799738
|
G | A | 5 | a0001c0001t0033g0198a0001c0001t0038g0196a0001c0001t0039g0195others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-10772C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145799738 | ||||||
chr1:145799741
|
C | T | 2 | a0001c0001t0006g0115a0001c0001t0066g0096 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.103-10775G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145799741 | ||||||
chr1:145799783
|
T | C | 1 | a0001c0001t0003g0223 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.103-10817A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145799783 | ||||||
chr1:145799842
|
C | T | 2 | a0001c0001t0032g0194a0001c0001t0051g0200 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.103-10876G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145799842 | ||||||
chr1:145799876
|
A | G | 218 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.103-10910T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145799876 | ||||||
chr1:145800069
|
T | G | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0250 | 3 | HG03491.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.103-11103A>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145800069 | ||||||
chr1:145800429
|
C | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(125): Show | 129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.103-11463G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145800429 | ||||||
chr1:145800588
|
A | G | 218 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.103-11622T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145800588 | ||||||
chr1:145800648
|
G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 4 | HG02129.hp2 NA18962.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-11682C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145800648 | ||||||
chr1:145800677
|
C | T | 3 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267 | 3 | HG02615.hp1 HG02895.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.103-11711G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145800677 | ||||||
chr1:145800740
|
G | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(127): Show | 131 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.103-11774C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145800740 | ||||||
chr1:145800898
|
A | G | 1 | a0001c0001t0002g0127 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.103-11932T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145800898 | ||||||
chr1:145800907
|
T | C | 3 | a0001c0001t0002g0127a0001c0001t0004g0037a0001c0003t0002g0270 | 3 | HG02074.hp1 HG02602.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.103-11941A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145800907 | ||||||
chr1:145800954
|
A | G | 2 | a0001c0001t0027g0268a0001c0001t0027g0269 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.103-11988T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145800954 | ||||||
chr1:145800967
|
G | A | 3 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131 | 3 | HG02922.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.103-12001C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145800967 | ||||||
chr1:145801155
|
G | A | 3 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267 | 3 | HG02615.hp1 HG02895.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.103-12189C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145801155 | ||||||
chr1:145801161
|
C | T | 1 | a0001c0001t0006g0115 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.103-12195G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145801161 | ||||||
chr1:145801337
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0024g0012others(1): Show | 4 | HG02896.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-12371C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145801337 | ||||||
chr1:145801355
|
G | C | 1 | a0001c0001t0001g0061 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.103-12389C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145801355 | ||||||
chr1:145801393
|
C | T | 1 | a0001c0001t0003g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.103-12427G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145801393 | ||||||
chr1:145801478
|
T | C | 1 | a0001c0001t0062g0052 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.103-12512A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145801478 | ||||||
chr1:145801718
|
A | G | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.103-12752T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145801718 | ||||||
chr1:145801891
|
G | A | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(126): Show | 130 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.103-12925C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145801891 | ||||||
chr1:145801970
|
T | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0028others(2): Show | 5 | HG02723.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-13004A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145801970 | ||||||
chr1:145801977
|
G | A | 1 | a0001c0001t0047g0151 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.103-13011C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145801977 | ||||||
chr1:145802074
|
C | T | 1 | a0001c0001t0067g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.103-13108G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145802074 | ||||||
chr1:145802195
|
C | G | 1 | a0001c0001t0038g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.103-13229G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145802195 | ||||||
chr1:145802298
|
C | G | 2 | a0001c0001t0002g0133a0001c0001t0002g0142 | 2 | NA18747.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.103-13332G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145802298 | ||||||
chr1:145802314
|
T | C | 1 | a0001c0001t0027g0269 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.103-13348A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145802314 | ||||||
chr1:145802375
|
G | C | 1 | a0001c0001t0002g0139 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.103-13409C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145802375 | ||||||
chr1:145802404
|
G | T | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.103-13438C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145802404 | ||||||
chr1:145802468
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.103-13502T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145802468 | ||||||
chr1:145802576
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.103-13610T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145802576 | ||||||
chr1:145802578
|
T | C | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.103-13612A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145802578 | ||||||
chr1:145802960
|
C | T | 1 | a0001c0001t0002g0145 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.103-13994G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145802960 | ||||||
chr1:145803129
|
A | G | 5 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131others(2): Show | 5 | HG02818.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-14163T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145803129 | ||||||
chr1:145803254
|
GT | G | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.103-14289delA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145803254 | ||||||
chr1:145803471
|
A | T | 1 | a0001c0001t0001g0106 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.103-14505T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145803471 | ||||||
chr1:145803983
|
G | A | 4 | a0001c0001t0018g0185a0001c0001t0018g0187a0001c0001t0032g0194others(1): Show | 4 | HG01884.hp1 HG03130.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-15017C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145803983 | ||||||
chr1:145804278
|
T | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.103-15312A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145804278 | ||||||
chr1:145804499
|
GCA | G | 19 | a0001c0001t0001g0046a0001c0001t0001g0085a0001c0001t0002g0148others(16): Show | 19 | HG01257.hp1 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.103-15535_103-1553 others(6): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145804499 | ||||||
chr1:145804499
|
GCACA | G | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(138): Show | 142 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.103-15537_103-1553 others(8): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145804499 | ||||||
chr1:145804499
|
GCACACA | G | 60 | a0001c0001t0001g0049a0001c0001t0003g0210a0001c0001t0003g0211others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.103-15539_103-1553 others(10): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145804499 | ||||||
chr1:145804537
|
A | G | 212 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(209): Show | 213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.103-15571T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145804537 | ||||||
chr1:145804546
|
A | T | 60 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.103-15580T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145804546 | ||||||
chr1:145804609
|
C | T | 13 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(10): Show | 13 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.103-15643G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145804609 | ||||||
chr1:145804971
|
C | G | 3 | a0001c0001t0002g0137a0001c0001t0002g0159a0001c0001t0002g0172 | 3 | HG01168.hp1 HG01169.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.103-16005G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145804971 | ||||||
chr1:145805047
|
A | T | 13 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(10): Show | 13 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.103-16081T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145805047 | ||||||
chr1:145805089
|
A | G | 8 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(5): Show | 8 | NA18940.hp2 NA18954.hp2 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-16123T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145805089 | ||||||
chr1:145805315
|
T | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.103-16349A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145805315 | ||||||
chr1:145805317
|
A | G | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.103-16351T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145805317 | ||||||
chr1:145805449
|
CA | C | 10 | a0001c0001t0018g0185a0001c0001t0018g0187a0001c0001t0030g0135others(7): Show | 10 | HG02572.hp1 HG02818.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.103-16484delT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145805449 | ||||||
chr1:145806273
|
G | A | 1 | a0001c0001t0061g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.103-17307C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145806273 | ||||||
chr1:145806689
|
C | T | 1 | a0001c0001t0063g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.102+17083G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145806689 | ||||||
chr1:145806875
|
G | A | 5 | a0001c0001t0005g0001a0001c0001t0005g0078a0001c0001t0005g0083others(2): Show | 6 | HG00733.hp1 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+16897C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145806875 | ||||||
chr1:145807110
|
C | T | 1 | a0001c0001t0067g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.102+16662G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145807110 | ||||||
chr1:145807375
|
G | A | 1 | a0001c0001t0003g0223 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.102+16397C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145807375 | ||||||
chr1:145807959
|
T | C | 1 | a0001c0001t0021g0128 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.102+15813A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145807959 | ||||||
chr1:145808023
|
G | C | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.102+15749C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145808023 | ||||||
chr1:145808056
|
CAT | C | 210 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.102+15714_102+1571 others(6): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145808056 | ||||||
chr1:145808197
|
G | A | 1 | a0001c0001t0043g0158 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.102+15575C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145808197 | ||||||
chr1:145808263
|
A | G | 1 | a0001c0001t0005g0113 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.102+15509T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145808263 | ||||||
chr1:145808303
|
T | A | 10 | a0001c0001t0003g0210a0001c0001t0003g0221a0001c0001t0003g0224others(7): Show | 10 | HG00738.hp1 HG01255.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.102+15469A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145808303 | ||||||
chr1:145808561
|
T | A | 5 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131others(2): Show | 5 | HG02818.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+15211A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145808561 | ||||||
chr1:145808861
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.102+14911T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145808861 | ||||||
chr1:145808904
|
G | T | 2 | a0001c0001t0068g0209a0001c0001t0069g0206 | 2 | NA18977.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.102+14868C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145808904 | ||||||
chr1:145808965
|
G | A | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(126): Show | 130 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.102+14807C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145808965 | ||||||
chr1:145809105
|
G | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.102+14667C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809105 | ||||||
chr1:145809183
|
A | AT | 5 | a0001c0001t0002g0139a0001c0001t0002g0165a0001c0001t0002g0166others(2): Show | 5 | HG01346.hp1 HG02165.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.102+14588dupA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809183 | ||||||
chr1:145809183
|
ATT | A | 9 | a0001c0001t0003g0211a0001c0001t0003g0215a0001c0001t0012g0129others(6): Show | 9 | HG01256.hp1 HG02258.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.102+14587_102+1458 others(6): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809183 | ||||||
chr1:145809183
|
ATTT | A | 73 | a0001c0001t0003g0210a0001c0001t0003g0214a0001c0001t0003g0216others(70): Show | 73 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.102+14586_102+1458 others(7): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809183 | ||||||
chr1:145809183
|
ATTTTT | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(128): Show | 132 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.102+14584_102+1458 others(9): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809183 | ||||||
chr1:145809488
|
A | ATT | 17 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(14): Show | 17 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.102+14282_102+1428 others(6): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809488 | ||||||
chr1:145809488
|
A | ATTTT | 46 | a0001c0001t0003g0214a0001c0001t0003g0215a0001c0001t0003g0216others(43): Show | 46 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.102+14280_102+1428 others(8): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809488 | ||||||
chr1:145809488
|
A | ATTTTT | 12 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0217others(9): Show | 12 | HG01123.hp1 HG01175.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.102+14279_102+1428 others(9): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809488 | ||||||
chr1:145809488
|
A | ATTTTTTT others(1): Show |
91 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(88): Show | 92 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.102+14276_102+1428 others(12): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809488 | ||||||
chr1:145809488
|
A | ATTTTTTT others(2): Show |
27 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0035others(24): Show | 27 | HG00438.hp1 HG00673.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.102+14275_102+1428 others(13): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809488 | ||||||
chr1:145809488
|
A | ATTTTTTT others(3): Show |
5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(2): Show | 5 | HG02895.hp1 HG02897.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+14274_102+1428 others(14): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809488 | ||||||
chr1:145809488
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0055g0093 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.102+14273_102+1428 others(15): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809488 | ||||||
chr1:145809488
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102+14272_102+1428 others(16): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809488 | ||||||
chr1:145809488
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0041g0199 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.102+14266_102+1428 others(22): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809488 | ||||||
chr1:145809488
|
A | ATTTTTTT others(12): Show |
1 | a0001c0001t0040g0197 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.102+14265_102+1428 others(23): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809488 | ||||||
chr1:145809488
|
A | ATTTTTTT others(13): Show |
1 | a0001c0001t0063g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.102+14264_102+1428 others(24): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809488 | ||||||
chr1:145809488
|
A | ATTTTTTT others(14): Show |
1 | a0001c0001t0038g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.102+14263_102+1428 others(25): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809488 | ||||||
chr1:145809488
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0039g0195 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.102+14283_102+1428 others(26): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809488 | ||||||
chr1:145809488
|
ATT | A | 5 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+14282_102+1428 others(6): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809488 | ||||||
chr1:145809557
|
C | T | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102+14215G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809557 | ||||||
chr1:145809609
|
A | G | 214 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.102+14163T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809609 | ||||||
chr1:145809954
|
G | A | 1 | a0001c0001t0017g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.102+13818C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145809954 | ||||||
chr1:145810060
|
G | A | 1 | a0001c0001t0024g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.102+13712C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145810060 | ||||||
chr1:145810411
|
C | T | 1 | a0001c0001t0009g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.102+13361G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145810411 | ||||||
chr1:145810557
|
C | G | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.102+13215G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145810557 | ||||||
chr1:145810640
|
C | T | 1 | a0001c0001t0004g0059 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.102+13132G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145810640 | ||||||
chr1:145810659
|
T | C | 1 | a0001c0001t0002g0174 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.102+13113A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145810659 | ||||||
chr1:145810664
|
A | G | 1 | a0001c0001t0021g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.102+13108T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145810664 | ||||||
chr1:145810696
|
G | A | 1 | a0001c0001t0006g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102+13076C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145810696 | ||||||
chr1:145810711
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.102+13061C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145810711 | ||||||
chr1:145810857
|
TTTTA | T | 5 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+12911_102+1291 others(8): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145810857 | ||||||
chr1:145810873
|
A | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0003g0242others(1): Show | 4 | HG00323.hp1 HG01928.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+12899T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145810873 | ||||||
chr1:145810877
|
T | A | 18 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.102+12895A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145810877 | ||||||
chr1:145810917
|
G | A | 1 | a0001c0001t0021g0128 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.102+12855C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145810917 | ||||||
chr1:145810935
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0025g0010 | 3 | HG03130.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.102+12837C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145810935 | ||||||
chr1:145811027
|
G | A | 2 | a0001c0001t0029g0084a0001c0001t0029g0088 | 2 | NA18962.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.102+12745C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811027 | ||||||
chr1:145811085
|
G | T | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.102+12687C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811085 | ||||||
chr1:145811181
|
T | C | 13 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(10): Show | 13 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.102+12591A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811181 | ||||||
chr1:145811259
|
C | T | 1 | a0001c0001t0053g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.102+12513G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811259 | ||||||
chr1:145811355
|
C | CA | 88 | a0001c0001t0001g0033a0001c0001t0001g0049a0001c0001t0001g0051others(85): Show | 88 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.102+12416dupT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811355 | ||||||
chr1:145811355
|
C | CAA | 12 | a0001c0001t0002g0150a0001c0001t0007g0189a0001c0001t0007g0191others(9): Show | 12 | HG01884.hp1 HG02055.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.102+12415_102+1241 others(6): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811355 | ||||||
chr1:145811651
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.102+12121T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811651 | ||||||
chr1:145811883
|
C | CA | 17 | a0001c0001t0002g0127a0001c0001t0002g0137a0001c0001t0002g0141others(14): Show | 17 | HG01106.hp2 HG01109.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.102+11888dupT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811883 | ||||||
chr1:145811883
|
CAAAAAA | C | 37 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0061others(34): Show | 38 | HG00558.hp2 HG00735.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.102+11883_102+1188 others(10): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811883 | ||||||
chr1:145811883
|
CAAAAAAA | C | 13 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0261others(10): Show | 13 | HG00741.hp1 HG01433.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.102+11882_102+1188 others(11): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811883 | ||||||
chr1:145811883
|
CAAAAAAA others(1): Show |
C | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(63): Show | 66 | HG00099.hp1 HG00438.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.102+11881_102+1188 others(12): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811883 | ||||||
chr1:145811899
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0041g0199 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.102+11862_102+1187 others(15): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811899 | ||||||
chr1:145811900
|
AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0011a0001c0001t0063g0264 | 2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.102+11862_102+1187 others(14): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811900 | ||||||
chr1:145811901
|
AAAAAAAA others(2): Show |
A | 13 | a0001c0001t0001g0054a0001c0001t0006g0055a0001c0001t0007g0193others(10): Show | 13 | HG02615.hp1 HG02818.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.102+11862_102+1187 others(13): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811901 | ||||||
chr1:145811901
|
AAAAAAAA others(4): Show |
A | 2 | a0001c0001t0033g0198a0001c0001t0040g0197 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.102+11860_102+1187 others(15): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811901 | ||||||
chr1:145811902
|
AAAAAAAA others(1): Show |
A | 6 | a0001c0001t0001g0056a0001c0001t0001g0090a0001c0001t0001g0101others(3): Show | 6 | HG00558.hp1 HG00673.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+11862_102+1186 others(12): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811902 | ||||||
chr1:145811906
|
A | T | 7 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0004g0110others(4): Show | 7 | HG00558.hp2 HG02129.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.102+11866T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811906 | ||||||
chr1:145811908
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0010g0203 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.102+11863_102+1186 others(28): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(16): Show |
3 | a0001c0001t0010g0202a0001c0001t0010g0204a0001c0001t0010g0205 | 3 | HG02723.hp2 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.102+11863_102+1186 others(27): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0003g0251 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.102+11863_102+1186 others(23): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0011g0208 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.102+11863_102+1186 others(25): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(9): Show |
3 | a0001c0001t0003g0258a0001c0001t0015g0218a0001c0001t0070g0249 | 3 | HG00323.hp2 HG00639.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.102+11863_102+1186 others(20): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0003g0233 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.102+11863_102+1186 others(22): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0011g0213 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.102+11863_102+1186 others(24): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(10): Show |
4 | a0001c0001t0003g0241a0001c0001t0003g0248a0001c0001t0003g0259others(1): Show | 4 | HG03669.hp2 HG04228.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+11863_102+1186 others(21): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(12): Show |
2 | a0001c0001t0011g0207a0001c0001t0011g0212 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.102+11863_102+1186 others(23): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0017g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.102+11863_102+1186 others(27): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(9): Show |
10 | a0001c0001t0003g0215a0001c0001t0003g0216a0001c0001t0003g0217others(7): Show | 10 | HG01123.hp1 HG01243.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.102+11863_102+1186 others(20): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0003g0211 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.102+11863_102+1186 others(22): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0028g0238 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.102+11863_102+1186 others(24): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0017g0252 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.102+11863_102+1186 others(28): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102+11863_102+1186 others(17): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(8): Show |
4 | a0001c0001t0003g0227a0001c0001t0015g0239a0001c0001t0016g0257others(1): Show | 4 | HG00099.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+11863_102+1186 others(19): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0003g0230 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.102+11863_102+1186 others(21): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0003g0245 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.102+11863_102+1186 others(23): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(9): Show |
10 | a0001c0001t0003g0214a0001c0001t0003g0223a0001c0001t0003g0224others(7): Show | 10 | HG00673.hp2 HG00733.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.102+11863_102+1186 others(20): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(11): Show |
3 | a0001c0001t0003g0210a0001c0001t0003g0244a0001c0001t0016g0260 | 3 | HG01496.hp1 HG02300.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.102+11863_102+1186 others(22): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(12): Show |
3 | a0001c0001t0003g0221a0001c0001t0003g0234a0001c0001t0003g0253 | 3 | HG00323.hp1 HG00738.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.102+11863_102+1186 others(23): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAAAA others(9): Show |
4 | a0001c0001t0003g0222a0001c0001t0003g0242a0001c0001t0003g0243others(1): Show | 4 | HG00735.hp1 HG01928.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+11863_102+1186 others(20): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAAATA others(9): Show |
1 | a0001c0001t0069g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.102+11863_102+1186 others(20): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | AAAAATAT others(10): Show |
1 | a0001c0001t0068g0209 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.102+11863_102+1186 others(21): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811908
|
A | T | 53 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0033others(50): Show | 54 | HG00558.hp2 HG00735.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.102+11864T>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811908 | ||||||
chr1:145811910
|
T | A | 37 | a0001c0001t0002g0127a0001c0001t0002g0132a0001c0001t0002g0133others(34): Show | 37 | HG00438.hp2 HG00741.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.102+11862A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811910 | ||||||
chr1:145811912
|
T | A | 6 | a0001c0001t0002g0132a0001c0001t0002g0138a0001c0001t0002g0141others(3): Show | 6 | HG00438.hp2 HG03453.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+11860A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811912 | ||||||
chr1:145811914
|
T | A | 1 | a0001c0001t0002g0141 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.102+11858A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811914 | ||||||
chr1:145811932
|
T | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0002g0141others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.102+11840A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811932 | ||||||
chr1:145811934
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0021g0178 | 2 | HG02818.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.102+11838G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145811934 | ||||||
chr1:145812072
|
C | T | 19 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0001t0007g0184others(16): Show | 19 | HG00323.hp2 HG01123.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.102+11700G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145812072 | ||||||
chr1:145812135
|
T | C | 7 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0001t0005g0006others(4): Show | 7 | HG00323.hp2 HG01123.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+11637A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145812135 | ||||||
chr1:145812186
|
A | G | 6 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0001t0015g0218others(3): Show | 6 | HG00323.hp2 HG01123.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+11586T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145812186 | ||||||
chr1:145812339
|
T | C | 16 | a0001c0001t0002g0176a0001c0001t0003g0216a0001c0001t0003g0217others(13): Show | 16 | HG00323.hp2 HG00558.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.102+11433A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145812339 | ||||||
chr1:145812417
|
G | C | 1 | a0001c0001t0048g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.102+11355C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145812417 | ||||||
chr1:145812432
|
C | T | 13 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(10): Show | 13 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.102+11340G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145812432 | ||||||
chr1:145812615
|
G | A | 13 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(10): Show | 13 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.102+11157C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145812615 | ||||||
chr1:145812638
|
T | C | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102+11134A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145812638 | ||||||
chr1:145812661
|
C | CA | 139 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(136): Show | 140 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.102+11110dupT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145812661 | ||||||
chr1:145812670
|
AC | A | 14 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(11): Show | 14 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.102+11101delG | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145812670 | ||||||
chr1:145812671
|
C | A | 199 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.102+11101G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145812671 | ||||||
chr1:145812818
|
G | A | 1 | a0001c0001t0016g0260 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.102+10954C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145812818 | ||||||
chr1:145812834
|
T | G | 134 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(131): Show | 135 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.102+10938A>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145812834 | ||||||
chr1:145812861
|
T | C | 199 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.102+10911A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145812861 | ||||||
chr1:145813022
|
T | TA | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.102+10749dupT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145813022 | ||||||
chr1:145813110
|
T | C | 3 | a0001c0001t0001g0061a0001c0001t0008g0089a0001c0001t0054g0114 | 3 | HG01106.hp1 HG01257.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.102+10662A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145813110 | ||||||
chr1:145813223
|
C | T | 1 | a0001c0001t0003g0251 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.102+10549G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145813223 | ||||||
chr1:145813384
|
C | T | 1 | a0001c0001t0013g0097 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.102+10388G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145813384 | ||||||
chr1:145813701
|
C | T | 2 | a0001c0001t0002g0134a0001c0001t0002g0145 | 2 | NA18939.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.102+10071G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145813701 | ||||||
chr1:145813785
|
T | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(126): Show | 130 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.102+9987A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145813785 | ||||||
chr1:145813973
|
C | A | 219 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.102+9799G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145813973 | ||||||
chr1:145814236
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.102+9536C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145814236 | ||||||
chr1:145814306
|
T | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.102+9466A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145814306 | ||||||
chr1:145814338
|
C | G | 1 | a0001c0001t0001g0106 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.102+9434G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145814338 | ||||||
chr1:145814456
|
A | G | 218 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.102+9316T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145814456 | ||||||
chr1:145814525
|
G | A | 1 | a0001c0001t0067g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.102+9247C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145814525 | ||||||
chr1:145814532
|
G | A | 1 | a0001c0001t0067g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.102+9240C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145814532 | ||||||
chr1:145814542
|
C | T | 1 | a0001c0001t0003g0259 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.102+9230G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145814542 | ||||||
chr1:145814850
|
A | G | 1 | a0001c0001t0002g0181 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.102+8922T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145814850 | ||||||
chr1:145814938
|
T | C | 1 | a0001c0001t0016g0257 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.102+8834A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145814938 | ||||||
chr1:145814943
|
AC | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(125): Show | 129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.102+8828delG | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145814943 | ||||||
chr1:145815170
|
C | T | 2 | a0001c0001t0027g0268a0001c0001t0027g0269 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.102+8602G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145815170 | ||||||
chr1:145815210
|
T | A | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102+8562A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145815210 | ||||||
chr1:145815336
|
C | T | 2 | a0001c0001t0002g0141a0001c0001t0002g0183 | 2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.102+8436G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145815336 | ||||||
chr1:145815560
|
A | G | 1 | a0001c0001t0067g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.102+8212T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145815560 | ||||||
chr1:145815595
|
G | A | 1 | a0001c0001t0020g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.102+8177C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145815595 | ||||||
chr1:145815613
|
A | G | 4 | a0001c0001t0002g0133a0001c0001t0002g0142a0001c0001t0002g0143others(1): Show | 4 | NA18747.hp2 NA18965.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+8159T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145815613 | ||||||
chr1:145815617
|
C | T | 64 | a0001c0001t0001g0106a0001c0001t0001g0118a0001c0001t0003g0210others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.102+8155G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145815617 | ||||||
chr1:145815672
|
A | C | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102+8100T>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145815672 | ||||||
chr1:145815672
|
A | G | 1 | a0001c0001t0005g0109 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.102+8100T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145815672 | ||||||
chr1:145815682
|
C | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(125): Show | 129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.102+8090G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145815682 | ||||||
chr1:145815815
|
G | A | 4 | a0001c0001t0010g0202a0001c0001t0010g0203a0001c0001t0010g0204others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+7957C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145815815 | ||||||
chr1:145815976
|
C | G | 7 | a0001c0001t0002g0141a0001c0001t0012g0129a0001c0001t0012g0130others(4): Show | 7 | HG02818.hp1 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+7796G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145815976 | ||||||
chr1:145816030
|
A | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0002g0139others(3): Show | 6 | HG02165.hp2 HG02280.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+7742T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816030 | ||||||
chr1:145816070
|
G | GT | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(121): Show | 125 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.102+7701dupA | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816070 | ||||||
chr1:145816070
|
G | GTT | 91 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0023others(88): Show | 91 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.102+7700_102+7701d others(4): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816070 | ||||||
chr1:145816070
|
G | GTTT | 6 | a0001c0001t0003g0216a0001c0001t0003g0219a0001c0001t0003g0220others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+7699_102+7701d others(5): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816070 | ||||||
chr1:145816070
|
G | GTTTT | 5 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG00099.hp1 HG01099.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+7698_102+7701d others(6): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816070 | ||||||
chr1:145816099
|
C | T | 58 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(55): Show | 58 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.102+7673G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816099 | ||||||
chr1:145816122
|
C | T | 1 | a0001c0001t0002g0140 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.102+7650G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816122 | ||||||
chr1:145816162
|
A | C | 69 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(66): Show | 69 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.102+7610T>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816162 | ||||||
chr1:145816187
|
G | A | 1 | a0001c0001t0005g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.102+7585C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816187 | ||||||
chr1:145816300
|
T | C | 4 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0021g0128others(1): Show | 4 | HG02818.hp1 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+7472A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816300 | ||||||
chr1:145816371
|
C | T | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.102+7401G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816371 | ||||||
chr1:145816405
|
G | A | 2 | a0001c0001t0007g0191a0001c0001t0007g0192 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.102+7367C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816405 | ||||||
chr1:145816436
|
T | C | 2 | a0001c0001t0018g0185a0001c0001t0018g0187 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.102+7336A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816436 | ||||||
chr1:145816725
|
CTTTCTT | C | 42 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0067others(39): Show | 43 | HG00438.hp1 HG00733.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.102+7041_102+7046d others(8): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816725 | ||||||
chr1:145816727
|
T | C | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0104 | 3 | HG01175.hp2 HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.102+7045A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816727 | ||||||
chr1:145816730
|
TTTTTCTT others(9): Show |
T | 1 | a0001c0001t0018g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.102+7026_102+7041d others(18): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816730 | ||||||
chr1:145816959
|
A | G | 1 | a0001c0001t0006g0115 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.102+6813T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145816959 | ||||||
chr1:145817077
|
G | A | 7 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0125others(4): Show | 7 | NA18940.hp2 NA18973.hp1 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+6695C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145817077 | ||||||
chr1:145817098
|
T | C | 3 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131 | 3 | HG02922.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.102+6674A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145817098 | ||||||
chr1:145817306
|
G | C | 63 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0003g0210others(60): Show | 63 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.102+6466C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145817306 | ||||||
chr1:145817432
|
G | A | 2 | a0001c0001t0027g0268a0001c0001t0027g0269 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.102+6340C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145817432 | ||||||
chr1:145817480
|
T | C | 5 | a0001c0001t0033g0198a0001c0001t0038g0196a0001c0001t0039g0195others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.102+6292A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145817480 | ||||||
chr1:145817518
|
A | G | 6 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0001t0015g0218others(3): Show | 6 | HG00323.hp2 HG01123.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+6254T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145817518 | ||||||
chr1:145817566
|
G | A | 1 | a0001c0001t0006g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102+6206C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145817566 | ||||||
chr1:145817656
|
C | T | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.102+6116G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145817656 | ||||||
chr1:145817693
|
C | T | 1 | a0001c0001t0056g0002 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.102+6079G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145817693 | ||||||
chr1:145817780
|
G | A | 3 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131 | 3 | HG02922.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.102+5992C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145817780 | ||||||
chr1:145817830
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.102+5942C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145817830 | ||||||
chr1:145817927
|
G | A | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(124): Show | 128 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.102+5845C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145817927 | ||||||
chr1:145817979
|
T | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.102+5793A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145817979 | ||||||
chr1:145818142
|
G | C | 1 | a0001c0001t0012g0131 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.102+5630C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145818142 | ||||||
chr1:145818162
|
T | C | 3 | a0001c0001t0003g0258a0001c0001t0007g0193a0001c0001t0021g0128 | 3 | HG00639.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.102+5610A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145818162 | ||||||
chr1:145818225
|
G | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(125): Show | 129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.102+5547C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145818225 | ||||||
chr1:145818270
|
A | G | 3 | a0001c0001t0003g0214a0001c0001t0003g0215a0001c0001t0055g0093 | 3 | HG00673.hp2 NA18964.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.102+5502T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145818270 | ||||||
chr1:145818344
|
G | A | 5 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+5428C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145818344 | ||||||
chr1:145818411
|
C | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(125): Show | 129 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.102+5361G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145818411 | ||||||
chr1:145818598
|
G | A | 2 | a0001c0001t0002g0168a0001c0001t0002g0177 | 2 | HG00741.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.102+5174C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145818598 | ||||||
chr1:145818671
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.102+5101A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145818671 | ||||||
chr1:145819135
|
G | T | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(118): Show | 122 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.102+4637C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145819135 | ||||||
chr1:145819271
|
C | CA | 16 | a0001c0001t0002g0127a0001c0001t0002g0132a0001c0001t0002g0133others(13): Show | 16 | HG00438.hp2 HG00741.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.102+4500dupT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145819271 | ||||||
chr1:145819271
|
CA | C | 19 | a0001c0001t0002g0134a0001c0001t0002g0136a0001c0001t0002g0137others(16): Show | 19 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.102+4500delT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145819271 | ||||||
chr1:145819271
|
CAA | C | 71 | a0001c0001t0001g0014a0001c0001t0001g0095a0001c0001t0001g0100others(68): Show | 71 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.102+4499_102+4500d others(4): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145819271 | ||||||
chr1:145819271
|
CAAA | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(102): Show | 106 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.102+4498_102+4500d others(5): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145819271 | ||||||
chr1:145819271
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0012g0129a0001c0001t0012g0130 | 2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.102+4489_102+4500d others(14): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145819271 | ||||||
chr1:145819271
|
CAAAAAAA others(6): Show |
C | 10 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(7): Show | 10 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.102+4488_102+4500d others(15): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145819271 | ||||||
chr1:145819271
|
CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0018g0185a0001c0001t0018g0187a0001c0001t0034g0186 | 3 | HG03130.hp1 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.102+4487_102+4500d others(16): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145819271 | ||||||
chr1:145819271
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0049g0237 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.102+4485_102+4500d others(18): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145819271 | ||||||
chr1:145819401
|
G | A | 1 | a0001c0001t0005g0113 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.102+4371C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145819401 | ||||||
chr1:145819575
|
A | C | 5 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+4197T>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145819575 | ||||||
chr1:145820033
|
A | G | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(134): Show | 138 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.102+3739T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145820033 | ||||||
chr1:145820140
|
G | A | 5 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131others(2): Show | 5 | HG02818.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+3632C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145820140 | ||||||
chr1:145820142
|
T | C | 1 | a0001c0001t0054g0114 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.102+3630A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145820142 | ||||||
chr1:145820338
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0009g0016a0001c0001t0009g0017 | 3 | NA18983.hp2 NA18986.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.102+3434T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145820338 | ||||||
chr1:145820452
|
A | G | 18 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.102+3320T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145820452 | ||||||
chr1:145820467
|
C | T | 1 | a0001c0001t0017g0235 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.102+3305G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145820467 | ||||||
chr1:145820468
|
A | G | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(135): Show | 139 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.102+3304T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145820468 | ||||||
chr1:145820612
|
T | C | 1 | a0001c0001t0032g0194 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.102+3160A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145820612 | ||||||
chr1:145820623
|
C | G | 199 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.102+3149G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145820623 | ||||||
chr1:145820635
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.102+3137G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145820635 | ||||||
chr1:145820637
|
G | A | 59 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.102+3135C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145820637 | ||||||
chr1:145820685
|
G | A | 4 | a0001c0001t0010g0202a0001c0001t0010g0203a0001c0001t0010g0204others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+3087C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145820685 | ||||||
chr1:145820869
|
T | C | 60 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.102+2903A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145820869 | ||||||
chr1:145821016
|
T | C | 18 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.102+2756A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821016 | ||||||
chr1:145821061
|
T | C | 18 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.102+2711A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821061 | ||||||
chr1:145821150
|
C | T | 1 | a0001c0001t0006g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.102+2622G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821150 | ||||||
chr1:145821191
|
T | C | 5 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131others(2): Show | 5 | HG02818.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+2581A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821191 | ||||||
chr1:145821289
|
T | C | 66 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(63): Show | 66 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.102+2483A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821289 | ||||||
chr1:145821371
|
T | C | 70 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(67): Show | 70 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.102+2401A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821371 | ||||||
chr1:145821457
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0003g0258a0001c0001t0016g0257 | 2 | HG00639.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.102+2303_102+2314d others(14): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821457 | ||||||
chr1:145821457
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0071g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.102+2302_102+2314d others(15): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821457 | ||||||
chr1:145821457
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0010g0204a0001c0001t0010g0205 | 2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.102+2300_102+2314d others(17): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821457 | ||||||
chr1:145821457
|
C | CTTTTTTT others(9): Show |
23 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0003g0243others(20): Show | 23 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.102+2299_102+2314d others(18): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821457 | ||||||
chr1:145821457
|
C | CTTTTTTT others(10): Show |
21 | a0001c0001t0003g0214a0001c0001t0003g0215a0001c0001t0003g0216others(18): Show | 21 | HG00323.hp2 HG00673.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.102+2298_102+2314d others(19): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821457 | ||||||
chr1:145821457
|
C | CTTTTTTT others(11): Show |
4 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0011g0212others(1): Show | 4 | HG02300.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+2297_102+2314d others(20): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821457 | ||||||
chr1:145821457
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0068g0209 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.102+2295_102+2314d others(22): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821457 | ||||||
chr1:145821457
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0011g0208 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.102+2293_102+2314d others(24): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821457 | ||||||
chr1:145821457
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0011g0207 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.102+2290_102+2314d others(27): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821457 | ||||||
chr1:145821457
|
CTT | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0119others(5): Show | 8 | HG01169.hp1 HG02258.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+2313_102+2314d others(4): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821457 | ||||||
chr1:145821457
|
CTTT | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0018others(132): Show | 136 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.102+2312_102+2314d others(5): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821457 | ||||||
chr1:145821457
|
CTTTT | C | 6 | a0001c0001t0006g0115a0001c0001t0007g0201a0001c0001t0051g0200others(3): Show | 6 | HG02083.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+2311_102+2314d others(6): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821457 | ||||||
chr1:145821491
|
G | A | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102+2281C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821491 | ||||||
chr1:145821687
|
C | T | 1 | a0001c0001t0069g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.102+2085G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821687 | ||||||
chr1:145821851
|
C | T | 1 | a0001c0001t0067g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.102+1921G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821851 | ||||||
chr1:145821915
|
G | A | 218 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.102+1857C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145821915 | ||||||
chr1:145822253
|
G | A | 1 | a0001c0001t0073g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102+1519C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145822253 | ||||||
chr1:145822259
|
T | C | 1 | a0001c0001t0077g0271 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.102+1513A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145822259 | ||||||
chr1:145822313
|
CA | C | 210 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.102+1458delT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145822313 | ||||||
chr1:145822481
|
G | T | 4 | a0001c0001t0010g0202a0001c0001t0010g0203a0001c0001t0010g0204others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+1291C>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145822481 | ||||||
chr1:145822513
|
T | A | 1 | a0001c0001t0001g0118 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.102+1259A>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145822513 | ||||||
chr1:145822540
|
C | G | 60 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0214others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.102+1232G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145822540 | ||||||
chr1:145822575
|
ACATT | A | 18 | a0001c0001t0007g0184a0001c0001t0007g0189a0001c0001t0007g0191others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.102+1193_102+1196d others(6): Show |
RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145822575 | ||||||
chr1:145822673
|
T | C | 3 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0020g0182 | 3 | NA18949.hp1 NA18969.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.102+1099A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145822673 | ||||||
chr1:145822702
|
C | G | 5 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+1070G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145822702 | ||||||
chr1:145822717
|
T | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(150): Show | 154 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.102+1055A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145822717 | ||||||
chr1:145822949
|
G | C | 1 | a0001c0001t0067g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.102+823C>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145822949 | ||||||
chr1:145823052
|
C | A | 8 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(5): Show | 8 | NA18940.hp2 NA18954.hp2 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+720G>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145823052 | ||||||
chr1:145823147
|
T | C | 187 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.102+625A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145823147 | ||||||
chr1:145823185
|
T | C | 1 | a0001c0001t0067g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.102+587A>G | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145823185 | ||||||
chr1:145823307
|
C | T | 4 | a0001c0001t0012g0129a0001c0001t0012g0130a0001c0001t0012g0131others(1): Show | 4 | HG02922.hp1 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+465G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145823307 | ||||||
chr1:145823504
|
C | G | 1 | a0001c0001t0002g0127 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.102+268G>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145823504 | ||||||
chr1:145823508
|
GA | G | 126 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(123): Show | 127 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.102+263delT | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145823508 | ||||||
chr1:145823537
|
A | G | 2 | a0001c0001t0005g0006a0001c0001t0037g0007 | 2 | HG01346.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.102+235T>C | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145823537 | ||||||
chr1:145823657
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0056g0002others(1): Show | 4 | HG00741.hp1 HG02145.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+115G>A | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145823657 | ||||||
chr1:145823714
|
G | A | 6 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0014g0267others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+58C>T | RNF115 | ENSG00000265491.5 | transcript | ENST00000582693.5 | protein_coding | 1/8 | chr1 | 145823714 |