geneid | 5981 |
---|---|
ensemblid | ENSG00000035928.17 |
hgncid | 9969 |
symbol | RFC1 |
name | replication factor C subunit 1 |
refseq_nuc | NM_002913.5 |
refseq_prot | NP_002904.3 |
ensembl_nuc | ENST00000349703.7 |
ensembl_prot | ENSP00000261424.4 |
mane_status | MANE Select |
chr | chr4 |
start | 39287456 |
end | 39366362 |
strand | - |
ver | v1.2 |
region | chr4:39287456-39366362 |
region5000 | chr4:39282456-39371362 |
regionname0 | RFC1_chr4_39287456_39366362 |
regionname5000 | RFC1_chr4_39282456_39371362 |
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 | 1147 | 261 | 70 | 52 | 103 | 8 | 26 | 79 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0002 | 0/0 | 1147 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0003 | 0/0 | 1147 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0004 | 0/0 | 1147 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0005 | 0/0 | 75 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0006 | 0/0 | 1147 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
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 | 1/0 | 3444 | 102 | 41 | 16 | 31 | 4 | 9 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
c0002 | 0/1 | 3444 | 95 | 2 | 27 | 50 | 4 | 11 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
c0003 | 0/0 | 3444 | 32 | 2 | 5 | 20 | 0 | 5 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
c0004 | 0/0 | 3444 | 26 | 22 | 4 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
c0005 | 0/0 | 3444 | 6 | 6 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
c0006 | 0/0 | 3444 | 5 | 5 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
c0007 | 0/0 | 3444 | 3 | 0 | 0 | 2 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
c0008 | 0/0 | 3444 | 2 | 2 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
c0009 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
c0010 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
c0011 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
c0012 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
c0013 | 0/0 | 3434 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
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 | 1427 | 151 | 58 | 23 | 52 | 4 | 14 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
t0002 | 0/1 | 1427 | 95 | 2 | 26 | 50 | 4 | 12 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
t0003 | 1/0 | 1427 | 14 | 13 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
t0004 | 0/0 | 1427 | 6 | 4 | 2 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
t0005 | 0/0 | 1427 | 2 | 2 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
t0006 | 0/0 | 1427 | 2 | 2 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
t0007 | 0/0 | 1427 | 2 | 2 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
t0008 | 0/0 | 1427 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
t0009 | 0/0 | 1427 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
t0010 | 0/0 | 1427 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
t0011 | 0/0 | 1427 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
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 | 2 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
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 | 1/0 | 3444 | 102 | 41 | 16 | 31 | 4 | 9 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0002 | 0/1 | 3444 | 95 | 2 | 27 | 50 | 4 | 11 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0003 | 0/0 | 3444 | 32 | 2 | 5 | 20 | 0 | 5 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0004 | 0/0 | 3444 | 26 | 22 | 4 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0007 | 0/0 | 3444 | 3 | 0 | 0 | 2 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0010 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0011 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0012 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0002c0005 | 0/0 | 3444 | 6 | 6 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0003c0006 | 0/0 | 3444 | 5 | 5 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0004c0008 | 0/0 | 3444 | 2 | 2 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0005c0013 | 0/0 | 3434 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0006c0009 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4870 | 82 | 24 | 16 | 29 | 4 | 9 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0001t0002 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0001t0003 | 1/0 | 4870 | 13 | 12 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0001t0005 | 0/0 | 4870 | 2 | 2 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0001t0007 | 0/0 | 4870 | 2 | 2 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0001t0008 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0001t0011 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0002t0001 | 0/0 | 4870 | 2 | 0 | 0 | 2 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0002t0002 | 0/1 | 4870 | 91 | 2 | 26 | 47 | 4 | 11 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0002t0009 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0002t0010 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0003t0001 | 0/0 | 4870 | 32 | 2 | 5 | 20 | 0 | 5 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0004t0001 | 0/0 | 4870 | 19 | 17 | 2 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0004t0004 | 0/0 | 4870 | 6 | 4 | 2 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0004t0006 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0007t0002 | 0/0 | 4870 | 3 | 0 | 0 | 2 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0010t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0011t0006 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0001c0012t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0002c0005t0001 | 0/0 | 4870 | 6 | 6 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0003c0006t0001 | 0/0 | 4870 | 5 | 5 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0004c0008t0001 | 0/0 | 4870 | 2 | 2 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0005c0013t0001 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
a0006c0009t0003 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | copy fasta | chr4 | 39282456 | 39371362 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0003g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0008g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0001t0011g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0009g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0002t0010g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0004g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0004t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0007t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0007t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0007t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0010t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0011t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0001c0012t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0002c0005t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0002c0005t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0002c0005t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0002c0005t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0002c0005t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0002c0005t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0003c0006t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0003c0006t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0003c0006t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0003c0006t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0003c0006t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0004c0008t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0004c0008t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0005c0013t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
a0006c0009t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | FIN | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0053 | EUR | FIN | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | CHS | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0143 | EAS | CHS | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0113 | EAS | CHS | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | CHS | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | CHS | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0149 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00642 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | CHS | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00733 | hp1 | a0001 | c0003 | t0001 | g0089 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0176 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0047 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0063 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0144 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0159 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0130 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0109 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0064 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01167 | hp1 | a0001 | c0004 | t0001 | g0027 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01167 | hp2 | a0001 | c0004 | t0004 | g0268 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0049 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01169 | hp1 | a0001 | c0004 | t0004 | g0271 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0251 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01175 | hp2 | a0001 | c0003 | t0001 | g0085 | AMR | PUR | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01255 | hp2 | a0001 | c0004 | t0001 | g0020 | AMR | CLM | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0129 | AMR | CLM | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0142 | AMR | CLM | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0128 | AMR | CLM | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0108 | AMR | CLM | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0235 | AMR | CLM | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0096 | AMR | CLM | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | IBS | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | IBS | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0098 | EUR | IBS | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | IBS | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01891 | hp1 | a0001 | c0004 | t0001 | g0029 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0110 | AMR | PEL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0111 | AMR | PEL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0135 | AMR | PEL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0102 | AMR | PEL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0107 | AMR | PEL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0160 | AMR | PEL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02004 | hp2 | a0001 | c0002 | t0010 | g0133 | AMR | PEL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02015 | hp1 | a0001 | c0003 | t0001 | g0052 | EAS | KHV | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02015 | hp2 | a0001 | c0007 | t0002 | g0120 | EAS | KHV | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0131 | EAS | KHV | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0154 | EAS | KHV | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0055 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | KHV | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02129 | hp1 | a0001 | c0003 | t0001 | g0057 | EAS | KHV | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0255 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | CDX | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02155 | hp2 | a0001 | c0003 | t0001 | g0067 | EAS | CDX | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0156 | AMR | PEL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02273 | hp2 | a0001 | c0003 | t0001 | g0069 | AMR | PEL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0082 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02451 | hp1 | a0002 | c0005 | t0001 | g0166 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02451 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02572 | hp2 | a0001 | c0004 | t0001 | g0046 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02615 | hp1 | a0001 | c0004 | t0001 | g0024 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02622 | hp1 | a0006 | c0009 | t0003 | g0028 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02630 | hp1 | a0002 | c0005 | t0001 | g0252 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02630 | hp2 | a0002 | c0005 | t0001 | g0165 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02647 | hp2 | a0001 | c0004 | t0001 | g0044 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0095 | SAS | PJL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0097 | SAS | PJL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02723 | hp1 | a0001 | c0004 | t0001 | g0022 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02723 | hp2 | a0003 | c0006 | t0001 | g0267 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0250 | SAS | PJL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02809 | hp1 | a0002 | c0005 | t0001 | g0164 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0026 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0079 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02818 | hp2 | a0002 | c0005 | t0001 | g0167 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02886 | hp1 | a0001 | c0004 | t0004 | g0272 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02886 | hp2 | a0001 | c0004 | t0001 | g0012 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02895 | hp1 | a0001 | c0004 | t0004 | g0273 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02895 | hp2 | a0001 | c0004 | t0001 | g0212 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02896 | hp2 | a0001 | c0004 | t0001 | g0094 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02897 | hp1 | a0001 | c0004 | t0004 | g0270 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02897 | hp2 | a0001 | c0004 | t0001 | g0092 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02970 | hp1 | a0001 | c0001 | t0007 | g0260 | AFR | ESN | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02970 | hp2 | a0004 | c0008 | t0001 | g0018 | AFR | ESN | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02976 | hp1 | a0001 | c0004 | t0004 | g0269 | AFR | ESN | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0178 | SAS | PJL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03041 | hp1 | a0001 | c0004 | t0001 | g0016 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03098 | hp1 | a0003 | c0006 | t0001 | g0263 | AFR | MSL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | MSL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0042 | AFR | ESN | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | MSL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | MSL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03225 | hp2 | a0001 | c0004 | t0001 | g0045 | AFR | MSL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0158 | SAS | PJL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | MSL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03453 | hp2 | a0001 | c0004 | t0001 | g0017 | AFR | MSL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03486 | hp2 | a0004 | c0008 | t0001 | g0019 | AFR | MSL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0123 | SAS | PJL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03490 | hp2 | a0001 | c0003 | t0001 | g0196 | SAS | PJL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03540 | hp2 | a0001 | c0011 | t0006 | g0031 | AFR | GWD | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0140 | SAS | PJL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03831 | hp2 | a0001 | c0003 | t0001 | g0169 | SAS | BEB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0126 | SAS | BEB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03927 | hp1 | a0001 | c0007 | t0002 | g0083 | SAS | BEB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0173 | SAS | STU | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG04115 | hp2 | a0001 | c0003 | t0001 | g0168 | SAS | STU | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0114 | SAS | BEB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG04228 | hp1 | a0001 | c0003 | t0001 | g0058 | SAS | STU | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0145 | SAS | STU | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18522 | hp1 | a0003 | c0006 | t0001 | g0264 | AFR | YRI | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | YRI | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18612 | hp1 | a0001 | c0007 | t0002 | g0004 | EAS | CHB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | CHB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | CHB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18906 | hp1 | a0001 | c0004 | t0001 | g0014 | AFR | YRI | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18906 | hp2 | a0003 | c0006 | t0001 | g0265 | AFR | YRI | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18944 | hp1 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18951 | hp1 | a0001 | c0003 | t0001 | g0066 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18951 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18961 | hp1 | a0001 | c0003 | t0001 | g0076 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18961 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18971 | hp1 | a0001 | c0003 | t0001 | g0060 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18972 | hp1 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18979 | hp2 | a0001 | c0003 | t0001 | g0078 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18982 | hp2 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18999 | hp1 | a0001 | c0001 | t0011 | g0274 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18999 | hp2 | a0001 | c0003 | t0001 | g0073 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19001 | hp1 | a0001 | c0003 | t0001 | g0077 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0137 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19003 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19005 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19009 | hp2 | a0001 | c0003 | t0001 | g0065 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19012 | hp2 | a0001 | c0003 | t0001 | g0087 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19043 | hp1 | a0001 | c0004 | t0006 | g0013 | AFR | LWK | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | LWK | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19058 | hp1 | a0001 | c0003 | t0001 | g0249 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19066 | hp2 | a0001 | c0002 | t0009 | g0170 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19079 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19079 | hp2 | a0001 | c0003 | t0001 | g0059 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19081 | hp1 | a0001 | c0003 | t0001 | g0074 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19082 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19083 | hp1 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19085 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19087 | hp2 | a0005 | c0013 | t0001 | g0005 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0155 | EUR | TSI | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0072 | EUR | TSI | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0136 | SAS | GIH | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | GIH | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0112 | AMR | CLM | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0239 | AMR | CLM | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02109 | hp1 | a0002 | c0005 | t0001 | g0163 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02109 | hp2 | a0003 | c0006 | t0001 | g0266 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02559 | hp1 | a0001 | c0004 | t0001 | g0021 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG02559 | hp2 | a0001 | c0012 | t0001 | g0003 | AFR | ACB | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
HG03471 | hp2 | a0001 | c0001 | t0008 | g0090 | AFR | MSL | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18955 | hp1 | a0001 | c0003 | t0001 | g0068 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA20300 | hp1 | a0001 | c0004 | t0001 | g0023 | AFR | USA | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA20300 | hp2 | a0001 | c0010 | t0001 | g0240 | AFR | USA | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | LWK | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0054 | AFR | LWK | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0070 | REF | REF | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0037 | REF | REF | RFC1_chr4_39282456_39371362 | RFC1 | chr4 | 39282456 | 39371362 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:39295708
|
G | T | 1 | a0003 | 5 | HG02109.hp2 HG02723.hp2 HG03098.hp1 others(2): Show |
missense_variant | MODERATE | c.2860C>A | p.Gln954Lys | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/25 | 2981/4870 | 2860/3444 | 954/1147 | chr4 | 39295708 | ||
chr4:39295724
|
C | T | 1 | a0006 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.2844G>A | p.Met948Ile | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/25 | 2965/4870 | 2844/3444 | 948/1147 | chr4 | 39295724 | ||
chr4:39304851
|
C | G | 1 | a0002 | 6 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
missense_variant | MODERATE | c.2073G>C | p.Glu691Asp | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 15/25 | 2194/4870 | 2073/3444 | 691/1147 | chr4 | 39304851 | ||
chr4:39308729
|
T | C | 1 | a0004 | 2 | HG02970.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.1792A>G | p.Ile598Val | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 13/25 | 1913/4870 | 1792/3444 | 598/1147 | chr4 | 39308729 | ||
chr4:39345430
|
CTTGGTTG others(3): Show |
C | 1 | a0005 | 1 | NA19087.hp2 | frameshift_variant | HIGH | c.169_178delAAGCAACC others(2): Show |
p.Lys57fs | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/25 | 299/4870 | 169/3444 | 57/1147 | chr4 | 39345430 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:39288842
|
T | C | 1 | a0001c0010 | 1 | NA20300.hp2 | splice_region_variant&synonymous_variant | LOW | c.3363A>G | p.Lys1121Lys | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 25/25 | 3484/4870 | 3363/3444 | 1121/1147 | chr4 | 39288842 | ||
chr4:39300286
|
G | A | 1 | a0001c0011 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.2664C>T | p.Tyr888Tyr | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 20/25 | 2785/4870 | 2664/3444 | 888/1147 | chr4 | 39300286 | ||
chr4:39300409
|
T | C | 2 | a0001c0002a0001c0007 | 98 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
synonymous_variant | LOW | c.2541A>G | p.Pro847Pro | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 20/25 | 2662/4870 | 2541/3444 | 847/1147 | chr4 | 39300409 | ||
chr4:39302305
|
A | G | 2 | a0001c0003a0001c0007 | 35 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(32): Show |
synonymous_variant | LOW | c.2508T>C | p.Ser836Ser | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/25 | 2629/4870 | 2508/3444 | 836/1147 | chr4 | 39302305 | ||
chr4:39304884
|
C | G | 2 | a0001c0004a0004c0008 | 28 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(25): Show |
synonymous_variant | LOW | c.2040G>C | p.Arg680Arg | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 15/25 | 2161/4870 | 2040/3444 | 680/1147 | chr4 | 39304884 | ||
chr4:39308688
|
G | C | 1 | a0001c0012 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.1833C>G | p.Leu611Leu | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 13/25 | 1954/4870 | 1833/3444 | 611/1147 | chr4 | 39308688 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:39287688
|
G | C | 8 | a0001c0001t0002a0001c0001t0005a0001c0002t0002others(5): Show | 101 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1073C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 25/25 | 1073 | chr4 | 39287688 | |||||
chr4:39287695
|
A | G | 1 | a0001c0001t0005 | 2 | HG02280.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1066T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 25/25 | 1066 | chr4 | 39287695 | |||||
chr4:39287853
|
A | G | 17 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(14): Show | 165 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*908T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 25/25 | 908 | chr4 | 39287853 | |||||
chr4:39287932
|
T | C | 1 | a0001c0002t0009 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*829A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 25/25 | 829 | chr4 | 39287932 | |||||
chr4:39288071
|
C | T | 1 | a0001c0001t0005 | 2 | HG02280.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*690G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 25/25 | 690 | chr4 | 39288071 | |||||
chr4:39288094
|
G | A | 1 | a0001c0002t0010 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*667C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 25/25 | 667 | chr4 | 39288094 | |||||
chr4:39288680
|
G | A | 1 | a0001c0001t0007 | 2 | HG02145.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*81C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 25/25 | 81 | chr4 | 39288680 | |||||
chr4:39288698
|
C | T | 1 | a0001c0001t0008 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*63G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 25/25 | 63 | chr4 | 39288698 | |||||
chr4:39366304
|
G | A | 1 | a0001c0004t0004 | 6 | HG01167.hp2 HG01169.hp1 HG02886.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/25 | chr4 | 39366304 | ||||||
chr4:39366333
|
T | G | 1 | a0001c0001t0011 | 1 | NA18999.hp1 | 5_prime_UTR_variant | MODIFIER | c.-92A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/25 | 92 | chr4 | 39366333 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:39288884
|
T | TTATGAGT others(31): Show |
2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3361-78_3361-41dup others(38): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 24/24 | chr4 | 39288884 | ||||||
chr4:39288917
|
C | A | 2 | a0001c0001t0005g0030a0001c0001t0005g0082 | 2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3361-73G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 24/24 | chr4 | 39288917 | ||||||
chr4:39288935
|
G | C | 4 | a0001c0001t0001g0198a0001c0001t0001g0202a0001c0001t0001g0238others(1): Show | 4 | HG02258.hp1 HG02717.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.3361-91C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 24/24 | chr4 | 39288935 | ||||||
chr4:39288975
|
A | T | 1 | a0001c0003t0001g0068 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3361-131T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 24/24 | chr4 | 39288975 | ||||||
chr4:39288996
|
T | C | 1 | a0001c0003t0001g0087 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3361-152A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 24/24 | chr4 | 39288996 | ||||||
chr4:39289448
|
A | C | 259 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(256): Show | 260 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(257): Show |
intron_variant | MODIFIER | c.3360+400T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 24/24 | chr4 | 39289448 | ||||||
chr4:39289462
|
G | A | 160 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(157): Show | 160 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(157): Show |
intron_variant | MODIFIER | c.3360+386C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 24/24 | chr4 | 39289462 | ||||||
chr4:39289493
|
C | T | 160 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(157): Show | 160 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(157): Show |
intron_variant | MODIFIER | c.3360+355G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 24/24 | chr4 | 39289493 | ||||||
chr4:39289763
|
T | C | 1 | a0001c0002t0002g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3360+85A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 24/24 | chr4 | 39289763 | ||||||
chr4:39290045
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.3169-6A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 23/24 | chr4 | 39290045 | ||||||
chr4:39290192
|
G | A | 160 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(157): Show | 160 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(157): Show |
intron_variant | MODIFIER | c.3169-153C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 23/24 | chr4 | 39290192 | ||||||
chr4:39290261
|
A | G | 2 | a0001c0001t0005g0030a0001c0001t0005g0082 | 2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3169-222T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 23/24 | chr4 | 39290261 | ||||||
chr4:39290371
|
TA | T | 160 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(157): Show | 160 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(157): Show |
intron_variant | MODIFIER | c.3169-333delT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 23/24 | chr4 | 39290371 | ||||||
chr4:39290536
|
T | G | 1 | a0001c0002t0002g0158 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3169-497A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 23/24 | chr4 | 39290536 | ||||||
chr4:39290646
|
T | C | 259 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(256): Show | 260 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(257): Show |
intron_variant | MODIFIER | c.3169-607A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 23/24 | chr4 | 39290646 | ||||||
chr4:39290651
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3169-612G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 23/24 | chr4 | 39290651 | ||||||
chr4:39290676
|
G | A | 1 | a0001c0004t0001g0042 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3169-637C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 23/24 | chr4 | 39290676 | ||||||
chr4:39290812
|
C | CA | 158 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(155): Show | 158 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(155): Show |
intron_variant | MODIFIER | c.3169-774dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 23/24 | chr4 | 39290812 | ||||||
chr4:39290882
|
T | G | 160 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(157): Show | 160 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(157): Show |
intron_variant | MODIFIER | c.3168+757A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 23/24 | chr4 | 39290882 | ||||||
chr4:39290995
|
G | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3168+644C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 23/24 | chr4 | 39290995 | ||||||
chr4:39291031
|
T | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0181a0001c0001t0001g0185others(3): Show | 6 | HG00597.hp1 NA18939.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.3168+608A>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 23/24 | chr4 | 39291031 | ||||||
chr4:39291178
|
G | T | 160 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(157): Show | 160 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(157): Show |
intron_variant | MODIFIER | c.3168+461C>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 23/24 | chr4 | 39291178 | ||||||
chr4:39292342
|
A | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2955-490T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39292342 | ||||||
chr4:39292417
|
G | C | 5 | a0001c0003t0001g0059a0001c0003t0001g0060a0001c0003t0001g0062others(2): Show | 5 | HG02155.hp2 NA18971.hp1 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.2955-565C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39292417 | ||||||
chr4:39292459
|
G | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0200a0001c0001t0001g0201others(1): Show | 4 | HG00323.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.2955-607C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39292459 | ||||||
chr4:39292615
|
A | ATTAT | 38 | a0001c0001t0001g0032a0001c0001t0001g0161a0001c0001t0001g0162others(35): Show | 38 | HG00323.hp1 HG01167.hp1 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.2955-767_2955-764d others(6): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39292615 | ||||||
chr4:39292615
|
A | ATTATTTA others(1): Show |
4 | a0001c0001t0001g0258a0001c0001t0001g0259a0002c0005t0001g0163others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2955-771_2955-764d others(10): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39292615 | ||||||
chr4:39292615
|
A | ATTATTTA others(5): Show |
2 | a0002c0005t0001g0164a0002c0005t0001g0165 | 2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2955-775_2955-764d others(14): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39292615 | ||||||
chr4:39292615
|
ATTAT | A | 87 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0216others(84): Show | 88 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.2955-767_2955-764d others(6): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39292615 | ||||||
chr4:39292615
|
ATTATTTA others(1): Show |
A | 5 | a0001c0001t0001g0006a0001c0001t0001g0199a0001c0001t0001g0207others(2): Show | 5 | HG01975.hp2 HG01978.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2955-771_2955-764d others(10): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39292615 | ||||||
chr4:39292615
|
ATTATTTA others(5): Show |
A | 3 | a0001c0001t0001g0008a0001c0001t0001g0220a0001c0011t0006g0031 | 3 | HG02615.hp2 HG03540.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2955-775_2955-764d others(14): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39292615 | ||||||
chr4:39292683
|
C | A | 1 | a0001c0002t0002g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2955-831G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39292683 | ||||||
chr4:39292791
|
G | A | 2 | a0001c0002t0002g0047a0001c0002t0002g0144 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2955-939C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39292791 | ||||||
chr4:39292808
|
A | AT | 12 | a0001c0003t0001g0054a0001c0003t0001g0056a0001c0003t0001g0057others(9): Show | 12 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2955-957dupA | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39292808 | ||||||
chr4:39292840
|
G | A | 1 | a0001c0001t0008g0090 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2955-988C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39292840 | ||||||
chr4:39292940
|
CAGCCTGT others(8): Show |
C | 1 | a0001c0003t0001g0089 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2955-1103_2955-108 others(19): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39292940 | ||||||
chr4:39293034
|
G | C | 3 | a0001c0001t0005g0030a0001c0001t0005g0082a0001c0011t0006g0031 | 3 | HG02280.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2955-1182C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39293034 | ||||||
chr4:39293933
|
T | C | 162 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(159): Show | 162 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(159): Show |
intron_variant | MODIFIER | c.2954+1681A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39293933 | ||||||
chr4:39294036
|
A | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0247 | 2 | HG01255.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2954+1578T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39294036 | ||||||
chr4:39294236
|
T | C | 1 | a0001c0001t0001g0221 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2954+1378A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39294236 | ||||||
chr4:39294308
|
G | T | 1 | a0001c0001t0001g0122 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2954+1306C>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39294308 | ||||||
chr4:39294410
|
G | A | 2 | a0001c0004t0001g0014a0001c0004t0006g0013 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2954+1204C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39294410 | ||||||
chr4:39294461
|
C | G | 2 | a0001c0001t0005g0030a0001c0001t0005g0082 | 2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2954+1153G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39294461 | ||||||
chr4:39294498
|
C | CCT | 162 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(159): Show | 162 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(159): Show |
intron_variant | MODIFIER | c.2954+1115_2954+111 others(6): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39294498 | ||||||
chr4:39294547
|
T | C | 162 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(159): Show | 162 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(159): Show |
intron_variant | MODIFIER | c.2954+1067A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39294547 | ||||||
chr4:39294730
|
T | C | 163 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(160): Show | 163 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(160): Show |
intron_variant | MODIFIER | c.2954+884A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39294730 | ||||||
chr4:39294799
|
T | C | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | NA19004.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.2954+815A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39294799 | ||||||
chr4:39294873
|
G | A | 1 | a0001c0003t0001g0068 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2954+741C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39294873 | ||||||
chr4:39294919
|
A | G | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2954+695T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39294919 | ||||||
chr4:39294926
|
C | A | 162 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(159): Show | 162 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(159): Show |
intron_variant | MODIFIER | c.2954+688G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39294926 | ||||||
chr4:39295142
|
A | G | 5 | a0003c0006t0001g0263a0003c0006t0001g0264a0003c0006t0001g0265others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2954+472T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39295142 | ||||||
chr4:39295336
|
T | C | 6 | a0002c0005t0001g0163a0002c0005t0001g0164a0002c0005t0001g0165others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2954+278A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39295336 | ||||||
chr4:39295407
|
CT | C | 3 | a0001c0001t0005g0030a0001c0001t0005g0082a0001c0011t0006g0031 | 3 | HG02280.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2954+206delA | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39295407 | ||||||
chr4:39295580
|
G | A | 38 | a0001c0001t0001g0010a0001c0001t0001g0091a0001c0001t0001g0162others(35): Show | 38 | HG00639.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.2954+34C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 22/24 | chr4 | 39295580 | ||||||
chr4:39295824
|
T | C | 2 | a0001c0004t0001g0044a0001c0004t0001g0045 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2809-65A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39295824 | ||||||
chr4:39295990
|
G | A | 1 | a0001c0002t0002g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2809-231C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39295990 | ||||||
chr4:39296053
|
C | T | 6 | a0001c0004t0001g0092a0001c0004t0001g0094a0001c0004t0001g0212others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2809-294G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296053 | ||||||
chr4:39296064
|
T | C | 161 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(158): Show | 161 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(158): Show |
intron_variant | MODIFIER | c.2809-305A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296064 | ||||||
chr4:39296212
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2809-453A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296212 | ||||||
chr4:39296222
|
C | T | 1 | a0001c0002t0002g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2809-463G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296222 | ||||||
chr4:39296250
|
CT | C | 81 | a0001c0001t0001g0025a0001c0001t0001g0161a0001c0001t0001g0180others(78): Show | 81 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(78): Show |
intron_variant | MODIFIER | c.2809-492delA | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296250 | ||||||
chr4:39296250
|
CTTT | C | 83 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 83 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.2809-494_2809-492d others(5): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296250 | ||||||
chr4:39296283
|
G | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0161a0001c0001t0001g0180others(1): Show | 4 | HG02486.hp1 HG03139.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2809-524C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296283 | ||||||
chr4:39296341
|
C | T | 7 | a0001c0002t0002g0107a0001c0002t0002g0108a0001c0002t0002g0109others(4): Show | 7 | HG01106.hp2 HG01123.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.2809-582G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296341 | ||||||
chr4:39296395
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2809-636G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296395 | ||||||
chr4:39296498
|
T | C | 259 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(256): Show | 260 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(257): Show |
intron_variant | MODIFIER | c.2809-739A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296498 | ||||||
chr4:39296507
|
G | C | 28 | a0001c0004t0001g0012a0001c0004t0001g0014a0001c0004t0001g0015others(25): Show | 28 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.2809-748C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296507 | ||||||
chr4:39296518
|
T | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 81 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.2809-759A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296518 | ||||||
chr4:39296550
|
A | G | 1 | a0001c0002t0002g0053 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2809-791T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296550 | ||||||
chr4:39296699
|
G | C | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2809-940C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296699 | ||||||
chr4:39296822
|
C | G | 10 | a0001c0001t0001g0025a0001c0001t0001g0161a0001c0001t0001g0180others(7): Show | 10 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2809-1063G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296822 | ||||||
chr4:39296872
|
A | G | 4 | a0001c0001t0001g0204a0001c0001t0001g0225a0001c0001t0001g0244others(1): Show | 4 | NA18943.hp1 NA18948.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.2809-1113T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296872 | ||||||
chr4:39296879
|
A | G | 4 | a0001c0001t0001g0204a0001c0001t0001g0225a0001c0001t0001g0244others(1): Show | 4 | NA18943.hp1 NA18948.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.2809-1120T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296879 | ||||||
chr4:39296884
|
T | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0181a0001c0001t0001g0185others(3): Show | 6 | HG00597.hp1 NA18939.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.2809-1125A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296884 | ||||||
chr4:39296901
|
C | G | 161 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(158): Show | 161 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(158): Show |
intron_variant | MODIFIER | c.2809-1142G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296901 | ||||||
chr4:39296986
|
C | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2809-1227G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39296986 | ||||||
chr4:39297281
|
G | T | 129 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 129 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.2809-1522C>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39297281 | ||||||
chr4:39297429
|
T | C | 161 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(158): Show | 161 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(158): Show |
intron_variant | MODIFIER | c.2809-1670A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39297429 | ||||||
chr4:39297552
|
T | A | 3 | a0001c0002t0002g0101a0001c0002t0002g0103a0001c0002t0002g0104 | 3 | NA18939.hp2 NA18944.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.2809-1793A>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39297552 | ||||||
chr4:39297571
|
C | T | 161 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(158): Show | 161 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(158): Show |
intron_variant | MODIFIER | c.2809-1812G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39297571 | ||||||
chr4:39297575
|
G | A | 1 | a0001c0002t0002g0097 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2809-1816C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39297575 | ||||||
chr4:39297617
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2809-1858G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39297617 | ||||||
chr4:39297646
|
A | G | 161 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(158): Show | 161 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(158): Show |
intron_variant | MODIFIER | c.2809-1887T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39297646 | ||||||
chr4:39297689
|
A | G | 1 | a0001c0003t0001g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2809-1930T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39297689 | ||||||
chr4:39297897
|
C | T | 1 | a0001c0002t0002g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2808+2124G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39297897 | ||||||
chr4:39297969
|
C | G | 2 | a0001c0004t0001g0044a0001c0004t0001g0045 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2808+2052G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39297969 | ||||||
chr4:39298080
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2808+1941C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39298080 | ||||||
chr4:39298116
|
C | G | 6 | a0002c0005t0001g0163a0002c0005t0001g0164a0002c0005t0001g0165others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2808+1905G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39298116 | ||||||
chr4:39298307
|
C | CAA | 79 | a0001c0001t0005g0030a0001c0001t0005g0082a0001c0002t0002g0002others(76): Show | 80 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.2808+1712_2808+171 others(6): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39298307 | ||||||
chr4:39298307
|
C | CAAA | 15 | a0001c0002t0002g0098a0001c0002t0002g0103a0001c0002t0002g0104others(12): Show | 15 | HG00597.hp2 HG00673.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.2808+1711_2808+171 others(7): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39298307 | ||||||
chr4:39298307
|
CAAAAAA | C | 98 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(95): Show | 98 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.2808+1708_2808+171 others(10): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39298307 | ||||||
chr4:39298307
|
CAAAAAAA | C | 64 | a0001c0001t0001g0213a0001c0001t0001g0261a0001c0001t0001g0262others(61): Show | 64 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.2808+1707_2808+171 others(11): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39298307 | ||||||
chr4:39298420
|
G | A | 2 | a0001c0002t0002g0047a0001c0002t0002g0144 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2808+1601C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39298420 | ||||||
chr4:39298578
|
C | T | 164 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(161): Show | 164 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(161): Show |
intron_variant | MODIFIER | c.2808+1443G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39298578 | ||||||
chr4:39298713
|
T | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2808+1308A>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39298713 | ||||||
chr4:39298844
|
C | T | 1 | a0001c0002t0002g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2808+1177G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39298844 | ||||||
chr4:39298881
|
G | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2808+1140C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39298881 | ||||||
chr4:39298929
|
C | T | 33 | a0001c0003t0001g0050a0001c0003t0001g0052a0001c0003t0001g0054others(30): Show | 33 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.2808+1092G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39298929 | ||||||
chr4:39298986
|
C | G | 165 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(162): Show | 165 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(162): Show |
intron_variant | MODIFIER | c.2808+1035G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39298986 | ||||||
chr4:39299008
|
C | A | 164 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(161): Show | 164 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(161): Show |
intron_variant | MODIFIER | c.2808+1013G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299008 | ||||||
chr4:39299031
|
T | C | 32 | a0001c0003t0001g0050a0001c0003t0001g0052a0001c0003t0001g0054others(29): Show | 32 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.2808+990A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299031 | ||||||
chr4:39299048
|
G | C | 1 | a0001c0003t0001g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2808+973C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299048 | ||||||
chr4:39299064
|
G | GC | 5 | a0003c0006t0001g0263a0003c0006t0001g0264a0003c0006t0001g0265others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2808+956dupG | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299064 | ||||||
chr4:39299067
|
C | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2808+954G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299067 | ||||||
chr4:39299111
|
C | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0237 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2808+910G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299111 | ||||||
chr4:39299326
|
C | T | 1 | a0001c0002t0002g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2808+695G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299326 | ||||||
chr4:39299329
|
G | A | 164 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(161): Show | 164 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(161): Show |
intron_variant | MODIFIER | c.2808+692C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299329 | ||||||
chr4:39299530
|
A | G | 28 | a0001c0004t0001g0012a0001c0004t0001g0014a0001c0004t0001g0015others(25): Show | 28 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.2808+491T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299530 | ||||||
chr4:39299610
|
C | CA | 10 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0041others(7): Show | 10 | HG02486.hp1 HG02615.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2808+410dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299610 | ||||||
chr4:39299610
|
CA | C | 6 | a0001c0001t0001g0215a0001c0001t0003g0033a0001c0001t0003g0038others(3): Show | 6 | HG00558.hp1 HG01515.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2808+410delT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299610 | ||||||
chr4:39299626
|
A | G | 1 | a0001c0004t0001g0014 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2808+395T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299626 | ||||||
chr4:39299714
|
T | C | 164 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(161): Show | 164 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(161): Show |
intron_variant | MODIFIER | c.2808+307A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299714 | ||||||
chr4:39299784
|
G | A | 1 | a0001c0003t0001g0056 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2808+237C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299784 | ||||||
chr4:39299952
|
G | A | 28 | a0001c0004t0001g0012a0001c0004t0001g0014a0001c0004t0001g0015others(25): Show | 28 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.2808+69C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299952 | ||||||
chr4:39299980
|
T | TA | 13 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0017others(10): Show | 13 | HG01255.hp2 HG02451.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.2808+40dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299980 | ||||||
chr4:39299985
|
G | C | 163 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(160): Show | 163 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(160): Show |
intron_variant | MODIFIER | c.2808+36C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 21/24 | chr4 | 39299985 | ||||||
chr4:39300213
|
G | A | 1 | a0001c0003t0001g0249 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2690+47C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 20/24 | chr4 | 39300213 | ||||||
chr4:39300436
|
C | T | 33 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0004t0001g0012others(30): Show | 33 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.2536-22G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39300436 | ||||||
chr4:39300629
|
T | G | 166 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(163): Show | 166 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(163): Show |
intron_variant | MODIFIER | c.2536-215A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39300629 | ||||||
chr4:39300658
|
C | T | 163 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(160): Show | 163 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(160): Show |
intron_variant | MODIFIER | c.2536-244G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39300658 | ||||||
chr4:39300809
|
G | C | 1 | a0001c0001t0001g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2536-395C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39300809 | ||||||
chr4:39300842
|
C | T | 131 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(128): Show | 131 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.2536-428G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39300842 | ||||||
chr4:39300977
|
G | A | 1 | a0001c0002t0002g0105 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2536-563C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39300977 | ||||||
chr4:39301045
|
A | G | 86 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 86 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.2536-631T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39301045 | ||||||
chr4:39301087
|
CGA | C | 5 | a0003c0006t0001g0263a0003c0006t0001g0264a0003c0006t0001g0265others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2536-675_2536-674d others(4): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39301087 | ||||||
chr4:39301088
|
GA | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 130 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.2536-675delT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39301088 | ||||||
chr4:39301089
|
A | G | 94 | a0001c0002t0002g0002a0001c0002t0002g0007a0001c0002t0002g0026others(91): Show | 95 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2536-675T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39301089 | ||||||
chr4:39301111
|
C | A | 2 | a0001c0001t0005g0030a0001c0001t0005g0082 | 2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2536-697G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39301111 | ||||||
chr4:39301175
|
C | G | 229 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(226): Show | 230 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.2536-761G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39301175 | ||||||
chr4:39301197
|
T | C | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2536-783A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39301197 | ||||||
chr4:39301246
|
G | A | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2536-832C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39301246 | ||||||
chr4:39301304
|
G | C | 5 | a0003c0006t0001g0263a0003c0006t0001g0264a0003c0006t0001g0265others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2536-890C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39301304 | ||||||
chr4:39301318
|
G | A | 2 | a0001c0002t0002g0142a0001c0002t0002g0251 | 2 | HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.2536-904C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39301318 | ||||||
chr4:39301481
|
T | C | 123 | a0001c0002t0002g0002a0001c0002t0002g0007a0001c0002t0002g0026others(120): Show | 124 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2535+797A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39301481 | ||||||
chr4:39301546
|
T | C | 4 | a0001c0003t0001g0066a0001c0003t0001g0068a0001c0003t0001g0073others(1): Show | 4 | NA18951.hp1 NA18955.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.2535+732A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39301546 | ||||||
chr4:39301697
|
G | A | 3 | a0001c0004t0001g0092a0001c0004t0001g0094a0001c0004t0001g0212 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2535+581C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39301697 | ||||||
chr4:39301847
|
T | C | 28 | a0001c0004t0001g0012a0001c0004t0001g0014a0001c0004t0001g0015others(25): Show | 28 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.2535+431A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39301847 | ||||||
chr4:39301859
|
T | C | 95 | a0001c0002t0002g0002a0001c0002t0002g0007a0001c0002t0002g0026others(92): Show | 96 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2535+419A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39301859 | ||||||
chr4:39301910
|
T | C | 1 | a0001c0003t0001g0069 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2535+368A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 19/24 | chr4 | 39301910 | ||||||
chr4:39302638
|
T | C | 3 | a0001c0004t0001g0012a0001c0004t0001g0027a0001c0004t0001g0029 | 3 | HG01167.hp1 HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2341-43A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 17/24 | chr4 | 39302638 | ||||||
chr4:39302702
|
C | T | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2340+35G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 17/24 | chr4 | 39302702 | ||||||
chr4:39302981
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0237 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2202+79G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 16/24 | chr4 | 39302981 | ||||||
chr4:39303298
|
GA | G | 19 | a0001c0001t0001g0226a0001c0001t0008g0090a0001c0004t0001g0012others(16): Show | 19 | HG01167.hp1 HG01169.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.2111-148delT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 15/24 | chr4 | 39303298 | ||||||
chr4:39303459
|
A | AT | 34 | a0001c0001t0001g0011a0001c0001t0001g0209a0001c0001t0001g0256others(31): Show | 34 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.2111-309dupA | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 15/24 | chr4 | 39303459 | ||||||
chr4:39303508
|
C | T | 1 | a0001c0001t0008g0090 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2111-357G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 15/24 | chr4 | 39303508 | ||||||
chr4:39303734
|
G | A | 1 | a0001c0002t0002g0235 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2111-583C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 15/24 | chr4 | 39303734 | ||||||
chr4:39304133
|
T | C | 5 | a0003c0006t0001g0263a0003c0006t0001g0264a0003c0006t0001g0265others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2110+681A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 15/24 | chr4 | 39304133 | ||||||
chr4:39304175
|
A | C | 4 | a0001c0002t0002g0141a0001c0002t0002g0150a0001c0002t0002g0151others(1): Show | 4 | NA18948.hp1 NA18964.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.2110+639T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 15/24 | chr4 | 39304175 | ||||||
chr4:39304317
|
C | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2110+497G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 15/24 | chr4 | 39304317 | ||||||
chr4:39304466
|
T | C | 6 | a0002c0005t0001g0163a0002c0005t0001g0164a0002c0005t0001g0165others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2110+348A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 15/24 | chr4 | 39304466 | ||||||
chr4:39305314
|
A | G | 7 | a0001c0004t0001g0021a0001c0004t0001g0023a0001c0004t0001g0044others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1996-386T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 14/24 | chr4 | 39305314 | ||||||
chr4:39305353
|
A | C | 259 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(256): Show | 260 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(257): Show |
intron_variant | MODIFIER | c.1996-425T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 14/24 | chr4 | 39305353 | ||||||
chr4:39305359
|
G | A | 1 | a0001c0002t0002g0097 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1996-431C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 14/24 | chr4 | 39305359 | ||||||
chr4:39305807
|
A | G | 1 | a0001c0003t0001g0075 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1995+785T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 14/24 | chr4 | 39305807 | ||||||
chr4:39306081
|
T | C | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1995+511A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 14/24 | chr4 | 39306081 | ||||||
chr4:39306167
|
C | T | 1 | a0001c0003t0001g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1995+425G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 14/24 | chr4 | 39306167 | ||||||
chr4:39306190
|
C | A | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0011g0274 | 3 | NA18999.hp1 NA19004.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1995+402G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 14/24 | chr4 | 39306190 | ||||||
chr4:39306331
|
C | T | 1 | a0001c0004t0006g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1995+261G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 14/24 | chr4 | 39306331 | ||||||
chr4:39306488
|
C | CCA | 147 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0025others(144): Show | 148 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.1995+102_1995+103d others(4): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 14/24 | chr4 | 39306488 | ||||||
chr4:39306488
|
C | CCACA | 4 | a0001c0002t0002g0118a0001c0002t0002g0121a0001c0002t0002g0123others(1): Show | 4 | HG00438.hp2 HG03490.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1995+100_1995+103d others(6): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 14/24 | chr4 | 39306488 | ||||||
chr4:39306567
|
G | A | 187 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(184): Show | 188 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.1995+25C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 14/24 | chr4 | 39306567 | ||||||
chr4:39306575
|
T | C | 1 | a0001c0002t0002g0235 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1995+17A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 14/24 | chr4 | 39306575 | ||||||
chr4:39306899
|
C | A | 1 | a0001c0002t0002g0175 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1886-198G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 13/24 | chr4 | 39306899 | ||||||
chr4:39307085
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1886-384C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 13/24 | chr4 | 39307085 | ||||||
chr4:39307142
|
T | A | 26 | a0001c0001t0001g0025a0001c0002t0002g0026a0001c0004t0001g0014others(23): Show | 26 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1886-441A>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 13/24 | chr4 | 39307142 | ||||||
chr4:39307165
|
A | T | 1 | a0001c0001t0001g0246 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1886-464T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 13/24 | chr4 | 39307165 | ||||||
chr4:39307304
|
G | A | 1 | a0001c0001t0003g0081 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1886-603C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 13/24 | chr4 | 39307304 | ||||||
chr4:39307308
|
G | A | 1 | a0001c0001t0003g0081 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1886-607C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 13/24 | chr4 | 39307308 | ||||||
chr4:39307735
|
C | A | 1 | a0002c0005t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1885+901G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 13/24 | chr4 | 39307735 | ||||||
chr4:39307735
|
C | CA | 122 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(119): Show | 122 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.1885+900dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 13/24 | chr4 | 39307735 | ||||||
chr4:39307873
|
T | C | 3 | a0001c0004t0001g0012a0001c0011t0006g0031a0002c0005t0001g0252 | 3 | HG02630.hp1 HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1885+763A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 13/24 | chr4 | 39307873 | ||||||
chr4:39308072
|
G | A | 5 | a0001c0001t0001g0122a0001c0002t0002g0140a0001c0002t0002g0146others(2): Show | 5 | HG02074.hp1 HG03710.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.1885+564C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 13/24 | chr4 | 39308072 | ||||||
chr4:39308091
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0237 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1885+545C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 13/24 | chr4 | 39308091 | ||||||
chr4:39308124
|
T | G | 1 | a0001c0001t0001g0185 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1885+512A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 13/24 | chr4 | 39308124 | ||||||
chr4:39309082
|
A | T | 1 | a0002c0005t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1489-50T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 12/24 | chr4 | 39309082 | ||||||
chr4:39309262
|
G | A | 33 | a0001c0001t0001g0061a0001c0002t0002g0072a0001c0002t0002g0251others(30): Show | 33 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1489-230C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 12/24 | chr4 | 39309262 | ||||||
chr4:39309469
|
C | T | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1489-437G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 12/24 | chr4 | 39309469 | ||||||
chr4:39309515
|
C | A | 1 | a0001c0002t0002g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1489-483G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 12/24 | chr4 | 39309515 | ||||||
chr4:39309603
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1489-571T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 12/24 | chr4 | 39309603 | ||||||
chr4:39309812
|
A | G | 1 | a0001c0003t0001g0060 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1489-780T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 12/24 | chr4 | 39309812 | ||||||
chr4:39310036
|
A | G | 258 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 259 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.1489-1004T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 12/24 | chr4 | 39310036 | ||||||
chr4:39310226
|
T | G | 1 | a0001c0002t0002g0172 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1489-1194A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 12/24 | chr4 | 39310226 | ||||||
chr4:39310341
|
G | C | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1488+1104C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 12/24 | chr4 | 39310341 | ||||||
chr4:39310374
|
C | A | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1488+1071G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 12/24 | chr4 | 39310374 | ||||||
chr4:39310806
|
T | C | 8 | a0001c0004t0001g0092a0001c0004t0001g0094a0001c0004t0004g0268others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1488+639A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 12/24 | chr4 | 39310806 | ||||||
chr4:39310850
|
G | C | 1 | a0001c0001t0001g0259 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1488+595C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 12/24 | chr4 | 39310850 | ||||||
chr4:39310904
|
C | T | 88 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(85): Show | 89 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1488+541G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 12/24 | chr4 | 39310904 | ||||||
chr4:39311056
|
G | A | 2 | a0001c0007t0002g0004a0001c0007t0002g0120 | 2 | HG02015.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1488+389C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 12/24 | chr4 | 39311056 | ||||||
chr4:39311127
|
C | T | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1488+318G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 12/24 | chr4 | 39311127 | ||||||
chr4:39311592
|
C | A | 1 | a0001c0001t0001g0202 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1384-43G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 11/24 | chr4 | 39311592 | ||||||
chr4:39311798
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1384-249G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 11/24 | chr4 | 39311798 | ||||||
chr4:39311850
|
G | C | 140 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.1384-301C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 11/24 | chr4 | 39311850 | ||||||
chr4:39311896
|
T | C | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1384-347A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 11/24 | chr4 | 39311896 | ||||||
chr4:39311987
|
G | GAA | 3 | a0001c0001t0001g0011a0001c0001t0007g0255a0001c0001t0007g0260 | 3 | HG02145.hp1 HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1384-440_1384-439d others(4): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 11/24 | chr4 | 39311987 | ||||||
chr4:39312080
|
T | C | 140 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 140 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.1384-531A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 11/24 | chr4 | 39312080 | ||||||
chr4:39312181
|
G | A | 2 | a0001c0002t0002g0047a0001c0002t0002g0144 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1383+571C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 11/24 | chr4 | 39312181 | ||||||
chr4:39312209
|
T | C | 136 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 136 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.1383+543A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 11/24 | chr4 | 39312209 | ||||||
chr4:39312259
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1383+493C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 11/24 | chr4 | 39312259 | ||||||
chr4:39312270
|
G | A | 1 | a0001c0002t0002g0109 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1383+482C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 11/24 | chr4 | 39312270 | ||||||
chr4:39312384
|
C | T | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | NA18945.hp1 NA18972.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1383+368G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 11/24 | chr4 | 39312384 | ||||||
chr4:39312411
|
T | C | 2 | a0001c0002t0002g0072a0001c0003t0001g0054 | 2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1383+341A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 11/24 | chr4 | 39312411 | ||||||
chr4:39312598
|
C | T | 1 | a0001c0004t0001g0024 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1383+154G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 11/24 | chr4 | 39312598 | ||||||
chr4:39312629
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1383+123A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 11/24 | chr4 | 39312629 | ||||||
chr4:39312647
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0180 | 2 | HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1383+105A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 11/24 | chr4 | 39312647 | ||||||
chr4:39313025
|
A | T | 2 | a0001c0002t0002g0160a0001c0002t0010g0133 | 2 | HG02004.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1204-94T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39313025 | ||||||
chr4:39313026
|
T | TCATCATA others(10): Show |
2 | a0001c0002t0002g0160a0001c0002t0010g0133 | 2 | HG02004.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1204-96_1204-95ins others(17): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39313026 | ||||||
chr4:39313127
|
G | A | 235 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(232): Show | 236 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.1204-196C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39313127 | ||||||
chr4:39313399
|
G | A | 2 | a0001c0001t0001g0025a0001c0002t0002g0026 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1204-468C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39313399 | ||||||
chr4:39313641
|
T | C | 5 | a0002c0005t0001g0163a0002c0005t0001g0164a0002c0005t0001g0165others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1204-710A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39313641 | ||||||
chr4:39313650
|
C | T | 2 | a0001c0004t0001g0044a0001c0004t0001g0045 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1204-719G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39313650 | ||||||
chr4:39313685
|
TGGGAAAA others(2): Show |
T | 35 | a0001c0001t0001g0061a0001c0002t0002g0072a0001c0002t0002g0251others(32): Show | 35 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1204-763_1204-755d others(11): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39313685 | ||||||
chr4:39313930
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1204-999A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39313930 | ||||||
chr4:39314605
|
A | C | 1 | a0001c0001t0001g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1204-1674T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39314605 | ||||||
chr4:39314643
|
G | A | 1 | a0001c0002t0002g0101 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1204-1712C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39314643 | ||||||
chr4:39315070
|
A | G | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1203+1845T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39315070 | ||||||
chr4:39315171
|
T | C | 164 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(161): Show | 164 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(161): Show |
intron_variant | MODIFIER | c.1203+1744A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39315171 | ||||||
chr4:39315328
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1203+1587A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39315328 | ||||||
chr4:39315701
|
T | C | 1 | a0001c0003t0001g0067 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1203+1214A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39315701 | ||||||
chr4:39315949
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1203+966C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39315949 | ||||||
chr4:39315953
|
G | A | 6 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | NA18945.hp1 NA18968.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203+962C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39315953 | ||||||
chr4:39315982
|
G | A | 2 | a0001c0002t0002g0125a0001c0002t0002g0179 | 2 | NA18970.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1203+933C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39315982 | ||||||
chr4:39316102
|
C | T | 1 | a0002c0005t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1203+813G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39316102 | ||||||
chr4:39316171
|
C | T | 136 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 136 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.1203+744G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39316171 | ||||||
chr4:39316205
|
G | A | 164 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(161): Show | 164 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(161): Show |
intron_variant | MODIFIER | c.1203+710C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39316205 | ||||||
chr4:39316205
|
G | C | 1 | a0001c0001t0003g0038 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1203+710C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39316205 | ||||||
chr4:39316442
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1203+473G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39316442 | ||||||
chr4:39316448
|
C | G | 1 | a0001c0004t0001g0024 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1203+467G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39316448 | ||||||
chr4:39316453
|
C | A | 21 | a0001c0001t0001g0061a0001c0003t0001g0050a0001c0003t0001g0052others(18): Show | 21 | HG02015.hp1 HG02074.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.1203+462G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39316453 | ||||||
chr4:39316799
|
T | C | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1203+116A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39316799 | ||||||
chr4:39316851
|
A | G | 1 | a0001c0002t0002g0118 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1203+64T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39316851 | ||||||
chr4:39316875
|
G | A | 1 | a0001c0004t0001g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1203+40C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 10/24 | chr4 | 39316875 | ||||||
chr4:39317086
|
A | G | 88 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(85): Show | 88 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1096-64T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39317086 | ||||||
chr4:39317162
|
G | A | 5 | a0003c0006t0001g0263a0003c0006t0001g0264a0003c0006t0001g0265others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096-140C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39317162 | ||||||
chr4:39317211
|
G | A | 1 | a0001c0003t0001g0196 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1096-189C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39317211 | ||||||
chr4:39317690
|
G | T | 2 | a0001c0002t0002g0053a0001c0002t0002g0070 | 2 | HG00323.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1096-668C>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39317690 | ||||||
chr4:39317747
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0224 | 2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1096-725G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39317747 | ||||||
chr4:39317795
|
TA | T | 138 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 138 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.1096-774delT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39317795 | ||||||
chr4:39317810
|
C | G | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1096-788G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39317810 | ||||||
chr4:39317942
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1096-920C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39317942 | ||||||
chr4:39318034
|
G | A | 1 | a0001c0002t0002g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1096-1012C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39318034 | ||||||
chr4:39318089
|
G | A | 1 | a0002c0005t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1096-1067C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39318089 | ||||||
chr4:39318144
|
G | A | 89 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(86): Show | 90 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1096-1122C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39318144 | ||||||
chr4:39318156
|
CA | C | 258 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 259 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.1096-1135delT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39318156 | ||||||
chr4:39318181
|
C | G | 5 | a0002c0005t0001g0163a0002c0005t0001g0164a0002c0005t0001g0165others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096-1159G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39318181 | ||||||
chr4:39318746
|
T | C | 230 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(227): Show | 231 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.1095+1637A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39318746 | ||||||
chr4:39318940
|
A | C | 2 | a0001c0011t0006g0031a0002c0005t0001g0252 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1095+1443T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39318940 | ||||||
chr4:39319011
|
T | C | 88 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(85): Show | 88 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1095+1372A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39319011 | ||||||
chr4:39319315
|
A | G | 2 | a0001c0001t0001g0011a0001c0004t0001g0212 | 2 | HG02145.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1095+1068T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39319315 | ||||||
chr4:39319450
|
A | C | 1 | a0001c0012t0001g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1095+933T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39319450 | ||||||
chr4:39319613
|
G | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0181others(13): Show | 16 | HG00597.hp1 HG00642.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1095+770C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39319613 | ||||||
chr4:39319768
|
C | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0180 | 2 | HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1095+615G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39319768 | ||||||
chr4:39319812
|
C | T | 1 | a0001c0004t0001g0023 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1095+571G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39319812 | ||||||
chr4:39319824
|
G | A | 2 | a0001c0004t0001g0014a0001c0004t0006g0013 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1095+559C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39319824 | ||||||
chr4:39319836
|
G | A | 1 | a0001c0001t0007g0260 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1095+547C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39319836 | ||||||
chr4:39320088
|
A | G | 258 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 259 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.1095+295T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39320088 | ||||||
chr4:39320171
|
G | C | 3 | a0001c0001t0001g0256a0001c0001t0007g0255a0001c0001t0007g0260 | 3 | HG02145.hp2 HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1095+212C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39320171 | ||||||
chr4:39320321
|
C | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1095+62G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39320321 | ||||||
chr4:39320349
|
C | CA | 9 | a0001c0001t0003g0036a0001c0002t0002g0026a0001c0004t0001g0012others(6): Show | 9 | HG01167.hp1 HG01891.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1095+33dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39320349 | ||||||
chr4:39320349
|
CA | C | 8 | a0001c0001t0001g0061a0001c0001t0005g0082a0001c0002t0002g0095others(5): Show | 8 | HG01978.hp1 HG01981.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1095+33delT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39320349 | ||||||
chr4:39320349
|
CAA | C | 131 | a0001c0001t0001g0122a0001c0001t0001g0191a0001c0001t0001g0230others(128): Show | 132 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.1095+32_1095+33del others(2): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39320349 | ||||||
chr4:39320349
|
CAAA | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(88): Show | 91 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.1095+31_1095+33del others(3): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39320349 | ||||||
chr4:39320365
|
A | C | 1 | a0001c0002t0002g0112 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1095+18T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 9/24 | chr4 | 39320365 | ||||||
chr4:39321612
|
T | C | 258 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 259 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.721-238A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39321612 | ||||||
chr4:39321641
|
G | T | 2 | a0001c0003t0001g0052a0001c0003t0001g0078 | 2 | HG02015.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.721-267C>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39321641 | ||||||
chr4:39321958
|
T | TA | 89 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(86): Show | 90 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.721-585_721-584ins others(1): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39321958 | ||||||
chr4:39322125
|
A | T | 3 | a0001c0001t0001g0256a0001c0001t0007g0255a0001c0001t0007g0260 | 3 | HG02145.hp2 HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.721-751T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39322125 | ||||||
chr4:39322175
|
G | A | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.721-801C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39322175 | ||||||
chr4:39322204
|
A | G | 254 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(251): Show | 255 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(252): Show |
intron_variant | MODIFIER | c.721-830T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39322204 | ||||||
chr4:39322380
|
C | A | 89 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(86): Show | 90 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.720+960G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39322380 | ||||||
chr4:39322404
|
C | CA | 5 | a0002c0005t0001g0163a0002c0005t0001g0164a0002c0005t0001g0165others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+935dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39322404 | ||||||
chr4:39322477
|
G | C | 1 | a0002c0005t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.720+863C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39322477 | ||||||
chr4:39322660
|
T | A | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.720+680A>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39322660 | ||||||
chr4:39322770
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0226 | 2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.720+570G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39322770 | ||||||
chr4:39322778
|
C | CA | 12 | a0001c0001t0001g0161a0001c0001t0001g0180a0001c0001t0001g0198others(9): Show | 12 | HG01975.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.720+561dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39322778 | ||||||
chr4:39322995
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.720+345C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39322995 | ||||||
chr4:39323159
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.720+181G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39323159 | ||||||
chr4:39323164
|
C | T | 2 | a0001c0011t0006g0031a0002c0005t0001g0252 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.720+176G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39323164 | ||||||
chr4:39323316
|
G | A | 1 | a0001c0001t0003g0043 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.720+24C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39323316 | ||||||
chr4:39323334
|
T | G | 1 | a0001c0003t0001g0075 | 1 | NA19085.hp1 | splice_region_variant&intron_variant | LOW | c.720+6A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39323334 | ||||||
chr4:39323337
|
C | A | 1 | a0001c0001t0008g0090 | 1 | HG03471.hp2 | splice_region_variant&intron_variant | LOW | c.720+3G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 7/24 | chr4 | 39323337 | ||||||
chr4:39323749
|
A | G | 258 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 259 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.643-332T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 6/24 | chr4 | 39323749 | ||||||
chr4:39324034
|
A | G | 1 | a0001c0001t0008g0090 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.643-617T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 6/24 | chr4 | 39324034 | ||||||
chr4:39324120
|
C | T | 1 | a0002c0005t0001g0164 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.643-703G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 6/24 | chr4 | 39324120 | ||||||
chr4:39324240
|
G | A | 2 | a0001c0003t0001g0059a0001c0003t0001g0065 | 2 | NA19009.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.643-823C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 6/24 | chr4 | 39324240 | ||||||
chr4:39324340
|
G | T | 1 | a0001c0001t0008g0090 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.643-923C>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 6/24 | chr4 | 39324340 | ||||||
chr4:39324512
|
C | T | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.643-1095G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 6/24 | chr4 | 39324512 | ||||||
chr4:39324572
|
A | C | 1 | a0002c0005t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.643-1155T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 6/24 | chr4 | 39324572 | ||||||
chr4:39324964
|
T | G | 1 | a0002c0005t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.643-1547A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 6/24 | chr4 | 39324964 | ||||||
chr4:39325230
|
C | G | 1 | a0001c0002t0002g0070 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.642+1333G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 6/24 | chr4 | 39325230 | ||||||
chr4:39325338
|
C | T | 20 | a0001c0001t0001g0025a0001c0002t0002g0026a0001c0004t0001g0012others(17): Show | 20 | HG01167.hp1 HG01255.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.642+1225G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 6/24 | chr4 | 39325338 | ||||||
chr4:39325399
|
G | A | 136 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 136 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.642+1164C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 6/24 | chr4 | 39325399 | ||||||
chr4:39325724
|
G | A | 136 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 136 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.642+839C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 6/24 | chr4 | 39325724 | ||||||
chr4:39325877
|
G | A | 2 | a0001c0003t0001g0249a0001c0003t0001g0250 | 2 | HG02738.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.642+686C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 6/24 | chr4 | 39325877 | ||||||
chr4:39325915
|
T | C | 1 | a0001c0002t0002g0118 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.642+648A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 6/24 | chr4 | 39325915 | ||||||
chr4:39326060
|
C | T | 4 | a0001c0003t0001g0056a0001c0003t0001g0074a0001c0003t0001g0075others(1): Show | 4 | NA18961.hp1 NA19005.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.642+503G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 6/24 | chr4 | 39326060 | ||||||
chr4:39326087
|
T | C | 2 | a0001c0004t0001g0014a0001c0004t0006g0013 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.642+476A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 6/24 | chr4 | 39326087 | ||||||
chr4:39326720
|
T | G | 1 | a0001c0002t0002g0159 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.565-80A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 5/24 | chr4 | 39326720 | ||||||
chr4:39326964
|
A | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0215 | 2 | HG00639.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.565-324T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 5/24 | chr4 | 39326964 | ||||||
chr4:39326978
|
T | C | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.565-338A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 5/24 | chr4 | 39326978 | ||||||
chr4:39327003
|
T | C | 1 | a0001c0002t0002g0098 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.565-363A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 5/24 | chr4 | 39327003 | ||||||
chr4:39327250
|
C | G | 230 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(227): Show | 231 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.564+274G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 5/24 | chr4 | 39327250 | ||||||
chr4:39327482
|
G | A | 136 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 136 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.564+42C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 5/24 | chr4 | 39327482 | ||||||
chr4:39327801
|
G | A | 1 | a0001c0002t0002g0128 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.332-45C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39327801 | ||||||
chr4:39327868
|
A | C | 5 | a0002c0005t0001g0163a0002c0005t0001g0164a0002c0005t0001g0165others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-112T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39327868 | ||||||
chr4:39328169
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.332-413T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39328169 | ||||||
chr4:39328180
|
CT | C | 90 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(87): Show | 91 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.332-425delA | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39328180 | ||||||
chr4:39328202
|
A | G | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.332-446T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39328202 | ||||||
chr4:39328246
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.332-490G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39328246 | ||||||
chr4:39328417
|
T | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0215 | 2 | HG00639.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.332-661A>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39328417 | ||||||
chr4:39328449
|
TA | T | 8 | a0001c0001t0001g0122a0001c0002t0002g0048a0001c0002t0002g0093others(5): Show | 8 | HG02155.hp1 NA18942.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.332-694delT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39328449 | ||||||
chr4:39328639
|
G | A | 2 | a0001c0002t0002g0113a0001c0002t0002g0147 | 2 | HG00558.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.332-883C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39328639 | ||||||
chr4:39328676
|
A | T | 90 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(87): Show | 91 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.332-920T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39328676 | ||||||
chr4:39328748
|
C | T | 230 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(227): Show | 231 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.332-992G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39328748 | ||||||
chr4:39329105
|
A | G | 2 | a0001c0003t0001g0063a0001c0003t0001g0064 | 2 | HG01069.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.332-1349T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329105 | ||||||
chr4:39329127
|
C | CA | 67 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 67 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.332-1372dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAA | 18 | a0001c0001t0001g0091a0001c0001t0001g0186a0001c0001t0001g0188others(15): Show | 18 | HG00597.hp1 HG00639.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.332-1373_332-1372d others(4): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAA | 10 | a0001c0001t0001g0187a0001c0001t0001g0206a0001c0001t0001g0219others(7): Show | 10 | HG00323.hp2 HG00558.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.332-1374_332-1372d others(5): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAA | 7 | a0001c0002t0002g0071a0001c0002t0002g0084a0001c0002t0002g0106others(4): Show | 7 | HG00438.hp1 HG02630.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.332-1375_332-1372d others(6): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(2): Show |
10 | a0001c0002t0002g0026a0001c0003t0001g0060a0001c0004t0001g0012others(7): Show | 10 | HG01167.hp1 HG02451.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.332-1380_332-1372d others(11): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(3): Show |
16 | a0001c0001t0001g0025a0001c0002t0002g0047a0001c0002t0002g0055others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.332-1381_332-1372d others(12): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(4): Show |
20 | a0001c0002t0002g0072a0001c0002t0002g0124a0001c0003t0001g0050others(17): Show | 20 | HG01069.hp2 HG01109.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.332-1382_332-1372d others(13): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(5): Show |
13 | a0001c0001t0001g0061a0001c0002t0002g0125a0001c0002t0002g0146others(10): Show | 13 | HG00733.hp1 HG02015.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.332-1383_332-1372d others(14): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(6): Show |
9 | a0001c0002t0002g0153a0001c0002t0002g0159a0001c0002t0002g0251others(6): Show | 9 | HG01074.hp2 HG01175.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.332-1384_332-1372d others(15): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(7): Show |
4 | a0001c0002t0002g0131a0002c0005t0001g0163a0002c0005t0001g0166others(1): Show | 4 | HG02027.hp1 HG02109.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-1385_332-1372d others(16): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(8): Show |
3 | a0001c0002t0002g0113a0001c0002t0002g0132a0001c0002t0002g0178 | 3 | HG00558.hp1 HG03017.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.332-1386_332-1372d others(17): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(9): Show |
1 | a0001c0002t0002g0098 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.332-1387_332-1372d others(18): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(10): Show |
4 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0147others(1): Show | 4 | HG00673.hp2 HG01106.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.332-1388_332-1372d others(19): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0180a0001c0002t0002g0110 | 2 | HG01952.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.332-1389_332-1372d others(20): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0161a0001c0002t0002g0049 | 2 | HG01168.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.332-1390_332-1372d others(21): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(14): Show |
1 | a0001c0002t0010g0133 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.332-1392_332-1372d others(23): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(15): Show |
5 | a0001c0001t0001g0122a0001c0002t0002g0070a0001c0002t0002g0107others(2): Show | 5 | HG01993.hp1 NA18961.hp2 NA19082.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-1393_332-1372d others(24): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(16): Show |
3 | a0001c0002t0002g0112a0001c0002t0002g0141a0001c0002t0002g0160 | 3 | HG01123.hp1 HG02004.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.332-1394_332-1372d others(25): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(17): Show |
2 | a0001c0002t0002g0115a0001c0002t0002g0116 | 2 | NA18942.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.332-1395_332-1372d others(26): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(18): Show |
1 | a0001c0002t0002g0148 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.332-1396_332-1372d others(27): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(20): Show |
2 | a0001c0002t0002g0140a0001c0002t0002g0177 | 2 | HG03710.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.332-1372_332-1371i others(29): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(22): Show |
2 | a0001c0002t0002g0145a0001c0007t0002g0083 | 2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.332-1372_332-1371i others(31): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(23): Show |
1 | a0001c0002t0002g0093 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.332-1372_332-1371i others(32): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(27): Show |
1 | a0001c0002t0002g0101 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.332-1372_332-1371i others(36): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(31): Show |
2 | a0001c0002t0002g0126a0001c0002t0002g0139 | 2 | HG03834.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.332-1372_332-1371i others(40): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(34): Show |
1 | a0001c0002t0002g0127 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.332-1372_332-1371i others(43): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(35): Show |
1 | a0001c0002t0002g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.332-1372_332-1371i others(44): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(36): Show |
1 | a0001c0002t0002g0142 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.332-1372_332-1371i others(45): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(38): Show |
1 | a0001c0002t0002g0114 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.332-1372_332-1371i others(47): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(41): Show |
1 | a0001c0002t0002g0157 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.332-1372_332-1371i others(50): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
C | CAAAAAAA others(42): Show |
1 | a0001c0002t0002g0135 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.332-1372_332-1371i others(51): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
CA | C | 12 | a0001c0001t0003g0033a0001c0001t0003g0038a0001c0001t0003g0039others(9): Show | 12 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.332-1372delT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
CAA | C | 8 | a0001c0003t0001g0066a0001c0003t0001g0067a0001c0003t0001g0068others(5): Show | 8 | HG02155.hp2 HG02273.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.332-1373_332-1372d others(4): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329127
|
CAAAAAAA | C | 8 | a0001c0002t0002g0096a0001c0002t0002g0102a0001c0002t0002g0128others(5): Show | 8 | HG00741.hp1 HG01261.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.332-1378_332-1372d others(9): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329127 | ||||||
chr4:39329365
|
A | G | 258 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 259 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.332-1609T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329365 | ||||||
chr4:39329395
|
G | C | 2 | a0001c0011t0006g0031a0002c0005t0001g0252 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.332-1639C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329395 | ||||||
chr4:39329447
|
G | A | 1 | a0003c0006t0001g0263 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.332-1691C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329447 | ||||||
chr4:39329451
|
G | A | 1 | a0001c0002t0002g0049 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.332-1695C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329451 | ||||||
chr4:39329528
|
T | C | 1 | a0001c0002t0002g0160 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.332-1772A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329528 | ||||||
chr4:39329555
|
C | G | 5 | a0002c0005t0001g0163a0002c0005t0001g0164a0002c0005t0001g0165others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-1799G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329555 | ||||||
chr4:39329656
|
G | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.332-1900C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329656 | ||||||
chr4:39329737
|
A | C | 7 | a0001c0001t0001g0161a0001c0001t0001g0180a0002c0005t0001g0163others(4): Show | 7 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-1981T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329737 | ||||||
chr4:39329912
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.332-2156C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329912 | ||||||
chr4:39329983
|
G | C | 1 | a0003c0006t0001g0267 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.332-2227C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39329983 | ||||||
chr4:39330044
|
T | A | 255 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(252): Show | 256 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(253): Show |
intron_variant | MODIFIER | c.332-2288A>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39330044 | ||||||
chr4:39330152
|
C | T | 1 | a0001c0002t0002g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.332-2396G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39330152 | ||||||
chr4:39330330
|
A | G | 1 | a0001c0002t0002g0158 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.332-2574T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39330330 | ||||||
chr4:39330609
|
G | C | 1 | a0001c0001t0003g0043 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.332-2853C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39330609 | ||||||
chr4:39330611
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.332-2855T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39330611 | ||||||
chr4:39330677
|
A | G | 3 | a0001c0001t0001g0211a0001c0001t0001g0245a0001c0010t0001g0240 | 3 | HG01074.hp1 HG02738.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.332-2921T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39330677 | ||||||
chr4:39330702
|
A | C | 1 | a0001c0001t0008g0090 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.332-2946T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39330702 | ||||||
chr4:39330778
|
A | G | 1 | a0001c0003t0001g0074 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.332-3022T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39330778 | ||||||
chr4:39330906
|
T | C | 2 | a0001c0011t0006g0031a0002c0005t0001g0252 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.332-3150A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39330906 | ||||||
chr4:39330996
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.332-3240T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39330996 | ||||||
chr4:39331385
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.332-3629C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39331385 | ||||||
chr4:39331447
|
G | A | 3 | a0001c0001t0001g0256a0001c0001t0007g0255a0001c0001t0007g0260 | 3 | HG02145.hp2 HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.332-3691C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39331447 | ||||||
chr4:39331499
|
G | A | 4 | a0001c0003t0001g0066a0001c0003t0001g0068a0001c0003t0001g0073others(1): Show | 4 | NA18951.hp1 NA18955.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.332-3743C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39331499 | ||||||
chr4:39331575
|
A | G | 2 | a0001c0001t0003g0040a0006c0009t0003g0028 | 2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.332-3819T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39331575 | ||||||
chr4:39331591
|
A | G | 2 | a0001c0003t0001g0249a0001c0003t0001g0250 | 2 | HG02738.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.332-3835T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39331591 | ||||||
chr4:39331810
|
A | G | 8 | a0001c0001t0001g0161a0001c0001t0001g0180a0001c0001t0008g0090others(5): Show | 8 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.332-4054T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39331810 | ||||||
chr4:39331813
|
A | C | 35 | a0001c0001t0001g0025a0001c0001t0001g0261a0001c0001t0001g0262others(32): Show | 35 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.332-4057T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39331813 | ||||||
chr4:39331820
|
T | C | 1 | a0002c0005t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.332-4064A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39331820 | ||||||
chr4:39331919
|
A | G | 259 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(256): Show | 260 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(257): Show |
intron_variant | MODIFIER | c.332-4163T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39331919 | ||||||
chr4:39332052
|
T | C | 8 | a0001c0002t0002g0125a0001c0002t0002g0146a0001c0002t0002g0153others(5): Show | 8 | HG02015.hp2 HG02040.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.332-4296A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39332052 | ||||||
chr4:39332332
|
T | C | 1 | a0002c0005t0001g0164 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.332-4576A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39332332 | ||||||
chr4:39332349
|
C | T | 136 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 136 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.332-4593G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39332349 | ||||||
chr4:39332441
|
G | T | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.332-4685C>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39332441 | ||||||
chr4:39332533
|
C | G | 1 | a0001c0002t0002g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.332-4777G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39332533 | ||||||
chr4:39332563
|
T | C | 6 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | NA18945.hp1 NA18968.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.332-4807A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39332563 | ||||||
chr4:39332755
|
C | T | 1 | a0001c0003t0001g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.332-4999G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39332755 | ||||||
chr4:39332767
|
T | C | 85 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(82): Show | 86 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.332-5011A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39332767 | ||||||
chr4:39332773
|
T | C | 1 | a0001c0003t0001g0089 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.332-5017A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39332773 | ||||||
chr4:39332958
|
T | C | 1 | a0001c0003t0001g0060 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.332-5202A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39332958 | ||||||
chr4:39333065
|
C | T | 1 | a0001c0002t0002g0096 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.332-5309G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39333065 | ||||||
chr4:39333163
|
A | G | 7 | a0001c0001t0001g0161a0001c0001t0001g0180a0002c0005t0001g0163others(4): Show | 7 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-5407T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39333163 | ||||||
chr4:39333416
|
A | G | 2 | a0001c0004t0001g0014a0001c0004t0006g0013 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.332-5660T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39333416 | ||||||
chr4:39333705
|
C | G | 2 | a0001c0011t0006g0031a0002c0005t0001g0252 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.332-5949G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39333705 | ||||||
chr4:39333855
|
G | A | 90 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(87): Show | 91 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.332-6099C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39333855 | ||||||
chr4:39333896
|
T | C | 7 | a0001c0001t0001g0161a0001c0001t0001g0180a0002c0005t0001g0163others(4): Show | 7 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-6140A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39333896 | ||||||
chr4:39333956
|
T | C | 1 | a0001c0002t0002g0147 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.332-6200A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39333956 | ||||||
chr4:39334120
|
A | G | 4 | a0001c0001t0001g0204a0001c0001t0001g0225a0001c0001t0001g0244others(1): Show | 4 | NA18943.hp1 NA18948.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.332-6364T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39334120 | ||||||
chr4:39334127
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.332-6371G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39334127 | ||||||
chr4:39334402
|
T | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.332-6646A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39334402 | ||||||
chr4:39334660
|
T | C | 2 | a0001c0011t0006g0031a0002c0005t0001g0252 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.332-6904A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39334660 | ||||||
chr4:39335006
|
A | C | 7 | a0001c0001t0001g0161a0001c0001t0001g0180a0002c0005t0001g0163others(4): Show | 7 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-7250T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39335006 | ||||||
chr4:39335033
|
T | C | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.332-7277A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39335033 | ||||||
chr4:39335075
|
T | G | 85 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 85 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.331+7270A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39335075 | ||||||
chr4:39335228
|
C | T | 1 | a0001c0003t0001g0076 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.331+7117G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39335228 | ||||||
chr4:39335229
|
A | T | 5 | a0002c0005t0001g0163a0002c0005t0001g0164a0002c0005t0001g0165others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+7116T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39335229 | ||||||
chr4:39335252
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.331+7093A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39335252 | ||||||
chr4:39335333
|
A | G | 85 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 85 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.331+7012T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39335333 | ||||||
chr4:39335495
|
A | T | 4 | a0001c0001t0001g0189a0001c0001t0001g0200a0001c0001t0001g0201others(1): Show | 4 | HG00323.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+6850T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39335495 | ||||||
chr4:39335605
|
C | T | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.331+6740G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39335605 | ||||||
chr4:39335651
|
G | C | 7 | a0001c0002t0002g0002a0001c0002t0002g0102a0001c0002t0002g0128others(4): Show | 8 | HG00642.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.331+6694C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39335651 | ||||||
chr4:39335746
|
G | A | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.331+6599C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39335746 | ||||||
chr4:39335750
|
T | C | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.331+6595A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39335750 | ||||||
chr4:39335798
|
C | T | 5 | a0001c0002t0002g0048a0001c0002t0002g0141a0001c0002t0002g0150others(2): Show | 5 | NA18948.hp1 NA18964.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+6547G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39335798 | ||||||
chr4:39335969
|
T | C | 5 | a0002c0005t0001g0163a0002c0005t0001g0164a0002c0005t0001g0165others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+6376A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39335969 | ||||||
chr4:39336014
|
T | C | 164 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(161): Show | 164 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(161): Show |
intron_variant | MODIFIER | c.331+6331A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39336014 | ||||||
chr4:39336094
|
C | G | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.331+6251G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39336094 | ||||||
chr4:39336328
|
C | CA | 258 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 259 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.331+6016dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39336328 | ||||||
chr4:39336575
|
G | A | 1 | a0001c0002t0002g0053 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.331+5770C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39336575 | ||||||
chr4:39336728
|
A | G | 1 | a0001c0004t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.331+5617T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39336728 | ||||||
chr4:39337041
|
G | A | 1 | a0001c0002t0002g0158 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.331+5304C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337041 | ||||||
chr4:39337140
|
C | T | 33 | a0001c0001t0001g0061a0001c0002t0002g0072a0001c0002t0002g0251others(30): Show | 33 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.331+5205G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337140 | ||||||
chr4:39337149
|
C | T | 3 | a0001c0002t0002g0156a0001c0002t0002g0157a0001c0002t0010g0133 | 3 | HG02004.hp2 HG02273.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.331+5196G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337149 | ||||||
chr4:39337239
|
C | A | 1 | a0002c0005t0001g0166 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.331+5106G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337239 | ||||||
chr4:39337374
|
C | CA | 35 | a0001c0001t0001g0061a0001c0001t0001g0247a0001c0002t0002g0072others(32): Show | 35 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.331+4970dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337374 | ||||||
chr4:39337435
|
A | AGATGCTA others(13): Show |
3 | a0001c0002t0002g0121a0001c0002t0002g0123a0001c0002t0002g0143 | 3 | HG00438.hp2 HG03490.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.331+4909_331+4910i others(22): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337435 | ||||||
chr4:39337435
|
A | AGATGCTA others(6): Show |
1 | a0001c0002t0002g0179 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.331+4909_331+4910i others(15): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337435 | ||||||
chr4:39337435
|
A | AGT | 60 | a0001c0001t0001g0006a0001c0001t0001g0181a0001c0001t0001g0190others(57): Show | 60 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.331+4908_331+4909d others(4): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337435 | ||||||
chr4:39337435
|
A | AGTGT | 12 | a0001c0001t0001g0122a0001c0002t0002g0049a0001c0002t0002g0051others(9): Show | 12 | HG00558.hp2 HG00597.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.331+4906_331+4909d others(6): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337435 | ||||||
chr4:39337435
|
A | AGTGTGT | 3 | a0001c0002t0002g0070a0001c0002t0002g0106a0001c0002t0002g0149 | 3 | HG00639.hp1 NA18954.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.331+4904_331+4909d others(8): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337435 | ||||||
chr4:39337435
|
AGT | A | 80 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(77): Show | 81 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.331+4908_331+4909d others(4): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337435 | ||||||
chr4:39337435
|
AGTGT | A | 31 | a0001c0001t0001g0025a0001c0001t0001g0161a0001c0001t0001g0162others(28): Show | 31 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.331+4906_331+4909d others(6): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337435 | ||||||
chr4:39337435
|
AGTGTGT | A | 23 | a0001c0001t0001g0032a0001c0001t0001g0262a0001c0002t0001g0232others(20): Show | 23 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.331+4904_331+4909d others(8): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337435 | ||||||
chr4:39337435
|
AGTGTGTG others(1): Show |
A | 16 | a0001c0001t0005g0030a0001c0004t0001g0012a0001c0004t0001g0014others(13): Show | 16 | HG01255.hp2 HG01891.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.331+4902_331+4909d others(10): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337435 | ||||||
chr4:39337435
|
AGTGTGTG others(3): Show |
A | 6 | a0001c0001t0001g0061a0001c0001t0001g0261a0001c0002t0002g0026others(3): Show | 6 | HG02074.hp2 HG02109.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.331+4900_331+4909d others(12): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337435 | ||||||
chr4:39337435
|
AGTGTGTG others(13): Show |
A | 3 | a0001c0001t0001g0256a0001c0001t0007g0255a0001c0001t0007g0260 | 3 | HG02145.hp2 HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.331+4890_331+4909d others(22): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337435 | ||||||
chr4:39337439
|
T | G | 1 | a0001c0001t0001g0244 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.331+4906A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337439 | ||||||
chr4:39337629
|
C | G | 5 | a0002c0005t0001g0163a0002c0005t0001g0164a0002c0005t0001g0165others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+4716G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337629 | ||||||
chr4:39337780
|
C | A | 90 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(87): Show | 91 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.331+4565G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39337780 | ||||||
chr4:39338313
|
T | C | 90 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(87): Show | 91 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.331+4032A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39338313 | ||||||
chr4:39338523
|
A | C | 1 | a0002c0005t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.331+3822T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39338523 | ||||||
chr4:39338977
|
C | A | 1 | a0001c0002t0002g0155 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.331+3368G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39338977 | ||||||
chr4:39339044
|
G | A | 90 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(87): Show | 91 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.331+3301C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39339044 | ||||||
chr4:39339082
|
C | CT | 30 | a0001c0001t0001g0025a0001c0001t0001g0261a0001c0001t0001g0262others(27): Show | 30 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.331+3262dupA | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39339082 | ||||||
chr4:39339197
|
C | T | 5 | a0002c0005t0001g0163a0002c0005t0001g0164a0002c0005t0001g0165others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+3148G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39339197 | ||||||
chr4:39339523
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.331+2822A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39339523 | ||||||
chr4:39339535
|
T | C | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.331+2810A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39339535 | ||||||
chr4:39339573
|
CATTTTTA others(3): Show |
C | 1 | a0001c0001t0001g0241 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.331+2762_331+2771d others(12): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39339573 | ||||||
chr4:39339580
|
A | T | 2 | a0001c0001t0003g0040a0006c0009t0003g0028 | 2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.331+2765T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39339580 | ||||||
chr4:39340257
|
T | A | 1 | a0001c0001t0008g0090 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.331+2088A>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39340257 | ||||||
chr4:39340543
|
C | T | 7 | a0001c0001t0001g0161a0001c0001t0001g0180a0002c0005t0001g0163others(4): Show | 7 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.331+1802G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39340543 | ||||||
chr4:39340929
|
C | G | 28 | a0001c0001t0001g0025a0001c0002t0002g0026a0001c0004t0001g0012others(25): Show | 28 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.331+1416G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39340929 | ||||||
chr4:39341086
|
A | AAGAAAAT others(7): Show |
1 | a0001c0003t0001g0069 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.331+1245_331+1258d others(16): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39341086 | ||||||
chr4:39341719
|
T | TTTTTCTC others(18): Show |
1 | a0001c0001t0001g0210 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.331+601_331+625dup others(25): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39341719 | ||||||
chr4:39341722
|
T | C | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.331+623A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39341722 | ||||||
chr4:39341862
|
C | T | 2 | a0001c0002t0002g0134a0001c0002t0002g0175 | 2 | HG00597.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.331+483G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39341862 | ||||||
chr4:39341997
|
C | A | 90 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(87): Show | 91 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.331+348G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39341997 | ||||||
chr4:39342007
|
AGATTATT others(8): Show |
A | 1 | a0001c0001t0001g0210 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.331+323_331+337del others(15): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39342007 | ||||||
chr4:39342159
|
C | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0180 | 2 | HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.331+186G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39342159 | ||||||
chr4:39342320
|
C | A | 90 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(87): Show | 91 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.331+25G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 4/24 | chr4 | 39342320 | ||||||
chr4:39342491
|
C | T | 1 | a0001c0001t0008g0090 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.209-24G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39342491 | ||||||
chr4:39342519
|
T | C | 3 | a0001c0001t0001g0256a0001c0001t0007g0255a0001c0001t0007g0260 | 3 | HG02145.hp2 HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.209-52A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39342519 | ||||||
chr4:39342578
|
T | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0197 | 2 | NA18969.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.209-111A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39342578 | ||||||
chr4:39342617
|
C | T | 226 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(223): Show | 227 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.209-150G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39342617 | ||||||
chr4:39342924
|
C | T | 1 | a0001c0002t0002g0095 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.209-457G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39342924 | ||||||
chr4:39342941
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.209-474G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39342941 | ||||||
chr4:39342978
|
C | G | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.209-511G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39342978 | ||||||
chr4:39342980
|
A | G | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | NA18945.hp1 NA18972.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.209-513T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39342980 | ||||||
chr4:39343021
|
T | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.209-554A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39343021 | ||||||
chr4:39343059
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.209-592A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39343059 | ||||||
chr4:39343175
|
A | G | 1 | a0001c0004t0001g0014 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.209-708T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39343175 | ||||||
chr4:39343199
|
T | TTTTAGTA others(23): Show |
1 | a0001c0001t0001g0209 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.209-762_209-733dup others(30): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39343199 | ||||||
chr4:39343341
|
G | C | 90 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(87): Show | 91 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.209-874C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39343341 | ||||||
chr4:39343834
|
G | A | 5 | a0003c0006t0001g0263a0003c0006t0001g0264a0003c0006t0001g0265others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-1367C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39343834 | ||||||
chr4:39343852
|
C | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0225a0001c0001t0002g0203 | 3 | NA18943.hp1 NA18948.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.209-1385G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39343852 | ||||||
chr4:39343910
|
C | T | 1 | a0001c0001t0003g0043 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.209-1443G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39343910 | ||||||
chr4:39344045
|
CAG | C | 4 | a0001c0001t0001g0025a0001c0002t0002g0026a0001c0004t0001g0014others(1): Show | 4 | HG02809.hp2 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+1354_208+1355d others(4): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39344045 | ||||||
chr4:39344109
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0237 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.208+1292C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39344109 | ||||||
chr4:39344396
|
AACAGTAT others(23): Show |
A | 1 | a0001c0003t0001g0074 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.208+975_208+1004de others(31): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39344396 | ||||||
chr4:39344537
|
G | A | 33 | a0001c0001t0001g0061a0001c0002t0002g0072a0001c0002t0002g0251others(30): Show | 33 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.208+864C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39344537 | ||||||
chr4:39344700
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0180 | 2 | HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.208+701C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39344700 | ||||||
chr4:39344713
|
A | AGGTAGAG others(13): Show |
1 | a0001c0001t0001g0192 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.208+668_208+687dup others(20): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39344713 | ||||||
chr4:39345371
|
A | G | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.208+30T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 3/24 | chr4 | 39345371 | ||||||
chr4:39345658
|
C | A | 1 | a0001c0001t0001g0244 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.133-182G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39345658 | ||||||
chr4:39345669
|
CGCCACAA others(28): Show |
C | 1 | a0001c0001t0001g0184 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.133-228_133-194del others(35): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39345669 | ||||||
chr4:39345766
|
T | A | 1 | a0001c0001t0001g0244 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.133-290A>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39345766 | ||||||
chr4:39345779
|
C | T | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.133-303G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39345779 | ||||||
chr4:39345822
|
A | G | 258 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 259 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.133-346T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39345822 | ||||||
chr4:39345878
|
A | G | 90 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(87): Show | 91 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.133-402T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39345878 | ||||||
chr4:39346214
|
C | T | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.133-738G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39346214 | ||||||
chr4:39346219
|
GTAATCCC others(3): Show |
G | 1 | a0001c0003t0001g0168 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.133-753_133-744del others(10): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39346219 | ||||||
chr4:39346224
|
C | G | 2 | a0001c0002t0002g0084a0001c0002t0002g0257 | 2 | NA18991.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.133-748G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39346224 | ||||||
chr4:39346331
|
CCAGGCGT others(38): Show |
C | 1 | a0001c0001t0001g0209 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.133-900_133-856del others(45): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39346331 | ||||||
chr4:39346575
|
G | A | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.133-1099C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39346575 | ||||||
chr4:39346610
|
A | T | 7 | a0001c0001t0001g0261a0001c0001t0001g0262a0003c0006t0001g0263others(4): Show | 7 | HG02109.hp2 HG02723.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.133-1134T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39346610 | ||||||
chr4:39346780
|
AGAAGAAG others(13): Show |
A | 1 | a0001c0001t0001g0009 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.133-1324_133-1305d others(22): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39346780 | ||||||
chr4:39346851
|
A | G | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.133-1375T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39346851 | ||||||
chr4:39346881
|
G | A | 1 | a0001c0002t0010g0133 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.133-1405C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39346881 | ||||||
chr4:39346977
|
T | C | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.133-1501A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39346977 | ||||||
chr4:39347093
|
A | G | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.133-1617T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39347093 | ||||||
chr4:39347147
|
T | A | 2 | a0001c0011t0006g0031a0002c0005t0001g0252 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.133-1671A>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39347147 | ||||||
chr4:39347342
|
T | TCCTCCTG others(75): Show |
1 | a0001c0003t0001g0078 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.133-1948_133-1867d others(84): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39347342 | ||||||
chr4:39347398
|
G | A | 3 | a0001c0001t0001g0195a0001c0001t0001g0237a0001c0001t0005g0030 | 3 | HG02257.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.133-1922C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39347398 | ||||||
chr4:39347506
|
A | G | 1 | a0001c0002t0002g0121 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.133-2030T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39347506 | ||||||
chr4:39347690
|
G | A | 3 | a0001c0001t0001g0256a0001c0001t0007g0255a0001c0001t0007g0260 | 3 | HG02145.hp2 HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.133-2214C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39347690 | ||||||
chr4:39347726
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.133-2250C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39347726 | ||||||
chr4:39347771
|
A | G | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.133-2295T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39347771 | ||||||
chr4:39348022
|
A | G | 2 | a0001c0002t0002g0072a0001c0003t0001g0054 | 2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.133-2546T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348022 | ||||||
chr4:39348094
|
T | C | 1 | a0001c0001t0008g0090 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.133-2618A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348094 | ||||||
chr4:39348100
|
AATTCTCA others(3): Show |
A | 1 | a0001c0002t0001g0232 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.133-2634_133-2625d others(12): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348100 | ||||||
chr4:39348188
|
G | GAGACAGG others(8): Show |
1 | a0001c0002t0002g0007 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.133-2727_133-2713d others(17): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348188 | ||||||
chr4:39348321
|
G | A | 164 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(161): Show | 164 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(161): Show |
intron_variant | MODIFIER | c.133-2845C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348321 | ||||||
chr4:39348336
|
T | C | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.133-2860A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348336 | ||||||
chr4:39348377
|
T | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0213 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.133-2901A>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348377 | ||||||
chr4:39348391
|
C | G | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.133-2915G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348391 | ||||||
chr4:39348404
|
C | T | 1 | a0001c0002t0002g0072 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.133-2928G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348404 | ||||||
chr4:39348414
|
C | G | 1 | a0001c0001t0001g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.132+2934G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348414 | ||||||
chr4:39348422
|
C | CAAAAAAG others(35): Show |
1 | a0003c0006t0001g0264 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.132+2884_132+2925d others(44): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348422 | ||||||
chr4:39348422
|
C | CAGAAAAG others(715): Show |
1 | a0001c0001t0001g0184 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.132+2925_132+2926i others(724): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348422 | ||||||
chr4:39348422
|
C | CAGAAAAG others(523): Show |
1 | a0001c0001t0001g0182 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.132+2925_132+2926i others(532): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348422 | ||||||
chr4:39348422
|
C | CAGAAAAG others(738): Show |
1 | a0001c0001t0001g0234 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.132+2925_132+2926i others(747): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348422 | ||||||
chr4:39348422
|
C | CAGAAAAG others(486): Show |
1 | a0001c0001t0001g0244 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.132+2925_132+2926i others(495): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348422 | ||||||
chr4:39348422
|
C | CAGAAAAG others(744): Show |
1 | a0001c0001t0001g0183 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.132+2925_132+2926i others(753): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348422 | ||||||
chr4:39348423
|
A | G | 1 | a0001c0002t0002g0072 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.132+2925T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348423 | ||||||
chr4:39348424
|
A | AAAAAG | 17 | a0001c0001t0001g0161a0001c0001t0001g0180a0001c0001t0003g0035others(14): Show | 17 | HG00639.hp1 HG01106.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.132+2919_132+2923d others(7): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(3): Show |
4 | a0001c0002t0002g0114a0001c0002t0002g0145a0002c0005t0001g0164others(1): Show | 4 | HG02451.hp1 HG02809.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+2914_132+2923d others(12): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(8): Show |
2 | a0001c0001t0001g0256a0002c0005t0001g0163 | 2 | HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.132+2909_132+2923d others(17): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(35): Show |
1 | a0001c0001t0001g0191 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(44): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(40): Show |
1 | a0001c0012t0001g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(49): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(13): Show |
4 | a0001c0001t0001g0195a0001c0001t0007g0255a0001c0001t0007g0260others(1): Show | 4 | HG02145.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+2904_132+2923d others(22): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(18): Show |
2 | a0001c0001t0001g0237a0001c0001t0001g0262 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.132+2899_132+2923d others(27): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(30): Show |
1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(39): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(28): Show |
2 | a0001c0001t0001g0261a0001c0011t0006g0031 | 2 | HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.132+2889_132+2923d others(37): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(33): Show |
1 | a0001c0001t0008g0090 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.132+2884_132+2923d others(42): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(40): Show |
4 | a0003c0006t0001g0263a0003c0006t0001g0265a0003c0006t0001g0266others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+2923_132+2924i others(49): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(592): Show |
1 | a0001c0001t0001g0206 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(601): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(93): Show |
1 | a0001c0001t0001g0253 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(102): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(98): Show |
1 | a0001c0001t0001g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(107): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(605): Show |
1 | a0001c0001t0001g0221 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(614): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(248): Show |
1 | a0001c0002t0002g0239 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(257): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(288): Show |
1 | a0001c0001t0001g0229 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(297): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(323): Show |
1 | a0001c0001t0001g0259 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(332): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(338): Show |
1 | a0001c0001t0001g0243 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(347): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(343): Show |
1 | a0001c0001t0001g0258 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(352): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(348): Show |
1 | a0001c0001t0001g0216 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(357): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(353): Show |
1 | a0001c0001t0001g0162 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(362): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(373): Show |
1 | a0001c0001t0001g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(382): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(378): Show |
2 | a0001c0001t0001g0223a0001c0001t0001g0242 | 2 | HG01981.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.132+2923_132+2924i others(387): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(393): Show |
1 | a0001c0001t0001g0193 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(402): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(413): Show |
1 | a0001c0001t0001g0213 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(422): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(423): Show |
2 | a0001c0001t0001g0210a0001c0001t0011g0274 | 2 | HG01168.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.132+2923_132+2924i others(432): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(428): Show |
1 | a0001c0010t0001g0240 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(437): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(438): Show |
2 | a0001c0001t0001g0190a0001c0001t0001g0247 | 2 | HG03471.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.132+2923_132+2924i others(447): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(463): Show |
1 | a0001c0001t0002g0203 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(472): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(473): Show |
2 | a0001c0001t0001g0198a0001c0001t0001g0248 | 2 | HG03017.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.132+2923_132+2924i others(482): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(488): Show |
1 | a0001c0001t0001g0192 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(497): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(493): Show |
1 | a0001c0001t0001g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(502): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(503): Show |
1 | a0001c0001t0001g0010 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(512): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(508): Show |
2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.132+2923_132+2924i others(517): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(528): Show |
1 | a0001c0001t0001g0194 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(537): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(533): Show |
1 | a0001c0001t0001g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(542): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(558): Show |
1 | a0005c0013t0001g0005 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(567): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(573): Show |
1 | a0001c0002t0001g0233 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(582): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(578): Show |
5 | a0001c0001t0001g0199a0001c0001t0001g0215a0001c0001t0001g0231others(2): Show | 5 | HG00733.hp2 HG01255.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+2923_132+2924i others(587): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(583): Show |
1 | a0001c0001t0001g0217 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(592): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(588): Show |
1 | a0001c0002t0002g0235 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(597): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(598): Show |
3 | a0001c0001t0001g0091a0001c0001t0001g0197a0001c0001t0001g0218 | 3 | HG00673.hp1 HG02129.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.132+2923_132+2924i others(607): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(618): Show |
1 | a0001c0001t0001g0185 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(627): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(628): Show |
1 | a0001c0002t0001g0232 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(637): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(633): Show |
1 | a0001c0001t0001g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(642): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(643): Show |
1 | a0001c0001t0001g0205 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(652): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(653): Show |
1 | a0001c0001t0001g0008 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(662): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(683): Show |
1 | a0001c0001t0001g0209 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(692): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(693): Show |
1 | a0001c0001t0001g0009 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(702): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(698): Show |
1 | a0001c0001t0001g0006 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(707): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(723): Show |
1 | a0001c0001t0001g0208 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(732): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(798): Show |
1 | a0001c0001t0001g0226 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(807): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(611): Show |
1 | a0001c0001t0001g0245 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(620): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(571): Show |
1 | a0001c0001t0001g0211 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(580): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(631): Show |
1 | a0001c0001t0001g0186 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(640): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(656): Show |
1 | a0001c0001t0001g0187 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(665): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(267): Show |
1 | a0001c0001t0001g0202 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(276): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(256): Show |
1 | a0001c0001t0001g0189 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(265): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(447): Show |
1 | a0001c0001t0001g0181 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(456): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(333): Show |
1 | a0001c0003t0001g0196 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(342): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(68): Show |
1 | a0001c0001t0001g0222 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(77): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAAGAA others(538): Show |
1 | a0001c0001t0001g0207 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.132+2923_132+2924i others(547): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | AAAAGGAA others(413): Show |
1 | a0001c0001t0001g0241 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.132+2923_132+2924i others(422): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
A | G | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG01978.hp2 NA18945.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+2924T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
AAAAAG | A | 53 | a0001c0001t0001g0041a0001c0001t0001g0122a0001c0002t0002g0002others(50): Show | 54 | HG00642.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.132+2919_132+2923d others(7): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
AAAAAGAA others(3): Show |
A | 14 | a0001c0001t0003g0001a0001c0001t0003g0040a0001c0002t0002g0097others(11): Show | 15 | HG00438.hp2 HG00558.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.132+2914_132+2923d others(12): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
AAAAAGAA others(8): Show |
A | 15 | a0001c0001t0001g0025a0001c0001t0005g0082a0001c0002t0002g0026others(12): Show | 15 | HG00597.hp2 HG00673.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.132+2909_132+2923d others(17): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348424
|
AAAAAGAA others(13): Show |
A | 1 | a0001c0004t0004g0272 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.132+2904_132+2923d others(22): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348424 | ||||||
chr4:39348426
|
A | AAGGGAAG others(2054): Show |
1 | a0001c0003t0001g0085 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.132+2921_132+2922i others(2063): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348426 | ||||||
chr4:39348426
|
A | AGGAAAGG others(3128): Show |
1 | a0001c0002t0002g0072 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.132+2921_132+2922i others(3137): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348426 | ||||||
chr4:39348426
|
A | AGGGAAGG others(3048): Show |
1 | a0001c0003t0001g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.132+2921_132+2922i others(3057): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348426 | ||||||
chr4:39348427
|
A | AAGAAGAG others(158): Show |
1 | a0001c0001t0001g0011 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.132+2920_132+2921i others(167): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348427 | ||||||
chr4:39348427
|
A | AGAAGAGA others(252): Show |
1 | a0001c0004t0001g0212 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.132+2920_132+2921i others(261): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348427 | ||||||
chr4:39348427
|
A | G | 1 | a0001c0003t0001g0077 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.132+2921T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348427 | ||||||
chr4:39348428
|
A | AAAAAAAA others(286): Show |
1 | a0001c0003t0001g0068 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.132+2919_132+2920i others(295): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348428 | ||||||
chr4:39348428
|
A | AAAAAGGA others(311): Show |
1 | a0001c0003t0001g0067 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.132+2919_132+2920i others(320): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348428 | ||||||
chr4:39348428
|
A | AAAAAGGA others(492): Show |
1 | a0001c0003t0001g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.132+2919_132+2920i others(501): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348428 | ||||||
chr4:39348428
|
A | AAAAGGAA others(429): Show |
1 | a0001c0003t0001g0073 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.132+2919_132+2920i others(438): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348428 | ||||||
chr4:39348428
|
A | AAAAGGAA others(390): Show |
1 | a0001c0003t0001g0066 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.132+2919_132+2920i others(399): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348428 | ||||||
chr4:39348428
|
A | AAAAGGAA others(435): Show |
1 | a0001c0003t0001g0087 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.132+2919_132+2920i others(444): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348428 | ||||||
chr4:39348428
|
A | AAAAGGAA others(482): Show |
1 | a0001c0003t0001g0168 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.132+2919_132+2920i others(491): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348428 | ||||||
chr4:39348428
|
A | AAAAGGAA others(498): Show |
1 | a0001c0003t0001g0250 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.132+2919_132+2920i others(507): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348428 | ||||||
chr4:39348428
|
A | AAAAGGAA others(470): Show |
1 | a0001c0003t0001g0249 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.132+2919_132+2920i others(479): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348428 | ||||||
chr4:39348428
|
A | G | 2 | a0001c0003t0001g0056a0001c0003t0001g0077 | 2 | NA19001.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.132+2920T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348428 | ||||||
chr4:39348429
|
G | A | 1 | a0001c0003t0001g0056 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.132+2919C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348429 | ||||||
chr4:39348430
|
A | G | 4 | a0001c0002t0002g0072a0001c0003t0001g0054a0001c0003t0001g0069others(1): Show | 4 | HG01175.hp2 HG02273.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+2918T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348430 | ||||||
chr4:39348431
|
A | G | 3 | a0001c0002t0002g0072a0001c0003t0001g0054a0001c0003t0001g0085 | 3 | HG01175.hp2 NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.132+2917T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348431 | ||||||
chr4:39348432
|
A | AAGAAAAG others(255): Show |
1 | a0001c0001t0001g0224 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.132+2915_132+2916i others(264): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348432 | ||||||
chr4:39348432
|
A | AAGAAAAG others(100): Show |
1 | a0001c0001t0001g0228 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.132+2915_132+2916i others(109): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348432 | ||||||
chr4:39348432
|
A | AAGAAAAG others(97): Show |
1 | a0001c0001t0001g0230 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.132+2915_132+2916i others(106): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348432 | ||||||
chr4:39348432
|
A | G | 3 | a0001c0001t0001g0011a0001c0003t0001g0077a0001c0004t0001g0212 | 3 | HG02145.hp1 HG02895.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.132+2916T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348432 | ||||||
chr4:39348433
|
A | G | 15 | a0001c0002t0002g0251a0001c0003t0001g0063a0001c0003t0001g0064others(12): Show | 15 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.132+2915T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348433 | ||||||
chr4:39348435
|
A | G | 4 | a0001c0002t0002g0072a0001c0003t0001g0054a0001c0003t0001g0069others(1): Show | 4 | HG01175.hp2 HG02273.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+2913T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348435 | ||||||
chr4:39348436
|
A | G | 3 | a0001c0002t0002g0072a0001c0003t0001g0054a0001c0003t0001g0085 | 3 | HG01175.hp2 NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.132+2912T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348436 | ||||||
chr4:39348437
|
A | AAGAAAAG others(100): Show |
1 | a0001c0001t0001g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.132+2910_132+2911i others(109): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348437 | ||||||
chr4:39348437
|
A | G | 3 | a0001c0001t0001g0011a0001c0003t0001g0077a0001c0004t0001g0212 | 3 | HG02145.hp1 HG02895.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.132+2911T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348437 | ||||||
chr4:39348438
|
A | AAG | 3 | a0001c0003t0001g0056a0001c0003t0001g0074a0001c0003t0001g0076 | 3 | NA18961.hp1 NA19005.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.132+2909_132+2910i others(4): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348438 | ||||||
chr4:39348438
|
A | G | 14 | a0001c0002t0002g0251a0001c0003t0001g0063a0001c0003t0001g0064others(11): Show | 14 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.132+2910T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348438 | ||||||
chr4:39348440
|
A | AAAAAAAG others(673): Show |
1 | a0001c0003t0001g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.132+2907_132+2908i others(682): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348440 | ||||||
chr4:39348440
|
A | G | 4 | a0001c0002t0002g0072a0001c0003t0001g0054a0001c0003t0001g0069others(1): Show | 4 | HG01175.hp2 HG02273.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+2908T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348440 | ||||||
chr4:39348441
|
A | G | 3 | a0001c0002t0002g0072a0001c0003t0001g0054a0001c0003t0001g0085 | 3 | HG01175.hp2 NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.132+2907T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348441 | ||||||
chr4:39348442
|
A | G | 3 | a0001c0001t0001g0011a0001c0003t0001g0077a0001c0004t0001g0212 | 3 | HG02145.hp1 HG02895.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.132+2906T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348442 | ||||||
chr4:39348443
|
A | AAAAGGAA others(284): Show |
1 | a0001c0003t0001g0050 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.132+2904_132+2905i others(293): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348443 | ||||||
chr4:39348443
|
A | AAAAGGAA others(464): Show |
1 | a0001c0001t0001g0061 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.132+2904_132+2905i others(473): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348443 | ||||||
chr4:39348443
|
A | AAAAGGAA others(2814): Show |
1 | a0001c0003t0001g0086 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.132+2904_132+2905i others(2823): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348443 | ||||||
chr4:39348443
|
A | AAAAGGGA others(542): Show |
1 | a0001c0003t0001g0060 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.132+2904_132+2905i others(551): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348443 | ||||||
chr4:39348443
|
A | AAAGGAAA others(591): Show |
1 | a0001c0003t0001g0078 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.132+2904_132+2905i others(600): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348443 | ||||||
chr4:39348443
|
A | AAAGGGAA others(374): Show |
1 | a0001c0003t0001g0065 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.132+2904_132+2905i others(383): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348443 | ||||||
chr4:39348443
|
A | AAAGGGAA others(447): Show |
1 | a0001c0003t0001g0059 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.132+2904_132+2905i others(456): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348443 | ||||||
chr4:39348443
|
A | AAAGGGAA others(445): Show |
1 | a0001c0003t0001g0062 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.132+2904_132+2905i others(454): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348443 | ||||||
chr4:39348443
|
A | G | 16 | a0001c0002t0002g0251a0001c0003t0001g0058a0001c0003t0001g0063others(13): Show | 16 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.132+2905T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348443 | ||||||
chr4:39348444
|
G | GAAAAGAA others(442): Show |
1 | a0001c0001t0001g0214 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.132+2903_132+2904i others(451): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348444 | ||||||
chr4:39348445
|
A | G | 6 | a0001c0002t0002g0072a0001c0003t0001g0052a0001c0003t0001g0054others(3): Show | 6 | HG01175.hp2 HG02015.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.132+2903T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348445 | ||||||
chr4:39348446
|
A | G | 3 | a0001c0002t0002g0072a0001c0003t0001g0054a0001c0003t0001g0085 | 3 | HG01175.hp2 NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.132+2902T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348446 | ||||||
chr4:39348447
|
A | AAGAGAAG others(85): Show |
1 | a0001c0001t0001g0088 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.132+2900_132+2901i others(94): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348447 | ||||||
chr4:39348447
|
A | G | 3 | a0001c0001t0001g0011a0001c0003t0001g0077a0001c0004t0001g0212 | 3 | HG02145.hp1 HG02895.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.132+2901T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348447 | ||||||
chr4:39348448
|
A | G | 21 | a0001c0001t0001g0061a0001c0002t0002g0251a0001c0003t0001g0050others(18): Show | 21 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.132+2900T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348448 | ||||||
chr4:39348450
|
A | AAAGGGAA others(678): Show |
1 | a0001c0003t0001g0058 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.132+2897_132+2898i others(687): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348450 | ||||||
chr4:39348450
|
A | G | 8 | a0001c0002t0002g0072a0001c0003t0001g0052a0001c0003t0001g0054others(5): Show | 8 | HG01175.hp2 HG02015.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.132+2898T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348450 | ||||||
chr4:39348451
|
A | G | 4 | a0001c0002t0002g0072a0001c0003t0001g0050a0001c0003t0001g0054others(1): Show | 4 | HG01175.hp2 NA18982.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+2897T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348451 | ||||||
chr4:39348452
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0088a0001c0003t0001g0077others(1): Show | 4 | HG02027.hp2 HG02145.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+2896T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348452 | ||||||
chr4:39348453
|
A | AGGGAAGG others(2267): Show |
1 | a0001c0003t0001g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.132+2894_132+2895i others(2276): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348453 | ||||||
chr4:39348453
|
A | G | 16 | a0001c0001t0001g0061a0001c0002t0002g0251a0001c0003t0001g0050others(13): Show | 16 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.132+2895T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348453 | ||||||
chr4:39348455
|
A | G | 11 | a0001c0002t0002g0072a0001c0003t0001g0052a0001c0003t0001g0054others(8): Show | 11 | HG01175.hp2 HG02015.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.132+2893T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348455 | ||||||
chr4:39348456
|
A | AAGAAGAG others(210): Show |
1 | a0001c0001t0001g0188 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.132+2891_132+2892i others(219): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348456 | ||||||
chr4:39348456
|
A | AAGGAAAG others(210): Show |
1 | a0001c0002t0002g0251 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.132+2891_132+2892i others(219): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348456 | ||||||
chr4:39348456
|
A | AAGGAAAG others(325): Show |
1 | a0001c0003t0001g0064 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.132+2891_132+2892i others(334): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348456 | ||||||
chr4:39348456
|
A | AAGGAAAG others(330): Show |
1 | a0001c0003t0001g0063 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.132+2891_132+2892i others(339): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348456 | ||||||
chr4:39348456
|
A | G | 3 | a0001c0002t0002g0072a0001c0003t0001g0054a0001c0003t0001g0085 | 3 | HG01175.hp2 NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.132+2892T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348456 | ||||||
chr4:39348457
|
A | C | 1 | a0001c0003t0001g0089 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.132+2891T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348457 | ||||||
chr4:39348457
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0088 | 2 | HG02027.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.132+2891T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348457 | ||||||
chr4:39348458
|
A | AAGGGAAG others(1446): Show |
1 | a0001c0003t0001g0074 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.132+2889_132+2890i others(1455): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348458 | ||||||
chr4:39348458
|
A | G | 12 | a0001c0001t0001g0061a0001c0003t0001g0050a0001c0003t0001g0057others(9): Show | 12 | HG00733.hp1 HG02074.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.132+2890T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348458 | ||||||
chr4:39348460
|
A | G | 11 | a0001c0002t0002g0072a0001c0002t0002g0251a0001c0003t0001g0052others(8): Show | 11 | HG01069.hp2 HG01109.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.132+2888T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348460 | ||||||
chr4:39348461
|
A | AAGGGAAG others(258): Show |
1 | a0001c0003t0001g0077 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.132+2886_132+2887i others(267): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348461 | ||||||
chr4:39348461
|
A | G | 3 | a0001c0002t0002g0072a0001c0003t0001g0050a0001c0003t0001g0054 | 3 | NA18982.hp2 NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.132+2887T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348461 | ||||||
chr4:39348462
|
A | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0088a0001c0003t0001g0056 | 3 | HG02027.hp2 HG02145.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.132+2886T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348462 | ||||||
chr4:39348463
|
A | AAGGGAAG others(1661): Show |
1 | a0001c0003t0001g0076 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.132+2884_132+2885i others(1670): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348463 | ||||||
chr4:39348463
|
A | G | 11 | a0001c0003t0001g0050a0001c0003t0001g0056a0001c0003t0001g0057others(8): Show | 11 | HG00733.hp1 HG02129.hp1 HG02273.hp2 others(8): Show |
intron_variant | MODIFIER | c.132+2885T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348463 | ||||||
chr4:39348465
|
A | AAAGGAAA others(689): Show |
1 | a0001c0003t0001g0069 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.132+2882_132+2883i others(698): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348465 | ||||||
chr4:39348465
|
A | G | 10 | a0001c0002t0002g0072a0001c0002t0002g0251a0001c0003t0001g0052others(7): Show | 10 | HG01069.hp2 HG01109.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.132+2883T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348465 | ||||||
chr4:39348466
|
A | AAGGGACG others(157): Show |
1 | a0001c0003t0001g0089 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.132+2881_132+2882i others(166): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348466 | ||||||
chr4:39348466
|
A | G | 8 | a0001c0002t0002g0072a0001c0002t0002g0251a0001c0003t0001g0054others(5): Show | 8 | HG01069.hp2 HG01109.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.132+2882T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348466 | ||||||
chr4:39348467
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.132+2881T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348467 | ||||||
chr4:39348468
|
A | G | 3 | a0001c0003t0001g0058a0001c0003t0001g0059a0001c0003t0001g0065 | 3 | HG04228.hp1 NA19009.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.132+2880T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348468 | ||||||
chr4:39348469
|
GAAAAGAA others(4): Show |
G | 1 | a0001c0004t0004g0268 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.132+2868_132+2878d others(13): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348469 | ||||||
chr4:39348470
|
A | AAAAGAAA others(705): Show |
1 | a0001c0001t0001g0219 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.132+2877_132+2878i others(714): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348470 | ||||||
chr4:39348470
|
A | AAAAGAAA others(599): Show |
1 | a0001c0001t0001g0225 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.132+2877_132+2878i others(608): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348470 | ||||||
chr4:39348470
|
A | G | 13 | a0001c0002t0002g0072a0001c0002t0002g0251a0001c0003t0001g0052others(10): Show | 13 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.132+2878T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348470 | ||||||
chr4:39348471
|
A | AAAAGGAA others(492): Show |
1 | a0001c0003t0001g0075 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.132+2876_132+2877i others(501): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348471 | ||||||
chr4:39348471
|
A | AGGGAAGG others(1673): Show |
1 | a0001c0003t0001g0056 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.132+2876_132+2877i others(1682): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348471 | ||||||
chr4:39348471
|
A | G | 6 | a0001c0002t0002g0072a0001c0003t0001g0054a0001c0003t0001g0074others(3): Show | 6 | HG00733.hp1 NA18961.hp1 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+2877T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348471 | ||||||
chr4:39348475
|
A | G | 14 | a0001c0002t0002g0072a0001c0002t0002g0251a0001c0003t0001g0052others(11): Show | 14 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.132+2873T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348475 | ||||||
chr4:39348476
|
A | G | 3 | a0001c0002t0002g0072a0001c0003t0001g0054a0001c0003t0001g0089 | 3 | HG00733.hp1 NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.132+2872T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348476 | ||||||
chr4:39348546
|
G | A | 1 | a0001c0003t0001g0056 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.132+2802C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348546 | ||||||
chr4:39348547
|
A | T | 1 | a0001c0003t0001g0056 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.132+2801T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348547 | ||||||
chr4:39348548
|
T | C | 1 | a0001c0003t0001g0056 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.132+2800A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348548 | ||||||
chr4:39348585
|
G | T | 1 | a0001c0003t0001g0078 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.132+2763C>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348585 | ||||||
chr4:39348883
|
T | TA | 258 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 259 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.132+2464_132+2465i others(3): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348883 | ||||||
chr4:39348936
|
T | C | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.132+2412A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39348936 | ||||||
chr4:39349071
|
A | AG | 258 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 259 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.132+2276_132+2277i others(3): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39349071 | ||||||
chr4:39349228
|
C | T | 5 | a0001c0001t0001g0211a0001c0001t0001g0245a0001c0001t0001g0258others(2): Show | 5 | HG01074.hp1 HG02486.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+2120G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39349228 | ||||||
chr4:39349396
|
G | A | 2 | a0001c0011t0006g0031a0002c0005t0001g0252 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.132+1952C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39349396 | ||||||
chr4:39349467
|
A | C | 1 | a0001c0003t0001g0078 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.132+1881T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39349467 | ||||||
chr4:39349527
|
A | G | 258 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 259 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.132+1821T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39349527 | ||||||
chr4:39349618
|
T | C | 1 | a0001c0002t0002g0177 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.132+1730A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39349618 | ||||||
chr4:39350188
|
G | GAA | 257 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(254): Show | 258 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(255): Show |
intron_variant | MODIFIER | c.132+1158_132+1159d others(4): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39350188 | ||||||
chr4:39350192
|
G | A | 1 | a0001c0003t0001g0073 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.132+1156C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39350192 | ||||||
chr4:39350220
|
T | A | 1 | a0001c0003t0001g0073 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.132+1128A>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39350220 | ||||||
chr4:39350248
|
C | T | 90 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(87): Show | 91 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.132+1100G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39350248 | ||||||
chr4:39350273
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.132+1075C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39350273 | ||||||
chr4:39350493
|
T | C | 3 | a0001c0004t0004g0269a0001c0004t0004g0270a0001c0004t0004g0273 | 3 | HG02895.hp1 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.132+855A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39350493 | ||||||
chr4:39350570
|
A | C | 1 | a0001c0001t0001g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.132+778T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39350570 | ||||||
chr4:39350656
|
A | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.132+692T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39350656 | ||||||
chr4:39350802
|
A | C | 1 | a0002c0005t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.132+546T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39350802 | ||||||
chr4:39350918
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.132+430G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39350918 | ||||||
chr4:39351032
|
C | T | 33 | a0001c0001t0001g0061a0001c0002t0002g0072a0001c0002t0002g0251others(30): Show | 33 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.132+316G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351032 | ||||||
chr4:39351066
|
C | T | 257 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(254): Show | 258 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(255): Show |
intron_variant | MODIFIER | c.132+282G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351066 | ||||||
chr4:39351077
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.132+271G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351077 | ||||||
chr4:39351093
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.132+255A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351093 | ||||||
chr4:39351168
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.132+180T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351168 | ||||||
chr4:39351183
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.132+165C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351183 | ||||||
chr4:39351200
|
G | A | 90 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(87): Show | 91 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.132+148C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351200 | ||||||
chr4:39351229
|
C | T | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.132+119G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351229 | ||||||
chr4:39351253
|
GA | G | 6 | a0001c0001t0001g0032a0001c0001t0003g0001a0001c0001t0003g0035others(3): Show | 7 | HG01891.hp2 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.132+94delT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351253 | ||||||
chr4:39351253
|
GAA | G | 16 | a0001c0001t0001g0041a0001c0001t0003g0033a0001c0001t0003g0034others(13): Show | 16 | HG00673.hp2 HG01891.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.132+93_132+94delTT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351253 | ||||||
chr4:39351253
|
GAAA | G | 44 | a0001c0001t0001g0025a0001c0001t0005g0030a0001c0001t0005g0082others(41): Show | 44 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.132+92_132+94delTT others(1): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351253 | ||||||
chr4:39351253
|
GAAAA | G | 71 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(68): Show | 72 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.132+91_132+94delTT others(2): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351253 | ||||||
chr4:39351253
|
GAAAAAAA others(2): Show |
G | 21 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0183others(18): Show | 21 | HG00597.hp1 HG00642.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.132+86_132+94delTT others(7): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351253 | ||||||
chr4:39351253
|
GAAAAAAA others(3): Show |
G | 71 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(68): Show | 71 | HG00323.hp1 HG00639.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.132+85_132+94delTT others(8): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351253 | ||||||
chr4:39351253
|
GAAAAAAA others(4): Show |
G | 9 | a0001c0001t0001g0161a0001c0001t0001g0180a0001c0001t0001g0261others(6): Show | 9 | HG01175.hp2 HG02273.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.132+84_132+94delTT others(9): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351253 | ||||||
chr4:39351253
|
GAAAAAAA others(5): Show |
G | 27 | a0001c0001t0001g0061a0001c0002t0002g0072a0001c0002t0002g0251others(24): Show | 27 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.132+83_132+94delTT others(10): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351253 | ||||||
chr4:39351253
|
GAAAAAAA others(6): Show |
G | 1 | a0001c0003t0001g0076 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.132+82_132+94delTT others(11): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351253 | ||||||
chr4:39351256
|
A | G | 1 | a0001c0002t0002g0147 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.132+92T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351256 | ||||||
chr4:39351257
|
A | G | 1 | a0001c0002t0002g0113 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.132+91T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351257 | ||||||
chr4:39351284
|
A | C | 1 | a0002c0005t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.132+64T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351284 | ||||||
chr4:39351290
|
T | C | 90 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(87): Show | 91 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.132+58A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351290 | ||||||
chr4:39351298
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.132+50C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 2/24 | chr4 | 39351298 | ||||||
chr4:39351502
|
C | T | 259 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(256): Show | 260 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(257): Show |
intron_variant | MODIFIER | c.4-26G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39351502 | ||||||
chr4:39351531
|
A | C | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4-55T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39351531 | ||||||
chr4:39351777
|
C | A | 1 | a0001c0002t0002g0051 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.4-301G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39351777 | ||||||
chr4:39351966
|
C | CA | 17 | a0001c0001t0001g0032a0001c0001t0001g0181a0001c0001t0001g0183others(14): Show | 17 | HG00597.hp1 HG00673.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.4-491dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39351966 | ||||||
chr4:39351966
|
CA | C | 10 | a0001c0001t0001g0221a0001c0002t0002g0107a0001c0003t0001g0057others(7): Show | 10 | HG01993.hp1 HG02109.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.4-491delT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39351966 | ||||||
chr4:39352004
|
G | A | 230 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(227): Show | 231 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.4-528C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39352004 | ||||||
chr4:39352206
|
A | T | 54 | a0001c0001t0001g0061a0001c0001t0001g0161a0001c0001t0001g0180others(51): Show | 54 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.4-730T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39352206 | ||||||
chr4:39352452
|
C | T | 7 | a0001c0002t0002g0107a0001c0002t0002g0108a0001c0002t0002g0109others(4): Show | 7 | HG01106.hp2 HG01123.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.4-976G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39352452 | ||||||
chr4:39352673
|
T | C | 2 | a0001c0002t0002g0047a0001c0002t0002g0144 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.4-1197A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39352673 | ||||||
chr4:39352837
|
C | T | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4-1361G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39352837 | ||||||
chr4:39352911
|
T | C | 2 | a0001c0001t0001g0190a0001c0001t0001g0224 | 2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4-1435A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39352911 | ||||||
chr4:39353027
|
G | GAC | 81 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 81 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.4-1553_4-1552dupGT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353027 | ||||||
chr4:39353027
|
G | GACAC | 5 | a0001c0001t0001g0214a0001c0001t0001g0217a0001c0001t0001g0218others(2): Show | 5 | HG00673.hp1 HG02040.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-1555_4-1552dupGT others(2): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353027 | ||||||
chr4:39353027
|
GAC | G | 37 | a0001c0001t0001g0061a0001c0002t0002g0051a0001c0002t0002g0053others(34): Show | 37 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.4-1553_4-1552delGT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353027 | ||||||
chr4:39353039
|
C | T | 1 | a0001c0002t0002g0106 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4-1563G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353039 | ||||||
chr4:39353158
|
T | C | 2 | a0001c0004t0001g0012a0001c0004t0001g0027 | 2 | HG01167.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4-1682A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353158 | ||||||
chr4:39353379
|
G | A | 29 | a0001c0001t0001g0025a0001c0002t0002g0026a0001c0003t0001g0079others(26): Show | 29 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.4-1903C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353379 | ||||||
chr4:39353397
|
C | CA | 40 | a0001c0001t0001g0025a0001c0001t0001g0161a0001c0001t0001g0180others(37): Show | 40 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.4-1922dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353397 | ||||||
chr4:39353397
|
C | CAA | 44 | a0001c0001t0001g0061a0001c0001t0001g0189a0001c0001t0001g0191others(41): Show | 44 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.4-1923_4-1922dupTT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353397 | ||||||
chr4:39353397
|
C | CAAA | 69 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0088others(66): Show | 69 | HG00323.hp2 HG00597.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.4-1924_4-1922dupTT others(1): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353397 | ||||||
chr4:39353397
|
C | CAAAA | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(83): Show | 87 | HG00558.hp1 HG00597.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.4-1925_4-1922dupTT others(2): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353397 | ||||||
chr4:39353397
|
C | CAAAAA | 11 | a0001c0001t0001g0183a0001c0001t0001g0245a0001c0002t0001g0233others(8): Show | 11 | HG00438.hp2 HG00741.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.4-1926_4-1922dupTT others(3): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353397 | ||||||
chr4:39353432
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4-1956C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353432 | ||||||
chr4:39353444
|
C | A | 2 | a0001c0001t0005g0030a0001c0001t0005g0082 | 2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4-1968G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353444 | ||||||
chr4:39353602
|
C | G | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4-2126G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353602 | ||||||
chr4:39353809
|
C | T | 141 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 141 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.4-2333G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353809 | ||||||
chr4:39353814
|
T | C | 169 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(166): Show | 169 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.4-2338A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353814 | ||||||
chr4:39353868
|
A | C | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4-2392T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353868 | ||||||
chr4:39353877
|
G | A | 3 | a0001c0001t0001g0256a0001c0001t0007g0255a0001c0001t0007g0260 | 3 | HG02145.hp2 HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.4-2401C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353877 | ||||||
chr4:39353881
|
G | A | 12 | a0001c0002t0002g0072a0001c0002t0002g0251a0001c0003t0001g0054others(9): Show | 12 | HG00733.hp1 HG01069.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.4-2405C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39353881 | ||||||
chr4:39354009
|
T | G | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4-2533A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39354009 | ||||||
chr4:39354133
|
C | T | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4-2657G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39354133 | ||||||
chr4:39354215
|
A | G | 85 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(82): Show | 86 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.4-2739T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39354215 | ||||||
chr4:39354346
|
G | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4-2870C>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39354346 | ||||||
chr4:39354723
|
G | C | 1 | a0001c0001t0001g0041 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4-3247C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39354723 | ||||||
chr4:39354749
|
C | CA | 12 | a0001c0001t0003g0036a0001c0001t0003g0039a0001c0001t0003g0043others(9): Show | 12 | HG00438.hp2 HG00741.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.4-3274dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39354749 | ||||||
chr4:39354749
|
CA | C | 114 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(111): Show | 114 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.4-3274delT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39354749 | ||||||
chr4:39354749
|
CAA | C | 29 | a0001c0001t0001g0025a0001c0001t0001g0206a0001c0002t0002g0026others(26): Show | 29 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.4-3275_4-3274delTT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39354749 | ||||||
chr4:39354749
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4-3283_4-3274delTT others(8): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39354749 | ||||||
chr4:39354749
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0012t0001g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4-3284_4-3274delTT others(9): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39354749 | ||||||
chr4:39354754
|
A | G | 2 | a0001c0002t0002g0103a0001c0002t0002g0104 | 2 | NA18939.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.4-3278T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39354754 | ||||||
chr4:39354772
|
A | C | 1 | a0001c0002t0002g0102 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.4-3296T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39354772 | ||||||
chr4:39355034
|
A | C | 1 | a0001c0003t0001g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4-3558T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355034 | ||||||
chr4:39355094
|
A | AATACACA others(3): Show |
1 | a0001c0001t0001g0181 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.4-3619_4-3618insGT others(8): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355094 | ||||||
chr4:39355096
|
A | AT | 4 | a0001c0001t0001g0190a0001c0001t0001g0195a0001c0001t0001g0237others(1): Show | 4 | HG02257.hp2 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-3621_4-3620insA | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355096 | ||||||
chr4:39355096
|
A | ATAC | 18 | a0001c0001t0001g0088a0001c0001t0001g0191a0001c0001t0001g0197others(15): Show | 18 | HG00741.hp2 HG01496.hp1 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.4-3621_4-3620insGT others(1): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355096 | ||||||
chr4:39355096
|
A | ATACAC | 16 | a0001c0001t0001g0008a0001c0001t0001g0091a0001c0001t0001g0162others(13): Show | 16 | HG00642.hp2 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.4-3621_4-3620insGT others(3): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355096 | ||||||
chr4:39355096
|
A | ATACACAC | 29 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(26): Show | 29 | HG00597.hp1 HG01074.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.4-3621_4-3620insGT others(5): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355096 | ||||||
chr4:39355096
|
A | ATACACAC others(2): Show |
11 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(8): Show | 11 | HG00639.hp2 HG00673.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.4-3621_4-3620insGT others(7): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355096 | ||||||
chr4:39355096
|
A | ATACACAC others(4): Show |
2 | a0001c0001t0001g0220a0001c0001t0001g0253 | 2 | HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.4-3621_4-3620insGT others(9): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355096 | ||||||
chr4:39355096
|
A | ATACACAC others(6): Show |
1 | a0001c0001t0001g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4-3621_4-3620insGT others(11): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355096 | ||||||
chr4:39355096
|
A | C | 4 | a0001c0001t0001g0181a0001c0001t0001g0189a0001c0001t0001g0221others(1): Show | 4 | HG00323.hp1 NA18612.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-3620T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355096 | ||||||
chr4:39355098
|
T | C | 86 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 86 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.4-3622A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355098 | ||||||
chr4:39355098
|
T | TAC | 20 | a0001c0001t0001g0025a0001c0001t0008g0090a0001c0002t0002g0026others(17): Show | 20 | HG00733.hp1 HG01167.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.4-3624_4-3623dupGT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355098 | ||||||
chr4:39355098
|
T | TACAC | 17 | a0001c0001t0001g0032a0001c0002t0002g0051a0001c0002t0002g0053others(14): Show | 17 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.4-3626_4-3623dupGT others(2): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355098 | ||||||
chr4:39355098
|
T | TACACAC | 6 | a0001c0002t0002g0251a0001c0003t0001g0052a0001c0003t0001g0085others(3): Show | 6 | HG01175.hp1 HG01175.hp2 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-3628_4-3623dupGT others(4): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355098 | ||||||
chr4:39355098
|
T | TACACACA others(1): Show |
6 | a0001c0001t0001g0011a0001c0002t0002g0055a0001c0003t0001g0054others(3): Show | 6 | HG02055.hp1 HG02145.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-3630_4-3623dupGT others(6): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355098 | ||||||
chr4:39355098
|
T | TACACACA others(3): Show |
1 | a0001c0003t0001g0056 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.4-3632_4-3623dupGT others(8): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355098 | ||||||
chr4:39355098
|
TAC | T | 15 | a0001c0001t0001g0041a0001c0001t0003g0001a0001c0001t0003g0033others(12): Show | 16 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.4-3624_4-3623delGT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355098 | ||||||
chr4:39355098
|
TACAC | T | 5 | a0001c0001t0001g0161a0001c0001t0001g0180a0001c0001t0001g0261others(2): Show | 5 | HG03139.hp1 HG03225.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-3626_4-3623delGT others(2): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355098 | ||||||
chr4:39355098
|
TACACACA others(1): Show |
T | 5 | a0001c0002t0002g0047a0001c0002t0002g0101a0001c0002t0002g0144others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-3630_4-3623delGT others(6): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355098 | ||||||
chr4:39355098
|
TACACACA others(3): Show |
T | 83 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0048others(80): Show | 84 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.4-3632_4-3623delGT others(8): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355098 | ||||||
chr4:39355098
|
TACACACA others(5): Show |
T | 2 | a0001c0002t0002g0097a0001c0002t0002g0100 | 2 | HG02698.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.4-3634_4-3623delGT others(10): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355098 | ||||||
chr4:39355098
|
TACACACA others(7): Show |
T | 3 | a0001c0004t0001g0015a0001c0004t0001g0016a0002c0005t0001g0252 | 3 | HG02451.hp2 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4-3636_4-3623delGT others(12): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355098 | ||||||
chr4:39355104
|
C | T | 2 | a0002c0005t0001g0164a0002c0005t0001g0165 | 2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.4-3628G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355104 | ||||||
chr4:39355108
|
C | T | 1 | a0002c0005t0001g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4-3632G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355108 | ||||||
chr4:39355138
|
A | G | 2 | a0001c0002t0001g0232a0001c0002t0001g0233 | 2 | NA18747.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.4-3662T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355138 | ||||||
chr4:39355142
|
G | C | 1 | a0001c0001t0001g0244 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4-3666C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355142 | ||||||
chr4:39355168
|
A | T | 2 | a0001c0002t0001g0232a0001c0002t0001g0233 | 2 | NA18747.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.4-3692T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355168 | ||||||
chr4:39355193
|
C | T | 3 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0230 | 3 | HG00642.hp2 HG00741.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.4-3717G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355193 | ||||||
chr4:39355351
|
C | T | 1 | a0001c0002t0002g0158 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4-3875G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355351 | ||||||
chr4:39355435
|
A | AAC | 4 | a0001c0001t0001g0194a0001c0001t0001g0229a0001c0003t0001g0052others(1): Show | 4 | HG02015.hp1 HG03831.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-3961_4-3960dupGT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355435 | ||||||
chr4:39355435
|
AAC | A | 16 | a0001c0004t0001g0012a0001c0004t0001g0015a0001c0004t0001g0016others(13): Show | 16 | HG01167.hp1 HG01255.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.4-3961_4-3960delGT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355435 | ||||||
chr4:39355563
|
A | AT | 85 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(82): Show | 86 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.4-4088dupA | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355563 | ||||||
chr4:39355751
|
A | C | 230 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(227): Show | 231 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.4-4275T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355751 | ||||||
chr4:39355785
|
C | T | 2 | a0001c0011t0006g0031a0002c0005t0001g0252 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4-4309G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39355785 | ||||||
chr4:39356000
|
C | CA | 14 | a0001c0001t0001g0011a0001c0001t0001g0088a0001c0001t0001g0185others(11): Show | 14 | HG01109.hp1 HG01175.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.4-4525dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39356000 | ||||||
chr4:39356000
|
C | CAA | 78 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(75): Show | 79 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.4-4526_4-4525dupTT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39356000 | ||||||
chr4:39356000
|
C | CAAA | 6 | a0001c0002t0002g0145a0001c0002t0002g0146a0001c0002t0002g0147others(3): Show | 6 | HG00673.hp2 HG03017.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-4527_4-4525dupTT others(1): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39356000 | ||||||
chr4:39356201
|
C | T | 84 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 84 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.4-4725G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39356201 | ||||||
chr4:39356252
|
A | G | 1 | a0001c0001t0005g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4-4776T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39356252 | ||||||
chr4:39356270
|
G | A | 3 | a0001c0002t0002g0049a0001c0002t0002g0098a0001c0002t0002g0159 | 3 | HG01074.hp2 HG01168.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.4-4794C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39356270 | ||||||
chr4:39356394
|
C | T | 1 | a0001c0002t0002g0099 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4-4918G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39356394 | ||||||
chr4:39356438
|
C | T | 230 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(227): Show | 231 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.4-4962G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39356438 | ||||||
chr4:39356503
|
A | T | 230 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(227): Show | 231 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.4-5027T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39356503 | ||||||
chr4:39356612
|
C | T | 1 | a0001c0001t0003g0039 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4-5136G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39356612 | ||||||
chr4:39357356
|
C | T | 1 | a0001c0002t0002g0098 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.4-5880G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39357356 | ||||||
chr4:39357442
|
T | C | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4-5966A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39357442 | ||||||
chr4:39357601
|
C | T | 20 | a0001c0001t0001g0025a0001c0002t0002g0026a0001c0004t0001g0012others(17): Show | 20 | HG01167.hp1 HG01255.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.4-6125G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39357601 | ||||||
chr4:39357615
|
C | CT | 7 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0258others(4): Show | 7 | HG00597.hp1 HG02055.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.4-6140dupA | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39357615 | ||||||
chr4:39357641
|
G | C | 2 | a0001c0011t0006g0031a0002c0005t0001g0252 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4-6165C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39357641 | ||||||
chr4:39357916
|
G | A | 39 | a0001c0001t0001g0061a0001c0001t0001g0226a0001c0002t0002g0051others(36): Show | 39 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.4-6440C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39357916 | ||||||
chr4:39358120
|
A | G | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4-6644T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39358120 | ||||||
chr4:39358190
|
A | G | 259 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(256): Show | 260 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(257): Show |
intron_variant | MODIFIER | c.4-6714T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39358190 | ||||||
chr4:39358268
|
G | A | 1 | a0001c0002t0002g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4-6792C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39358268 | ||||||
chr4:39358304
|
T | C | 3 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0230 | 3 | HG00642.hp2 HG00741.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.4-6828A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39358304 | ||||||
chr4:39358378
|
G | C | 8 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0180others(5): Show | 8 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.4-6902C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39358378 | ||||||
chr4:39358656
|
A | G | 2 | a0001c0011t0006g0031a0002c0005t0001g0252 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4-7180T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39358656 | ||||||
chr4:39358905
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3+7334T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39358905 | ||||||
chr4:39359012
|
A | G | 1 | a0001c0002t0002g0097 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3+7227T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39359012 | ||||||
chr4:39359042
|
G | C | 1 | a0001c0004t0001g0012 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3+7197C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39359042 | ||||||
chr4:39359049
|
T | C | 2 | a0001c0001t0001g0025a0001c0002t0002g0026 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3+7190A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39359049 | ||||||
chr4:39359064
|
C | A | 1 | a0001c0002t0002g0179 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3+7175G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39359064 | ||||||
chr4:39359436
|
A | G | 3 | a0001c0001t0001g0256a0001c0001t0007g0255a0001c0001t0007g0260 | 3 | HG02145.hp2 HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3+6803T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39359436 | ||||||
chr4:39359449
|
A | G | 85 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(82): Show | 86 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.3+6790T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39359449 | ||||||
chr4:39359554
|
C | T | 1 | a0001c0002t0002g0049 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3+6685G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39359554 | ||||||
chr4:39359589
|
G | A | 2 | a0001c0011t0006g0031a0002c0005t0001g0252 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3+6650C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39359589 | ||||||
chr4:39359821
|
C | CA | 7 | a0001c0001t0001g0011a0001c0001t0001g0229a0001c0001t0001g0246others(4): Show | 7 | HG00733.hp2 HG02145.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+6417dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39359821 | ||||||
chr4:39359931
|
T | C | 86 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 86 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.3+6308A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39359931 | ||||||
chr4:39360040
|
T | C | 5 | a0002c0005t0001g0163a0002c0005t0001g0164a0002c0005t0001g0165others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+6199A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39360040 | ||||||
chr4:39360053
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3+6186T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39360053 | ||||||
chr4:39360088
|
C | T | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3+6151G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39360088 | ||||||
chr4:39360219
|
G | A | 1 | a0001c0003t0001g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3+6020C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39360219 | ||||||
chr4:39360243
|
G | A | 38 | a0001c0001t0001g0061a0001c0001t0011g0274a0001c0002t0002g0053others(35): Show | 38 | HG00323.hp2 HG00438.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.3+5996C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39360243 | ||||||
chr4:39360357
|
G | T | 141 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 141 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.3+5882C>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39360357 | ||||||
chr4:39360364
|
G | T | 1 | a0001c0003t0001g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3+5875C>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39360364 | ||||||
chr4:39360518
|
T | TTAAAA | 7 | a0001c0002t0002g0153a0001c0002t0002g0154a0001c0002t0002g0155others(4): Show | 7 | HG02040.hp1 HG02074.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+5716_3+5720dupTT others(3): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39360518 | ||||||
chr4:39360518
|
T | TTAAAATA others(3): Show |
2 | a0001c0001t0005g0030a0001c0002t0002g0158 | 2 | HG03239.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3+5711_3+5720dupTT others(8): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39360518 | ||||||
chr4:39360518
|
TTAAAATA others(3): Show |
T | 142 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 142 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.3+5711_3+5720delTT others(8): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39360518 | ||||||
chr4:39360603
|
C | T | 38 | a0001c0001t0001g0061a0001c0002t0002g0051a0001c0002t0002g0053others(35): Show | 38 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.3+5636G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39360603 | ||||||
chr4:39360737
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3+5502T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39360737 | ||||||
chr4:39360817
|
C | T | 1 | a0001c0002t0009g0170 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3+5422G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39360817 | ||||||
chr4:39360938
|
G | A | 5 | a0002c0005t0001g0163a0002c0005t0001g0164a0002c0005t0001g0165others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+5301C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39360938 | ||||||
chr4:39361013
|
T | A | 258 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 259 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.3+5226A>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39361013 | ||||||
chr4:39361028
|
A | G | 1 | a0001c0003t0001g0085 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3+5211T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39361028 | ||||||
chr4:39361048
|
T | C | 1 | a0001c0002t0002g0159 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3+5191A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39361048 | ||||||
chr4:39361272
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3+4967G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39361272 | ||||||
chr4:39361321
|
G | A | 55 | a0001c0001t0001g0061a0001c0001t0001g0088a0001c0001t0001g0161others(52): Show | 55 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.3+4918C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39361321 | ||||||
chr4:39361583
|
T | C | 1 | a0001c0003t0001g0077 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3+4656A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39361583 | ||||||
chr4:39361814
|
C | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0180 | 2 | HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3+4425G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39361814 | ||||||
chr4:39361944
|
C | T | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3+4295G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39361944 | ||||||
chr4:39362026
|
G | A | 2 | a0001c0011t0006g0031a0002c0005t0001g0252 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3+4213C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39362026 | ||||||
chr4:39362202
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3+4037C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39362202 | ||||||
chr4:39362243
|
G | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0247 | 2 | HG01255.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.3+3996C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39362243 | ||||||
chr4:39362463
|
G | A | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0180 | 3 | HG03139.hp1 HG03540.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3+3776C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39362463 | ||||||
chr4:39362807
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3+3432G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39362807 | ||||||
chr4:39362994
|
G | A | 1 | a0001c0003t0001g0089 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3+3245C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39362994 | ||||||
chr4:39363068
|
C | G | 85 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 85 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.3+3171G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39363068 | ||||||
chr4:39363175
|
T | G | 1 | a0001c0003t0001g0078 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3+3064A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39363175 | ||||||
chr4:39363214
|
T | C | 1 | a0001c0011t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3+3025A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39363214 | ||||||
chr4:39363236
|
T | C | 56 | a0001c0001t0001g0061a0001c0001t0001g0088a0001c0001t0001g0161others(53): Show | 56 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.3+3003A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39363236 | ||||||
chr4:39363247
|
G | A | 5 | a0003c0006t0001g0263a0003c0006t0001g0264a0003c0006t0001g0265others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3+2992C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39363247 | ||||||
chr4:39363474
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3+2765C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39363474 | ||||||
chr4:39363500
|
C | T | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3+2739G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39363500 | ||||||
chr4:39363531
|
T | C | 39 | a0001c0001t0001g0061a0001c0001t0001g0088a0001c0002t0002g0051others(36): Show | 39 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.3+2708A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39363531 | ||||||
chr4:39363618
|
G | T | 1 | a0001c0002t0002g0160 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3+2621C>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39363618 | ||||||
chr4:39363619
|
G | A | 1 | a0001c0002t0002g0160 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3+2620C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39363619 | ||||||
chr4:39363899
|
AAAAG | A | 7 | a0001c0001t0001g0186a0001c0001t0001g0193a0001c0001t0001g0248others(4): Show | 7 | HG00639.hp2 HG01496.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.3+2336_3+2339delCT others(2): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39363899 | ||||||
chr4:39363900
|
AAAG | A | 248 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(245): Show | 249 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(246): Show |
intron_variant | MODIFIER | c.3+2336_3+2338delCT others(1): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39363900 | ||||||
chr4:39363901
|
AAG | A | 8 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0003t0001g0079others(5): Show | 8 | HG02109.hp2 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.3+2336_3+2337delCT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39363901 | ||||||
chr4:39363934
|
G | A | 28 | a0001c0001t0001g0025a0001c0002t0002g0026a0001c0004t0001g0012others(25): Show | 28 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.3+2305C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39363934 | ||||||
chr4:39364080
|
TA | T | 134 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(131): Show | 134 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.3+2158delT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39364080 | ||||||
chr4:39364080
|
TAA | T | 17 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0180others(14): Show | 17 | HG00323.hp2 HG00558.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.3+2157_3+2158delTT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39364080 | ||||||
chr4:39364097
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3+2142T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39364097 | ||||||
chr4:39364100
|
A | G | 142 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 142 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.3+2139T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39364100 | ||||||
chr4:39364121
|
A | G | 1 | a0001c0001t0005g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3+2118T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39364121 | ||||||
chr4:39364266
|
G | GA | 85 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(82): Show | 86 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.3+1972dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39364266 | ||||||
chr4:39364266
|
GA | G | 144 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(141): Show | 144 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.3+1972delT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39364266 | ||||||
chr4:39364268
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3+1971T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39364268 | ||||||
chr4:39364345
|
G | C | 5 | a0002c0005t0001g0163a0002c0005t0001g0164a0002c0005t0001g0165others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+1894C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39364345 | ||||||
chr4:39364849
|
G | A | 1 | a0001c0001t0008g0090 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3+1390C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39364849 | ||||||
chr4:39364872
|
T | C | 1 | a0001c0002t0002g0049 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3+1367A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39364872 | ||||||
chr4:39364970
|
T | C | 87 | a0001c0001t0001g0122a0001c0002t0002g0002a0001c0002t0002g0047others(84): Show | 88 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.3+1269A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39364970 | ||||||
chr4:39365055
|
A | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1184T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365055 | ||||||
chr4:39365057
|
T | G | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1182A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365057 | ||||||
chr4:39365058
|
T | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1181A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365058 | ||||||
chr4:39365061
|
A | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1178T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365061 | ||||||
chr4:39365064
|
T | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1175A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365064 | ||||||
chr4:39365067
|
A | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1172T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365067 | ||||||
chr4:39365070
|
A | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1169T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365070 | ||||||
chr4:39365071
|
C | T | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1168G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365071 | ||||||
chr4:39365073
|
T | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1166A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365073 | ||||||
chr4:39365074
|
A | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1165T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365074 | ||||||
chr4:39365076
|
T | A | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1163A>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365076 | ||||||
chr4:39365077
|
A | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1162T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365077 | ||||||
chr4:39365079
|
T | G | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1160A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365079 | ||||||
chr4:39365084
|
T | G | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1155A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365084 | ||||||
chr4:39365087
|
T | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1152A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365087 | ||||||
chr4:39365089
|
C | G | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1150G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365089 | ||||||
chr4:39365090
|
A | G | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1149T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365090 | ||||||
chr4:39365092
|
T | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1147A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365092 | ||||||
chr4:39365093
|
G | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1146C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365093 | ||||||
chr4:39365095
|
T | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1144A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365095 | ||||||
chr4:39365100
|
T | G | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1139A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365100 | ||||||
chr4:39365105
|
A | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1134T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365105 | ||||||
chr4:39365106
|
A | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1133T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365106 | ||||||
chr4:39365107
|
A | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1132T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365107 | ||||||
chr4:39365108
|
A | G | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1131T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365108 | ||||||
chr4:39365112
|
G | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1127C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365112 | ||||||
chr4:39365114
|
T | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1125A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365114 | ||||||
chr4:39365115
|
T | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1124A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365115 | ||||||
chr4:39365121
|
A | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1118T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365121 | ||||||
chr4:39365122
|
T | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1117A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365122 | ||||||
chr4:39365131
|
C | G | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1108G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365131 | ||||||
chr4:39365133
|
G | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1106C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365133 | ||||||
chr4:39365136
|
T | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1103A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365136 | ||||||
chr4:39365138
|
G | A | 2 | a0001c0002t0001g0232a0001c0002t0001g0233 | 2 | NA18747.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.3+1101C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365138 | ||||||
chr4:39365138
|
G | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1101C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365138 | ||||||
chr4:39365139
|
A | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1100T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365139 | ||||||
chr4:39365140
|
T | A | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1099A>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365140 | ||||||
chr4:39365143
|
G | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1096C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365143 | ||||||
chr4:39365144
|
G | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1095C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365144 | ||||||
chr4:39365145
|
G | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1094C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365145 | ||||||
chr4:39365146
|
T | G | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1093A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365146 | ||||||
chr4:39365148
|
G | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1091C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365148 | ||||||
chr4:39365149
|
A | C | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1090T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365149 | ||||||
chr4:39365151
|
A | G | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1088T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365151 | ||||||
chr4:39365152
|
T | G | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1087A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365152 | ||||||
chr4:39365153
|
G | GA | 62 | a0001c0001t0001g0061a0001c0001t0001g0161a0001c0001t0001g0162others(59): Show | 62 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.3+1085dupT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365153 | ||||||
chr4:39365153
|
G | GAA | 17 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0180others(14): Show | 17 | HG00323.hp1 HG00597.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.3+1084_3+1085dupTT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365153 | ||||||
chr4:39365153
|
G | GAAA | 56 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(53): Show | 56 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.3+1083_3+1085dupTT others(1): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365153 | ||||||
chr4:39365153
|
G | GAAAA | 20 | a0001c0001t0001g0011a0001c0001t0001g0184a0001c0001t0001g0234others(17): Show | 20 | HG00733.hp2 HG01123.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.3+1082_3+1085dupTT others(2): Show |
RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365153 | ||||||
chr4:39365153
|
GA | G | 23 | a0001c0001t0001g0025a0001c0002t0002g0026a0001c0002t0002g0093others(20): Show | 23 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.3+1085delT | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365153 | ||||||
chr4:39365154
|
A | G | 1 | a0001c0004t0001g0027 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3+1085T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365154 | ||||||
chr4:39365262
|
A | T | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | NA18945.hp1 NA18972.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3+977T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365262 | ||||||
chr4:39365315
|
G | GC | 95 | a0001c0001t0001g0122a0001c0001t0001g0161a0001c0001t0001g0162others(92): Show | 96 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.3+923dupG | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365315 | ||||||
chr4:39365315
|
GC | G | 79 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 79 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.3+923delG | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365315 | ||||||
chr4:39365375
|
G | A | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3+864C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365375 | ||||||
chr4:39365484
|
G | A | 1 | a0001c0001t0007g0260 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3+755C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365484 | ||||||
chr4:39365604
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3+635A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365604 | ||||||
chr4:39365668
|
C | G | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+571G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365668 | ||||||
chr4:39365671
|
T | G | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+568A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365671 | ||||||
chr4:39365672
|
G | C | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+567C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365672 | ||||||
chr4:39365674
|
A | G | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+565T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365674 | ||||||
chr4:39365677
|
C | T | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+562G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365677 | ||||||
chr4:39365678
|
A | T | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+561T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365678 | ||||||
chr4:39365680
|
C | G | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+559G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365680 | ||||||
chr4:39365682
|
A | G | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+557T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365682 | ||||||
chr4:39365683
|
A | T | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+556T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365683 | ||||||
chr4:39365686
|
A | G | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+553T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365686 | ||||||
chr4:39365688
|
A | C | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+551T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365688 | ||||||
chr4:39365690
|
T | C | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+549A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365690 | ||||||
chr4:39365693
|
A | G | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+546T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365693 | ||||||
chr4:39365694
|
A | T | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+545T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365694 | ||||||
chr4:39365696
|
A | T | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+543T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365696 | ||||||
chr4:39365699
|
C | A | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+540G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365699 | ||||||
chr4:39365700
|
T | A | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+539A>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365700 | ||||||
chr4:39365701
|
C | A | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+538G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365701 | ||||||
chr4:39365704
|
C | A | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+535G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365704 | ||||||
chr4:39365705
|
A | G | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+534T>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365705 | ||||||
chr4:39365707
|
G | T | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+532C>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365707 | ||||||
chr4:39365708
|
C | G | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+531G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365708 | ||||||
chr4:39365708
|
C | T | 7 | a0001c0001t0001g0261a0001c0001t0001g0262a0003c0006t0001g0263others(4): Show | 7 | HG02109.hp2 HG02723.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+531G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365708 | ||||||
chr4:39365709
|
C | G | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+530G>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365709 | ||||||
chr4:39365716
|
C | T | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+523G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365716 | ||||||
chr4:39365719
|
A | C | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+520T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365719 | ||||||
chr4:39365720
|
A | T | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+519T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365720 | ||||||
chr4:39365721
|
C | A | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+518G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365721 | ||||||
chr4:39365723
|
C | A | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+516G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365723 | ||||||
chr4:39365724
|
C | A | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+515G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365724 | ||||||
chr4:39365726
|
C | T | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+513G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365726 | ||||||
chr4:39365727
|
T | G | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+512A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365727 | ||||||
chr4:39365730
|
G | A | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+509C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365730 | ||||||
chr4:39365731
|
G | T | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+508C>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365731 | ||||||
chr4:39365733
|
G | A | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+506C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365733 | ||||||
chr4:39365736
|
C | A | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+503G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365736 | ||||||
chr4:39365737
|
G | T | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+502C>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365737 | ||||||
chr4:39365738
|
T | G | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+501A>C | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365738 | ||||||
chr4:39365744
|
A | C | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+495T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365744 | ||||||
chr4:39365745
|
C | A | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+494G>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365745 | ||||||
chr4:39365746
|
G | A | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+493C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365746 | ||||||
chr4:39365747
|
A | T | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+492T>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365747 | ||||||
chr4:39365749
|
C | T | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+490G>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365749 | ||||||
chr4:39365750
|
G | C | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+489C>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365750 | ||||||
chr4:39365751
|
G | T | 1 | a0001c0007t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3+488C>A | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39365751 | ||||||
chr4:39366034
|
T | C | 81 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(78): Show | 81 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.3+205A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39366034 | ||||||
chr4:39366068
|
T | C | 7 | a0001c0001t0001g0261a0001c0001t0001g0262a0003c0006t0001g0263others(4): Show | 7 | HG02109.hp2 HG02723.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+171A>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39366068 | ||||||
chr4:39366204
|
G | A | 5 | a0003c0006t0001g0263a0003c0006t0001g0264a0003c0006t0001g0265others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3+35C>T | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39366204 | ||||||
chr4:39366205
|
A | C | 1 | a0001c0012t0001g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3+34T>G | RFC1 | ENSG00000035928.17 | transcript | ENST00000349703.7 | protein_coding | 1/24 | chr4 | 39366205 |