geneid | 5990 |
---|---|
ensemblid | ENSG00000087903.13 |
hgncid | 9983 |
symbol | RFX2 |
name | regulatory factor X2 |
refseq_nuc | NM_000635.4 |
refseq_prot | NP_000626.2 |
ensembl_nuc | ENST00000303657.10 |
ensembl_prot | ENSP00000306335.4 |
mane_status | MANE Select |
chr | chr19 |
start | 5993164 |
end | 6110500 |
strand | - |
ver | v1.2 |
region | chr19:5993164-6110500 |
region5000 | chr19:5988164-6115500 |
regionname0 | RFX2_chr19_5993164_6110500 |
regionname5000 | RFX2_chr19_5988164_6115500 |
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 | 723 | 222 | 81 | 44 | 60 | 6 | 29 | 43 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0002 | 0/0 | 723 | 70 | 10 | 15 | 29 | 4 | 12 | 15 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0003 | 0/0 | 723 | 9 | 0 | 0 | 9 | 0 | 0 | 7 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0004 | 0/0 | 723 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0005 | 0/0 | 723 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0006 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0007 | 0/0 | 723 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0008 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0009 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2172 | 193 | 55 | 43 | 58 | 6 | 29 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
c0002 | 0/0 | 2172 | 64 | 10 | 15 | 23 | 4 | 12 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
c0003 | 0/0 | 2172 | 14 | 13 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
c0004 | 0/0 | 2172 | 13 | 13 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
c0005 | 0/0 | 2172 | 9 | 0 | 0 | 9 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
c0006 | 0/0 | 2172 | 5 | 0 | 0 | 5 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
c0007 | 0/0 | 2172 | 2 | 0 | 0 | 2 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
c0008 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
c0009 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
c0010 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
c0011 | 0/0 | 2172 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
c0012 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
c0013 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
c0014 | 0/0 | 2172 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
c0015 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
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 | 1/0 | 1788 | 236 | 68 | 44 | 84 | 3 | 36 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0002 | 0/1 | 1785 | 24 | 6 | 7 | 4 | 1 | 5 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0003 | 0/0 | 1785 | 16 | 3 | 5 | 4 | 4 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0004 | 0/0 | 1788 | 6 | 6 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0005 | 0/0 | 1788 | 6 | 6 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0006 | 0/0 | 1788 | 4 | 0 | 0 | 4 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0007 | 0/0 | 1784 | 3 | 0 | 1 | 0 | 2 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0008 | 0/0 | 1788 | 2 | 0 | 1 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0009 | 0/0 | 1785 | 2 | 2 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0010 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0011 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0012 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0013 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0014 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0015 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0016 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0017 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
t0018 | 0/0 | 1785 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2172 | 193 | 55 | 43 | 58 | 6 | 29 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0003 | 0/0 | 2172 | 14 | 13 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0004 | 0/0 | 2172 | 13 | 13 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0007 | 0/0 | 2172 | 2 | 0 | 0 | 2 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0002c0002 | 0/0 | 2172 | 64 | 10 | 15 | 23 | 4 | 12 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0002c0006 | 0/0 | 2172 | 5 | 0 | 0 | 5 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0002c0015 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0003c0005 | 0/0 | 2172 | 9 | 0 | 0 | 9 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0004c0008 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0004c0013 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0005c0014 | 0/0 | 2172 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0006c0009 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0007c0011 | 0/0 | 2172 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0008c0012 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0009c0010 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3959 | 152 | 40 | 37 | 47 | 3 | 24 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0001t0002 | 0/1 | 3956 | 15 | 3 | 2 | 4 | 1 | 4 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0001t0003 | 0/0 | 3956 | 6 | 3 | 2 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0001t0004 | 0/0 | 3959 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0001t0005 | 0/0 | 3959 | 5 | 5 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0001t0006 | 0/0 | 3959 | 4 | 0 | 0 | 4 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0001t0007 | 0/0 | 3955 | 2 | 0 | 1 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0001t0008 | 0/0 | 3959 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0001t0009 | 0/0 | 3956 | 2 | 2 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0001t0012 | 0/0 | 3959 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0001t0013 | 0/0 | 3959 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0001t0015 | 0/0 | 3959 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0001t0016 | 0/0 | 3959 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0001t0017 | 0/0 | 3956 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0003t0001 | 0/0 | 3959 | 7 | 6 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0003t0004 | 0/0 | 3959 | 5 | 5 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0003t0011 | 0/0 | 3959 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0003t0014 | 0/0 | 3959 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0004t0001 | 0/0 | 3959 | 13 | 13 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0001c0007t0001 | 0/0 | 3959 | 2 | 0 | 0 | 2 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0002c0002t0001 | 0/0 | 3959 | 46 | 9 | 5 | 21 | 0 | 11 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0002c0002t0002 | 0/0 | 3956 | 7 | 1 | 5 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0002c0002t0003 | 0/0 | 3956 | 7 | 0 | 3 | 1 | 3 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0002c0002t0007 | 0/0 | 3955 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0002c0002t0008 | 0/0 | 3959 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0002c0002t0010 | 0/0 | 3959 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0002c0002t0018 | 0/0 | 3956 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0002c0006t0001 | 0/0 | 3959 | 3 | 0 | 0 | 3 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0002c0006t0003 | 0/0 | 3956 | 2 | 0 | 0 | 2 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0002c0015t0001 | 0/0 | 3959 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0003c0005t0001 | 0/0 | 3959 | 8 | 0 | 0 | 8 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0003c0005t0003 | 0/0 | 3956 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0004c0008t0002 | 0/0 | 3956 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0004c0013t0002 | 0/0 | 3956 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0005c0014t0001 | 0/0 | 3959 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0006c0009t0005 | 0/0 | 3959 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0007c0011t0001 | 0/0 | 3959 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0008c0012t0001 | 0/0 | 3959 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
a0009c0010t0001 | 0/0 | 3959 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | copy fasta | chr19 | 5988164 | 6115500 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0002g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0007g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0007g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0008g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0009g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0012g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0013g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0015g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0016g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0001t0017g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0003t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0003t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0003t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0003t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0003t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0003t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0003t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0003t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0003t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0003t0011g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0003t0014g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0004t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0004t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0004t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0004t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0004t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0004t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0004t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0004t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0004t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0004t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0004t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0007t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0001c0007t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0007g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0008g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0010g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0002t0018g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0006t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0006t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0006t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0006t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0006t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0002c0015t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0003c0005t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0003c0005t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0003c0005t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0003c0005t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0003c0005t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0003c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0003c0005t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0003c0005t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0003c0005t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0004c0008t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0004c0013t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0005c0014t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0006c0009t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0007c0011t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0008c0012t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
a0009c0010t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0007 | g0267 | EUR | GBR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | GBR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0233 | EUR | FIN | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | CHS | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | CHS | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00544 | hp1 | a0002 | c0015 | t0001 | g0181 | EAS | CHS | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | CHS | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00642 | hp2 | a0002 | c0002 | t0003 | g0076 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | CHS | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00741 | hp1 | a0001 | c0001 | t0007 | g0013 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0155 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01167 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0207 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01192 | hp2 | a0002 | c0002 | t0003 | g0057 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01255 | hp1 | a0002 | c0002 | t0003 | g0056 | AMR | CLM | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01255 | hp2 | a0001 | c0001 | t0012 | g0157 | AMR | CLM | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01256 | hp2 | a0002 | c0002 | t0008 | g0062 | AMR | CLM | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0074 | AMR | CLM | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0212 | AMR | CLM | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01515 | hp1 | a0002 | c0002 | t0003 | g0075 | EUR | IBS | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | IBS | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01884 | hp2 | a0001 | c0004 | t0001 | g0292 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01891 | hp2 | a0001 | c0004 | t0001 | g0294 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0204 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01934 | hp1 | a0002 | c0002 | t0018 | g0215 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01934 | hp2 | a0001 | c0003 | t0001 | g0259 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01975 | hp1 | a0007 | c0011 | t0001 | g0146 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | KHV | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02027 | hp1 | a0003 | c0005 | t0001 | g0045 | EAS | KHV | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02027 | hp2 | a0002 | c0006 | t0001 | g0214 | EAS | KHV | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0302 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | KHV | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | KHV | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02129 | hp2 | a0002 | c0002 | t0003 | g0081 | EAS | KHV | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02135 | hp1 | a0002 | c0006 | t0001 | g0208 | EAS | KHV | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | KHV | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0193 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0077 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02155 | hp1 | a0003 | c0005 | t0001 | g0046 | EAS | CDX | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02155 | hp2 | a0001 | c0001 | t0016 | g0027 | EAS | CDX | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02165 | hp1 | a0002 | c0006 | t0001 | g0100 | EAS | CDX | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CDX | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0295 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02258 | hp2 | a0001 | c0003 | t0001 | g0260 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02280 | hp1 | a0001 | c0003 | t0001 | g0258 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02523 | hp2 | a0002 | c0006 | t0003 | g0095 | EAS | KHV | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02572 | hp1 | a0001 | c0003 | t0004 | g0275 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0066 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02615 | hp1 | a0001 | c0001 | t0015 | g0287 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02622 | hp2 | a0001 | c0004 | t0001 | g0012 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0307 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02647 | hp1 | a0004 | c0008 | t0002 | g0284 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0231 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0192 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0097 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0083 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0303 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0257 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0191 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02895 | hp2 | a0001 | c0004 | t0001 | g0038 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02922 | hp2 | a0001 | c0004 | t0001 | g0279 | AFR | ESN | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02970 | hp2 | a0001 | c0003 | t0011 | g0263 | AFR | ESN | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02976 | hp1 | a0001 | c0003 | t0001 | g0255 | AFR | ESN | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02976 | hp2 | a0001 | c0004 | t0001 | g0280 | AFR | ESN | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03041 | hp2 | a0001 | c0004 | t0001 | g0293 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | MSL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0304 | AFR | ESN | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03195 | hp1 | a0001 | c0003 | t0004 | g0269 | AFR | ESN | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0281 | AFR | ESN | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0230 | AFR | MSL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03225 | hp1 | a0001 | c0003 | t0004 | g0268 | AFR | MSL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03225 | hp2 | a0001 | c0004 | t0001 | g0278 | AFR | MSL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0070 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03453 | hp2 | a0001 | c0001 | t0009 | g0291 | AFR | MSL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0306 | AFR | MSL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0265 | AFR | MSL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03491 | hp1 | a0005 | c0014 | t0001 | g0174 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03516 | hp1 | a0001 | c0004 | t0001 | g0277 | AFR | ESN | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0256 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03540 | hp2 | a0001 | c0004 | t0001 | g0283 | AFR | GWD | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0195 | AFR | MSL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03579 | hp2 | a0004 | c0013 | t0002 | g0251 | AFR | MSL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0058 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0201 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0299 | SAS | STU | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0199 | SAS | STU | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0205 | SAS | BEB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0298 | SAS | BEB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG04184 | hp1 | a0001 | c0001 | t0008 | g0301 | SAS | BEB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0071 | SAS | STU | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | STU | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | STU | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | YRI | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18612 | hp1 | a0009 | c0010 | t0001 | g0047 | EAS | CHB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | CHB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | YRI | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18906 | hp2 | a0001 | c0004 | t0001 | g0276 | AFR | YRI | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18943 | hp1 | a0002 | c0006 | t0003 | g0096 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18944 | hp1 | a0001 | c0007 | t0001 | g0107 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18953 | hp1 | a0003 | c0005 | t0003 | g0020 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18973 | hp2 | a0003 | c0005 | t0001 | g0049 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18983 | hp1 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18983 | hp2 | a0003 | c0005 | t0001 | g0052 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19000 | hp1 | a0003 | c0005 | t0001 | g0048 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19003 | hp1 | a0002 | c0002 | t0010 | g0061 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19005 | hp1 | a0001 | c0001 | t0006 | g0217 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0158 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19011 | hp2 | a0008 | c0012 | t0001 | g0151 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19030 | hp1 | a0001 | c0001 | t0009 | g0245 | AFR | LWK | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | LWK | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19043 | hp1 | a0001 | c0003 | t0014 | g0261 | AFR | LWK | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0190 | AFR | LWK | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19055 | hp2 | a0001 | c0007 | t0001 | g0273 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19064 | hp1 | a0001 | c0001 | t0006 | g0173 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19066 | hp2 | a0003 | c0005 | t0001 | g0050 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19077 | hp1 | a0003 | c0005 | t0001 | g0051 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19077 | hp2 | a0001 | c0001 | t0017 | g0239 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19085 | hp2 | a0003 | c0005 | t0001 | g0197 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19090 | hp2 | a0001 | c0001 | t0013 | g0176 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA19240 | hp2 | a0001 | c0004 | t0001 | g0282 | AFR | YRI | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA20752 | hp1 | a0002 | c0002 | t0007 | g0126 | EUR | TSI | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA20752 | hp2 | a0002 | c0002 | t0003 | g0098 | EUR | TSI | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA20805 | hp1 | a0002 | c0002 | t0003 | g0125 | EUR | TSI | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | TSI | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0297 | SAS | GIH | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | GIH | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0087 | AMR | CLM | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02109 | hp1 | a0001 | c0003 | t0004 | g0262 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02109 | hp2 | a0006 | c0009 | t0005 | g0305 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0194 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0247 | AFR | MSL | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG06807 | hp1 | a0002 | c0002 | t0002 | g0073 | AFR | USA | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | USA | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | USA | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
NA20300 | hp2 | a0001 | c0003 | t0004 | g0264 | AFR | USA | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0169 | REF | REF | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | RFX2_chr19_5988164_6115500 | RFX2 | chr19 | 5988164 | 6115500 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:5994875
|
C | T | 1 | a0008 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.2132G>A | p.Arg711Gln | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 2248/3959 | 2132/2172 | 711/723 | chr19 | 5994875 | ||
chr19:5994902
|
C | A | 1 | a0004 | 2 | HG02647.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.2105G>T | p.Arg702Leu | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 2221/3959 | 2105/2172 | 702/723 | chr19 | 5994902 | ||
chr19:5994929
|
C | T | 1 | a0009 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.2078G>A | p.Arg693His | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 2194/3959 | 2078/2172 | 693/723 | chr19 | 5994929 | ||
chr19:5997106
|
C | T | 1 | a0007 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.1967G>A | p.Arg656His | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/18 | 2083/3959 | 1967/2172 | 656/723 | chr19 | 5997106 | ||
chr19:6008177
|
A | C | 2 | a0003a0009 | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
missense_variant | MODERATE | c.1063T>G | p.Phe355Val | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 10/18 | 1179/3959 | 1063/2172 | 355/723 | chr19 | 6008177 | ||
chr19:6010166
|
C | T | 1 | a0006 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.985G>A | p.Val329Met | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/18 | 1101/3959 | 985/2172 | 329/723 | chr19 | 6010166 | ||
chr19:6040149
|
G | A | 1 | a0005 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.353C>T | p.Thr118Ile | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/18 | 469/3959 | 353/2172 | 118/723 | chr19 | 6040149 | ||
chr19:6042048
|
C | T | 1 | a0002 | 70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
missense_variant | MODERATE | c.256G>A | p.Ala86Thr | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/18 | 372/3959 | 256/2172 | 86/723 | chr19 | 6042048 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:5997105
|
G | A | 1 | a0001c0007 | 2 | NA18944.hp1 NA19055.hp2 |
synonymous_variant | LOW | c.1968C>T | p.Arg656Arg | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/18 | 2084/3959 | 1968/2172 | 656/723 | chr19 | 5997105 | ||
chr19:6007034
|
G | A | 2 | a0003c0005a0009c0010 | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
synonymous_variant | LOW | c.1380C>T | p.Pro460Pro | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/18 | 1496/3959 | 1380/2172 | 460/723 | chr19 | 6007034 | ||
chr19:6007713
|
G | A | 2 | a0003c0005a0009c0010 | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
synonymous_variant | LOW | c.1224C>T | p.Asp408Asp | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 11/18 | 1340/3959 | 1224/2172 | 408/723 | chr19 | 6007713 | ||
chr19:6040136
|
C | T | 2 | a0001c0004a0004c0008 | 14 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(11): Show |
synonymous_variant | LOW | c.366G>A | p.Ser122Ser | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/18 | 482/3959 | 366/2172 | 122/723 | chr19 | 6040136 | ||
chr19:6044208
|
C | T | 1 | a0001c0003 | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
synonymous_variant | LOW | c.165G>A | p.Gln55Gln | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/18 | 281/3959 | 165/2172 | 55/723 | chr19 | 6044208 | ||
chr19:6044211
|
A | T | 1 | a0001c0003 | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
synonymous_variant | LOW | c.162T>A | p.Val54Val | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/18 | 278/3959 | 162/2172 | 54/723 | chr19 | 6044211 | ||
chr19:6047440
|
C | T | 2 | a0002c0006a0002c0015 | 6 | HG00544.hp1 HG02027.hp2 HG02135.hp1 others(3): Show |
synonymous_variant | LOW | c.57G>A | p.Ser19Ser | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/18 | 173/3959 | 57/2172 | 19/723 | chr19 | 6047440 | ||
chr19:6047451
|
G | A | 1 | a0002c0015 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.46C>T | p.Leu16Leu | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/18 | 162/3959 | 46/2172 | 16/723 | chr19 | 6047451 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:5993225
|
G | A | 1 | a0001c0001t0015 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1610C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 1610 | chr19 | 5993225 | |||||
chr19:5993459
|
C | T | 5 | a0001c0001t0002a0001c0001t0017a0002c0002t0002others(2): Show | 25 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1376G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 1376 | chr19 | 5993459 | |||||
chr19:5993586
|
T | C | 2 | a0001c0001t0004a0001c0003t0004 | 6 | HG02109.hp1 HG02572.hp1 HG03195.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1249A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 1249 | chr19 | 5993586 | |||||
chr19:5993769
|
ATATT | A | 2 | a0001c0001t0007a0002c0002t0007 | 3 | HG00140.hp1 HG00741.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1062_*1065delAATA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 1062 | chr19 | 5993769 | |||||
chr19:5993885
|
G | T | 5 | a0001c0001t0002a0001c0001t0017a0002c0002t0002others(2): Show | 25 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*950C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 950 | chr19 | 5993885 | |||||
chr19:5993911
|
C | T | 1 | a0001c0003t0014 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*924G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 924 | chr19 | 5993911 | |||||
chr19:5994123
|
C | T | 1 | a0001c0001t0013 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*712G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 712 | chr19 | 5994123 | |||||
chr19:5994140
|
G | A | 1 | a0001c0001t0017 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*695C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 695 | chr19 | 5994140 | |||||
chr19:5994199
|
C | T | 1 | a0001c0001t0012 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*636G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 636 | chr19 | 5994199 | |||||
chr19:5994209
|
G | A | 2 | a0001c0001t0008a0002c0002t0008 | 2 | HG01256.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*626C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 626 | chr19 | 5994209 | |||||
chr19:5994239
|
G | C | 1 | a0002c0002t0018 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*596C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 596 | chr19 | 5994239 | |||||
chr19:5994322
|
C | G | 7 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(4): Show | 31 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*513G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 513 | chr19 | 5994322 | |||||
chr19:5994347
|
G | A | 1 | a0001c0001t0016 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*488C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 488 | chr19 | 5994347 | |||||
chr19:5994693
|
T | A | 1 | a0002c0002t0010 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*142A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 142 | chr19 | 5994693 | |||||
chr19:5994763
|
C | T | 1 | a0001c0003t0011 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*72G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 72 | chr19 | 5994763 | |||||
chr19:5994765
|
G | T | 1 | a0002c0002t0010 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*70C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 70 | chr19 | 5994765 | |||||
chr19:5994812
|
CGAG | C | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(8): Show | 44 | HG00323.hp2 HG00642.hp2 HG01074.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*20_*22delCTC | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 18/18 | 20 | chr19 | 5994812 | |||||
chr19:6110407
|
G | C | 2 | a0001c0001t0005a0006c0009t0005 | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-23C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/18 | 62911 | chr19 | 6110407 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:5995107
|
C | A | 1 | a0002c0002t0010g0061 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2057-157G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 17/17 | chr19 | 5995107 | ||||||
chr19:5995259
|
A | G | 43 | a0001c0001t0002g0011a0001c0001t0002g0030a0001c0001t0002g0031others(40): Show | 44 | HG00323.hp2 HG00642.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.2057-309T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 17/17 | chr19 | 5995259 | ||||||
chr19:5995374
|
C | T | 1 | a0001c0001t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2056+227G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 17/17 | chr19 | 5995374 | ||||||
chr19:5995439
|
T | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(150): Show | 154 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.2056+162A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 17/17 | chr19 | 5995439 | ||||||
chr19:5995458
|
C | T | 1 | a0001c0001t0009g0245 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2056+143G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 17/17 | chr19 | 5995458 | ||||||
chr19:5995571
|
T | C | 43 | a0001c0001t0002g0011a0001c0001t0002g0030a0001c0001t0002g0031others(40): Show | 44 | HG00323.hp2 HG00642.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.2056+30A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 17/17 | chr19 | 5995571 | ||||||
chr19:5995573
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0091a0002c0002t0001g0191others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2056+28C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 17/17 | chr19 | 5995573 | ||||||
chr19:5995586
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2056+15G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 17/17 | chr19 | 5995586 | ||||||
chr19:5995984
|
G | A | 2 | a0001c0001t0009g0245a0001c0001t0009g0291 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2014-341C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/17 | chr19 | 5995984 | ||||||
chr19:5996037
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0152a0001c0001t0001g0241 | 3 | HG02683.hp1 HG03831.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2014-394G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/17 | chr19 | 5996037 | ||||||
chr19:5996052
|
A | T | 2 | a0001c0001t0005g0304a0001c0004t0001g0279 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2014-409T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/17 | chr19 | 5996052 | ||||||
chr19:5996252
|
A | ACACAAAC others(59): Show |
1 | a0001c0001t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2014-610_2014-609i others(68): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/17 | chr19 | 5996252 | ||||||
chr19:5996252
|
A | ACACAAAC others(59): Show |
125 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0017others(122): Show | 125 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2014-610_2014-609i others(68): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/17 | chr19 | 5996252 | ||||||
chr19:5996252
|
A | ACACAAAC others(57): Show |
24 | a0001c0001t0002g0011a0001c0001t0002g0030a0001c0001t0002g0031others(21): Show | 25 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.2014-610_2014-609i others(66): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/17 | chr19 | 5996252 | ||||||
chr19:5996288
|
G | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0040a0002c0002t0001g0065others(3): Show | 6 | HG00673.hp2 HG02523.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.2014-645C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/17 | chr19 | 5996288 | ||||||
chr19:5996350
|
C | T | 6 | a0001c0004t0001g0038a0001c0004t0001g0283a0002c0002t0001g0190others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2014-707G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/17 | chr19 | 5996350 | ||||||
chr19:5996367
|
C | T | 1 | a0001c0003t0001g0255 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2013+693G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/17 | chr19 | 5996367 | ||||||
chr19:5996428
|
T | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0017others(135): Show | 139 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.2013+632A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/17 | chr19 | 5996428 | ||||||
chr19:5996473
|
T | A | 1 | a0002c0002t0001g0070 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2013+587A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/17 | chr19 | 5996473 | ||||||
chr19:5996677
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(1): Show | 4 | HG02486.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2013+383G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/17 | chr19 | 5996677 | ||||||
chr19:5996753
|
T | C | 163 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(160): Show | 164 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.2013+307A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/17 | chr19 | 5996753 | ||||||
chr19:5996894
|
C | T | 1 | a0001c0003t0004g0262 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2013+166G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/17 | chr19 | 5996894 | ||||||
chr19:5996948
|
C | T | 2 | a0001c0007t0001g0107a0001c0007t0001g0273 | 2 | NA18944.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2013+112G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/17 | chr19 | 5996948 | ||||||
chr19:5996968
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0054a0001c0001t0001g0184others(1): Show | 4 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.2013+92G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 16/17 | chr19 | 5996968 | ||||||
chr19:5997225
|
C | T | 1 | a0002c0002t0001g0212 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1860-12G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5997225 | ||||||
chr19:5997437
|
G | A | 1 | a0001c0001t0008g0301 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1860-224C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5997437 | ||||||
chr19:5997443
|
C | G | 8 | a0001c0001t0001g0053a0001c0001t0001g0135a0001c0001t0001g0240others(5): Show | 8 | HG00741.hp2 HG02280.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1860-230G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5997443 | ||||||
chr19:5997484
|
G | A | 14 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0233others(11): Show | 14 | HG00323.hp2 HG00642.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1860-271C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5997484 | ||||||
chr19:5997569
|
G | C | 4 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(1): Show | 4 | HG02965.hp1 HG03098.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1860-356C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5997569 | ||||||
chr19:5997624
|
C | T | 44 | a0001c0001t0001g0220a0001c0001t0002g0011a0001c0001t0002g0030others(41): Show | 45 | HG00323.hp2 HG00642.hp2 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.1860-411G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5997624 | ||||||
chr19:5997643
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1860-430G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5997643 | ||||||
chr19:5997674
|
C | T | 2 | a0002c0002t0001g0297a0002c0002t0001g0298 | 2 | HG03942.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1860-461G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5997674 | ||||||
chr19:5997675
|
C | T | 1 | a0002c0002t0001g0083 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1860-462G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5997675 | ||||||
chr19:5997960
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1860-747T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5997960 | ||||||
chr19:5998068
|
G | C | 1 | a0001c0004t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1860-855C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5998068 | ||||||
chr19:5998075
|
G | A | 43 | a0001c0001t0001g0220a0001c0001t0002g0011a0001c0001t0002g0031others(40): Show | 44 | HG00323.hp2 HG00642.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.1860-862C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5998075 | ||||||
chr19:5998231
|
C | G | 25 | a0001c0001t0001g0220a0001c0001t0002g0011a0001c0001t0002g0030others(22): Show | 26 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1860-1018G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5998231 | ||||||
chr19:5998293
|
G | GCAAC | 3 | a0001c0001t0001g0004a0001c0001t0008g0301a0002c0002t0008g0062 | 3 | HG01256.hp2 HG04184.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1860-1084_1860-108 others(8): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5998293 | ||||||
chr19:5998388
|
A | C | 2 | a0004c0008t0002g0284a0004c0013t0002g0251 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1860-1175T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5998388 | ||||||
chr19:5998401
|
C | A | 8 | a0001c0001t0001g0053a0001c0001t0001g0135a0001c0001t0001g0240others(5): Show | 8 | HG00741.hp2 HG02280.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1860-1188G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5998401 | ||||||
chr19:5998456
|
A | G | 41 | a0001c0001t0001g0220a0001c0001t0002g0011a0001c0001t0002g0030others(38): Show | 42 | HG00323.hp2 HG00642.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.1860-1243T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5998456 | ||||||
chr19:5998545
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0007g0267 | 2 | HG00140.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1860-1332C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5998545 | ||||||
chr19:5998592
|
C | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0240a0001c0001t0001g0252 | 3 | HG00741.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1860-1379G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5998592 | ||||||
chr19:5998771
|
G | A | 1 | a0001c0001t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1860-1558C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5998771 | ||||||
chr19:5998812
|
C | T | 1 | a0002c0002t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1860-1599G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5998812 | ||||||
chr19:5998879
|
T | G | 14 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0233others(11): Show | 14 | HG00323.hp2 HG00642.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1860-1666A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5998879 | ||||||
chr19:5998954
|
C | T | 1 | a0001c0001t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1860-1741G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5998954 | ||||||
chr19:5999334
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1860-2121C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5999334 | ||||||
chr19:5999361
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1860-2148C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5999361 | ||||||
chr19:5999472
|
G | A | 14 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0233others(11): Show | 14 | HG00323.hp2 HG00642.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1860-2259C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5999472 | ||||||
chr19:5999587
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1859+2228G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5999587 | ||||||
chr19:5999658
|
C | T | 8 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0091others(5): Show | 8 | HG01934.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1859+2157G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5999658 | ||||||
chr19:5999673
|
G | T | 25 | a0001c0001t0001g0220a0001c0001t0002g0011a0001c0001t0002g0030others(22): Show | 26 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1859+2142C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5999673 | ||||||
chr19:5999784
|
G | A | 6 | a0001c0004t0001g0038a0001c0004t0001g0283a0002c0002t0001g0190others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1859+2031C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5999784 | ||||||
chr19:5999806
|
G | A | 5 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0306others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1859+2009C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 5999806 | ||||||
chr19:6000001
|
T | C | 1 | a0001c0001t0009g0291 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1859+1814A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6000001 | ||||||
chr19:6000072
|
C | T | 1 | a0001c0001t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1859+1743G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6000072 | ||||||
chr19:6000076
|
C | T | 7 | a0001c0001t0001g0036a0001c0001t0004g0247a0001c0003t0004g0262others(4): Show | 7 | HG02109.hp1 HG02572.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1859+1739G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6000076 | ||||||
chr19:6000277
|
G | A | 4 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0008g0301others(1): Show | 4 | HG01256.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1859+1538C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6000277 | ||||||
chr19:6000302
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0024others(73): Show | 76 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1859+1513G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6000302 | ||||||
chr19:6000638
|
C | T | 1 | a0002c0002t0001g0205 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1859+1177G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6000638 | ||||||
chr19:6000685
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1859+1130G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6000685 | ||||||
chr19:6000758
|
C | G | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1859+1057G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6000758 | ||||||
chr19:6000796
|
G | T | 1 | a0001c0004t0001g0292 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1859+1019C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6000796 | ||||||
chr19:6000918
|
CT | C | 3 | a0001c0001t0001g0148a0001c0001t0001g0236a0002c0006t0003g0095 | 3 | HG01069.hp2 HG02523.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1859+896delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6000918 | ||||||
chr19:6000972
|
C | G | 1 | a0001c0001t0001g0300 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1859+843G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6000972 | ||||||
chr19:6001111
|
T | C | 1 | a0001c0001t0004g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1859+704A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6001111 | ||||||
chr19:6001274
|
C | T | 1 | a0003c0005t0001g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1859+541G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6001274 | ||||||
chr19:6001472
|
C | G | 1 | a0002c0002t0002g0001 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1859+343G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6001472 | ||||||
chr19:6001540
|
G | C | 1 | a0001c0001t0001g0025 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1859+275C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6001540 | ||||||
chr19:6001654
|
G | T | 1 | a0001c0001t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1859+161C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6001654 | ||||||
chr19:6001666
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1859+149C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 15/17 | chr19 | 6001666 | ||||||
chr19:6002259
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1651-236G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 14/17 | chr19 | 6002259 | ||||||
chr19:6002277
|
T | C | 17 | a0001c0001t0001g0036a0001c0001t0001g0184a0001c0001t0003g0018others(14): Show | 17 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1651-254A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 14/17 | chr19 | 6002277 | ||||||
chr19:6002470
|
G | A | 1 | a0002c0002t0001g0203 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1650+251C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 14/17 | chr19 | 6002470 | ||||||
chr19:6002564
|
G | A | 2 | a0001c0001t0003g0155a0001c0001t0003g0156 | 2 | HG01074.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1650+157C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 14/17 | chr19 | 6002564 | ||||||
chr19:6002607
|
G | A | 1 | a0001c0001t0002g0188 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1650+114C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 14/17 | chr19 | 6002607 | ||||||
chr19:6002620
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1650+101C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 14/17 | chr19 | 6002620 | ||||||
chr19:6002642
|
C | T | 4 | a0001c0001t0001g0101a0001c0001t0001g0168a0001c0001t0016g0027others(1): Show | 4 | HG00423.hp1 HG02155.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.1650+79G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 14/17 | chr19 | 6002642 | ||||||
chr19:6002690
|
C | T | 8 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0091others(5): Show | 8 | HG01934.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1650+31G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 14/17 | chr19 | 6002690 | ||||||
chr19:6002906
|
A | G | 45 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0053others(42): Show | 46 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.1501-36T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6002906 | ||||||
chr19:6003035
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0223 | 2 | HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1501-165C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003035 | ||||||
chr19:6003055
|
G | A | 1 | a0001c0004t0001g0294 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1501-185C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003055 | ||||||
chr19:6003065
|
C | T | 6 | a0001c0001t0001g0036a0001c0001t0004g0247a0001c0003t0004g0262others(3): Show | 6 | HG02109.hp1 HG02572.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1501-195G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003065 | ||||||
chr19:6003127
|
C | T | 25 | a0001c0001t0001g0189a0001c0001t0001g0220a0001c0001t0002g0011others(22): Show | 26 | HG00140.hp2 HG00642.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.1501-257G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003127 | ||||||
chr19:6003484
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1501-614T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003484 | ||||||
chr19:6003515
|
A | G | 171 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(168): Show | 171 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.1501-645T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003515 | ||||||
chr19:6003563
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1500+638C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003563 | ||||||
chr19:6003668
|
A | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 153 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1500+533T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003668 | ||||||
chr19:6003711
|
A | T | 6 | a0001c0001t0004g0247a0001c0003t0004g0262a0001c0003t0004g0264others(3): Show | 6 | HG02109.hp1 HG02572.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1500+490T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003711 | ||||||
chr19:6003714
|
C | T | 1 | a0001c0004t0001g0281 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1500+487G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003714 | ||||||
chr19:6003757
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1500+444G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003757 | ||||||
chr19:6003774
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1500+427C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003774 | ||||||
chr19:6003775
|
T | C | 3 | a0001c0001t0001g0135a0001c0001t0003g0018a0001c0001t0003g0019 | 3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1500+426A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003775 | ||||||
chr19:6003778
|
C | CA | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00597.hp2 HG00673.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1500+422dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003778 | ||||||
chr19:6003778
|
CA | C | 12 | a0001c0001t0001g0119a0001c0001t0001g0168a0001c0001t0002g0188others(9): Show | 12 | HG01943.hp1 HG02165.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1500+422delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003778 | ||||||
chr19:6003778
|
CAAAAAAA others(1): Show |
C | 83 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0023others(80): Show | 83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1500+415_1500+422d others(10): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003778 | ||||||
chr19:6003778
|
CAAAAAAA others(2): Show |
C | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(14): Show | 17 | HG01952.hp1 HG01975.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.1500+414_1500+422d others(11): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003778 | ||||||
chr19:6003778
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0054a0001c0001t0001g0250 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1500+412_1500+422d others(13): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003778 | ||||||
chr19:6003826
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1500+375C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6003826 | ||||||
chr19:6004094
|
G | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(250): Show | 254 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.1500+107C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6004094 | ||||||
chr19:6004124
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1500+77G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 13/17 | chr19 | 6004124 | ||||||
chr19:6004368
|
T | C | 1 | a0002c0002t0001g0298 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1403-70A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6004368 | ||||||
chr19:6004389
|
G | A | 1 | a0001c0001t0002g0299 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1403-91C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6004389 | ||||||
chr19:6004406
|
T | C | 1 | a0002c0002t0001g0295 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1403-108A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6004406 | ||||||
chr19:6004414
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1403-116C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6004414 | ||||||
chr19:6004429
|
C | T | 9 | a0001c0003t0001g0256a0001c0003t0001g0257a0001c0003t0001g0258others(6): Show | 9 | HG01934.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1403-131G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6004429 | ||||||
chr19:6004665
|
G | A | 1 | a0005c0014t0001g0174 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1403-367C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6004665 | ||||||
chr19:6004728
|
C | A | 5 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(2): Show | 5 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.1403-430G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6004728 | ||||||
chr19:6004747
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1403-449G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6004747 | ||||||
chr19:6004800
|
TA | T | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 116 | HG00423.hp1 HG00544.hp1 HG00673.hp2 others(113): Show |
intron_variant | MODIFIER | c.1403-503delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6004800 | ||||||
chr19:6004894
|
G | A | 7 | a0001c0001t0001g0053a0001c0001t0001g0054a0003c0005t0001g0045others(4): Show | 7 | HG01109.hp2 HG02027.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1403-596C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6004894 | ||||||
chr19:6004910
|
G | A | 1 | a0001c0001t0017g0239 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1403-612C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6004910 | ||||||
chr19:6004916
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1403-618G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6004916 | ||||||
chr19:6004917
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1403-619C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6004917 | ||||||
chr19:6004957
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0003g0009 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1403-659T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6004957 | ||||||
chr19:6004993
|
C | A | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1403-695G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6004993 | ||||||
chr19:6005021
|
A | C | 6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1403-723T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6005021 | ||||||
chr19:6005061
|
G | T | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1403-763C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6005061 | ||||||
chr19:6005151
|
T | C | 23 | a0001c0001t0001g0028a0001c0001t0001g0088a0001c0001t0001g0089others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.1403-853A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6005151 | ||||||
chr19:6005326
|
C | T | 1 | a0002c0002t0001g0209 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1403-1028G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6005326 | ||||||
chr19:6005404
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1403-1106G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6005404 | ||||||
chr19:6005502
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1403-1204C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6005502 | ||||||
chr19:6005526
|
G | A | 10 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(7): Show | 10 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1403-1228C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6005526 | ||||||
chr19:6005582
|
T | G | 1 | a0001c0001t0002g0170 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1403-1284A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6005582 | ||||||
chr19:6005908
|
A | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1402+1104T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6005908 | ||||||
chr19:6005938
|
G | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1402+1074C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6005938 | ||||||
chr19:6005940
|
A | C | 22 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0091others(19): Show | 22 | HG01884.hp2 HG01891.hp2 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.1402+1072T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6005940 | ||||||
chr19:6005967
|
G | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1402+1045C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6005967 | ||||||
chr19:6005975
|
C | A | 1 | a0001c0001t0001g0179 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1402+1037G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6005975 | ||||||
chr19:6006021
|
G | A | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(42): Show | 45 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.1402+991C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006021 | ||||||
chr19:6006166
|
A | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1402+846T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006166 | ||||||
chr19:6006171
|
T | C | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(42): Show | 45 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.1402+841A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006171 | ||||||
chr19:6006223
|
C | A | 1 | a0001c0001t0001g0164 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1402+789G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006223 | ||||||
chr19:6006287
|
G | A | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(42): Show | 45 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.1402+725C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006287 | ||||||
chr19:6006293
|
T | TG | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1402+718dupC | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006293 | ||||||
chr19:6006324
|
A | G | 6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1402+688T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006324 | ||||||
chr19:6006353
|
C | T | 6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1402+659G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006353 | ||||||
chr19:6006460
|
A | AT | 7 | a0001c0001t0001g0123a0001c0001t0001g0133a0001c0001t0001g0185others(4): Show | 7 | HG00438.hp1 HG00544.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.1402+551dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006460 | ||||||
chr19:6006460
|
AT | A | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 90 | HG00323.hp1 HG00741.hp2 HG01074.hp1 others(87): Show |
intron_variant | MODIFIER | c.1402+551delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006460 | ||||||
chr19:6006611
|
G | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1402+401C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006611 | ||||||
chr19:6006663
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0003g0009 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1402+349A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006663 | ||||||
chr19:6006709
|
C | G | 10 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(7): Show | 10 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1402+303G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006709 | ||||||
chr19:6006730
|
G | A | 3 | a0001c0004t0001g0292a0001c0004t0001g0293a0001c0004t0001g0294 | 3 | HG01884.hp2 HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1402+282C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006730 | ||||||
chr19:6006758
|
A | AT | 32 | a0001c0001t0001g0010a0001c0001t0001g0136a0001c0001t0001g0240others(29): Show | 32 | HG00741.hp2 HG02055.hp2 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1402+253dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006758 | ||||||
chr19:6006781
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1402+231G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006781 | ||||||
chr19:6006796
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1402+216G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006796 | ||||||
chr19:6006806
|
T | A | 18 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0091others(15): Show | 18 | HG01934.hp2 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1402+206A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006806 | ||||||
chr19:6006827
|
A | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1402+185T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006827 | ||||||
chr19:6006972
|
G | C | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1402+40C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006972 | ||||||
chr19:6006999
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0003g0009 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1402+13C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 12/17 | chr19 | 6006999 | ||||||
chr19:6007265
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0002g0188 | 2 | HG01943.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1248-99T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 11/17 | chr19 | 6007265 | ||||||
chr19:6007343
|
G | A | 17 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(14): Show | 17 | HG02055.hp2 HG02109.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1248-177C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 11/17 | chr19 | 6007343 | ||||||
chr19:6007371
|
G | A | 6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1248-205C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 11/17 | chr19 | 6007371 | ||||||
chr19:6007429
|
T | C | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1247+261A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 11/17 | chr19 | 6007429 | ||||||
chr19:6007623
|
A | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1247+67T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 11/17 | chr19 | 6007623 | ||||||
chr19:6007672
|
C | T | 2 | a0002c0002t0001g0067a0002c0002t0001g0206 | 2 | NA18967.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1247+18G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 11/17 | chr19 | 6007672 | ||||||
chr19:6008335
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1016-111T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6008335 | ||||||
chr19:6008375
|
C | CT | 8 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(5): Show | 8 | HG02071.hp2 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1016-152dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6008375 | ||||||
chr19:6008375
|
CT | C | 27 | a0001c0001t0001g0150a0001c0001t0001g0274a0001c0001t0004g0247others(24): Show | 27 | HG02055.hp2 HG02109.hp2 HG02622.hp2 others(24): Show |
intron_variant | MODIFIER | c.1016-152delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6008375 | ||||||
chr19:6008379
|
T | C | 5 | a0001c0001t0001g0285a0001c0001t0001g0300a0001c0001t0003g0018others(2): Show | 5 | HG02080.hp1 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1016-155A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6008379 | ||||||
chr19:6008494
|
G | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1016-270C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6008494 | ||||||
chr19:6008665
|
A | G | 156 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 157 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1016-441T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6008665 | ||||||
chr19:6008675
|
A | AT | 12 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0090others(9): Show | 12 | HG01175.hp1 HG01496.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.1016-452dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6008675 | ||||||
chr19:6008675
|
AT | A | 71 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(68): Show | 71 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.1016-452delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6008675 | ||||||
chr19:6008960
|
G | A | 6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1016-736C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6008960 | ||||||
chr19:6009044
|
C | T | 6 | a0001c0001t0002g0104a0001c0001t0002g0169a0001c0001t0002g0171others(3): Show | 6 | HG01943.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.1016-820G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6009044 | ||||||
chr19:6009138
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1016-914G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6009138 | ||||||
chr19:6009156
|
C | T | 19 | a0002c0002t0001g0092a0002c0002t0001g0097a0002c0002t0002g0001others(16): Show | 20 | HG00544.hp1 HG00642.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1016-932G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6009156 | ||||||
chr19:6009408
|
A | G | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 81 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(78): Show |
intron_variant | MODIFIER | c.1015+728T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6009408 | ||||||
chr19:6009411
|
C | T | 49 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(46): Show | 49 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.1015+725G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6009411 | ||||||
chr19:6009434
|
T | C | 157 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 158 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.1015+702A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6009434 | ||||||
chr19:6009570
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1015+566C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6009570 | ||||||
chr19:6009794
|
G | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1015+342C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6009794 | ||||||
chr19:6009851
|
C | T | 1 | a0002c0002t0001g0059 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1015+285G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6009851 | ||||||
chr19:6010006
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0064 | 2 | HG03017.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1015+130G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6010006 | ||||||
chr19:6010021
|
G | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1015+115C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6010021 | ||||||
chr19:6010053
|
A | G | 38 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(35): Show | 38 | HG00741.hp2 HG02027.hp1 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.1015+83T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6010053 | ||||||
chr19:6010102
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1015+34C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6010102 | ||||||
chr19:6010116
|
G | C | 8 | a0003c0005t0001g0046a0003c0005t0001g0048a0003c0005t0001g0049others(5): Show | 8 | HG02155.hp1 NA18612.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.1015+20C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6010116 | ||||||
chr19:6010124
|
C | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0166 | 2 | NA18966.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1015+12G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 9/17 | chr19 | 6010124 | ||||||
chr19:6010369
|
C | T | 1 | a0001c0001t0007g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.900-118G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6010369 | ||||||
chr19:6010402
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.900-151C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6010402 | ||||||
chr19:6010469
|
G | A | 1 | a0002c0002t0001g0072 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.900-218C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6010469 | ||||||
chr19:6010561
|
T | C | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.900-310A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6010561 | ||||||
chr19:6010857
|
C | T | 1 | a0001c0001t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.900-606G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6010857 | ||||||
chr19:6010906
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.900-655G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6010906 | ||||||
chr19:6010914
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.900-663G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6010914 | ||||||
chr19:6010971
|
C | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.900-720G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6010971 | ||||||
chr19:6010993
|
T | G | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 81 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(78): Show |
intron_variant | MODIFIER | c.900-742A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6010993 | ||||||
chr19:6011111
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0003g0009 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.900-860C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6011111 | ||||||
chr19:6011130
|
A | T | 80 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(77): Show | 80 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.900-879T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6011130 | ||||||
chr19:6011137
|
T | TTAAAA | 14 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0184others(11): Show | 14 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.900-891_900-887dup others(5): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6011137 | ||||||
chr19:6011137
|
T | TTAAAATA others(3): Show |
30 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(27): Show | 30 | HG01243.hp2 HG01891.hp2 HG01934.hp2 others(27): Show |
intron_variant | MODIFIER | c.900-896_900-887dup others(10): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6011137 | ||||||
chr19:6011332
|
G | A | 1 | a0001c0001t0002g0030 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.900-1081C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6011332 | ||||||
chr19:6011354
|
C | T | 1 | a0002c0002t0001g0070 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.900-1103G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6011354 | ||||||
chr19:6011358
|
T | C | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.900-1107A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6011358 | ||||||
chr19:6011379
|
G | A | 3 | a0001c0004t0001g0292a0001c0004t0001g0293a0001c0004t0001g0294 | 3 | HG01884.hp2 HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.900-1128C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6011379 | ||||||
chr19:6011432
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.900-1181G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6011432 | ||||||
chr19:6011435
|
T | G | 28 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(25): Show | 28 | HG00741.hp2 HG02055.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.900-1184A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6011435 | ||||||
chr19:6011600
|
C | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.900-1349G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6011600 | ||||||
chr19:6011749
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.899+1237G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6011749 | ||||||
chr19:6011797
|
C | A | 2 | a0001c0001t0001g0242a0001c0001t0001g0244 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.899+1189G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6011797 | ||||||
chr19:6011909
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.899+1077A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6011909 | ||||||
chr19:6011966
|
T | C | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.899+1020A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6011966 | ||||||
chr19:6012150
|
T | C | 1 | a0001c0001t0001g0222 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.899+836A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6012150 | ||||||
chr19:6012165
|
T | A | 1 | a0001c0001t0006g0026 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.899+821A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6012165 | ||||||
chr19:6012257
|
CT | C | 17 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(14): Show | 17 | HG02055.hp2 HG02109.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.899+728delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6012257 | ||||||
chr19:6012451
|
G | T | 33 | a0001c0001t0001g0010a0001c0001t0001g0240a0001c0001t0001g0252others(30): Show | 33 | HG00741.hp2 HG02027.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.899+535C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6012451 | ||||||
chr19:6012525
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.899+461G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6012525 | ||||||
chr19:6012602
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.899+384G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6012602 | ||||||
chr19:6012636
|
G | A | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.899+350C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6012636 | ||||||
chr19:6012759
|
T | G | 1 | a0001c0004t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.899+227A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6012759 | ||||||
chr19:6012771
|
A | T | 17 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(14): Show | 17 | HG02055.hp2 HG02109.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.899+215T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6012771 | ||||||
chr19:6012852
|
G | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.899+134C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 8/17 | chr19 | 6012852 | ||||||
chr19:6013191
|
C | CT | 11 | a0001c0003t0004g0269a0003c0005t0001g0045a0003c0005t0001g0046others(8): Show | 11 | HG02027.hp1 HG02155.hp1 HG03195.hp1 others(8): Show |
intron_variant | MODIFIER | c.780-87dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6013191 | ||||||
chr19:6013254
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.780-149G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6013254 | ||||||
chr19:6013375
|
G | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.780-270C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6013375 | ||||||
chr19:6013434
|
C | T | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.780-329G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6013434 | ||||||
chr19:6013478
|
G | A | 1 | a0001c0001t0002g0227 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.780-373C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6013478 | ||||||
chr19:6013494
|
C | CT | 72 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(69): Show | 72 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(69): Show |
intron_variant | MODIFIER | c.780-390dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6013494 | ||||||
chr19:6013494
|
C | CTTT | 6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.780-392_780-390dup others(3): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6013494 | ||||||
chr19:6013535
|
C | T | 12 | a0001c0001t0004g0247a0001c0004t0001g0012a0001c0004t0001g0276others(9): Show | 12 | HG02622.hp2 HG02647.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.780-430G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6013535 | ||||||
chr19:6013664
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.780-559C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6013664 | ||||||
chr19:6013725
|
G | A | 23 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(20): Show | 23 | HG00741.hp2 HG02055.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.780-620C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6013725 | ||||||
chr19:6013734
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.780-629G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6013734 | ||||||
chr19:6013800
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0043 | 2 | NA18955.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.780-695A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6013800 | ||||||
chr19:6013829
|
G | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.780-724C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6013829 | ||||||
chr19:6013979
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.780-874G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6013979 | ||||||
chr19:6014168
|
T | G | 1 | a0001c0001t0001g0032 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.780-1063A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6014168 | ||||||
chr19:6014297
|
G | A | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.780-1192C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6014297 | ||||||
chr19:6014307
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.780-1202G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6014307 | ||||||
chr19:6014472
|
C | A | 1 | a0001c0001t0001g0041 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.780-1367G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6014472 | ||||||
chr19:6014518
|
C | T | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.780-1413G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6014518 | ||||||
chr19:6014534
|
C | T | 16 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(13): Show | 16 | HG00741.hp2 HG02622.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.780-1429G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6014534 | ||||||
chr19:6014579
|
C | G | 6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.780-1474G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6014579 | ||||||
chr19:6014621
|
G | A | 70 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0183others(67): Show | 71 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.779+1469C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6014621 | ||||||
chr19:6014659
|
A | G | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.779+1431T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6014659 | ||||||
chr19:6014974
|
A | C | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 81 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(78): Show |
intron_variant | MODIFIER | c.779+1116T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6014974 | ||||||
chr19:6015012
|
C | A | 47 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(44): Show | 47 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.779+1078G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6015012 | ||||||
chr19:6015055
|
T | C | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 81 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(78): Show |
intron_variant | MODIFIER | c.779+1035A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6015055 | ||||||
chr19:6015058
|
T | A | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.779+1032A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6015058 | ||||||
chr19:6015107
|
C | T | 1 | a0002c0002t0001g0070 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.779+983G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6015107 | ||||||
chr19:6015108
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0141 | 2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.779+982C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6015108 | ||||||
chr19:6015289
|
G | T | 12 | a0001c0001t0004g0247a0001c0004t0001g0012a0001c0004t0001g0276others(9): Show | 12 | HG02622.hp2 HG02647.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.779+801C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6015289 | ||||||
chr19:6015495
|
GTT | G | 4 | a0001c0001t0001g0300a0001c0001t0003g0018a0001c0001t0003g0019others(1): Show | 4 | HG02080.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.779+593_779+594del others(2): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6015495 | ||||||
chr19:6015643
|
C | G | 2 | a0001c0001t0001g0010a0001c0001t0003g0009 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.779+447G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6015643 | ||||||
chr19:6015803
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.779+287C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6015803 | ||||||
chr19:6015882
|
G | A | 47 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(44): Show | 47 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.779+208C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6015882 | ||||||
chr19:6015983
|
C | T | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.779+107G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 7/17 | chr19 | 6015983 | ||||||
chr19:6016417
|
G | A | 1 | a0001c0001t0009g0291 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.598-146C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6016417 | ||||||
chr19:6016425
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.598-154G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6016425 | ||||||
chr19:6016539
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0266 | 2 | NA19012.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.598-268G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6016539 | ||||||
chr19:6016634
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.598-363C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6016634 | ||||||
chr19:6016653
|
A | G | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 81 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(78): Show |
intron_variant | MODIFIER | c.598-382T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6016653 | ||||||
chr19:6016681
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0003g0009 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.598-410C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6016681 | ||||||
chr19:6017016
|
ACTGAGAT others(2): Show |
A | 8 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(5): Show | 8 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.598-754_598-746del others(9): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6017016 | ||||||
chr19:6017017
|
CTGAGATC others(6): Show |
C | 1 | a0001c0001t0001g0122 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.598-759_598-747del others(13): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6017017 | ||||||
chr19:6017069
|
A | G | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(12): Show | 15 | HG00741.hp2 HG02486.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.598-798T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6017069 | ||||||
chr19:6017151
|
C | G | 1 | a0001c0004t0001g0293 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.598-880G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6017151 | ||||||
chr19:6017184
|
G | A | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-913C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6017184 | ||||||
chr19:6017195
|
T | C | 1 | a0002c0002t0002g0074 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.598-924A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6017195 | ||||||
chr19:6017383
|
T | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(35): Show | 38 | HG00741.hp2 HG01109.hp2 HG02027.hp1 others(35): Show |
intron_variant | MODIFIER | c.598-1112A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6017383 | ||||||
chr19:6017384
|
G | A | 1 | a0001c0004t0001g0281 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.598-1113C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6017384 | ||||||
chr19:6017567
|
G | A | 4 | a0001c0001t0001g0300a0001c0001t0003g0018a0001c0001t0003g0019others(1): Show | 4 | HG02080.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-1296C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6017567 | ||||||
chr19:6017666
|
G | A | 1 | a0001c0003t0014g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.598-1395C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6017666 | ||||||
chr19:6018025
|
AG | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.598-1755delC | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6018025 | ||||||
chr19:6018036
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0091others(1): Show | 4 | HG02055.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.598-1765G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6018036 | ||||||
chr19:6018195
|
C | A | 11 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(8): Show | 11 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.598-1924G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6018195 | ||||||
chr19:6018203
|
C | G | 1 | a0002c0002t0001g0295 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.598-1932G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6018203 | ||||||
chr19:6018221
|
T | A | 1 | a0001c0001t0001g0002 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.598-1950A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6018221 | ||||||
chr19:6018245
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.598-1974G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6018245 | ||||||
chr19:6018328
|
G | A | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.598-2057C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6018328 | ||||||
chr19:6018498
|
G | C | 1 | a0001c0001t0001g0289 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.598-2227C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6018498 | ||||||
chr19:6018535
|
G | A | 22 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(19): Show | 22 | HG00741.hp2 HG02615.hp1 HG02622.hp2 others(19): Show |
intron_variant | MODIFIER | c.598-2264C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6018535 | ||||||
chr19:6018697
|
G | A | 9 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(6): Show | 9 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-2426C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6018697 | ||||||
chr19:6018709
|
G | A | 9 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(6): Show | 9 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-2438C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6018709 | ||||||
chr19:6018891
|
G | GT | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.598-2621dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6018891 | ||||||
chr19:6018916
|
G | A | 12 | a0001c0001t0004g0247a0001c0004t0001g0012a0001c0004t0001g0276others(9): Show | 12 | HG02622.hp2 HG02647.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.598-2645C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6018916 | ||||||
chr19:6018948
|
C | T | 10 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(7): Show | 10 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.598-2677G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6018948 | ||||||
chr19:6018954
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-2683C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6018954 | ||||||
chr19:6019037
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.598-2766A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019037 | ||||||
chr19:6019123
|
G | A | 14 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(11): Show | 14 | HG00741.hp2 HG02027.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.598-2852C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019123 | ||||||
chr19:6019356
|
A | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.598-3085T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019356 | ||||||
chr19:6019428
|
G | A | 29 | a0001c0001t0001g0101a0001c0001t0001g0102a0002c0002t0001g0092others(26): Show | 30 | HG00544.hp1 HG00642.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.598-3157C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019428 | ||||||
chr19:6019510
|
GTA | G | 9 | a0003c0005t0001g0045a0003c0005t0001g0048a0003c0005t0001g0049others(6): Show | 9 | HG02027.hp1 NA18612.hp1 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-3241_598-3240d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019510 | ||||||
chr19:6019512
|
A | ATG | 166 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(163): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.598-3243_598-3242d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019512 | ||||||
chr19:6019512
|
A | ATGTG | 17 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0130others(14): Show | 17 | HG01069.hp1 HG01192.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.598-3245_598-3242d others(6): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019512 | ||||||
chr19:6019512
|
A | ATGTGTG | 13 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0053others(10): Show | 13 | HG01891.hp2 HG02055.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.598-3247_598-3242d others(8): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019512 | ||||||
chr19:6019512
|
A | ATGTGTGT others(1): Show |
7 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0002g0196others(4): Show | 7 | HG00741.hp2 HG01884.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.598-3249_598-3242d others(10): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019512 | ||||||
chr19:6019512
|
A | ATGTGTGT others(3): Show |
6 | a0001c0001t0001g0054a0001c0001t0001g0286a0001c0001t0001g0288others(3): Show | 6 | HG01109.hp2 HG02615.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-3251_598-3242d others(12): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019512 | ||||||
chr19:6019512
|
A | ATGTGTGT others(5): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(3): Show | 6 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-3253_598-3242d others(14): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019512 | ||||||
chr19:6019512
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0001g0289 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.598-3255_598-3242d others(16): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019512 | ||||||
chr19:6019512
|
A | G | 1 | a0003c0005t0001g0046 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.598-3241T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019512 | ||||||
chr19:6019512
|
ATG | A | 4 | a0001c0001t0001g0113a0001c0001t0002g0299a0002c0002t0002g0001others(1): Show | 5 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-3243_598-3242d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019512 | ||||||
chr19:6019512
|
ATGTG | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0128others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-3245_598-3242d others(6): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019512 | ||||||
chr19:6019544
|
G | GTGTA | 3 | a0001c0003t0001g0256a0001c0003t0001g0258a0001c0003t0011g0263 | 3 | HG02280.hp1 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.598-3274_598-3273i others(6): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019544 | ||||||
chr19:6019544
|
G | GTGTGTA | 11 | a0001c0003t0001g0255a0001c0003t0001g0257a0001c0003t0001g0259others(8): Show | 11 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.598-3274_598-3273i others(8): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019544 | ||||||
chr19:6019546
|
A | G | 52 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 52 | HG01123.hp1 HG01243.hp2 HG01891.hp1 others(49): Show |
intron_variant | MODIFIER | c.598-3275T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019546 | ||||||
chr19:6019561
|
CT | C | 40 | a0001c0001t0001g0164a0001c0003t0001g0255a0001c0003t0001g0256others(37): Show | 40 | HG01884.hp2 HG01891.hp2 HG01934.hp2 others(37): Show |
intron_variant | MODIFIER | c.598-3291delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019561 | ||||||
chr19:6019585
|
G | GAT | 82 | a0001c0001t0001g0025a0001c0001t0001g0041a0001c0001t0001g0055others(79): Show | 83 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.598-3316_598-3315d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019585 | ||||||
chr19:6019585
|
G | GATAT | 19 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0296others(16): Show | 19 | HG00741.hp2 HG01123.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.598-3318_598-3315d others(6): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019585 | ||||||
chr19:6019585
|
G | GATATAT | 10 | a0001c0001t0001g0254a0001c0003t0001g0256a0001c0003t0004g0268others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.598-3320_598-3315d others(8): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019585 | ||||||
chr19:6019585
|
G | GATATATA others(3): Show |
5 | a0001c0004t0001g0279a0001c0004t0001g0280a0001c0004t0001g0281others(2): Show | 5 | HG02922.hp2 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-3324_598-3315d others(12): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019585 | ||||||
chr19:6019585
|
G | GATATATA others(7): Show |
5 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(2): Show | 5 | HG02647.hp1 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-3328_598-3315d others(16): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019585 | ||||||
chr19:6019585
|
GAT | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.598-3316_598-3315d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019585 | ||||||
chr19:6019605
|
T | TA | 3 | a0001c0001t0001g0040a0001c0001t0001g0103a0001c0001t0001g0167 | 3 | HG01192.hp1 NA18964.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.598-3335_598-3334i others(3): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019605 | ||||||
chr19:6019631
|
C | T | 1 | a0001c0001t0013g0176 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.598-3360G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019631 | ||||||
chr19:6019648
|
G | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.598-3377C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019648 | ||||||
chr19:6019700
|
C | T | 1 | a0002c0002t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.598-3429G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019700 | ||||||
chr19:6019708
|
C | T | 10 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(7): Show | 10 | HG01934.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.598-3437G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019708 | ||||||
chr19:6019820
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.598-3549G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019820 | ||||||
chr19:6019887
|
T | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG02080.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-3616A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019887 | ||||||
chr19:6019956
|
C | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.598-3685G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019956 | ||||||
chr19:6019967
|
G | A | 23 | a0001c0001t0001g0024a0001c0001t0001g0105a0001c0001t0001g0106others(20): Show | 23 | HG00597.hp2 HG00735.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.598-3696C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6019967 | ||||||
chr19:6020250
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.598-3979G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6020250 | ||||||
chr19:6020318
|
A | C | 1 | a0001c0001t0001g0254 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.598-4047T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6020318 | ||||||
chr19:6020426
|
C | G | 79 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(76): Show | 79 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(76): Show |
intron_variant | MODIFIER | c.598-4155G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6020426 | ||||||
chr19:6020611
|
A | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.598-4340T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6020611 | ||||||
chr19:6020672
|
G | A | 1 | a0002c0002t0001g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.598-4401C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6020672 | ||||||
chr19:6020750
|
T | C | 21 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0133others(18): Show | 21 | HG00140.hp2 HG01256.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.598-4479A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6020750 | ||||||
chr19:6020764
|
G | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0224a0001c0001t0001g0237 | 3 | HG00621.hp1 HG03017.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.598-4493C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6020764 | ||||||
chr19:6020939
|
G | A | 1 | a0002c0002t0001g0093 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.598-4668C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6020939 | ||||||
chr19:6021127
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.598-4856T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6021127 | ||||||
chr19:6021179
|
G | T | 6 | a0001c0003t0014g0261a0001c0004t0001g0012a0001c0004t0001g0038others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-4908C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6021179 | ||||||
chr19:6021195
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.598-4924G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6021195 | ||||||
chr19:6021294
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.597+4869C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6021294 | ||||||
chr19:6021418
|
G | A | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.597+4745C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6021418 | ||||||
chr19:6021523
|
G | A | 21 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0133others(18): Show | 21 | HG00140.hp2 HG01256.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.597+4640C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6021523 | ||||||
chr19:6021679
|
G | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(13): Show | 16 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.597+4484C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6021679 | ||||||
chr19:6021761
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.597+4402A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6021761 | ||||||
chr19:6021843
|
T | C | 79 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(76): Show | 79 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(76): Show |
intron_variant | MODIFIER | c.597+4320A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6021843 | ||||||
chr19:6021887
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.597+4276A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6021887 | ||||||
chr19:6021914
|
G | T | 4 | a0001c0004t0001g0038a0001c0004t0001g0292a0001c0004t0001g0293others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.597+4249C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6021914 | ||||||
chr19:6021964
|
G | C | 1 | a0001c0001t0001g0032 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.597+4199C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6021964 | ||||||
chr19:6022099
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.597+4064G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6022099 | ||||||
chr19:6022169
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.597+3994G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6022169 | ||||||
chr19:6022260
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.597+3903G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6022260 | ||||||
chr19:6022412
|
C | T | 1 | a0001c0004t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.597+3751G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6022412 | ||||||
chr19:6022514
|
C | A | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.597+3649G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6022514 | ||||||
chr19:6022547
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.597+3616G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6022547 | ||||||
chr19:6022560
|
C | T | 11 | a0001c0001t0016g0027a0003c0005t0001g0045a0003c0005t0001g0046others(8): Show | 11 | HG02027.hp1 HG02155.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.597+3603G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6022560 | ||||||
chr19:6022581
|
T | C | 20 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(17): Show | 20 | HG00741.hp2 HG02027.hp1 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.597+3582A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6022581 | ||||||
chr19:6022591
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0166 | 2 | NA18966.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.597+3572G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6022591 | ||||||
chr19:6022634
|
C | T | 6 | a0001c0001t0001g0253a0002c0002t0001g0068a0002c0002t0001g0077others(3): Show | 6 | HG01074.hp1 HG01081.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+3529G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6022634 | ||||||
chr19:6022741
|
C | A | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.597+3422G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6022741 | ||||||
chr19:6022943
|
C | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.597+3220G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6022943 | ||||||
chr19:6023099
|
G | C | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.597+3064C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6023099 | ||||||
chr19:6023151
|
A | G | 153 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 154 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.597+3012T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6023151 | ||||||
chr19:6023336
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.597+2827T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6023336 | ||||||
chr19:6023376
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.597+2787C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6023376 | ||||||
chr19:6023391
|
A | G | 4 | a0001c0001t0001g0300a0001c0001t0003g0018a0001c0001t0003g0019others(1): Show | 4 | HG02080.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+2772T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6023391 | ||||||
chr19:6023406
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0186 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.597+2757G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6023406 | ||||||
chr19:6023500
|
C | T | 2 | a0002c0006t0003g0095a0002c0006t0003g0096 | 2 | HG02523.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.597+2663G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6023500 | ||||||
chr19:6023508
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.597+2655A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6023508 | ||||||
chr19:6023612
|
C | T | 1 | a0002c0002t0001g0078 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.597+2551G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6023612 | ||||||
chr19:6023684
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.597+2479G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6023684 | ||||||
chr19:6023865
|
C | T | 2 | a0002c0002t0003g0056a0002c0002t0003g0057 | 2 | HG01192.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.597+2298G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6023865 | ||||||
chr19:6023873
|
A | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.597+2290T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6023873 | ||||||
chr19:6023920
|
C | T | 2 | a0001c0001t0006g0158a0001c0001t0006g0173 | 2 | NA19007.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.597+2243G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6023920 | ||||||
chr19:6023940
|
C | T | 1 | a0001c0001t0007g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.597+2223G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6023940 | ||||||
chr19:6023977
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.597+2186C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6023977 | ||||||
chr19:6024023
|
A | G | 11 | a0001c0001t0001g0014a0003c0005t0001g0045a0003c0005t0001g0046others(8): Show | 11 | HG01358.hp2 HG02027.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.597+2140T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024023 | ||||||
chr19:6024041
|
A | G | 1 | a0001c0001t0002g0137 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.597+2122T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024041 | ||||||
chr19:6024204
|
G | A | 4 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0178others(1): Show | 4 | HG01884.hp1 HG02004.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+1959C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024204 | ||||||
chr19:6024376
|
A | G | 1 | a0001c0001t0002g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.597+1787T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024376 | ||||||
chr19:6024577
|
G | A | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 58 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(55): Show |
intron_variant | MODIFIER | c.597+1586C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024577 | ||||||
chr19:6024591
|
A | G | 12 | a0001c0001t0001g0014a0002c0002t0001g0063a0003c0005t0001g0045others(9): Show | 12 | HG01358.hp2 HG02027.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.597+1572T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024591 | ||||||
chr19:6024647
|
A | G | 4 | a0002c0002t0001g0065a0002c0002t0001g0200a0002c0002t0001g0203others(1): Show | 4 | HG00423.hp1 HG00673.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.597+1516T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024647 | ||||||
chr19:6024687
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.597+1476C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024687 | ||||||
chr19:6024716
|
A | AGTGAGGA others(22): Show |
2 | a0001c0001t0001g0189a0002c0002t0001g0209 | 2 | HG00140.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.597+1418_597+1446d others(31): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024716 | ||||||
chr19:6024716
|
AGTGAGGA others(22): Show |
A | 4 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0089others(1): Show | 4 | HG01515.hp1 HG02055.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+1418_597+1446d others(31): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024716 | ||||||
chr19:6024716
|
AGTGAGGA others(51): Show |
A | 1 | a0001c0001t0002g0196 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.597+1389_597+1446d others(60): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024716 | ||||||
chr19:6024716
|
AGTGAGGA others(80): Show |
A | 16 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(13): Show | 16 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.597+1360_597+1446d others(89): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024716 | ||||||
chr19:6024731
|
G | GAGGACGG others(138): Show |
1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.597+1431_597+1432i others(147): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024731 | ||||||
chr19:6024744
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.597+1419G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024744 | ||||||
chr19:6024789
|
GAGGACGG others(109): Show |
G | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.597+1258_597+1373d others(2): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024789 | ||||||
chr19:6024818
|
G | GAGGACGG others(22): Show |
35 | a0001c0001t0001g0010a0001c0001t0001g0242a0001c0001t0001g0243others(32): Show | 35 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.597+1344_597+1345i others(31): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024818 | ||||||
chr19:6024847
|
G | C | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(42): Show | 45 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.597+1316C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024847 | ||||||
chr19:6024847
|
G | GAGGACGG others(22): Show |
11 | a0001c0003t0004g0275a0001c0004t0001g0012a0001c0004t0001g0276others(8): Show | 11 | HG02572.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.597+1315_597+1316i others(31): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024847 | ||||||
chr19:6024847
|
G | GAGGACGG others(109): Show |
2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.597+1315_597+1316i others(118): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024847 | ||||||
chr19:6024876
|
G | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0053others(52): Show | 55 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(52): Show |
intron_variant | MODIFIER | c.597+1287C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024876 | ||||||
chr19:6024876
|
G | GAGGACGG others(22): Show |
5 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(2): Show | 5 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+1258_597+1286d others(31): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024876 | ||||||
chr19:6024876
|
G | GAGGACGG others(51): Show |
4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+1229_597+1286d others(60): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024876 | ||||||
chr19:6024905
|
C | G | 2 | a0001c0001t0001g0159a0007c0011t0001g0146 | 2 | HG01975.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.597+1258G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6024905 | ||||||
chr19:6025124
|
A | G | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(60): Show | 63 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(60): Show |
intron_variant | MODIFIER | c.597+1039T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6025124 | ||||||
chr19:6025145
|
A | G | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 69 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(66): Show |
intron_variant | MODIFIER | c.597+1018T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6025145 | ||||||
chr19:6025220
|
C | T | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.597+943G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6025220 | ||||||
chr19:6025234
|
G | A | 9 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(6): Show | 9 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.597+929C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6025234 | ||||||
chr19:6025687
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.597+476C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6025687 | ||||||
chr19:6025715
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.597+448A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6025715 | ||||||
chr19:6025737
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.597+426G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6025737 | ||||||
chr19:6025784
|
C | CT | 21 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0089others(18): Show | 21 | HG00438.hp1 HG01243.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.597+378dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6025784 | ||||||
chr19:6025784
|
CT | C | 9 | a0003c0005t0001g0046a0003c0005t0001g0048a0003c0005t0001g0049others(6): Show | 9 | HG02155.hp1 NA18612.hp1 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.597+378delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6025784 | ||||||
chr19:6025879
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.597+284C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6025879 | ||||||
chr19:6026110
|
A | G | 1 | a0001c0001t0002g0188 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.597+53T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 6/17 | chr19 | 6026110 | ||||||
chr19:6026255
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.523-18T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6026255 | ||||||
chr19:6026351
|
G | C | 5 | a0002c0002t0001g0068a0002c0002t0001g0077a0002c0002t0001g0094others(2): Show | 5 | HG01074.hp1 HG01081.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.523-114C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6026351 | ||||||
chr19:6026381
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.523-144G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6026381 | ||||||
chr19:6026441
|
C | T | 14 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(11): Show | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.523-204G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6026441 | ||||||
chr19:6026622
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.523-385C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6026622 | ||||||
chr19:6026776
|
G | A | 1 | a0001c0003t0001g0258 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.523-539C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6026776 | ||||||
chr19:6026780
|
G | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-543C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6026780 | ||||||
chr19:6026808
|
T | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-571A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6026808 | ||||||
chr19:6026933
|
C | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-696G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6026933 | ||||||
chr19:6026956
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.523-719C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6026956 | ||||||
chr19:6026982
|
C | T | 5 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0178others(2): Show | 5 | HG01884.hp1 HG02004.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.523-745G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6026982 | ||||||
chr19:6027006
|
C | T | 3 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0290 | 3 | HG02965.hp1 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.523-769G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6027006 | ||||||
chr19:6027025
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.523-788C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6027025 | ||||||
chr19:6027050
|
C | T | 14 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(11): Show | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.523-813G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6027050 | ||||||
chr19:6027149
|
T | C | 20 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(17): Show | 20 | HG00741.hp2 HG02027.hp1 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.523-912A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6027149 | ||||||
chr19:6027150
|
T | TAAAACAC others(2): Show |
10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-914_523-913ins others(9): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6027150 | ||||||
chr19:6027215
|
G | T | 9 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(6): Show | 9 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.523-978C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6027215 | ||||||
chr19:6027227
|
G | A | 10 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(7): Show | 10 | HG00741.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.523-990C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6027227 | ||||||
chr19:6027367
|
C | G | 14 | a0001c0004t0001g0012a0001c0004t0001g0038a0001c0004t0001g0276others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.523-1130G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6027367 | ||||||
chr19:6027414
|
G | A | 9 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(6): Show | 9 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.523-1177C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6027414 | ||||||
chr19:6027436
|
C | T | 1 | a0002c0002t0001g0080 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.523-1199G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6027436 | ||||||
chr19:6027468
|
C | T | 4 | a0001c0003t0004g0262a0001c0003t0004g0268a0001c0003t0004g0269others(1): Show | 4 | HG02109.hp1 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.523-1231G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6027468 | ||||||
chr19:6027517
|
G | A | 10 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(7): Show | 10 | HG00741.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.523-1280C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6027517 | ||||||
chr19:6027535
|
C | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-1298G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6027535 | ||||||
chr19:6027569
|
C | T | 1 | a0004c0013t0002g0251 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.523-1332G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6027569 | ||||||
chr19:6027609
|
T | A | 1 | a0001c0001t0001g0237 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.523-1372A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6027609 | ||||||
chr19:6028017
|
C | T | 1 | a0002c0002t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.523-1780G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6028017 | ||||||
chr19:6028105
|
A | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.523-1868T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6028105 | ||||||
chr19:6028204
|
T | C | 1 | a0002c0015t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.523-1967A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6028204 | ||||||
chr19:6028204
|
T | TA | 16 | a0001c0001t0001g0300a0001c0001t0008g0301a0001c0004t0001g0012others(13): Show | 16 | HG01884.hp2 HG01891.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.523-1968dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6028204 | ||||||
chr19:6028215
|
AC | A | 14 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(11): Show | 14 | HG00741.hp2 HG02027.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.523-1979delG | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6028215 | ||||||
chr19:6028216
|
C | A | 134 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 135 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.523-1979G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6028216 | ||||||
chr19:6028293
|
C | T | 1 | a0002c0002t0003g0075 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.523-2056G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6028293 | ||||||
chr19:6028425
|
G | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-2188C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6028425 | ||||||
chr19:6028462
|
G | A | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 69 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(66): Show |
intron_variant | MODIFIER | c.523-2225C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6028462 | ||||||
chr19:6028489
|
A | G | 1 | a0002c0002t0003g0057 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.523-2252T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6028489 | ||||||
chr19:6028626
|
T | C | 1 | a0005c0014t0001g0174 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.523-2389A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6028626 | ||||||
chr19:6028670
|
G | A | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.523-2433C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6028670 | ||||||
chr19:6028707
|
TA | T | 8 | a0001c0001t0001g0101a0001c0001t0001g0253a0001c0001t0001g0286others(5): Show | 8 | HG01891.hp1 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.523-2471delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6028707 | ||||||
chr19:6028783
|
T | C | 14 | a0001c0004t0001g0012a0001c0004t0001g0038a0001c0004t0001g0276others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.523-2546A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6028783 | ||||||
chr19:6028806
|
G | A | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 59 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(56): Show |
intron_variant | MODIFIER | c.523-2569C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6028806 | ||||||
chr19:6028812
|
C | T | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.523-2575G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6028812 | ||||||
chr19:6029076
|
C | CA | 69 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0101others(66): Show | 70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.523-2840dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6029076 | ||||||
chr19:6029076
|
CA | C | 61 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(58): Show | 61 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(58): Show |
intron_variant | MODIFIER | c.523-2840delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6029076 | ||||||
chr19:6029199
|
C | T | 9 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(6): Show | 9 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.523-2962G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6029199 | ||||||
chr19:6029256
|
C | CA | 12 | a0001c0001t0001g0168a0001c0001t0001g0224a0003c0005t0001g0045others(9): Show | 12 | HG00621.hp1 HG02027.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.523-3020dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6029256 | ||||||
chr19:6029295
|
A | G | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.523-3058T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6029295 | ||||||
chr19:6029395
|
C | A | 6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.523-3158G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6029395 | ||||||
chr19:6029552
|
T | A | 1 | a0001c0001t0002g0227 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.523-3315A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6029552 | ||||||
chr19:6030198
|
C | G | 1 | a0002c0002t0001g0209 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.523-3961G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6030198 | ||||||
chr19:6030241
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.523-4004G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6030241 | ||||||
chr19:6030266
|
G | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-4029C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6030266 | ||||||
chr19:6030368
|
G | A | 1 | a0002c0002t0002g0073 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.523-4131C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6030368 | ||||||
chr19:6030781
|
T | A | 2 | a0001c0001t0001g0300a0001c0001t0008g0301 | 2 | HG02080.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.523-4544A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6030781 | ||||||
chr19:6030813
|
T | C | 16 | a0001c0001t0001g0010a0001c0001t0001g0053a0001c0001t0001g0054others(13): Show | 16 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.523-4576A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6030813 | ||||||
chr19:6030853
|
G | A | 1 | a0001c0003t0001g0255 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.523-4616C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6030853 | ||||||
chr19:6030989
|
C | A | 8 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0147others(5): Show | 8 | HG00621.hp2 HG01069.hp2 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.523-4752G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6030989 | ||||||
chr19:6030998
|
A | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-4761T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6030998 | ||||||
chr19:6031160
|
C | T | 14 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(11): Show | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.523-4923G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6031160 | ||||||
chr19:6031175
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.523-4938A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6031175 | ||||||
chr19:6031213
|
C | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-4976G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6031213 | ||||||
chr19:6031253
|
G | A | 15 | a0001c0001t0004g0247a0001c0004t0001g0012a0001c0004t0001g0038others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.523-5016C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6031253 | ||||||
chr19:6031383
|
CT | C | 9 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(6): Show | 9 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.523-5147delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6031383 | ||||||
chr19:6031423
|
C | CT | 188 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(185): Show | 189 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.523-5187dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6031423 | ||||||
chr19:6031423
|
C | CTT | 44 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0035others(41): Show | 44 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.523-5188_523-5187d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6031423 | ||||||
chr19:6031423
|
C | CTTT | 12 | a0001c0001t0001g0017a0001c0001t0006g0217a0001c0004t0001g0012others(9): Show | 12 | HG02027.hp1 HG02155.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.523-5189_523-5187d others(5): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6031423 | ||||||
chr19:6031423
|
CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.523-5194_523-5187d others(10): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6031423 | ||||||
chr19:6031423
|
CTTTTTTT others(3): Show |
C | 1 | a0002c0002t0001g0072 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.523-5196_523-5187d others(12): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6031423 | ||||||
chr19:6031523
|
A | AGGT | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-5289_523-5287d others(5): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6031523 | ||||||
chr19:6031974
|
G | A | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 59 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(56): Show |
intron_variant | MODIFIER | c.523-5737C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6031974 | ||||||
chr19:6031979
|
G | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-5742C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6031979 | ||||||
chr19:6032109
|
T | C | 5 | a0003c0005t0001g0049a0003c0005t0001g0050a0003c0005t0001g0051others(2): Show | 5 | NA18973.hp2 NA18983.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-5872A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6032109 | ||||||
chr19:6032184
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-5947G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6032184 | ||||||
chr19:6032320
|
C | T | 2 | a0002c0002t0001g0083a0002c0002t0002g0201 | 2 | HG02738.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.523-6083G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6032320 | ||||||
chr19:6032379
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-6142G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6032379 | ||||||
chr19:6032532
|
C | T | 10 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(7): Show | 10 | HG01934.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-6295G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6032532 | ||||||
chr19:6032900
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0222a0001c0001t0001g0223others(1): Show | 4 | HG02071.hp1 HG03927.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.523-6663G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6032900 | ||||||
chr19:6032940
|
C | G | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.523-6703G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6032940 | ||||||
chr19:6032950
|
AG | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0224a0001c0001t0001g0237 | 3 | HG00621.hp1 HG03017.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.523-6714delC | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6032950 | ||||||
chr19:6032985
|
C | T | 1 | a0004c0013t0002g0251 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.523-6748G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6032985 | ||||||
chr19:6033187
|
T | C | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.522+6793A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6033187 | ||||||
chr19:6033205
|
C | A | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.522+6775G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6033205 | ||||||
chr19:6033242
|
T | A | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.522+6738A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6033242 | ||||||
chr19:6033456
|
G | C | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+6524C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6033456 | ||||||
chr19:6033523
|
T | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.522+6457A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6033523 | ||||||
chr19:6033608
|
A | G | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.522+6372T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6033608 | ||||||
chr19:6033615
|
C | CA | 67 | a0001c0001t0001g0010a0001c0001t0001g0044a0001c0001t0001g0055others(64): Show | 67 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.522+6364dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6033615 | ||||||
chr19:6033615
|
C | CAA | 68 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0111others(65): Show | 69 | HG00597.hp1 HG00642.hp2 HG01123.hp2 others(66): Show |
intron_variant | MODIFIER | c.522+6363_522+6364d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6033615 | ||||||
chr19:6033615
|
C | CAAA | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG00544.hp1 HG01891.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.522+6362_522+6364d others(5): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6033615 | ||||||
chr19:6033629
|
A | C | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+6351T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6033629 | ||||||
chr19:6033758
|
T | C | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.522+6222A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6033758 | ||||||
chr19:6033835
|
T | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0238a0001c0001t0017g0239 | 3 | NA18747.hp2 NA18994.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.522+6145A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6033835 | ||||||
chr19:6033965
|
T | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.522+6015A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6033965 | ||||||
chr19:6034227
|
A | AT | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(28): Show | 31 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.522+5752dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6034227 | ||||||
chr19:6034227
|
AT | A | 34 | a0001c0001t0001g0010a0001c0001t0001g0053a0001c0001t0001g0054others(31): Show | 34 | HG00323.hp2 HG01109.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.522+5752delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6034227 | ||||||
chr19:6034474
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+5506C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6034474 | ||||||
chr19:6034487
|
A | G | 1 | a0001c0001t0001g0015 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.522+5493T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6034487 | ||||||
chr19:6034508
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0002g0011 | 2 | HG03831.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.522+5472A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6034508 | ||||||
chr19:6034656
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.522+5324G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6034656 | ||||||
chr19:6034765
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.522+5215C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6034765 | ||||||
chr19:6034787
|
T | C | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.522+5193A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6034787 | ||||||
chr19:6034918
|
C | T | 4 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0002g0170others(1): Show | 4 | NA18747.hp1 NA18944.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+5062G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6034918 | ||||||
chr19:6034964
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.522+5016C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6034964 | ||||||
chr19:6035023
|
C | T | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.522+4957G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035023 | ||||||
chr19:6035039
|
G | T | 1 | a0002c0002t0001g0295 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.522+4941C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035039 | ||||||
chr19:6035086
|
T | A | 14 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(11): Show | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.522+4894A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035086 | ||||||
chr19:6035097
|
G | T | 73 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(70): Show | 73 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(70): Show |
intron_variant | MODIFIER | c.522+4883C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035097 | ||||||
chr19:6035154
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.522+4826A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035154 | ||||||
chr19:6035156
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.522+4824C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035156 | ||||||
chr19:6035168
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | HG01109.hp2 HG02451.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+4812G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035168 | ||||||
chr19:6035207
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.522+4773G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035207 | ||||||
chr19:6035385
|
T | G | 1 | a0001c0001t0001g0179 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.522+4595A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035385 | ||||||
chr19:6035601
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0166 | 2 | NA18966.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.522+4379C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035601 | ||||||
chr19:6035610
|
G | A | 29 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(26): Show | 29 | HG00741.hp2 HG02027.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.522+4370C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035610 | ||||||
chr19:6035845
|
TGG | T | 22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(19): Show | 22 | HG02027.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.522+4133_522+4134d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035845 | ||||||
chr19:6035848
|
G | GGT | 18 | a0001c0001t0001g0021a0001c0001t0001g0285a0001c0001t0001g0300others(15): Show | 19 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.522+4131_522+4132i others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035848 | ||||||
chr19:6035848
|
G | GGTGT | 8 | a0001c0001t0001g0010a0001c0001t0001g0102a0001c0001t0008g0301others(5): Show | 8 | HG01192.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.522+4131_522+4132i others(6): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035848 | ||||||
chr19:6035848
|
G | GGTGTGT | 20 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0101others(17): Show | 20 | HG00544.hp1 HG01109.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.522+4131_522+4132i others(8): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035848 | ||||||
chr19:6035848
|
G | GGTGTGTG others(1): Show |
7 | a0002c0002t0001g0092a0002c0002t0001g0192a0002c0002t0001g0193others(4): Show | 7 | HG02015.hp2 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.522+4131_522+4132i others(10): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035848 | ||||||
chr19:6035848
|
G | GGTGTGTG others(3): Show |
2 | a0002c0002t0018g0215a0002c0006t0003g0095 | 2 | HG01934.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.522+4131_522+4132i others(12): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035848 | ||||||
chr19:6035848
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.522+4132C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035848 | ||||||
chr19:6035848
|
GGGGTGTG others(1): Show |
G | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.522+4124_522+4131d others(10): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035848 | ||||||
chr19:6035850
|
G | GGGTGTGT others(4): Show |
1 | a0001c0001t0001g0248 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.522+4129_522+4130i others(13): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035850 | ||||||
chr19:6035850
|
G | GGT | 29 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0055others(26): Show | 29 | HG00642.hp1 HG01074.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.522+4128_522+4129d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035850 | ||||||
chr19:6035850
|
G | GGTGT | 11 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0211others(8): Show | 11 | HG01175.hp1 HG01433.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.522+4126_522+4129d others(6): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035850 | ||||||
chr19:6035850
|
G | GGTGTGTG others(3): Show |
3 | a0001c0001t0001g0243a0001c0001t0001g0246a0001c0001t0001g0250 | 3 | HG01243.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.522+4120_522+4129d others(12): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035850 | ||||||
chr19:6035850
|
G | GGTGTGTG others(5): Show |
1 | a0001c0001t0009g0245 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.522+4118_522+4129d others(14): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035850 | ||||||
chr19:6035850
|
G | GT | 3 | a0001c0001t0001g0133a0001c0001t0001g0154a0001c0001t0001g0237 | 3 | HG03831.hp1 HG04204.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.522+4129_522+4130i others(3): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035850 | ||||||
chr19:6035850
|
G | T | 84 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0021others(81): Show | 85 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.522+4130C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035850 | ||||||
chr19:6035850
|
GGT | G | 7 | a0001c0001t0001g0099a0001c0001t0001g0103a0001c0001t0001g0131others(4): Show | 7 | HG00735.hp1 HG01192.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.522+4128_522+4129d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035850 | ||||||
chr19:6035852
|
T | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0236 | 2 | NA19065.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.522+4128A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035852 | ||||||
chr19:6035916
|
A | G | 11 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(8): Show | 11 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.522+4064T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035916 | ||||||
chr19:6035968
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.522+4012G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6035968 | ||||||
chr19:6036047
|
T | C | 1 | a0003c0005t0001g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.522+3933A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6036047 | ||||||
chr19:6036152
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.522+3828G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6036152 | ||||||
chr19:6036206
|
C | T | 6 | a0001c0001t0002g0104a0001c0001t0002g0169a0001c0001t0002g0171others(3): Show | 6 | HG01943.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.522+3774G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6036206 | ||||||
chr19:6036275
|
A | G | 15 | a0001c0001t0004g0247a0001c0004t0001g0012a0001c0004t0001g0038others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.522+3705T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6036275 | ||||||
chr19:6036618
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0288 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.522+3362G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6036618 | ||||||
chr19:6036982
|
T | C | 1 | a0003c0005t0003g0020 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.522+2998A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6036982 | ||||||
chr19:6037025
|
C | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0244 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.522+2955G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6037025 | ||||||
chr19:6037051
|
G | A | 1 | a0002c0002t0001g0072 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.522+2929C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6037051 | ||||||
chr19:6037177
|
G | A | 1 | a0002c0006t0001g0214 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.522+2803C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6037177 | ||||||
chr19:6037218
|
A | G | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.522+2762T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6037218 | ||||||
chr19:6037289
|
G | GA | 74 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0101others(71): Show | 75 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.522+2690dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6037289 | ||||||
chr19:6037289
|
GA | G | 22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(19): Show | 22 | HG01109.hp2 HG02080.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.522+2690delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6037289 | ||||||
chr19:6037350
|
T | C | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.522+2630A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6037350 | ||||||
chr19:6037457
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.522+2523T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6037457 | ||||||
chr19:6037709
|
C | A | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.522+2271G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6037709 | ||||||
chr19:6037837
|
T | C | 1 | a0003c0005t0001g0050 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.522+2143A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6037837 | ||||||
chr19:6037848
|
C | A | 25 | a0001c0001t0001g0024a0001c0001t0001g0105a0001c0001t0001g0106others(22): Show | 25 | HG00597.hp2 HG00735.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.522+2132G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6037848 | ||||||
chr19:6037894
|
A | T | 6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.522+2086T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6037894 | ||||||
chr19:6038159
|
T | A | 30 | a0001c0001t0001g0010a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 30 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.522+1821A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6038159 | ||||||
chr19:6038232
|
C | T | 9 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(6): Show | 9 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.522+1748G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6038232 | ||||||
chr19:6038289
|
T | C | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(12): Show | 15 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.522+1691A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6038289 | ||||||
chr19:6038298
|
G | C | 6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.522+1682C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6038298 | ||||||
chr19:6038328
|
G | GA | 138 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0021others(135): Show | 139 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.522+1651dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6038328 | ||||||
chr19:6038328
|
G | GAA | 59 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0028others(56): Show | 59 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.522+1650_522+1651d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6038328 | ||||||
chr19:6038328
|
G | GAAA | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0132others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.522+1649_522+1651d others(5): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6038328 | ||||||
chr19:6038328
|
GA | G | 26 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(23): Show | 26 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.522+1651delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6038328 | ||||||
chr19:6038339
|
A | AC | 37 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0211others(34): Show | 37 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.522+1640_522+1641i others(3): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6038339 | ||||||
chr19:6038360
|
C | T | 4 | a0001c0001t0001g0300a0001c0001t0003g0018a0001c0001t0003g0019others(1): Show | 4 | HG02080.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+1620G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6038360 | ||||||
chr19:6038410
|
A | T | 6 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0144others(3): Show | 6 | HG01070.hp1 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.522+1570T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6038410 | ||||||
chr19:6038502
|
A | T | 2 | a0001c0001t0001g0234a0001c0001t0003g0233 | 2 | HG00323.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.522+1478T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6038502 | ||||||
chr19:6038758
|
C | T | 6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.522+1222G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6038758 | ||||||
chr19:6039010
|
C | G | 4 | a0001c0003t0004g0262a0001c0003t0004g0268a0001c0003t0004g0269others(1): Show | 4 | HG02109.hp1 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+970G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6039010 | ||||||
chr19:6039339
|
G | A | 10 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(7): Show | 10 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.522+641C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6039339 | ||||||
chr19:6039472
|
A | T | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+508T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6039472 | ||||||
chr19:6039481
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+499C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6039481 | ||||||
chr19:6039510
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.522+470A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6039510 | ||||||
chr19:6039541
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(12): Show | 15 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.522+439C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6039541 | ||||||
chr19:6039572
|
G | A | 1 | a0001c0001t0005g0303 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.522+408C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6039572 | ||||||
chr19:6039656
|
G | C | 9 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(6): Show | 9 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.522+324C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6039656 | ||||||
chr19:6039741
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.522+239G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6039741 | ||||||
chr19:6039779
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+201C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6039779 | ||||||
chr19:6039837
|
C | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0053a0001c0001t0001g0054others(15): Show | 18 | HG01109.hp2 HG01934.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.522+143G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 5/17 | chr19 | 6039837 | ||||||
chr19:6040416
|
A | T | 1 | a0001c0001t0001g0042 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.261-175T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6040416 | ||||||
chr19:6040775
|
CA | C | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0032others(11): Show | 14 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.261-535delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6040775 | ||||||
chr19:6040813
|
C | T | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-572G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6040813 | ||||||
chr19:6040858
|
T | C | 153 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 154 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.261-617A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6040858 | ||||||
chr19:6040981
|
G | A | 24 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(21): Show | 24 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.261-740C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6040981 | ||||||
chr19:6041013
|
G | T | 1 | a0001c0001t0002g0030 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.261-772C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6041013 | ||||||
chr19:6041039
|
G | T | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.261-798C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6041039 | ||||||
chr19:6041137
|
T | C | 14 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(11): Show | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.261-896A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6041137 | ||||||
chr19:6041192
|
T | A | 306 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(303): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.260+852A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6041192 | ||||||
chr19:6041209
|
C | T | 18 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(15): Show | 18 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.260+835G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6041209 | ||||||
chr19:6041336
|
G | C | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.260+708C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6041336 | ||||||
chr19:6041343
|
C | A | 1 | a0001c0001t0001g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.260+701G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6041343 | ||||||
chr19:6041416
|
A | G | 1 | a0003c0005t0001g0050 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.260+628T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6041416 | ||||||
chr19:6041529
|
C | T | 28 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0242others(25): Show | 28 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.260+515G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6041529 | ||||||
chr19:6041606
|
C | CT | 8 | a0001c0001t0001g0136a0001c0001t0001g0234a0001c0001t0001g0271others(5): Show | 8 | HG00140.hp1 HG00323.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.260+437dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6041606 | ||||||
chr19:6041606
|
CT | C | 59 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0135others(56): Show | 59 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(56): Show |
intron_variant | MODIFIER | c.260+437delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6041606 | ||||||
chr19:6041606
|
CTT | C | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.260+436_260+437del others(2): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6041606 | ||||||
chr19:6041669
|
C | A | 1 | a0001c0001t0001g0134 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.260+375G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6041669 | ||||||
chr19:6041713
|
A | C | 1 | a0002c0002t0001g0093 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.260+331T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6041713 | ||||||
chr19:6041904
|
T | C | 1 | a0001c0004t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.260+140A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 4/17 | chr19 | 6041904 | ||||||
chr19:6042144
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.181-21G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6042144 | ||||||
chr19:6042209
|
G | C | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.181-86C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6042209 | ||||||
chr19:6042362
|
C | T | 9 | a0002c0002t0001g0063a0002c0002t0001g0065a0002c0002t0001g0072others(6): Show | 9 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(6): Show |
intron_variant | MODIFIER | c.181-239G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6042362 | ||||||
chr19:6042372
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.181-249G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6042372 | ||||||
chr19:6042454
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.181-331T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6042454 | ||||||
chr19:6042501
|
T | G | 14 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(11): Show | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.181-378A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6042501 | ||||||
chr19:6042505
|
T | G | 82 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(79): Show | 82 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(79): Show |
intron_variant | MODIFIER | c.181-382A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6042505 | ||||||
chr19:6042525
|
T | G | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-402A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6042525 | ||||||
chr19:6042795
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.181-672C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6042795 | ||||||
chr19:6043048
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.181-925G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6043048 | ||||||
chr19:6043051
|
C | T | 9 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(6): Show | 9 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.181-928G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6043051 | ||||||
chr19:6043196
|
G | T | 1 | a0002c0002t0001g0059 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.180+997C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6043196 | ||||||
chr19:6043288
|
C | G | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 69 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(66): Show |
intron_variant | MODIFIER | c.180+905G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6043288 | ||||||
chr19:6043294
|
C | T | 1 | a0002c0002t0001g0086 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.180+899G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6043294 | ||||||
chr19:6043359
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.180+834G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6043359 | ||||||
chr19:6043378
|
T | C | 1 | a0002c0006t0003g0095 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.180+815A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6043378 | ||||||
chr19:6043423
|
G | C | 14 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(11): Show | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.180+770C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6043423 | ||||||
chr19:6043585
|
T | G | 1 | a0002c0002t0001g0190 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.180+608A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6043585 | ||||||
chr19:6043732
|
C | T | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(14): Show | 17 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.180+461G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6043732 | ||||||
chr19:6043734
|
A | G | 1 | a0001c0001t0007g0267 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.180+459T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6043734 | ||||||
chr19:6043831
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.180+362G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6043831 | ||||||
chr19:6043881
|
C | T | 14 | a0001c0004t0001g0012a0001c0004t0001g0038a0001c0004t0001g0276others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.180+312G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6043881 | ||||||
chr19:6044033
|
T | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+160A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6044033 | ||||||
chr19:6044178
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.180+15C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 3/17 | chr19 | 6044178 | ||||||
chr19:6044458
|
C | A | 1 | a0001c0001t0001g0222 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.91-176G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6044458 | ||||||
chr19:6044538
|
C | T | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-256G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6044538 | ||||||
chr19:6044591
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.91-309G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6044591 | ||||||
chr19:6044682
|
AG | A | 26 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0001t0001g0084others(23): Show | 26 | HG00621.hp2 HG01069.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.91-401delC | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6044682 | ||||||
chr19:6044687
|
A | C | 26 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0001t0001g0084others(23): Show | 26 | HG00621.hp2 HG01069.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.91-405T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6044687 | ||||||
chr19:6044714
|
C | T | 30 | a0001c0001t0001g0101a0001c0001t0001g0102a0002c0002t0001g0092others(27): Show | 31 | HG00544.hp1 HG00642.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.91-432G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6044714 | ||||||
chr19:6044725
|
G | A | 1 | a0002c0002t0001g0069 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.91-443C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6044725 | ||||||
chr19:6044897
|
A | G | 79 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(76): Show | 79 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(76): Show |
intron_variant | MODIFIER | c.91-615T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6044897 | ||||||
chr19:6044956
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(14): Show | 17 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.91-674C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6044956 | ||||||
chr19:6045051
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-769G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6045051 | ||||||
chr19:6045082
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.91-800G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6045082 | ||||||
chr19:6045163
|
CCT | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-883_91-882delAG | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6045163 | ||||||
chr19:6045253
|
G | A | 42 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0242others(39): Show | 42 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.91-971C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6045253 | ||||||
chr19:6045300
|
CCA | C | 11 | a0001c0001t0001g0017a0001c0001t0001g0108a0001c0001t0001g0236others(8): Show | 11 | HG03669.hp2 HG03704.hp1 HG04199.hp2 others(8): Show |
intron_variant | MODIFIER | c.91-1020_91-1019del others(2): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6045300 | ||||||
chr19:6045334
|
C | T | 10 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(7): Show | 10 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.91-1052G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6045334 | ||||||
chr19:6045357
|
C | T | 14 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(11): Show | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.91-1075G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6045357 | ||||||
chr19:6045534
|
T | C | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(54): Show | 57 | HG00741.hp2 HG01109.hp2 HG01884.hp2 others(54): Show |
intron_variant | MODIFIER | c.91-1252A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6045534 | ||||||
chr19:6045551
|
C | T | 4 | a0002c0002t0001g0072a0002c0002t0001g0078a0002c0002t0001g0080others(1): Show | 4 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-1269G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6045551 | ||||||
chr19:6045658
|
G | GT | 15 | a0001c0001t0009g0245a0001c0003t0004g0262a0001c0003t0004g0268others(12): Show | 15 | HG02027.hp1 HG02109.hp1 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-1377dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6045658 | ||||||
chr19:6045666
|
G | T | 78 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(75): Show | 78 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(75): Show |
intron_variant | MODIFIER | c.91-1384C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6045666 | ||||||
chr19:6045668
|
T | TG | 10 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(7): Show | 10 | HG01934.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.91-1387_91-1386ins others(1): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6045668 | ||||||
chr19:6045669
|
T | G | 9 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(6): Show | 9 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.91-1387A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6045669 | ||||||
chr19:6045740
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.91-1458G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6045740 | ||||||
chr19:6046173
|
C | T | 4 | a0001c0001t0001g0120a0002c0002t0001g0191a0002c0002t0001g0230others(1): Show | 4 | HG00735.hp2 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+1234G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046173 | ||||||
chr19:6046438
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+969C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046438 | ||||||
chr19:6046442
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+965C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046442 | ||||||
chr19:6046503
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.90+904G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046503 | ||||||
chr19:6046553
|
C | T | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(14): Show | 17 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.90+854G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046553 | ||||||
chr19:6046554
|
G | A | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+853C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046554 | ||||||
chr19:6046563
|
C | A | 21 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(18): Show | 21 | HG00741.hp2 HG02055.hp2 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.90+844G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046563 | ||||||
chr19:6046563
|
C | CA | 11 | a0001c0001t0001g0016a0001c0001t0001g0133a0001c0001t0001g0136others(8): Show | 11 | HG01891.hp1 HG02258.hp1 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.90+843dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046563 | ||||||
chr19:6046564
|
A | C | 1 | a0002c0002t0003g0098 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.90+843T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046564 | ||||||
chr19:6046587
|
C | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(14): Show | 17 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.90+820G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046587 | ||||||
chr19:6046605
|
C | CT | 106 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0023others(103): Show | 107 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.90+801dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046605 | ||||||
chr19:6046605
|
C | CTT | 11 | a0001c0001t0001g0248a0001c0001t0002g0299a0001c0003t0001g0257others(8): Show | 11 | HG00642.hp2 HG01192.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+800_90+801dupAA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046605 | ||||||
chr19:6046605
|
CT | C | 10 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0134others(7): Show | 10 | HG01074.hp2 HG01169.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.90+801delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046605 | ||||||
chr19:6046605
|
CTTTT | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+798_90+801delAA others(2): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046605 | ||||||
chr19:6046605
|
CTTTTTTT others(3): Show |
C | 4 | a0001c0004t0001g0038a0001c0004t0001g0292a0001c0004t0001g0293others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+792_90+801delAA others(8): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046605 | ||||||
chr19:6046605
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+791_90+801delAA others(9): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046605 | ||||||
chr19:6046753
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0003g0009 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.90+654A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046753 | ||||||
chr19:6046794
|
G | T | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+613C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046794 | ||||||
chr19:6046848
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+559G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046848 | ||||||
chr19:6046920
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+487G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046920 | ||||||
chr19:6046930
|
A | AT | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG02155.hp1 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.90+476dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046930 | ||||||
chr19:6046930
|
AT | A | 37 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0102others(34): Show | 37 | HG00741.hp2 HG01109.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.90+476delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046930 | ||||||
chr19:6046968
|
G | A | 14 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(11): Show | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.90+439C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6046968 | ||||||
chr19:6047027
|
A | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+380T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6047027 | ||||||
chr19:6047073
|
T | C | 1 | a0001c0001t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.90+334A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6047073 | ||||||
chr19:6047108
|
C | G | 9 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(6): Show | 9 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.90+299G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6047108 | ||||||
chr19:6047340
|
C | T | 4 | a0001c0001t0001g0300a0001c0001t0003g0018a0001c0001t0003g0019others(1): Show | 4 | HG02080.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+67G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6047340 | ||||||
chr19:6047398
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.90+9C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6047398 | ||||||
chr19:6047399
|
C | T | 12 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(9): Show | 12 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.90+8G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 2/17 | chr19 | 6047399 | ||||||
chr19:6047526
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8-22A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6047526 | ||||||
chr19:6047706
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-8-202C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6047706 | ||||||
chr19:6047736
|
A | G | 4 | a0001c0004t0001g0038a0001c0004t0001g0292a0001c0004t0001g0293others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-232T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6047736 | ||||||
chr19:6047767
|
C | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-263G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6047767 | ||||||
chr19:6047787
|
A | G | 3 | a0001c0001t0001g0033a0001c0001t0001g0175a0001c0001t0001g0235 | 3 | HG01167.hp2 HG04184.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-8-283T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6047787 | ||||||
chr19:6047879
|
T | C | 10 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(7): Show | 10 | HG00741.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-375A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6047879 | ||||||
chr19:6047952
|
G | A | 42 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0242others(39): Show | 42 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.-8-448C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6047952 | ||||||
chr19:6048237
|
A | G | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-733T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6048237 | ||||||
chr19:6048517
|
T | A | 1 | a0001c0001t0001g0183 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-8-1013A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6048517 | ||||||
chr19:6048593
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(14): Show | 17 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-1089C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6048593 | ||||||
chr19:6048632
|
G | A | 1 | a0002c0002t0002g0074 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-8-1128C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6048632 | ||||||
chr19:6048651
|
A | T | 5 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(2): Show | 5 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1147T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6048651 | ||||||
chr19:6048673
|
G | A | 14 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(11): Show | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-1169C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6048673 | ||||||
chr19:6048707
|
T | G | 27 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(24): Show | 27 | HG00741.hp2 HG02055.hp2 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.-8-1203A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6048707 | ||||||
chr19:6048714
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-8-1210A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6048714 | ||||||
chr19:6048906
|
G | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-8-1402C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6048906 | ||||||
chr19:6048960
|
G | T | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1456C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6048960 | ||||||
chr19:6049158
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1654C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6049158 | ||||||
chr19:6049244
|
GGTAGCAT others(2): Show |
G | 18 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(15): Show | 18 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-8-1749_-8-1741del others(9): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6049244 | ||||||
chr19:6049333
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-8-1829T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6049333 | ||||||
chr19:6049664
|
G | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(15): Show | 18 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-8-2160C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6049664 | ||||||
chr19:6049679
|
C | A | 7 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(4): Show | 7 | HG00735.hp2 HG01928.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-2175G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6049679 | ||||||
chr19:6050108
|
A | C | 1 | a0001c0001t0008g0301 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-8-2604T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6050108 | ||||||
chr19:6050351
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-2847A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6050351 | ||||||
chr19:6050458
|
T | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-2954A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6050458 | ||||||
chr19:6050481
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-8-2977C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6050481 | ||||||
chr19:6050595
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0166 | 2 | NA18966.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-8-3091T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6050595 | ||||||
chr19:6050914
|
A | C | 10 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(7): Show | 10 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-3410T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6050914 | ||||||
chr19:6051011
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8-3507C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6051011 | ||||||
chr19:6051234
|
T | TA | 10 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(7): Show | 10 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-3731dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6051234 | ||||||
chr19:6051439
|
G | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(15): Show | 18 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-8-3935C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6051439 | ||||||
chr19:6051620
|
GAAAC | G | 14 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(11): Show | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-4120_-8-4117del others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6051620 | ||||||
chr19:6051909
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0002g0011 | 2 | HG02280.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-8-4405C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6051909 | ||||||
chr19:6051910
|
C | A | 1 | a0001c0001t0002g0299 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-8-4406G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6051910 | ||||||
chr19:6052003
|
G | A | 7 | a0001c0001t0002g0011a0001c0001t0005g0302a0001c0001t0005g0303others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-4499C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6052003 | ||||||
chr19:6052022
|
T | C | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 155 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.-8-4518A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6052022 | ||||||
chr19:6052034
|
C | T | 1 | a0002c0002t0001g0210 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-8-4530G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6052034 | ||||||
chr19:6052161
|
C | T | 12 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(9): Show | 12 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8-4657G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6052161 | ||||||
chr19:6052278
|
A | T | 1 | a0002c0002t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-8-4774T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6052278 | ||||||
chr19:6052298
|
A | C | 1 | a0001c0001t0001g0187 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-8-4794T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6052298 | ||||||
chr19:6052822
|
T | C | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-5318A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6052822 | ||||||
chr19:6052945
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-8-5441T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6052945 | ||||||
chr19:6052951
|
G | A | 1 | a0003c0005t0003g0020 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-8-5447C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6052951 | ||||||
chr19:6053005
|
C | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(15): Show | 18 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-8-5501G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6053005 | ||||||
chr19:6053029
|
T | C | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-5525A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6053029 | ||||||
chr19:6053193
|
A | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(8): Show | 11 | HG02080.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8-5689T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6053193 | ||||||
chr19:6053614
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-8-6110A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6053614 | ||||||
chr19:6053861
|
TG | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(15): Show | 18 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-8-6358delC | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6053861 | ||||||
chr19:6053921
|
A | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-6417T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6053921 | ||||||
chr19:6053955
|
C | CA | 74 | a0001c0001t0001g0022a0001c0001t0001g0055a0001c0001t0001g0064others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.-8-6452dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6053955 | ||||||
chr19:6053955
|
CA | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(11): Show | 14 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-6452delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6053955 | ||||||
chr19:6054000
|
T | G | 2 | a0003c0005t0001g0045a0003c0005t0003g0020 | 2 | HG02027.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.-8-6496A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6054000 | ||||||
chr19:6054096
|
CA | C | 9 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(6): Show | 9 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-6593delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6054096 | ||||||
chr19:6054124
|
C | T | 1 | a0001c0001t0005g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-8-6620G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6054124 | ||||||
chr19:6054182
|
A | G | 1 | a0004c0013t0002g0251 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-8-6678T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6054182 | ||||||
chr19:6054249
|
T | C | 1 | a0001c0001t0002g0031 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-8-6745A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6054249 | ||||||
chr19:6054287
|
CAT | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0222a0001c0001t0006g0217 | 3 | NA19003.hp2 NA19005.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-8-6785_-8-6784del others(2): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6054287 | ||||||
chr19:6054630
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-8-7126C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6054630 | ||||||
chr19:6054831
|
C | A | 151 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 152 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.-8-7327G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6054831 | ||||||
chr19:6055165
|
T | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-8-7661A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6055165 | ||||||
chr19:6055168
|
C | G | 6 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0144others(3): Show | 6 | HG01070.hp1 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-7664G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6055168 | ||||||
chr19:6055182
|
C | G | 20 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(17): Show | 20 | HG01109.hp2 HG02055.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-7678G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6055182 | ||||||
chr19:6055396
|
G | A | 1 | a0002c0002t0010g0061 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-8-7892C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6055396 | ||||||
chr19:6055411
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-8-7907A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6055411 | ||||||
chr19:6055570
|
C | T | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-8066G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6055570 | ||||||
chr19:6055687
|
T | C | 14 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(11): Show | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-8183A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6055687 | ||||||
chr19:6055859
|
C | G | 1 | a0002c0002t0001g0069 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-8-8355G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6055859 | ||||||
chr19:6055934
|
C | T | 14 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(11): Show | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-8430G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6055934 | ||||||
chr19:6055960
|
A | G | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-8456T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6055960 | ||||||
chr19:6055995
|
T | TA | 14 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(11): Show | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-8492dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6055995 | ||||||
chr19:6056053
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-8-8549T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6056053 | ||||||
chr19:6056229
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-8-8725G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6056229 | ||||||
chr19:6056318
|
T | G | 14 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(11): Show | 14 | HG01934.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-8814A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6056318 | ||||||
chr19:6056512
|
C | T | 1 | a0001c0001t0001g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8-9008G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6056512 | ||||||
chr19:6056528
|
C | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-9024G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6056528 | ||||||
chr19:6056712
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0088others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-9208C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6056712 | ||||||
chr19:6056798
|
G | A | 6 | a0002c0002t0001g0070a0002c0002t0001g0079a0002c0002t0001g0205others(3): Show | 6 | HG03239.hp2 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-9294C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6056798 | ||||||
chr19:6057236
|
G | T | 10 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257others(7): Show | 10 | HG01934.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-9732C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6057236 | ||||||
chr19:6057287
|
G | A | 2 | a0002c0002t0002g0001a0002c0002t0002g0087 | 3 | HG01123.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-8-9783C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6057287 | ||||||
chr19:6057585
|
C | T | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-10081G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6057585 | ||||||
chr19:6057620
|
G | A | 4 | a0001c0001t0001g0300a0001c0001t0003g0018a0001c0001t0003g0019others(1): Show | 4 | HG02080.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-10116C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6057620 | ||||||
chr19:6057640
|
C | T | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-10136G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6057640 | ||||||
chr19:6057716
|
T | C | 1 | a0002c0002t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-8-10212A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6057716 | ||||||
chr19:6057842
|
A | C | 1 | a0001c0001t0001g0090 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-8-10338T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6057842 | ||||||
chr19:6057894
|
G | C | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-10390C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6057894 | ||||||
chr19:6057898
|
T | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(27): Show | 30 | HG01109.hp2 HG02027.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.-8-10394A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6057898 | ||||||
chr19:6058009
|
G | A | 1 | a0001c0004t0001g0293 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-8-10505C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6058009 | ||||||
chr19:6058111
|
A | T | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8-10607T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6058111 | ||||||
chr19:6058135
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-8-10631G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6058135 | ||||||
chr19:6058277
|
C | T | 1 | a0002c0002t0002g0207 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-8-10773G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6058277 | ||||||
chr19:6058535
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-8-11031G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6058535 | ||||||
chr19:6058536
|
A | G | 72 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(69): Show | 72 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.-8-11032T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6058536 | ||||||
chr19:6058599
|
GT | G | 24 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(21): Show | 24 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-8-11096delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6058599 | ||||||
chr19:6058630
|
G | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-11126C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6058630 | ||||||
chr19:6058713
|
T | C | 18 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(15): Show | 18 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.-8-11209A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6058713 | ||||||
chr19:6058733
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0211 | 2 | HG01175.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-8-11229A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6058733 | ||||||
chr19:6058855
|
A | G | 1 | a0002c0002t0001g0069 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-8-11351T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6058855 | ||||||
chr19:6058971
|
C | T | 204 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(201): Show | 205 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.-8-11467G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6058971 | ||||||
chr19:6059002
|
CAGAGTCT others(18): Show |
C | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8-11523_-8-11499d others(27): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059002 | ||||||
chr19:6059029
|
G | C | 28 | a0001c0001t0001g0108a0001c0001t0001g0234a0001c0001t0001g0236others(25): Show | 28 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8-11525C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059029 | ||||||
chr19:6059073
|
T | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0300a0001c0001t0003g0009others(3): Show | 6 | HG02080.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-11569A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059073 | ||||||
chr19:6059091
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-8-11587G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059091 | ||||||
chr19:6059245
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8-11741C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059245 | ||||||
chr19:6059295
|
A | C | 2 | a0001c0001t0001g0021a0001c0001t0002g0030 | 2 | HG02523.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-8-11791T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059295 | ||||||
chr19:6059320
|
A | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-11816T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059320 | ||||||
chr19:6059364
|
A | G | 21 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(18): Show | 21 | HG01109.hp2 HG02055.hp2 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.-8-11860T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059364 | ||||||
chr19:6059372
|
C | T | 21 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(18): Show | 21 | HG01109.hp2 HG02055.hp2 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.-8-11868G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059372 | ||||||
chr19:6059502
|
T | C | 1 | a0001c0001t0001g0270 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-8-11998A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059502 | ||||||
chr19:6059585
|
C | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-8-12081G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059585 | ||||||
chr19:6059615
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-8-12111G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059615 | ||||||
chr19:6059646
|
T | C | 1 | a0001c0004t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-8-12142A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059646 | ||||||
chr19:6059652
|
T | C | 13 | a0001c0004t0001g0012a0001c0004t0001g0276a0001c0004t0001g0277others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8-12148A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059652 | ||||||
chr19:6059695
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0224 | 2 | HG00621.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-8-12191C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059695 | ||||||
chr19:6059706
|
C | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(28): Show | 31 | HG01109.hp2 HG02027.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.-8-12202G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059706 | ||||||
chr19:6059738
|
AAC | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-12236_-8-12235d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059738 | ||||||
chr19:6059829
|
A | G | 21 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(18): Show | 21 | HG01109.hp2 HG02055.hp2 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.-8-12325T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059829 | ||||||
chr19:6059961
|
T | TG | 30 | a0001c0001t0001g0108a0001c0001t0001g0234a0001c0001t0001g0236others(27): Show | 30 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8-12458dupC | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059961 | ||||||
chr19:6059964
|
G | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0129a0001c0001t0001g0300others(4): Show | 7 | HG01256.hp1 HG02080.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-12460C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6059964 | ||||||
chr19:6060055
|
T | A | 1 | a0001c0001t0001g0119 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-8-12551A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6060055 | ||||||
chr19:6060194
|
C | G | 14 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(11): Show | 14 | HG00741.hp2 HG02027.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8-12690G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6060194 | ||||||
chr19:6060313
|
A | G | 1 | a0001c0001t0016g0027 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-8-12809T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6060313 | ||||||
chr19:6060475
|
C | A | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-12971G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6060475 | ||||||
chr19:6060614
|
A | G | 76 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 76 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-13110T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6060614 | ||||||
chr19:6060630
|
A | G | 199 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(196): Show | 200 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.-8-13126T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6060630 | ||||||
chr19:6060705
|
C | T | 7 | a0001c0001t0002g0011a0001c0001t0005g0302a0001c0001t0005g0303others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-13201G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6060705 | ||||||
chr19:6060720
|
T | C | 167 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(164): Show | 168 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.-8-13216A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6060720 | ||||||
chr19:6060873
|
C | A | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 166 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.-8-13369G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6060873 | ||||||
chr19:6060939
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-8-13435T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6060939 | ||||||
chr19:6060956
|
C | T | 7 | a0001c0001t0002g0011a0001c0001t0005g0302a0001c0001t0005g0303others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-13452G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6060956 | ||||||
chr19:6060999
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-13495G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6060999 | ||||||
chr19:6061036
|
G | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-8-13532C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6061036 | ||||||
chr19:6061065
|
C | T | 1 | a0001c0003t0001g0258 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-8-13561G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6061065 | ||||||
chr19:6061071
|
G | A | 1 | a0001c0001t0002g0030 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-8-13567C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6061071 | ||||||
chr19:6061394
|
AC | A | 162 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(159): Show | 163 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.-8-13891delG | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6061394 | ||||||
chr19:6061447
|
T | A | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-8-13943A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6061447 | ||||||
chr19:6061455
|
T | C | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-13951A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6061455 | ||||||
chr19:6061561
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-8-14057G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6061561 | ||||||
chr19:6061613
|
C | T | 1 | a0001c0004t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-8-14109G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6061613 | ||||||
chr19:6061688
|
C | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-8-14184G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6061688 | ||||||
chr19:6061996
|
ACAACAAC others(36): Show |
A | 1 | a0001c0001t0001g0024 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-8-14535_-8-14493d others(45): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6061996 | ||||||
chr19:6062237
|
C | A | 13 | a0001c0004t0001g0012a0001c0004t0001g0276a0001c0004t0001g0277others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8-14733G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6062237 | ||||||
chr19:6062263
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8-14759C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6062263 | ||||||
chr19:6062264
|
T | C | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 94 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(91): Show |
intron_variant | MODIFIER | c.-8-14760A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6062264 | ||||||
chr19:6062286
|
C | T | 1 | a0002c0006t0001g0208 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-8-14782G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6062286 | ||||||
chr19:6062293
|
G | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0252 | 2 | HG00741.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-8-14789C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6062293 | ||||||
chr19:6062340
|
G | C | 1 | a0001c0001t0001g0007 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-8-14836C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6062340 | ||||||
chr19:6062500
|
A | G | 1 | a0001c0001t0001g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8-14996T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6062500 | ||||||
chr19:6062523
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-8-15019C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6062523 | ||||||
chr19:6062717
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-15213C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6062717 | ||||||
chr19:6062835
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-15331G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6062835 | ||||||
chr19:6062933
|
G | A | 9 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(6): Show | 9 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-15429C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6062933 | ||||||
chr19:6063191
|
G | T | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-15687C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6063191 | ||||||
chr19:6063192
|
G | T | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-15688C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6063192 | ||||||
chr19:6063243
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-8-15739G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6063243 | ||||||
chr19:6063365
|
G | A | 1 | a0001c0003t0001g0256 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-15861C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6063365 | ||||||
chr19:6063398
|
G | C | 3 | a0002c0002t0001g0059a0002c0002t0001g0060a0002c0002t0001g0198 | 3 | HG02080.hp2 NA19063.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-8-15894C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6063398 | ||||||
chr19:6063463
|
G | C | 1 | a0001c0001t0001g0007 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-8-15959C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6063463 | ||||||
chr19:6063601
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-16097C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6063601 | ||||||
chr19:6063742
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-8-16238G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6063742 | ||||||
chr19:6063758
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-8-16254G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6063758 | ||||||
chr19:6063765
|
G | C | 1 | a0001c0001t0001g0238 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-8-16261C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6063765 | ||||||
chr19:6064111
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-8-16607A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6064111 | ||||||
chr19:6064186
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(8): Show | 11 | HG02080.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8-16682G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6064186 | ||||||
chr19:6064236
|
C | T | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-16732G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6064236 | ||||||
chr19:6064247
|
G | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-16743C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6064247 | ||||||
chr19:6064393
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-8-16889C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6064393 | ||||||
chr19:6064438
|
G | A | 24 | a0001c0001t0001g0024a0001c0001t0001g0101a0001c0001t0001g0102others(21): Show | 24 | HG00597.hp2 HG00735.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.-8-16934C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6064438 | ||||||
chr19:6064505
|
A | G | 28 | a0001c0001t0001g0108a0001c0001t0001g0234a0001c0001t0001g0236others(25): Show | 28 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8-17001T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6064505 | ||||||
chr19:6064567
|
C | G | 9 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(6): Show | 9 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-17063G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6064567 | ||||||
chr19:6064599
|
C | T | 2 | a0002c0006t0003g0095a0002c0006t0003g0096 | 2 | HG02523.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.-8-17095G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6064599 | ||||||
chr19:6064636
|
C | A | 1 | a0002c0006t0001g0100 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-8-17132G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6064636 | ||||||
chr19:6064672
|
A | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-17168T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6064672 | ||||||
chr19:6064787
|
T | G | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-8-17283A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6064787 | ||||||
chr19:6064928
|
C | T | 2 | a0001c0003t0004g0268a0001c0003t0004g0269 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-8-17424G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6064928 | ||||||
chr19:6064934
|
C | G | 4 | a0002c0002t0001g0065a0002c0002t0001g0200a0002c0002t0001g0203others(1): Show | 4 | HG00423.hp1 HG00673.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-17430G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6064934 | ||||||
chr19:6065029
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-8-17525C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6065029 | ||||||
chr19:6065061
|
T | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-17557A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6065061 | ||||||
chr19:6065386
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0130a0001c0001t0001g0168others(1): Show | 4 | HG00621.hp1 HG03017.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-17882G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6065386 | ||||||
chr19:6065553
|
G | A | 3 | a0002c0002t0001g0058a0002c0002t0001g0066a0002c0002t0001g0071 | 3 | HG02602.hp1 HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-8-18049C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6065553 | ||||||
chr19:6066077
|
C | T | 1 | a0001c0003t0001g0258 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-8-18573G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6066077 | ||||||
chr19:6066164
|
A | C | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-8-18660T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6066164 | ||||||
chr19:6066205
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-8-18701C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6066205 | ||||||
chr19:6066316
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-8-18812G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6066316 | ||||||
chr19:6066650
|
T | C | 10 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(7): Show | 10 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-19146A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6066650 | ||||||
chr19:6067314
|
G | C | 1 | a0001c0001t0001g0007 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-8-19810C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6067314 | ||||||
chr19:6067646
|
G | C | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-20142C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6067646 | ||||||
chr19:6067730
|
G | T | 21 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(18): Show | 21 | HG01109.hp2 HG02055.hp2 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.-8-20226C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6067730 | ||||||
chr19:6067790
|
G | A | 1 | a0001c0001t0004g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-8-20286C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6067790 | ||||||
chr19:6067793
|
GGGTCAAC others(9): Show |
G | 1 | a0001c0001t0005g0307 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-8-20305_-8-20290d others(18): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6067793 | ||||||
chr19:6067914
|
A | G | 4 | a0002c0002t0001g0079a0002c0002t0001g0205a0002c0002t0001g0297others(1): Show | 4 | HG03831.hp2 HG03942.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-20410T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6067914 | ||||||
chr19:6067969
|
G | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-8-20465C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6067969 | ||||||
chr19:6068017
|
T | C | 13 | a0001c0004t0001g0012a0001c0004t0001g0276a0001c0004t0001g0277others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8-20513A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6068017 | ||||||
chr19:6068173
|
G | A | 1 | a0002c0002t0001g0080 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-8-20669C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6068173 | ||||||
chr19:6068176
|
T | C | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-20672A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6068176 | ||||||
chr19:6068517
|
T | C | 27 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(24): Show | 27 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-8-21013A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6068517 | ||||||
chr19:6068519
|
G | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-8-21015C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6068519 | ||||||
chr19:6068542
|
C | G | 162 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(159): Show | 163 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.-8-21038G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6068542 | ||||||
chr19:6068662
|
C | G | 1 | a0001c0001t0001g0300 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-8-21158G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6068662 | ||||||
chr19:6068665
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-8-21161C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6068665 | ||||||
chr19:6068866
|
G | T | 27 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(24): Show | 27 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-8-21362C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6068866 | ||||||
chr19:6068890
|
A | C | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-21386T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6068890 | ||||||
chr19:6068912
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-8-21408A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6068912 | ||||||
chr19:6069243
|
T | C | 3 | a0001c0004t0001g0292a0001c0004t0001g0293a0001c0004t0001g0294 | 3 | HG01884.hp2 HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-8-21739A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069243 | ||||||
chr19:6069252
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-8-21748A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069252 | ||||||
chr19:6069326
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-21822G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069326 | ||||||
chr19:6069363
|
A | G | 1 | a0001c0004t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-8-21859T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069363 | ||||||
chr19:6069431
|
A | G | 21 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(18): Show | 21 | HG01109.hp2 HG02055.hp2 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.-8-21927T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069431 | ||||||
chr19:6069584
|
T | C | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8-22080A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069584 | ||||||
chr19:6069896
|
G | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008 | 3 | HG02486.hp1 HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-8-22392C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069896 | ||||||
chr19:6069908
|
A | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0211 | 2 | HG01175.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-8-22404T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069908 | ||||||
chr19:6069981
|
T | C | 3 | a0002c0002t0001g0191a0002c0002t0001g0230a0002c0002t0001g0231 | 3 | HG02647.hp2 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-8-22477A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069981 | ||||||
chr19:6069986
|
T | TGGATGGG others(478): Show |
1 | a0001c0001t0001g0148 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-8-22483_-8-22482i others(487): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069986 | ||||||
chr19:6069986
|
T | TGGATGGG others(458): Show |
1 | a0002c0002t0001g0200 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-8-22483_-8-22482i others(467): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069986 | ||||||
chr19:6069986
|
T | TGGATGGG others(463): Show |
2 | a0001c0001t0001g0253a0002c0006t0001g0214 | 2 | HG01891.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.-8-22483_-8-22482i others(472): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069986 | ||||||
chr19:6069986
|
T | TGGATGGG others(468): Show |
84 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0143others(81): Show | 85 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-8-22483_-8-22482i others(477): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069986 | ||||||
chr19:6069986
|
T | TGGATGGG others(473): Show |
41 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0033others(38): Show | 41 | HG00140.hp2 HG01123.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.-8-22483_-8-22482i others(482): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069986 | ||||||
chr19:6069986
|
T | TGGATGGG others(478): Show |
72 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(69): Show | 72 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.-8-22483_-8-22482i others(487): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069986 | ||||||
chr19:6069986
|
T | TGGATGGG others(483): Show |
25 | a0001c0001t0001g0024a0001c0001t0001g0105a0001c0001t0001g0106others(22): Show | 25 | HG00597.hp2 HG00735.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.-8-22483_-8-22482i others(492): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069986 | ||||||
chr19:6069986
|
T | TGGATGGG others(488): Show |
2 | a0001c0001t0006g0158a0001c0001t0006g0173 | 2 | NA19007.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-8-22483_-8-22482i others(497): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069986 | ||||||
chr19:6069986
|
T | TGGATGGG others(693): Show |
1 | a0001c0001t0001g0300 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-8-22483_-8-22482i others(702): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069986 | ||||||
chr19:6069986
|
T | TGGATGGG others(688): Show |
22 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0054others(19): Show | 22 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-8-22483_-8-22482i others(697): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069986 | ||||||
chr19:6069986
|
T | TGGATGGG others(709): Show |
6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-22483_-8-22482i others(718): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069986 | ||||||
chr19:6069989
|
A | ATGGGATG others(1114): Show |
4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-22486_-8-22485i others(1123): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069989 | ||||||
chr19:6069998
|
G | A | 45 | a0001c0001t0001g0010a0001c0001t0001g0234a0001c0001t0001g0236others(42): Show | 45 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.-8-22494C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6069998 | ||||||
chr19:6070019
|
G | A | 45 | a0001c0001t0001g0010a0001c0001t0001g0234a0001c0001t0001g0236others(42): Show | 45 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.-8-22515C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070019 | ||||||
chr19:6070033
|
A | AGGATG | 20 | a0001c0001t0001g0055a0001c0001t0001g0145a0001c0001t0001g0152others(17): Show | 20 | HG01943.hp1 HG02055.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8-22534_-8-22530d others(7): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070033 | ||||||
chr19:6070033
|
A | G | 45 | a0001c0001t0001g0010a0001c0001t0001g0234a0001c0001t0001g0236others(42): Show | 45 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.-8-22529T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070033 | ||||||
chr19:6070038
|
G | GGAATGGG others(790): Show |
8 | a0003c0005t0001g0046a0003c0005t0001g0048a0003c0005t0001g0049others(5): Show | 8 | HG02155.hp1 NA18612.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-22535_-8-22534i others(799): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070038 | ||||||
chr19:6070038
|
G | GGAATGGG others(785): Show |
2 | a0003c0005t0001g0045a0003c0005t0003g0020 | 2 | HG02027.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.-8-22535_-8-22534i others(794): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070038 | ||||||
chr19:6070038
|
G | GGAATGGG others(463): Show |
3 | a0002c0002t0001g0067a0002c0002t0001g0194a0002c0002t0001g0209 | 3 | HG02135.hp2 HG02486.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-8-22535_-8-22534i others(472): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070038 | ||||||
chr19:6070038
|
G | GGAATGGG others(688): Show |
1 | a0001c0003t0004g0264 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-8-22535_-8-22534i others(697): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070038 | ||||||
chr19:6070038
|
G | GGAATGGG others(683): Show |
27 | a0001c0001t0001g0010a0001c0001t0001g0234a0001c0001t0001g0236others(24): Show | 27 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-8-22535_-8-22534i others(692): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070038 | ||||||
chr19:6070038
|
G | GGAATGGG others(479): Show |
4 | a0001c0003t0004g0262a0001c0003t0004g0268a0001c0003t0004g0269others(1): Show | 4 | HG02109.hp1 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-22535_-8-22534i others(488): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070038 | ||||||
chr19:6070074
|
T | TGGATG | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-22575_-8-22571d others(7): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070074 | ||||||
chr19:6070095
|
T | TGGATG | 11 | a0001c0001t0001g0130a0003c0005t0001g0045a0003c0005t0001g0046others(8): Show | 11 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8-22596_-8-22592d others(7): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070095 | ||||||
chr19:6070095
|
TGGATG | T | 11 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(8): Show | 11 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-22596_-8-22592d others(7): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070095 | ||||||
chr19:6070170
|
A | AATGGG | 3 | a0001c0004t0001g0292a0001c0004t0001g0293a0001c0004t0001g0294 | 3 | HG01884.hp2 HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-8-22671_-8-22667d others(7): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070170 | ||||||
chr19:6070170
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-22666T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070170 | ||||||
chr19:6070179
|
G | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-22675C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070179 | ||||||
chr19:6070181
|
A | ATGGGATG others(253): Show |
3 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG02559.hp1 HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-8-22678_-8-22677i others(262): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070181 | ||||||
chr19:6070181
|
A | ATGGGATG others(710): Show |
1 | a0001c0001t0001g0054 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-8-22678_-8-22677i others(719): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070181 | ||||||
chr19:6070181
|
A | ATGGGATG others(730): Show |
3 | a0001c0001t0005g0303a0001c0001t0005g0306a0001c0001t0005g0307 | 3 | HG02630.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-8-22678_-8-22677i others(739): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070181 | ||||||
chr19:6070181
|
A | ATGGGATG others(715): Show |
1 | a0001c0001t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-8-22678_-8-22677i others(724): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070181 | ||||||
chr19:6070181
|
A | ATGGGATG others(725): Show |
1 | a0001c0001t0005g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-8-22678_-8-22677i others(734): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070181 | ||||||
chr19:6070181
|
A | ATGGGATG others(705): Show |
1 | a0001c0001t0001g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-8-22678_-8-22677i others(714): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070181 | ||||||
chr19:6070181
|
A | ATGGGATG others(710): Show |
1 | a0001c0004t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-8-22678_-8-22677i others(719): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070181 | ||||||
chr19:6070181
|
A | ATGGGATG others(725): Show |
2 | a0001c0001t0005g0302a0006c0009t0005g0305 | 2 | HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-8-22678_-8-22677i others(734): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070181 | ||||||
chr19:6070181
|
A | ATGGGATG others(705): Show |
2 | a0001c0001t0001g0010a0001c0001t0003g0009 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-8-22678_-8-22677i others(714): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070181 | ||||||
chr19:6070181
|
A | ATGGGATG others(700): Show |
4 | a0001c0001t0001g0300a0001c0001t0003g0018a0001c0001t0003g0019others(1): Show | 4 | HG02080.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-22678_-8-22677i others(709): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070181 | ||||||
chr19:6070181
|
A | ATGGGATG others(690): Show |
1 | a0001c0001t0001g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8-22678_-8-22677i others(699): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070181 | ||||||
chr19:6070192
|
T | TGGGATGG others(227): Show |
1 | a0001c0001t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-8-22689_-8-22688i others(236): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070192 | ||||||
chr19:6070206
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-8-22702C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070206 | ||||||
chr19:6070207
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-8-22703T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070207 | ||||||
chr19:6070219
|
G | GT | 20 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(17): Show | 20 | HG01109.hp2 HG02055.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-22716_-8-22715i others(3): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070219 | ||||||
chr19:6070231
|
G | A | 20 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(17): Show | 20 | HG01109.hp2 HG02055.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-22727C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(726): Show |
1 | a0002c0002t0003g0075 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(735): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(716): Show |
1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(725): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(716): Show |
1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(725): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(716): Show |
2 | a0001c0001t0001g0240a0001c0001t0001g0252 | 2 | HG00741.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(725): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(731): Show |
1 | a0001c0001t0009g0291 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(740): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(721): Show |
4 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0290others(1): Show | 4 | HG02615.hp1 HG02965.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(730): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(721): Show |
1 | a0002c0002t0001g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(730): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(716): Show |
7 | a0002c0002t0001g0190a0002c0002t0001g0192a0002c0002t0001g0193others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(725): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(706): Show |
1 | a0002c0002t0001g0295 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(715): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(612): Show |
7 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(4): Show | 7 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(621): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(721): Show |
1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(730): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(711): Show |
2 | a0001c0001t0001g0254a0001c0001t0001g0296 | 2 | HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(720): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(711): Show |
2 | a0001c0001t0001g0099a0001c0001t0001g0103 | 2 | HG00735.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(720): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(727): Show |
2 | a0001c0001t0003g0155a0001c0001t0003g0156 | 2 | HG01074.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(736): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(706): Show |
1 | a0001c0001t0001g0028 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(715): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(716): Show |
1 | a0001c0001t0001g0289 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(725): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(716): Show |
1 | a0002c0006t0001g0100 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(725): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(716): Show |
1 | a0001c0001t0001g0014 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(725): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(716): Show |
7 | a0001c0001t0001g0216a0002c0002t0001g0092a0002c0002t0002g0001others(4): Show | 8 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(725): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(711): Show |
16 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0140others(13): Show | 16 | HG00544.hp1 HG00621.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(720): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(706): Show |
1 | a0001c0001t0001g0122 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(715): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(701): Show |
1 | a0001c0001t0001g0109 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(710): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(716): Show |
2 | a0001c0001t0001g0023a0001c0001t0001g0036 | 2 | HG02735.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(725): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(721): Show |
2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(730): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(711): Show |
8 | a0001c0001t0001g0150a0001c0001t0001g0161a0001c0001t0001g0211others(5): Show | 8 | HG00741.hp1 HG01175.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(720): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(711): Show |
6 | a0001c0001t0001g0042a0001c0001t0001g0154a0001c0001t0001g0159others(3): Show | 6 | HG01123.hp1 HG02165.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(720): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(706): Show |
1 | a0008c0012t0001g0151 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(715): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(711): Show |
1 | a0001c0001t0002g0188 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(720): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(685): Show |
1 | a0002c0002t0002g0073 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(694): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(706): Show |
140 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(137): Show | 140 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(715): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(701): Show |
1 | a0002c0002t0010g0061 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(710): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(607): Show |
2 | a0001c0004t0001g0281a0001c0004t0001g0282 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(616): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(721): Show |
1 | a0001c0001t0003g0233 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(730): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(716): Show |
9 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0238others(6): Show | 9 | HG00140.hp1 HG01069.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(725): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(711): Show |
3 | a0001c0001t0001g0237a0001c0003t0004g0262a0001c0003t0004g0275 | 3 | HG02109.hp1 HG02572.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(720): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(711): Show |
1 | a0001c0003t0001g0257 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(720): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(706): Show |
9 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0258others(6): Show | 9 | HG01934.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(715): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(701): Show |
1 | a0001c0001t0001g0168 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(710): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(696): Show |
1 | a0001c0001t0001g0017 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(705): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(696): Show |
10 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(7): Show | 10 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(705): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(721): Show |
9 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(6): Show | 9 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(730): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(716): Show |
1 | a0003c0005t0001g0050 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(725): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(711): Show |
1 | a0001c0004t0001g0292 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(720): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(706): Show |
1 | a0001c0001t0002g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-8-22728_-8-22727i others(715): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(701): Show |
8 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0144others(5): Show | 8 | HG01993.hp1 HG03017.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(710): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(706): Show |
2 | a0001c0004t0001g0293a0001c0004t0001g0294 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(715): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(706): Show |
2 | a0001c0003t0004g0268a0001c0003t0004g0269 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-8-22728_-8-22727i others(715): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070231
|
G | GATGGGAT others(19): Show |
1 | a0001c0001t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-8-22753_-8-22728d others(28): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070231 | ||||||
chr19:6070403
|
G | A | 74 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 74 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.-8-22899C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070403 | ||||||
chr19:6070460
|
G | T | 26 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(23): Show | 26 | HG00140.hp1 HG01069.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.-8-22956C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070460 | ||||||
chr19:6070685
|
A | G | 44 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0211others(41): Show | 44 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.-8-23181T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070685 | ||||||
chr19:6070748
|
C | G | 1 | a0001c0001t0009g0291 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8-23244G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6070748 | ||||||
chr19:6071149
|
G | C | 1 | a0001c0001t0001g0164 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-8-23645C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6071149 | ||||||
chr19:6071168
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-8-23664A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6071168 | ||||||
chr19:6071260
|
A | C | 1 | a0001c0001t0002g0104 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-8-23756T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6071260 | ||||||
chr19:6071364
|
G | T | 7 | a0001c0001t0002g0011a0001c0001t0005g0302a0001c0001t0005g0303others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-23860C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6071364 | ||||||
chr19:6071423
|
A | G | 10 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(7): Show | 10 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-23919T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6071423 | ||||||
chr19:6071462
|
C | T | 2 | a0001c0001t0001g0266a0001c0007t0001g0273 | 2 | NA19012.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-8-23958G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6071462 | ||||||
chr19:6071748
|
TA | T | 161 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(158): Show | 162 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.-8-24245delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6071748 | ||||||
chr19:6071791
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-8-24287A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6071791 | ||||||
chr19:6071833
|
A | T | 1 | a0002c0002t0001g0060 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-8-24329T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6071833 | ||||||
chr19:6071880
|
T | C | 12 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(9): Show | 12 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8-24376A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6071880 | ||||||
chr19:6072005
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-8-24501C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6072005 | ||||||
chr19:6072020
|
C | A | 17 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(14): Show | 17 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-24516G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6072020 | ||||||
chr19:6072027
|
A | G | 1 | a0001c0001t0002g0170 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-8-24523T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6072027 | ||||||
chr19:6072073
|
G | T | 1 | a0001c0003t0004g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-8-24569C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6072073 | ||||||
chr19:6072131
|
G | GAATAA | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-24628_-8-24627i others(7): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6072131 | ||||||
chr19:6072187
|
A | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-24683T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6072187 | ||||||
chr19:6072483
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-8-24979C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6072483 | ||||||
chr19:6072550
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-8-25046A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6072550 | ||||||
chr19:6072649
|
G | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-25145C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6072649 | ||||||
chr19:6072659
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-8-25155A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6072659 | ||||||
chr19:6072757
|
G | GA | 22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(19): Show | 22 | HG01109.hp2 HG02055.hp2 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.-8-25254dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6072757 | ||||||
chr19:6072859
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-8-25355C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6072859 | ||||||
chr19:6073042
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-8-25538G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6073042 | ||||||
chr19:6073066
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-8-25562C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6073066 | ||||||
chr19:6073129
|
A | C | 1 | a0002c0002t0001g0086 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-8-25625T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6073129 | ||||||
chr19:6073358
|
T | C | 40 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(37): Show | 40 | HG01109.hp2 HG02027.hp1 HG02055.hp2 others(37): Show |
intron_variant | MODIFIER | c.-8-25854A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6073358 | ||||||
chr19:6073371
|
G | A | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(53): Show | 56 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8-25867C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6073371 | ||||||
chr19:6073423
|
C | T | 6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-25919G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6073423 | ||||||
chr19:6073424
|
G | A | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8-25920C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6073424 | ||||||
chr19:6073495
|
C | T | 88 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 88 | HG00140.hp1 HG01069.hp1 HG01109.hp2 others(85): Show |
intron_variant | MODIFIER | c.-8-25991G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6073495 | ||||||
chr19:6073496
|
C | T | 88 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 88 | HG00140.hp1 HG01069.hp1 HG01109.hp2 others(85): Show |
intron_variant | MODIFIER | c.-8-25992G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6073496 | ||||||
chr19:6073759
|
C | T | 9 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(6): Show | 9 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-26255G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6073759 | ||||||
chr19:6073779
|
G | C | 26 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(23): Show | 26 | HG00140.hp1 HG01069.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.-8-26275C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6073779 | ||||||
chr19:6074336
|
A | G | 20 | a0002c0002t0001g0092a0002c0002t0001g0097a0002c0002t0001g0295others(17): Show | 21 | HG00544.hp1 HG00642.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8-26832T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6074336 | ||||||
chr19:6074394
|
C | T | 28 | a0002c0002t0001g0092a0002c0002t0001g0097a0002c0002t0001g0190others(25): Show | 29 | HG00544.hp1 HG00642.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.-8-26890G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6074394 | ||||||
chr19:6074410
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-26906G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6074410 | ||||||
chr19:6074426
|
G | A | 41 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0001g0060others(38): Show | 41 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.-8-26922C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6074426 | ||||||
chr19:6074465
|
T | C | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-26961A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6074465 | ||||||
chr19:6074691
|
G | T | 1 | a0002c0002t0001g0086 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-8-27187C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6074691 | ||||||
chr19:6074699
|
G | A | 28 | a0002c0002t0001g0092a0002c0002t0001g0097a0002c0002t0001g0190others(25): Show | 29 | HG00544.hp1 HG00642.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.-8-27195C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6074699 | ||||||
chr19:6074891
|
A | C | 7 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(4): Show | 7 | HG00741.hp2 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-27387T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6074891 | ||||||
chr19:6074928
|
C | G | 5 | a0002c0002t0001g0190a0002c0002t0001g0192a0002c0002t0001g0193others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-27424G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6074928 | ||||||
chr19:6074994
|
A | ATG | 6 | a0002c0002t0001g0070a0002c0002t0001g0079a0002c0002t0001g0205others(3): Show | 6 | HG03239.hp2 HG03831.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-27492_-8-27491d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6074994 | ||||||
chr19:6075200
|
T | G | 4 | a0001c0003t0004g0262a0001c0003t0004g0268a0001c0003t0004g0269others(1): Show | 4 | HG02109.hp1 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-27696A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6075200 | ||||||
chr19:6075201
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-8-27697A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6075201 | ||||||
chr19:6075218
|
A | G | 18 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(15): Show | 18 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.-8-27714T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6075218 | ||||||
chr19:6075272
|
T | TGGA | 9 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(6): Show | 9 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-27771_-8-27769d others(5): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6075272 | ||||||
chr19:6075272
|
T | TGGAGGAG others(5): Show |
2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-8-27780_-8-27769d others(14): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6075272 | ||||||
chr19:6075442
|
G | A | 1 | a0002c0002t0001g0080 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-8-27938C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6075442 | ||||||
chr19:6075590
|
A | G | 3 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254 | 3 | HG00741.hp2 HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-8-28086T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6075590 | ||||||
chr19:6075622
|
T | C | 1 | a0001c0001t0002g0031 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-8-28118A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6075622 | ||||||
chr19:6075656
|
G | A | 2 | a0002c0002t0002g0207a0002c0002t0008g0062 | 2 | HG01175.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.-8-28152C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6075656 | ||||||
chr19:6075702
|
G | A | 26 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(23): Show | 26 | HG00140.hp1 HG01069.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.-8-28198C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6075702 | ||||||
chr19:6075720
|
A | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-28216T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6075720 | ||||||
chr19:6075947
|
G | A | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-8-28443C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6075947 | ||||||
chr19:6075952
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(8): Show | 11 | HG02080.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8-28448G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6075952 | ||||||
chr19:6076033
|
T | C | 1 | a0001c0001t0002g0170 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-8-28529A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6076033 | ||||||
chr19:6076046
|
T | A | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-28542A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6076046 | ||||||
chr19:6076138
|
G | A | 7 | a0001c0001t0002g0011a0001c0001t0005g0302a0001c0001t0005g0303others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-28634C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6076138 | ||||||
chr19:6076201
|
A | G | 18 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(15): Show | 18 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.-8-28697T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6076201 | ||||||
chr19:6076204
|
C | T | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-28700G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6076204 | ||||||
chr19:6076269
|
G | A | 26 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(23): Show | 26 | HG00140.hp1 HG01069.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.-8-28765C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6076269 | ||||||
chr19:6076644
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-8-29140C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6076644 | ||||||
chr19:6076677
|
G | A | 26 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(23): Show | 26 | HG00140.hp1 HG01069.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.-8-29173C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6076677 | ||||||
chr19:6076749
|
A | T | 1 | a0001c0001t0001g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-8-29245T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6076749 | ||||||
chr19:6077048
|
A | G | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(90): Show | 93 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(90): Show |
intron_variant | MODIFIER | c.-8-29544T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6077048 | ||||||
chr19:6077109
|
A | G | 1 | a0001c0001t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-8-29605T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6077109 | ||||||
chr19:6077216
|
G | A | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8-29712C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6077216 | ||||||
chr19:6077220
|
A | G | 66 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(63): Show | 66 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.-8-29716T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6077220 | ||||||
chr19:6077308
|
A | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-29804T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6077308 | ||||||
chr19:6077367
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-8-29863G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6077367 | ||||||
chr19:6077811
|
G | T | 1 | a0001c0001t0001g0115 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-8-30307C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6077811 | ||||||
chr19:6077875
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-30371C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6077875 | ||||||
chr19:6077894
|
C | A | 20 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0242others(17): Show | 20 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-30390G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6077894 | ||||||
chr19:6077934
|
C | T | 1 | a0002c0002t0001g0077 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-8-30430G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6077934 | ||||||
chr19:6077936
|
C | T | 1 | a0001c0001t0002g0188 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-8-30432G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6077936 | ||||||
chr19:6077980
|
C | CA | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 19 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8-30477dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6077980 | ||||||
chr19:6077980
|
CA | C | 58 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0132others(55): Show | 58 | HG00140.hp1 HG01069.hp1 HG01243.hp2 others(55): Show |
intron_variant | MODIFIER | c.-8-30477delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6077980 | ||||||
chr19:6078008
|
G | A | 1 | a0001c0004t0001g0277 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-8-30504C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6078008 | ||||||
chr19:6078145
|
A | G | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(60): Show | 63 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.-8-30641T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6078145 | ||||||
chr19:6078169
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-8-30665G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6078169 | ||||||
chr19:6078176
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-8-30672C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6078176 | ||||||
chr19:6078311
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-8-30807A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6078311 | ||||||
chr19:6078338
|
T | TA | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(39): Show | 42 | HG00140.hp1 HG01069.hp1 HG01934.hp2 others(39): Show |
intron_variant | MODIFIER | c.-8-30835dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6078338 | ||||||
chr19:6078338
|
T | TAA | 7 | a0001c0001t0002g0011a0001c0001t0005g0302a0001c0001t0005g0303others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-30836_-8-30835d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6078338 | ||||||
chr19:6078338
|
T | TAAAA | 18 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(15): Show | 18 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.-8-30838_-8-30835d others(6): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6078338 | ||||||
chr19:6078367
|
C | T | 1 | a0003c0005t0001g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-8-30863G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6078367 | ||||||
chr19:6078532
|
C | T | 1 | a0004c0008t0002g0284 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-8-31028G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6078532 | ||||||
chr19:6078834
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-8-31330A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6078834 | ||||||
chr19:6078965
|
G | A | 18 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(15): Show | 18 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9+31428C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6078965 | ||||||
chr19:6078993
|
C | T | 3 | a0001c0004t0001g0292a0001c0004t0001g0293a0001c0004t0001g0294 | 3 | HG01884.hp2 HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-9+31400G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6078993 | ||||||
chr19:6079056
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-9+31337C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6079056 | ||||||
chr19:6079068
|
G | A | 1 | a0002c0002t0001g0204 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-9+31325C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6079068 | ||||||
chr19:6079174
|
A | C | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-9+31219T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6079174 | ||||||
chr19:6079221
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-9+31172G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6079221 | ||||||
chr19:6079349
|
T | TAAAAGGA others(359): Show |
1 | a0001c0001t0001g0274 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-9+31043_-9+31044i others(368): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6079349 | ||||||
chr19:6079587
|
A | G | 44 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(41): Show | 44 | HG00140.hp1 HG01069.hp1 HG01934.hp2 others(41): Show |
intron_variant | MODIFIER | c.-9+30806T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6079587 | ||||||
chr19:6079625
|
C | G | 2 | a0001c0001t0001g0266a0001c0007t0001g0273 | 2 | NA19012.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-9+30768G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6079625 | ||||||
chr19:6079696
|
G | T | 13 | a0001c0004t0001g0012a0001c0004t0001g0276a0001c0004t0001g0277others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9+30697C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6079696 | ||||||
chr19:6079746
|
C | T | 44 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(41): Show | 44 | HG00140.hp1 HG01069.hp1 HG01934.hp2 others(41): Show |
intron_variant | MODIFIER | c.-9+30647G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6079746 | ||||||
chr19:6079760
|
C | G | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+30633G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6079760 | ||||||
chr19:6079884
|
C | CA | 13 | a0001c0001t0001g0028a0001c0001t0001g0053a0001c0001t0001g0054others(10): Show | 13 | HG01109.hp2 HG01358.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+30508dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6079884 | ||||||
chr19:6079884
|
CA | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(27): Show | 30 | HG00642.hp2 HG00741.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+30508delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6079884 | ||||||
chr19:6079884
|
CAA | C | 53 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(50): Show | 53 | HG00140.hp1 HG01069.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.-9+30507_-9+30508d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6079884 | ||||||
chr19:6080127
|
T | C | 1 | a0001c0001t0002g0225 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-9+30266A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080127 | ||||||
chr19:6080202
|
A | ATG | 35 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0044others(32): Show | 35 | HG00323.hp2 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-9+30189_-9+30190d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080202 | ||||||
chr19:6080202
|
A | ATGTG | 14 | a0001c0001t0001g0053a0001c0001t0001g0088a0001c0001t0001g0089others(11): Show | 14 | HG01433.hp2 HG01934.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+30187_-9+30190d others(6): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080202 | ||||||
chr19:6080202
|
A | ATGTGTG | 3 | a0001c0001t0001g0010a0001c0001t0001g0129a0001c0001t0003g0009 | 3 | HG01256.hp1 HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-9+30185_-9+30190d others(8): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080202 | ||||||
chr19:6080202
|
A | ATGTGTGT others(3): Show |
9 | a0001c0001t0001g0234a0001c0001t0001g0270a0001c0001t0001g0272others(6): Show | 9 | HG00140.hp1 HG01069.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+30181_-9+30190d others(12): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080202 | ||||||
chr19:6080202
|
A | ATGTGTGT others(5): Show |
4 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0271others(1): Show | 4 | HG03669.hp2 NA18747.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+30179_-9+30190d others(14): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080202 | ||||||
chr19:6080202
|
A | ATGTGTGT others(7): Show |
4 | a0001c0003t0001g0258a0001c0003t0001g0259a0001c0003t0001g0260others(1): Show | 4 | HG01934.hp2 HG02258.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+30177_-9+30190d others(16): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080202 | ||||||
chr19:6080202
|
A | ATGTGTGT others(9): Show |
5 | a0001c0001t0001g0236a0001c0001t0001g0266a0001c0003t0001g0257others(2): Show | 5 | HG02886.hp1 HG03486.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+30175_-9+30190d others(18): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080202 | ||||||
chr19:6080202
|
A | ATGTGTGT others(11): Show |
3 | a0001c0001t0017g0239a0001c0003t0001g0255a0001c0003t0001g0256 | 3 | HG02976.hp1 HG03540.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-9+30173_-9+30190d others(20): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080202 | ||||||
chr19:6080202
|
A | ATGTGTGT others(13): Show |
1 | a0001c0003t0004g0264 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-9+30171_-9+30190d others(22): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080202 | ||||||
chr19:6080202
|
ATG | A | 26 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(23): Show | 26 | HG00741.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.-9+30189_-9+30190d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080202 | ||||||
chr19:6080202
|
ATGTG | A | 5 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(2): Show | 5 | HG02965.hp1 HG03098.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+30187_-9+30190d others(6): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080202 | ||||||
chr19:6080240
|
A | G | 1 | a0002c0002t0008g0062 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-9+30153T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080240 | ||||||
chr19:6080254
|
C | CAG | 7 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0286others(4): Show | 7 | HG01070.hp1 HG01070.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+30137_-9+30138d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080254 | ||||||
chr19:6080448
|
G | C | 1 | a0001c0001t0001g0037 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-9+29945C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080448 | ||||||
chr19:6080453
|
G | A | 18 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(15): Show | 18 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9+29940C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080453 | ||||||
chr19:6080471
|
C | G | 44 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(41): Show | 44 | HG00140.hp1 HG01069.hp1 HG01934.hp2 others(41): Show |
intron_variant | MODIFIER | c.-9+29922G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080471 | ||||||
chr19:6080510
|
G | T | 1 | a0002c0002t0001g0063 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-9+29883C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080510 | ||||||
chr19:6080612
|
A | G | 5 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(2): Show | 5 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+29781T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080612 | ||||||
chr19:6080618
|
C | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-9+29775G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080618 | ||||||
chr19:6080644
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-9+29749C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080644 | ||||||
chr19:6080735
|
A | C | 1 | a0002c0002t0001g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-9+29658T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080735 | ||||||
chr19:6080838
|
C | G | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+29555G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080838 | ||||||
chr19:6080878
|
A | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+29515T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080878 | ||||||
chr19:6080961
|
G | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-9+29432C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6080961 | ||||||
chr19:6081035
|
C | CA | 13 | a0001c0001t0001g0036a0001c0001t0001g0089a0001c0001t0001g0128others(10): Show | 13 | HG00140.hp2 HG01081.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+29357dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6081035 | ||||||
chr19:6081035
|
CA | C | 55 | a0001c0001t0001g0108a0001c0001t0001g0111a0001c0001t0001g0112others(52): Show | 55 | HG00741.hp2 HG01243.hp2 HG01256.hp2 others(52): Show |
intron_variant | MODIFIER | c.-9+29357delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6081035 | ||||||
chr19:6081035
|
CAA | C | 38 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(35): Show | 38 | HG00140.hp1 HG01069.hp1 HG01934.hp2 others(35): Show |
intron_variant | MODIFIER | c.-9+29356_-9+29357d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6081035 | ||||||
chr19:6081055
|
A | T | 13 | a0001c0004t0001g0012a0001c0004t0001g0276a0001c0004t0001g0277others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9+29338T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6081055 | ||||||
chr19:6081152
|
A | G | 1 | a0001c0001t0001g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-9+29241T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6081152 | ||||||
chr19:6081230
|
C | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0175a0001c0001t0001g0235 | 3 | HG01167.hp2 HG04184.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-9+29163G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6081230 | ||||||
chr19:6081307
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-9+29086G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6081307 | ||||||
chr19:6081405
|
T | C | 1 | a0001c0001t0008g0301 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-9+28988A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6081405 | ||||||
chr19:6081427
|
C | G | 1 | a0001c0001t0002g0171 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-9+28966G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6081427 | ||||||
chr19:6081625
|
G | C | 1 | a0002c0002t0001g0297 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-9+28768C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6081625 | ||||||
chr19:6081656
|
T | C | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 62 | HG00140.hp1 HG01069.hp1 HG01243.hp2 others(59): Show |
intron_variant | MODIFIER | c.-9+28737A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6081656 | ||||||
chr19:6081715
|
G | A | 7 | a0001c0001t0002g0011a0001c0001t0005g0302a0001c0001t0005g0303others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+28678C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6081715 | ||||||
chr19:6081728
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-9+28665C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6081728 | ||||||
chr19:6081815
|
C | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(16): Show | 19 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-9+28578G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6081815 | ||||||
chr19:6081819
|
G | A | 1 | a0001c0003t0001g0265 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-9+28574C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6081819 | ||||||
chr19:6081825
|
C | A | 4 | a0001c0001t0001g0139a0001c0001t0001g0178a0001c0001t0001g0221others(1): Show | 4 | HG01884.hp1 HG02004.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+28568G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6081825 | ||||||
chr19:6082156
|
C | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-9+28237G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6082156 | ||||||
chr19:6082293
|
C | CA | 31 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0222others(28): Show | 31 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.-9+28099dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6082293 | ||||||
chr19:6082293
|
C | CAA | 20 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(17): Show | 20 | HG00741.hp2 HG02027.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+28098_-9+28099d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6082293 | ||||||
chr19:6082293
|
CA | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0088others(98): Show | 102 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-9+28099delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6082293 | ||||||
chr19:6082494
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+27899C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6082494 | ||||||
chr19:6082506
|
C | T | 1 | a0002c0002t0001g0072 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-9+27887G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6082506 | ||||||
chr19:6082670
|
G | A | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-9+27723C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6082670 | ||||||
chr19:6082762
|
G | T | 1 | a0001c0001t0001g0044 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-9+27631C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6082762 | ||||||
chr19:6082767
|
G | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-9+27626C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6082767 | ||||||
chr19:6082768
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+27625G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6082768 | ||||||
chr19:6082873
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+27520C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6082873 | ||||||
chr19:6082873
|
G | C | 3 | a0001c0001t0001g0129a0001c0001t0001g0152a0001c0001t0001g0189 | 3 | HG00140.hp2 HG01256.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-9+27520C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6082873 | ||||||
chr19:6083088
|
G | A | 4 | a0001c0003t0004g0262a0001c0003t0004g0268a0001c0003t0004g0269others(1): Show | 4 | HG02109.hp1 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+27305C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6083088 | ||||||
chr19:6083192
|
C | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0285 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-9+27201G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6083192 | ||||||
chr19:6083270
|
A | C | 18 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(15): Show | 18 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9+27123T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6083270 | ||||||
chr19:6083530
|
G | T | 12 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(9): Show | 12 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-9+26863C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6083530 | ||||||
chr19:6083548
|
G | GT | 15 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0084others(12): Show | 15 | HG01934.hp2 HG02080.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+26844dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6083548 | ||||||
chr19:6083548
|
G | GTT | 36 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0240others(33): Show | 36 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.-9+26843_-9+26844d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6083548 | ||||||
chr19:6083548
|
GT | G | 70 | a0001c0001t0001g0010a0001c0001t0001g0128a0002c0002t0001g0058others(67): Show | 71 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.-9+26844delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6083548 | ||||||
chr19:6083744
|
T | A | 77 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(74): Show | 77 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.-9+26649A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6083744 | ||||||
chr19:6083829
|
C | T | 1 | a0002c0006t0001g0214 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-9+26564G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6083829 | ||||||
chr19:6083916
|
A | G | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+26477T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6083916 | ||||||
chr19:6083951
|
C | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+26442G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6083951 | ||||||
chr19:6083983
|
C | T | 1 | a0002c0006t0001g0100 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-9+26410G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6083983 | ||||||
chr19:6083990
|
A | C | 26 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0001g0012others(23): Show | 26 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-9+26403T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6083990 | ||||||
chr19:6084282
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0186 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-9+26111T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6084282 | ||||||
chr19:6084332
|
C | A | 1 | a0001c0001t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+26061G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6084332 | ||||||
chr19:6084639
|
C | CTTTTTTT | 10 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(7): Show | 10 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9+25753_-9+25754i others(9): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6084639 | ||||||
chr19:6084643
|
C | CTTTCTTT others(4): Show |
1 | a0001c0001t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+25749_-9+25750i others(13): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6084643 | ||||||
chr19:6084643
|
C | CTTTTTT | 9 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(6): Show | 9 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+25744_-9+25749d others(8): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6084643 | ||||||
chr19:6084643
|
C | CTTTTTTT others(3): Show |
41 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0234others(38): Show | 41 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.-9+25749_-9+25750i others(12): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6084643 | ||||||
chr19:6084643
|
C | CTTTTTTT others(4): Show |
22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(19): Show | 22 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-9+25749_-9+25750i others(13): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6084643 | ||||||
chr19:6084643
|
C | T | 12 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(9): Show | 12 | HG01243.hp2 HG01891.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-9+25750G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6084643 | ||||||
chr19:6084896
|
C | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9+25497G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6084896 | ||||||
chr19:6084900
|
G | A | 72 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0211others(69): Show | 73 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.-9+25493C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6084900 | ||||||
chr19:6084933
|
G | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9+25460C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6084933 | ||||||
chr19:6084981
|
C | T | 72 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0211others(69): Show | 73 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.-9+25412G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6084981 | ||||||
chr19:6085026
|
T | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0162a0001c0001t0001g0185 | 3 | HG00438.hp1 NA18973.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-9+25367A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6085026 | ||||||
chr19:6085110
|
T | C | 74 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0101others(71): Show | 75 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.-9+25283A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6085110 | ||||||
chr19:6085173
|
CCTGT | C | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+25216_-9+25219d others(6): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6085173 | ||||||
chr19:6085182
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0006g0217 | 2 | NA19003.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-9+25211C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6085182 | ||||||
chr19:6085209
|
C | T | 1 | a0002c0006t0001g0100 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-9+25184G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6085209 | ||||||
chr19:6085287
|
GTCTT | G | 6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+25102_-9+25105d others(6): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6085287 | ||||||
chr19:6085420
|
T | G | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-9+24973A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6085420 | ||||||
chr19:6085444
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-9+24949G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6085444 | ||||||
chr19:6085547
|
T | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9+24846A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6085547 | ||||||
chr19:6085646
|
C | T | 1 | a0001c0001t0003g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-9+24747G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6085646 | ||||||
chr19:6086024
|
C | A | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(90): Show | 93 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(90): Show |
intron_variant | MODIFIER | c.-9+24369G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6086024 | ||||||
chr19:6086071
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-9+24322C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6086071 | ||||||
chr19:6086091
|
C | CA | 9 | a0001c0001t0001g0187a0001c0001t0009g0245a0002c0002t0001g0069others(6): Show | 9 | HG01123.hp1 HG01175.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+24301dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6086091 | ||||||
chr19:6086091
|
C | CAA | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+24300_-9+24301d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6086091 | ||||||
chr19:6086091
|
CA | C | 201 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 202 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.-9+24301delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6086091 | ||||||
chr19:6086091
|
CAA | C | 8 | a0001c0001t0001g0036a0001c0001t0001g0130a0001c0001t0005g0302others(5): Show | 8 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+24300_-9+24301d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6086091 | ||||||
chr19:6086172
|
A | C | 1 | a0001c0001t0002g0299 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-9+24221T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6086172 | ||||||
chr19:6086625
|
C | T | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-9+23768G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6086625 | ||||||
chr19:6086636
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+23757C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6086636 | ||||||
chr19:6086693
|
T | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0250 | 2 | HG01243.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-9+23700A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6086693 | ||||||
chr19:6086701
|
C | T | 13 | a0001c0004t0001g0012a0001c0004t0001g0276a0001c0004t0001g0277others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9+23692G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6086701 | ||||||
chr19:6086733
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9+23660G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6086733 | ||||||
chr19:6086833
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0064 | 2 | HG03017.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-9+23560A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6086833 | ||||||
chr19:6086833
|
T | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0300a0001c0001t0003g0009others(3): Show | 6 | HG02080.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+23560A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6086833 | ||||||
chr19:6086994
|
CT | C | 30 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0240others(27): Show | 30 | HG00741.hp2 HG01109.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+23398delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6086994 | ||||||
chr19:6086998
|
T | C | 26 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(23): Show | 26 | HG00140.hp1 HG01069.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.-9+23395A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6086998 | ||||||
chr19:6087125
|
T | C | 18 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(15): Show | 18 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9+23268A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6087125 | ||||||
chr19:6087145
|
A | T | 1 | a0001c0001t0016g0027 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-9+23248T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6087145 | ||||||
chr19:6087151
|
G | A | 30 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0240others(27): Show | 30 | HG00741.hp2 HG01109.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+23242C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6087151 | ||||||
chr19:6087439
|
G | A | 7 | a0001c0001t0002g0011a0001c0001t0005g0302a0001c0001t0005g0303others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+22954C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6087439 | ||||||
chr19:6087617
|
G | A | 9 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(6): Show | 9 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+22776C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6087617 | ||||||
chr19:6087859
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-9+22534C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6087859 | ||||||
chr19:6087994
|
T | G | 27 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(24): Show | 27 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9+22399A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6087994 | ||||||
chr19:6088014
|
G | T | 4 | a0001c0001t0001g0300a0001c0001t0003g0018a0001c0001t0003g0019others(1): Show | 4 | HG02080.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+22379C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6088014 | ||||||
chr19:6088076
|
G | C | 92 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 92 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(89): Show |
intron_variant | MODIFIER | c.-9+22317C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6088076 | ||||||
chr19:6088211
|
C | CT | 44 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0089others(41): Show | 44 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.-9+22181dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6088211 | ||||||
chr19:6088211
|
CT | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0175others(23): Show | 27 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.-9+22181delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6088211 | ||||||
chr19:6088211
|
CTT | C | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(28): Show | 31 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-9+22180_-9+22181d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6088211 | ||||||
chr19:6088441
|
C | T | 6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+21952G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6088441 | ||||||
chr19:6088455
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-9+21938G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6088455 | ||||||
chr19:6088514
|
A | AT | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(60): Show | 63 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.-9+21878dupA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6088514 | ||||||
chr19:6088670
|
T | G | 27 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(24): Show | 27 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9+21723A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6088670 | ||||||
chr19:6088695
|
G | A | 3 | a0001c0004t0001g0292a0001c0004t0001g0293a0001c0004t0001g0294 | 3 | HG01884.hp2 HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-9+21698C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6088695 | ||||||
chr19:6088772
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-9+21621C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6088772 | ||||||
chr19:6088792
|
G | A | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+21601C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6088792 | ||||||
chr19:6088809
|
T | C | 27 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(24): Show | 27 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9+21584A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6088809 | ||||||
chr19:6088817
|
T | C | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(90): Show | 93 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(90): Show |
intron_variant | MODIFIER | c.-9+21576A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6088817 | ||||||
chr19:6088892
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-9+21501G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6088892 | ||||||
chr19:6089041
|
T | C | 10 | a0001c0004t0001g0012a0001c0004t0001g0276a0001c0004t0001g0277others(7): Show | 10 | HG02622.hp2 HG02647.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9+21352A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6089041 | ||||||
chr19:6089061
|
A | G | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+21332T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6089061 | ||||||
chr19:6089454
|
G | A | 2 | a0001c0001t0001g0216a0001c0001t0002g0104 | 2 | HG02738.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-9+20939C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6089454 | ||||||
chr19:6089476
|
T | C | 2 | a0001c0001t0001g0166a0001c0001t0013g0176 | 2 | NA18966.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-9+20917A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6089476 | ||||||
chr19:6089534
|
G | C | 1 | a0001c0001t0009g0291 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-9+20859C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6089534 | ||||||
chr19:6089593
|
G | A | 1 | a0002c0002t0001g0092 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-9+20800C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6089593 | ||||||
chr19:6089604
|
C | A | 1 | a0001c0001t0001g0178 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-9+20789G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6089604 | ||||||
chr19:6089813
|
C | T | 14 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(11): Show | 14 | HG00741.hp2 HG02027.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+20580G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6089813 | ||||||
chr19:6089818
|
T | C | 2 | a0001c0001t0001g0099a0002c0002t0003g0057 | 2 | HG00735.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-9+20575A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6089818 | ||||||
chr19:6089986
|
G | T | 3 | a0002c0002t0001g0079a0002c0002t0001g0297a0002c0002t0001g0298 | 3 | HG03942.hp2 HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-9+20407C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6089986 | ||||||
chr19:6090040
|
C | A | 1 | a0001c0001t0001g0238 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-9+20353G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6090040 | ||||||
chr19:6090090
|
T | A | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9+20303A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6090090 | ||||||
chr19:6090123
|
G | C | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-9+20270C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6090123 | ||||||
chr19:6090240
|
T | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+20153A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6090240 | ||||||
chr19:6090245
|
A | G | 10 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(7): Show | 10 | HG01243.hp2 HG02559.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9+20148T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6090245 | ||||||
chr19:6090328
|
G | A | 1 | a0002c0002t0001g0071 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-9+20065C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6090328 | ||||||
chr19:6090370
|
C | CA | 20 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(17): Show | 20 | HG02145.hp1 HG02615.hp1 HG02647.hp1 others(17): Show |
intron_variant | MODIFIER | c.-9+20022dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6090370 | ||||||
chr19:6090370
|
CA | C | 12 | a0001c0001t0004g0247a0002c0002t0001g0078a0003c0005t0001g0045others(9): Show | 12 | HG00597.hp1 HG02027.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9+20022delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6090370 | ||||||
chr19:6090589
|
C | T | 21 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0240others(18): Show | 21 | HG00741.hp2 HG01109.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+19804G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6090589 | ||||||
chr19:6090598
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-9+19795A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6090598 | ||||||
chr19:6091047
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-9+19346C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6091047 | ||||||
chr19:6091226
|
G | A | 26 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(23): Show | 26 | HG00140.hp1 HG01069.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.-9+19167C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6091226 | ||||||
chr19:6091262
|
C | G | 1 | a0001c0001t0008g0301 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-9+19131G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6091262 | ||||||
chr19:6091391
|
T | C | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+19002A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6091391 | ||||||
chr19:6091408
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-9+18985T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6091408 | ||||||
chr19:6091448
|
C | CA | 8 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0001g0177others(5): Show | 8 | HG00544.hp2 HG00741.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+18944dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6091448 | ||||||
chr19:6091448
|
CA | C | 6 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0003t0001g0255others(3): Show | 6 | HG01109.hp2 HG01515.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+18944delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6091448 | ||||||
chr19:6091564
|
G | A | 1 | a0002c0002t0001g0213 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-9+18829C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6091564 | ||||||
chr19:6091914
|
T | A | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+18479A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6091914 | ||||||
chr19:6092005
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-9+18388G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6092005 | ||||||
chr19:6092147
|
T | G | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-9+18246A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6092147 | ||||||
chr19:6092253
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-9+18140T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6092253 | ||||||
chr19:6092376
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-9+18017C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6092376 | ||||||
chr19:6092767
|
G | A | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-9+17626C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6092767 | ||||||
chr19:6092944
|
C | T | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9+17449G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6092944 | ||||||
chr19:6092953
|
T | TA | 15 | a0001c0001t0001g0010a0001c0001t0001g0178a0001c0004t0001g0012others(12): Show | 15 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9+17439dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6092953 | ||||||
chr19:6093049
|
C | A | 1 | a0001c0001t0001g0168 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-9+17344G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6093049 | ||||||
chr19:6093049
|
C | T | 9 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(6): Show | 9 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+17344G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6093049 | ||||||
chr19:6093385
|
A | T | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(42): Show | 45 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.-9+17008T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6093385 | ||||||
chr19:6093483
|
C | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9+16910G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6093483 | ||||||
chr19:6093827
|
A | G | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+16566T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6093827 | ||||||
chr19:6094024
|
T | A | 1 | a0001c0001t0001g0035 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-9+16369A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6094024 | ||||||
chr19:6094163
|
C | T | 1 | a0002c0002t0001g0063 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-9+16230G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6094163 | ||||||
chr19:6094229
|
CTTTT | C | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+16160_-9+16163d others(6): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6094229 | ||||||
chr19:6094261
|
T | G | 2 | a0002c0002t0001g0192a0002c0002t0001g0193 | 2 | HG02145.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-9+16132A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6094261 | ||||||
chr19:6094359
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-9+16034C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6094359 | ||||||
chr19:6094468
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-9+15925G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6094468 | ||||||
chr19:6094675
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-9+15718C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6094675 | ||||||
chr19:6094791
|
T | A | 5 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(2): Show | 5 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+15602A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6094791 | ||||||
chr19:6094858
|
G | A | 27 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(24): Show | 27 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9+15535C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6094858 | ||||||
chr19:6094899
|
C | G | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0001g0038 | 3 | HG01109.hp2 HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-9+15494G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6094899 | ||||||
chr19:6094904
|
G | A | 1 | a0001c0001t0009g0291 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-9+15489C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6094904 | ||||||
chr19:6094989
|
A | G | 1 | a0001c0001t0002g0188 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-9+15404T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6094989 | ||||||
chr19:6095034
|
C | T | 1 | a0001c0004t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-9+15359G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6095034 | ||||||
chr19:6095045
|
G | C | 2 | a0001c0001t0001g0010a0001c0001t0003g0009 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-9+15348C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6095045 | ||||||
chr19:6095060
|
C | T | 13 | a0001c0004t0001g0012a0001c0004t0001g0276a0001c0004t0001g0277others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9+15333G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6095060 | ||||||
chr19:6095091
|
G | A | 2 | a0002c0002t0003g0075a0002c0002t0003g0076 | 2 | HG00642.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.-9+15302C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6095091 | ||||||
chr19:6095092
|
A | G | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+15301T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6095092 | ||||||
chr19:6095177
|
G | C | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-9+15216C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6095177 | ||||||
chr19:6095199
|
A | G | 27 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(24): Show | 27 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9+15194T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6095199 | ||||||
chr19:6095334
|
T | C | 1 | a0002c0002t0002g0073 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-9+15059A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6095334 | ||||||
chr19:6095348
|
A | G | 32 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(29): Show | 32 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.-9+15045T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6095348 | ||||||
chr19:6095420
|
G | A | 41 | a0001c0001t0001g0064a0002c0002t0001g0058a0002c0002t0001g0059others(38): Show | 41 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.-9+14973C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6095420 | ||||||
chr19:6095463
|
G | A | 72 | a0001c0001t0001g0064a0001c0001t0001g0099a0001c0001t0001g0101others(69): Show | 73 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.-9+14930C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6095463 | ||||||
chr19:6095494
|
T | C | 9 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(6): Show | 9 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+14899A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6095494 | ||||||
chr19:6095557
|
G | A | 1 | a0002c0002t0002g0073 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-9+14836C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6095557 | ||||||
chr19:6095919
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-9+14474G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6095919 | ||||||
chr19:6095949
|
G | T | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 165 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9+14444C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6095949 | ||||||
chr19:6096157
|
T | G | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-9+14236A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096157 | ||||||
chr19:6096389
|
T | C | 75 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0099others(72): Show | 76 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.-9+14004A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096389 | ||||||
chr19:6096406
|
T | C | 23 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0102others(20): Show | 24 | HG00544.hp1 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.-9+13987A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096406 | ||||||
chr19:6096424
|
T | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0036 | 2 | HG02735.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-9+13969A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096424 | ||||||
chr19:6096430
|
TTTTTG | T | 61 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0234others(58): Show | 61 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.-9+13958_-9+13962d others(7): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096430 | ||||||
chr19:6096430
|
TTTTTGTT others(8): Show |
T | 18 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(15): Show | 18 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9+13948_-9+13962d others(17): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096430 | ||||||
chr19:6096430
|
TTTTTGTT others(13): Show |
T | 13 | a0001c0004t0001g0012a0001c0004t0001g0276a0001c0004t0001g0277others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9+13943_-9+13962d others(22): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096430 | ||||||
chr19:6096469
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-9+13924A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096469 | ||||||
chr19:6096507
|
C | T | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+13886G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096507 | ||||||
chr19:6096547
|
T | C | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+13846A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096547 | ||||||
chr19:6096596
|
A | G | 27 | a0001c0001t0001g0005a0001c0001t0001g0234a0001c0001t0001g0236others(24): Show | 27 | HG00140.hp1 HG01069.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.-9+13797T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096596 | ||||||
chr19:6096602
|
A | G | 1 | a0001c0001t0006g0026 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-9+13791T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096602 | ||||||
chr19:6096603
|
T | C | 1 | a0001c0001t0006g0026 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-9+13790A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096603 | ||||||
chr19:6096609
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0006g0026 | 2 | HG00323.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-9+13784T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096609 | ||||||
chr19:6096636
|
C | T | 5 | a0003c0005t0001g0049a0003c0005t0001g0050a0003c0005t0001g0051others(2): Show | 5 | NA18973.hp2 NA18983.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+13757G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096636 | ||||||
chr19:6096648
|
A | G | 303 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(300): Show | 304 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.-9+13745T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096648 | ||||||
chr19:6096651
|
TTAGCCAG others(5): Show |
T | 1 | a0002c0002t0001g0077 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-9+13730_-9+13741d others(14): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096651 | ||||||
chr19:6096668
|
G | A | 1 | a0002c0002t0001g0077 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-9+13725C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096668 | ||||||
chr19:6096725
|
C | T | 2 | a0001c0001t0001g0108a0001c0007t0001g0107 | 2 | NA18944.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-9+13668G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096725 | ||||||
chr19:6096731
|
G | T | 4 | a0001c0001t0001g0300a0001c0001t0003g0018a0001c0001t0003g0019others(1): Show | 4 | HG02080.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+13662C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096731 | ||||||
chr19:6096971
|
C | T | 11 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(8): Show | 11 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9+13422G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6096971 | ||||||
chr19:6097140
|
G | A | 92 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 92 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(89): Show |
intron_variant | MODIFIER | c.-9+13253C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6097140 | ||||||
chr19:6097453
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0168 | 2 | HG02004.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-9+12940T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6097453 | ||||||
chr19:6097475
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-9+12918C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6097475 | ||||||
chr19:6097497
|
C | T | 1 | a0002c0002t0008g0062 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-9+12896G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6097497 | ||||||
chr19:6097498
|
G | A | 26 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(23): Show | 26 | HG00140.hp1 HG01069.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.-9+12895C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6097498 | ||||||
chr19:6097511
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-9+12882C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6097511 | ||||||
chr19:6097519
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-9+12874C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6097519 | ||||||
chr19:6097561
|
G | A | 26 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0001g0012others(23): Show | 26 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-9+12832C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6097561 | ||||||
chr19:6097591
|
AATT | A | 26 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0001g0012others(23): Show | 26 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-9+12799_-9+12801d others(5): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6097591 | ||||||
chr19:6097659
|
C | T | 1 | a0001c0004t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-9+12734G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6097659 | ||||||
chr19:6097950
|
A | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+12443T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6097950 | ||||||
chr19:6097970
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-9+12423G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6097970 | ||||||
chr19:6098222
|
C | A | 48 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0240others(45): Show | 48 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.-9+12171G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098222 | ||||||
chr19:6098366
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-9+12027T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098366 | ||||||
chr19:6098372
|
C | T | 1 | a0001c0001t0002g0188 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-9+12021G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098372 | ||||||
chr19:6098629
|
T | C | 44 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0242others(41): Show | 44 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.-9+11764A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098629 | ||||||
chr19:6098644
|
G | A | 1 | a0001c0004t0001g0283 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-9+11749C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098644 | ||||||
chr19:6098660
|
A | T | 18 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(15): Show | 18 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9+11733T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098660 | ||||||
chr19:6098722
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+11671G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098722 | ||||||
chr19:6098727
|
G | C | 9 | a0001c0004t0001g0276a0001c0004t0001g0277a0001c0004t0001g0278others(6): Show | 9 | HG02647.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+11666C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098727 | ||||||
chr19:6098789
|
C | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-9+11604G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098789 | ||||||
chr19:6098839
|
A | G | 4 | a0001c0001t0001g0103a0001c0001t0001g0216a0001c0001t0002g0104others(1): Show | 4 | HG00323.hp2 HG01192.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+11554T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098839 | ||||||
chr19:6098856
|
T | C | 7 | a0001c0001t0002g0011a0001c0001t0005g0302a0001c0001t0005g0303others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+11537A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098856 | ||||||
chr19:6098965
|
C | CA | 83 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0055others(80): Show | 84 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-9+11427dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098965 | ||||||
chr19:6098965
|
C | CAA | 29 | a0001c0001t0001g0037a0001c0001t0001g0179a0001c0001t0001g0243others(26): Show | 29 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.-9+11426_-9+11427d others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098965 | ||||||
chr19:6098965
|
C | CAAA | 9 | a0001c0001t0001g0252a0001c0004t0001g0276a0001c0004t0001g0278others(6): Show | 9 | HG00741.hp2 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+11425_-9+11427d others(5): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098965 | ||||||
chr19:6098965
|
C | CAAAA | 6 | a0001c0001t0001g0240a0001c0001t0001g0253a0001c0001t0001g0254others(3): Show | 6 | HG01891.hp1 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+11424_-9+11427d others(6): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098965 | ||||||
chr19:6098965
|
CAAAA | C | 24 | a0001c0001t0001g0234a0001c0001t0001g0237a0001c0001t0001g0238others(21): Show | 24 | HG00140.hp1 HG01934.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-9+11424_-9+11427d others(6): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098965 | ||||||
chr19:6098965
|
CAAAAAA | C | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+11422_-9+11427d others(8): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098965 | ||||||
chr19:6098965
|
CAAAAAAA others(7): Show |
C | 14 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0001g0038others(11): Show | 14 | HG01109.hp2 HG02027.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+11414_-9+11427d others(16): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098965 | ||||||
chr19:6098965
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+11413_-9+11427d others(17): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098965 | ||||||
chr19:6098965
|
CAAAAAAA others(9): Show |
C | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(14): Show | 17 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-9+11412_-9+11427d others(18): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6098965 | ||||||
chr19:6099016
|
G | T | 1 | a0001c0001t0001g0187 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-9+11377C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6099016 | ||||||
chr19:6099515
|
AT | A | 11 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(8): Show | 11 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9+10877delA | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6099515 | ||||||
chr19:6100196
|
G | T | 1 | a0001c0001t0001g0274 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-9+10197C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6100196 | ||||||
chr19:6100216
|
T | A | 1 | a0001c0001t0001g0237 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-9+10177A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6100216 | ||||||
chr19:6100223
|
G | C | 7 | a0001c0001t0002g0011a0001c0001t0005g0302a0001c0001t0005g0303others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+10170C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6100223 | ||||||
chr19:6100285
|
AGGGGAG | A | 27 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(24): Show | 27 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9+10102_-9+10107d others(8): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6100285 | ||||||
chr19:6100326
|
A | G | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+10067T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6100326 | ||||||
chr19:6100422
|
A | G | 167 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(164): Show | 168 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.-9+9971T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6100422 | ||||||
chr19:6100462
|
C | T | 23 | a0001c0001t0001g0024a0001c0001t0001g0105a0001c0001t0001g0106others(20): Show | 23 | HG00597.hp2 HG00735.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.-9+9931G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6100462 | ||||||
chr19:6100464
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | NA18982.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-9+9929C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6100464 | ||||||
chr19:6100697
|
C | T | 26 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0001g0012others(23): Show | 26 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-9+9696G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6100697 | ||||||
chr19:6100812
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-9+9581T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6100812 | ||||||
chr19:6100835
|
A | AT | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+9557_-9+9558ins others(1): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6100835 | ||||||
chr19:6100839
|
GAATT | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0300a0001c0001t0003g0009others(3): Show | 6 | HG02080.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+9550_-9+9553del others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6100839 | ||||||
chr19:6100843
|
TAATTAAT others(34): Show |
T | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-9+9509_-9+9549del others(41): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6100843 | ||||||
chr19:6100884
|
G | GAATT | 79 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(76): Show | 79 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.-9+9505_-9+9508dup others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6100884 | ||||||
chr19:6100884
|
G | GAATTATA others(24): Show |
13 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0001g0038others(10): Show | 13 | HG01109.hp2 HG02027.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+9508_-9+9509ins others(31): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6100884 | ||||||
chr19:6101018
|
C | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0216a0001c0001t0002g0104 | 3 | HG01192.hp1 HG02738.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-9+9375G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6101018 | ||||||
chr19:6101212
|
T | C | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(90): Show | 93 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(90): Show |
intron_variant | MODIFIER | c.-9+9181A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6101212 | ||||||
chr19:6101305
|
A | G | 2 | a0001c0004t0001g0279a0001c0004t0001g0280 | 2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-9+9088T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6101305 | ||||||
chr19:6101431
|
G | A | 14 | a0001c0001t0001g0285a0001c0004t0001g0012a0001c0004t0001g0276others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9+8962C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6101431 | ||||||
chr19:6101502
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-9+8891C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6101502 | ||||||
chr19:6102072
|
T | G | 64 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(61): Show | 64 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.-9+8321A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6102072 | ||||||
chr19:6102115
|
C | T | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+8278G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6102115 | ||||||
chr19:6102170
|
T | C | 91 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(88): Show | 91 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.-9+8223A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6102170 | ||||||
chr19:6102504
|
C | G | 2 | a0001c0001t0001g0300a0001c0001t0008g0301 | 2 | HG02080.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-9+7889G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6102504 | ||||||
chr19:6102593
|
T | C | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9+7800A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6102593 | ||||||
chr19:6102670
|
C | T | 1 | a0001c0004t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-9+7723G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6102670 | ||||||
chr19:6102696
|
T | C | 2 | a0001c0004t0001g0293a0001c0004t0001g0294 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-9+7697A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6102696 | ||||||
chr19:6102752
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+7641G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6102752 | ||||||
chr19:6102769
|
G | T | 27 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(24): Show | 27 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9+7624C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6102769 | ||||||
chr19:6102953
|
G | A | 1 | a0002c0002t0001g0210 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-9+7440C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6102953 | ||||||
chr19:6103088
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-9+7305G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6103088 | ||||||
chr19:6103206
|
T | C | 13 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0001g0038others(10): Show | 13 | HG01109.hp2 HG02027.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+7187A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6103206 | ||||||
chr19:6103273
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-9+7120A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6103273 | ||||||
chr19:6103358
|
T | C | 48 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0240others(45): Show | 48 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.-9+7035A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6103358 | ||||||
chr19:6103365
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-9+7028G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6103365 | ||||||
chr19:6103430
|
C | T | 13 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0001g0038others(10): Show | 13 | HG01109.hp2 HG02027.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+6963G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6103430 | ||||||
chr19:6103685
|
T | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0186 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-9+6708A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6103685 | ||||||
chr19:6103745
|
T | G | 14 | a0001c0001t0001g0285a0001c0004t0001g0012a0001c0004t0001g0276others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9+6648A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6103745 | ||||||
chr19:6103914
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9+6479G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6103914 | ||||||
chr19:6104046
|
A | C | 35 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(32): Show | 35 | HG00741.hp2 HG01243.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.-9+6347T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104046 | ||||||
chr19:6104090
|
A | G | 163 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(160): Show | 164 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.-9+6303T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104090 | ||||||
chr19:6104167
|
C | G | 1 | a0001c0001t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+6226G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104167 | ||||||
chr19:6104280
|
A | T | 13 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0001g0038others(10): Show | 13 | HG01109.hp2 HG02027.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+6113T>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104280 | ||||||
chr19:6104383
|
C | A | 13 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0001g0038others(10): Show | 13 | HG01109.hp2 HG02027.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+6010G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104383 | ||||||
chr19:6104413
|
C | CAAAAAAT others(169): Show |
1 | a0001c0004t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-9+5979_-9+5980ins others(176): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104413 | ||||||
chr19:6104413
|
C | CAAAAAAT others(168): Show |
7 | a0003c0005t0001g0046a0003c0005t0001g0049a0003c0005t0001g0051others(4): Show | 7 | HG02155.hp1 NA18612.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+5979_-9+5980ins others(175): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104413 | ||||||
chr19:6104413
|
C | CAAAAAAT others(169): Show |
3 | a0003c0005t0001g0045a0003c0005t0001g0048a0003c0005t0001g0050 | 3 | HG02027.hp1 NA19000.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-9+5979_-9+5980ins others(176): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104413 | ||||||
chr19:6104413
|
C | CAAAAAAT others(170): Show |
2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-9+5979_-9+5980ins others(177): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104413 | ||||||
chr19:6104430
|
G | A | 13 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0001g0038others(10): Show | 13 | HG01109.hp2 HG02027.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+5963C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104430 | ||||||
chr19:6104568
|
C | CA | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 85 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-9+5824dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104568 | ||||||
chr19:6104568
|
C | CAAAA | 11 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0001g0038others(8): Show | 11 | HG01109.hp2 HG02027.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9+5821_-9+5824dup others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104568 | ||||||
chr19:6104634
|
T | C | 27 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(24): Show | 27 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9+5759A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104634 | ||||||
chr19:6104680
|
T | C | 35 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(32): Show | 35 | HG00741.hp2 HG01243.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.-9+5713A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104680 | ||||||
chr19:6104694
|
A | C | 1 | a0001c0001t0001g0044 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-9+5699T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104694 | ||||||
chr19:6104699
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0252 | 2 | HG00741.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-9+5694T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104699 | ||||||
chr19:6104715
|
A | G | 27 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(24): Show | 27 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9+5678T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104715 | ||||||
chr19:6104842
|
T | C | 1 | a0001c0004t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-9+5551A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104842 | ||||||
chr19:6104975
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0300a0001c0001t0003g0009others(1): Show | 4 | HG02080.hp1 HG02451.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+5418C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104975 | ||||||
chr19:6104979
|
G | T | 2 | a0001c0001t0001g0010a0001c0001t0003g0009 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-9+5414C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6104979 | ||||||
chr19:6105115
|
TCA | T | 13 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0001g0038others(10): Show | 13 | HG01109.hp2 HG02027.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+5276_-9+5277del others(2): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6105115 | ||||||
chr19:6105118
|
CA | C | 22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(19): Show | 22 | HG01884.hp2 HG01891.hp2 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.-9+5274delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6105118 | ||||||
chr19:6105163
|
T | C | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-9+5230A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6105163 | ||||||
chr19:6105198
|
A | G | 27 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(24): Show | 27 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9+5195T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6105198 | ||||||
chr19:6105234
|
T | G | 10 | a0003c0005t0001g0045a0003c0005t0001g0046a0003c0005t0001g0048others(7): Show | 10 | HG02027.hp1 HG02155.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9+5159A>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6105234 | ||||||
chr19:6105289
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-9+5104A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6105289 | ||||||
chr19:6105351
|
C | G | 48 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0240others(45): Show | 48 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.-9+5042G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6105351 | ||||||
chr19:6105579
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0001g0038 | 3 | HG01109.hp2 HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-9+4814C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6105579 | ||||||
chr19:6105582
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-9+4811C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6105582 | ||||||
chr19:6105602
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-9+4791C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6105602 | ||||||
chr19:6105722
|
C | G | 1 | a0001c0001t0001g0090 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-9+4671G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6105722 | ||||||
chr19:6105796
|
G | C | 64 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(61): Show | 64 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.-9+4597C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6105796 | ||||||
chr19:6105833
|
G | T | 13 | a0001c0004t0001g0012a0001c0004t0001g0276a0001c0004t0001g0277others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9+4560C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6105833 | ||||||
chr19:6106044
|
G | A | 1 | a0002c0002t0001g0213 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-9+4349C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6106044 | ||||||
chr19:6106067
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-9+4326G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6106067 | ||||||
chr19:6106230
|
C | CCCAT | 104 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(101): Show | 105 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.-9+4159_-9+4162dup others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6106230 | ||||||
chr19:6106230
|
C | CCCATCCA others(1): Show |
31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(28): Show | 31 | HG01192.hp2 HG01255.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.-9+4155_-9+4162dup others(8): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6106230 | ||||||
chr19:6106230
|
C | CCCATCCA others(5): Show |
1 | a0003c0005t0001g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-9+4151_-9+4162dup others(12): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6106230 | ||||||
chr19:6106230
|
CCCAT | C | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0189others(1): Show | 4 | HG00140.hp2 HG01123.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+4159_-9+4162del others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6106230 | ||||||
chr19:6106230
|
CCCATCCA others(13): Show |
C | 6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+4143_-9+4162del others(20): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6106230 | ||||||
chr19:6106452
|
C | A | 91 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(88): Show | 91 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.-9+3941G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6106452 | ||||||
chr19:6106483
|
T | A | 8 | a0002c0002t0001g0190a0002c0002t0001g0191a0002c0002t0001g0192others(5): Show | 8 | HG02145.hp1 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+3910A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6106483 | ||||||
chr19:6106609
|
C | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(13): Show | 16 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-9+3784G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6106609 | ||||||
chr19:6106631
|
C | T | 13 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0001g0038others(10): Show | 13 | HG01109.hp2 HG02027.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+3762G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6106631 | ||||||
chr19:6106638
|
G | A | 1 | a0001c0004t0001g0038 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-9+3755C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6106638 | ||||||
chr19:6106667
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0300a0001c0001t0003g0009others(1): Show | 4 | HG02080.hp1 HG02451.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+3726C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6106667 | ||||||
chr19:6106762
|
T | C | 5 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(2): Show | 5 | HG02165.hp2 NA18955.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+3631A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6106762 | ||||||
chr19:6106850
|
T | C | 78 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(75): Show | 78 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(75): Show |
intron_variant | MODIFIER | c.-9+3543A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6106850 | ||||||
chr19:6107017
|
C | A | 78 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(75): Show | 78 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(75): Show |
intron_variant | MODIFIER | c.-9+3376G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107017 | ||||||
chr19:6107070
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0002g0196 | 2 | NA18953.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-9+3323G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107070 | ||||||
chr19:6107076
|
A | C | 4 | a0001c0001t0001g0240a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+3317T>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107076 | ||||||
chr19:6107157
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+3236C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107157 | ||||||
chr19:6107222
|
G | A | 78 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(75): Show | 78 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(75): Show |
intron_variant | MODIFIER | c.-9+3171C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107222 | ||||||
chr19:6107339
|
G | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(13): Show | 16 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-9+3054C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107339 | ||||||
chr19:6107355
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-9+3038C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107355 | ||||||
chr19:6107420
|
T | C | 7 | a0001c0001t0002g0011a0001c0001t0005g0302a0001c0001t0005g0303others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+2973A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107420 | ||||||
chr19:6107480
|
G | A | 10 | a0001c0001t0001g0285a0001c0004t0001g0276a0001c0004t0001g0277others(7): Show | 10 | HG02647.hp1 HG02723.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9+2913C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107480 | ||||||
chr19:6107550
|
C | G | 78 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(75): Show | 78 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(75): Show |
intron_variant | MODIFIER | c.-9+2843G>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107550 | ||||||
chr19:6107616
|
C | CA | 47 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0016others(44): Show | 47 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.-9+2776dupT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107616 | ||||||
chr19:6107616
|
C | CAA | 6 | a0001c0001t0001g0232a0001c0001t0001g0248a0001c0001t0001g0249others(3): Show | 6 | HG01243.hp2 HG02071.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+2775_-9+2776dup others(2): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107616 | ||||||
chr19:6107616
|
C | CAAA | 7 | a0001c0001t0001g0005a0001c0001t0001g0252a0001c0001t0001g0253others(4): Show | 7 | HG00741.hp2 HG01891.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+2774_-9+2776dup others(3): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107616 | ||||||
chr19:6107616
|
C | CAAAA | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(4): Show | 7 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+2773_-9+2776dup others(4): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107616 | ||||||
chr19:6107616
|
C | CAAAAAA | 6 | a0001c0004t0001g0278a0001c0004t0001g0279a0001c0004t0001g0280others(3): Show | 6 | HG02922.hp2 HG02976.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+2771_-9+2776dup others(6): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107616 | ||||||
chr19:6107616
|
C | CAAAAAAA others(1): Show |
9 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0015g0287others(6): Show | 9 | HG02280.hp1 HG02615.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+2769_-9+2776dup others(8): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107616 | ||||||
chr19:6107616
|
C | CAAAAAAA others(2): Show |
8 | a0001c0001t0001g0290a0001c0001t0009g0291a0001c0003t0001g0259others(5): Show | 8 | HG01891.hp2 HG01934.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+2768_-9+2776dup others(9): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107616 | ||||||
chr19:6107616
|
C | CAAAAAAA others(3): Show |
12 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0237others(9): Show | 12 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9+2767_-9+2776dup others(10): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107616 | ||||||
chr19:6107616
|
C | CAAAAAAA others(4): Show |
8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0274others(5): Show | 8 | HG02080.hp1 HG02572.hp1 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+2766_-9+2776dup others(11): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107616 | ||||||
chr19:6107616
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0008g0301 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-9+2765_-9+2776dup others(12): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107616 | ||||||
chr19:6107616
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-9+2754_-9+2776dup others(23): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107616 | ||||||
chr19:6107616
|
C | CAAAAAAA others(19): Show |
1 | a0001c0001t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+2751_-9+2776dup others(26): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107616 | ||||||
chr19:6107616
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-9+2776_-9+2777ins others(32): Show |
RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107616 | ||||||
chr19:6107616
|
CA | C | 25 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(22): Show | 25 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.-9+2776delT | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107616 | ||||||
chr19:6107880
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(1): Show | 4 | NA18747.hp2 NA18994.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+2513G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6107880 | ||||||
chr19:6108355
|
C | T | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-9+2038G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6108355 | ||||||
chr19:6108477
|
T | A | 14 | a0001c0001t0001g0285a0001c0004t0001g0012a0001c0004t0001g0276others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9+1916A>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6108477 | ||||||
chr19:6108707
|
G | C | 1 | a0001c0001t0001g0235 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-9+1686C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6108707 | ||||||
chr19:6108836
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+1557G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6108836 | ||||||
chr19:6108909
|
G | A | 6 | a0001c0001t0001g0286a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 6 | HG02615.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+1484C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6108909 | ||||||
chr19:6108967
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+1426G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6108967 | ||||||
chr19:6108973
|
G | C | 2 | a0001c0001t0005g0306a0001c0001t0005g0307 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-9+1420C>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6108973 | ||||||
chr19:6109024
|
G | T | 1 | a0001c0001t0001g0017 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-9+1369C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6109024 | ||||||
chr19:6109052
|
G | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-9+1341C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6109052 | ||||||
chr19:6109336
|
G | T | 6 | a0001c0001t0005g0302a0001c0001t0005g0303a0001c0001t0005g0304others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+1057C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6109336 | ||||||
chr19:6109424
|
G | T | 2 | a0001c0001t0001g0014a0001c0001t0007g0013 | 2 | HG00741.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-9+969C>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6109424 | ||||||
chr19:6109566
|
G | A | 77 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 77 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(74): Show |
intron_variant | MODIFIER | c.-9+827C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6109566 | ||||||
chr19:6109664
|
T | C | 3 | a0001c0004t0001g0292a0001c0004t0001g0293a0001c0004t0001g0294 | 3 | HG01884.hp2 HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-9+729A>G | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6109664 | ||||||
chr19:6109821
|
C | A | 1 | a0002c0002t0001g0295 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-9+572G>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6109821 | ||||||
chr19:6109888
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-9+505C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6109888 | ||||||
chr19:6109994
|
G | A | 2 | a0002c0002t0001g0297a0002c0002t0001g0298 | 2 | HG03942.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-9+399C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6109994 | ||||||
chr19:6110185
|
A | G | 1 | a0001c0004t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-9+208T>C | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6110185 | ||||||
chr19:6110213
|
C | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(13): Show | 16 | HG02055.hp2 HG02080.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-9+180G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6110213 | ||||||
chr19:6110236
|
C | CG | 306 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(303): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-9+156dupC | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6110236 | ||||||
chr19:6110288
|
G | A | 1 | a0001c0001t0002g0299 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-9+105C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6110288 | ||||||
chr19:6110299
|
G | A | 2 | a0001c0001t0001g0300a0001c0001t0008g0301 | 2 | HG02080.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-9+94C>T | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6110299 | ||||||
chr19:6110320
|
G | GC | 306 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(303): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-9+72dupG | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6110320 | ||||||
chr19:6110344
|
C | T | 1 | a0001c0001t0001g0002 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-9+49G>A | RFX2 | ENSG00000087903.13 | transcript | ENST00000303657.10 | protein_coding | 1/17 | chr19 | 6110344 |