geneid | 27291 |
---|---|
ensemblid | ENSG00000166024.14 |
hgncid | 23512 |
symbol | R3HCC1L |
name | R3H domain and coiled-coil containing 1 like |
refseq_nuc | NM_001351015.2 |
refseq_prot | NP_001337944.2 |
ensembl_nuc | ENST00000298999.8 |
ensembl_prot | ENSP00000298999.3 |
mane_status | MANE Select |
chr | chr10 |
start | 98134657 |
end | 98244897 |
strand | + |
ver | v1.2 |
region | chr10:98134657-98244897 |
region5000 | chr10:98129657-98249897 |
regionname0 | R3HCC1L_chr10_98134657_98244897 |
regionname5000 | R3HCC1L_chr10_98129657_98249897 |
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 | 0/1 | 778 | 210 | 49 | 27 | 107 | 6 | 20 | 85 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0002 | 0/0 | 778 | 98 | 8 | 20 | 51 | 4 | 15 | 38 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0003 | 0/0 | 778 | 42 | 13 | 10 | 7 | 7 | 5 | 6 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0004 | 0/0 | 778 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0005 | 0/0 | 778 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0006 | 1/0 | 778 | 3 | 2 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0007 | 0/0 | 778 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0008 | 0/0 | 778 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0009 | 0/0 | 778 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0010 | 0/0 | 778 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0011 | 0/0 | 778 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0012 | 0/0 | 778 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0013 | 0/0 | 778 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0014 | 0/0 | 778 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0015 | 0/0 | 778 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0016 | 0/0 | 778 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0017 | 0/0 | 778 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0018 | 0/0 | 778 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0019 | 0/0 | 778 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0020 | 0/0 | 778 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0021 | 0/0 | 778 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0022 | 0/0 | 778 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0023 | 0/0 | 778 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0024 | 0/0 | 778 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
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 | 0/1 | 2337 | 207 | 46 | 27 | 107 | 6 | 20 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0002 | 0/0 | 2337 | 98 | 8 | 20 | 51 | 4 | 15 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0003 | 0/0 | 2337 | 40 | 11 | 10 | 7 | 7 | 5 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0004 | 0/0 | 2337 | 7 | 7 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0005 | 1/0 | 2337 | 3 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0006 | 0/0 | 2337 | 3 | 0 | 0 | 3 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0007 | 0/0 | 2337 | 3 | 2 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0008 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0009 | 0/0 | 2337 | 2 | 0 | 1 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0010 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0011 | 0/0 | 2337 | 2 | 0 | 2 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0012 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0013 | 0/0 | 2337 | 2 | 1 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0014 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0015 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0016 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0017 | 0/0 | 2337 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0018 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0019 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0020 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0021 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0022 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0023 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0024 | 0/0 | 2337 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0025 | 0/0 | 2337 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0026 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
c0027 | 0/0 | 2337 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1057 | 167 | 23 | 28 | 86 | 6 | 24 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
t0002 | 1/1 | 1057 | 137 | 25 | 23 | 70 | 5 | 12 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
t0003 | 0/0 | 1057 | 40 | 9 | 12 | 7 | 7 | 5 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
t0004 | 0/0 | 1057 | 20 | 20 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
t0005 | 0/0 | 1057 | 7 | 7 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
t0006 | 0/0 | 1056 | 5 | 5 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
t0007 | 0/0 | 1057 | 3 | 3 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
t0008 | 0/0 | 1057 | 2 | 0 | 0 | 2 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
t0009 | 0/0 | 1057 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
t0010 | 0/0 | 1057 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
t0011 | 0/0 | 1057 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
t0012 | 0/0 | 1057 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
t0013 | 0/0 | 1057 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
t0014 | 0/0 | 1057 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
t0015 | 0/0 | 1057 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 11 | 0 | 3 | 7 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0002 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0008 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0250 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0255 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
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 | 0/1 | 2337 | 207 | 46 | 27 | 107 | 6 | 20 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0001c0010 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0001c0020 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0002c0002 | 0/0 | 2337 | 98 | 8 | 20 | 51 | 4 | 15 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0003c0003 | 0/0 | 2337 | 40 | 11 | 10 | 7 | 7 | 5 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0003c0012 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0004c0004 | 0/0 | 2337 | 7 | 7 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0005c0007 | 0/0 | 2337 | 3 | 2 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0006c0005 | 1/0 | 2337 | 3 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0007c0006 | 0/0 | 2337 | 3 | 0 | 0 | 3 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0008c0014 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0009c0009 | 0/0 | 2337 | 2 | 0 | 1 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0010c0011 | 0/0 | 2337 | 2 | 0 | 2 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0011c0008 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0012c0013 | 0/0 | 2337 | 2 | 1 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0013c0015 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0014c0016 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0015c0025 | 0/0 | 2337 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0016c0023 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0017c0019 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0018c0021 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0019c0022 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0020c0024 | 0/0 | 2337 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0021c0018 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0022c0017 | 0/0 | 2337 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0023c0026 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0024c0027 | 0/0 | 2337 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3393 | 55 | 7 | 7 | 33 | 1 | 7 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0001c0001t0002 | 0/1 | 3393 | 129 | 22 | 19 | 70 | 5 | 12 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0001c0001t0004 | 0/0 | 3393 | 9 | 9 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0001c0001t0006 | 0/0 | 3392 | 5 | 5 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0001c0001t0007 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0001c0001t0008 | 0/0 | 3393 | 2 | 0 | 0 | 2 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0001c0001t0010 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0001c0001t0011 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0001c0001t0012 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0001c0001t0013 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0001c0001t0014 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0001c0001t0015 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0001c0010t0007 | 0/0 | 3393 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0001c0020t0004 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0002c0002t0001 | 0/0 | 3393 | 97 | 8 | 20 | 50 | 4 | 15 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0002c0002t0009 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0003c0003t0003 | 0/0 | 3393 | 33 | 4 | 10 | 7 | 7 | 5 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0003c0003t0005 | 0/0 | 3393 | 7 | 7 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0003c0012t0003 | 0/0 | 3393 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0004c0004t0004 | 0/0 | 3393 | 7 | 7 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0005c0007t0003 | 0/0 | 3393 | 3 | 2 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0006c0005t0002 | 1/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0006c0005t0004 | 0/0 | 3393 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0007c0006t0001 | 0/0 | 3393 | 3 | 0 | 0 | 3 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0008c0014t0001 | 0/0 | 3393 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0009c0009t0001 | 0/0 | 3393 | 2 | 0 | 1 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0010c0011t0002 | 0/0 | 3393 | 2 | 0 | 2 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0011c0008t0001 | 0/0 | 3393 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0012c0013t0002 | 0/0 | 3393 | 2 | 1 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0013c0015t0001 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0014c0016t0001 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0015c0025t0001 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0016c0023t0002 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0017c0019t0003 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0018c0021t0002 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0019c0022t0001 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0020c0024t0003 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0021c0018t0001 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0022c0017t0002 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0023c0026t0004 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
a0024c0027t0001 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | copy fasta | chr10 | 98129657 | 98249897 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0255 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0004g0002 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0008g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0010g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0011g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0012g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0013g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0014g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0001t0015g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0010t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0010t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0001c0020t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0001 | 0/0 | 9 | 0 | 3 | 5 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0002c0002t0009g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0003t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0012t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0003c0012t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0004c0004t0004g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0004c0004t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0004c0004t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0004c0004t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0004c0004t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0004c0004t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0005c0007t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0005c0007t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0005c0007t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0006c0005t0002g0250 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0006c0005t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0006c0005t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0007c0006t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0007c0006t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0008c0014t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0008c0014t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0009c0009t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0009c0009t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0010c0011t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0010c0011t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0011c0008t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0012c0013t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0012c0013t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0013c0015t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0014c0016t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0015c0025t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0016c0023t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0017c0019t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0018c0021t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0019c0022t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0020c0024t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0021c0018t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0022c0017t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0023c0026t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
a0024c0027t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0235 | EUR | GBR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00099 | hp2 | a0003 | c0003 | t0003 | g0157 | EUR | GBR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00140 | hp1 | a0003 | c0003 | t0003 | g0017 | EUR | GBR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0042 | EUR | GBR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0052 | EUR | FIN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00280 | hp2 | a0003 | c0003 | t0003 | g0161 | EUR | FIN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00323 | hp1 | a0003 | c0003 | t0003 | g0190 | EUR | FIN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0063 | EUR | FIN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | CHS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | CHS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | CHS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | CHS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | CHS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | CHS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0337 | EAS | CHS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | CHS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00639 | hp1 | a0003 | c0003 | t0003 | g0175 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0142 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0345 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00733 | hp1 | a0003 | c0003 | t0003 | g0183 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00733 | hp2 | a0010 | c0011 | t0002 | g0291 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01069 | hp1 | a0003 | c0003 | t0003 | g0177 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0104 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0099 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0068 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01099 | hp1 | a0020 | c0024 | t0003 | g0179 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01099 | hp2 | a0010 | c0011 | t0002 | g0334 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01109 | hp2 | a0009 | c0009 | t0001 | g0090 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01168 | hp1 | a0001 | c0001 | t0012 | g0292 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01175 | hp2 | a0003 | c0003 | t0003 | g0181 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01255 | hp1 | a0005 | c0007 | t0003 | g0232 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0071 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0107 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01256 | hp2 | a0003 | c0003 | t0003 | g0180 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0102 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0288 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01258 | hp1 | a0003 | c0003 | t0003 | g0168 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01346 | hp1 | a0022 | c0017 | t0002 | g0335 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0077 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01358 | hp1 | a0003 | c0003 | t0003 | g0170 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0055 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01496 | hp1 | a0012 | c0013 | t0002 | g0206 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01496 | hp2 | a0003 | c0003 | t0003 | g0162 | AMR | CLM | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01515 | hp2 | a0003 | c0003 | t0003 | g0186 | EUR | IBS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01516 | hp1 | a0003 | c0003 | t0003 | g0185 | EUR | IBS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0141 | EUR | IBS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01517 | hp1 | a0003 | c0003 | t0003 | g0187 | EUR | IBS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0301 | EUR | IBS | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01891 | hp1 | a0013 | c0015 | t0001 | g0137 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01891 | hp2 | a0003 | c0003 | t0005 | g0227 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0045 | AMR | PEL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | PEL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0075 | AMR | PEL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | PEL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0051 | AMR | PEL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PEL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG01981 | hp2 | a0003 | c0003 | t0003 | g0017 | AMR | PEL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02055 | hp1 | a0003 | c0003 | t0003 | g0184 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02055 | hp2 | a0004 | c0004 | t0004 | g0148 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02056 | hp2 | a0003 | c0003 | t0003 | g0166 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0041 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02148 | hp1 | a0003 | c0003 | t0003 | g0174 | AMR | PEL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | PEL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | CDX | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | CDX | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CDX | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | CDX | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02257 | hp1 | a0004 | c0004 | t0004 | g0016 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0049 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PEL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | PEL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02451 | hp1 | a0003 | c0012 | t0003 | g0159 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02451 | hp2 | a0004 | c0004 | t0004 | g0016 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | KHV | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02615 | hp2 | a0003 | c0003 | t0005 | g0224 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02630 | hp1 | a0003 | c0003 | t0005 | g0225 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02647 | hp2 | a0012 | c0013 | t0002 | g0207 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02683 | hp2 | a0015 | c0025 | t0001 | g0210 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0043 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0073 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02717 | hp2 | a0004 | c0004 | t0004 | g0145 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02735 | hp1 | a0001 | c0001 | t0014 | g0266 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0095 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0044 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02738 | hp2 | a0003 | c0003 | t0003 | g0163 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0244 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02818 | hp1 | a0003 | c0012 | t0003 | g0158 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02818 | hp2 | a0001 | c0010 | t0007 | g0028 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02895 | hp2 | a0003 | c0003 | t0003 | g0169 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0120 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02922 | hp1 | a0017 | c0019 | t0003 | g0027 | AFR | ESN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02922 | hp2 | a0001 | c0010 | t0007 | g0029 | AFR | ESN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02970 | hp1 | a0004 | c0004 | t0004 | g0146 | AFR | ESN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0088 | AFR | ESN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02976 | hp1 | a0004 | c0004 | t0004 | g0152 | AFR | ESN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0247 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03041 | hp2 | a0003 | c0003 | t0005 | g0228 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0023 | AFR | MSL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | MSL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03139 | hp1 | a0006 | c0005 | t0004 | g0149 | AFR | ESN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03139 | hp2 | a0001 | c0001 | t0010 | g0205 | AFR | ESN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03195 | hp2 | a0003 | c0003 | t0005 | g0226 | AFR | ESN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | MSL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03225 | hp2 | a0021 | c0018 | t0001 | g0191 | AFR | MSL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0268 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0082 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03453 | hp1 | a0014 | c0016 | t0001 | g0112 | AFR | MSL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | MSL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03486 | hp1 | a0005 | c0007 | t0003 | g0233 | AFR | MSL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | MSL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03490 | hp1 | a0003 | c0003 | t0003 | g0171 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0069 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03492 | hp2 | a0003 | c0003 | t0003 | g0173 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03516 | hp1 | a0005 | c0007 | t0003 | g0231 | AFR | ESN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | ESN | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03540 | hp1 | a0003 | c0003 | t0005 | g0229 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03540 | hp2 | a0006 | c0005 | t0004 | g0150 | AFR | GWD | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0208 | AFR | MSL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | MSL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | STU | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | STU | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0054 | SAS | PJL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0140 | SAS | BEB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0274 | SAS | BEB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0304 | SAS | BEB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0047 | SAS | BEB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0046 | SAS | BEB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03942 | hp2 | a0003 | c0003 | t0003 | g0176 | SAS | BEB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | STU | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0300 | SAS | BEB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | BEB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | STU | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0305 | SAS | STU | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG04204 | hp1 | a0003 | c0003 | t0003 | g0172 | SAS | STU | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG04228 | hp1 | a0024 | c0027 | t0001 | g0076 | SAS | STU | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18522 | hp1 | a0016 | c0023 | t0002 | g0223 | AFR | YRI | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18522 | hp2 | a0008 | c0014 | t0001 | g0103 | AFR | YRI | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18747 | hp1 | a0001 | c0001 | t0015 | g0022 | EAS | CHB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18747 | hp2 | a0002 | c0002 | t0009 | g0093 | EAS | CHB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18906 | hp1 | a0001 | c0020 | t0004 | g0151 | AFR | YRI | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18906 | hp2 | a0023 | c0026 | t0004 | g0144 | AFR | YRI | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18953 | hp2 | a0003 | c0003 | t0003 | g0165 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18956 | hp1 | a0001 | c0001 | t0008 | g0119 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18963 | hp1 | a0003 | c0003 | t0003 | g0164 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18964 | hp1 | a0003 | c0003 | t0003 | g0167 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18965 | hp1 | a0003 | c0003 | t0003 | g0160 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18975 | hp1 | a0007 | c0006 | t0001 | g0001 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18984 | hp1 | a0003 | c0003 | t0003 | g0178 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18985 | hp2 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18993 | hp1 | a0007 | c0006 | t0001 | g0081 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19006 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | LWK | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0222 | AFR | LWK | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19043 | hp1 | a0008 | c0014 | t0001 | g0070 | AFR | LWK | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | LWK | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19078 | hp1 | a0001 | c0001 | t0011 | g0320 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19079 | hp1 | a0003 | c0003 | t0003 | g0189 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19081 | hp2 | a0007 | c0006 | t0001 | g0001 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | YRI | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA19240 | hp2 | a0004 | c0004 | t0004 | g0147 | AFR | YRI | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA20129 | hp1 | a0011 | c0008 | t0001 | g0009 | AFR | ASW | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | ASW | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | TSI | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | TSI | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0318 | EUR | TSI | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA20805 | hp2 | a0009 | c0009 | t0001 | g0091 | EUR | TSI | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | GIH | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0062 | SAS | GIH | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0242 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02486 | hp1 | a0003 | c0003 | t0005 | g0230 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02486 | hp2 | a0011 | c0008 | t0001 | g0009 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02559 | hp1 | a0018 | c0021 | t0002 | g0254 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG02559 | hp2 | a0001 | c0001 | t0013 | g0199 | AFR | ACB | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0245 | AFR | MSL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG03471 | hp2 | a0019 | c0022 | t0001 | g0031 | AFR | MSL | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG06807 | hp1 | a0001 | c0001 | t0006 | g0241 | AFR | USA | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
HG06807 | hp2 | a0003 | c0003 | t0003 | g0182 | AFR | USA | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0050 | AFR | USA | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0280 | AFR | USA | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0344 | AFR | LWK | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
NA21309 | hp2 | a0003 | c0003 | t0003 | g0188 | AFR | LWK | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0255 | REF | REF | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
homoSapiens_grch38 | hp1 | a0006 | c0005 | t0002 | g0250 | REF | REF | R3HCC1L_chr10_98129657_98249897 | R3HCC1L | chr10 | 98129657 | 98249897 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:98208296
|
T | C | 1 | a0013 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.182T>C | p.Val61Ala | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 499/3393 | 182/2337 | 61/778 | chr10 | 98208296 | ||
chr10:98208577
|
G | A | 1 | a0014 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.463G>A | p.Val155Met | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 780/3393 | 463/2337 | 155/778 | chr10 | 98208577 | ||
chr10:98208608
|
A | G | 1 | a0024 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.494A>G | p.Gln165Arg | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 811/3393 | 494/2337 | 165/778 | chr10 | 98208608 | ||
chr10:98208686
|
A | C | 1 | a0023 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.572A>C | p.His191Pro | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 889/3393 | 572/2337 | 191/778 | chr10 | 98208686 | ||
chr10:98208734
|
T | C | 1 | a0022 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.620T>C | p.Ile207Thr | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 937/3393 | 620/2337 | 207/778 | chr10 | 98208734 | ||
chr10:98208778
|
A | G | 1 | a0008 | 2 | NA18522.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.664A>G | p.Arg222Gly | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 981/3393 | 664/2337 | 222/778 | chr10 | 98208778 | ||
chr10:98208828
|
A | C | 1 | a0012 | 2 | HG01496.hp1 HG02647.hp2 |
missense_variant | MODERATE | c.714A>C | p.Lys238Asn | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 1031/3393 | 714/2337 | 238/778 | chr10 | 98208828 | ||
chr10:98208844
|
G | C | 1 | a0021 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.730G>C | p.Glu244Gln | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 1047/3393 | 730/2337 | 244/778 | chr10 | 98208844 | ||
chr10:98208895
|
A | G | 1 | a0005 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.781A>G | p.Ser261Gly | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 1098/3393 | 781/2337 | 261/778 | chr10 | 98208895 | ||
chr10:98208913
|
A | G | 1 | a0015 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.799A>G | p.Thr267Ala | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 1116/3393 | 799/2337 | 267/778 | chr10 | 98208913 | ||
chr10:98208986
|
G | T | 1 | a0020 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.872G>T | p.Gly291Val | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 1189/3393 | 872/2337 | 291/778 | chr10 | 98208986 | ||
chr10:98209255
|
A | T | 1 | a0016 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.1141A>T | p.Thr381Ser | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 1458/3393 | 1141/2337 | 381/778 | chr10 | 98209255 | ||
chr10:98209483
|
G | A | 1 | a0011 | 2 | HG02486.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.1369G>A | p.Glu457Lys | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 1686/3393 | 1369/2337 | 457/778 | chr10 | 98209483 | ||
chr10:98209633
|
A | C | 2 | a0011a0019 | 3 | HG02486.hp2 HG03471.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.1519A>C | p.Ile507Leu | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 1836/3393 | 1519/2337 | 507/778 | chr10 | 98209633 | ||
chr10:98209718
|
A | C | 3 | a0003a0005a0020 | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
missense_variant | MODERATE | c.1604A>C | p.Asp535Ala | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 1921/3393 | 1604/2337 | 535/778 | chr10 | 98209718 | ||
chr10:98209741
|
G | C | 1 | a0009 | 2 | HG01109.hp2 NA20805.hp2 |
missense_variant | MODERATE | c.1627G>C | p.Val543Leu | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 1944/3393 | 1627/2337 | 543/778 | chr10 | 98209741 | ||
chr10:98209750
|
C | T | 1 | a0010 | 2 | HG00733.hp2 HG01099.hp2 |
missense_variant | MODERATE | c.1636C>T | p.Pro546Ser | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 1953/3393 | 1636/2337 | 546/778 | chr10 | 98209750 | ||
chr10:98209811
|
A | G | 9 | a0002a0007a0008others(6): Show | 111 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(108): Show |
missense_variant | MODERATE | c.1697A>G | p.His566Arg | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 2014/3393 | 1697/2337 | 566/778 | chr10 | 98209811 | ||
chr10:98231651
|
A | G | 23 | a0001a0002a0003others(20): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
missense_variant | MODERATE | c.1925A>G | p.His642Arg | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/10 | 2242/3393 | 1925/2337 | 642/778 | chr10 | 98231651 | ||
chr10:98235434
|
C | T | 1 | a0018 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.2042C>T | p.Ala681Val | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 8/10 | 2359/3393 | 2042/2337 | 681/778 | chr10 | 98235434 | ||
chr10:98235490
|
G | T | 1 | a0004 | 7 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
missense_variant | MODERATE | c.2098G>T | p.Ala700Ser | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 8/10 | 2415/3393 | 2098/2337 | 700/778 | chr10 | 98235490 | ||
chr10:98236048
|
G | A | 1 | a0007 | 3 | NA18975.hp1 NA18993.hp1 NA19081.hp2 |
missense_variant | MODERATE | c.2153G>A | p.Arg718His | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/10 | 2470/3393 | 2153/2337 | 718/778 | chr10 | 98236048 | ||
chr10:98236125
|
G | A | 1 | a0017 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.2230G>A | p.Glu744Lys | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/10 | 2547/3393 | 2230/2337 | 744/778 | chr10 | 98236125 | ||
chr10:98236125
|
G | C | 2 | a0012a0016 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
missense_variant | MODERATE | c.2230G>C | p.Glu744Gln | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/10 | 2547/3393 | 2230/2337 | 744/778 | chr10 | 98236125 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:98209653
|
T | C | 1 | a0013c0015 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.1539T>C | p.Gly513Gly | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 1856/3393 | 1539/2337 | 513/778 | chr10 | 98209653 | ||
chr10:98209893
|
A | G | 1 | a0003c0012 | 2 | HG02451.hp1 HG02818.hp1 |
synonymous_variant | LOW | c.1779A>G | p.Leu593Leu | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/10 | 2096/3393 | 1779/2337 | 593/778 | chr10 | 98209893 | ||
chr10:98236070
|
A | C | 1 | a0001c0010 | 2 | HG02818.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.2175A>C | p.Leu725Leu | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/10 | 2492/3393 | 2175/2337 | 725/778 | chr10 | 98236070 | ||
chr10:98236124
|
C | T | 1 | a0001c0020 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.2229C>T | p.Thr743Thr | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/10 | 2546/3393 | 2229/2337 | 743/778 | chr10 | 98236124 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:98134693
|
G | A | 1 | a0002c0002t0009 | 1 | NA18747.hp2 | 5_prime_UTR_variant | MODIFIER | c.-281G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/10 | 73422 | chr10 | 98134693 | |||||
chr10:98162926
|
G | A | 5 | a0001c0001t0004a0001c0020t0004a0004c0004t0004others(2): Show | 20 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-169G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 3/10 | 45189 | chr10 | 98162926 | |||||
chr10:98163349
|
C | T | 1 | a0001c0001t0015 | 1 | NA18747.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/10 | chr10 | 98163349 | ||||||
chr10:98163350
|
G | A | 1 | a0001c0001t0010 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-62G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/10 | 44765 | chr10 | 98163350 | |||||
chr10:98163380
|
A | G | 5 | a0001c0001t0004a0001c0020t0004a0004c0004t0004others(2): Show | 20 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-32A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/10 | 44735 | chr10 | 98163380 | |||||
chr10:98244241
|
A | G | 1 | a0001c0001t0010 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*83A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 10/10 | 83 | chr10 | 98244241 | |||||
chr10:98244281
|
G | A | 1 | a0001c0001t0011 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*123G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 10/10 | 123 | chr10 | 98244281 | |||||
chr10:98244359
|
A | G | 1 | a0003c0003t0005 | 7 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*201A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 10/10 | 201 | chr10 | 98244359 | |||||
chr10:98244406
|
A | G | 1 | a0001c0001t0014 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*248A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 10/10 | 248 | chr10 | 98244406 | |||||
chr10:98244464
|
TC | T | 1 | a0001c0001t0006 | 5 | HG02109.hp1 HG02809.hp1 HG03209.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*308delC | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 10/10 | 308 | INFO_REALIGN_3_PRIME | chr10 | 98244464 | ||||
chr10:98244603
|
G | A | 6 | a0003c0003t0003a0003c0003t0005a0003c0012t0003others(3): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*445G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 10/10 | 445 | chr10 | 98244603 | |||||
chr10:98244684
|
G | C | 23 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(20): Show | 221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*526G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 10/10 | 526 | chr10 | 98244684 | |||||
chr10:98244726
|
A | G | 1 | a0001c0001t0013 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*568A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 10/10 | 568 | chr10 | 98244726 | |||||
chr10:98244757
|
G | A | 2 | a0001c0001t0008a0001c0001t0012 | 3 | HG01168.hp1 NA18956.hp1 NA18985.hp2 |
3_prime_UTR_variant | MODIFIER | c.*599G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 10/10 | 599 | chr10 | 98244757 | |||||
chr10:98244779
|
G | T | 2 | a0001c0001t0007a0001c0010t0007 | 3 | HG02818.hp2 HG02922.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*621G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 10/10 | 621 | chr10 | 98244779 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:98134781
|
C | T | 1 | a0001c0001t0002g0346 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-268+75C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98134781 | ||||||
chr10:98134785
|
G | A | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-268+79G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98134785 | ||||||
chr10:98135185
|
G | A | 1 | a0001c0001t0002g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-268+479G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98135185 | ||||||
chr10:98135229
|
A | G | 1 | a0001c0001t0002g0345 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-268+523A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98135229 | ||||||
chr10:98135383
|
G | A | 2 | a0001c0001t0002g0025a0001c0001t0002g0026 | 2 | HG01978.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-268+677G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98135383 | ||||||
chr10:98135465
|
C | T | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-268+759C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98135465 | ||||||
chr10:98135489
|
T | C | 227 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(224): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.-268+783T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98135489 | ||||||
chr10:98135497
|
G | T | 1 | a0001c0001t0002g0343 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-268+791G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98135497 | ||||||
chr10:98135726
|
C | A | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-268+1020C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98135726 | ||||||
chr10:98135803
|
C | G | 1 | a0001c0001t0002g0342 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-268+1097C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98135803 | ||||||
chr10:98135841
|
A | G | 1 | a0002c0002t0001g0234 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-268+1135A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98135841 | ||||||
chr10:98136017
|
G | GT | 37 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(34): Show | 42 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.-268+1327dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98136017 | |||||
chr10:98136167
|
G | A | 226 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(223): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.-268+1461G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98136167 | ||||||
chr10:98136461
|
C | G | 67 | a0001c0001t0002g0008a0001c0001t0002g0020a0001c0001t0002g0021others(64): Show | 71 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-268+1755C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98136461 | ||||||
chr10:98136490
|
T | C | 2 | a0001c0010t0007g0028a0001c0010t0007g0029 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-268+1784T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98136490 | ||||||
chr10:98136558
|
A | G | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-268+1852A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98136558 | ||||||
chr10:98136563
|
C | T | 10 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(7): Show | 10 | HG01255.hp1 HG01891.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-268+1857C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98136563 | ||||||
chr10:98136578
|
G | C | 1 | a0001c0001t0002g0282 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-268+1872G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98136578 | ||||||
chr10:98136691
|
A | G | 1 | a0001c0001t0002g0281 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-268+1985A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98136691 | ||||||
chr10:98136743
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-268+2037G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98136743 | ||||||
chr10:98136808
|
G | T | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-268+2102G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98136808 | ||||||
chr10:98136995
|
G | T | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-268+2289G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98136995 | ||||||
chr10:98137019
|
G | A | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-268+2313G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98137019 | ||||||
chr10:98137771
|
A | G | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-268+3065A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98137771 | ||||||
chr10:98137976
|
T | TCAAGATG others(314): Show |
1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-268+3286_-268+328 others(325): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98137976 | |||||
chr10:98138025
|
A | G | 227 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(224): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.-268+3319A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98138025 | ||||||
chr10:98138034
|
C | T | 2 | a0001c0001t0002g0278a0001c0001t0002g0279 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-268+3328C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98138034 | ||||||
chr10:98138131
|
A | G | 38 | a0001c0001t0007g0023a0001c0010t0007g0028a0001c0010t0007g0029others(35): Show | 39 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.-268+3425A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98138131 | ||||||
chr10:98138376
|
A | T | 226 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(223): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.-268+3670A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98138376 | ||||||
chr10:98138511
|
T | C | 227 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(224): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.-268+3805T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98138511 | ||||||
chr10:98138524
|
T | C | 226 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(223): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.-268+3818T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98138524 | ||||||
chr10:98138528
|
TA | T | 7 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-268+3834delA | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98138528 | |||||
chr10:98138703
|
C | T | 3 | a0002c0002t0001g0154a0002c0002t0001g0155a0002c0002t0001g0156 | 3 | HG02080.hp1 HG02135.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-268+3997C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98138703 | ||||||
chr10:98138846
|
G | A | 1 | a0001c0001t0008g0030 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-268+4140G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98138846 | ||||||
chr10:98138949
|
T | G | 10 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(7): Show | 10 | HG01255.hp1 HG01891.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-268+4243T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98138949 | ||||||
chr10:98139491
|
C | A | 2 | a0011c0008t0001g0009a0019c0022t0001g0031 | 3 | HG02486.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-268+4785C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98139491 | ||||||
chr10:98139661
|
T | TA | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-268+4956dupA | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98139661 | |||||
chr10:98139837
|
G | A | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-268+5131G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98139837 | ||||||
chr10:98139917
|
T | A | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-268+5211T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98139917 | ||||||
chr10:98139946
|
G | A | 10 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(7): Show | 10 | HG01255.hp1 HG01891.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-268+5240G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98139946 | ||||||
chr10:98140216
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-268+5510C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98140216 | ||||||
chr10:98140246
|
G | A | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-268+5540G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98140246 | ||||||
chr10:98140508
|
C | T | 1 | a0016c0023t0002g0223 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-268+5802C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98140508 | ||||||
chr10:98140723
|
C | T | 14 | a0001c0001t0004g0002a0001c0001t0004g0220a0001c0001t0004g0221others(11): Show | 20 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-268+6017C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98140723 | ||||||
chr10:98140783
|
G | A | 2 | a0002c0002t0001g0032a0002c0002t0001g0033 | 2 | NA18997.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-268+6077G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98140783 | ||||||
chr10:98140815
|
C | T | 1 | a0003c0003t0003g0190 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-268+6109C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98140815 | ||||||
chr10:98140817
|
GTTAACTA others(23): Show |
G | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-268+6116_-268+614 others(34): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98140817 | |||||
chr10:98140873
|
G | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0034others(6): Show | 13 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-268+6167G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98140873 | ||||||
chr10:98140900
|
AT | A | 3 | a0001c0001t0002g0283a0001c0001t0002g0284a0001c0001t0002g0285 | 3 | NA18951.hp1 NA18967.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.-268+6195delT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98140900 | ||||||
chr10:98141002
|
G | C | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-268+6296G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98141002 | ||||||
chr10:98141027
|
T | C | 1 | a0002c0002t0001g0041 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-268+6321T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98141027 | ||||||
chr10:98141162
|
G | A | 1 | a0001c0001t0002g0286 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-268+6456G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98141162 | ||||||
chr10:98141343
|
T | A | 1 | a0019c0022t0001g0031 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-268+6637T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98141343 | ||||||
chr10:98141374
|
T | C | 1 | a0001c0001t0002g0236 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-268+6668T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98141374 | ||||||
chr10:98141378
|
A | G | 13 | a0001c0001t0004g0002a0001c0001t0004g0220a0001c0001t0004g0221others(10): Show | 19 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-268+6672A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98141378 | ||||||
chr10:98141543
|
A | G | 1 | a0004c0004t0004g0152 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-268+6837A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98141543 | ||||||
chr10:98141722
|
T | G | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-268+7016T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98141722 | ||||||
chr10:98141959
|
A | T | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-268+7253A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98141959 | ||||||
chr10:98142301
|
C | G | 7 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-268+7595C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98142301 | ||||||
chr10:98142374
|
G | A | 11 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(8): Show | 11 | HG01255.hp1 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-268+7668G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98142374 | ||||||
chr10:98142617
|
G | A | 1 | a0003c0003t0003g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-268+7911G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98142617 | ||||||
chr10:98142634
|
T | C | 37 | a0001c0010t0007g0028a0001c0010t0007g0029a0003c0003t0003g0017others(34): Show | 38 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.-268+7928T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98142634 | ||||||
chr10:98142796
|
C | G | 11 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(8): Show | 11 | HG01255.hp1 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-268+8090C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98142796 | ||||||
chr10:98142811
|
T | C | 225 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(222): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.-268+8105T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98142811 | ||||||
chr10:98142941
|
A | C | 156 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(153): Show | 186 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.-268+8235A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98142941 | ||||||
chr10:98142968
|
C | CA | 39 | a0001c0010t0007g0028a0001c0010t0007g0029a0002c0002t0001g0042others(36): Show | 40 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.-268+8272dupA | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98142968 | |||||
chr10:98143172
|
C | T | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-268+8466C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98143172 | ||||||
chr10:98143388
|
G | A | 144 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(141): Show | 169 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.-268+8682G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98143388 | ||||||
chr10:98143453
|
G | A | 1 | a0001c0001t0002g0287 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-268+8747G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98143453 | ||||||
chr10:98143466
|
A | G | 1 | a0003c0003t0003g0189 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-268+8760A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98143466 | ||||||
chr10:98143538
|
G | A | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-268+8832G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98143538 | ||||||
chr10:98143599
|
G | A | 1 | a0002c0002t0001g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-268+8893G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98143599 | ||||||
chr10:98143631
|
G | A | 1 | a0003c0012t0003g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-268+8925G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98143631 | ||||||
chr10:98143769
|
C | T | 2 | a0002c0002t0001g0141a0002c0002t0001g0142 | 2 | HG00642.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-268+9063C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98143769 | ||||||
chr10:98143770
|
G | A | 1 | a0002c0002t0001g0044 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-268+9064G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98143770 | ||||||
chr10:98143886
|
C | T | 1 | a0002c0002t0001g0140 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-268+9180C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98143886 | ||||||
chr10:98143921
|
T | C | 225 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(222): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.-268+9215T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98143921 | ||||||
chr10:98143947
|
C | T | 214 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(211): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.-268+9241C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98143947 | ||||||
chr10:98144089
|
T | G | 225 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(222): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.-268+9383T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98144089 | ||||||
chr10:98144129
|
A | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(52): Show | 62 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-268+9423A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98144129 | ||||||
chr10:98144164
|
A | G | 225 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(222): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.-268+9458A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98144164 | ||||||
chr10:98144236
|
G | A | 1 | a0001c0001t0002g0288 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-268+9530G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98144236 | ||||||
chr10:98144300
|
C | T | 1 | a0010c0011t0002g0334 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-268+9594C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98144300 | ||||||
chr10:98144332
|
C | T | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0277 | 3 | HG01978.hp2 HG02300.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-268+9626C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98144332 | ||||||
chr10:98144412
|
C | T | 225 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(222): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.-268+9706C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98144412 | ||||||
chr10:98144503
|
C | T | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-268+9797C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98144503 | ||||||
chr10:98144589
|
C | T | 8 | a0003c0003t0003g0181a0003c0003t0003g0182a0003c0003t0003g0183others(5): Show | 8 | HG00733.hp1 HG01175.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.-268+9883C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98144589 | ||||||
chr10:98144600
|
G | A | 1 | a0002c0002t0001g0045 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-268+9894G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98144600 | ||||||
chr10:98144686
|
A | G | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-268+9980A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98144686 | ||||||
chr10:98144779
|
C | T | 1 | a0003c0003t0003g0190 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-268+10073C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98144779 | ||||||
chr10:98144835
|
A | T | 1 | a0001c0001t0002g0276 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-268+10129A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98144835 | ||||||
chr10:98144867
|
A | T | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-268+10161A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98144867 | ||||||
chr10:98145201
|
T | C | 10 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0211others(7): Show | 10 | HG01943.hp2 NA18939.hp2 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.-268+10495T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98145201 | ||||||
chr10:98145333
|
T | G | 38 | a0001c0001t0007g0023a0001c0010t0007g0028a0001c0010t0007g0029others(35): Show | 39 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.-268+10627T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98145333 | ||||||
chr10:98145366
|
A | C | 1 | a0001c0001t0002g0333 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-268+10660A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98145366 | ||||||
chr10:98145725
|
C | T | 2 | a0011c0008t0001g0009a0019c0022t0001g0031 | 3 | HG02486.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-267-10368C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98145725 | ||||||
chr10:98145807
|
G | A | 1 | a0001c0001t0002g0289 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-267-10286G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98145807 | ||||||
chr10:98145831
|
C | A | 215 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(212): Show | 248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.-267-10262C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98145831 | ||||||
chr10:98145860
|
A | T | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-267-10233A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98145860 | ||||||
chr10:98145948
|
C | CA | 58 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(55): Show | 65 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.-267-10134dupA | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98145948 | |||||
chr10:98146033
|
T | C | 2 | a0002c0002t0001g0046a0002c0002t0001g0047 | 2 | HG03927.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-267-10060T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98146033 | ||||||
chr10:98146068
|
G | A | 224 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(221): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.-267-10025G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98146068 | ||||||
chr10:98146069
|
T | A | 1 | a0003c0003t0003g0180 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-267-10024T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98146069 | ||||||
chr10:98146176
|
C | CTT | 225 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(222): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.-267-9912_-267-991 others(6): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98146176 | |||||
chr10:98146425
|
G | C | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-267-9668G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98146425 | ||||||
chr10:98146552
|
G | A | 37 | a0001c0010t0007g0028a0001c0010t0007g0029a0003c0003t0003g0017others(34): Show | 38 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.-267-9541G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98146552 | ||||||
chr10:98146693
|
C | A | 1 | a0001c0001t0002g0237 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-267-9400C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98146693 | ||||||
chr10:98146700
|
C | G | 1 | a0001c0001t0001g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-267-9393C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98146700 | ||||||
chr10:98146992
|
C | A | 7 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-267-9101C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98146992 | ||||||
chr10:98147025
|
A | G | 86 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0005others(83): Show | 103 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-267-9068A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98147025 | ||||||
chr10:98147049
|
T | G | 1 | a0023c0026t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-267-9044T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98147049 | ||||||
chr10:98147195
|
C | T | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-267-8898C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98147195 | ||||||
chr10:98147219
|
A | G | 1 | a0002c0002t0001g0108 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-267-8874A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98147219 | ||||||
chr10:98147252
|
A | G | 1 | a0001c0001t0002g0275 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-267-8841A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98147252 | ||||||
chr10:98147483
|
C | T | 13 | a0001c0001t0004g0002a0001c0001t0004g0220a0001c0001t0004g0221others(10): Show | 19 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-267-8610C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98147483 | ||||||
chr10:98147592
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-267-8501T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98147592 | ||||||
chr10:98147676
|
C | T | 31 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(28): Show | 38 | HG01081.hp2 HG01496.hp1 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.-267-8417C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98147676 | ||||||
chr10:98147733
|
A | G | 7 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-267-8360A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98147733 | ||||||
chr10:98147766
|
A | G | 18 | a0001c0001t0002g0022a0001c0001t0002g0283a0001c0001t0002g0284others(15): Show | 18 | HG00597.hp2 HG00621.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.-267-8327A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98147766 | ||||||
chr10:98147831
|
G | A | 1 | a0003c0003t0003g0181 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-267-8262G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98147831 | ||||||
chr10:98148157
|
C | T | 225 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(222): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.-267-7936C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98148157 | ||||||
chr10:98148302
|
T | G | 1 | a0001c0001t0002g0238 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-267-7791T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98148302 | ||||||
chr10:98148341
|
A | G | 2 | a0003c0003t0003g0190a0020c0024t0003g0179 | 2 | HG00323.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-267-7752A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98148341 | ||||||
chr10:98148359
|
C | T | 7 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-267-7734C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98148359 | ||||||
chr10:98148393
|
A | G | 2 | a0001c0010t0007g0028a0001c0010t0007g0029 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-267-7700A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98148393 | ||||||
chr10:98148588
|
A | G | 1 | a0002c0002t0001g0107 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-267-7505A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98148588 | ||||||
chr10:98148615
|
G | C | 1 | a0001c0001t0002g0143 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-267-7478G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98148615 | ||||||
chr10:98148672
|
G | A | 1 | a0023c0026t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-267-7421G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98148672 | ||||||
chr10:98148737
|
C | G | 1 | a0001c0001t0001g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-267-7356C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98148737 | ||||||
chr10:98148951
|
T | G | 1 | a0002c0002t0001g0048 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-267-7142T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98148951 | ||||||
chr10:98149029
|
G | T | 11 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(8): Show | 11 | HG01255.hp1 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-267-7064G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98149029 | ||||||
chr10:98149097
|
G | A | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-267-6996G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98149097 | ||||||
chr10:98149246
|
G | C | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-267-6847G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98149246 | ||||||
chr10:98149335
|
G | A | 1 | a0001c0001t0002g0192 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-267-6758G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98149335 | ||||||
chr10:98149428
|
G | A | 35 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(32): Show | 36 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.-267-6665G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98149428 | ||||||
chr10:98149437
|
T | G | 3 | a0002c0002t0001g0049a0002c0002t0001g0050a0002c0002t0001g0051 | 3 | HG01978.hp1 HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-267-6656T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98149437 | ||||||
chr10:98149449
|
A | G | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-267-6644A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98149449 | ||||||
chr10:98149862
|
T | C | 2 | a0003c0012t0003g0158a0003c0012t0003g0159 | 2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-267-6231T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98149862 | ||||||
chr10:98150062
|
G | A | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-267-6031G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98150062 | ||||||
chr10:98150276
|
C | T | 86 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0005others(83): Show | 103 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-267-5817C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98150276 | ||||||
chr10:98150377
|
T | C | 1 | a0001c0001t0002g0239 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-267-5716T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98150377 | ||||||
chr10:98150407
|
C | CT | 3 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0040 | 6 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.-267-5682dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98150407 | |||||
chr10:98150655
|
C | T | 7 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-267-5438C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98150655 | ||||||
chr10:98150706
|
T | A | 1 | a0001c0001t0002g0343 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-267-5387T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98150706 | ||||||
chr10:98150816
|
T | C | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-267-5277T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98150816 | ||||||
chr10:98150834
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-267-5259C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98150834 | ||||||
chr10:98150905
|
A | G | 2 | a0002c0002t0001g0041a0013c0015t0001g0137 | 2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-267-5188A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98150905 | ||||||
chr10:98150956
|
G | A | 1 | a0002c0002t0001g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-267-5137G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98150956 | ||||||
chr10:98150974
|
C | T | 8 | a0003c0003t0003g0181a0003c0003t0003g0182a0003c0003t0003g0183others(5): Show | 8 | HG00733.hp1 HG01175.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.-267-5119C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98150974 | ||||||
chr10:98150975
|
G | T | 1 | a0002c0002t0001g0106 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-267-5118G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98150975 | ||||||
chr10:98151044
|
G | A | 7 | a0001c0001t0004g0220a0004c0004t0004g0016a0004c0004t0004g0145others(4): Show | 8 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-267-5049G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98151044 | ||||||
chr10:98151169
|
A | G | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-267-4924A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98151169 | ||||||
chr10:98151485
|
C | T | 2 | a0001c0001t0002g0321a0001c0001t0011g0320 | 2 | NA18956.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.-267-4608C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98151485 | ||||||
chr10:98151629
|
A | G | 1 | a0001c0001t0002g0333 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-267-4464A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98151629 | ||||||
chr10:98151636
|
T | G | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-267-4457T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98151636 | ||||||
chr10:98151909
|
T | G | 1 | a0016c0023t0002g0223 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-267-4184T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98151909 | ||||||
chr10:98152077
|
C | T | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-267-4016C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152077 | ||||||
chr10:98152084
|
C | G | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-267-4009C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152084 | ||||||
chr10:98152101
|
C | A | 1 | a0001c0001t0002g0290 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-267-3992C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152101 | ||||||
chr10:98152259
|
A | G | 6 | a0004c0004t0004g0016a0004c0004t0004g0145a0004c0004t0004g0146others(3): Show | 7 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-267-3834A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152259 | ||||||
chr10:98152298
|
A | C | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-267-3795A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152298 | ||||||
chr10:98152303
|
C | T | 2 | a0001c0001t0002g0339a0001c0001t0002g0340 | 2 | HG00558.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-267-3790C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152303 | ||||||
chr10:98152304
|
G | A | 226 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(223): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.-267-3789G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152304 | ||||||
chr10:98152321
|
C | T | 1 | a0001c0001t0002g0282 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-267-3772C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152321 | ||||||
chr10:98152340
|
A | G | 1 | a0004c0004t0004g0016 | 2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-267-3753A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152340 | ||||||
chr10:98152346
|
T | C | 225 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(222): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.-267-3747T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152346 | ||||||
chr10:98152377
|
C | T | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-267-3716C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152377 | ||||||
chr10:98152388
|
T | G | 1 | a0002c0002t0001g0053 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-267-3705T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152388 | ||||||
chr10:98152409
|
C | T | 1 | a0003c0003t0005g0229 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-267-3684C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152409 | ||||||
chr10:98152428
|
G | C | 3 | a0001c0001t0012g0292a0010c0011t0002g0291a0010c0011t0002g0334 | 3 | HG00733.hp2 HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-267-3665G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152428 | ||||||
chr10:98152444
|
C | A | 1 | a0002c0002t0001g0054 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-267-3649C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152444 | ||||||
chr10:98152444
|
C | T | 2 | a0001c0001t0002g0236a0001c0001t0002g0274 | 2 | HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-267-3649C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152444 | ||||||
chr10:98152472
|
GCCTCTTC others(263): Show |
G | 87 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0005others(84): Show | 104 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.-267-3616_-267-334 others(4): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98152472 | |||||
chr10:98152481
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-267-3612C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152481 | ||||||
chr10:98152530
|
A | G | 1 | a0001c0001t0002g0237 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-267-3563A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152530 | ||||||
chr10:98152557
|
C | T | 1 | a0001c0001t0002g0289 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-267-3536C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152557 | ||||||
chr10:98152568
|
C | T | 2 | a0001c0001t0002g0236a0001c0001t0002g0274 | 2 | HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-267-3525C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152568 | ||||||
chr10:98152609
|
A | C | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-267-3484A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152609 | ||||||
chr10:98152621
|
G | A | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-267-3472G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152621 | ||||||
chr10:98152641
|
C | T | 1 | a0012c0013t0002g0207 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-267-3452C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152641 | ||||||
chr10:98152642
|
A | G | 139 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(136): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-267-3451A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152642 | ||||||
chr10:98152674
|
C | T | 7 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-267-3419C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152674 | ||||||
chr10:98152787
|
C | T | 212 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(209): Show | 239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-267-3306C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152787 | ||||||
chr10:98152791
|
C | G | 1 | a0008c0014t0001g0103 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-267-3302C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152791 | ||||||
chr10:98152791
|
C | T | 2 | a0002c0002t0001g0104a0002c0002t0001g0105 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-267-3302C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152791 | ||||||
chr10:98152803
|
C | T | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-267-3290C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152803 | ||||||
chr10:98152844
|
G | A | 2 | a0001c0001t0001g0113a0014c0016t0001g0112 | 2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-267-3249G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152844 | ||||||
chr10:98152862
|
G | A | 1 | a0001c0001t0002g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-267-3231G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152862 | ||||||
chr10:98152864
|
C | T | 226 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(223): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.-267-3229C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152864 | ||||||
chr10:98152917
|
C | T | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-267-3176C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152917 | ||||||
chr10:98152925
|
C | T | 180 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(177): Show | 212 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.-267-3168C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152925 | ||||||
chr10:98152930
|
T | C | 226 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(223): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.-267-3163T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152930 | ||||||
chr10:98152934
|
C | T | 55 | a0001c0001t0004g0002a0001c0001t0004g0220a0001c0001t0004g0221others(52): Show | 62 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.-267-3159C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98152934 | ||||||
chr10:98152945
|
T | TG | 33 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(30): Show | 40 | HG01081.hp2 HG01496.hp1 HG02055.hp2 others(37): Show |
intron_variant | MODIFIER | c.-267-3142dupG | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98152945 | |||||
chr10:98153010
|
C | T | 2 | a0002c0002t0001g0032a0002c0002t0001g0033 | 2 | NA18997.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-267-3083C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98153010 | ||||||
chr10:98153041
|
G | A | 46 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.-267-3052G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98153041 | ||||||
chr10:98153050
|
C | T | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-267-3043C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98153050 | ||||||
chr10:98153087
|
C | T | 1 | a0004c0004t0004g0152 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-267-3006C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98153087 | ||||||
chr10:98153217
|
T | C | 1 | a0001c0001t0002g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-267-2876T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98153217 | ||||||
chr10:98153301
|
A | G | 1 | a0001c0001t0002g0338 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-267-2792A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98153301 | ||||||
chr10:98153326
|
C | T | 7 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-267-2767C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98153326 | ||||||
chr10:98153375
|
T | A | 67 | a0001c0001t0002g0008a0001c0001t0002g0020a0001c0001t0002g0021others(64): Show | 71 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-267-2718T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98153375 | ||||||
chr10:98153420
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-267-2673G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98153420 | ||||||
chr10:98153558
|
C | A | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-267-2535C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98153558 | ||||||
chr10:98153609
|
T | TA | 11 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(8): Show | 11 | HG01433.hp2 HG01978.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-267-2462dupA | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98153609 | |||||
chr10:98153609
|
TA | T | 49 | a0001c0001t0001g0038a0001c0001t0001g0111a0001c0001t0001g0139others(46): Show | 50 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.-267-2462delA | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98153609 | |||||
chr10:98153627
|
A | G | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-267-2466A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98153627 | ||||||
chr10:98153803
|
CA | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(156): Show | 184 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.-267-2274delA | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98153803 | |||||
chr10:98153938
|
C | T | 1 | a0001c0001t0002g0321 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-267-2155C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98153938 | ||||||
chr10:98153955
|
A | G | 1 | a0001c0001t0004g0222 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-267-2138A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98153955 | ||||||
chr10:98154011
|
A | G | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-267-2082A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98154011 | ||||||
chr10:98154073
|
G | A | 1 | a0014c0016t0001g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-267-2020G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98154073 | ||||||
chr10:98154157
|
G | A | 1 | a0002c0002t0001g0056 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-267-1936G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98154157 | ||||||
chr10:98154182
|
C | CA | 37 | a0001c0001t0002g0020a0001c0001t0002g0022a0001c0001t0002g0246others(34): Show | 38 | HG00597.hp2 HG01109.hp1 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.-267-1890dupA | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98154182 | |||||
chr10:98154182
|
CA | C | 117 | a0001c0001t0001g0118a0001c0001t0002g0018a0001c0001t0002g0193others(114): Show | 141 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-267-1890delA | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98154182 | |||||
chr10:98154182
|
CAA | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(93): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-267-1891_-267-189 others(6): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98154182 | |||||
chr10:98154274
|
T | A | 1 | a0001c0001t0002g0343 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-267-1819T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98154274 | ||||||
chr10:98154348
|
G | T | 1 | a0001c0001t0001g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-267-1745G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98154348 | ||||||
chr10:98154357
|
G | A | 2 | a0011c0008t0001g0009a0019c0022t0001g0031 | 3 | HG02486.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-267-1736G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98154357 | ||||||
chr10:98154372
|
T | A | 14 | a0001c0001t0004g0002a0001c0001t0004g0220a0001c0001t0004g0221others(11): Show | 20 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-267-1721T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98154372 | ||||||
chr10:98154504
|
C | T | 226 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(223): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.-267-1589C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98154504 | ||||||
chr10:98154526
|
A | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 6 | NA18943.hp1 NA18972.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.-267-1567A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98154526 | ||||||
chr10:98154602
|
T | TAGCCACA others(1): Show |
14 | a0001c0001t0004g0002a0001c0001t0004g0220a0001c0001t0004g0221others(11): Show | 20 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-267-1490_-267-148 others(12): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98154602 | |||||
chr10:98154620
|
G | A | 2 | a0001c0010t0007g0028a0001c0010t0007g0029 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-267-1473G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98154620 | ||||||
chr10:98154952
|
T | C | 10 | a0002c0002t0001g0053a0002c0002t0001g0057a0002c0002t0001g0058others(7): Show | 10 | HG02040.hp2 HG02080.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.-267-1141T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98154952 | ||||||
chr10:98154969
|
A | G | 1 | a0001c0001t0002g0343 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-267-1124A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98154969 | ||||||
chr10:98155025
|
G | A | 4 | a0002c0002t0001g0042a0002c0002t0001g0052a0002c0002t0001g0062others(1): Show | 4 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(1): Show |
intron_variant | MODIFIER | c.-267-1068G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98155025 | ||||||
chr10:98155061
|
C | A | 1 | a0001c0001t0002g0339 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-267-1032C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98155061 | ||||||
chr10:98155383
|
T | C | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-267-710T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98155383 | ||||||
chr10:98155511
|
A | G | 1 | a0002c0002t0001g0100 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-267-582A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98155511 | ||||||
chr10:98155699
|
C | T | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-267-394C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98155699 | ||||||
chr10:98155747
|
A | G | 1 | a0003c0003t0003g0176 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-267-346A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98155747 | ||||||
chr10:98155802
|
G | GT | 12 | a0001c0001t0001g0015a0001c0001t0001g0132a0001c0001t0001g0133others(9): Show | 13 | HG00642.hp2 HG01074.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.-267-279dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98155802 | |||||
chr10:98155881
|
T | C | 2 | a0011c0008t0001g0009a0019c0022t0001g0031 | 3 | HG02486.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-267-212T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | chr10 | 98155881 | ||||||
chr10:98156052
|
AT | A | 15 | a0001c0001t0001g0035a0001c0001t0002g0301a0001c0001t0002g0302others(12): Show | 15 | HG01517.hp2 HG02735.hp2 HG02897.hp2 others(12): Show |
intron_variant | MODIFIER | c.-267-25delT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 98156052 | |||||
chr10:98156691
|
G | A | 13 | a0001c0001t0004g0002a0001c0001t0004g0220a0001c0001t0004g0221others(10): Show | 19 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-213+544G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98156691 | ||||||
chr10:98156751
|
T | G | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-213+604T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98156751 | ||||||
chr10:98156940
|
C | A | 145 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(142): Show | 170 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.-213+793C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98156940 | ||||||
chr10:98157005
|
A | G | 11 | a0001c0001t0002g0020a0001c0001t0002g0282a0001c0001t0002g0287others(8): Show | 12 | HG01934.hp2 HG01981.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.-213+858A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98157005 | ||||||
chr10:98157089
|
C | G | 1 | a0001c0001t0002g0341 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-213+942C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98157089 | ||||||
chr10:98157184
|
T | G | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-213+1037T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98157184 | ||||||
chr10:98157352
|
A | G | 1 | a0016c0023t0002g0223 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-213+1205A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98157352 | ||||||
chr10:98157373
|
A | G | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-213+1226A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98157373 | ||||||
chr10:98157453
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-213+1306T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98157453 | ||||||
chr10:98157454
|
C | T | 225 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(222): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.-213+1307C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98157454 | ||||||
chr10:98157508
|
C | T | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-213+1361C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98157508 | ||||||
chr10:98157533
|
T | C | 2 | a0001c0010t0007g0028a0001c0010t0007g0029 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-213+1386T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98157533 | ||||||
chr10:98157559
|
T | C | 226 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(223): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.-213+1412T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98157559 | ||||||
chr10:98157636
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-213+1489G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98157636 | ||||||
chr10:98157799
|
C | T | 1 | a0002c0002t0001g0051 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-213+1652C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98157799 | ||||||
chr10:98157829
|
C | G | 1 | a0001c0001t0002g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-213+1682C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98157829 | ||||||
chr10:98157977
|
G | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0219 | 3 | HG01192.hp2 HG01433.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-213+1830G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98157977 | ||||||
chr10:98158000
|
G | A | 69 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(66): Show | 82 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.-213+1853G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98158000 | ||||||
chr10:98158056
|
C | T | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-213+1909C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98158056 | ||||||
chr10:98158177
|
C | A | 7 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-213+2030C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98158177 | ||||||
chr10:98158278
|
G | T | 2 | a0005c0007t0003g0232a0005c0007t0003g0233 | 2 | HG01255.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-213+2131G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98158278 | ||||||
chr10:98158450
|
C | T | 1 | a0003c0003t0003g0175 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-213+2303C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98158450 | ||||||
chr10:98158496
|
T | A | 1 | a0002c0002t0001g0054 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-213+2349T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98158496 | ||||||
chr10:98158791
|
G | C | 14 | a0001c0001t0004g0002a0001c0001t0004g0220a0001c0001t0004g0221others(11): Show | 20 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-213+2644G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98158791 | ||||||
chr10:98158810
|
C | CT | 10 | a0001c0001t0001g0110a0001c0001t0014g0266a0002c0002t0001g0156others(7): Show | 11 | HG00140.hp1 HG00323.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.-213+2677dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 98158810 | |||||
chr10:98158810
|
CT | C | 8 | a0003c0003t0003g0181a0003c0003t0003g0182a0003c0003t0003g0183others(5): Show | 8 | HG00733.hp1 HG01175.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.-213+2677delT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 98158810 | |||||
chr10:98158882
|
C | A | 1 | a0001c0001t0002g0322 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-213+2735C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98158882 | ||||||
chr10:98158921
|
C | T | 1 | a0003c0003t0005g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-213+2774C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98158921 | ||||||
chr10:98159190
|
T | C | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-213+3043T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98159190 | ||||||
chr10:98159219
|
A | G | 226 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(223): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.-213+3072A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98159219 | ||||||
chr10:98159231
|
ATTG | A | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-213+3087_-213+308 others(7): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 98159231 | |||||
chr10:98159368
|
T | C | 13 | a0001c0001t0004g0002a0001c0001t0004g0220a0001c0001t0004g0221others(10): Show | 19 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-213+3221T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98159368 | ||||||
chr10:98159423
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-213+3276C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98159423 | ||||||
chr10:98159759
|
C | G | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-212-3124C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98159759 | ||||||
chr10:98160232
|
T | C | 1 | a0002c0002t0001g0068 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-212-2651T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98160232 | ||||||
chr10:98160233
|
C | T | 1 | a0001c0001t0004g0222 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-212-2650C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98160233 | ||||||
chr10:98160358
|
A | G | 1 | a0002c0002t0009g0093 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-212-2525A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98160358 | ||||||
chr10:98160542
|
G | A | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-212-2341G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98160542 | ||||||
chr10:98160570
|
C | A | 1 | a0001c0001t0002g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-212-2313C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98160570 | ||||||
chr10:98160609
|
T | C | 1 | a0003c0003t0005g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-212-2274T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98160609 | ||||||
chr10:98160710
|
C | G | 1 | a0001c0001t0004g0221 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-212-2173C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98160710 | ||||||
chr10:98160753
|
T | C | 1 | a0006c0005t0004g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-212-2130T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98160753 | ||||||
chr10:98160756
|
G | A | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-212-2127G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98160756 | ||||||
chr10:98160905
|
C | G | 1 | a0023c0026t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-212-1978C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98160905 | ||||||
chr10:98160927
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-212-1956A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98160927 | ||||||
chr10:98161156
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-212-1727G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98161156 | ||||||
chr10:98161272
|
T | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(52): Show | 62 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-212-1611T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98161272 | ||||||
chr10:98161308
|
G | A | 2 | a0001c0001t0002g0007a0001c0001t0002g0235 | 4 | HG00099.hp1 HG00738.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-212-1575G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98161308 | ||||||
chr10:98161710
|
A | G | 16 | a0001c0001t0002g0019a0001c0001t0002g0143a0001c0001t0002g0239others(13): Show | 17 | HG00544.hp1 HG02040.hp1 NA18942.hp1 others(14): Show |
intron_variant | MODIFIER | c.-212-1173A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98161710 | ||||||
chr10:98161727
|
A | C | 2 | a0001c0001t0002g0268a0001c0001t0002g0281 | 2 | HG01074.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-212-1156A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98161727 | ||||||
chr10:98161796
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-212-1087C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98161796 | ||||||
chr10:98161833
|
A | G | 1 | a0002c0002t0001g0006 | 3 | HG03491.hp2 HG03492.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-212-1050A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98161833 | ||||||
chr10:98161901
|
A | G | 1 | a0015c0025t0001g0210 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-212-982A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98161901 | ||||||
chr10:98161965
|
G | A | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-212-918G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98161965 | ||||||
chr10:98162018
|
A | T | 1 | a0003c0003t0005g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-212-865A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98162018 | ||||||
chr10:98162205
|
A | G | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-212-678A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98162205 | ||||||
chr10:98162208
|
T | C | 2 | a0003c0003t0003g0182a0003c0003t0003g0183 | 2 | HG00733.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-212-675T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98162208 | ||||||
chr10:98162212
|
T | C | 1 | a0003c0003t0003g0161 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-212-671T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98162212 | ||||||
chr10:98162232
|
A | C | 2 | a0002c0002t0001g0012a0002c0002t0001g0092 | 3 | HG02155.hp1 NA18971.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-212-651A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98162232 | ||||||
chr10:98162270
|
T | A | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-212-613T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98162270 | ||||||
chr10:98162569
|
G | A | 1 | a0002c0002t0001g0069 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-212-314G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98162569 | ||||||
chr10:98162580
|
C | T | 1 | a0014c0016t0001g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-212-303C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98162580 | ||||||
chr10:98162655
|
T | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(52): Show | 62 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-212-228T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98162655 | ||||||
chr10:98162666
|
G | A | 1 | a0001c0001t0002g0281 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-212-217G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98162666 | ||||||
chr10:98162672
|
T | TTG | 18 | a0001c0001t0002g0246a0001c0001t0002g0247a0001c0001t0002g0273others(15): Show | 24 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-212-189_-212-188d others(4): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 98162672 | |||||
chr10:98162672
|
TTG | T | 5 | a0001c0001t0001g0211a0001c0001t0001g0218a0001c0001t0002g0258others(2): Show | 5 | NA18522.hp2 NA18950.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.-212-189_-212-188d others(4): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 98162672 | |||||
chr10:98162672
|
TTGTG | T | 5 | a0001c0001t0007g0023a0001c0010t0007g0028a0001c0010t0007g0029others(2): Show | 5 | HG02818.hp2 HG02922.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-212-191_-212-188d others(6): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 98162672 | |||||
chr10:98162703
|
T | C | 6 | a0001c0001t0002g0020a0001c0001t0002g0287a0001c0001t0002g0295others(3): Show | 7 | HG01981.hp1 HG02148.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.-212-180T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98162703 | ||||||
chr10:98162729
|
A | G | 3 | a0003c0003t0003g0171a0003c0003t0003g0172a0003c0003t0003g0173 | 3 | HG03490.hp1 HG03492.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-212-154A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98162729 | ||||||
chr10:98162752
|
C | T | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-212-131C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98162752 | ||||||
chr10:98162796
|
C | T | 2 | a0009c0009t0001g0090a0009c0009t0001g0091 | 2 | HG01109.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-212-87C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98162796 | ||||||
chr10:98162818
|
C | T | 1 | a0001c0001t0002g0258 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-212-65C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 2/9 | chr10 | 98162818 | ||||||
chr10:98163486
|
T | C | 1 | a0001c0001t0002g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-15+89T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98163486 | ||||||
chr10:98163584
|
T | C | 1 | a0001c0001t0002g0249 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-15+187T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98163584 | ||||||
chr10:98163627
|
C | T | 1 | a0002c0002t0001g0089 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-15+230C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98163627 | ||||||
chr10:98163646
|
C | T | 1 | a0001c0001t0006g0245 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-15+249C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98163646 | ||||||
chr10:98163826
|
T | G | 89 | a0001c0001t0002g0007a0001c0001t0002g0235a0002c0002t0001g0001others(86): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.-15+429T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98163826 | ||||||
chr10:98163940
|
A | T | 1 | a0001c0001t0002g0265 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-15+543A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98163940 | ||||||
chr10:98164006
|
C | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(140): Show | 168 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.-15+609C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98164006 | ||||||
chr10:98164090
|
G | T | 5 | a0003c0003t0003g0161a0003c0003t0003g0168a0003c0003t0003g0169others(2): Show | 5 | HG00280.hp2 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+693G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98164090 | ||||||
chr10:98164159
|
G | T | 2 | a0003c0003t0003g0166a0003c0003t0003g0167 | 2 | HG02056.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-15+762G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98164159 | ||||||
chr10:98164326
|
C | T | 2 | a0001c0001t0002g0278a0001c0001t0002g0279 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-15+929C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98164326 | ||||||
chr10:98164562
|
G | A | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-15+1165G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98164562 | ||||||
chr10:98164569
|
T | A | 1 | a0001c0001t0002g0303 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-15+1172T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98164569 | ||||||
chr10:98164868
|
G | T | 2 | a0002c0002t0001g0088a0002c0002t0001g0280 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-15+1471G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98164868 | ||||||
chr10:98164895
|
A | G | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-15+1498A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98164895 | ||||||
chr10:98164965
|
A | C | 1 | a0001c0001t0002g0329 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-15+1568A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98164965 | ||||||
chr10:98165001
|
C | T | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-15+1604C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98165001 | ||||||
chr10:98165029
|
G | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0219 | 3 | HG01192.hp2 HG01433.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-15+1632G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98165029 | ||||||
chr10:98165300
|
A | G | 6 | a0004c0004t0004g0016a0004c0004t0004g0145a0004c0004t0004g0146others(3): Show | 7 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+1903A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98165300 | ||||||
chr10:98165397
|
G | A | 89 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0005others(86): Show | 107 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-15+2000G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98165397 | ||||||
chr10:98165423
|
C | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(52): Show | 62 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-15+2026C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98165423 | ||||||
chr10:98165549
|
C | T | 1 | a0003c0003t0005g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-15+2152C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98165549 | ||||||
chr10:98165759
|
C | T | 1 | a0002c0002t0001g0054 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-15+2362C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98165759 | ||||||
chr10:98165909
|
T | C | 226 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(223): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.-15+2512T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98165909 | ||||||
chr10:98165969
|
C | T | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-15+2572C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98165969 | ||||||
chr10:98165970
|
G | A | 1 | a0010c0011t0002g0291 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-15+2573G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98165970 | ||||||
chr10:98166122
|
C | T | 226 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(223): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.-15+2725C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98166122 | ||||||
chr10:98166284
|
G | A | 1 | a0002c0002t0001g0071 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-15+2887G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98166284 | ||||||
chr10:98166305
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-15+2908C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98166305 | ||||||
chr10:98166322
|
A | G | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-15+2925A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98166322 | ||||||
chr10:98166514
|
T | A | 179 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(176): Show | 211 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-15+3117T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98166514 | ||||||
chr10:98166531
|
G | A | 3 | a0001c0001t0002g0024a0001c0001t0002g0304a0001c0001t0002g0305 | 3 | HG03654.hp2 HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-15+3134G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98166531 | ||||||
chr10:98166779
|
C | T | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-15+3382C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98166779 | ||||||
chr10:98166813
|
G | T | 86 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0005others(83): Show | 103 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-15+3416G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98166813 | ||||||
chr10:98166879
|
A | G | 1 | a0003c0003t0003g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-15+3482A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98166879 | ||||||
chr10:98166898
|
C | T | 225 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(222): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.-15+3501C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98166898 | ||||||
chr10:98166937
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-15+3540T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98166937 | ||||||
chr10:98166946
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-15+3549T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98166946 | ||||||
chr10:98166950
|
C | T | 1 | a0001c0001t0002g0303 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-15+3553C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98166950 | ||||||
chr10:98167034
|
G | T | 1 | a0001c0001t0002g0203 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-15+3637G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98167034 | ||||||
chr10:98167101
|
T | A | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-15+3704T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98167101 | ||||||
chr10:98167102
|
A | G | 87 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0005others(84): Show | 104 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.-15+3705A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98167102 | ||||||
chr10:98167376
|
C | A | 1 | a0001c0001t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-15+3979C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98167376 | ||||||
chr10:98167391
|
A | G | 1 | a0001c0001t0006g0244 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-15+3994A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98167391 | ||||||
chr10:98167429
|
C | T | 3 | a0001c0001t0002g0344a0001c0010t0007g0028a0001c0010t0007g0029 | 3 | HG02818.hp2 HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-15+4032C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98167429 | ||||||
chr10:98167430
|
G | A | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-15+4033G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98167430 | ||||||
chr10:98167535
|
A | G | 4 | a0002c0002t0001g0085a0002c0002t0001g0086a0002c0002t0001g0087others(1): Show | 4 | HG00597.hp1 HG02015.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+4138A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98167535 | ||||||
chr10:98167547
|
A | T | 2 | a0001c0010t0007g0028a0001c0010t0007g0029 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-15+4150A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98167547 | ||||||
chr10:98167653
|
T | C | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-15+4256T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98167653 | ||||||
chr10:98167686
|
GGGACTTT others(14): Show |
G | 1 | a0001c0001t0002g0337 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-15+4304_-15+4324d others(23): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98167686 | |||||
chr10:98167689
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0040 | 6 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+4292A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98167689 | ||||||
chr10:98167697
|
A | C | 1 | a0001c0001t0002g0193 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-15+4300A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98167697 | ||||||
chr10:98167757
|
C | G | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-15+4360C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98167757 | ||||||
chr10:98167799
|
A | G | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-15+4402A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98167799 | ||||||
chr10:98167896
|
A | G | 5 | a0003c0003t0003g0160a0003c0003t0003g0165a0003c0003t0003g0166others(2): Show | 5 | HG02056.hp2 NA18953.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+4499A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98167896 | ||||||
chr10:98168027
|
G | A | 1 | a0002c0002t0001g0072 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-15+4630G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98168027 | ||||||
chr10:98168176
|
T | C | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-15+4779T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98168176 | ||||||
chr10:98168204
|
G | C | 167 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(164): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.-15+4807G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98168204 | ||||||
chr10:98168221
|
G | A | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-15+4824G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98168221 | ||||||
chr10:98168235
|
T | C | 2 | a0001c0001t0002g0251a0001c0001t0002g0270 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-15+4838T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98168235 | ||||||
chr10:98168288
|
A | G | 1 | a0002c0002t0001g0099 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-15+4891A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98168288 | ||||||
chr10:98168413
|
C | T | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-15+5016C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98168413 | ||||||
chr10:98168441
|
G | A | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-15+5044G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98168441 | ||||||
chr10:98168534
|
T | A | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-15+5137T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98168534 | ||||||
chr10:98168907
|
A | T | 1 | a0002c0002t0001g0045 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-15+5510A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98168907 | ||||||
chr10:98168955
|
G | A | 1 | a0022c0017t0002g0335 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-15+5558G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98168955 | ||||||
chr10:98168986
|
A | C | 1 | a0001c0001t0002g0336 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-15+5589A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98168986 | ||||||
chr10:98169039
|
G | C | 1 | a0002c0002t0001g0073 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-15+5642G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98169039 | ||||||
chr10:98169068
|
G | A | 1 | a0002c0002t0001g0073 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-15+5671G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98169068 | ||||||
chr10:98169488
|
T | C | 2 | a0012c0013t0002g0206a0012c0013t0002g0207 | 2 | HG01496.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-15+6091T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98169488 | ||||||
chr10:98169609
|
T | C | 1 | a0003c0003t0005g0224 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-15+6212T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98169609 | ||||||
chr10:98169903
|
T | C | 120 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(117): Show | 127 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.-15+6506T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98169903 | ||||||
chr10:98169930
|
G | C | 1 | a0002c0002t0001g0073 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-15+6533G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98169930 | ||||||
chr10:98170143
|
A | G | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-15+6746A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98170143 | ||||||
chr10:98170274
|
C | G | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-15+6877C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98170274 | ||||||
chr10:98170275
|
C | T | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-15+6878C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98170275 | ||||||
chr10:98170277
|
C | G | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-15+6880C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98170277 | ||||||
chr10:98170380
|
A | G | 2 | a0002c0002t0001g0041a0013c0015t0001g0137 | 2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-15+6983A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98170380 | ||||||
chr10:98170426
|
C | T | 7 | a0001c0001t0004g0220a0004c0004t0004g0016a0004c0004t0004g0145others(4): Show | 8 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+7029C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98170426 | ||||||
chr10:98170470
|
A | G | 1 | a0001c0001t0002g0273 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-15+7073A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98170470 | ||||||
chr10:98170472
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-15+7075C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98170472 | ||||||
chr10:98170606
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-15+7209G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98170606 | ||||||
chr10:98170778
|
A | G | 1 | a0002c0002t0001g0084 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-15+7381A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98170778 | ||||||
chr10:98170857
|
A | C | 2 | a0001c0001t0002g0339a0001c0001t0002g0340 | 2 | HG00558.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-15+7460A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98170857 | ||||||
chr10:98170908
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-15+7511T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98170908 | ||||||
chr10:98170913
|
G | T | 1 | a0001c0001t0002g0203 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-15+7516G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98170913 | ||||||
chr10:98171073
|
A | C | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-15+7676A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98171073 | ||||||
chr10:98171208
|
T | A | 1 | a0001c0001t0002g0265 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-15+7811T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98171208 | ||||||
chr10:98171686
|
A | C | 1 | a0002c0002t0001g0083 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-15+8289A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98171686 | ||||||
chr10:98171789
|
G | A | 333 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(330): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-15+8392G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98171789 | ||||||
chr10:98171943
|
T | G | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-15+8546T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98171943 | ||||||
chr10:98172083
|
G | A | 5 | a0001c0001t0001g0110a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | NA18967.hp1 NA18977.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+8686G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98172083 | ||||||
chr10:98172133
|
T | C | 1 | a0001c0001t0002g0337 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-15+8736T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98172133 | ||||||
chr10:98172204
|
C | T | 2 | a0001c0001t0002g0314a0001c0001t0002g0333 | 2 | HG02080.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.-15+8807C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98172204 | ||||||
chr10:98172312
|
G | T | 1 | a0003c0003t0003g0190 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-15+8915G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98172312 | ||||||
chr10:98172324
|
G | A | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-15+8927G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98172324 | ||||||
chr10:98172389
|
G | A | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-15+8992G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98172389 | ||||||
chr10:98172442
|
A | G | 1 | a0003c0003t0003g0164 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-15+9045A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98172442 | ||||||
chr10:98172511
|
G | A | 4 | a0003c0003t0003g0168a0003c0003t0003g0169a0003c0003t0003g0170others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+9114G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98172511 | ||||||
chr10:98172522
|
G | A | 2 | a0002c0002t0001g0041a0013c0015t0001g0137 | 2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-15+9125G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98172522 | ||||||
chr10:98172563
|
C | T | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-15+9166C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98172563 | ||||||
chr10:98172660
|
C | T | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-15+9263C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98172660 | ||||||
chr10:98173034
|
T | A | 1 | a0002c0002t0001g0099 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-15+9637T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98173034 | ||||||
chr10:98173065
|
G | C | 1 | a0002c0002t0001g0062 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-15+9668G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98173065 | ||||||
chr10:98173333
|
A | G | 333 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(330): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-15+9936A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98173333 | ||||||
chr10:98173386
|
G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(48): Show | 58 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.-15+9989G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98173386 | ||||||
chr10:98173507
|
C | T | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-15+10110C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98173507 | ||||||
chr10:98173608
|
G | A | 1 | a0010c0011t0002g0291 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-15+10211G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98173608 | ||||||
chr10:98173761
|
C | T | 1 | a0001c0001t0002g0305 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-15+10364C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98173761 | ||||||
chr10:98174248
|
T | C | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-15+10851T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98174248 | ||||||
chr10:98174577
|
T | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0114a0001c0001t0001g0116others(12): Show | 16 | HG01192.hp2 HG01361.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+11180T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98174577 | ||||||
chr10:98174844
|
A | G | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-15+11447A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98174844 | ||||||
chr10:98174890
|
C | A | 1 | a0001c0001t0001g0110 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-15+11493C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98174890 | ||||||
chr10:98174905
|
A | G | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-15+11508A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98174905 | ||||||
chr10:98174911
|
G | A | 1 | a0002c0002t0001g0032 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-15+11514G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98174911 | ||||||
chr10:98174966
|
T | A | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-15+11569T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98174966 | ||||||
chr10:98175014
|
A | G | 1 | a0002c0002t0001g0094 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-15+11617A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98175014 | ||||||
chr10:98175072
|
C | T | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-15+11675C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98175072 | ||||||
chr10:98175075
|
G | A | 8 | a0001c0001t0002g0195a0003c0003t0005g0224a0003c0003t0005g0225others(5): Show | 8 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+11678G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98175075 | ||||||
chr10:98175403
|
C | G | 2 | a0011c0008t0001g0009a0019c0022t0001g0031 | 3 | HG02486.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-15+12006C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98175403 | ||||||
chr10:98175495
|
G | A | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-15+12098G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98175495 | ||||||
chr10:98175509
|
T | C | 1 | a0001c0001t0002g0237 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-15+12112T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98175509 | ||||||
chr10:98176061
|
A | G | 1 | a0001c0001t0002g0286 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-15+12664A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98176061 | ||||||
chr10:98176118
|
G | A | 2 | a0001c0001t0002g0204a0001c0001t0002g0293 | 2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-15+12721G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98176118 | ||||||
chr10:98176188
|
A | C | 82 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0005others(79): Show | 99 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.-15+12791A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98176188 | ||||||
chr10:98176223
|
C | T | 334 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(331): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.-15+12826C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98176223 | ||||||
chr10:98176425
|
T | C | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-15+13028T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98176425 | ||||||
chr10:98176457
|
C | G | 5 | a0001c0001t0006g0241a0001c0001t0006g0242a0001c0001t0006g0243others(2): Show | 5 | HG02109.hp1 HG02809.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+13060C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98176457 | ||||||
chr10:98176558
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-15+13161T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98176558 | ||||||
chr10:98176765
|
TCTTTA | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 7 | NA18941.hp2 NA18951.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+13374_-15+1337 others(9): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98176765 | |||||
chr10:98176788
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-15+13391A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98176788 | ||||||
chr10:98176792
|
G | A | 1 | a0001c0001t0002g0337 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-15+13395G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98176792 | ||||||
chr10:98176849
|
CT | C | 7 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+13461delT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98176849 | |||||
chr10:98176856
|
T | G | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-15+13459T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98176856 | ||||||
chr10:98177020
|
T | A | 1 | a0001c0001t0002g0238 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-15+13623T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98177020 | ||||||
chr10:98177044
|
A | G | 2 | a0001c0010t0007g0028a0001c0010t0007g0029 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-15+13647A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98177044 | ||||||
chr10:98177070
|
G | A | 2 | a0003c0003t0003g0168a0003c0003t0003g0180 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-15+13673G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98177070 | ||||||
chr10:98177081
|
G | A | 1 | a0006c0005t0004g0150 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-15+13684G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98177081 | ||||||
chr10:98177191
|
C | G | 1 | a0001c0001t0002g0276 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-15+13794C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98177191 | ||||||
chr10:98177247
|
T | C | 1 | a0001c0001t0002g0322 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-15+13850T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98177247 | ||||||
chr10:98177311
|
C | T | 1 | a0003c0003t0003g0174 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-15+13914C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98177311 | ||||||
chr10:98177442
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-15+14045C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98177442 | ||||||
chr10:98177515
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-15+14118G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98177515 | ||||||
chr10:98177658
|
G | T | 1 | a0001c0001t0002g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-15+14261G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98177658 | ||||||
chr10:98177744
|
C | G | 1 | a0009c0009t0001g0091 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-15+14347C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98177744 | ||||||
chr10:98177769
|
T | C | 167 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(164): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.-15+14372T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98177769 | ||||||
chr10:98177809
|
A | G | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-15+14412A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98177809 | ||||||
chr10:98177894
|
T | C | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-15+14497T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98177894 | ||||||
chr10:98177937
|
T | C | 1 | a0001c0001t0002g0273 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-15+14540T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98177937 | ||||||
chr10:98178008
|
C | G | 1 | a0002c0002t0001g0082 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-15+14611C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98178008 | ||||||
chr10:98178033
|
T | C | 1 | a0003c0003t0003g0161 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-15+14636T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98178033 | ||||||
chr10:98178174
|
T | G | 1 | a0004c0004t0004g0146 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-15+14777T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98178174 | ||||||
chr10:98178227
|
G | A | 1 | a0001c0001t0002g0275 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-15+14830G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98178227 | ||||||
chr10:98178370
|
G | T | 1 | a0002c0002t0001g0062 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-15+14973G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98178370 | ||||||
chr10:98178478
|
A | G | 1 | a0001c0001t0002g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-15+15081A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98178478 | ||||||
chr10:98178544
|
C | T | 1 | a0001c0001t0002g0026 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-15+15147C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98178544 | ||||||
chr10:98178642
|
A | C | 1 | a0022c0017t0002g0335 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-15+15245A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98178642 | ||||||
chr10:98179060
|
C | G | 1 | a0022c0017t0002g0335 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-15+15663C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98179060 | ||||||
chr10:98179114
|
T | G | 1 | a0002c0002t0001g0074 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-15+15717T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98179114 | ||||||
chr10:98179178
|
A | G | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-15+15781A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98179178 | ||||||
chr10:98179322
|
A | C | 1 | a0016c0023t0002g0223 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-15+15925A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98179322 | ||||||
chr10:98179439
|
C | G | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-15+16042C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98179439 | ||||||
chr10:98179495
|
G | A | 2 | a0001c0010t0007g0028a0001c0010t0007g0029 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-15+16098G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98179495 | ||||||
chr10:98179589
|
G | T | 1 | a0002c0002t0001g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-15+16192G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98179589 | ||||||
chr10:98179627
|
C | T | 33 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(30): Show | 34 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.-15+16230C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98179627 | ||||||
chr10:98179632
|
G | A | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-15+16235G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98179632 | ||||||
chr10:98179802
|
A | G | 329 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(326): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.-15+16405A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98179802 | ||||||
chr10:98180157
|
G | A | 1 | a0004c0004t0004g0152 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-15+16760G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98180157 | ||||||
chr10:98180184
|
G | T | 1 | a0002c0002t0001g0108 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-15+16787G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98180184 | ||||||
chr10:98180272
|
G | A | 1 | a0001c0001t0002g0295 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-15+16875G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98180272 | ||||||
chr10:98180323
|
C | T | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-15+16926C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98180323 | ||||||
chr10:98180391
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-15+16994A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98180391 | ||||||
chr10:98180439
|
T | G | 1 | a0001c0001t0002g0259 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-15+17042T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98180439 | ||||||
chr10:98180482
|
C | T | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-15+17085C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98180482 | ||||||
chr10:98180483
|
G | A | 1 | a0002c0002t0001g0082 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-15+17086G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98180483 | ||||||
chr10:98180920
|
C | T | 7 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+17523C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98180920 | ||||||
chr10:98180935
|
A | G | 1 | a0001c0001t0002g0192 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-15+17538A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98180935 | ||||||
chr10:98180972
|
C | T | 1 | a0008c0014t0001g0070 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-15+17575C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98180972 | ||||||
chr10:98181548
|
A | G | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-15+18151A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98181548 | ||||||
chr10:98181635
|
C | T | 5 | a0003c0003t0003g0161a0003c0003t0003g0168a0003c0003t0003g0169others(2): Show | 5 | HG00280.hp2 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+18238C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98181635 | ||||||
chr10:98181694
|
T | C | 3 | a0002c0002t0001g0069a0002c0002t0001g0073a0002c0002t0001g0082 | 3 | HG02698.hp2 HG03239.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.-15+18297T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98181694 | ||||||
chr10:98181803
|
C | T | 1 | a0001c0001t0002g0328 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-15+18406C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98181803 | ||||||
chr10:98181804
|
G | A | 1 | a0003c0003t0005g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-15+18407G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98181804 | ||||||
chr10:98181943
|
T | C | 333 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(330): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-15+18546T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98181943 | ||||||
chr10:98182020
|
G | C | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-15+18623G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98182020 | ||||||
chr10:98182088
|
C | G | 1 | a0016c0023t0002g0223 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-15+18691C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98182088 | ||||||
chr10:98182126
|
T | C | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-15+18729T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98182126 | ||||||
chr10:98182284
|
G | T | 1 | a0002c0002t0001g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+18887G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98182284 | ||||||
chr10:98182319
|
C | G | 2 | a0012c0013t0002g0206a0012c0013t0002g0207 | 2 | HG01496.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-15+18922C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98182319 | ||||||
chr10:98182543
|
G | A | 3 | a0001c0001t0002g0239a0001c0001t0002g0260a0001c0001t0002g0336 | 3 | HG00544.hp1 HG02040.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-15+19146G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98182543 | ||||||
chr10:98182653
|
A | G | 2 | a0002c0002t0001g0032a0002c0002t0001g0033 | 2 | NA18997.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-15+19256A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98182653 | ||||||
chr10:98182850
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-15+19453A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98182850 | ||||||
chr10:98182864
|
C | T | 1 | a0005c0007t0003g0231 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-15+19467C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98182864 | ||||||
chr10:98182901
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-15+19504G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98182901 | ||||||
chr10:98182982
|
C | T | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-15+19585C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98182982 | ||||||
chr10:98183056
|
A | G | 1 | a0003c0003t0003g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-15+19659A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98183056 | ||||||
chr10:98183083
|
C | T | 3 | a0001c0001t0002g0268a0001c0001t0002g0281a0001c0001t0002g0345 | 3 | HG00642.hp2 HG01074.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-15+19686C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98183083 | ||||||
chr10:98183160
|
C | T | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-15+19763C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98183160 | ||||||
chr10:98183165
|
G | A | 87 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0005others(84): Show | 104 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.-15+19768G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98183165 | ||||||
chr10:98183331
|
C | CT | 114 | a0001c0001t0001g0215a0001c0001t0002g0007a0001c0001t0002g0008others(111): Show | 121 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.-15+19950dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98183331 | |||||
chr10:98183331
|
CT | C | 61 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0018others(58): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.-15+19950delT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98183331 | |||||
chr10:98183453
|
G | A | 1 | a0002c0002t0001g0033 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-15+20056G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98183453 | ||||||
chr10:98183811
|
C | T | 87 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0005others(84): Show | 104 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.-15+20414C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98183811 | ||||||
chr10:98183949
|
C | T | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-15+20552C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98183949 | ||||||
chr10:98183958
|
G | GT | 24 | a0001c0001t0001g0110a0001c0001t0001g0126a0001c0001t0001g0214others(21): Show | 25 | HG01081.hp2 HG01934.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-15+20576dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98183958 | |||||
chr10:98183958
|
G | GTTTTTTT others(1): Show |
27 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0161others(24): Show | 28 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.-15+20569_-15+2057 others(12): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98183958 | |||||
chr10:98183958
|
G | GTTTTTTT others(2): Show |
6 | a0003c0003t0003g0160a0003c0003t0003g0170a0003c0003t0003g0174others(3): Show | 6 | HG00639.hp1 HG00733.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+20568_-15+2057 others(13): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98183958 | |||||
chr10:98183958
|
G | GTTTTTTT others(13): Show |
1 | a0005c0007t0003g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-15+20576_-15+2057 others(24): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98183958 | |||||
chr10:98183958
|
G | GTTTTTTT others(15): Show |
2 | a0003c0012t0003g0159a0005c0007t0003g0231 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-15+20576_-15+2057 others(26): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98183958 | |||||
chr10:98183958
|
G | GTTTTTTT others(20): Show |
1 | a0003c0012t0003g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-15+20576_-15+2057 others(31): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98183958 | |||||
chr10:98183958
|
GT | G | 7 | a0001c0001t0002g0272a0001c0001t0002g0297a0001c0001t0002g0298others(4): Show | 7 | NA18942.hp2 NA18946.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+20576delT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98183958 | |||||
chr10:98183958
|
GTT | G | 115 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(112): Show | 122 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.-15+20575_-15+2057 others(6): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98183958 | |||||
chr10:98183992
|
T | C | 2 | a0002c0002t0001g0117a0002c0002t0001g0120 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-15+20595T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98183992 | ||||||
chr10:98184059
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-15+20662G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98184059 | ||||||
chr10:98184129
|
C | T | 1 | a0002c0002t0001g0044 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-15+20732C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98184129 | ||||||
chr10:98184521
|
G | C | 1 | a0003c0003t0003g0184 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-15+21124G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98184521 | ||||||
chr10:98184575
|
A | G | 333 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(330): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-15+21178A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98184575 | ||||||
chr10:98184607
|
C | T | 6 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0227others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+21210C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98184607 | ||||||
chr10:98184715
|
A | G | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-15+21318A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98184715 | ||||||
chr10:98184779
|
C | A | 3 | a0003c0003t0003g0171a0003c0003t0003g0172a0003c0003t0003g0173 | 3 | HG03490.hp1 HG03492.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-15+21382C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98184779 | ||||||
chr10:98184824
|
G | A | 1 | a0002c0002t0001g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-15+21427G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98184824 | ||||||
chr10:98184873
|
T | C | 1 | a0002c0002t0001g0075 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-15+21476T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98184873 | ||||||
chr10:98185008
|
T | C | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-15+21611T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98185008 | ||||||
chr10:98185030
|
A | G | 1 | a0001c0001t0008g0119 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-15+21633A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98185030 | ||||||
chr10:98185394
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-15+21997G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98185394 | ||||||
chr10:98185440
|
T | G | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-15+22043T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98185440 | ||||||
chr10:98185793
|
G | T | 51 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(48): Show | 58 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.-14-22308G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98185793 | ||||||
chr10:98186311
|
G | A | 2 | a0005c0007t0003g0232a0005c0007t0003g0233 | 2 | HG01255.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-14-21790G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98186311 | ||||||
chr10:98186463
|
C | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(141): Show | 169 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.-14-21638C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98186463 | ||||||
chr10:98186571
|
C | T | 346 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(343): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.-14-21530C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98186571 | ||||||
chr10:98186574
|
T | C | 1 | a0001c0020t0004g0151 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-14-21527T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98186574 | ||||||
chr10:98186736
|
A | G | 1 | a0002c0002t0001g0061 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-14-21365A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98186736 | ||||||
chr10:98186847
|
T | G | 1 | a0001c0001t0002g0252 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-14-21254T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98186847 | ||||||
chr10:98187312
|
C | T | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-14-20789C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98187312 | ||||||
chr10:98187388
|
G | C | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-14-20713G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98187388 | ||||||
chr10:98187409
|
GTCATAA | G | 46 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.-14-20686_-14-2068 others(10): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98187409 | |||||
chr10:98187540
|
A | G | 1 | a0001c0001t0002g0332 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-14-20561A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98187540 | ||||||
chr10:98187660
|
A | G | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-20441A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98187660 | ||||||
chr10:98187730
|
C | CT | 46 | a0001c0001t0001g0034a0001c0001t0002g0264a0001c0001t0002g0287others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.-14-20349dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98187730 | |||||
chr10:98187730
|
C | CTT | 9 | a0003c0003t0003g0174a0003c0003t0003g0188a0003c0003t0005g0224others(6): Show | 9 | HG01891.hp2 HG02148.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-14-20350_-14-2034 others(6): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98187730 | |||||
chr10:98187730
|
CT | C | 25 | a0001c0001t0001g0038a0001c0001t0001g0113a0001c0001t0001g0130others(22): Show | 25 | HG00099.hp1 HG00323.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-14-20349delT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98187730 | |||||
chr10:98187757
|
G | T | 42 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(39): Show | 43 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.-14-20344G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98187757 | ||||||
chr10:98187812
|
C | T | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-14-20289C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98187812 | ||||||
chr10:98187963
|
G | A | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-20138G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98187963 | ||||||
chr10:98188014
|
G | A | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-14-20087G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98188014 | ||||||
chr10:98188063
|
T | G | 1 | a0003c0003t0003g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-14-20038T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98188063 | ||||||
chr10:98188106
|
CAAATT | C | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-14-19992_-14-1998 others(9): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98188106 | |||||
chr10:98188196
|
G | A | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-14-19905G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98188196 | ||||||
chr10:98188212
|
A | G | 1 | a0001c0001t0001g0014 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-14-19889A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98188212 | ||||||
chr10:98188329
|
A | G | 1 | a0023c0026t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-14-19772A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98188329 | ||||||
chr10:98188479
|
C | G | 46 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.-14-19622C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98188479 | ||||||
chr10:98188496
|
A | G | 1 | a0001c0001t0002g0252 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-14-19605A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98188496 | ||||||
chr10:98188690
|
T | C | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-14-19411T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98188690 | ||||||
chr10:98188732
|
G | A | 93 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0005others(90): Show | 111 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.-14-19369G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98188732 | ||||||
chr10:98188749
|
C | T | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-14-19352C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98188749 | ||||||
chr10:98189021
|
G | A | 8 | a0003c0003t0003g0181a0003c0003t0003g0182a0003c0003t0003g0183others(5): Show | 8 | HG00733.hp1 HG01175.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-19080G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98189021 | ||||||
chr10:98189057
|
T | C | 12 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0194others(9): Show | 13 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14-19044T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98189057 | ||||||
chr10:98189105
|
G | C | 46 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.-14-18996G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98189105 | ||||||
chr10:98189174
|
T | C | 1 | a0001c0001t0002g0342 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-14-18927T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98189174 | ||||||
chr10:98189410
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-14-18691G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98189410 | ||||||
chr10:98189503
|
T | C | 333 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(330): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-14-18598T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98189503 | ||||||
chr10:98189567
|
T | C | 2 | a0002c0002t0001g0046a0002c0002t0001g0047 | 2 | HG03927.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-14-18534T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98189567 | ||||||
chr10:98189696
|
A | G | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-18405A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98189696 | ||||||
chr10:98189772
|
A | C | 1 | a0002c0002t0001g0060 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-14-18329A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98189772 | ||||||
chr10:98190029
|
G | A | 1 | a0002c0002t0001g0074 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-14-18072G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98190029 | ||||||
chr10:98190041
|
A | G | 1 | a0001c0001t0002g0331 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-14-18060A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98190041 | ||||||
chr10:98190056
|
A | G | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-14-18045A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98190056 | ||||||
chr10:98190094
|
T | G | 4 | a0002c0002t0001g0006a0002c0002t0001g0043a0002c0002t0001g0077others(1): Show | 6 | HG01346.hp2 HG02698.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-18007T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98190094 | ||||||
chr10:98190156
|
C | T | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-14-17945C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98190156 | ||||||
chr10:98190223
|
G | T | 2 | a0001c0010t0007g0028a0001c0010t0007g0029 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-14-17878G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98190223 | ||||||
chr10:98190300
|
T | G | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-14-17801T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98190300 | ||||||
chr10:98190604
|
T | A | 5 | a0002c0002t0001g0088a0002c0002t0001g0208a0002c0002t0001g0280others(2): Show | 5 | HG02970.hp2 HG03579.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-17497T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98190604 | ||||||
chr10:98190676
|
T | C | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-17425T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98190676 | ||||||
chr10:98190741
|
T | C | 53 | a0001c0001t0002g0007a0001c0001t0002g0019a0001c0001t0002g0025others(50): Show | 56 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.-14-17360T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98190741 | ||||||
chr10:98190828
|
A | C | 1 | a0022c0017t0002g0335 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-14-17273A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98190828 | ||||||
chr10:98191289
|
A | G | 46 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.-14-16812A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98191289 | ||||||
chr10:98191441
|
A | ATAGATGT others(6): Show |
45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-14-16658_-14-1664 others(17): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98191441 | |||||
chr10:98191462
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-14-16639G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98191462 | ||||||
chr10:98191493
|
T | C | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-14-16608T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98191493 | ||||||
chr10:98191547
|
A | G | 1 | a0002c0002t0001g0095 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-14-16554A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98191547 | ||||||
chr10:98191894
|
G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(48): Show | 58 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.-14-16207G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98191894 | ||||||
chr10:98191915
|
C | T | 1 | a0002c0002t0001g0045 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-14-16186C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98191915 | ||||||
chr10:98191985
|
T | C | 334 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(331): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.-14-16116T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98191985 | ||||||
chr10:98192005
|
A | C | 1 | a0001c0001t0001g0218 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-14-16096A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98192005 | ||||||
chr10:98192056
|
C | T | 1 | a0002c0002t0001g0087 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-14-16045C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98192056 | ||||||
chr10:98192394
|
T | G | 1 | a0001c0001t0001g0217 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-14-15707T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98192394 | ||||||
chr10:98192463
|
A | G | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-14-15638A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98192463 | ||||||
chr10:98192558
|
T | C | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-14-15543T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98192558 | ||||||
chr10:98192715
|
A | G | 6 | a0004c0004t0004g0016a0004c0004t0004g0145a0004c0004t0004g0146others(3): Show | 7 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-15386A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98192715 | ||||||
chr10:98192777
|
C | G | 134 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0018others(131): Show | 142 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-14-15324C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98192777 | ||||||
chr10:98192880
|
A | T | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-15221A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98192880 | ||||||
chr10:98193071
|
A | T | 1 | a0002c0002t0001g0044 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-14-15030A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98193071 | ||||||
chr10:98193097
|
TCAA | T | 82 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0005others(79): Show | 99 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.-14-14999_-14-1499 others(7): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98193097 | |||||
chr10:98193513
|
A | G | 167 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(164): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.-14-14588A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98193513 | ||||||
chr10:98193551
|
C | T | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-14-14550C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98193551 | ||||||
chr10:98193626
|
C | T | 2 | a0001c0001t0004g0002a0001c0001t0004g0221 | 7 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-14475C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98193626 | ||||||
chr10:98193757
|
A | G | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-14-14344A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98193757 | ||||||
chr10:98193986
|
T | C | 2 | a0003c0003t0003g0190a0020c0024t0003g0179 | 2 | HG00323.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-14-14115T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98193986 | ||||||
chr10:98194014
|
C | A | 2 | a0001c0010t0007g0028a0001c0010t0007g0029 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-14-14087C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98194014 | ||||||
chr10:98194038
|
AAAG | A | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-14-14057_-14-1405 others(7): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98194038 | |||||
chr10:98194132
|
A | G | 42 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(39): Show | 43 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.-14-13969A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98194132 | ||||||
chr10:98194136
|
A | T | 46 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.-14-13965A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98194136 | ||||||
chr10:98194141
|
G | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0125a0001c0001t0001g0129 | 4 | HG00639.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-13960G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98194141 | ||||||
chr10:98194222
|
A | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(141): Show | 169 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.-14-13879A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98194222 | ||||||
chr10:98194254
|
G | A | 1 | a0001c0010t0007g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-13847G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98194254 | ||||||
chr10:98194410
|
A | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(52): Show | 62 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-14-13691A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98194410 | ||||||
chr10:98194545
|
G | A | 345 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(342): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.-14-13556G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98194545 | ||||||
chr10:98194781
|
C | CTGT | 46 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.-14-13319_-14-1331 others(7): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98194781 | |||||
chr10:98194943
|
T | C | 2 | a0003c0003t0003g0017a0003c0003t0003g0174 | 3 | HG00140.hp1 HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.-14-13158T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98194943 | ||||||
chr10:98195407
|
C | CTA | 6 | a0002c0002t0001g0071a0002c0002t0001g0083a0002c0002t0001g0141others(3): Show | 6 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-12691_-14-1269 others(6): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98195407 | |||||
chr10:98195445
|
CT | C | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0194others(10): Show | 14 | HG00323.hp1 HG01081.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-14-12642delT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98195445 | |||||
chr10:98195473
|
C | G | 1 | a0001c0001t0002g0306 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-14-12628C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98195473 | ||||||
chr10:98195593
|
AC | A | 117 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(114): Show | 124 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.-14-12507delC | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98195593 | ||||||
chr10:98195594
|
C | A | 57 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(54): Show | 59 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.-14-12507C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98195594 | ||||||
chr10:98195596
|
A | C | 2 | a0001c0001t0001g0014a0002c0002t0001g0047 | 3 | HG02615.hp1 HG02886.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-14-12505A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98195596 | ||||||
chr10:98195603
|
A | C | 54 | a0001c0001t0002g0007a0001c0001t0002g0019a0001c0001t0002g0025others(51): Show | 57 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.-14-12498A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98195603 | ||||||
chr10:98195702
|
C | A | 2 | a0001c0001t0002g0236a0001c0001t0002g0274 | 2 | HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-14-12399C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98195702 | ||||||
chr10:98195812
|
T | G | 3 | a0001c0001t0007g0023a0001c0010t0007g0028a0001c0010t0007g0029 | 3 | HG02818.hp2 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-14-12289T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98195812 | ||||||
chr10:98195877
|
A | G | 1 | a0001c0001t0002g0194 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-14-12224A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98195877 | ||||||
chr10:98195894
|
G | A | 2 | a0003c0003t0003g0017a0003c0003t0003g0174 | 3 | HG00140.hp1 HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.-14-12207G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98195894 | ||||||
chr10:98196436
|
T | C | 1 | a0004c0004t0004g0145 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-14-11665T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98196436 | ||||||
chr10:98196570
|
T | C | 1 | a0001c0001t0002g0201 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-14-11531T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98196570 | ||||||
chr10:98196640
|
G | A | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-11461G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98196640 | ||||||
chr10:98196925
|
T | C | 1 | a0001c0001t0002g0327 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-14-11176T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98196925 | ||||||
chr10:98196945
|
C | T | 1 | a0003c0003t0003g0181 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-14-11156C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98196945 | ||||||
chr10:98197094
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0002g0333 | 2 | HG00639.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.-14-11007C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98197094 | ||||||
chr10:98197207
|
GC | G | 145 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(142): Show | 170 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.-14-10886delC | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98197207 | |||||
chr10:98197282
|
G | T | 1 | a0002c0002t0001g0051 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-14-10819G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98197282 | ||||||
chr10:98197436
|
A | G | 1 | a0001c0001t0002g0328 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-14-10665A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98197436 | ||||||
chr10:98197514
|
G | A | 6 | a0001c0001t0001g0111a0001c0001t0001g0126a0001c0001t0001g0128others(3): Show | 6 | HG01975.hp2 HG02015.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-10587G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98197514 | ||||||
chr10:98197524
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-14-10577G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98197524 | ||||||
chr10:98197548
|
T | G | 1 | a0001c0001t0002g0204 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-14-10553T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98197548 | ||||||
chr10:98197750
|
A | G | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-14-10351A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98197750 | ||||||
chr10:98197965
|
A | G | 2 | a0011c0008t0001g0009a0019c0022t0001g0031 | 3 | HG02486.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-14-10136A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98197965 | ||||||
chr10:98198059
|
G | A | 1 | a0001c0001t0002g0294 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-14-10042G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98198059 | ||||||
chr10:98198282
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-14-9819A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98198282 | ||||||
chr10:98198325
|
T | C | 333 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(330): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-14-9776T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98198325 | ||||||
chr10:98198411
|
C | T | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-14-9690C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98198411 | ||||||
chr10:98198500
|
A | AT | 316 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(313): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.-14-9599dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98198500 | |||||
chr10:98198523
|
A | G | 3 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0277 | 3 | HG01978.hp2 HG02300.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-14-9578A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98198523 | ||||||
chr10:98198540
|
C | T | 1 | a0019c0022t0001g0031 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-14-9561C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98198540 | ||||||
chr10:98198549
|
G | GA | 164 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(161): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.-14-9540dupA | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98198549 | |||||
chr10:98198549
|
GA | G | 6 | a0001c0001t0001g0014a0001c0010t0007g0028a0001c0010t0007g0029others(3): Show | 7 | HG01496.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-9540delA | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98198549 | |||||
chr10:98198787
|
C | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0037 | 3 | NA18972.hp1 NA19012.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-14-9314C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98198787 | ||||||
chr10:98198931
|
T | C | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-14-9170T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98198931 | ||||||
chr10:98198941
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-14-9160A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98198941 | ||||||
chr10:98199048
|
G | A | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-9053G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98199048 | ||||||
chr10:98199050
|
A | AT | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-14-9044dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98199050 | |||||
chr10:98199094
|
C | G | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-14-9007C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98199094 | ||||||
chr10:98199254
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-14-8847G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98199254 | ||||||
chr10:98199443
|
AT | A | 14 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(11): Show | 15 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-14-8648delT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98199443 | |||||
chr10:98199451
|
T | C | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-8650T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98199451 | ||||||
chr10:98199854
|
A | G | 1 | a0002c0002t0001g0077 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-14-8247A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98199854 | ||||||
chr10:98199986
|
T | C | 1 | a0001c0001t0002g0299 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-14-8115T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98199986 | ||||||
chr10:98200121
|
A | G | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-14-7980A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98200121 | ||||||
chr10:98200235
|
A | G | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-14-7866A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98200235 | ||||||
chr10:98200255
|
TTGAG | T | 87 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0005others(84): Show | 104 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.-14-7844_-14-7841d others(6): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98200255 | |||||
chr10:98200268
|
G | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(52): Show | 62 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-14-7833G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98200268 | ||||||
chr10:98200455
|
T | C | 1 | a0001c0001t0002g0193 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-14-7646T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98200455 | ||||||
chr10:98200476
|
C | G | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-14-7625C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98200476 | ||||||
chr10:98200532
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-14-7569T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98200532 | ||||||
chr10:98200581
|
A | G | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-14-7520A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98200581 | ||||||
chr10:98200753
|
C | A | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-14-7348C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98200753 | ||||||
chr10:98200886
|
C | T | 1 | a0001c0001t0002g0346 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-14-7215C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98200886 | ||||||
chr10:98200952
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-14-7149G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98200952 | ||||||
chr10:98200982
|
A | G | 1 | a0002c0002t0001g0044 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-14-7119A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98200982 | ||||||
chr10:98200990
|
C | T | 46 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.-14-7111C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98200990 | ||||||
chr10:98201240
|
C | G | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-14-6861C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98201240 | ||||||
chr10:98201281
|
T | G | 1 | a0023c0026t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-14-6820T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98201281 | ||||||
chr10:98201401
|
A | G | 46 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.-14-6700A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98201401 | ||||||
chr10:98201537
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-14-6564G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98201537 | ||||||
chr10:98201602
|
A | G | 2 | a0001c0010t0007g0028a0001c0010t0007g0029 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-14-6499A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98201602 | ||||||
chr10:98201655
|
A | G | 1 | a0003c0003t0003g0170 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-14-6446A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98201655 | ||||||
chr10:98201709
|
A | G | 1 | a0002c0002t0001g0077 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-14-6392A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98201709 | ||||||
chr10:98201728
|
T | C | 2 | a0002c0002t0001g0117a0002c0002t0001g0120 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-14-6373T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98201728 | ||||||
chr10:98201876
|
A | G | 1 | a0001c0001t0002g0299 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-14-6225A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98201876 | ||||||
chr10:98201881
|
A | AT | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-14-6200dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98201881 | |||||
chr10:98201881
|
AT | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(63): Show | 72 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.-14-6200delT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98201881 | |||||
chr10:98201881
|
ATT | A | 202 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0035others(199): Show | 227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-14-6201_-14-6200d others(4): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98201881 | |||||
chr10:98201881
|
ATTT | A | 12 | a0001c0001t0002g0238a0001c0001t0002g0247a0001c0001t0002g0251others(9): Show | 12 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-14-6202_-14-6200d others(5): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98201881 | |||||
chr10:98201901
|
T | A | 188 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(185): Show | 203 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.-14-6200T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98201901 | ||||||
chr10:98201921
|
A | G | 1 | a0002c0002t0001g0108 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-14-6180A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98201921 | ||||||
chr10:98202053
|
T | C | 1 | a0001c0001t0002g0337 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-14-6048T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98202053 | ||||||
chr10:98202123
|
A | T | 1 | a0001c0001t0002g0298 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-14-5978A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98202123 | ||||||
chr10:98202516
|
G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(48): Show | 58 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.-14-5585G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98202516 | ||||||
chr10:98202576
|
G | A | 1 | a0001c0001t0002g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14-5525G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98202576 | ||||||
chr10:98202659
|
C | T | 2 | a0008c0014t0001g0070a0008c0014t0001g0103 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-14-5442C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98202659 | ||||||
chr10:98202694
|
T | A | 333 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(330): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-14-5407T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98202694 | ||||||
chr10:98202858
|
G | GA | 12 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0194others(9): Show | 13 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14-5229dupA | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98202858 | |||||
chr10:98202858
|
GA | G | 7 | a0001c0001t0001g0121a0001c0010t0007g0028a0001c0010t0007g0029others(4): Show | 7 | HG01496.hp1 HG02027.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-5229delA | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98202858 | |||||
chr10:98202869
|
A | G | 1 | a0002c0002t0001g0053 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-14-5232A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98202869 | ||||||
chr10:98203072
|
T | C | 3 | a0002c0002t0001g0005a0002c0002t0001g0078a0002c0002t0001g0079 | 5 | NA18950.hp1 NA18991.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-5029T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98203072 | ||||||
chr10:98203213
|
T | G | 1 | a0001c0001t0002g0346 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-14-4888T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98203213 | ||||||
chr10:98203248
|
G | A | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-14-4853G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98203248 | ||||||
chr10:98203626
|
G | A | 1 | a0002c0002t0001g0080 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-14-4475G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98203626 | ||||||
chr10:98203883
|
A | C | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-4218A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98203883 | ||||||
chr10:98203963
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-14-4138G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98203963 | ||||||
chr10:98203989
|
G | T | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-14-4112G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98203989 | ||||||
chr10:98204136
|
C | T | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-14-3965C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98204136 | ||||||
chr10:98204137
|
G | A | 2 | a0003c0003t0005g0227a0003c0003t0005g0229 | 2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-14-3964G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98204137 | ||||||
chr10:98204376
|
C | G | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-14-3725C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98204376 | ||||||
chr10:98204542
|
C | T | 1 | a0001c0020t0004g0151 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-14-3559C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98204542 | ||||||
chr10:98204727
|
A | T | 1 | a0001c0001t0002g0299 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-14-3374A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98204727 | ||||||
chr10:98204734
|
A | C | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-14-3367A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98204734 | ||||||
chr10:98204748
|
C | T | 333 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(330): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-14-3353C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98204748 | ||||||
chr10:98204898
|
T | C | 5 | a0001c0001t0002g0303a0001c0001t0002g0307a0001c0001t0002g0308others(2): Show | 5 | HG01975.hp1 NA18948.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-3203T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98204898 | ||||||
chr10:98205011
|
G | A | 3 | a0001c0001t0012g0292a0010c0011t0002g0291a0010c0011t0002g0334 | 3 | HG00733.hp2 HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-14-3090G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98205011 | ||||||
chr10:98205169
|
C | T | 3 | a0001c0001t0002g0253a0001c0001t0002g0256a0001c0001t0002g0257 | 3 | HG01175.hp1 HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-14-2932C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98205169 | ||||||
chr10:98205302
|
C | G | 345 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(342): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.-14-2799C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98205302 | ||||||
chr10:98205313
|
AACTAGAA others(22): Show |
A | 2 | a0001c0001t0002g0236a0001c0001t0002g0274 | 2 | HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-14-2785_-14-2757d others(31): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98205313 | |||||
chr10:98205618
|
C | A | 1 | a0002c0002t0001g0054 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-14-2483C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98205618 | ||||||
chr10:98206043
|
C | A | 2 | a0011c0008t0001g0009a0019c0022t0001g0031 | 3 | HG02486.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-14-2058C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98206043 | ||||||
chr10:98206110
|
T | G | 3 | a0002c0002t0001g0006a0002c0002t0001g0043a0024c0027t0001g0076 | 5 | HG02698.hp1 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-1991T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98206110 | ||||||
chr10:98206157
|
C | T | 1 | a0002c0002t0001g0087 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-14-1944C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98206157 | ||||||
chr10:98206253
|
C | CG | 332 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(329): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.-14-1848_-14-1847i others(3): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98206253 | ||||||
chr10:98206281
|
T | C | 2 | a0001c0001t0002g0309a0001c0001t0002g0310 | 2 | HG02132.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.-14-1820T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98206281 | ||||||
chr10:98206327
|
TAA | T | 6 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0227others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-1759_-14-1758d others(4): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98206327 | |||||
chr10:98206350
|
A | G | 1 | a0001c0001t0011g0320 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-14-1751A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98206350 | ||||||
chr10:98206438
|
T | G | 1 | a0002c0002t0001g0065 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-14-1663T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98206438 | ||||||
chr10:98206465
|
G | T | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-14-1636G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98206465 | ||||||
chr10:98206598
|
CATT | C | 330 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(327): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.-14-1490_-14-1488d others(5): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr10 | 98206598 | |||||
chr10:98206646
|
G | A | 1 | a0002c0002t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-14-1455G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98206646 | ||||||
chr10:98206698
|
A | G | 5 | a0002c0002t0001g0042a0002c0002t0001g0052a0002c0002t0001g0054others(2): Show | 5 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-1403A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98206698 | ||||||
chr10:98206802
|
C | A | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-1299C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98206802 | ||||||
chr10:98206821
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-14-1280G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98206821 | ||||||
chr10:98207080
|
G | A | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-1021G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98207080 | ||||||
chr10:98207096
|
C | T | 1 | a0001c0001t0002g0337 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-14-1005C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98207096 | ||||||
chr10:98207324
|
G | T | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-777G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98207324 | ||||||
chr10:98207328
|
T | C | 1 | a0005c0007t0003g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-14-773T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98207328 | ||||||
chr10:98207358
|
A | G | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-14-743A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98207358 | ||||||
chr10:98207454
|
A | T | 1 | a0001c0001t0002g0200 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-14-647A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98207454 | ||||||
chr10:98207550
|
C | T | 2 | a0002c0002t0001g0059a0002c0002t0001g0101 | 2 | NA18966.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.-14-551C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98207550 | ||||||
chr10:98207668
|
T | G | 1 | a0001c0001t0002g0337 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-14-433T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98207668 | ||||||
chr10:98207811
|
C | G | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-14-290C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 4/9 | chr10 | 98207811 | ||||||
chr10:98210091
|
A | G | 6 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0227others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1785+192A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98210091 | ||||||
chr10:98210159
|
G | A | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1785+260G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98210159 | ||||||
chr10:98210165
|
G | A | 333 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(330): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1785+266G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98210165 | ||||||
chr10:98210519
|
C | T | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1785+620C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98210519 | ||||||
chr10:98210522
|
A | G | 5 | a0001c0001t0001g0110a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | NA18967.hp1 NA18977.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.1785+623A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98210522 | ||||||
chr10:98210580
|
T | G | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1785+681T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98210580 | ||||||
chr10:98210601
|
T | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0035others(1): Show | 5 | NA18972.hp1 NA18983.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1785+702T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98210601 | ||||||
chr10:98210854
|
G | A | 1 | a0002c0002t0001g0083 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1785+955G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98210854 | ||||||
chr10:98210874
|
A | C | 2 | a0001c0001t0002g0204a0001c0001t0002g0293 | 2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1785+975A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98210874 | ||||||
chr10:98211265
|
A | C | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1785+1366A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98211265 | ||||||
chr10:98211366
|
A | G | 1 | a0001c0020t0004g0151 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1785+1467A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98211366 | ||||||
chr10:98211467
|
A | G | 51 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(48): Show | 58 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1785+1568A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98211467 | ||||||
chr10:98211500
|
T | G | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1785+1601T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98211500 | ||||||
chr10:98211709
|
G | T | 1 | a0002c0002t0001g0077 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1785+1810G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98211709 | ||||||
chr10:98212081
|
A | G | 1 | a0001c0001t0002g0294 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1785+2182A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98212081 | ||||||
chr10:98212091
|
G | A | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.1785+2192G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98212091 | ||||||
chr10:98212093
|
A | G | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1785+2194A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98212093 | ||||||
chr10:98212355
|
T | A | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1785+2456T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98212355 | ||||||
chr10:98212366
|
T | G | 91 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0005others(88): Show | 108 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1785+2467T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98212366 | ||||||
chr10:98212460
|
C | T | 1 | a0002c0002t0001g0079 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1785+2561C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98212460 | ||||||
chr10:98212739
|
G | A | 346 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(343): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.1785+2840G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98212739 | ||||||
chr10:98212916
|
C | G | 87 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0005others(84): Show | 104 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1785+3017C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98212916 | ||||||
chr10:98212932
|
A | G | 1 | a0003c0003t0003g0176 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1785+3033A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98212932 | ||||||
chr10:98212977
|
G | A | 8 | a0003c0003t0003g0181a0003c0003t0003g0182a0003c0003t0003g0183others(5): Show | 8 | HG00733.hp1 HG01175.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1785+3078G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98212977 | ||||||
chr10:98213064
|
CT | C | 4 | a0001c0001t0002g0303a0001c0001t0002g0307a0001c0001t0002g0308others(1): Show | 4 | HG01975.hp1 NA18948.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1785+3169delT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 98213064 | |||||
chr10:98213136
|
A | G | 3 | a0001c0001t0007g0023a0001c0010t0007g0028a0001c0010t0007g0029 | 3 | HG02818.hp2 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1785+3237A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98213136 | ||||||
chr10:98213659
|
T | G | 2 | a0002c0002t0001g0005a0002c0002t0001g0079 | 4 | NA18950.hp1 NA19007.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.1785+3760T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98213659 | ||||||
chr10:98213667
|
C | A | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1785+3768C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98213667 | ||||||
chr10:98213714
|
A | C | 1 | a0001c0001t0002g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1785+3815A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98213714 | ||||||
chr10:98213839
|
G | A | 333 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(330): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1785+3940G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98213839 | ||||||
chr10:98213986
|
A | G | 1 | a0002c0002t0001g0077 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1785+4087A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98213986 | ||||||
chr10:98214043
|
C | A | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.1785+4144C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98214043 | ||||||
chr10:98214081
|
C | T | 1 | a0001c0001t0002g0310 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1785+4182C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98214081 | ||||||
chr10:98214114
|
T | C | 1 | a0001c0001t0002g0193 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1785+4215T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98214114 | ||||||
chr10:98214151
|
A | G | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1785+4252A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98214151 | ||||||
chr10:98214310
|
T | C | 1 | a0002c0002t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1785+4411T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98214310 | ||||||
chr10:98214325
|
T | C | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.1785+4426T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98214325 | ||||||
chr10:98214332
|
T | C | 1 | a0015c0025t0001g0210 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1785+4433T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98214332 | ||||||
chr10:98214334
|
G | A | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1785+4435G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98214334 | ||||||
chr10:98214709
|
A | G | 1 | a0002c0002t0001g0044 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1785+4810A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98214709 | ||||||
chr10:98214722
|
A | G | 1 | a0022c0017t0002g0335 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1785+4823A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98214722 | ||||||
chr10:98214902
|
C | T | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1785+5003C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98214902 | ||||||
chr10:98215019
|
T | G | 1 | a0001c0001t0001g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1785+5120T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98215019 | ||||||
chr10:98215057
|
C | T | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.1785+5158C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98215057 | ||||||
chr10:98215404
|
AT | A | 54 | a0001c0001t0002g0007a0001c0001t0002g0019a0001c0001t0002g0025others(51): Show | 57 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1785+5514delT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 98215404 | |||||
chr10:98215472
|
T | G | 1 | a0003c0003t0003g0172 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1785+5573T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98215472 | ||||||
chr10:98215482
|
C | A | 2 | a0011c0008t0001g0009a0019c0022t0001g0031 | 3 | HG02486.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1785+5583C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98215482 | ||||||
chr10:98215905
|
G | A | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1785+6006G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98215905 | ||||||
chr10:98215940
|
A | G | 2 | a0001c0001t0004g0002a0001c0001t0004g0221 | 7 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1785+6041A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98215940 | ||||||
chr10:98215969
|
C | T | 1 | a0001c0001t0002g0289 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1785+6070C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98215969 | ||||||
chr10:98215970
|
A | G | 333 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(330): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1785+6071A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98215970 | ||||||
chr10:98216212
|
T | C | 2 | a0012c0013t0002g0206a0012c0013t0002g0207 | 2 | HG01496.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1785+6313T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98216212 | ||||||
chr10:98216317
|
C | T | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.1785+6418C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98216317 | ||||||
chr10:98216323
|
A | G | 2 | a0008c0014t0001g0070a0008c0014t0001g0103 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1785+6424A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98216323 | ||||||
chr10:98216414
|
T | G | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1785+6515T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98216414 | ||||||
chr10:98216483
|
A | G | 3 | a0001c0001t0002g0344a0001c0010t0007g0028a0001c0010t0007g0029 | 3 | HG02818.hp2 HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1785+6584A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98216483 | ||||||
chr10:98216767
|
G | A | 1 | a0002c0002t0001g0077 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1785+6868G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98216767 | ||||||
chr10:98216838
|
C | G | 1 | a0002c0002t0001g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1785+6939C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98216838 | ||||||
chr10:98216854
|
A | G | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.1785+6955A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98216854 | ||||||
chr10:98216865
|
T | C | 333 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(330): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1785+6966T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98216865 | ||||||
chr10:98216982
|
A | G | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.1785+7083A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98216982 | ||||||
chr10:98217096
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1785+7197T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98217096 | ||||||
chr10:98217100
|
C | T | 1 | a0001c0001t0002g0238 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1785+7201C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98217100 | ||||||
chr10:98217317
|
A | G | 1 | a0001c0001t0002g0275 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1785+7418A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98217317 | ||||||
chr10:98217404
|
T | C | 1 | a0003c0003t0005g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1785+7505T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98217404 | ||||||
chr10:98217610
|
A | G | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1785+7711A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98217610 | ||||||
chr10:98217664
|
G | A | 3 | a0001c0001t0007g0023a0001c0010t0007g0028a0001c0010t0007g0029 | 3 | HG02818.hp2 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1785+7765G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98217664 | ||||||
chr10:98217797
|
T | G | 1 | a0008c0014t0001g0103 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1785+7898T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98217797 | ||||||
chr10:98217988
|
A | G | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1785+8089A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98217988 | ||||||
chr10:98218110
|
G | C | 2 | a0011c0008t0001g0009a0019c0022t0001g0031 | 3 | HG02486.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1785+8211G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98218110 | ||||||
chr10:98218607
|
C | T | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1785+8708C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98218607 | ||||||
chr10:98218635
|
A | G | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1785+8736A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98218635 | ||||||
chr10:98218658
|
G | A | 333 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(330): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1785+8759G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98218658 | ||||||
chr10:98218868
|
G | A | 1 | a0002c0002t0001g0073 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1785+8969G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98218868 | ||||||
chr10:98219071
|
T | A | 1 | a0002c0002t0001g0059 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1785+9172T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98219071 | ||||||
chr10:98219262
|
C | T | 2 | a0001c0001t0002g0306a0001c0001t0002g0315 | 2 | NA18961.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1785+9363C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98219262 | ||||||
chr10:98219447
|
C | T | 1 | a0003c0003t0003g0172 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1785+9548C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98219447 | ||||||
chr10:98219492
|
T | A | 2 | a0001c0001t0002g0313a0001c0001t0002g0316 | 2 | NA18960.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1785+9593T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98219492 | ||||||
chr10:98219557
|
A | G | 1 | a0001c0001t0002g0249 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1785+9658A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98219557 | ||||||
chr10:98219719
|
CTTATCTG others(10): Show |
C | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1785+9822_1785+983 others(21): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 98219719 | |||||
chr10:98219904
|
A | G | 1 | a0001c0001t0002g0290 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1785+10005A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98219904 | ||||||
chr10:98219969
|
T | A | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1785+10070T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98219969 | ||||||
chr10:98219997
|
C | T | 2 | a0001c0001t0002g0339a0001c0001t0002g0340 | 2 | HG00558.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1785+10098C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98219997 | ||||||
chr10:98220315
|
T | G | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.1785+10416T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98220315 | ||||||
chr10:98220370
|
C | CT | 91 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0005others(88): Show | 109 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1785+10481dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 98220370 | |||||
chr10:98220386
|
C | CT | 45 | a0002c0002t0001g0100a0003c0003t0003g0017a0003c0003t0003g0157others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.1785+10501dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 98220386 | |||||
chr10:98220386
|
CT | C | 9 | a0001c0001t0001g0217a0001c0001t0002g0019a0001c0001t0002g0278others(6): Show | 10 | HG01109.hp1 HG01943.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1785+10501delT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 98220386 | |||||
chr10:98220400
|
T | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0286a0001c0001t0002g0302 | 4 | NA18985.hp1 NA19000.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.1785+10501T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98220400 | ||||||
chr10:98220404
|
C | G | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1785+10505C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98220404 | ||||||
chr10:98220406
|
C | CT | 35 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(32): Show | 36 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.1785+10508dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 98220406 | |||||
chr10:98220423
|
T | C | 33 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(30): Show | 34 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.1785+10524T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98220423 | ||||||
chr10:98220454
|
A | G | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1785+10555A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98220454 | ||||||
chr10:98220491
|
C | T | 1 | a0003c0003t0003g0172 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1785+10592C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98220491 | ||||||
chr10:98220530
|
C | T | 7 | a0002c0002t0001g0004a0002c0002t0001g0011a0002c0002t0001g0064others(4): Show | 10 | HG01361.hp2 NA18941.hp1 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.1785+10631C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98220530 | ||||||
chr10:98220550
|
C | T | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1785+10651C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98220550 | ||||||
chr10:98220569
|
T | C | 314 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(311): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1785+10670T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98220569 | ||||||
chr10:98220599
|
A | G | 53 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(50): Show | 60 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.1785+10700A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98220599 | ||||||
chr10:98220625
|
G | A | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1785+10726G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98220625 | ||||||
chr10:98220674
|
C | T | 2 | a0001c0010t0007g0028a0001c0010t0007g0029 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1785+10775C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98220674 | ||||||
chr10:98221018
|
C | G | 2 | a0001c0001t0002g0192a0001c0001t0002g0194 | 2 | HG01081.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1786-10494C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221018 | ||||||
chr10:98221125
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1786-10387G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221125 | ||||||
chr10:98221206
|
G | A | 1 | a0009c0009t0001g0090 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1786-10306G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221206 | ||||||
chr10:98221304
|
G | A | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1786-10208G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221304 | ||||||
chr10:98221320
|
T | G | 3 | a0001c0001t0002g0268a0001c0001t0002g0281a0001c0001t0002g0345 | 3 | HG00642.hp2 HG01074.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1786-10192T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221320 | ||||||
chr10:98221376
|
T | G | 4 | a0001c0001t0001g0218a0002c0002t0001g0006a0002c0002t0001g0043others(1): Show | 6 | HG02698.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.1786-10136T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221376 | ||||||
chr10:98221385
|
T | G | 2 | a0002c0002t0001g0104a0002c0002t0001g0105 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1786-10127T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221385 | ||||||
chr10:98221461
|
A | G | 7 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1786-10051A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221461 | ||||||
chr10:98221518
|
C | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(141): Show | 169 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1786-9994C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221518 | ||||||
chr10:98221571
|
G | A | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1786-9941G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221571 | ||||||
chr10:98221591
|
A | C | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.1786-9921A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221591 | ||||||
chr10:98221650
|
G | T | 6 | a0001c0001t0006g0241a0001c0001t0006g0242a0001c0001t0006g0243others(3): Show | 6 | HG02109.hp1 HG02809.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1786-9862G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221650 | ||||||
chr10:98221697
|
A | G | 1 | a0011c0008t0001g0009 | 2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1786-9815A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221697 | ||||||
chr10:98221700
|
G | A | 53 | a0001c0001t0002g0007a0001c0001t0002g0019a0001c0001t0002g0025others(50): Show | 56 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1786-9812G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221700 | ||||||
chr10:98221728
|
A | G | 4 | a0001c0001t0002g0021a0001c0001t0002g0286a0001c0001t0002g0302others(1): Show | 5 | NA18985.hp1 NA18986.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.1786-9784A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221728 | ||||||
chr10:98221759
|
C | G | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1786-9753C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221759 | ||||||
chr10:98221761
|
A | G | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1786-9751A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221761 | ||||||
chr10:98221858
|
T | G | 1 | a0001c0001t0002g0277 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1786-9654T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221858 | ||||||
chr10:98221859
|
C | T | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1786-9653C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221859 | ||||||
chr10:98221892
|
G | A | 2 | a0001c0010t0007g0028a0001c0010t0007g0029 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1786-9620G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221892 | ||||||
chr10:98221933
|
G | C | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1786-9579G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98221933 | ||||||
chr10:98222026
|
C | T | 2 | a0002c0002t0001g0104a0002c0002t0001g0105 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1786-9486C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98222026 | ||||||
chr10:98222096
|
T | A | 1 | a0001c0001t0002g0290 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1786-9416T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98222096 | ||||||
chr10:98222120
|
T | C | 6 | a0001c0001t0002g0249a0001c0001t0002g0251a0001c0001t0002g0253others(3): Show | 6 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1786-9392T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98222120 | ||||||
chr10:98222208
|
G | A | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1786-9304G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98222208 | ||||||
chr10:98222218
|
T | C | 1 | a0022c0017t0002g0335 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1786-9294T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98222218 | ||||||
chr10:98222344
|
C | G | 1 | a0002c0002t0001g0055 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1786-9168C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98222344 | ||||||
chr10:98222466
|
A | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(142): Show | 170 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.1786-9046A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98222466 | ||||||
chr10:98222549
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1786-8963G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98222549 | ||||||
chr10:98222573
|
G | A | 2 | a0002c0002t0001g0050a0002c0002t0001g0088 | 2 | HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1786-8939G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98222573 | ||||||
chr10:98222639
|
A | G | 2 | a0005c0007t0003g0232a0005c0007t0003g0233 | 2 | HG01255.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1786-8873A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98222639 | ||||||
chr10:98222694
|
A | G | 1 | a0003c0012t0003g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1786-8818A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98222694 | ||||||
chr10:98222785
|
C | T | 1 | a0023c0026t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1786-8727C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98222785 | ||||||
chr10:98222791
|
G | A | 4 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0198others(1): Show | 4 | HG02109.hp2 HG02809.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1786-8721G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98222791 | ||||||
chr10:98222999
|
A | C | 316 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(313): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1786-8513A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98222999 | ||||||
chr10:98223033
|
T | C | 2 | a0005c0007t0003g0232a0005c0007t0003g0233 | 2 | HG01255.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1786-8479T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98223033 | ||||||
chr10:98223169
|
A | G | 1 | a0003c0003t0003g0176 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1786-8343A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98223169 | ||||||
chr10:98223278
|
G | C | 333 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(330): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1786-8234G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98223278 | ||||||
chr10:98223360
|
C | T | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1786-8152C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98223360 | ||||||
chr10:98223367
|
A | T | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1786-8145A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98223367 | ||||||
chr10:98223553
|
T | C | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.1786-7959T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98223553 | ||||||
chr10:98223747
|
C | G | 6 | a0004c0004t0004g0016a0004c0004t0004g0145a0004c0004t0004g0146others(3): Show | 7 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1786-7765C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98223747 | ||||||
chr10:98223838
|
T | G | 1 | a0001c0001t0002g0247 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1786-7674T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98223838 | ||||||
chr10:98223841
|
G | A | 1 | a0002c0002t0001g0060 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1786-7671G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98223841 | ||||||
chr10:98223875
|
C | A | 1 | a0002c0002t0001g0141 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1786-7637C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98223875 | ||||||
chr10:98224011
|
G | A | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1786-7501G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98224011 | ||||||
chr10:98224091
|
C | G | 1 | a0002c0002t0001g0071 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1786-7421C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98224091 | ||||||
chr10:98224309
|
C | G | 2 | a0002c0002t0001g0069a0002c0002t0001g0082 | 2 | HG03239.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1786-7203C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98224309 | ||||||
chr10:98224367
|
A | G | 1 | a0001c0001t0002g0324 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1786-7145A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98224367 | ||||||
chr10:98224379
|
A | G | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1786-7133A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98224379 | ||||||
chr10:98224642
|
C | T | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1786-6870C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98224642 | ||||||
chr10:98224729
|
T | C | 1 | a0003c0003t0003g0166 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1786-6783T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98224729 | ||||||
chr10:98224778
|
C | A | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1786-6734C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98224778 | ||||||
chr10:98224836
|
A | G | 2 | a0001c0010t0007g0028a0001c0010t0007g0029 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1786-6676A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98224836 | ||||||
chr10:98224852
|
A | G | 1 | a0001c0001t0002g0249 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1786-6660A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98224852 | ||||||
chr10:98225007
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1786-6505A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98225007 | ||||||
chr10:98225070
|
T | C | 1 | a0001c0001t0012g0292 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1786-6442T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98225070 | ||||||
chr10:98225464
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1786-6048T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98225464 | ||||||
chr10:98225477
|
A | C | 1 | a0004c0004t0004g0145 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1786-6035A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98225477 | ||||||
chr10:98225533
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1786-5979G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98225533 | ||||||
chr10:98225642
|
T | G | 1 | a0002c0002t0001g0074 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1786-5870T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98225642 | ||||||
chr10:98225892
|
G | A | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1786-5620G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98225892 | ||||||
chr10:98226018
|
T | G | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1786-5494T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98226018 | ||||||
chr10:98226101
|
A | G | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1786-5411A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98226101 | ||||||
chr10:98226250
|
G | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1786-5262G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98226250 | ||||||
chr10:98226403
|
G | A | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1786-5109G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98226403 | ||||||
chr10:98226793
|
C | T | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1786-4719C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98226793 | ||||||
chr10:98226793
|
CGTTTAAG others(11): Show |
C | 2 | a0002c0002t0001g0069a0002c0002t0001g0082 | 2 | HG03239.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1786-4712_1786-469 others(22): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 98226793 | |||||
chr10:98226824
|
T | C | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.1786-4688T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98226824 | ||||||
chr10:98226881
|
A | C | 144 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(141): Show | 169 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1786-4631A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98226881 | ||||||
chr10:98226971
|
T | C | 1 | a0001c0001t0002g0332 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1786-4541T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98226971 | ||||||
chr10:98227161
|
T | C | 2 | a0001c0001t0004g0002a0001c0001t0004g0221 | 7 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1786-4351T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98227161 | ||||||
chr10:98227258
|
A | G | 1 | a0001c0001t0002g0193 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1786-4254A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98227258 | ||||||
chr10:98227373
|
A | G | 1 | a0002c0002t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1786-4139A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98227373 | ||||||
chr10:98227527
|
G | A | 332 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(329): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1786-3985G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98227527 | ||||||
chr10:98227576
|
GT | G | 318 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(315): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1786-3919delT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 98227576 | |||||
chr10:98227576
|
GTT | G | 6 | a0001c0001t0002g0246a0001c0001t0002g0312a0002c0002t0001g0096others(3): Show | 6 | HG01496.hp1 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1786-3920_1786-391 others(6): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 98227576 | |||||
chr10:98227578
|
T | G | 3 | a0001c0001t0002g0024a0001c0001t0002g0204a0001c0001t0002g0293 | 3 | HG02630.hp2 HG03654.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1786-3934T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98227578 | ||||||
chr10:98227579
|
T | G | 1 | a0003c0003t0003g0163 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1786-3933T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98227579 | ||||||
chr10:98227580
|
T | G | 34 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(31): Show | 35 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.1786-3932T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98227580 | ||||||
chr10:98227581
|
T | G | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1786-3931T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98227581 | ||||||
chr10:98227802
|
A | G | 2 | a0001c0001t0002g0278a0001c0001t0002g0279 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1786-3710A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98227802 | ||||||
chr10:98227887
|
C | T | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1786-3625C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98227887 | ||||||
chr10:98227977
|
A | G | 7 | a0003c0003t0003g0181a0003c0003t0003g0182a0003c0003t0003g0183others(4): Show | 7 | HG00733.hp1 HG01175.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1786-3535A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98227977 | ||||||
chr10:98228187
|
A | G | 1 | a0001c0001t0002g0343 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1786-3325A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98228187 | ||||||
chr10:98228199
|
A | G | 1 | a0001c0001t0006g0245 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1786-3313A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98228199 | ||||||
chr10:98228561
|
T | C | 1 | a0002c0002t0001g0080 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1786-2951T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98228561 | ||||||
chr10:98228801
|
T | G | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1786-2711T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98228801 | ||||||
chr10:98228855
|
T | G | 1 | a0003c0003t0003g0176 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1786-2657T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98228855 | ||||||
chr10:98229055
|
T | G | 1 | a0015c0025t0001g0210 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1786-2457T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98229055 | ||||||
chr10:98229064
|
C | T | 4 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0198others(1): Show | 4 | HG02109.hp2 HG02809.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1786-2448C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98229064 | ||||||
chr10:98229065
|
A | G | 333 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(330): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1786-2447A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98229065 | ||||||
chr10:98229108
|
C | T | 2 | a0011c0008t0001g0009a0019c0022t0001g0031 | 3 | HG02486.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1786-2404C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98229108 | ||||||
chr10:98229139
|
G | A | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1786-2373G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98229139 | ||||||
chr10:98229154
|
G | A | 1 | a0002c0002t0001g0065 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1786-2358G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98229154 | ||||||
chr10:98229379
|
G | GT | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.1786-2130dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 98229379 | |||||
chr10:98229463
|
A | G | 46 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.1786-2049A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98229463 | ||||||
chr10:98229639
|
G | C | 1 | a0002c0002t0001g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1786-1873G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98229639 | ||||||
chr10:98229792
|
G | C | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1786-1720G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98229792 | ||||||
chr10:98229858
|
G | C | 1 | a0003c0003t0003g0162 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1786-1654G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98229858 | ||||||
chr10:98229869
|
A | G | 2 | a0001c0001t0002g0278a0001c0001t0002g0279 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1786-1643A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98229869 | ||||||
chr10:98230042
|
C | CT | 134 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0018others(131): Show | 142 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.1786-1463dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 98230042 | |||||
chr10:98230122
|
T | A | 3 | a0002c0002t0001g0083a0002c0002t0001g0141a0002c0002t0001g0142 | 3 | HG00642.hp1 HG00735.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1786-1390T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98230122 | ||||||
chr10:98230202
|
G | T | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1786-1310G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98230202 | ||||||
chr10:98230204
|
C | T | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1786-1308C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98230204 | ||||||
chr10:98230272
|
C | T | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1786-1240C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98230272 | ||||||
chr10:98230284
|
T | G | 49 | a0002c0002t0001g0041a0002c0002t0001g0117a0002c0002t0001g0120others(46): Show | 50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1786-1228T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98230284 | ||||||
chr10:98230367
|
G | A | 2 | a0001c0010t0007g0028a0001c0010t0007g0029 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1786-1145G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98230367 | ||||||
chr10:98230368
|
T | C | 1 | a0002c0002t0001g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1786-1144T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98230368 | ||||||
chr10:98230417
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1786-1095C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98230417 | ||||||
chr10:98230552
|
A | G | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1786-960A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98230552 | ||||||
chr10:98230736
|
G | A | 195 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(192): Show | 221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.1786-776G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98230736 | ||||||
chr10:98230743
|
G | A | 1 | a0002c0002t0001g0045 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1786-769G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98230743 | ||||||
chr10:98230850
|
T | C | 1 | a0002c0002t0001g0094 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1786-662T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98230850 | ||||||
chr10:98231437
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1786-75G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98231437 | ||||||
chr10:98231483
|
C | T | 1 | a0021c0018t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1786-29C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 5/9 | chr10 | 98231483 | ||||||
chr10:98231843
|
A | G | 3 | a0001c0001t0007g0023a0001c0010t0007g0028a0001c0010t0007g0029 | 3 | HG02818.hp2 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1961+156A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | chr10 | 98231843 | ||||||
chr10:98231901
|
T | C | 3 | a0001c0001t0007g0023a0001c0010t0007g0028a0001c0010t0007g0029 | 3 | HG02818.hp2 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1961+214T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | chr10 | 98231901 | ||||||
chr10:98231917
|
A | G | 1 | a0002c0002t0001g0092 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1961+230A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | chr10 | 98231917 | ||||||
chr10:98232449
|
T | A | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.1961+762T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | chr10 | 98232449 | ||||||
chr10:98232786
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 5 | NA18941.hp2 NA18951.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.1961+1099G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | chr10 | 98232786 | ||||||
chr10:98232874
|
C | G | 1 | a0001c0001t0002g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1961+1187C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | chr10 | 98232874 | ||||||
chr10:98233277
|
G | A | 46 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.1962-1169G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | chr10 | 98233277 | ||||||
chr10:98233357
|
G | A | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1962-1089G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | chr10 | 98233357 | ||||||
chr10:98233488
|
G | A | 2 | a0003c0003t0003g0165a0003c0003t0003g0178 | 2 | NA18953.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1962-958G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | chr10 | 98233488 | ||||||
chr10:98233563
|
G | C | 12 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0194others(9): Show | 13 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1962-883G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | chr10 | 98233563 | ||||||
chr10:98233608
|
A | G | 3 | a0001c0001t0006g0243a0001c0001t0006g0244a0001c0001t0006g0245 | 3 | HG02809.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1962-838A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | chr10 | 98233608 | ||||||
chr10:98233878
|
C | G | 51 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(48): Show | 58 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1962-568C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | chr10 | 98233878 | ||||||
chr10:98234088
|
CTCCTCTG others(2): Show |
C | 51 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(48): Show | 58 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1962-351_1962-343d others(11): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr10 | 98234088 | |||||
chr10:98234125
|
G | T | 42 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(39): Show | 43 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.1962-321G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | chr10 | 98234125 | ||||||
chr10:98234173
|
C | T | 2 | a0011c0008t0001g0009a0019c0022t0001g0031 | 3 | HG02486.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1962-273C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | chr10 | 98234173 | ||||||
chr10:98234203
|
T | C | 2 | a0001c0001t0004g0220a0001c0001t0004g0222 | 2 | NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1962-243T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | chr10 | 98234203 | ||||||
chr10:98234224
|
C | T | 1 | a0001c0001t0006g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1962-222C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 6/9 | chr10 | 98234224 | ||||||
chr10:98234976
|
G | A | 2 | a0003c0012t0003g0158a0003c0012t0003g0159 | 2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2033-449G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 7/9 | chr10 | 98234976 | ||||||
chr10:98235245
|
A | G | 2 | a0003c0012t0003g0158a0003c0012t0003g0159 | 2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2033-180A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 7/9 | chr10 | 98235245 | ||||||
chr10:98235972
|
G | T | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2129-52G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 8/9 | chr10 | 98235972 | ||||||
chr10:98236016
|
C | T | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
splice_region_variant&intron_variant | LOW | c.2129-8C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 8/9 | chr10 | 98236016 | ||||||
chr10:98236375
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2269+211G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98236375 | ||||||
chr10:98236672
|
C | T | 1 | a0006c0005t0004g0150 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2269+508C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98236672 | ||||||
chr10:98236680
|
T | A | 1 | a0001c0001t0002g0258 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2269+516T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98236680 | ||||||
chr10:98236971
|
T | C | 1 | a0003c0003t0003g0172 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2269+807T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98236971 | ||||||
chr10:98237035
|
G | A | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2269+871G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98237035 | ||||||
chr10:98237077
|
C | A | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2269+913C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98237077 | ||||||
chr10:98237140
|
G | C | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2269+976G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98237140 | ||||||
chr10:98237169
|
T | C | 1 | a0002c0002t0001g0032 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2269+1005T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98237169 | ||||||
chr10:98237293
|
A | G | 46 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.2269+1129A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98237293 | ||||||
chr10:98237471
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2269+1307C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98237471 | ||||||
chr10:98237620
|
A | G | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2269+1456A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98237620 | ||||||
chr10:98237681
|
A | C | 1 | a0001c0001t0002g0328 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2269+1517A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98237681 | ||||||
chr10:98237863
|
T | G | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2269+1699T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98237863 | ||||||
chr10:98238064
|
A | G | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.2269+1900A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98238064 | ||||||
chr10:98238096
|
T | C | 1 | a0001c0001t0002g0305 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2269+1932T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98238096 | ||||||
chr10:98238533
|
A | T | 1 | a0001c0001t0006g0241 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2269+2369A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98238533 | ||||||
chr10:98238576
|
TGAGTTTA | T | 7 | a0003c0003t0005g0224a0003c0003t0005g0225a0003c0003t0005g0226others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2269+2416_2269+242 others(11): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr10 | 98238576 | |||||
chr10:98239046
|
T | C | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2269+2882T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98239046 | ||||||
chr10:98239089
|
A | G | 4 | a0002c0002t0001g0006a0002c0002t0001g0043a0002c0002t0001g0077others(1): Show | 6 | HG01346.hp2 HG02698.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.2269+2925A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98239089 | ||||||
chr10:98239213
|
G | A | 6 | a0002c0002t0001g0071a0002c0002t0001g0083a0002c0002t0001g0141others(3): Show | 6 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2269+3049G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98239213 | ||||||
chr10:98239303
|
A | G | 1 | a0001c0001t0002g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2269+3139A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98239303 | ||||||
chr10:98239454
|
C | G | 333 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(330): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.2269+3290C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98239454 | ||||||
chr10:98239586
|
C | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(144): Show | 172 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.2269+3422C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98239586 | ||||||
chr10:98239780
|
C | A | 2 | a0001c0001t0008g0030a0001c0001t0008g0119 | 2 | NA18956.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2269+3616C>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98239780 | ||||||
chr10:98239899
|
T | C | 1 | a0023c0026t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2269+3735T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98239899 | ||||||
chr10:98240174
|
C | T | 1 | a0001c0001t0010g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2270-3917C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98240174 | ||||||
chr10:98240176
|
C | T | 1 | a0002c0002t0001g0234 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2270-3915C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98240176 | ||||||
chr10:98240238
|
G | A | 45 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.2270-3853G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98240238 | ||||||
chr10:98240255
|
G | A | 3 | a0012c0013t0002g0206a0012c0013t0002g0207a0016c0023t0002g0223 | 3 | HG01496.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2270-3836G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98240255 | ||||||
chr10:98240365
|
T | A | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2270-3726T>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98240365 | ||||||
chr10:98240797
|
A | AT | 205 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0014others(202): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.2270-3279dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr10 | 98240797 | |||||
chr10:98240797
|
A | ATT | 88 | a0001c0001t0001g0139a0001c0001t0001g0214a0001c0001t0002g0257others(85): Show | 105 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2270-3280_2270-327 others(6): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr10 | 98240797 | |||||
chr10:98240797
|
A | ATTT | 6 | a0002c0002t0001g0049a0002c0002t0001g0067a0002c0002t0001g0117others(3): Show | 6 | HG01891.hp1 HG02257.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2270-3281_2270-327 others(7): Show |
R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr10 | 98240797 | |||||
chr10:98240797
|
A | T | 1 | a0001c0001t0002g0238 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2270-3294A>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98240797 | ||||||
chr10:98240831
|
T | C | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2270-3260T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98240831 | ||||||
chr10:98240868
|
A | G | 145 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(142): Show | 170 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.2270-3223A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98240868 | ||||||
chr10:98240888
|
A | C | 46 | a0003c0003t0003g0017a0003c0003t0003g0157a0003c0003t0003g0160others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.2270-3203A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98240888 | ||||||
chr10:98241006
|
T | C | 1 | a0001c0001t0002g0311 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2270-3085T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98241006 | ||||||
chr10:98241163
|
C | T | 3 | a0005c0007t0003g0231a0005c0007t0003g0232a0005c0007t0003g0233 | 3 | HG01255.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2270-2928C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98241163 | ||||||
chr10:98241181
|
G | A | 1 | a0001c0001t0002g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2270-2910G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98241181 | ||||||
chr10:98241205
|
C | T | 1 | a0001c0001t0002g0305 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2270-2886C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98241205 | ||||||
chr10:98241488
|
A | G | 1 | a0001c0001t0013g0199 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2270-2603A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98241488 | ||||||
chr10:98241559
|
A | G | 1 | a0005c0007t0003g0231 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2270-2532A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98241559 | ||||||
chr10:98241900
|
A | C | 2 | a0001c0001t0008g0030a0001c0001t0008g0119 | 2 | NA18956.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2270-2191A>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98241900 | ||||||
chr10:98241967
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2270-2124G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98241967 | ||||||
chr10:98242166
|
G | A | 1 | a0001c0001t0006g0241 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2270-1925G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98242166 | ||||||
chr10:98242243
|
G | C | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2270-1848G>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98242243 | ||||||
chr10:98242408
|
G | A | 1 | a0005c0007t0003g0231 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2270-1683G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98242408 | ||||||
chr10:98242495
|
A | G | 1 | a0002c0002t0001g0208 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2270-1596A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98242495 | ||||||
chr10:98242642
|
A | G | 334 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(331): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.2270-1449A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98242642 | ||||||
chr10:98242661
|
C | G | 1 | a0017c0019t0003g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2270-1430C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98242661 | ||||||
chr10:98242707
|
T | C | 4 | a0002c0002t0001g0006a0002c0002t0001g0043a0002c0002t0001g0077others(1): Show | 6 | HG01346.hp2 HG02698.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.2270-1384T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98242707 | ||||||
chr10:98243012
|
T | C | 1 | a0002c0002t0001g0101 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2270-1079T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98243012 | ||||||
chr10:98243084
|
C | CT | 8 | a0003c0003t0003g0181a0003c0003t0003g0182a0003c0003t0003g0183others(5): Show | 8 | HG00733.hp1 HG01175.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.2270-1006dupT | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr10 | 98243084 | |||||
chr10:98243196
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2270-895C>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98243196 | ||||||
chr10:98243440
|
A | G | 1 | a0001c0001t0007g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2270-651A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98243440 | ||||||
chr10:98243485
|
T | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(52): Show | 62 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.2270-606T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98243485 | ||||||
chr10:98243545
|
G | A | 3 | a0001c0001t0012g0292a0010c0011t0002g0291a0010c0011t0002g0334 | 3 | HG00733.hp2 HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.2270-546G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98243545 | ||||||
chr10:98243547
|
A | G | 3 | a0001c0001t0012g0292a0010c0011t0002g0291a0010c0011t0002g0334 | 3 | HG00733.hp2 HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.2270-544A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98243547 | ||||||
chr10:98243723
|
G | A | 13 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0193others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.2270-368G>A | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98243723 | ||||||
chr10:98243791
|
T | G | 12 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0194others(9): Show | 13 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2270-300T>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98243791 | ||||||
chr10:98243829
|
A | G | 12 | a0001c0001t0002g0018a0001c0001t0002g0192a0001c0001t0002g0194others(9): Show | 13 | HG01081.hp2 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2270-262A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98243829 | ||||||
chr10:98243859
|
A | G | 2 | a0001c0010t0007g0028a0001c0010t0007g0029 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2270-232A>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98243859 | ||||||
chr10:98243978
|
G | T | 1 | a0001c0001t0002g0343 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2270-113G>T | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98243978 | ||||||
chr10:98243990
|
C | G | 1 | a0001c0001t0002g0290 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2270-101C>G | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98243990 | ||||||
chr10:98244028
|
T | C | 121 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(118): Show | 128 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.2270-63T>C | R3HCC1L | ENSG00000166024.14 | transcript | ENST00000298999.8 | protein_coding | 9/9 | chr10 | 98244028 |