geneid | 727 |
---|---|
ensemblid | ENSG00000106804.10 |
hgncid | 1331 |
symbol | C5 |
name | complement C5 |
refseq_nuc | NM_001735.3 |
refseq_prot | NP_001726.2 |
ensembl_nuc | ENST00000223642.3 |
ensembl_prot | ENSP00000223642.1 |
mane_status | MANE Select |
chr | chr9 |
start | 120952335 |
end | 121050275 |
strand | - |
ver | v1.2 |
region | chr9:120952335-121050275 |
region5000 | chr9:120947335-121055275 |
regionname0 | C5_chr9_120952335_121050275 |
regionname5000 | C5_chr9_120947335_121055275 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1676 | 98 | 31 | 19 | 33 | 6 | 8 | 27 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0002 | 0/0 | 1676 | 70 | 3 | 19 | 36 | 4 | 8 | 30 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0003 | 0/1 | 1676 | 56 | 20 | 5 | 30 | 0 | 0 | 22 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0004 | 0/0 | 1676 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0005 | 0/0 | 1676 | 7 | 0 | 0 | 7 | 0 | 0 | 4 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0006 | 0/0 | 1676 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0007 | 0/0 | 1676 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0008 | 0/0 | 1676 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0009 | 0/0 | 1676 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0010 | 0/0 | 1676 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0011 | 0/0 | 1676 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0012 | 0/0 | 1676 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0013 | 0/0 | 1676 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0014 | 0/0 | 1676 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0015 | 0/0 | 1676 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0016 | 0/0 | 1676 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0017 | 0/0 | 1676 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0018 | 0/0 | 1676 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0019 | 0/0 | 1676 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 5031 | 83 | 26 | 19 | 27 | 4 | 6 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0002 | 0/0 | 5031 | 69 | 3 | 19 | 35 | 4 | 8 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0003 | 0/1 | 5031 | 36 | 4 | 1 | 30 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0004 | 0/0 | 5031 | 20 | 16 | 4 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0005 | 0/0 | 5031 | 10 | 9 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0006 | 0/0 | 5031 | 8 | 1 | 0 | 3 | 2 | 2 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0007 | 0/0 | 5031 | 7 | 0 | 0 | 7 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0008 | 0/0 | 5031 | 6 | 6 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0009 | 0/0 | 5031 | 4 | 4 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0010 | 0/0 | 5031 | 4 | 0 | 4 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0011 | 0/0 | 5031 | 3 | 3 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0012 | 0/0 | 5031 | 3 | 3 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0013 | 0/0 | 5031 | 3 | 0 | 0 | 3 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0014 | 0/0 | 5031 | 3 | 3 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0015 | 0/0 | 5031 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0016 | 0/0 | 5031 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0017 | 0/0 | 5031 | 2 | 0 | 0 | 2 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0018 | 0/0 | 5031 | 2 | 0 | 0 | 2 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0019 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0020 | 0/0 | 5031 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0021 | 0/0 | 5031 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0022 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0023 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0024 | 0/0 | 5031 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0025 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0026 | 0/0 | 5031 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
c0027 | 0/0 | 5031 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 434 | 270 | 81 | 47 | 114 | 10 | 16 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
t0002 | 0/0 | 434 | 4 | 4 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
t0003 | 0/0 | 434 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
t0004 | 0/0 | 434 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
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 | 3 | 0 | 0 | 3 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0011 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0026 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 5031 | 83 | 26 | 19 | 27 | 4 | 6 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0001c0006 | 0/0 | 5031 | 8 | 1 | 0 | 3 | 2 | 2 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0001c0016 | 0/0 | 5031 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0001c0018 | 0/0 | 5031 | 2 | 0 | 0 | 2 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0001c0019 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0001c0022 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0001c0024 | 0/0 | 5031 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0002c0002 | 0/0 | 5031 | 69 | 3 | 19 | 35 | 4 | 8 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0002c0026 | 0/0 | 5031 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0003c0003 | 0/1 | 5031 | 36 | 4 | 1 | 30 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0003c0004 | 0/0 | 5031 | 20 | 16 | 4 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0004c0005 | 0/0 | 5031 | 10 | 9 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0005c0007 | 0/0 | 5031 | 7 | 0 | 0 | 7 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0006c0008 | 0/0 | 5031 | 6 | 6 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0007c0009 | 0/0 | 5031 | 4 | 4 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0008c0010 | 0/0 | 5031 | 4 | 0 | 4 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0009c0012 | 0/0 | 5031 | 3 | 3 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0010c0014 | 0/0 | 5031 | 3 | 3 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0011c0013 | 0/0 | 5031 | 3 | 0 | 0 | 3 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0012c0011 | 0/0 | 5031 | 3 | 3 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0013c0015 | 0/0 | 5031 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0014c0017 | 0/0 | 5031 | 2 | 0 | 0 | 2 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0015c0020 | 0/0 | 5031 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0016c0027 | 0/0 | 5031 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0017c0025 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0018c0023 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0019c0021 | 0/0 | 5031 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5464 | 82 | 26 | 18 | 27 | 4 | 6 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0001c0001t0004 | 0/0 | 5464 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0001c0006t0001 | 0/0 | 5464 | 8 | 1 | 0 | 3 | 2 | 2 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0001c0016t0001 | 0/0 | 5464 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0001c0018t0001 | 0/0 | 5464 | 2 | 0 | 0 | 2 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0001c0019t0001 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0001c0022t0001 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0001c0024t0001 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0002c0002t0001 | 0/0 | 5464 | 69 | 3 | 19 | 35 | 4 | 8 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0002c0026t0001 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0003c0003t0001 | 0/1 | 5464 | 36 | 4 | 1 | 30 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0003c0004t0001 | 0/0 | 5464 | 19 | 15 | 4 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0003c0004t0003 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0004c0005t0001 | 0/0 | 5464 | 6 | 5 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0004c0005t0002 | 0/0 | 5464 | 4 | 4 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0005c0007t0001 | 0/0 | 5464 | 7 | 0 | 0 | 7 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0006c0008t0001 | 0/0 | 5464 | 6 | 6 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0007c0009t0001 | 0/0 | 5464 | 4 | 4 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0008c0010t0001 | 0/0 | 5464 | 4 | 0 | 4 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0009c0012t0001 | 0/0 | 5464 | 3 | 3 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0010c0014t0001 | 0/0 | 5464 | 3 | 3 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0011c0013t0001 | 0/0 | 5464 | 3 | 0 | 0 | 3 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0012c0011t0001 | 0/0 | 5464 | 3 | 3 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0013c0015t0001 | 0/0 | 5464 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0014c0017t0001 | 0/0 | 5464 | 2 | 0 | 0 | 2 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0015c0020t0001 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0016c0027t0001 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0017c0025t0001 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0018c0023t0001 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
a0019c0021t0001 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | copy fasta | chr9 | 120947335 | 121055275 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0011 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0006t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0006t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0006t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0006t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0006t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0006t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0006t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0006t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0016t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0018t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0018t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0019t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0022t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0001c0024t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0002c0026t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0026 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0003c0004t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0004c0005t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0004c0005t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0004c0005t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0004c0005t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0004c0005t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0004c0005t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0004c0005t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0004c0005t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0004c0005t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0005c0007t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0005c0007t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0005c0007t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0005c0007t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0005c0007t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0005c0007t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0005c0007t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0006c0008t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0006c0008t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0006c0008t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0006c0008t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0006c0008t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0006c0008t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0007c0009t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0007c0009t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0007c0009t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0007c0009t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0008c0010t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0008c0010t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0008c0010t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0008c0010t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0009c0012t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0009c0012t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0009c0012t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0010c0014t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0010c0014t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0011c0013t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0011c0013t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0011c0013t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0012c0011t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0012c0011t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0013c0015t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0013c0015t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0014c0017t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0014c0017t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0015c0020t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0016c0027t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0017c0025t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0018c0023t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
a0019c0021t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0006 | t0001 | g0197 | EUR | GBR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0122 | EUR | FIN | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | FIN | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0151 | EUR | FIN | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00323 | hp2 | a0001 | c0006 | t0001 | g0201 | EUR | FIN | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | CHS | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00408 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | CHS | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00438 | hp1 | a0003 | c0003 | t0001 | g0033 | EAS | CHS | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00438 | hp2 | a0015 | c0020 | t0001 | g0021 | EAS | CHS | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00597 | hp1 | a0003 | c0003 | t0001 | g0014 | EAS | CHS | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00597 | hp2 | a0001 | c0024 | t0001 | g0070 | EAS | CHS | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | CHS | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00621 | hp2 | a0003 | c0003 | t0001 | g0053 | EAS | CHS | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00639 | hp1 | a0004 | c0005 | t0001 | g0218 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0140 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00738 | hp1 | a0008 | c0010 | t0001 | g0199 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0138 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0136 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01074 | hp2 | a0003 | c0004 | t0001 | g0031 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0137 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01109 | hp1 | a0003 | c0004 | t0001 | g0059 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0264 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0110 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01175 | hp2 | a0008 | c0010 | t0001 | g0210 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01243 | hp2 | a0003 | c0003 | t0001 | g0046 | AMR | PUR | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0125 | AMR | CLM | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0168 | AMR | CLM | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0153 | AMR | CLM | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01261 | hp2 | a0003 | c0004 | t0001 | g0016 | AMR | CLM | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0126 | AMR | CLM | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0121 | EUR | IBS | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0118 | EUR | IBS | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01884 | hp1 | a0001 | c0022 | t0001 | g0229 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01884 | hp2 | a0001 | c0006 | t0001 | g0204 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01891 | hp1 | a0004 | c0005 | t0002 | g0212 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0129 | AMR | PEL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0113 | AMR | PEL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0154 | AMR | PEL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0157 | AMR | PEL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01981 | hp2 | a0008 | c0010 | t0001 | g0200 | AMR | PEL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | PEL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02015 | hp1 | a0001 | c0018 | t0001 | g0248 | EAS | KHV | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02015 | hp2 | a0003 | c0003 | t0001 | g0052 | EAS | KHV | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02027 | hp1 | a0001 | c0006 | t0001 | g0194 | EAS | KHV | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | KHV | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02040 | hp2 | a0019 | c0021 | t0001 | g0245 | EAS | KHV | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02055 | hp1 | a0003 | c0003 | t0001 | g0067 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | KHV | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02129 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | KHV | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | KHV | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02132 | hp1 | a0003 | c0003 | t0001 | g0051 | EAS | KHV | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02132 | hp2 | a0005 | c0007 | t0001 | g0263 | EAS | KHV | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02135 | hp1 | a0005 | c0007 | t0001 | g0260 | EAS | KHV | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02135 | hp2 | a0001 | c0018 | t0001 | g0244 | EAS | KHV | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02145 | hp1 | a0003 | c0004 | t0001 | g0063 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02148 | hp1 | a0003 | c0004 | t0001 | g0032 | AMR | PEL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0072 | AMR | PEL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02155 | hp1 | a0003 | c0003 | t0001 | g0045 | EAS | CDX | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | CDX | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02257 | hp2 | a0003 | c0004 | t0001 | g0056 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02258 | hp2 | a0006 | c0008 | t0001 | g0104 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02280 | hp1 | a0004 | c0005 | t0002 | g0215 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0178 | AMR | PEL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02293 | hp2 | a0008 | c0010 | t0001 | g0198 | AMR | PEL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02451 | hp1 | a0003 | c0004 | t0001 | g0024 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02451 | hp2 | a0007 | c0009 | t0001 | g0208 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02572 | hp2 | a0003 | c0003 | t0001 | g0061 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02630 | hp2 | a0003 | c0004 | t0001 | g0028 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02647 | hp2 | a0004 | c0005 | t0001 | g0004 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02717 | hp2 | a0001 | c0016 | t0001 | g0003 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02809 | hp1 | a0012 | c0011 | t0001 | g0006 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02809 | hp2 | a0003 | c0004 | t0001 | g0025 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02818 | hp2 | a0006 | c0008 | t0001 | g0069 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02886 | hp1 | a0003 | c0004 | t0001 | g0020 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02886 | hp2 | a0007 | c0009 | t0001 | g0206 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02895 | hp1 | a0007 | c0009 | t0001 | g0207 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02895 | hp2 | a0009 | c0012 | t0001 | g0066 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02896 | hp1 | a0004 | c0005 | t0001 | g0004 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02897 | hp1 | a0009 | c0012 | t0001 | g0062 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02965 | hp1 | a0012 | c0011 | t0001 | g0226 | AFR | ESN | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02965 | hp2 | a0003 | c0004 | t0001 | g0060 | AFR | ESN | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02970 | hp1 | a0003 | c0004 | t0001 | g0058 | AFR | ESN | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02976 | hp1 | a0010 | c0014 | t0001 | g0005 | AFR | ESN | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0114 | SAS | PJL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03017 | hp2 | a0001 | c0006 | t0001 | g0203 | SAS | PJL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03098 | hp1 | a0001 | c0016 | t0001 | g0003 | AFR | MSL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03098 | hp2 | a0003 | c0003 | t0001 | g0065 | AFR | MSL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03130 | hp1 | a0010 | c0014 | t0001 | g0219 | AFR | ESN | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03130 | hp2 | a0004 | c0005 | t0002 | g0213 | AFR | ESN | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03195 | hp1 | a0017 | c0025 | t0001 | g0223 | AFR | ESN | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03195 | hp2 | a0006 | c0008 | t0001 | g0241 | AFR | ESN | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03209 | hp1 | a0009 | c0012 | t0001 | g0064 | AFR | MSL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03209 | hp2 | a0003 | c0003 | t0001 | g0057 | AFR | MSL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03225 | hp2 | a0007 | c0009 | t0001 | g0209 | AFR | MSL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0112 | SAS | PJL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03453 | hp2 | a0003 | c0004 | t0001 | g0019 | AFR | MSL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03486 | hp2 | a0006 | c0008 | t0001 | g0105 | AFR | MSL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0148 | SAS | PJL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0123 | SAS | PJL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03540 | hp2 | a0003 | c0004 | t0001 | g0018 | AFR | GWD | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03579 | hp1 | a0004 | c0005 | t0001 | g0216 | AFR | MSL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03579 | hp2 | a0018 | c0023 | t0001 | g0205 | AFR | MSL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0169 | SAS | PJL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0133 | SAS | PJL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0130 | SAS | BEB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | YRI | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18747 | hp1 | a0005 | c0007 | t0001 | g0261 | EAS | CHB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18747 | hp2 | a0016 | c0027 | t0001 | g0107 | EAS | CHB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18906 | hp1 | a0003 | c0004 | t0001 | g0023 | AFR | YRI | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18906 | hp2 | a0001 | c0019 | t0001 | g0225 | AFR | YRI | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18939 | hp2 | a0003 | c0003 | t0001 | g0050 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18942 | hp1 | a0003 | c0003 | t0001 | g0035 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18944 | hp1 | a0005 | c0007 | t0001 | g0262 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18946 | hp2 | a0005 | c0007 | t0001 | g0116 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18948 | hp2 | a0001 | c0006 | t0001 | g0196 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18950 | hp1 | a0003 | c0003 | t0001 | g0038 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18950 | hp2 | a0011 | c0013 | t0001 | g0143 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18952 | hp1 | a0014 | c0017 | t0001 | g0079 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18954 | hp1 | a0005 | c0007 | t0001 | g0115 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18954 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18959 | hp1 | a0002 | c0026 | t0001 | g0174 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18974 | hp1 | a0003 | c0003 | t0001 | g0036 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18978 | hp2 | a0003 | c0003 | t0001 | g0039 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18980 | hp1 | a0003 | c0003 | t0001 | g0034 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18980 | hp2 | a0005 | c0007 | t0001 | g0259 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18981 | hp1 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18986 | hp1 | a0003 | c0003 | t0001 | g0013 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18989 | hp1 | a0003 | c0003 | t0001 | g0049 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18990 | hp1 | a0011 | c0013 | t0001 | g0142 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18992 | hp1 | a0003 | c0003 | t0001 | g0055 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18992 | hp2 | a0014 | c0017 | t0001 | g0089 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18993 | hp1 | a0003 | c0003 | t0001 | g0040 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19004 | hp2 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19007 | hp2 | a0003 | c0003 | t0001 | g0044 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19012 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19030 | hp2 | a0003 | c0004 | t0001 | g0015 | AFR | LWK | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19043 | hp1 | a0004 | c0005 | t0001 | g0217 | AFR | LWK | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19055 | hp1 | a0003 | c0003 | t0001 | g0043 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19060 | hp1 | a0003 | c0003 | t0001 | g0041 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19062 | hp1 | a0001 | c0006 | t0001 | g0195 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19062 | hp2 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19070 | hp1 | a0011 | c0013 | t0001 | g0146 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19070 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19083 | hp2 | a0003 | c0003 | t0001 | g0037 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19089 | hp2 | a0003 | c0003 | t0001 | g0054 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19090 | hp1 | a0003 | c0003 | t0001 | g0047 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA20129 | hp1 | a0004 | c0005 | t0002 | g0214 | AFR | ASW | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA20129 | hp2 | a0006 | c0008 | t0001 | g0106 | AFR | ASW | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0152 | SAS | GIH | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA20905 | hp2 | a0001 | c0006 | t0001 | g0202 | SAS | GIH | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0111 | AMR | CLM | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02109 | hp1 | a0003 | c0004 | t0001 | g0022 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02486 | hp1 | a0013 | c0015 | t0001 | g0221 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0127 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02559 | hp1 | a0013 | c0015 | t0001 | g0220 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG02559 | hp2 | a0003 | c0004 | t0001 | g0027 | AFR | ACB | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03471 | hp1 | a0012 | c0011 | t0001 | g0006 | AFR | MSL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG03471 | hp2 | a0004 | c0005 | t0001 | g0211 | AFR | MSL | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG06807 | hp1 | a0003 | c0004 | t0003 | g0029 | AFR | USA | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
HG06807 | hp2 | a0010 | c0014 | t0001 | g0005 | AFR | USA | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0222 | AFR | USA | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA20300 | hp2 | a0006 | c0008 | t0001 | g0240 | AFR | USA | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA21309 | hp1 | a0003 | c0004 | t0001 | g0017 | AFR | LWK | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0001 | g0026 | REF | REF | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0011 | REF | REF | C5_chr9_120947335_121055275 | C5 | chr9 | 120947335 | 121055275 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:120963648
|
T | G | 1 | a0008 | 4 | HG00738.hp1 HG01175.hp2 HG01981.hp2 others(1): Show |
missense_variant | MODERATE | c.4311A>C | p.Glu1437Asp | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 34/41 | 4340/5464 | 4311/5031 | 1437/1676 | chr9 | 120963648 | ||
chr9:120974867
|
C | T | 4 | a0006a0009a0010others(1): Show | 13 | HG02258.hp2 HG02818.hp2 HG02895.hp2 others(10): Show |
missense_variant | MODERATE | c.3929G>A | p.Ser1310Asn | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/41 | 3958/5464 | 3929/5031 | 1310/1676 | chr9 | 120974867 | ||
chr9:120976792
|
T | C | 1 | a0015 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.3772A>G | p.Ser1258Gly | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/41 | 3801/5464 | 3772/5031 | 1258/1676 | chr9 | 120976792 | ||
chr9:120976794
|
G | C | 1 | a0017 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.3770C>G | p.Thr1257Ser | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/41 | 3799/5464 | 3770/5031 | 1257/1676 | chr9 | 120976794 | ||
chr9:120989595
|
G | T | 1 | a0006 | 6 | HG02258.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
missense_variant | MODERATE | c.3127C>A | p.Gln1043Lys | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 24/41 | 3156/5464 | 3127/5031 | 1043/1676 | chr9 | 120989595 | ||
chr9:120989689
|
C | G | 1 | a0013 | 2 | HG02486.hp1 HG02559.hp1 |
missense_variant | MODERATE | c.3033G>C | p.Glu1011Asp | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 24/41 | 3062/5464 | 3033/5031 | 1011/1676 | chr9 | 120989689 | ||
chr9:120991236
|
C | A | 1 | a0005 | 7 | HG02132.hp2 HG02135.hp1 NA18747.hp1 others(4): Show |
missense_variant | MODERATE | c.2896G>T | p.Asp966Tyr | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 23/41 | 2925/5464 | 2896/5031 | 966/1676 | chr9 | 120991236 | ||
chr9:120997554
|
C | T | 1 | a0007 | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
missense_variant | MODERATE | c.2783G>A | p.Arg928Gln | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 21/41 | 2812/5464 | 2783/5031 | 928/1676 | chr9 | 120997554 | ||
chr9:120997683
|
C | T | 1 | a0011 | 3 | NA18950.hp2 NA18990.hp1 NA19070.hp1 |
missense_variant | MODERATE | c.2654G>A | p.Arg885His | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 21/41 | 2683/5464 | 2654/5031 | 885/1676 | chr9 | 120997683 | ||
chr9:121006922
|
C | T | 4 | a0002a0005a0011others(1): Show | 81 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(78): Show |
missense_variant | MODERATE | c.2404G>A | p.Val802Ile | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 19/41 | 2433/5464 | 2404/5031 | 802/1676 | chr9 | 121006922 | ||
chr9:121017818
|
G | A | 1 | a0014 | 2 | NA18952.hp1 NA18992.hp2 |
missense_variant | MODERATE | c.1541C>T | p.Thr514Met | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 13/41 | 1570/5464 | 1541/5031 | 514/1676 | chr9 | 121017818 | ||
chr9:121020137
|
T | C | 2 | a0004a0010 | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
missense_variant | MODERATE | c.1345A>G | p.Arg449Gly | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/41 | 1374/5464 | 1345/5031 | 449/1676 | chr9 | 121020137 | ||
chr9:121027190
|
T | A | 1 | a0016 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.843A>T | p.Glu281Asp | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 8/41 | 872/5464 | 843/5031 | 281/1676 | chr9 | 121027190 | ||
chr9:121034828
|
C | G | 1 | a0019 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.559G>C | p.Asp187His | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/41 | 588/5464 | 559/5031 | 187/1676 | chr9 | 121034828 | ||
chr9:121037940
|
C | T | 4 | a0003a0009a0013others(1): Show | 62 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(59): Show |
missense_variant | MODERATE | c.433G>A | p.Val145Ile | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/41 | 462/5464 | 433/5031 | 145/1676 | chr9 | 121037940 | ||
chr9:121043097
|
G | T | 1 | a0012 | 3 | HG02809.hp1 HG02965.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.328C>A | p.His110Asn | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/41 | 357/5464 | 328/5031 | 110/1676 | chr9 | 121043097 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:120953825
|
T | C | 3 | a0008c0010a0010c0014a0018c0023 | 8 | HG00738.hp1 HG01175.hp2 HG01981.hp2 others(5): Show |
synonymous_variant | LOW | c.4806A>G | p.Lys1602Lys | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 40/41 | 4835/5464 | 4806/5031 | 1602/1676 | chr9 | 120953825 | ||
chr9:120963693
|
C | T | 6 | a0001c0024a0002c0026a0003c0003others(3): Show | 50 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(47): Show |
synonymous_variant | LOW | c.4266G>A | p.Ala1422Ala | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 34/41 | 4295/5464 | 4266/5031 | 1422/1676 | chr9 | 120963693 | ||
chr9:120976895
|
G | T | 1 | a0001c0016 | 2 | HG02717.hp2 HG03098.hp1 |
synonymous_variant | LOW | c.3669C>A | p.Pro1223Pro | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/41 | 3698/5464 | 3669/5031 | 1223/1676 | chr9 | 120976895 | ||
chr9:120982742
|
A | G | 1 | a0001c0022 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.3303T>C | p.Cys1101Cys | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 26/41 | 3332/5464 | 3303/5031 | 1101/1676 | chr9 | 120982742 | ||
chr9:120989596
|
C | T | 1 | a0006c0008 | 6 | HG02258.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
synonymous_variant | LOW | c.3126G>A | p.Lys1042Lys | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 24/41 | 3155/5464 | 3126/5031 | 1042/1676 | chr9 | 120989596 | ||
chr9:121017503
|
C | T | 2 | a0004c0005a0010c0014 | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
synonymous_variant | LOW | c.1725G>A | p.Leu575Leu | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 14/41 | 1754/5464 | 1725/5031 | 575/1676 | chr9 | 121017503 | ||
chr9:121017727
|
G | A | 5 | a0002c0002a0002c0026a0005c0007others(2): Show | 81 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(78): Show |
synonymous_variant | LOW | c.1632C>T | p.Tyr544Tyr | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 13/41 | 1661/5464 | 1632/5031 | 544/1676 | chr9 | 121017727 | ||
chr9:121020000
|
G | A | 2 | a0004c0005a0010c0014 | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
synonymous_variant | LOW | c.1482C>T | p.Asp494Asp | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/41 | 1511/5464 | 1482/5031 | 494/1676 | chr9 | 121020000 | ||
chr9:121020021
|
G | A | 4 | a0001c0006a0004c0005a0008c0010others(1): Show | 25 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
synonymous_variant | LOW | c.1461C>T | p.Thr487Thr | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/41 | 1490/5464 | 1461/5031 | 487/1676 | chr9 | 121020021 | ||
chr9:121021656
|
T | C | 11 | a0001c0006a0001c0018a0003c0003others(8): Show | 90 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(87): Show |
synonymous_variant | LOW | c.1155A>G | p.Gly385Gly | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 11/41 | 1184/5464 | 1155/5031 | 385/1676 | chr9 | 121021656 | ||
chr9:121043119
|
C | T | 1 | a0001c0019 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.306G>A | p.Val102Val | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/41 | 335/5464 | 306/5031 | 102/1676 | chr9 | 121043119 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:120952500
|
C | T | 1 | a0003c0004t0003 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*239G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 41/41 | 239 | chr9 | 120952500 | |||||
chr9:120952628
|
T | G | 1 | a0004c0005t0002 | 4 | HG01891.hp1 HG02280.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*111A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 41/41 | 111 | chr9 | 120952628 | |||||
chr9:121050270
|
G | A | 1 | a0001c0001t0004 | 1 | HG01169.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-24C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/41 | chr9 | 121050270 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:120952889
|
T | C | 2 | a0002c0002t0001g0110a0002c0002t0001g0118 | 2 | HG01175.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.4902-21A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 40/40 | chr9 | 120952889 | ||||||
chr9:120952932
|
A | AT | 7 | a0008c0010t0001g0198a0008c0010t0001g0199a0008c0010t0001g0200others(4): Show | 8 | HG00738.hp1 HG01175.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.4902-65dupA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 40/40 | chr9 | 120952932 | ||||||
chr9:120953009
|
T | C | 90 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0001g0076others(87): Show | 97 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.4902-141A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 40/40 | chr9 | 120953009 | ||||||
chr9:120953012
|
C | T | 3 | a0010c0014t0001g0005a0010c0014t0001g0219a0018c0023t0001g0205 | 4 | HG02976.hp1 HG03130.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4902-144G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 40/40 | chr9 | 120953012 | ||||||
chr9:120953058
|
G | A | 6 | a0003c0004t0001g0019a0003c0004t0001g0027a0003c0004t0001g0058others(3): Show | 6 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.4902-190C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 40/40 | chr9 | 120953058 | ||||||
chr9:120953160
|
G | A | 3 | a0010c0014t0001g0005a0010c0014t0001g0219a0018c0023t0001g0205 | 4 | HG02976.hp1 HG03130.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4902-292C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 40/40 | chr9 | 120953160 | ||||||
chr9:120953209
|
C | T | 23 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(20): Show | 25 | HG00639.hp2 HG00735.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.4902-341G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 40/40 | chr9 | 120953209 | ||||||
chr9:120953218
|
C | T | 87 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0080others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.4902-350G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 40/40 | chr9 | 120953218 | ||||||
chr9:120953426
|
A | C | 3 | a0010c0014t0001g0005a0010c0014t0001g0219a0018c0023t0001g0205 | 4 | HG02976.hp1 HG03130.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4901+304T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 40/40 | chr9 | 120953426 | ||||||
chr9:120953673
|
T | C | 1 | a0002c0002t0001g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4901+57A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 40/40 | chr9 | 120953673 | ||||||
chr9:120953945
|
G | A | 2 | a0010c0014t0001g0005a0010c0014t0001g0219 | 3 | HG02976.hp1 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4763-77C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120953945 | ||||||
chr9:120953982
|
C | T | 2 | a0005c0007t0001g0115a0005c0007t0001g0116 | 2 | NA18946.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.4763-114G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120953982 | ||||||
chr9:120954385
|
A | T | 1 | a0001c0001t0001g0076 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.4763-517T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120954385 | ||||||
chr9:120954403
|
T | C | 82 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(79): Show | 89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.4763-535A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120954403 | ||||||
chr9:120954463
|
T | A | 7 | a0001c0001t0001g0068a0003c0004t0001g0018a0003c0004t0001g0022others(4): Show | 7 | HG02109.hp1 HG02451.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4763-595A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120954463 | ||||||
chr9:120954562
|
T | C | 82 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(79): Show | 89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.4763-694A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120954562 | ||||||
chr9:120955003
|
AAG | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0235 | 3 | HG02145.hp2 HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4763-1137_4763-113 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120955003 | ||||||
chr9:120955111
|
C | A | 89 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0001g0224others(86): Show | 96 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.4763-1243G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120955111 | ||||||
chr9:120955296
|
T | C | 2 | a0001c0001t0001g0088a0002c0002t0001g0136 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.4763-1428A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120955296 | ||||||
chr9:120955504
|
T | C | 1 | a0002c0002t0001g0110 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.4763-1636A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120955504 | ||||||
chr9:120955562
|
C | A | 89 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0001g0224others(86): Show | 96 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.4763-1694G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120955562 | ||||||
chr9:120955871
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4762+1414C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120955871 | ||||||
chr9:120956152
|
G | C | 3 | a0003c0003t0001g0036a0003c0003t0001g0049a0003c0003t0001g0050 | 3 | NA18939.hp2 NA18974.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.4762+1133C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120956152 | ||||||
chr9:120956285
|
C | T | 7 | a0008c0010t0001g0198a0008c0010t0001g0199a0008c0010t0001g0200others(4): Show | 8 | HG00738.hp1 HG01175.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.4762+1000G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120956285 | ||||||
chr9:120956293
|
C | G | 23 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(20): Show | 25 | HG00639.hp2 HG00735.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.4762+992G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120956293 | ||||||
chr9:120956305
|
T | A | 23 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(20): Show | 25 | HG00639.hp2 HG00735.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.4762+980A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120956305 | ||||||
chr9:120956593
|
T | C | 1 | a0002c0002t0001g0179 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.4762+692A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120956593 | ||||||
chr9:120956736
|
C | A | 30 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(27): Show | 33 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.4762+549G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120956736 | ||||||
chr9:120956794
|
T | C | 1 | a0003c0003t0001g0048 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4762+491A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120956794 | ||||||
chr9:120956902
|
A | G | 1 | a0002c0002t0001g0072 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4762+383T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120956902 | ||||||
chr9:120957045
|
T | C | 2 | a0001c0018t0001g0244a0019c0021t0001g0245 | 2 | HG02040.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.4762+240A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120957045 | ||||||
chr9:120957057
|
G | A | 82 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(79): Show | 89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.4762+228C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 39/40 | chr9 | 120957057 | ||||||
chr9:120957496
|
C | T | 1 | a0001c0022t0001g0229 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4679-128G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120957496 | ||||||
chr9:120957559
|
C | T | 3 | a0010c0014t0001g0005a0010c0014t0001g0219a0018c0023t0001g0205 | 4 | HG02976.hp1 HG03130.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4679-191G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120957559 | ||||||
chr9:120957980
|
C | A | 2 | a0001c0018t0001g0244a0019c0021t0001g0245 | 2 | HG02040.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.4679-612G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120957980 | ||||||
chr9:120958205
|
T | C | 23 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(20): Show | 25 | HG00639.hp2 HG00735.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.4679-837A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120958205 | ||||||
chr9:120958262
|
T | A | 23 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(20): Show | 25 | HG00639.hp2 HG00735.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.4679-894A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120958262 | ||||||
chr9:120958325
|
T | C | 1 | a0003c0003t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4679-957A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120958325 | ||||||
chr9:120958567
|
C | CT | 23 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(20): Show | 25 | HG00639.hp2 HG00735.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.4679-1200dupA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120958567 | ||||||
chr9:120958610
|
A | T | 82 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(79): Show | 89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.4679-1242T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120958610 | ||||||
chr9:120958661
|
A | T | 1 | a0003c0003t0001g0048 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4679-1293T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120958661 | ||||||
chr9:120958787
|
A | C | 3 | a0003c0003t0001g0057a0003c0003t0001g0061a0004c0005t0001g0218 | 3 | HG00639.hp1 HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4679-1419T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120958787 | ||||||
chr9:120958807
|
T | C | 2 | a0003c0004t0001g0028a0003c0004t0003g0029 | 2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4679-1439A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120958807 | ||||||
chr9:120958906
|
T | C | 82 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(79): Show | 89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.4678+1342A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120958906 | ||||||
chr9:120959232
|
A | ATTTC | 17 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0100others(14): Show | 18 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.4678+1012_4678+101 others(8): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120959232 | ||||||
chr9:120959232
|
ATTTC | A | 87 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.4678+1012_4678+101 others(8): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120959232 | ||||||
chr9:120959232
|
ATTTCTTT others(1): Show |
A | 53 | a0001c0001t0001g0068a0001c0018t0001g0244a0001c0024t0001g0070others(50): Show | 57 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.4678+1008_4678+101 others(12): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120959232 | ||||||
chr9:120959232
|
ATTTCTTT others(9): Show |
A | 30 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(27): Show | 33 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.4678+1000_4678+101 others(20): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120959232 | ||||||
chr9:120959291
|
TG | T | 82 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(79): Show | 89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.4678+956delC | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120959291 | ||||||
chr9:120959371
|
G | A | 4 | a0008c0010t0001g0198a0008c0010t0001g0199a0008c0010t0001g0200others(1): Show | 4 | HG00738.hp1 HG01175.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.4678+877C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120959371 | ||||||
chr9:120959449
|
G | A | 52 | a0001c0018t0001g0244a0001c0024t0001g0070a0002c0026t0001g0174others(49): Show | 56 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.4678+799C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120959449 | ||||||
chr9:120959556
|
C | T | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.4678+692G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120959556 | ||||||
chr9:120959611
|
T | G | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4678+637A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120959611 | ||||||
chr9:120959870
|
G | A | 197 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0030others(194): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.4678+378C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120959870 | ||||||
chr9:120959917
|
A | G | 4 | a0008c0010t0001g0198a0008c0010t0001g0199a0008c0010t0001g0200others(1): Show | 4 | HG00738.hp1 HG01175.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.4678+331T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120959917 | ||||||
chr9:120960081
|
T | TA | 82 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(79): Show | 89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.4678+166dupT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 38/40 | chr9 | 120960081 | ||||||
chr9:120960596
|
C | T | 1 | a0001c0018t0001g0248 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4589-259G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 37/40 | chr9 | 120960596 | ||||||
chr9:120960734
|
C | G | 7 | a0001c0001t0001g0068a0003c0004t0001g0018a0003c0004t0001g0022others(4): Show | 7 | HG02109.hp1 HG02451.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4589-397G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 37/40 | chr9 | 120960734 | ||||||
chr9:120960772
|
C | T | 4 | a0008c0010t0001g0198a0008c0010t0001g0199a0008c0010t0001g0200others(1): Show | 4 | HG00738.hp1 HG01175.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.4589-435G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 37/40 | chr9 | 120960772 | ||||||
chr9:120960834
|
T | C | 7 | a0001c0001t0001g0068a0003c0004t0001g0018a0003c0004t0001g0022others(4): Show | 7 | HG02109.hp1 HG02451.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4589-497A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 37/40 | chr9 | 120960834 | ||||||
chr9:120961018
|
C | T | 1 | a0003c0003t0001g0044 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.4588+464G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 37/40 | chr9 | 120961018 | ||||||
chr9:120961024
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | NA18948.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.4588+458C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 37/40 | chr9 | 120961024 | ||||||
chr9:120961073
|
T | C | 89 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(86): Show | 89 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.4588+409A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 37/40 | chr9 | 120961073 | ||||||
chr9:120961112
|
C | A | 82 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(79): Show | 89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.4588+370G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 37/40 | chr9 | 120961112 | ||||||
chr9:120961132
|
G | A | 30 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(27): Show | 33 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.4588+350C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 37/40 | chr9 | 120961132 | ||||||
chr9:120961179
|
T | G | 259 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(256): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.4588+303A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 37/40 | chr9 | 120961179 | ||||||
chr9:120961256
|
G | A | 7 | a0008c0010t0001g0198a0008c0010t0001g0199a0008c0010t0001g0200others(4): Show | 8 | HG00738.hp1 HG01175.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.4588+226C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 37/40 | chr9 | 120961256 | ||||||
chr9:120961333
|
C | G | 23 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(20): Show | 25 | HG00639.hp2 HG00735.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.4588+149G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 37/40 | chr9 | 120961333 | ||||||
chr9:120961904
|
A | C | 1 | a0001c0001t0001g0181 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.4505-339T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 36/40 | chr9 | 120961904 | ||||||
chr9:120961960
|
G | A | 2 | a0001c0001t0001g0068a0003c0004t0001g0022 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4505-395C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 36/40 | chr9 | 120961960 | ||||||
chr9:120962101
|
T | C | 3 | a0010c0014t0001g0005a0010c0014t0001g0219a0018c0023t0001g0205 | 4 | HG02976.hp1 HG03130.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4505-536A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 36/40 | chr9 | 120962101 | ||||||
chr9:120962230
|
A | G | 82 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(79): Show | 89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.4504+441T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 36/40 | chr9 | 120962230 | ||||||
chr9:120962280
|
T | C | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4504+391A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 36/40 | chr9 | 120962280 | ||||||
chr9:120962308
|
T | A | 1 | a0002c0002t0001g0072 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4504+363A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 36/40 | chr9 | 120962308 | ||||||
chr9:120962358
|
A | C | 2 | a0006c0008t0001g0240a0006c0008t0001g0241 | 2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4504+313T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 36/40 | chr9 | 120962358 | ||||||
chr9:120963113
|
G | T | 1 | a0003c0003t0001g0061 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4324-146C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 34/40 | chr9 | 120963113 | ||||||
chr9:120963246
|
G | A | 30 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(27): Show | 33 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.4324-279C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 34/40 | chr9 | 120963246 | ||||||
chr9:120963261
|
T | C | 23 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(20): Show | 25 | HG00639.hp2 HG00735.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.4324-294A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 34/40 | chr9 | 120963261 | ||||||
chr9:120963350
|
C | CA | 22 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(19): Show | 23 | HG00639.hp2 HG00735.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.4323+285dupT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 34/40 | chr9 | 120963350 | ||||||
chr9:120963498
|
C | T | 7 | a0008c0010t0001g0198a0008c0010t0001g0199a0008c0010t0001g0200others(4): Show | 8 | HG00738.hp1 HG01175.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.4323+138G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 34/40 | chr9 | 120963498 | ||||||
chr9:120963504
|
C | CAA | 25 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0228others(22): Show | 27 | HG00639.hp2 HG00735.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.4323+130_4323+131d others(4): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 34/40 | chr9 | 120963504 | ||||||
chr9:120963504
|
CA | C | 8 | a0001c0001t0001g0068a0001c0001t0001g0096a0003c0004t0001g0018others(5): Show | 8 | HG01123.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4323+131delT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 34/40 | chr9 | 120963504 | ||||||
chr9:120963627
|
A | T | 1 | a0003c0003t0001g0014 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4323+9T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 34/40 | chr9 | 120963627 | ||||||
chr9:120963751
|
A | G | 7 | a0008c0010t0001g0198a0008c0010t0001g0199a0008c0010t0001g0200others(4): Show | 8 | HG00738.hp1 HG01175.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.4221-13T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120963751 | ||||||
chr9:120963867
|
T | C | 46 | a0001c0024t0001g0070a0002c0026t0001g0174a0003c0003t0001g0001others(43): Show | 50 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.4221-129A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120963867 | ||||||
chr9:120964064
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4221-326C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120964064 | ||||||
chr9:120964127
|
A | C | 1 | a0001c0001t0001g0242 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4221-389T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120964127 | ||||||
chr9:120964306
|
C | T | 1 | a0018c0023t0001g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4221-568G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120964306 | ||||||
chr9:120964379
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0242 | 3 | HG02109.hp2 HG02258.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4221-641A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120964379 | ||||||
chr9:120964398
|
G | A | 2 | a0001c0018t0001g0244a0019c0021t0001g0245 | 2 | HG02040.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.4221-660C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120964398 | ||||||
chr9:120964447
|
C | T | 6 | a0003c0004t0001g0019a0003c0004t0001g0027a0003c0004t0001g0058others(3): Show | 6 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.4221-709G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120964447 | ||||||
chr9:120964471
|
GCAAA | G | 4 | a0008c0010t0001g0198a0008c0010t0001g0199a0008c0010t0001g0200others(1): Show | 4 | HG00738.hp1 HG01175.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.4221-737_4221-734d others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120964471 | ||||||
chr9:120965162
|
A | T | 4 | a0008c0010t0001g0198a0008c0010t0001g0199a0008c0010t0001g0200others(1): Show | 4 | HG00738.hp1 HG01175.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.4221-1424T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120965162 | ||||||
chr9:120965255
|
G | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0100a0001c0001t0001g0101others(4): Show | 8 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.4221-1517C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120965255 | ||||||
chr9:120965521
|
A | AAAAT | 15 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0243others(12): Show | 15 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.4221-1787_4221-178 others(8): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120965521 | ||||||
chr9:120965521
|
AAAAT | A | 65 | a0001c0001t0001g0068a0001c0001t0001g0100a0001c0001t0001g0101others(62): Show | 70 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.4221-1787_4221-178 others(8): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120965521 | ||||||
chr9:120965521
|
AAAATAAA others(1): Show |
A | 17 | a0001c0001t0001g0010a0001c0001t0001g0189a0001c0001t0001g0234others(14): Show | 18 | HG00738.hp1 HG01175.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.4221-1791_4221-178 others(12): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120965521 | ||||||
chr9:120965521
|
AAAATAAA others(5): Show |
A | 23 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(20): Show | 25 | HG00639.hp2 HG00735.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.4221-1795_4221-178 others(16): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120965521 | ||||||
chr9:120965521
|
AAAATAAA others(9): Show |
A | 1 | a0017c0025t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4221-1799_4221-178 others(20): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120965521 | ||||||
chr9:120965714
|
T | G | 1 | a0007c0009t0001g0208 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4221-1976A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120965714 | ||||||
chr9:120965716
|
C | T | 82 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(79): Show | 89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.4221-1978G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120965716 | ||||||
chr9:120965765
|
G | A | 1 | a0002c0002t0001g0164 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4221-2027C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120965765 | ||||||
chr9:120966272
|
A | G | 52 | a0001c0018t0001g0244a0001c0024t0001g0070a0002c0026t0001g0174others(49): Show | 56 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.4221-2534T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120966272 | ||||||
chr9:120966335
|
T | C | 82 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(79): Show | 89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.4221-2597A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120966335 | ||||||
chr9:120966342
|
T | C | 8 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(5): Show | 9 | HG01891.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.4221-2604A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120966342 | ||||||
chr9:120966655
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4220+2406C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120966655 | ||||||
chr9:120966680
|
G | T | 46 | a0001c0024t0001g0070a0002c0026t0001g0174a0003c0003t0001g0001others(43): Show | 50 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.4220+2381C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120966680 | ||||||
chr9:120966707
|
G | A | 2 | a0001c0018t0001g0244a0019c0021t0001g0245 | 2 | HG02040.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.4220+2354C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120966707 | ||||||
chr9:120967066
|
C | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0256 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4220+1995G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120967066 | ||||||
chr9:120967153
|
G | A | 30 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(27): Show | 33 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.4220+1908C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120967153 | ||||||
chr9:120967209
|
G | A | 1 | a0007c0009t0001g0208 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4220+1852C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120967209 | ||||||
chr9:120967259
|
C | CA | 36 | a0001c0001t0001g0009a0001c0001t0001g0074a0001c0001t0001g0090others(33): Show | 39 | HG00639.hp2 HG00735.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.4220+1801dupT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120967259 | ||||||
chr9:120967259
|
CA | C | 53 | a0001c0018t0001g0244a0001c0024t0001g0070a0002c0002t0001g0161others(50): Show | 57 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.4220+1801delT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120967259 | ||||||
chr9:120967595
|
A | C | 1 | a0002c0002t0001g0179 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.4220+1466T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120967595 | ||||||
chr9:120967618
|
G | A | 7 | a0008c0010t0001g0198a0008c0010t0001g0199a0008c0010t0001g0200others(4): Show | 8 | HG00738.hp1 HG01175.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.4220+1443C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120967618 | ||||||
chr9:120967684
|
T | C | 30 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(27): Show | 33 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.4220+1377A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120967684 | ||||||
chr9:120967717
|
C | A | 6 | a0001c0018t0001g0244a0003c0004t0001g0015a0003c0004t0001g0023others(3): Show | 6 | HG02040.hp2 HG02135.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.4220+1344G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120967717 | ||||||
chr9:120967722
|
TC | T | 6 | a0004c0005t0001g0004a0004c0005t0001g0216a0004c0005t0002g0212others(3): Show | 7 | HG01891.hp1 HG02280.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.4220+1338delG | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120967722 | ||||||
chr9:120967723
|
C | A | 46 | a0001c0018t0001g0244a0001c0024t0001g0070a0002c0026t0001g0174others(43): Show | 49 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.4220+1338G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120967723 | ||||||
chr9:120967724
|
T | A | 6 | a0004c0005t0001g0004a0004c0005t0001g0216a0004c0005t0002g0212others(3): Show | 7 | HG01891.hp1 HG02280.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.4220+1337A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120967724 | ||||||
chr9:120968022
|
A | G | 30 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(27): Show | 33 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.4220+1039T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120968022 | ||||||
chr9:120968276
|
A | G | 82 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(79): Show | 89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.4220+785T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120968276 | ||||||
chr9:120968290
|
T | C | 23 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(20): Show | 25 | HG00639.hp2 HG00735.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.4220+771A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120968290 | ||||||
chr9:120968356
|
C | T | 5 | a0003c0004t0001g0018a0007c0009t0001g0206a0007c0009t0001g0207others(2): Show | 5 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.4220+705G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120968356 | ||||||
chr9:120968411
|
C | T | 46 | a0001c0024t0001g0070a0002c0026t0001g0174a0003c0003t0001g0001others(43): Show | 50 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.4220+650G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120968411 | ||||||
chr9:120968466
|
AC | A | 3 | a0010c0014t0001g0005a0010c0014t0001g0219a0018c0023t0001g0205 | 4 | HG02976.hp1 HG03130.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4220+594delG | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120968466 | ||||||
chr9:120968558
|
A | C | 1 | a0001c0001t0001g0087 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4220+503T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120968558 | ||||||
chr9:120968696
|
T | C | 1 | a0002c0002t0001g0176 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.4220+365A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120968696 | ||||||
chr9:120968909
|
C | A | 7 | a0001c0001t0001g0068a0003c0004t0001g0018a0003c0004t0001g0022others(4): Show | 7 | HG02109.hp1 HG02451.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4220+152G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 33/40 | chr9 | 120968909 | ||||||
chr9:120969130
|
G | A | 53 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0227others(50): Show | 57 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.4163-12C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 32/40 | chr9 | 120969130 | ||||||
chr9:120969306
|
G | GAAGTCTT others(23): Show |
26 | a0001c0001t0001g0227a0001c0016t0001g0003a0003c0004t0001g0017others(23): Show | 28 | HG00738.hp1 HG01175.hp2 HG01981.hp2 others(25): Show |
intron_variant | MODIFIER | c.4163-189_4163-188i others(32): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 32/40 | chr9 | 120969306 | ||||||
chr9:120969372
|
A | C | 6 | a0001c0001t0001g0192a0002c0002t0001g0156a0002c0002t0001g0158others(3): Show | 6 | HG03654.hp2 NA18946.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.4163-254T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 32/40 | chr9 | 120969372 | ||||||
chr9:120969378
|
A | T | 3 | a0003c0003t0001g0036a0003c0003t0001g0049a0003c0003t0001g0050 | 3 | NA18939.hp2 NA18974.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.4163-260T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 32/40 | chr9 | 120969378 | ||||||
chr9:120969649
|
G | A | 1 | a0011c0013t0001g0143 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.4162+521C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 32/40 | chr9 | 120969649 | ||||||
chr9:120969900
|
T | G | 2 | a0001c0001t0001g0099a0002c0002t0001g0159 | 2 | NA18939.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.4162+270A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 32/40 | chr9 | 120969900 | ||||||
chr9:120970274
|
A | G | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.4081-23T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120970274 | ||||||
chr9:120970371
|
A | C | 3 | a0002c0002t0001g0114a0002c0002t0001g0130a0002c0002t0001g0133 | 3 | HG03017.hp1 HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.4081-120T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120970371 | ||||||
chr9:120970376
|
G | T | 3 | a0002c0002t0001g0114a0002c0002t0001g0130a0002c0002t0001g0133 | 3 | HG03017.hp1 HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.4081-125C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120970376 | ||||||
chr9:120970611
|
C | T | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4081-360G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120970611 | ||||||
chr9:120970855
|
A | C | 99 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0006t0001g0194others(96): Show | 105 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.4081-604T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120970855 | ||||||
chr9:120970893
|
T | C | 30 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0006t0001g0194others(27): Show | 32 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.4081-642A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120970893 | ||||||
chr9:120971029
|
A | G | 29 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0006t0001g0194others(26): Show | 31 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.4081-778T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120971029 | ||||||
chr9:120971147
|
G | T | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.4080+783C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120971147 | ||||||
chr9:120971171
|
C | CA | 6 | a0001c0001t0001g0228a0001c0001t0001g0235a0002c0002t0001g0149others(3): Show | 6 | HG02040.hp1 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.4080+758dupT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120971171 | ||||||
chr9:120971171
|
C | CAA | 30 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0006t0001g0194others(27): Show | 32 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.4080+757_4080+758d others(4): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120971171 | ||||||
chr9:120971194
|
A | G | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4080+736T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120971194 | ||||||
chr9:120971338
|
A | G | 1 | a0001c0001t0001g0252 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.4080+592T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120971338 | ||||||
chr9:120971352
|
C | T | 13 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0006t0001g0194others(10): Show | 13 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4080+578G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120971352 | ||||||
chr9:120971353
|
G | A | 1 | a0002c0002t0001g0124 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.4080+577C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120971353 | ||||||
chr9:120971362
|
T | C | 1 | a0008c0010t0001g0210 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4080+568A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120971362 | ||||||
chr9:120971450
|
G | T | 1 | a0017c0025t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4080+480C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120971450 | ||||||
chr9:120971673
|
G | A | 1 | a0003c0003t0001g0061 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4080+257C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120971673 | ||||||
chr9:120971726
|
C | T | 9 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(6): Show | 9 | HG02258.hp2 HG02818.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.4080+204G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120971726 | ||||||
chr9:120971736
|
C | T | 1 | a0017c0025t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4080+194G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 31/40 | chr9 | 120971736 | ||||||
chr9:120972009
|
GAAAC | G | 84 | a0001c0006t0001g0204a0001c0016t0001g0003a0003c0003t0001g0001others(81): Show | 90 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.4018-21_4018-18del others(4): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120972009 | ||||||
chr9:120972041
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4018-49T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120972041 | ||||||
chr9:120972212
|
C | A | 1 | a0002c0002t0001g0169 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4018-220G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120972212 | ||||||
chr9:120972223
|
A | G | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4018-231T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120972223 | ||||||
chr9:120972240
|
G | C | 1 | a0002c0002t0001g0155 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4018-248C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120972240 | ||||||
chr9:120972303
|
C | T | 1 | a0002c0002t0001g0123 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.4018-311G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120972303 | ||||||
chr9:120972724
|
G | A | 1 | a0003c0004t0001g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4018-732C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120972724 | ||||||
chr9:120972755
|
C | G | 1 | a0017c0025t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4018-763G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120972755 | ||||||
chr9:120973013
|
T | C | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4018-1021A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120973013 | ||||||
chr9:120973205
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0190 | 2 | NA19003.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.4018-1213C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120973205 | ||||||
chr9:120973277
|
A | T | 13 | a0003c0004t0001g0015a0003c0004t0001g0022a0003c0004t0001g0023others(10): Show | 14 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.4018-1285T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120973277 | ||||||
chr9:120973425
|
G | C | 3 | a0010c0014t0001g0005a0010c0014t0001g0219a0018c0023t0001g0205 | 4 | HG02976.hp1 HG03130.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4017+1354C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120973425 | ||||||
chr9:120973514
|
C | A | 1 | a0006c0008t0001g0105 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4017+1265G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120973514 | ||||||
chr9:120973641
|
CT | C | 11 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0012others(8): Show | 14 | HG00408.hp2 HG00438.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.4017+1137delA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120973641 | ||||||
chr9:120973790
|
C | T | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.4017+989G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120973790 | ||||||
chr9:120973851
|
C | T | 1 | a0003c0004t0001g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4017+928G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120973851 | ||||||
chr9:120973852
|
G | A | 13 | a0003c0004t0001g0015a0003c0004t0001g0022a0003c0004t0001g0023others(10): Show | 14 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.4017+927C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120973852 | ||||||
chr9:120973861
|
C | T | 1 | a0002c0002t0001g0179 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.4017+918G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120973861 | ||||||
chr9:120973877
|
G | A | 1 | a0003c0003t0001g0039 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.4017+902C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120973877 | ||||||
chr9:120973973
|
C | CA | 69 | a0001c0006t0001g0204a0001c0018t0001g0244a0001c0018t0001g0248others(66): Show | 73 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.4017+805dupT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120973973 | ||||||
chr9:120974140
|
C | T | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4017+639G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120974140 | ||||||
chr9:120974260
|
T | G | 1 | a0002c0002t0001g0193 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4017+519A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120974260 | ||||||
chr9:120974459
|
C | T | 12 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(9): Show | 13 | HG02258.hp2 HG02818.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.4017+320G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120974459 | ||||||
chr9:120974740
|
C | T | 69 | a0001c0006t0001g0204a0001c0018t0001g0244a0001c0018t0001g0248others(66): Show | 73 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.4017+39G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120974740 | ||||||
chr9:120974762
|
G | C | 100 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(97): Show | 106 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.4017+17C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 30/40 | chr9 | 120974762 | ||||||
chr9:120975024
|
T | C | 1 | a0003c0003t0001g0037 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.3865-93A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/40 | chr9 | 120975024 | ||||||
chr9:120975026
|
G | T | 1 | a0012c0011t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3865-95C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/40 | chr9 | 120975026 | ||||||
chr9:120975172
|
T | G | 1 | a0003c0003t0001g0048 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3865-241A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/40 | chr9 | 120975172 | ||||||
chr9:120975392
|
C | T | 1 | a0003c0004t0001g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3865-461G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/40 | chr9 | 120975392 | ||||||
chr9:120975442
|
G | A | 56 | a0001c0006t0001g0204a0001c0018t0001g0244a0001c0018t0001g0248others(53): Show | 59 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.3865-511C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/40 | chr9 | 120975442 | ||||||
chr9:120975837
|
T | C | 69 | a0001c0006t0001g0204a0001c0018t0001g0244a0001c0018t0001g0248others(66): Show | 73 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.3864+863A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/40 | chr9 | 120975837 | ||||||
chr9:120975917
|
A | G | 1 | a0004c0005t0001g0217 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3864+783T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/40 | chr9 | 120975917 | ||||||
chr9:120975970
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3864+730G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/40 | chr9 | 120975970 | ||||||
chr9:120976085
|
C | T | 1 | a0002c0002t0001g0113 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3864+615G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/40 | chr9 | 120976085 | ||||||
chr9:120976238
|
T | A | 1 | a0001c0001t0001g0097 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3864+462A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/40 | chr9 | 120976238 | ||||||
chr9:120976289
|
A | C | 1 | a0001c0001t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3864+411T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/40 | chr9 | 120976289 | ||||||
chr9:120976317
|
G | A | 13 | a0003c0004t0001g0015a0003c0004t0001g0022a0003c0004t0001g0023others(10): Show | 14 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.3864+383C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/40 | chr9 | 120976317 | ||||||
chr9:120976530
|
T | C | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3864+170A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/40 | chr9 | 120976530 | ||||||
chr9:120976590
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3864+110A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 29/40 | chr9 | 120976590 | ||||||
chr9:120976926
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3659-21A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 28/40 | chr9 | 120976926 | ||||||
chr9:120977189
|
C | T | 1 | a0005c0007t0001g0261 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3659-284G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 28/40 | chr9 | 120977189 | ||||||
chr9:120977282
|
C | T | 10 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(7): Show | 10 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.3659-377G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 28/40 | chr9 | 120977282 | ||||||
chr9:120977715
|
C | T | 106 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(103): Show | 108 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.3659-810G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 28/40 | chr9 | 120977715 | ||||||
chr9:120977845
|
T | C | 1 | a0001c0001t0001g0010 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3659-940A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 28/40 | chr9 | 120977845 | ||||||
chr9:120978160
|
C | T | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3659-1255G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 28/40 | chr9 | 120978160 | ||||||
chr9:120978206
|
C | T | 106 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(103): Show | 108 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.3659-1301G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 28/40 | chr9 | 120978206 | ||||||
chr9:120978248
|
A | G | 10 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(7): Show | 10 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.3659-1343T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 28/40 | chr9 | 120978248 | ||||||
chr9:120978479
|
T | A | 1 | a0002c0002t0001g0175 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3659-1574A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 28/40 | chr9 | 120978479 | ||||||
chr9:120978720
|
C | T | 2 | a0003c0004t0001g0020a0003c0004t0001g0056 | 2 | HG02257.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3658+1363G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 28/40 | chr9 | 120978720 | ||||||
chr9:120978920
|
C | A | 1 | a0003c0003t0001g0026 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3658+1163G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 28/40 | chr9 | 120978920 | ||||||
chr9:120979072
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3658+1011C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 28/40 | chr9 | 120979072 | ||||||
chr9:120979165
|
C | A | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3658+918G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 28/40 | chr9 | 120979165 | ||||||
chr9:120979232
|
G | T | 3 | a0010c0014t0001g0005a0010c0014t0001g0219a0018c0023t0001g0205 | 4 | HG02976.hp1 HG03130.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3658+851C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 28/40 | chr9 | 120979232 | ||||||
chr9:120979544
|
G | T | 4 | a0001c0001t0001g0088a0002c0002t0001g0125a0002c0002t0001g0129others(1): Show | 4 | HG01069.hp2 HG01255.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.3658+539C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 28/40 | chr9 | 120979544 | ||||||
chr9:120980338
|
C | G | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3487-84G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 27/40 | chr9 | 120980338 | ||||||
chr9:120980418
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3487-164C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 27/40 | chr9 | 120980418 | ||||||
chr9:120980540
|
G | A | 181 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(178): Show | 186 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.3487-286C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 27/40 | chr9 | 120980540 | ||||||
chr9:120980585
|
A | C | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3487-331T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 27/40 | chr9 | 120980585 | ||||||
chr9:120980659
|
C | T | 56 | a0001c0006t0001g0204a0003c0003t0001g0001a0003c0003t0001g0002others(53): Show | 60 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.3487-405G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 27/40 | chr9 | 120980659 | ||||||
chr9:120980677
|
G | A | 1 | a0003c0004t0001g0015 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3487-423C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 27/40 | chr9 | 120980677 | ||||||
chr9:120980741
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3487-487C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 27/40 | chr9 | 120980741 | ||||||
chr9:120980843
|
C | T | 1 | a0003c0004t0001g0015 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3487-589G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 27/40 | chr9 | 120980843 | ||||||
chr9:120980848
|
C | T | 2 | a0003c0004t0001g0031a0003c0004t0001g0032 | 2 | HG01074.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.3487-594G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 27/40 | chr9 | 120980848 | ||||||
chr9:120980934
|
G | C | 1 | a0001c0001t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3487-680C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 27/40 | chr9 | 120980934 | ||||||
chr9:120981030
|
T | C | 3 | a0010c0014t0001g0005a0010c0014t0001g0219a0018c0023t0001g0205 | 4 | HG02976.hp1 HG03130.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3487-776A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 27/40 | chr9 | 120981030 | ||||||
chr9:120981061
|
C | T | 2 | a0002c0002t0001g0152a0002c0002t0001g0153 | 2 | HG01261.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3486+783G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 27/40 | chr9 | 120981061 | ||||||
chr9:120981128
|
G | A | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3486+716C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 27/40 | chr9 | 120981128 | ||||||
chr9:120981402
|
G | A | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3486+442C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 27/40 | chr9 | 120981402 | ||||||
chr9:120981434
|
G | T | 9 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(6): Show | 9 | HG02258.hp2 HG02818.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.3486+410C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 27/40 | chr9 | 120981434 | ||||||
chr9:120981643
|
C | T | 20 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(17): Show | 20 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.3486+201G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 27/40 | chr9 | 120981643 | ||||||
chr9:120981974
|
A | G | 10 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(7): Show | 10 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.3391-35T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 26/40 | chr9 | 120981974 | ||||||
chr9:120982219
|
C | T | 20 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(17): Show | 20 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.3391-280G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 26/40 | chr9 | 120982219 | ||||||
chr9:120982256
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3391-317G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 26/40 | chr9 | 120982256 | ||||||
chr9:120982289
|
C | T | 1 | a0017c0025t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3391-350G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 26/40 | chr9 | 120982289 | ||||||
chr9:120982300
|
G | A | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3390+355C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 26/40 | chr9 | 120982300 | ||||||
chr9:120982439
|
T | C | 9 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(6): Show | 9 | HG02258.hp2 HG02818.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.3390+216A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 26/40 | chr9 | 120982439 | ||||||
chr9:120982646
|
T | C | 9 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(6): Show | 9 | HG02258.hp2 HG02818.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.3390+9A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 26/40 | chr9 | 120982646 | ||||||
chr9:120982851
|
G | A | 1 | a0002c0002t0001g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3231-37C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120982851 | ||||||
chr9:120983057
|
T | C | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3231-243A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120983057 | ||||||
chr9:120983538
|
T | C | 11 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(8): Show | 11 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.3231-724A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120983538 | ||||||
chr9:120983799
|
TA | T | 13 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0001g0227others(10): Show | 13 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.3231-986delT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120983799 | ||||||
chr9:120983977
|
G | A | 180 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(177): Show | 186 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.3231-1163C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120983977 | ||||||
chr9:120984160
|
T | C | 86 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0087others(83): Show | 86 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.3231-1346A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120984160 | ||||||
chr9:120984206
|
AT | A | 176 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(173): Show | 182 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.3231-1393delA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120984206 | ||||||
chr9:120984216
|
TG | T | 4 | a0002c0002t0001g0072a0002c0002t0001g0111a0002c0002t0001g0126others(1): Show | 4 | HG01123.hp1 HG01361.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.3231-1403delC | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120984216 | ||||||
chr9:120984252
|
G | T | 9 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(6): Show | 9 | HG02258.hp2 HG02818.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.3231-1438C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120984252 | ||||||
chr9:120984315
|
G | A | 2 | a0006c0008t0001g0240a0006c0008t0001g0241 | 2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3231-1501C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120984315 | ||||||
chr9:120984377
|
T | C | 1 | a0003c0003t0001g0057 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3231-1563A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120984377 | ||||||
chr9:120984518
|
T | C | 20 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(17): Show | 20 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.3231-1704A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120984518 | ||||||
chr9:120984521
|
G | A | 53 | a0001c0006t0001g0204a0003c0003t0001g0001a0003c0003t0001g0002others(50): Show | 56 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.3231-1707C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120984521 | ||||||
chr9:120984696
|
AATAGGT | A | 86 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0087others(83): Show | 86 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.3231-1888_3231-188 others(10): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120984696 | ||||||
chr9:120984714
|
C | CT | 11 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0080others(8): Show | 12 | HG02145.hp2 HG02572.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.3231-1901dupA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120984714 | ||||||
chr9:120984714
|
CT | C | 18 | a0001c0001t0001g0098a0001c0001t0001g0101a0001c0001t0001g0181others(15): Show | 19 | HG00408.hp2 HG01934.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.3231-1901delA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120984714 | ||||||
chr9:120984714
|
CTT | C | 142 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0087others(139): Show | 145 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.3231-1902_3231-190 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120984714 | ||||||
chr9:120984714
|
CTTT | C | 20 | a0001c0001t0001g0073a0002c0002t0001g0114a0002c0002t0001g0119others(17): Show | 21 | HG00621.hp1 HG01256.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.3231-1903_3231-190 others(7): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120984714 | ||||||
chr9:120984754
|
C | G | 3 | a0001c0001t0001g0090a0014c0017t0001g0079a0014c0017t0001g0089 | 3 | NA18952.hp1 NA18975.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.3231-1940G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120984754 | ||||||
chr9:120985038
|
C | A | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3231-2224G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120985038 | ||||||
chr9:120985057
|
G | C | 56 | a0001c0006t0001g0204a0003c0003t0001g0001a0003c0003t0001g0002others(53): Show | 60 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.3231-2243C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120985057 | ||||||
chr9:120985156
|
C | T | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3231-2342G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120985156 | ||||||
chr9:120985390
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3231-2576C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120985390 | ||||||
chr9:120985476
|
C | G | 13 | a0003c0004t0001g0015a0003c0004t0001g0022a0003c0004t0001g0023others(10): Show | 14 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.3231-2662G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120985476 | ||||||
chr9:120985528
|
T | G | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3231-2714A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120985528 | ||||||
chr9:120985562
|
AATAG | A | 11 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(8): Show | 11 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.3231-2752_3231-274 others(8): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120985562 | ||||||
chr9:120985663
|
G | A | 180 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(177): Show | 186 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.3231-2849C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120985663 | ||||||
chr9:120985716
|
A | G | 1 | a0002c0002t0001g0157 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3231-2902T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120985716 | ||||||
chr9:120985875
|
A | T | 76 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(73): Show | 80 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.3231-3061T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120985875 | ||||||
chr9:120985955
|
C | T | 1 | a0009c0012t0001g0064 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3230+3091G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120985955 | ||||||
chr9:120986366
|
T | TA | 165 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(162): Show | 170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.3230+2679dupT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120986366 | ||||||
chr9:120986383
|
G | A | 1 | a0001c0024t0001g0070 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3230+2663C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120986383 | ||||||
chr9:120986477
|
A | T | 52 | a0001c0006t0001g0204a0003c0003t0001g0001a0003c0003t0001g0002others(49): Show | 55 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.3230+2569T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120986477 | ||||||
chr9:120986515
|
G | A | 1 | a0002c0002t0001g0126 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3230+2531C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120986515 | ||||||
chr9:120986552
|
G | C | 23 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(20): Show | 23 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.3230+2494C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120986552 | ||||||
chr9:120986621
|
T | TGTGGGGC others(27): Show |
11 | a0003c0004t0001g0015a0003c0004t0001g0022a0004c0005t0001g0004others(8): Show | 12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3230+2391_3230+242 others(38): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120986621 | ||||||
chr9:120986621
|
T | TGTGGGGC others(61): Show |
3 | a0003c0004t0001g0023a0003c0004t0001g0024a0003c0004t0001g0025 | 3 | HG02451.hp1 HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3230+2424_3230+242 others(72): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120986621 | ||||||
chr9:120986704
|
C | G | 1 | a0008c0010t0001g0200 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3230+2342G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120986704 | ||||||
chr9:120986924
|
T | C | 1 | a0005c0007t0001g0263 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3230+2122A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120986924 | ||||||
chr9:120987207
|
A | G | 1 | a0002c0002t0001g0173 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3230+1839T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120987207 | ||||||
chr9:120987434
|
GGAGATCG others(3): Show |
G | 5 | a0003c0003t0001g0065a0003c0003t0001g0067a0009c0012t0001g0062others(2): Show | 5 | HG02055.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3230+1602_3230+161 others(14): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120987434 | ||||||
chr9:120987441
|
G | A | 18 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(15): Show | 18 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.3230+1605C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120987441 | ||||||
chr9:120987445
|
C | T | 5 | a0003c0003t0001g0065a0003c0003t0001g0067a0009c0012t0001g0062others(2): Show | 5 | HG02055.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3230+1601G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120987445 | ||||||
chr9:120987446
|
C | G | 5 | a0003c0003t0001g0065a0003c0003t0001g0067a0009c0012t0001g0062others(2): Show | 5 | HG02055.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3230+1600G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120987446 | ||||||
chr9:120987569
|
C | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0243a0001c0001t0001g0246 | 3 | HG01123.hp2 HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.3230+1477G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120987569 | ||||||
chr9:120987636
|
C | CA | 94 | a0001c0001t0001g0091a0001c0001t0001g0181a0001c0006t0001g0194others(91): Show | 94 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.3230+1409dupT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120987636 | ||||||
chr9:120987636
|
CA | C | 60 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0012others(57): Show | 63 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.3230+1409delT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120987636 | ||||||
chr9:120987674
|
C | A | 1 | a0004c0005t0001g0218 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3230+1372G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120987674 | ||||||
chr9:120987680
|
TTAAAG | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0243a0001c0001t0001g0246others(6): Show | 10 | HG00099.hp2 HG00738.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.3230+1361_3230+136 others(9): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120987680 | ||||||
chr9:120987855
|
C | T | 1 | a0003c0003t0001g0061 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3230+1191G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120987855 | ||||||
chr9:120987859
|
C | T | 81 | a0002c0002t0001g0071a0002c0002t0001g0072a0002c0002t0001g0109others(78): Show | 81 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.3230+1187G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120987859 | ||||||
chr9:120988137
|
G | C | 1 | a0004c0005t0002g0214 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3230+909C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120988137 | ||||||
chr9:120988303
|
G | A | 1 | a0001c0006t0001g0203 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3230+743C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120988303 | ||||||
chr9:120988577
|
G | C | 8 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(5): Show | 9 | HG01891.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.3230+469C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120988577 | ||||||
chr9:120988678
|
T | C | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3230+368A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120988678 | ||||||
chr9:120988732
|
G | A | 1 | a0002c0002t0001g0118 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.3230+314C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120988732 | ||||||
chr9:120988829
|
A | G | 1 | a0003c0003t0001g0057 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3230+217T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120988829 | ||||||
chr9:120988909
|
C | T | 1 | a0002c0002t0001g0147 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3230+137G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120988909 | ||||||
chr9:120989029
|
C | G | 1 | a0003c0004t0001g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3230+17G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 25/40 | chr9 | 120989029 | ||||||
chr9:120989289
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3155-168A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 24/40 | chr9 | 120989289 | ||||||
chr9:120989354
|
A | C | 2 | a0004c0005t0001g0004a0004c0005t0001g0216 | 3 | HG02647.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3154+214T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 24/40 | chr9 | 120989354 | ||||||
chr9:120989370
|
C | T | 11 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(8): Show | 11 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.3154+198G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 24/40 | chr9 | 120989370 | ||||||
chr9:120989383
|
A | G | 18 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(15): Show | 18 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.3154+185T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 24/40 | chr9 | 120989383 | ||||||
chr9:120989438
|
G | T | 6 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(3): Show | 6 | HG02258.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.3154+130C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 24/40 | chr9 | 120989438 | ||||||
chr9:120989522
|
A | G | 125 | a0001c0018t0001g0244a0001c0018t0001g0248a0002c0002t0001g0071others(122): Show | 128 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.3154+46T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 24/40 | chr9 | 120989522 | ||||||
chr9:120989810
|
T | C | 2 | a0002c0002t0001g0170a0002c0002t0001g0175 | 2 | NA18964.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2942-30A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 23/40 | chr9 | 120989810 | ||||||
chr9:120989961
|
CA | C | 6 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 6 | HG02572.hp2 NA18967.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.2942-182delT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 23/40 | chr9 | 120989961 | ||||||
chr9:120989964
|
A | C | 1 | a0003c0003t0001g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2942-184T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 23/40 | chr9 | 120989964 | ||||||
chr9:120989965
|
A | C | 1 | a0004c0005t0001g0218 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2942-185T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 23/40 | chr9 | 120989965 | ||||||
chr9:120990518
|
C | T | 6 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(3): Show | 6 | HG02258.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2941+673G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 23/40 | chr9 | 120990518 | ||||||
chr9:120990579
|
C | T | 3 | a0006c0008t0001g0104a0006c0008t0001g0105a0006c0008t0001g0106 | 3 | HG02258.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2941+612G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 23/40 | chr9 | 120990579 | ||||||
chr9:120990583
|
T | C | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2941+608A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 23/40 | chr9 | 120990583 | ||||||
chr9:120990864
|
G | A | 1 | a0002c0002t0001g0132 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2941+327C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 23/40 | chr9 | 120990864 | ||||||
chr9:120990975
|
T | C | 18 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(15): Show | 18 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.2941+216A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 23/40 | chr9 | 120990975 | ||||||
chr9:120990998
|
G | A | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2941+193C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 23/40 | chr9 | 120990998 | ||||||
chr9:120991150
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2941+41G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 23/40 | chr9 | 120991150 | ||||||
chr9:120991297
|
T | C | 11 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(8): Show | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2852-17A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120991297 | ||||||
chr9:120991322
|
G | T | 12 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(9): Show | 12 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.2852-42C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120991322 | ||||||
chr9:120991566
|
C | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(8): Show | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2852-286G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120991566 | ||||||
chr9:120991764
|
A | G | 1 | a0001c0001t0004g0264 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2852-484T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120991764 | ||||||
chr9:120991770
|
T | C | 1 | a0003c0004t0001g0017 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2852-490A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120991770 | ||||||
chr9:120991936
|
A | G | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2852-656T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120991936 | ||||||
chr9:120991965
|
T | C | 3 | a0003c0004t0001g0023a0003c0004t0001g0024a0003c0004t0001g0025 | 3 | HG02451.hp1 HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2852-685A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120991965 | ||||||
chr9:120992615
|
C | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | NA18948.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2852-1335G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120992615 | ||||||
chr9:120992682
|
G | A | 1 | a0003c0003t0001g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2852-1402C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120992682 | ||||||
chr9:120993105
|
T | A | 11 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(8): Show | 11 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2852-1825A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120993105 | ||||||
chr9:120993214
|
T | G | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2852-1934A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120993214 | ||||||
chr9:120993396
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2852-2116T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120993396 | ||||||
chr9:120993421
|
T | TTA | 81 | a0002c0002t0001g0071a0002c0002t0001g0072a0002c0002t0001g0109others(78): Show | 81 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.2852-2143_2852-214 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120993421 | ||||||
chr9:120993435
|
A | T | 1 | a0017c0025t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2852-2155T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120993435 | ||||||
chr9:120993445
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2852-2165G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120993445 | ||||||
chr9:120993567
|
T | C | 179 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(176): Show | 185 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.2852-2287A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120993567 | ||||||
chr9:120993613
|
G | A | 81 | a0002c0002t0001g0071a0002c0002t0001g0072a0002c0002t0001g0109others(78): Show | 81 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.2852-2333C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120993613 | ||||||
chr9:120993615
|
G | T | 3 | a0001c0001t0001g0090a0014c0017t0001g0079a0014c0017t0001g0089 | 3 | NA18952.hp1 NA18975.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.2852-2335C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120993615 | ||||||
chr9:120993624
|
G | A | 8 | a0003c0003t0001g0014a0003c0003t0001g0036a0003c0003t0001g0039others(5): Show | 8 | HG00597.hp1 HG02015.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.2852-2344C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120993624 | ||||||
chr9:120993665
|
G | A | 1 | a0017c0025t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2852-2385C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120993665 | ||||||
chr9:120993681
|
C | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(8): Show | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2852-2401G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120993681 | ||||||
chr9:120993708
|
C | T | 6 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(3): Show | 6 | HG02258.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2852-2428G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120993708 | ||||||
chr9:120993722
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2852-2442C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120993722 | ||||||
chr9:120993882
|
C | T | 116 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(113): Show | 119 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.2851+2358G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120993882 | ||||||
chr9:120994088
|
T | C | 6 | a0002c0002t0001g0109a0002c0002t0001g0119a0002c0002t0001g0120others(3): Show | 6 | HG00621.hp1 HG02071.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.2851+2152A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120994088 | ||||||
chr9:120994367
|
G | C | 1 | a0002c0002t0001g0117 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2851+1873C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120994367 | ||||||
chr9:120994400
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2851+1840A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120994400 | ||||||
chr9:120994412
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2851+1828C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120994412 | ||||||
chr9:120994460
|
G | A | 1 | a0007c0009t0001g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2851+1780C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120994460 | ||||||
chr9:120994592
|
CA | C | 97 | a0001c0016t0001g0003a0002c0002t0001g0071a0002c0002t0001g0072others(94): Show | 100 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.2851+1647delT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120994592 | ||||||
chr9:120994603
|
T | A | 18 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(15): Show | 18 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.2851+1637A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120994603 | ||||||
chr9:120994687
|
T | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG01069.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.2851+1553A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120994687 | ||||||
chr9:120994705
|
C | T | 18 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(15): Show | 18 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.2851+1535G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120994705 | ||||||
chr9:120994909
|
A | C | 109 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(106): Show | 112 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.2851+1331T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120994909 | ||||||
chr9:120994922
|
GA | G | 84 | a0001c0001t0001g0008a0002c0002t0001g0071a0002c0002t0001g0072others(81): Show | 85 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.2851+1317delT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120994922 | ||||||
chr9:120995109
|
A | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0185 | 2 | NA18944.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.2851+1131T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120995109 | ||||||
chr9:120995134
|
G | A | 116 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(113): Show | 119 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.2851+1106C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120995134 | ||||||
chr9:120995342
|
G | C | 11 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(8): Show | 11 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2851+898C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120995342 | ||||||
chr9:120995820
|
C | CT | 99 | a0001c0001t0001g0077a0001c0006t0001g0194a0001c0006t0001g0195others(96): Show | 100 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.2851+419dupA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120995820 | ||||||
chr9:120995820
|
C | CTT | 12 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(9): Show | 14 | HG00639.hp1 HG01891.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.2851+418_2851+419d others(4): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120995820 | ||||||
chr9:120995820
|
CT | C | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0228others(2): Show | 5 | HG01069.hp2 HG01243.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.2851+419delA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120995820 | ||||||
chr9:120995921
|
C | T | 6 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(3): Show | 6 | HG02258.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2851+319G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120995921 | ||||||
chr9:120996147
|
T | C | 82 | a0002c0002t0001g0071a0002c0002t0001g0072a0002c0002t0001g0109others(79): Show | 82 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.2851+93A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 22/40 | chr9 | 120996147 | ||||||
chr9:120996354
|
A | G | 12 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(9): Show | 12 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.2791-54T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 21/40 | chr9 | 120996354 | ||||||
chr9:120996362
|
G | C | 1 | a0003c0003t0001g0050 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2791-62C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 21/40 | chr9 | 120996362 | ||||||
chr9:120996539
|
C | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(8): Show | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2791-239G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 21/40 | chr9 | 120996539 | ||||||
chr9:120996592
|
G | T | 7 | a0001c0001t0001g0068a0006c0008t0001g0069a0006c0008t0001g0104others(4): Show | 7 | HG02258.hp2 HG02818.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2791-292C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 21/40 | chr9 | 120996592 | ||||||
chr9:120996649
|
T | G | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2791-349A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 21/40 | chr9 | 120996649 | ||||||
chr9:120996727
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2791-427C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 21/40 | chr9 | 120996727 | ||||||
chr9:120996766
|
G | A | 98 | a0001c0016t0001g0003a0002c0002t0001g0071a0002c0002t0001g0072others(95): Show | 101 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.2791-466C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 21/40 | chr9 | 120996766 | ||||||
chr9:120996843
|
G | A | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2791-543C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 21/40 | chr9 | 120996843 | ||||||
chr9:120996974
|
G | A | 116 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(113): Show | 119 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.2790+573C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 21/40 | chr9 | 120996974 | ||||||
chr9:120997082
|
C | A | 1 | a0001c0001t0001g0008 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2790+465G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 21/40 | chr9 | 120997082 | ||||||
chr9:120997318
|
T | G | 1 | a0001c0001t0001g0092 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2790+229A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 21/40 | chr9 | 120997318 | ||||||
chr9:120997427
|
T | C | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2790+120A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 21/40 | chr9 | 120997427 | ||||||
chr9:120997485
|
C | T | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2790+62G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 21/40 | chr9 | 120997485 | ||||||
chr9:120997788
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2563-14C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120997788 | ||||||
chr9:120997789
|
A | T | 1 | a0001c0001t0001g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2563-15T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120997789 | ||||||
chr9:120997808
|
A | AT | 6 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(3): Show | 6 | HG02258.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2563-35dupA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120997808 | ||||||
chr9:120997808
|
AT | A | 85 | a0001c0001t0001g0068a0001c0016t0001g0003a0002c0002t0001g0071others(82): Show | 86 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2563-35delA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120997808 | ||||||
chr9:120997829
|
G | C | 82 | a0002c0002t0001g0071a0002c0002t0001g0072a0002c0002t0001g0109others(79): Show | 82 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.2563-55C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120997829 | ||||||
chr9:120997895
|
C | T | 89 | a0001c0001t0001g0068a0002c0002t0001g0071a0002c0002t0001g0072others(86): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.2563-121G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120997895 | ||||||
chr9:120997952
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2563-178C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120997952 | ||||||
chr9:120998045
|
C | T | 81 | a0002c0002t0001g0071a0002c0002t0001g0072a0002c0002t0001g0109others(78): Show | 81 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.2563-271G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120998045 | ||||||
chr9:120998087
|
T | G | 1 | a0003c0004t0001g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2563-313A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120998087 | ||||||
chr9:120998198
|
G | A | 9 | a0003c0003t0001g0065a0003c0003t0001g0067a0003c0004t0001g0058others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2563-424C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120998198 | ||||||
chr9:120998385
|
C | G | 1 | a0002c0002t0001g0164 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2563-611G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120998385 | ||||||
chr9:120998954
|
T | A | 3 | a0002c0002t0001g0167a0002c0002t0001g0171a0002c0002t0001g0172 | 3 | NA18970.hp2 NA19010.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2563-1180A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120998954 | ||||||
chr9:120999016
|
C | T | 1 | a0006c0008t0001g0106 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2563-1242G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120999016 | ||||||
chr9:120999040
|
C | A | 2 | a0005c0007t0001g0260a0005c0007t0001g0262 | 2 | HG02135.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.2563-1266G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120999040 | ||||||
chr9:120999194
|
C | T | 1 | a0003c0004t0001g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2563-1420G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120999194 | ||||||
chr9:120999363
|
G | T | 1 | a0001c0001t0001g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2563-1589C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120999363 | ||||||
chr9:120999844
|
A | C | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2563-2070T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120999844 | ||||||
chr9:120999990
|
C | T | 1 | a0003c0003t0001g0061 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2563-2216G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 120999990 | ||||||
chr9:121000043
|
G | A | 83 | a0001c0001t0001g0068a0002c0002t0001g0071a0002c0002t0001g0072others(80): Show | 83 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.2563-2269C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121000043 | ||||||
chr9:121000058
|
C | CA | 15 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(12): Show | 15 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.2563-2285dupT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121000058 | ||||||
chr9:121000058
|
C | CAA | 59 | a0001c0018t0001g0244a0001c0018t0001g0248a0003c0003t0001g0001others(56): Show | 62 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.2563-2286_2563-228 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121000058 | ||||||
chr9:121000121
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2563-2347T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121000121 | ||||||
chr9:121000137
|
T | G | 1 | a0002c0002t0001g0161 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2563-2363A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121000137 | ||||||
chr9:121000318
|
T | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0235a0001c0001t0001g0239 | 4 | HG02145.hp2 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2563-2544A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121000318 | ||||||
chr9:121000398
|
T | A | 156 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(153): Show | 159 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.2563-2624A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121000398 | ||||||
chr9:121000401
|
T | C | 1 | a0001c0006t0001g0204 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2563-2627A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121000401 | ||||||
chr9:121000509
|
T | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0228a0001c0001t0001g0242others(2): Show | 6 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2563-2735A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121000509 | ||||||
chr9:121000702
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2563-2928G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121000702 | ||||||
chr9:121000728
|
T | C | 94 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(91): Show | 94 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.2563-2954A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121000728 | ||||||
chr9:121000745
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2563-2971C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121000745 | ||||||
chr9:121001368
|
T | C | 4 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(1): Show | 4 | HG02258.hp2 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2563-3594A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121001368 | ||||||
chr9:121001478
|
T | C | 1 | a0007c0009t0001g0206 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2563-3704A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121001478 | ||||||
chr9:121001602
|
T | C | 62 | a0001c0018t0001g0244a0001c0018t0001g0248a0003c0003t0001g0001others(59): Show | 65 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.2563-3828A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121001602 | ||||||
chr9:121001667
|
A | G | 1 | a0002c0002t0001g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2563-3893T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121001667 | ||||||
chr9:121001916
|
C | G | 169 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(166): Show | 175 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.2562+4003G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121001916 | ||||||
chr9:121002085
|
A | G | 3 | a0001c0018t0001g0244a0001c0018t0001g0248a0019c0021t0001g0245 | 3 | HG02015.hp1 HG02040.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.2562+3834T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002085 | ||||||
chr9:121002134
|
ATATATGT others(3): Show |
A | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2562+3775_2562+378 others(14): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002134 | ||||||
chr9:121002175
|
T | G | 83 | a0001c0001t0001g0084a0002c0002t0001g0071a0002c0002t0001g0072others(80): Show | 83 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.2562+3744A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002175 | ||||||
chr9:121002183
|
G | T | 1 | a0015c0020t0001g0021 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2562+3736C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002183 | ||||||
chr9:121002197
|
CGTATATA others(25): Show |
C | 41 | a0002c0002t0001g0109a0002c0002t0001g0110a0002c0002t0001g0113others(38): Show | 41 | HG00280.hp1 HG00408.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.2562+3690_2562+372 others(36): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002197 | ||||||
chr9:121002212
|
A | G | 40 | a0001c0001t0001g0084a0002c0002t0001g0071a0002c0002t0001g0072others(37): Show | 40 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.2562+3707T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002212 | ||||||
chr9:121002214
|
ACG | A | 39 | a0001c0001t0001g0084a0002c0002t0001g0071a0002c0002t0001g0072others(36): Show | 39 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2562+3703_2562+370 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002214 | ||||||
chr9:121002215
|
C | T | 1 | a0002c0002t0001g0117 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2562+3704G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002215 | ||||||
chr9:121002216
|
G | A | 2 | a0002c0002t0001g0117a0017c0025t0001g0223 | 2 | HG02257.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2562+3703C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002216 | ||||||
chr9:121002216
|
GTA | G | 19 | a0001c0001t0001g0008a0001c0001t0001g0073a0001c0001t0001g0074others(16): Show | 21 | HG01109.hp2 HG01169.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2562+3701_2562+370 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002216 | ||||||
chr9:121002216
|
GTATATA | G | 52 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0012others(49): Show | 55 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.2562+3697_2562+370 others(10): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002216 | ||||||
chr9:121002216
|
GTATATAT others(23): Show |
G | 1 | a0003c0004t0001g0016 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2562+3673_2562+370 others(34): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002216 | ||||||
chr9:121002222
|
A | ACG | 12 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(9): Show | 12 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.2562+3696_2562+369 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002222 | ||||||
chr9:121002222
|
A | ACGTATAT others(3): Show |
4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2562+3696_2562+369 others(14): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002222 | ||||||
chr9:121002222
|
A | ATG | 22 | a0001c0016t0001g0003a0001c0018t0001g0244a0001c0018t0001g0248others(19): Show | 25 | HG00438.hp2 HG00639.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2562+3696_2562+369 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002222 | ||||||
chr9:121002222
|
A | ATGTATAT others(27): Show |
4 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(1): Show | 4 | HG02258.hp2 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2562+3696_2562+369 others(38): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002222 | ||||||
chr9:121002222
|
A | G | 1 | a0002c0002t0001g0117 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2562+3697T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002222 | ||||||
chr9:121002222
|
ATATATAT others(33): Show |
A | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2562+3657_2562+369 others(44): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002222 | ||||||
chr9:121002224
|
A | G | 39 | a0001c0001t0001g0084a0002c0002t0001g0071a0002c0002t0001g0072others(36): Show | 39 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2562+3695T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002224 | ||||||
chr9:121002226
|
A | G | 1 | a0002c0002t0001g0123 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2562+3693T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002226 | ||||||
chr9:121002229
|
T | C | 12 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(9): Show | 12 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.2562+3690A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002229 | ||||||
chr9:121002230
|
G | A | 40 | a0001c0001t0001g0084a0002c0002t0001g0071a0002c0002t0001g0072others(37): Show | 40 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.2562+3689C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002230 | ||||||
chr9:121002230
|
G | GTA | 4 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(1): Show | 4 | HG02258.hp2 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2562+3687_2562+368 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002230 | ||||||
chr9:121002234
|
A | G | 40 | a0001c0001t0001g0084a0002c0002t0001g0071a0002c0002t0001g0072others(37): Show | 40 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.2562+3685T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002234 | ||||||
chr9:121002237
|
T | C | 1 | a0002c0002t0001g0123 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2562+3682A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002237 | ||||||
chr9:121002238
|
G | A | 40 | a0001c0001t0001g0084a0002c0002t0001g0071a0002c0002t0001g0072others(37): Show | 40 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.2562+3681C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002238 | ||||||
chr9:121002238
|
GTATATGT others(21): Show |
G | 1 | a0003c0004t0001g0017 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2562+3653_2562+368 others(32): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002238 | ||||||
chr9:121002242
|
ATG | A | 10 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(7): Show | 10 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.2562+3675_2562+367 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002242 | ||||||
chr9:121002244
|
G | A | 53 | a0001c0006t0001g0204a0002c0002t0001g0123a0003c0003t0001g0001others(50): Show | 56 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2562+3675C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002244 | ||||||
chr9:121002244
|
GTATATAT others(13): Show |
G | 9 | a0001c0018t0001g0244a0001c0018t0001g0248a0003c0003t0001g0026others(6): Show | 9 | HG00438.hp2 HG01074.hp2 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.2562+3655_2562+367 others(24): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002244 | ||||||
chr9:121002246
|
A | G | 49 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0014others(46): Show | 52 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.2562+3673T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002246 | ||||||
chr9:121002252
|
A | G | 23 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(20): Show | 25 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.2562+3667T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002252 | ||||||
chr9:121002253
|
T | C | 40 | a0001c0001t0001g0084a0002c0002t0001g0071a0002c0002t0001g0072others(37): Show | 40 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.2562+3666A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002253 | ||||||
chr9:121002254
|
G | A | 12 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(9): Show | 12 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.2562+3665C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002254 | ||||||
chr9:121002254
|
G | GTA | 41 | a0002c0002t0001g0109a0002c0002t0001g0110a0002c0002t0001g0113others(38): Show | 41 | HG00280.hp1 HG00408.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.2562+3663_2562+366 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002254 | ||||||
chr9:121002254
|
GTA | G | 12 | a0003c0003t0001g0057a0003c0003t0001g0061a0003c0003t0001g0065others(9): Show | 12 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2562+3663_2562+366 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002254 | ||||||
chr9:121002258
|
ATATG | A | 40 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0012others(37): Show | 43 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.2562+3657_2562+366 others(8): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002258 | ||||||
chr9:121002260
|
A | ATATG | 11 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(8): Show | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2562+3658_2562+365 others(8): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002260 | ||||||
chr9:121002262
|
G | A | 11 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(8): Show | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2562+3657C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002262 | ||||||
chr9:121002263
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2562+3656A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002263 | ||||||
chr9:121002264
|
A | G | 41 | a0001c0001t0001g0068a0003c0003t0001g0001a0003c0003t0001g0002others(38): Show | 44 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.2562+3655T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002264 | ||||||
chr9:121002270
|
A | G | 39 | a0002c0002t0001g0071a0002c0002t0001g0072a0002c0002t0001g0111others(36): Show | 39 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2562+3649T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002270 | ||||||
chr9:121002272
|
G | A | 39 | a0002c0002t0001g0071a0002c0002t0001g0072a0002c0002t0001g0111others(36): Show | 39 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2562+3647C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002272 | ||||||
chr9:121002274
|
A | G | 1 | a0002c0002t0001g0123 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2562+3645T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002274 | ||||||
chr9:121002276
|
A | G | 1 | a0002c0002t0001g0123 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2562+3643T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002276 | ||||||
chr9:121002281
|
C | T | 40 | a0001c0001t0001g0084a0002c0002t0001g0071a0002c0002t0001g0072others(37): Show | 40 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.2562+3638G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002281 | ||||||
chr9:121002282
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2562+3637C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002282 | ||||||
chr9:121002284
|
A | G | 41 | a0001c0001t0001g0084a0002c0002t0001g0071a0002c0002t0001g0072others(38): Show | 41 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.2562+3635T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002284 | ||||||
chr9:121002286
|
A | G | 41 | a0001c0001t0001g0084a0002c0002t0001g0071a0002c0002t0001g0072others(38): Show | 41 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.2562+3633T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002286 | ||||||
chr9:121002288
|
A | G | 41 | a0001c0001t0001g0084a0002c0002t0001g0071a0002c0002t0001g0072others(38): Show | 41 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.2562+3631T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002288 | ||||||
chr9:121002289
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2562+3630A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002289 | ||||||
chr9:121002292
|
A | G | 41 | a0001c0001t0001g0084a0002c0002t0001g0071a0002c0002t0001g0072others(38): Show | 41 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.2562+3627T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002292 | ||||||
chr9:121002294
|
A | G | 41 | a0001c0001t0001g0084a0002c0002t0001g0071a0002c0002t0001g0072others(38): Show | 41 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.2562+3625T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002294 | ||||||
chr9:121002296
|
A | G | 41 | a0001c0001t0001g0084a0002c0002t0001g0071a0002c0002t0001g0072others(38): Show | 41 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.2562+3623T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002296 | ||||||
chr9:121002297
|
T | C | 11 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(8): Show | 11 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2562+3622A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002297 | ||||||
chr9:121002298
|
G | A | 4 | a0002c0002t0001g0109a0002c0002t0001g0119a0002c0002t0001g0144others(1): Show | 4 | HG00621.hp1 NA18951.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.2562+3621C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002298 | ||||||
chr9:121002300
|
A | G | 10 | a0002c0002t0001g0072a0002c0002t0001g0111a0002c0002t0001g0125others(7): Show | 10 | HG00735.hp2 HG01074.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.2562+3619T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002300 | ||||||
chr9:121002302
|
A | G | 2 | a0002c0002t0001g0109a0002c0002t0001g0144 | 2 | NA18951.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2562+3617T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002302 | ||||||
chr9:121002304
|
A | G | 3 | a0001c0001t0001g0068a0002c0002t0001g0109a0002c0002t0001g0144 | 3 | HG03486.hp1 NA18951.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2562+3615T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002304 | ||||||
chr9:121002306
|
A | G | 2 | a0002c0002t0001g0109a0002c0002t0001g0144 | 2 | NA18951.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2562+3613T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002306 | ||||||
chr9:121002308
|
A | G | 6 | a0002c0002t0001g0109a0002c0002t0001g0110a0002c0002t0001g0130others(3): Show | 6 | HG01175.hp1 HG03195.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.2562+3611T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002308 | ||||||
chr9:121002308
|
ATG | A | 12 | a0002c0002t0001g0117a0002c0002t0001g0179a0003c0003t0001g0014others(9): Show | 12 | HG00597.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2562+3609_2562+361 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002308 | ||||||
chr9:121002308
|
ATGTG | A | 9 | a0002c0002t0001g0071a0002c0002t0001g0125a0002c0002t0001g0127others(6): Show | 9 | HG01255.hp1 HG02293.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2562+3607_2562+361 others(8): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002308 | ||||||
chr9:121002308
|
ATGTGTG | A | 25 | a0002c0002t0001g0072a0002c0002t0001g0111a0002c0002t0001g0114others(22): Show | 25 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.2562+3605_2562+361 others(10): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002308 | ||||||
chr9:121002310
|
G | A | 5 | a0001c0001t0001g0068a0002c0002t0001g0112a0002c0002t0001g0150others(2): Show | 5 | HG01993.hp1 HG03239.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2562+3609C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002310 | ||||||
chr9:121002312
|
G | A | 18 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(15): Show | 18 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.2562+3607C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002312 | ||||||
chr9:121002312
|
GTGTGTAT others(7): Show |
G | 12 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(9): Show | 14 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.2562+3593_2562+360 others(18): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002312 | ||||||
chr9:121002314
|
G | A | 25 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(22): Show | 25 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.2562+3605C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002314 | ||||||
chr9:121002314
|
G | GTA | 3 | a0001c0018t0001g0248a0003c0003t0001g0026a0003c0004t0001g0056 | 3 | HG02015.hp1 HG02257.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2562+3604_2562+360 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002314 | ||||||
chr9:121002314
|
G | GTATATAT others(5): Show |
1 | a0017c0025t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2562+3604_2562+360 others(16): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002314 | ||||||
chr9:121002314
|
GTGTA | G | 5 | a0003c0004t0001g0017a0007c0009t0001g0206a0007c0009t0001g0207others(2): Show | 5 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2562+3601_2562+360 others(8): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002314 | ||||||
chr9:121002314
|
GTGTATAT others(7): Show |
G | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2562+3591_2562+360 others(18): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002314 | ||||||
chr9:121002316
|
G | A | 96 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(93): Show | 99 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.2562+3603C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002316 | ||||||
chr9:121002316
|
G | GTA | 7 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0081others(4): Show | 8 | HG01109.hp2 HG01978.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2562+3601_2562+360 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002316 | ||||||
chr9:121002316
|
G | GTGTATAT others(5): Show |
2 | a0002c0002t0001g0109a0002c0002t0001g0144 | 2 | NA18951.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2562+3602_2562+360 others(16): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002316 | ||||||
chr9:121002316
|
G | GTGTGTGT others(9): Show |
1 | a0002c0002t0001g0121 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2562+3602_2562+360 others(20): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002316 | ||||||
chr9:121002316
|
G | GTGTGTGT others(11): Show |
1 | a0002c0002t0001g0122 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2562+3602_2562+360 others(22): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002316 | ||||||
chr9:121002316
|
G | GTGTGTGT others(13): Show |
1 | a0002c0002t0001g0160 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2562+3602_2562+360 others(24): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002316 | ||||||
chr9:121002316
|
G | GTGTGTGT others(13): Show |
1 | a0002c0002t0001g0157 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2562+3602_2562+360 others(24): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002316 | ||||||
chr9:121002316
|
G | GTGTGTGT others(13): Show |
28 | a0002c0002t0001g0110a0002c0002t0001g0124a0002c0002t0001g0128others(25): Show | 28 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.2562+3602_2562+360 others(24): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002316 | ||||||
chr9:121002316
|
G | GTGTGTGT others(11): Show |
1 | a0002c0002t0001g0113 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2562+3602_2562+360 others(22): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002316 | ||||||
chr9:121002316
|
G | GTGTGTGT others(13): Show |
6 | a0002c0002t0001g0129a0002c0002t0001g0135a0002c0002t0001g0145others(3): Show | 6 | HG01070.hp1 HG01928.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.2562+3602_2562+360 others(24): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002316 | ||||||
chr9:121002318
|
A | ATG | 3 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196 | 3 | HG02027.hp1 NA18948.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2562+3600_2562+360 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002318 | ||||||
chr9:121002318
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0224a0001c0001t0001g0231others(3): Show | 7 | HG00639.hp2 HG00735.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2562+3601T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002318 | ||||||
chr9:121002320
|
A | G | 7 | a0001c0006t0001g0201a0001c0006t0001g0202a0001c0006t0001g0203others(4): Show | 7 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.2562+3599T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002320 | ||||||
chr9:121002341
|
T | C | 4 | a0001c0001t0001g0247a0001c0001t0001g0251a0001c0001t0001g0252others(1): Show | 4 | HG00099.hp2 HG03195.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.2562+3578A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002341 | ||||||
chr9:121002341
|
TAC | T | 3 | a0003c0003t0001g0035a0003c0003t0001g0053a0003c0004t0001g0059 | 3 | HG00621.hp2 HG01109.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.2562+3576_2562+357 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002341 | ||||||
chr9:121002341
|
TACAC | T | 35 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0012others(32): Show | 38 | HG00408.hp2 HG00438.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.2562+3574_2562+357 others(8): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002341 | ||||||
chr9:121002343
|
C | T | 125 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0016t0001g0003others(122): Show | 128 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.2562+3576G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002343 | ||||||
chr9:121002345
|
C | CATATATA others(3): Show |
11 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(8): Show | 11 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2562+3573_2562+357 others(14): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002345 | ||||||
chr9:121002345
|
C | T | 99 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0018t0001g0244others(96): Show | 99 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.2562+3574G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002345 | ||||||
chr9:121002713
|
G | A | 12 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(9): Show | 12 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.2562+3206C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121002713 | ||||||
chr9:121003000
|
A | G | 1 | a0002c0002t0001g0119 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2562+2919T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121003000 | ||||||
chr9:121003059
|
A | T | 1 | a0002c0002t0001g0117 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2562+2860T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121003059 | ||||||
chr9:121003078
|
G | A | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2562+2841C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121003078 | ||||||
chr9:121003223
|
G | A | 1 | a0002c0002t0001g0118 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2562+2696C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121003223 | ||||||
chr9:121003787
|
ACTCT | A | 8 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(5): Show | 9 | HG01891.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2562+2128_2562+213 others(8): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121003787 | ||||||
chr9:121003932
|
A | G | 173 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(170): Show | 179 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.2562+1987T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121003932 | ||||||
chr9:121003993
|
C | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | HG02071.hp2 NA18951.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2562+1926G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121003993 | ||||||
chr9:121004248
|
A | C | 12 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(9): Show | 12 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.2562+1671T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121004248 | ||||||
chr9:121004339
|
G | GTA | 8 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0235others(5): Show | 9 | HG02145.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2562+1578_2562+157 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121004339 | ||||||
chr9:121004511
|
T | C | 169 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(166): Show | 175 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.2562+1408A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121004511 | ||||||
chr9:121004526
|
T | C | 169 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(166): Show | 175 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.2562+1393A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121004526 | ||||||
chr9:121004721
|
G | C | 169 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(166): Show | 175 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.2562+1198C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121004721 | ||||||
chr9:121004727
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2562+1192G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121004727 | ||||||
chr9:121004983
|
T | TA | 190 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0068others(187): Show | 199 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.2562+935dupT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121004983 | ||||||
chr9:121005010
|
T | C | 1 | a0004c0005t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2562+909A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121005010 | ||||||
chr9:121005430
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2562+489C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121005430 | ||||||
chr9:121005870
|
A | C | 1 | a0003c0004t0001g0023 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2562+49T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 20/40 | chr9 | 121005870 | ||||||
chr9:121006171
|
T | A | 1 | a0018c0023t0001g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2423-113A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 19/40 | chr9 | 121006171 | ||||||
chr9:121006579
|
C | T | 1 | a0003c0003t0001g0057 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2422+325G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 19/40 | chr9 | 121006579 | ||||||
chr9:121007182
|
C | T | 1 | a0001c0006t0001g0195 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2349-205G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 18/40 | chr9 | 121007182 | ||||||
chr9:121007376
|
T | C | 1 | a0001c0018t0001g0248 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2349-399A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 18/40 | chr9 | 121007376 | ||||||
chr9:121007480
|
G | A | 2 | a0001c0016t0001g0003a0018c0023t0001g0205 | 3 | HG02717.hp2 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2349-503C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 18/40 | chr9 | 121007480 | ||||||
chr9:121007564
|
T | A | 164 | a0001c0001t0001g0068a0001c0006t0001g0194a0001c0006t0001g0195others(161): Show | 169 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.2349-587A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 18/40 | chr9 | 121007564 | ||||||
chr9:121007716
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2348+692G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 18/40 | chr9 | 121007716 | ||||||
chr9:121008158
|
A | C | 175 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(172): Show | 181 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.2348+250T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 18/40 | chr9 | 121008158 | ||||||
chr9:121008559
|
T | C | 1 | a0002c0026t0001g0174 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2258-61A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121008559 | ||||||
chr9:121008732
|
T | C | 23 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(20): Show | 25 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.2258-234A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121008732 | ||||||
chr9:121008758
|
C | T | 2 | a0004c0005t0001g0004a0004c0005t0001g0216 | 3 | HG02647.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2258-260G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121008758 | ||||||
chr9:121008848
|
T | C | 8 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(5): Show | 8 | HG00099.hp1 HG00738.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2258-350A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121008848 | ||||||
chr9:121008873
|
T | G | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2258-375A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121008873 | ||||||
chr9:121008903
|
C | T | 62 | a0001c0018t0001g0244a0001c0018t0001g0248a0003c0003t0001g0001others(59): Show | 65 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.2258-405G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121008903 | ||||||
chr9:121008927
|
C | CACAA | 26 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0016t0001g0003others(23): Show | 28 | HG00735.hp2 HG01074.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.2258-433_2258-430d others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121008927 | ||||||
chr9:121008927
|
C | CACAAACA others(1): Show |
131 | a0001c0001t0001g0068a0001c0018t0001g0244a0001c0018t0001g0248others(128): Show | 135 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.2258-437_2258-430d others(10): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121008927 | ||||||
chr9:121008927
|
C | CACAAACA others(5): Show |
3 | a0002c0002t0001g0112a0013c0015t0001g0221a0017c0025t0001g0223 | 3 | HG02486.hp1 HG03195.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2258-441_2258-430d others(14): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121008927 | ||||||
chr9:121009105
|
T | C | 2 | a0004c0005t0002g0212a0004c0005t0002g0213 | 2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2258-607A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121009105 | ||||||
chr9:121009215
|
T | C | 23 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(20): Show | 25 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.2258-717A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121009215 | ||||||
chr9:121009249
|
A | G | 2 | a0003c0004t0001g0016a0003c0004t0001g0017 | 2 | HG01261.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2258-751T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121009249 | ||||||
chr9:121009323
|
A | G | 3 | a0001c0001t0001g0073a0001c0001t0001g0074a0017c0025t0001g0223 | 3 | HG01109.hp2 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2258-825T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121009323 | ||||||
chr9:121009497
|
G | A | 1 | a0018c0023t0001g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2258-999C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121009497 | ||||||
chr9:121009499
|
G | A | 1 | a0012c0011t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2258-1001C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121009499 | ||||||
chr9:121009521
|
T | C | 23 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(20): Show | 25 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.2258-1023A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121009521 | ||||||
chr9:121009594
|
C | A | 1 | a0002c0002t0001g0128 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2258-1096G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121009594 | ||||||
chr9:121010260
|
T | G | 1 | a0002c0002t0001g0129 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2258-1762A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121010260 | ||||||
chr9:121010840
|
G | T | 257 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(254): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.2258-2342C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121010840 | ||||||
chr9:121010883
|
C | T | 1 | a0004c0005t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2258-2385G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121010883 | ||||||
chr9:121011018
|
T | C | 1 | a0006c0008t0001g0069 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2258-2520A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121011018 | ||||||
chr9:121011098
|
T | A | 23 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(20): Show | 25 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.2258-2600A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121011098 | ||||||
chr9:121011188
|
C | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0074a0017c0025t0001g0223 | 3 | HG01109.hp2 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2257+2685G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121011188 | ||||||
chr9:121011491
|
A | T | 1 | a0004c0005t0001g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2257+2382T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121011491 | ||||||
chr9:121011545
|
A | AAC | 180 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(177): Show | 186 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.2257+2327_2257+232 others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121011545 | ||||||
chr9:121011551
|
T | A | 1 | a0007c0009t0001g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2257+2322A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121011551 | ||||||
chr9:121011825
|
A | T | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2257+2048T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121011825 | ||||||
chr9:121011982
|
GA | G | 11 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(8): Show | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2257+1890delT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121011982 | ||||||
chr9:121012185
|
G | A | 177 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(174): Show | 183 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.2257+1688C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121012185 | ||||||
chr9:121012327
|
C | T | 23 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(20): Show | 25 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.2257+1546G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121012327 | ||||||
chr9:121012458
|
G | C | 2 | a0003c0004t0001g0031a0003c0004t0001g0032 | 2 | HG01074.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2257+1415C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121012458 | ||||||
chr9:121012470
|
C | T | 1 | a0004c0005t0001g0218 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2257+1403G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121012470 | ||||||
chr9:121012480
|
C | T | 1 | a0015c0020t0001g0021 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2257+1393G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121012480 | ||||||
chr9:121012594
|
A | G | 1 | a0018c0023t0001g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2257+1279T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121012594 | ||||||
chr9:121012611
|
T | C | 12 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(9): Show | 12 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.2257+1262A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121012611 | ||||||
chr9:121012902
|
T | C | 1 | a0003c0003t0001g0039 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2257+971A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121012902 | ||||||
chr9:121013235
|
G | A | 23 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(20): Show | 25 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.2257+638C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121013235 | ||||||
chr9:121013275
|
C | T | 1 | a0001c0006t0001g0195 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2257+598G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121013275 | ||||||
chr9:121013312
|
C | T | 1 | a0017c0025t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2257+561G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121013312 | ||||||
chr9:121013318
|
G | GA | 66 | a0001c0001t0001g0235a0001c0018t0001g0244a0002c0002t0001g0156others(63): Show | 69 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.2257+554dupT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121013318 | ||||||
chr9:121013318
|
G | GGAAA | 11 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(8): Show | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2257+554_2257+555i others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121013318 | ||||||
chr9:121013318
|
G | GGAAAAA | 11 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(8): Show | 11 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.2257+554_2257+555i others(8): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121013318 | ||||||
chr9:121013318
|
GA | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0243a0001c0001t0001g0247others(2): Show | 6 | HG00099.hp2 HG00738.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.2257+554delT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121013318 | ||||||
chr9:121013482
|
G | C | 180 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(177): Show | 186 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.2257+391C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121013482 | ||||||
chr9:121013699
|
T | G | 1 | a0002c0026t0001g0174 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2257+174A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121013699 | ||||||
chr9:121013729
|
A | AT | 23 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(20): Show | 25 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.2257+143dupA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 17/40 | chr9 | 121013729 | ||||||
chr9:121014091
|
G | A | 1 | a0003c0003t0001g0053 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2060-21C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 16/40 | chr9 | 121014091 | ||||||
chr9:121014112
|
G | C | 23 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(20): Show | 25 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.2060-42C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 16/40 | chr9 | 121014112 | ||||||
chr9:121014119
|
T | A | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | HG02071.hp2 NA18951.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2060-49A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 16/40 | chr9 | 121014119 | ||||||
chr9:121014637
|
A | G | 5 | a0003c0004t0001g0025a0006c0008t0001g0069a0006c0008t0001g0104others(2): Show | 5 | HG02258.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2059+562T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 16/40 | chr9 | 121014637 | ||||||
chr9:121015827
|
T | C | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1996+427A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 15/40 | chr9 | 121015827 | ||||||
chr9:121015870
|
C | T | 148 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(145): Show | 151 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1996+384G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 15/40 | chr9 | 121015870 | ||||||
chr9:121015879
|
G | A | 1 | a0002c0002t0001g0222 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1996+375C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 15/40 | chr9 | 121015879 | ||||||
chr9:121016050
|
C | T | 1 | a0002c0002t0001g0177 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1996+204G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 15/40 | chr9 | 121016050 | ||||||
chr9:121016410
|
A | C | 23 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(20): Show | 25 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1867-27T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 14/40 | chr9 | 121016410 | ||||||
chr9:121016833
|
A | G | 2 | a0002c0002t0001g0136a0002c0002t0001g0138 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1867-450T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 14/40 | chr9 | 121016833 | ||||||
chr9:121016842
|
C | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(8): Show | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1867-459G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 14/40 | chr9 | 121016842 | ||||||
chr9:121016850
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1867-467C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 14/40 | chr9 | 121016850 | ||||||
chr9:121017007
|
A | T | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1866+355T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 14/40 | chr9 | 121017007 | ||||||
chr9:121017153
|
T | C | 1 | a0012c0011t0001g0006 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1866+209A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 14/40 | chr9 | 121017153 | ||||||
chr9:121017342
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1866+20G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 14/40 | chr9 | 121017342 | ||||||
chr9:121017550
|
G | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0236 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1717-39C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 13/40 | chr9 | 121017550 | ||||||
chr9:121017551
|
T | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0236 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1717-40A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 13/40 | chr9 | 121017551 | ||||||
chr9:121018019
|
G | A | 2 | a0003c0004t0001g0028a0003c0004t0003g0029 | 2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1507-167C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018019 | ||||||
chr9:121018028
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1507-176G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018028 | ||||||
chr9:121018188
|
G | A | 1 | a0015c0020t0001g0021 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1507-336C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018188 | ||||||
chr9:121018189
|
T | G | 23 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(20): Show | 25 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1507-337A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018189 | ||||||
chr9:121018252
|
C | CA | 67 | a0001c0001t0001g0007a0001c0001t0001g0073a0001c0001t0001g0075others(64): Show | 71 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1507-401dupT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018252 | ||||||
chr9:121018252
|
C | CAA | 12 | a0001c0001t0001g0074a0001c0001t0001g0253a0003c0003t0001g0014others(9): Show | 12 | HG00597.hp1 HG01109.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1507-402_1507-401d others(4): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018252 | ||||||
chr9:121018252
|
CA | C | 12 | a0001c0001t0001g0093a0001c0001t0001g0102a0001c0001t0001g0192others(9): Show | 12 | HG01069.hp1 HG01255.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1507-401delT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018252 | ||||||
chr9:121018252
|
CAAAA | C | 7 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(4): Show | 8 | HG01891.hp1 HG02280.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1507-404_1507-401d others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018252 | ||||||
chr9:121018252
|
CAAAAA | C | 16 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(13): Show | 17 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.1507-405_1507-401d others(7): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018252 | ||||||
chr9:121018366
|
G | A | 84 | a0001c0001t0001g0073a0001c0001t0001g0074a0002c0002t0001g0071others(81): Show | 84 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1507-514C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018366 | ||||||
chr9:121018419
|
A | G | 23 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(20): Show | 25 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1507-567T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018419 | ||||||
chr9:121018431
|
G | A | 1 | a0018c0023t0001g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1507-579C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018431 | ||||||
chr9:121018578
|
A | AAAGG | 15 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0076others(12): Show | 18 | HG00099.hp2 HG00597.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1507-730_1507-727d others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018578 | ||||||
chr9:121018578
|
A | AAAGGAAG others(1): Show |
5 | a0001c0001t0001g0243a0001c0001t0001g0246a0001c0018t0001g0244others(2): Show | 5 | HG00639.hp1 HG01169.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1507-734_1507-727d others(10): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018578 | ||||||
chr9:121018578
|
AAAGG | A | 21 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(18): Show | 21 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1507-730_1507-727d others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018578 | ||||||
chr9:121018578
|
AAAGGAAG others(1): Show |
A | 85 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0016t0001g0003others(82): Show | 86 | HG00280.hp1 HG00408.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.1507-734_1507-727d others(10): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018578 | ||||||
chr9:121018578
|
AAAGGAAG others(5): Show |
A | 66 | a0001c0001t0001g0068a0001c0001t0001g0087a0001c0001t0001g0088others(63): Show | 69 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1507-738_1507-727d others(14): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018578 | ||||||
chr9:121018603
|
A | C | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-751T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018603 | ||||||
chr9:121018605
|
G | A | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-753C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018605 | ||||||
chr9:121018609
|
G | A | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-757C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018609 | ||||||
chr9:121018615
|
A | G | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-763T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018615 | ||||||
chr9:121018619
|
C | G | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-767G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018619 | ||||||
chr9:121018621
|
A | G | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-769T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018621 | ||||||
chr9:121018623
|
A | G | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-771T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018623 | ||||||
chr9:121018625
|
A | G | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-773T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018625 | ||||||
chr9:121018627
|
A | G | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-775T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018627 | ||||||
chr9:121018633
|
G | A | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-781C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018633 | ||||||
chr9:121018635
|
G | A | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-783C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018635 | ||||||
chr9:121018637
|
G | A | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-785C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018637 | ||||||
chr9:121018639
|
G | A | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-787C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018639 | ||||||
chr9:121018641
|
G | A | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-789C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018641 | ||||||
chr9:121018643
|
G | A | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-791C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018643 | ||||||
chr9:121018645
|
G | A | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-793C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018645 | ||||||
chr9:121018646
|
G | A | 1 | a0005c0007t0001g0262 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1507-794C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018646 | ||||||
chr9:121018646
|
G | GGAAAGAA others(10): Show |
166 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(163): Show | 171 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1507-795_1507-794i others(19): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018646 | ||||||
chr9:121018647
|
G | GAAAGAAA others(6): Show |
4 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(1): Show | 4 | HG02258.hp2 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1507-808_1507-796d others(15): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018647 | ||||||
chr9:121018658
|
A | AGAAAAGA others(14): Show |
1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1507-807_1507-806i others(23): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018658 | ||||||
chr9:121018662
|
G | A | 1 | a0002c0002t0001g0177 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1507-810C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018662 | ||||||
chr9:121018666
|
G | A | 1 | a0002c0002t0001g0177 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1507-814C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018666 | ||||||
chr9:121018678
|
A | G | 1 | a0002c0002t0001g0177 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1507-826T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018678 | ||||||
chr9:121018684
|
G | A | 1 | a0002c0002t0001g0177 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1507-832C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018684 | ||||||
chr9:121018686
|
G | A | 1 | a0002c0002t0001g0177 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1507-834C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018686 | ||||||
chr9:121018688
|
G | A | 1 | a0002c0002t0001g0177 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1507-836C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018688 | ||||||
chr9:121018724
|
AGAAG | A | 4 | a0002c0002t0001g0149a0002c0002t0001g0175a0004c0005t0002g0212others(1): Show | 4 | HG01891.hp1 HG02040.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1507-876_1507-873d others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018724 | ||||||
chr9:121018736
|
G | GGAAA | 27 | a0001c0001t0001g0073a0001c0001t0001g0074a0002c0002t0001g0110others(24): Show | 27 | HG00408.hp1 HG00621.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1507-885_1507-884i others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018736 | ||||||
chr9:121018738
|
AAGGAAAG others(5): Show |
A | 4 | a0002c0002t0001g0176a0008c0010t0001g0198a0010c0014t0001g0005others(1): Show | 5 | HG02293.hp2 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1507-898_1507-887d others(14): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018738 | ||||||
chr9:121018738
|
AAGGAAAG others(9): Show |
A | 17 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.1507-902_1507-887d others(18): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018738 | ||||||
chr9:121018738
|
AAGGAAAG others(13): Show |
A | 1 | a0004c0005t0001g0217 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1507-906_1507-887d others(22): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018738 | ||||||
chr9:121018740
|
G | A | 80 | a0001c0001t0001g0073a0001c0001t0001g0074a0002c0002t0001g0071others(77): Show | 80 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1507-888C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018740 | ||||||
chr9:121018740
|
G | GGAAA | 17 | a0003c0003t0001g0014a0003c0003t0001g0026a0003c0003t0001g0061others(14): Show | 17 | HG00438.hp2 HG00597.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1507-892_1507-889d others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018740 | ||||||
chr9:121018740
|
G | GGAAAGAA others(1): Show |
20 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0012others(17): Show | 23 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.1507-889_1507-888i others(10): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018740 | ||||||
chr9:121018742
|
A | AAAGAAAG others(5): Show |
12 | a0003c0003t0001g0037a0003c0003t0001g0038a0003c0003t0001g0041others(9): Show | 12 | HG01109.hp1 HG02145.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.1507-891_1507-890i others(14): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018742 | ||||||
chr9:121018742
|
A | AAAGAAAG others(13): Show |
1 | a0003c0004t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1507-891_1507-890i others(22): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018742 | ||||||
chr9:121018742
|
A | AAAGAAAG others(1): Show |
43 | a0002c0002t0001g0072a0002c0002t0001g0109a0002c0002t0001g0112others(40): Show | 43 | HG00323.hp1 HG00735.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1507-891_1507-890i others(10): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018742 | ||||||
chr9:121018742
|
A | AAAGAAAG others(5): Show |
8 | a0002c0002t0001g0071a0002c0002t0001g0121a0002c0002t0001g0122others(5): Show | 8 | HG00280.hp1 HG01515.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.1507-891_1507-890i others(14): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018742 | ||||||
chr9:121018742
|
A | AAAGG | 16 | a0001c0001t0001g0030a0001c0001t0001g0081a0001c0001t0001g0086others(13): Show | 16 | HG01069.hp2 HG01884.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.1507-894_1507-891d others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018742 | ||||||
chr9:121018742
|
AAAGG | A | 31 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0083others(28): Show | 33 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1507-894_1507-891d others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018742 | ||||||
chr9:121018742
|
AAAGGAAG others(1): Show |
A | 4 | a0001c0001t0001g0250a0001c0024t0001g0070a0012c0011t0001g0006others(1): Show | 5 | HG00597.hp2 HG02809.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1507-898_1507-891d others(10): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018742 | ||||||
chr9:121018742
|
AAAGGAAG others(5): Show |
A | 6 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(3): Show | 6 | HG02258.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1507-902_1507-891d others(14): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018742 | ||||||
chr9:121018742
|
AAAGGAAG others(9): Show |
A | 3 | a0001c0001t0001g0068a0001c0001t0001g0230a0001c0016t0001g0003 | 4 | HG02717.hp2 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1507-906_1507-891d others(18): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018742 | ||||||
chr9:121018746
|
G | A | 30 | a0002c0002t0001g0114a0002c0002t0001g0130a0002c0002t0001g0131others(27): Show | 30 | HG00438.hp2 HG01074.hp2 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.1507-894C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018746 | ||||||
chr9:121018750
|
G | A | 6 | a0002c0002t0001g0133a0002c0002t0001g0149a0002c0002t0001g0175others(3): Show | 6 | HG02040.hp1 HG02155.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.1507-898C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018750 | ||||||
chr9:121018754
|
G | A | 5 | a0002c0002t0001g0133a0002c0002t0001g0176a0008c0010t0001g0198others(2): Show | 6 | HG02293.hp2 HG02976.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1507-902C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018754 | ||||||
chr9:121018758
|
G | A | 22 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(19): Show | 23 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1507-906C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018758 | ||||||
chr9:121018762
|
G | A | 5 | a0001c0001t0001g0068a0006c0008t0001g0069a0006c0008t0001g0104others(2): Show | 5 | HG02258.hp2 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1507-910C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018762 | ||||||
chr9:121018766
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1507-914C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018766 | ||||||
chr9:121018802
|
A | G | 2 | a0003c0004t0001g0018a0005c0007t0001g0261 | 2 | HG03540.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1507-950T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121018802 | ||||||
chr9:121019051
|
C | T | 23 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(20): Show | 25 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1506+925G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121019051 | ||||||
chr9:121019140
|
T | TA | 22 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(19): Show | 24 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.1506+835dupT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121019140 | ||||||
chr9:121019157
|
G | A | 148 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(145): Show | 151 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1506+819C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121019157 | ||||||
chr9:121019273
|
T | C | 2 | a0001c0016t0001g0003a0018c0023t0001g0205 | 3 | HG02717.hp2 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1506+703A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121019273 | ||||||
chr9:121019349
|
C | T | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1506+627G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121019349 | ||||||
chr9:121019369
|
A | C | 23 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(20): Show | 25 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1506+607T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121019369 | ||||||
chr9:121019440
|
C | T | 1 | a0001c0018t0001g0244 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1506+536G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121019440 | ||||||
chr9:121019485
|
C | G | 23 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(20): Show | 25 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1506+491G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121019485 | ||||||
chr9:121019492
|
G | A | 148 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(145): Show | 151 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1506+484C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121019492 | ||||||
chr9:121019572
|
T | C | 3 | a0006c0008t0001g0104a0006c0008t0001g0105a0006c0008t0001g0106 | 3 | HG02258.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1506+404A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121019572 | ||||||
chr9:121019716
|
C | A | 2 | a0004c0005t0001g0004a0004c0005t0001g0216 | 3 | HG02647.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1506+260G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121019716 | ||||||
chr9:121019860
|
C | T | 173 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(170): Show | 179 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.1506+116G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 12/40 | chr9 | 121019860 | ||||||
chr9:121020244
|
T | A | 1 | a0003c0004t0001g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1303-65A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 11/40 | chr9 | 121020244 | ||||||
chr9:121020620
|
A | G | 2 | a0001c0016t0001g0003a0018c0023t0001g0205 | 3 | HG02717.hp2 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1303-441T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 11/40 | chr9 | 121020620 | ||||||
chr9:121020653
|
C | T | 1 | a0003c0004t0001g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1303-474G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 11/40 | chr9 | 121020653 | ||||||
chr9:121020778
|
T | G | 151 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(148): Show | 154 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1303-599A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 11/40 | chr9 | 121020778 | ||||||
chr9:121020999
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0190 | 2 | NA19003.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1302+510A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 11/40 | chr9 | 121020999 | ||||||
chr9:121021039
|
C | T | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1302+470G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 11/40 | chr9 | 121021039 | ||||||
chr9:121021128
|
T | C | 2 | a0002c0002t0001g0164a0002c0002t0001g0165 | 2 | HG02155.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1302+381A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 11/40 | chr9 | 121021128 | ||||||
chr9:121021147
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0190 | 2 | NA19003.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1302+362G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 11/40 | chr9 | 121021147 | ||||||
chr9:121021272
|
C | T | 1 | a0003c0003t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1302+237G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 11/40 | chr9 | 121021272 | ||||||
chr9:121021309
|
T | C | 1 | a0003c0003t0001g0014 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1302+200A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 11/40 | chr9 | 121021309 | ||||||
chr9:121021715
|
A | G | 85 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(82): Show | 90 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1117-21T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121021715 | ||||||
chr9:121021889
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1117-195A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121021889 | ||||||
chr9:121021949
|
T | A | 4 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(1): Show | 4 | HG02258.hp2 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1117-255A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121021949 | ||||||
chr9:121022029
|
T | A | 4 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(1): Show | 4 | HG02258.hp2 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1117-335A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121022029 | ||||||
chr9:121022070
|
T | G | 62 | a0001c0018t0001g0244a0001c0018t0001g0248a0003c0003t0001g0001others(59): Show | 65 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1117-376A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121022070 | ||||||
chr9:121022220
|
C | T | 81 | a0002c0002t0001g0071a0002c0002t0001g0072a0002c0002t0001g0109others(78): Show | 81 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1117-526G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121022220 | ||||||
chr9:121022298
|
CAT | C | 175 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(172): Show | 180 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1117-606_1117-605d others(4): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121022298 | ||||||
chr9:121022314
|
T | C | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1117-620A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121022314 | ||||||
chr9:121022322
|
C | A | 2 | a0013c0015t0001g0220a0013c0015t0001g0221 | 2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1117-628G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121022322 | ||||||
chr9:121022334
|
G | C | 1 | a0018c0023t0001g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1117-640C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121022334 | ||||||
chr9:121022519
|
C | T | 1 | a0001c0006t0001g0201 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1117-825G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121022519 | ||||||
chr9:121022527
|
G | A | 4 | a0006c0008t0001g0069a0006c0008t0001g0104a0006c0008t0001g0105others(1): Show | 4 | HG02258.hp2 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1117-833C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121022527 | ||||||
chr9:121022647
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1116+757T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121022647 | ||||||
chr9:121022700
|
T | A | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1116+704A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121022700 | ||||||
chr9:121022724
|
G | A | 85 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(82): Show | 90 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1116+680C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121022724 | ||||||
chr9:121022879
|
G | A | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116+525C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121022879 | ||||||
chr9:121022922
|
G | A | 85 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(82): Show | 90 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1116+482C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121022922 | ||||||
chr9:121022971
|
A | G | 84 | a0001c0001t0001g0073a0001c0001t0001g0074a0002c0002t0001g0071others(81): Show | 84 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1116+433T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121022971 | ||||||
chr9:121022998
|
CAT | C | 12 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(9): Show | 12 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1116+404_1116+405d others(4): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121022998 | ||||||
chr9:121023267
|
G | A | 80 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(77): Show | 85 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.1116+137C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 10/40 | chr9 | 121023267 | ||||||
chr9:121023724
|
A | G | 1 | a0017c0025t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1001-205T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121023724 | ||||||
chr9:121023757
|
C | T | 74 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(71): Show | 77 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1001-238G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121023757 | ||||||
chr9:121023892
|
G | T | 1 | a0002c0002t0001g0120 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1001-373C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121023892 | ||||||
chr9:121023990
|
C | T | 1 | a0001c0001t0001g0007 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1001-471G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121023990 | ||||||
chr9:121023997
|
A | G | 85 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(82): Show | 90 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1001-478T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121023997 | ||||||
chr9:121024058
|
C | T | 12 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(9): Show | 12 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1001-539G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024058 | ||||||
chr9:121024151
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1001-632G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024151 | ||||||
chr9:121024213
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1001-694G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024213 | ||||||
chr9:121024236
|
GGGGAGGG others(36): Show |
G | 1 | a0003c0004t0001g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1001-760_1001-718d others(45): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024236 | ||||||
chr9:121024240
|
AGGGGGGA others(1): Show |
A | 37 | a0001c0006t0001g0195a0001c0006t0001g0196a0001c0006t0001g0197others(34): Show | 39 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1001-729_1001-722d others(10): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024240 | ||||||
chr9:121024241
|
GGGGGGAG others(14): Show |
G | 43 | a0001c0018t0001g0244a0001c0018t0001g0248a0003c0003t0001g0001others(40): Show | 46 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.1001-743_1001-723d others(23): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024241 | ||||||
chr9:121024241
|
GGGGGGAG others(54): Show |
G | 1 | a0001c0006t0001g0204 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1001-783_1001-723d others(63): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024241 | ||||||
chr9:121024245
|
G | A | 2 | a0003c0003t0001g0038a0003c0004t0001g0063 | 2 | HG02145.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1001-726C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024245 | ||||||
chr9:121024246
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1001-727C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024246 | ||||||
chr9:121024247
|
A | G | 1 | a0003c0003t0001g0038 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1001-728T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024247 | ||||||
chr9:121024249
|
G | GGGGAGGG others(6): Show |
1 | a0001c0001t0001g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1001-743_1001-731d others(15): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024249 | ||||||
chr9:121024253
|
A | G | 1 | a0001c0006t0001g0194 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1001-734T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024253 | ||||||
chr9:121024253
|
AGGGGGGA others(7): Show |
A | 1 | a0003c0003t0001g0038 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1001-748_1001-735d others(16): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024253 | ||||||
chr9:121024254
|
G | A | 1 | a0001c0006t0001g0194 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1001-735C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024254 | ||||||
chr9:121024262
|
T | G | 37 | a0001c0006t0001g0195a0001c0006t0001g0196a0001c0006t0001g0197others(34): Show | 39 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1001-743A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024262 | ||||||
chr9:121024263
|
G | C | 1 | a0001c0001t0001g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1001-744C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024263 | ||||||
chr9:121024268
|
G | GGGGGAGG others(4): Show |
4 | a0001c0001t0001g0075a0001c0001t0001g0183a0001c0001t0001g0190others(1): Show | 4 | HG02027.hp2 NA18946.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-760_1001-750d others(13): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024268 | ||||||
chr9:121024268
|
GGGGGAGG others(4): Show |
G | 2 | a0005c0007t0001g0115a0005c0007t0001g0116 | 2 | NA18946.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1001-760_1001-750d others(13): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024268 | ||||||
chr9:121024268
|
GGGGGAGG others(44): Show |
G | 1 | a0018c0023t0001g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1001-800_1001-750d others(53): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024268 | ||||||
chr9:121024273
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1001-754T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024273 | ||||||
chr9:121024274
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1001-755C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024274 | ||||||
chr9:121024275
|
G | T | 39 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(36): Show | 41 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1001-756C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024275 | ||||||
chr9:121024279
|
A | AG | 82 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(79): Show | 87 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1001-761dupC | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024279 | ||||||
chr9:121024279
|
A | AGGGAGGG others(21): Show |
1 | a0001c0001t0001g0080 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1001-761_1001-760i others(30): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024279 | ||||||
chr9:121024290
|
A | AGGGGAGG others(17): Show |
1 | a0001c0001t0001g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1001-772_1001-771i others(26): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024290 | ||||||
chr9:121024290
|
A | G | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | NA18971.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1001-771T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024290 | ||||||
chr9:121024291
|
G | A | 11 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(8): Show | 11 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1001-772C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024291 | ||||||
chr9:121024302
|
C | G | 1 | a0001c0001t0001g0080 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1001-783G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024302 | ||||||
chr9:121024302
|
C | T | 48 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(45): Show | 48 | HG00597.hp2 HG01069.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.1001-783G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024302 | ||||||
chr9:121024308
|
G | GGGGGAGG others(4): Show |
3 | a0001c0001t0001g0068a0002c0002t0001g0150a0002c0002t0001g0222 | 3 | HG03486.hp1 NA18942.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1001-800_1001-790d others(13): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024308 | ||||||
chr9:121024308
|
GGGGGAGG others(4): Show |
G | 3 | a0002c0002t0001g0155a0013c0015t0001g0220a0013c0015t0001g0221 | 3 | HG01993.hp1 HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1001-800_1001-790d others(13): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024308 | ||||||
chr9:121024311
|
G | T | 1 | a0002c0002t0001g0109 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1001-792C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024311 | ||||||
chr9:121024313
|
A | G | 2 | a0002c0002t0001g0109a0002c0002t0001g0156 | 2 | NA18978.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1001-794T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024313 | ||||||
chr9:121024313
|
AG | A | 47 | a0002c0002t0001g0071a0002c0002t0001g0072a0002c0002t0001g0111others(44): Show | 47 | HG00280.hp1 HG00408.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1001-795delC | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024313 | ||||||
chr9:121024314
|
G | A | 1 | a0002c0002t0001g0109 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1001-795C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024314 | ||||||
chr9:121024324
|
A | AGGGGGAG others(11): Show |
2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | NA18948.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1001-806_1001-805i others(20): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024324 | ||||||
chr9:121024324
|
A | AGGGGGAG others(11): Show |
6 | a0001c0001t0001g0099a0001c0001t0001g0191a0006c0008t0001g0069others(3): Show | 6 | HG02258.hp2 HG02818.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-823_1001-806d others(20): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024324 | ||||||
chr9:121024324
|
A | AGGGGGAG others(12): Show |
30 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(27): Show | 30 | HG00597.hp2 HG01069.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1001-824_1001-806d others(21): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024324 | ||||||
chr9:121024324
|
A | AGGGGGAG others(13): Show |
2 | a0001c0001t0001g0181a0001c0001t0001g0192 | 2 | NA18946.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1001-825_1001-806d others(22): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024324 | ||||||
chr9:121024324
|
A | AGGGGGAG others(23): Show |
1 | a0001c0001t0001g0095 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1001-806_1001-805i others(32): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024324 | ||||||
chr9:121024324
|
A | AGGGGGAG others(41): Show |
1 | a0001c0001t0001g0093 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1001-806_1001-805i others(50): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024324 | ||||||
chr9:121024324
|
A | AGGGGGAG others(43): Show |
1 | a0001c0001t0001g0092 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1001-806_1001-805i others(52): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024324 | ||||||
chr9:121024324
|
A | AGGGGGAG others(13): Show |
1 | a0001c0001t0004g0264 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1001-806_1001-805i others(22): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024324 | ||||||
chr9:121024324
|
A | AGGGGGAG others(12): Show |
2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1001-806_1001-805i others(21): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024324 | ||||||
chr9:121024335
|
A | AGGGGGAG others(14): Show |
1 | a0001c0001t0001g0182 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1001-817_1001-816i others(23): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024335 | ||||||
chr9:121024344
|
G | A | 85 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(82): Show | 90 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1001-825C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024344 | ||||||
chr9:121024350
|
A | T | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1001-831T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024350 | ||||||
chr9:121024361
|
A | AG | 82 | a0001c0001t0001g0080a0001c0006t0001g0194a0001c0006t0001g0195others(79): Show | 87 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1001-843dupC | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024361 | ||||||
chr9:121024361
|
A | AGG | 9 | a0003c0003t0001g0014a0003c0003t0001g0047a0003c0003t0001g0049others(6): Show | 9 | HG00597.hp1 HG00639.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1001-844_1001-843d others(4): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024361 | ||||||
chr9:121024368
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1001-849T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024368 | ||||||
chr9:121024556
|
G | A | 1 | a0018c0023t0001g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1000+898C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024556 | ||||||
chr9:121024693
|
C | T | 11 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(8): Show | 11 | HG01081.hp2 HG01123.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000+761G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024693 | ||||||
chr9:121024712
|
T | C | 39 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(36): Show | 39 | HG00597.hp2 HG01081.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.1000+742A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024712 | ||||||
chr9:121024777
|
C | A | 1 | a0003c0004t0001g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1000+677G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024777 | ||||||
chr9:121024781
|
C | T | 1 | a0003c0003t0001g0041 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1000+673G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024781 | ||||||
chr9:121024813
|
C | T | 62 | a0001c0018t0001g0244a0001c0018t0001g0248a0003c0003t0001g0001others(59): Show | 65 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1000+641G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024813 | ||||||
chr9:121024966
|
A | G | 1 | a0017c0025t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1000+488T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024966 | ||||||
chr9:121024975
|
A | G | 1 | a0003c0004t0001g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1000+479T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121024975 | ||||||
chr9:121025064
|
G | T | 3 | a0001c0001t0001g0090a0014c0017t0001g0079a0014c0017t0001g0089 | 3 | NA18952.hp1 NA18975.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1000+390C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121025064 | ||||||
chr9:121025102
|
T | C | 11 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(8): Show | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1000+352A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121025102 | ||||||
chr9:121025244
|
G | A | 4 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000+210C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121025244 | ||||||
chr9:121025288
|
A | G | 134 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(131): Show | 134 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.1000+166T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121025288 | ||||||
chr9:121025419
|
T | C | 2 | a0001c0001t0001g0091a0003c0003t0001g0046 | 2 | HG01243.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1000+35A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121025419 | ||||||
chr9:121025419
|
T | TAC | 8 | a0001c0016t0001g0003a0004c0005t0001g0218a0007c0009t0001g0206others(5): Show | 10 | HG00639.hp1 HG02451.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1000+33_1000+34dup others(2): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121025419 | ||||||
chr9:121025419
|
T | TACAC | 9 | a0001c0001t0001g0010a0001c0001t0001g0243a0001c0001t0001g0246others(6): Show | 10 | HG00099.hp2 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1000+31_1000+34dup others(4): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121025419 | ||||||
chr9:121025419
|
T | TACACAC | 25 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0001t0001g0080others(22): Show | 26 | HG01069.hp1 HG01071.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.1000+29_1000+34dup others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121025419 | ||||||
chr9:121025419
|
T | TACACACA others(1): Show |
83 | a0001c0001t0001g0068a0001c0001t0001g0088a0001c0001t0001g0090others(80): Show | 83 | HG00280.hp1 HG00408.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.1000+27_1000+34dup others(8): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121025419 | ||||||
chr9:121025419
|
T | TACACACA others(3): Show |
58 | a0001c0001t0001g0075a0001c0001t0001g0081a0001c0001t0001g0082others(55): Show | 58 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1000+25_1000+34dup others(10): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121025419 | ||||||
chr9:121025419
|
T | TACACACA others(5): Show |
35 | a0001c0001t0001g0077a0001c0001t0001g0085a0001c0018t0001g0244others(32): Show | 38 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1000+23_1000+34dup others(12): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121025419 | ||||||
chr9:121025419
|
T | TACACACA others(7): Show |
8 | a0003c0003t0001g0040a0003c0003t0001g0041a0003c0003t0001g0055others(5): Show | 8 | HG02148.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1000+21_1000+34dup others(14): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121025419 | ||||||
chr9:121025425
|
C | CACACACA others(5): Show |
1 | a0003c0003t0001g0045 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1000+28_1000+29ins others(12): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 9/40 | chr9 | 121025425 | ||||||
chr9:121025721
|
G | A | 4 | a0001c0001t0001g0243a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG00099.hp2 HG00738.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-141C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 8/40 | chr9 | 121025721 | ||||||
chr9:121025992
|
G | A | 1 | a0002c0002t0001g0177 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.874-412C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 8/40 | chr9 | 121025992 | ||||||
chr9:121026114
|
T | A | 1 | a0001c0001t0001g0080 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.874-534A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 8/40 | chr9 | 121026114 | ||||||
chr9:121026114
|
T | C | 219 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(216): Show | 224 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.874-534A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 8/40 | chr9 | 121026114 | ||||||
chr9:121026115
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.874-535A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 8/40 | chr9 | 121026115 | ||||||
chr9:121026118
|
C | G | 1 | a0001c0001t0001g0080 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.874-538G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 8/40 | chr9 | 121026118 | ||||||
chr9:121026122
|
C | G | 1 | a0001c0001t0001g0080 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.874-542G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 8/40 | chr9 | 121026122 | ||||||
chr9:121026142
|
T | C | 1 | a0002c0002t0001g0134 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.874-562A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 8/40 | chr9 | 121026142 | ||||||
chr9:121026230
|
A | G | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.874-650T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 8/40 | chr9 | 121026230 | ||||||
chr9:121026285
|
T | C | 220 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(217): Show | 225 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.874-705A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 8/40 | chr9 | 121026285 | ||||||
chr9:121026772
|
G | C | 1 | a0002c0002t0001g0135 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.873+388C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 8/40 | chr9 | 121026772 | ||||||
chr9:121026939
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.873+221G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 8/40 | chr9 | 121026939 | ||||||
chr9:121027340
|
T | A | 5 | a0001c0016t0001g0003a0007c0009t0001g0206a0007c0009t0001g0207others(2): Show | 6 | HG02451.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-66A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121027340 | ||||||
chr9:121027356
|
C | T | 84 | a0001c0001t0001g0073a0001c0001t0001g0074a0002c0002t0001g0071others(81): Show | 84 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.759-82G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121027356 | ||||||
chr9:121027424
|
T | C | 8 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(5): Show | 9 | HG01891.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.759-150A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121027424 | ||||||
chr9:121027486
|
C | A | 1 | a0002c0002t0001g0156 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.759-212G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121027486 | ||||||
chr9:121027575
|
C | G | 8 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(5): Show | 9 | HG01891.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.759-301G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121027575 | ||||||
chr9:121027616
|
G | T | 1 | a0002c0002t0001g0156 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.759-342C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121027616 | ||||||
chr9:121027740
|
G | A | 49 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(46): Show | 49 | HG00597.hp2 HG01069.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.759-466C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121027740 | ||||||
chr9:121027777
|
G | A | 1 | a0002c0002t0001g0178 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.759-503C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121027777 | ||||||
chr9:121028164
|
G | C | 1 | a0001c0001t0001g0230 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.759-890C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121028164 | ||||||
chr9:121028343
|
C | T | 134 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(131): Show | 134 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.759-1069G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121028343 | ||||||
chr9:121028521
|
A | T | 3 | a0004c0005t0001g0218a0010c0014t0001g0005a0010c0014t0001g0219 | 4 | HG00639.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-1247T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121028521 | ||||||
chr9:121028746
|
G | A | 2 | a0002c0002t0001g0136a0002c0002t0001g0138 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.759-1472C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121028746 | ||||||
chr9:121028854
|
T | C | 220 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(217): Show | 225 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.758+1543A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121028854 | ||||||
chr9:121029186
|
T | C | 1 | a0002c0002t0001g0071 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.758+1211A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121029186 | ||||||
chr9:121029641
|
C | T | 9 | a0003c0003t0001g0065a0003c0003t0001g0067a0003c0004t0001g0058others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.758+756G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121029641 | ||||||
chr9:121029658
|
C | A | 220 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(217): Show | 225 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.758+739G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121029658 | ||||||
chr9:121029682
|
G | C | 3 | a0001c0018t0001g0244a0001c0018t0001g0248a0019c0021t0001g0245 | 3 | HG02015.hp1 HG02040.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.758+715C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121029682 | ||||||
chr9:121029727
|
G | T | 134 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(131): Show | 134 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.758+670C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121029727 | ||||||
chr9:121029747
|
G | C | 1 | a0003c0004t0001g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.758+650C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121029747 | ||||||
chr9:121030015
|
T | C | 1 | a0001c0006t0001g0204 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.758+382A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121030015 | ||||||
chr9:121030191
|
T | C | 12 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(9): Show | 12 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.758+206A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 7/40 | chr9 | 121030191 | ||||||
chr9:121030628
|
G | A | 74 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(71): Show | 77 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.668-141C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 6/40 | chr9 | 121030628 | ||||||
chr9:121030711
|
A | G | 12 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(9): Show | 12 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.668-224T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 6/40 | chr9 | 121030711 | ||||||
chr9:121031119
|
A | G | 1 | a0018c0023t0001g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.668-632T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 6/40 | chr9 | 121031119 | ||||||
chr9:121031257
|
GTTAC | G | 134 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(131): Show | 134 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.668-774_668-771del others(4): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 6/40 | chr9 | 121031257 | ||||||
chr9:121031328
|
G | C | 1 | a0018c0023t0001g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.667+785C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 6/40 | chr9 | 121031328 | ||||||
chr9:121031648
|
C | T | 1 | a0017c0025t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.667+465G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 6/40 | chr9 | 121031648 | ||||||
chr9:121031753
|
A | G | 1 | a0003c0003t0001g0044 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.667+360T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 6/40 | chr9 | 121031753 | ||||||
chr9:121032404
|
G | A | 1 | a0002c0002t0001g0155 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.585-209C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121032404 | ||||||
chr9:121032427
|
T | A | 1 | a0018c0023t0001g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.585-232A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121032427 | ||||||
chr9:121032455
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.585-260A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121032455 | ||||||
chr9:121032478
|
T | C | 2 | a0003c0004t0001g0031a0003c0004t0001g0032 | 2 | HG01074.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.585-283A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121032478 | ||||||
chr9:121032544
|
C | T | 3 | a0001c0001t0001g0073a0001c0001t0001g0074a0017c0025t0001g0223 | 3 | HG01109.hp2 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.585-349G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121032544 | ||||||
chr9:121032682
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.585-487G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121032682 | ||||||
chr9:121032825
|
C | T | 1 | a0002c0002t0001g0113 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.585-630G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121032825 | ||||||
chr9:121032927
|
C | G | 222 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(219): Show | 228 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.585-732G>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121032927 | ||||||
chr9:121033010
|
A | ATG | 84 | a0001c0001t0001g0090a0002c0002t0001g0071a0002c0002t0001g0072others(81): Show | 84 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.585-817_585-816dup others(2): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033010 | ||||||
chr9:121033010
|
A | ATGTG | 52 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(49): Show | 55 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.585-816_585-815ins others(4): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033010 | ||||||
chr9:121033010
|
A | ATGTGTG | 8 | a0003c0003t0001g0039a0003c0003t0001g0042a0003c0003t0001g0044others(5): Show | 8 | HG01981.hp2 HG02055.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.585-816_585-815ins others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033010 | ||||||
chr9:121033010
|
ATGGG | A | 11 | a0001c0001t0001g0192a0004c0005t0001g0004a0004c0005t0001g0211others(8): Show | 13 | HG01891.hp1 HG02280.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.585-819_585-816del others(4): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033010 | ||||||
chr9:121033011
|
TGG | T | 9 | a0001c0001t0001g0073a0001c0001t0001g0074a0003c0004t0001g0020others(6): Show | 9 | HG00639.hp1 HG01109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.585-818_585-817del others(2): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033011 | ||||||
chr9:121033013
|
G | T | 197 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0076others(194): Show | 200 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.585-818C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033013 | ||||||
chr9:121033013
|
GGT | G | 2 | a0012c0011t0001g0006a0012c0011t0001g0226 | 3 | HG02809.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.585-820_585-819del others(2): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033013 | ||||||
chr9:121033040
|
A | G | 1 | a0002c0002t0001g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.585-845T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033040 | ||||||
chr9:121033044
|
A | G | 1 | a0002c0002t0001g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.585-849T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033044 | ||||||
chr9:121033046
|
G | A | 1 | a0002c0002t0001g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.585-851C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033046 | ||||||
chr9:121033075
|
T | TAC | 49 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(46): Show | 49 | HG00597.hp2 HG01069.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.585-882_585-881dup others(2): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033075 | ||||||
chr9:121033416
|
T | C | 217 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(214): Show | 222 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.585-1221A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033416 | ||||||
chr9:121033464
|
GAGCCAGG others(3): Show |
G | 2 | a0014c0017t0001g0079a0014c0017t0001g0089 | 2 | NA18952.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.585-1279_585-1270d others(12): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033464 | ||||||
chr9:121033761
|
G | A | 48 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(45): Show | 48 | HG00597.hp2 HG01069.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.584+1042C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033761 | ||||||
chr9:121033902
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.584+901A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033902 | ||||||
chr9:121033902
|
TTTCC | T | 82 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(79): Show | 87 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.584+897_584+900del others(4): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033902 | ||||||
chr9:121033906
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.584+897G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121033906 | ||||||
chr9:121034070
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.584+733C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121034070 | ||||||
chr9:121034108
|
C | T | 5 | a0001c0016t0001g0003a0007c0009t0001g0206a0007c0009t0001g0207others(2): Show | 6 | HG02451.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.584+695G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121034108 | ||||||
chr9:121034451
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.584+352G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121034451 | ||||||
chr9:121034452
|
G | A | 11 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(8): Show | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.584+351C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121034452 | ||||||
chr9:121034454
|
C | T | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | NA18971.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.584+349G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 5/40 | chr9 | 121034454 | ||||||
chr9:121035046
|
T | A | 222 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(219): Show | 228 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.493-152A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121035046 | ||||||
chr9:121035150
|
C | CT | 217 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(214): Show | 222 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.493-257_493-256ins others(1): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121035150 | ||||||
chr9:121035194
|
CAACA | C | 6 | a0001c0016t0001g0003a0003c0004t0001g0015a0007c0009t0001g0206others(3): Show | 7 | HG02451.hp2 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.493-304_493-301del others(4): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121035194 | ||||||
chr9:121035240
|
A | G | 1 | a0002c0002t0001g0156 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.493-346T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121035240 | ||||||
chr9:121035265
|
C | T | 217 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(214): Show | 222 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.493-371G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121035265 | ||||||
chr9:121035388
|
C | T | 2 | a0001c0006t0001g0195a0001c0006t0001g0196 | 2 | NA18948.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.493-494G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121035388 | ||||||
chr9:121035413
|
C | T | 217 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(214): Show | 222 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.493-519G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121035413 | ||||||
chr9:121035434
|
A | T | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.493-540T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121035434 | ||||||
chr9:121035735
|
AT | A | 16 | a0001c0001t0001g0224a0001c0001t0001g0231a0001c0001t0001g0232others(13): Show | 16 | HG00639.hp2 HG00735.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.493-842delA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121035735 | ||||||
chr9:121035928
|
T | C | 1 | a0003c0003t0001g0041 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.493-1034A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121035928 | ||||||
chr9:121035969
|
G | C | 1 | a0001c0006t0001g0204 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.493-1075C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121035969 | ||||||
chr9:121036043
|
C | T | 81 | a0002c0002t0001g0071a0002c0002t0001g0072a0002c0002t0001g0109others(78): Show | 81 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.493-1149G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121036043 | ||||||
chr9:121036146
|
G | C | 1 | a0001c0006t0001g0195 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.493-1252C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121036146 | ||||||
chr9:121036165
|
T | C | 1 | a0006c0008t0001g0105 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.493-1271A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121036165 | ||||||
chr9:121036214
|
G | A | 2 | a0002c0002t0001g0152a0002c0002t0001g0153 | 2 | HG01261.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.493-1320C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121036214 | ||||||
chr9:121036391
|
A | T | 1 | a0003c0004t0001g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.492+1490T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121036391 | ||||||
chr9:121036506
|
G | A | 1 | a0018c0023t0001g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.492+1375C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121036506 | ||||||
chr9:121036582
|
T | A | 1 | a0001c0006t0001g0204 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.492+1299A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121036582 | ||||||
chr9:121036611
|
AC | A | 134 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(131): Show | 134 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.492+1269delG | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121036611 | ||||||
chr9:121036803
|
T | C | 1 | a0002c0002t0001g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.492+1078A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121036803 | ||||||
chr9:121036839
|
C | T | 1 | a0003c0003t0001g0034 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.492+1042G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121036839 | ||||||
chr9:121036882
|
G | GT | 8 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(5): Show | 8 | HG00099.hp1 HG01934.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.492+998dupA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121036882 | ||||||
chr9:121037237
|
T | C | 4 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(1): Show | 4 | HG00099.hp1 HG02027.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.492+644A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121037237 | ||||||
chr9:121037302
|
G | GT | 7 | a0001c0016t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(4): Show | 8 | HG02451.hp2 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.492+578dupA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121037302 | ||||||
chr9:121037302
|
GT | G | 105 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(102): Show | 108 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.492+578delA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121037302 | ||||||
chr9:121037303
|
T | G | 1 | a0003c0003t0001g0039 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.492+578A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121037303 | ||||||
chr9:121037406
|
C | T | 71 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(68): Show | 74 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.492+475G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121037406 | ||||||
chr9:121037425
|
C | T | 3 | a0008c0010t0001g0198a0008c0010t0001g0199a0008c0010t0001g0210 | 3 | HG00738.hp1 HG01175.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.492+456G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121037425 | ||||||
chr9:121037440
|
A | AGTAGCT | 166 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0006t0001g0194others(163): Show | 171 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.492+435_492+440dup others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121037440 | ||||||
chr9:121037486
|
G | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0224a0001c0001t0001g0231others(2): Show | 6 | HG00639.hp2 HG00735.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.492+395C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121037486 | ||||||
chr9:121037496
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.492+385T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121037496 | ||||||
chr9:121037554
|
A | C | 2 | a0006c0008t0001g0104a0006c0008t0001g0106 | 2 | HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.492+327T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121037554 | ||||||
chr9:121037679
|
T | G | 1 | a0003c0003t0001g0057 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.492+202A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121037679 | ||||||
chr9:121037816
|
T | A | 79 | a0002c0002t0001g0071a0002c0002t0001g0072a0002c0002t0001g0109others(76): Show | 79 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.492+65A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 4/40 | chr9 | 121037816 | ||||||
chr9:121038122
|
T | C | 1 | a0004c0005t0001g0217 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.422-171A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121038122 | ||||||
chr9:121038209
|
C | A | 5 | a0001c0016t0001g0003a0007c0009t0001g0206a0007c0009t0001g0207others(2): Show | 6 | HG02451.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.422-258G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121038209 | ||||||
chr9:121038921
|
C | T | 5 | a0001c0016t0001g0003a0007c0009t0001g0206a0007c0009t0001g0207others(2): Show | 6 | HG02451.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.422-970G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121038921 | ||||||
chr9:121039380
|
T | C | 1 | a0006c0008t0001g0069 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.422-1429A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121039380 | ||||||
chr9:121039552
|
G | C | 1 | a0003c0004t0001g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.422-1601C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121039552 | ||||||
chr9:121039705
|
G | C | 1 | a0001c0024t0001g0070 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.422-1754C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121039705 | ||||||
chr9:121039762
|
C | T | 1 | a0003c0003t0001g0033 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.422-1811G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121039762 | ||||||
chr9:121040164
|
G | T | 5 | a0001c0016t0001g0003a0007c0009t0001g0206a0007c0009t0001g0207others(2): Show | 6 | HG02451.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.422-2213C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121040164 | ||||||
chr9:121040165
|
A | T | 5 | a0001c0016t0001g0003a0007c0009t0001g0206a0007c0009t0001g0207others(2): Show | 6 | HG02451.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.422-2214T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121040165 | ||||||
chr9:121040539
|
A | T | 1 | a0001c0001t0001g0230 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.421+2465T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121040539 | ||||||
chr9:121040711
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.421+2293A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121040711 | ||||||
chr9:121040870
|
G | A | 11 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(8): Show | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.421+2134C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121040870 | ||||||
chr9:121040952
|
CT | C | 136 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0076others(133): Show | 137 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.421+2051delA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121040952 | ||||||
chr9:121041009
|
C | T | 63 | a0001c0001t0001g0030a0001c0006t0001g0194a0001c0006t0001g0195others(60): Show | 66 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.421+1995G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121041009 | ||||||
chr9:121041088
|
C | T | 1 | a0003c0003t0001g0026 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.421+1916G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121041088 | ||||||
chr9:121041297
|
C | CTTTTT | 63 | a0002c0002t0001g0113a0002c0002t0001g0114a0002c0002t0001g0117others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.421+1702_421+1706d others(7): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121041297 | ||||||
chr9:121041297
|
C | CTTTTTT | 96 | a0001c0001t0001g0030a0001c0001t0001g0076a0001c0001t0001g0077others(93): Show | 101 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.421+1701_421+1706d others(8): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121041297 | ||||||
chr9:121041297
|
C | CTTTTTTT | 49 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0078others(46): Show | 49 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.421+1700_421+1706d others(9): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121041297 | ||||||
chr9:121041297
|
C | CTTTTTTT others(1): Show |
9 | a0001c0001t0001g0073a0001c0006t0001g0194a0001c0006t0001g0195others(6): Show | 9 | HG01175.hp2 HG02027.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.421+1699_421+1706d others(10): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121041297 | ||||||
chr9:121041297
|
CTTTTTTT others(3): Show |
C | 1 | a0012c0011t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.421+1697_421+1706d others(12): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121041297 | ||||||
chr9:121041327
|
C | T | 1 | a0001c0022t0001g0229 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.421+1677G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121041327 | ||||||
chr9:121041488
|
A | G | 1 | a0007c0009t0001g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.421+1516T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121041488 | ||||||
chr9:121041566
|
A | G | 218 | a0001c0001t0001g0030a0001c0001t0001g0068a0001c0001t0001g0073others(215): Show | 223 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.421+1438T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121041566 | ||||||
chr9:121041598
|
ATTC | A | 2 | a0003c0004t0001g0031a0003c0004t0001g0032 | 2 | HG01074.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.421+1403_421+1405d others(5): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121041598 | ||||||
chr9:121041766
|
T | TA | 28 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0012others(25): Show | 31 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.421+1237dupT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121041766 | ||||||
chr9:121041854
|
C | T | 11 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(8): Show | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.421+1150G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121041854 | ||||||
chr9:121042303
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | NA18948.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.421+701A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121042303 | ||||||
chr9:121042498
|
C | T | 45 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(42): Show | 45 | HG00597.hp2 HG01069.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.421+506G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121042498 | ||||||
chr9:121042859
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.421+145T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121042859 | ||||||
chr9:121042871
|
G | T | 1 | a0001c0001t0001g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.421+133C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 3/40 | chr9 | 121042871 | ||||||
chr9:121043270
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.259-104A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121043270 | ||||||
chr9:121043402
|
A | G | 1 | a0004c0005t0001g0218 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-236T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121043402 | ||||||
chr9:121043700
|
C | CT | 34 | a0001c0001t0001g0224a0001c0001t0001g0243a0001c0018t0001g0244others(31): Show | 36 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.259-535dupA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121043700 | ||||||
chr9:121043700
|
C | CTT | 111 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(108): Show | 111 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.259-536_259-535dup others(2): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121043700 | ||||||
chr9:121043700
|
C | CTTT | 6 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(3): Show | 6 | HG02027.hp2 HG03654.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-537_259-535dup others(3): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121043700 | ||||||
chr9:121043700
|
CT | C | 5 | a0001c0006t0001g0204a0007c0009t0001g0206a0007c0009t0001g0207others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-535delA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121043700 | ||||||
chr9:121043929
|
T | A | 1 | a0017c0025t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.259-763A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121043929 | ||||||
chr9:121044240
|
C | T | 3 | a0003c0004t0001g0019a0003c0004t0001g0020a0003c0004t0001g0056 | 3 | HG02257.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.259-1074G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121044240 | ||||||
chr9:121044347
|
C | T | 1 | a0018c0023t0001g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.259-1181G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121044347 | ||||||
chr9:121044376
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.259-1210A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121044376 | ||||||
chr9:121044425
|
G | A | 3 | a0001c0001t0001g0249a0013c0015t0001g0220a0013c0015t0001g0221 | 3 | HG00738.hp2 HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.259-1259C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121044425 | ||||||
chr9:121044458
|
A | C | 60 | a0001c0001t0001g0030a0003c0003t0001g0001a0003c0003t0001g0002others(57): Show | 63 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.259-1292T>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121044458 | ||||||
chr9:121044552
|
G | A | 1 | a0001c0001t0001g0242 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.259-1386C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121044552 | ||||||
chr9:121044743
|
T | C | 8 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(5): Show | 9 | HG01891.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.258+1448A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121044743 | ||||||
chr9:121044947
|
T | C | 11 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(8): Show | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.258+1244A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121044947 | ||||||
chr9:121044948
|
C | CT | 9 | a0001c0001t0001g0073a0001c0001t0001g0074a0002c0002t0001g0222others(6): Show | 9 | HG01109.hp2 HG01175.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.258+1242dupA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121044948 | ||||||
chr9:121044948
|
CT | C | 5 | a0001c0001t0001g0108a0001c0001t0001g0258a0002c0002t0001g0179others(2): Show | 5 | HG01070.hp2 NA18992.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+1242delA | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121044948 | ||||||
chr9:121045104
|
A | G | 4 | a0001c0006t0001g0194a0001c0006t0001g0195a0001c0006t0001g0196others(1): Show | 4 | HG00099.hp1 HG02027.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+1087T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121045104 | ||||||
chr9:121045108
|
G | A | 1 | a0003c0004t0001g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.258+1083C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121045108 | ||||||
chr9:121045212
|
A | G | 13 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(10): Show | 13 | HG02071.hp2 NA18944.hp2 NA18946.hp1 others(10): Show |
intron_variant | MODIFIER | c.258+979T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121045212 | ||||||
chr9:121045260
|
T | C | 24 | a0002c0002t0001g0156a0002c0002t0001g0157a0002c0002t0001g0158others(21): Show | 24 | HG00408.hp1 HG01256.hp2 HG01978.hp2 others(21): Show |
intron_variant | MODIFIER | c.258+931A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121045260 | ||||||
chr9:121045942
|
T | C | 218 | a0001c0001t0001g0030a0001c0001t0001g0068a0001c0001t0001g0073others(215): Show | 223 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.258+249A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121045942 | ||||||
chr9:121045971
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.258+220C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121045971 | ||||||
chr9:121045984
|
C | A | 9 | a0001c0001t0001g0010a0001c0001t0001g0243a0001c0001t0001g0246others(6): Show | 10 | HG00099.hp2 HG00738.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.258+207G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 2/40 | chr9 | 121045984 | ||||||
chr9:121046685
|
C | A | 80 | a0002c0002t0001g0071a0002c0002t0001g0072a0002c0002t0001g0109others(77): Show | 80 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.66-302G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121046685 | ||||||
chr9:121046688
|
G | T | 1 | a0003c0003t0001g0057 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.66-305C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121046688 | ||||||
chr9:121046720
|
G | T | 1 | a0002c0002t0001g0072 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.66-337C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121046720 | ||||||
chr9:121046770
|
C | T | 1 | a0002c0002t0001g0071 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.66-387G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121046770 | ||||||
chr9:121046826
|
G | A | 218 | a0001c0001t0001g0030a0001c0001t0001g0068a0001c0001t0001g0073others(215): Show | 223 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.66-443C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121046826 | ||||||
chr9:121047261
|
G | C | 218 | a0001c0001t0001g0030a0001c0001t0001g0068a0001c0001t0001g0073others(215): Show | 223 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.66-878C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121047261 | ||||||
chr9:121047302
|
A | G | 1 | a0012c0011t0001g0006 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.66-919T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121047302 | ||||||
chr9:121047459
|
G | A | 223 | a0001c0001t0001g0030a0001c0001t0001g0068a0001c0001t0001g0073others(220): Show | 229 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.66-1076C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121047459 | ||||||
chr9:121047612
|
C | T | 134 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(131): Show | 134 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.66-1229G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121047612 | ||||||
chr9:121047766
|
G | C | 3 | a0004c0005t0001g0218a0010c0014t0001g0005a0010c0014t0001g0219 | 4 | HG00639.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.66-1383C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121047766 | ||||||
chr9:121047844
|
AGAG | A | 5 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208others(2): Show | 5 | HG02451.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.66-1464_66-1462del others(3): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121047844 | ||||||
chr9:121047847
|
G | A | 1 | a0001c0016t0001g0003 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.66-1464C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121047847 | ||||||
chr9:121047915
|
A | T | 1 | a0001c0024t0001g0070 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.66-1532T>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121047915 | ||||||
chr9:121047952
|
C | A | 3 | a0007c0009t0001g0206a0007c0009t0001g0207a0007c0009t0001g0208 | 3 | HG02451.hp2 HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.66-1569G>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121047952 | ||||||
chr9:121048169
|
A | G | 50 | a0001c0001t0001g0030a0003c0003t0001g0001a0003c0003t0001g0002others(47): Show | 53 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.66-1786T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121048169 | ||||||
chr9:121048238
|
G | A | 1 | a0007c0009t0001g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66-1855C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121048238 | ||||||
chr9:121048308
|
T | C | 222 | a0001c0001t0001g0030a0001c0001t0001g0068a0001c0001t0001g0073others(219): Show | 228 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.65+1874A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121048308 | ||||||
chr9:121048401
|
G | A | 13 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(10): Show | 13 | HG02071.hp2 NA18944.hp2 NA18946.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+1781C>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121048401 | ||||||
chr9:121048442
|
T | C | 1 | a0002c0002t0001g0193 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.65+1740A>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121048442 | ||||||
chr9:121048605
|
C | T | 133 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0074others(130): Show | 133 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.65+1577G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121048605 | ||||||
chr9:121048705
|
T | A | 61 | a0001c0001t0001g0030a0003c0003t0001g0001a0003c0003t0001g0002others(58): Show | 64 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.65+1477A>T | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121048705 | ||||||
chr9:121048760
|
G | T | 222 | a0001c0001t0001g0030a0001c0001t0001g0068a0001c0001t0001g0073others(219): Show | 228 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.65+1422C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121048760 | ||||||
chr9:121048763
|
G | GGTTACT | 255 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(252): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.65+1418_65+1419ins others(6): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121048763 | ||||||
chr9:121048862
|
G | C | 11 | a0004c0005t0001g0004a0004c0005t0001g0211a0004c0005t0001g0216others(8): Show | 13 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+1320C>G | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121048862 | ||||||
chr9:121048866
|
G | T | 1 | a0006c0008t0001g0069 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.65+1316C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121048866 | ||||||
chr9:121049087
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.65+1095T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121049087 | ||||||
chr9:121049230
|
G | T | 1 | a0003c0003t0001g0014 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.65+952C>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121049230 | ||||||
chr9:121049354
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.65+828T>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121049354 | ||||||
chr9:121049417
|
C | T | 2 | a0003c0003t0001g0012a0003c0003t0001g0013 | 2 | NA18986.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.65+765G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121049417 | ||||||
chr9:121049439
|
C | T | 60 | a0001c0001t0001g0030a0003c0003t0001g0001a0003c0003t0001g0002others(57): Show | 63 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.65+743G>A | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121049439 | ||||||
chr9:121049772
|
T | G | 2 | a0013c0015t0001g0220a0013c0015t0001g0221 | 2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.65+410A>C | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121049772 | ||||||
chr9:121049958
|
TA | T | 221 | a0001c0001t0001g0030a0001c0001t0001g0068a0001c0001t0001g0073others(218): Show | 227 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.65+223delT | C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121049958 | ||||||
chr9:121050051
|
AGAT | A | 5 | a0005c0007t0001g0259a0005c0007t0001g0260a0005c0007t0001g0261others(2): Show | 5 | HG02132.hp2 HG02135.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.65+128_65+130delAT others(1): Show |
C5 | ENSG00000106804.10 | transcript | ENST00000223642.3 | protein_coding | 1/40 | chr9 | 121050051 |