geneid | 952 |
---|---|
ensemblid | ENSG00000004468.13 |
hgncid | 1667 |
symbol | CD38 |
name | CD38 molecule |
refseq_nuc | NM_001775.4 |
refseq_prot | NP_001766.2 |
ensembl_nuc | ENST00000226279.8 |
ensembl_prot | ENSP00000226279.2 |
mane_status | MANE Select |
chr | chr4 |
start | 15778328 |
end | 15853232 |
strand | + |
ver | v1.2 |
region | chr4:15778328-15853232 |
region5000 | chr4:15773328-15858232 |
regionname0 | CD38_chr4_15778328_15853232 |
regionname5000 | CD38_chr4_15773328_15858232 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 300 | 341 | 76 | 66 | 149 | 12 | 36 | 121 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0002 | 0/0 | 300 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 903 | 298 | 70 | 61 | 121 | 12 | 32 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
c0002 | 0/0 | 903 | 39 | 6 | 4 | 25 | 0 | 4 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
c0003 | 0/0 | 903 | 3 | 0 | 0 | 3 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
c0004 | 0/0 | 903 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
c0005 | 0/0 | 903 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
c0006 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4718 | 67 | 1 | 20 | 36 | 4 | 6 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0002 | 0/1 | 4717 | 61 | 5 | 16 | 22 | 5 | 12 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0003 | 0/0 | 4720 | 29 | 1 | 13 | 11 | 2 | 2 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0004 | 0/0 | 4717 | 22 | 4 | 1 | 11 | 1 | 5 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0005 | 0/0 | 4720 | 16 | 0 | 2 | 13 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0006 | 0/0 | 4718 | 16 | 0 | 0 | 15 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0007 | 0/0 | 4720 | 10 | 2 | 3 | 4 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0008 | 0/0 | 4717 | 9 | 0 | 0 | 9 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0009 | 0/0 | 4720 | 7 | 2 | 1 | 3 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0010 | 0/0 | 4721 | 6 | 0 | 1 | 3 | 0 | 2 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0011 | 0/0 | 4717 | 6 | 6 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0012 | 0/0 | 4720 | 4 | 0 | 0 | 4 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0013 | 0/0 | 4719 | 4 | 0 | 0 | 3 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0014 | 0/0 | 4721 | 4 | 1 | 0 | 1 | 0 | 2 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0015 | 0/0 | 4719 | 3 | 2 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0016 | 0/0 | 4721 | 3 | 2 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0017 | 0/0 | 4717 | 3 | 3 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0018 | 0/0 | 4717 | 3 | 0 | 3 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0019 | 0/0 | 4717 | 3 | 3 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0020 | 0/0 | 4717 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0021 | 0/0 | 4720 | 2 | 0 | 0 | 1 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0022 | 0/0 | 4718 | 2 | 1 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0023 | 0/0 | 4717 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0024 | 0/0 | 4719 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0025 | 0/0 | 4717 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0026 | 0/0 | 4717 | 2 | 1 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0027 | 0/0 | 4717 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0028 | 0/0 | 4718 | 2 | 1 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0029 | 0/0 | 4717 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0030 | 0/0 | 4718 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0031 | 0/0 | 4717 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0032 | 0/0 | 4719 | 2 | 1 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0033 | 0/0 | 4717 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0034 | 0/0 | 4718 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0035 | 0/0 | 4719 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0036 | 0/0 | 4717 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0037 | 0/0 | 4717 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0038 | 0/0 | 4717 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0039 | 0/0 | 4721 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0040 | 0/0 | 4718 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0041 | 0/0 | 4720 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0042 | 0/0 | 4717 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0043 | 0/0 | 4717 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0044 | 0/0 | 4720 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0045 | 0/0 | 4719 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0046 | 0/0 | 4717 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0047 | 0/0 | 4718 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0048 | 0/0 | 4717 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0049 | 0/0 | 4717 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0050 | 0/0 | 4718 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0051 | 0/0 | 4718 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0052 | 1/0 | 4718 | 1 | 0 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0053 | 0/0 | 4718 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0054 | 0/0 | 4718 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0055 | 0/0 | 4720 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0056 | 0/0 | 4720 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0057 | 0/0 | 4717 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0058 | 0/0 | 4721 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0059 | 0/0 | 4718 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0060 | 0/0 | 4717 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0061 | 0/0 | 4719 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0062 | 0/0 | 4709 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0063 | 0/0 | 4719 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0064 | 0/0 | 4719 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0065 | 0/0 | 4718 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0066 | 0/0 | 4719 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0067 | 0/0 | 4719 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0068 | 0/0 | 4721 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0069 | 0/0 | 4720 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0070 | 0/0 | 4717 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0071 | 0/0 | 4718 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0072 | 0/0 | 4709 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
t0073 | 0/0 | 4717 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
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 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0191 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0231 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 903 | 298 | 70 | 61 | 121 | 12 | 32 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002 | 0/0 | 903 | 39 | 6 | 4 | 25 | 0 | 4 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0004 | 0/0 | 903 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0005 | 0/0 | 903 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0006 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0002c0003 | 0/0 | 903 | 3 | 0 | 0 | 3 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5620 | 59 | 1 | 20 | 28 | 4 | 6 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0002 | 0/1 | 5619 | 60 | 5 | 16 | 21 | 5 | 12 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0003 | 0/0 | 5622 | 23 | 0 | 13 | 6 | 2 | 2 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0004 | 0/0 | 5619 | 20 | 4 | 1 | 9 | 1 | 5 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0005 | 0/0 | 5622 | 6 | 0 | 0 | 6 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0006 | 0/0 | 5620 | 15 | 0 | 0 | 15 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0007 | 0/0 | 5622 | 6 | 2 | 2 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0008 | 0/0 | 5619 | 9 | 0 | 0 | 9 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0009 | 0/0 | 5622 | 6 | 2 | 0 | 3 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0010 | 0/0 | 5623 | 5 | 0 | 1 | 3 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0011 | 0/0 | 5619 | 6 | 6 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0013 | 0/0 | 5621 | 4 | 0 | 0 | 3 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0014 | 0/0 | 5623 | 4 | 1 | 0 | 1 | 0 | 2 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0015 | 0/0 | 5621 | 3 | 2 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0016 | 0/0 | 5623 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0017 | 0/0 | 5619 | 3 | 3 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0018 | 0/0 | 5619 | 3 | 0 | 3 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0019 | 0/0 | 5619 | 3 | 3 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0020 | 0/0 | 5619 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0021 | 0/0 | 5622 | 2 | 0 | 0 | 1 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0022 | 0/0 | 5620 | 2 | 1 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0023 | 0/0 | 5619 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0024 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0025 | 0/0 | 5619 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0026 | 0/0 | 5619 | 2 | 1 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0028 | 0/0 | 5620 | 2 | 1 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0030 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0031 | 0/0 | 5619 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0032 | 0/0 | 5621 | 2 | 1 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0033 | 0/0 | 5619 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0034 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0035 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0036 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0038 | 0/0 | 5619 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0039 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0040 | 0/0 | 5620 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0041 | 0/0 | 5622 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0042 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0043 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0044 | 0/0 | 5622 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0045 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0046 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0047 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0048 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0049 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0050 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0051 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0052 | 1/0 | 5620 | 1 | 0 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0053 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0054 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0055 | 0/0 | 5622 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0056 | 0/0 | 5622 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0057 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0058 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0059 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0060 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0061 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0062 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0063 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0064 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0065 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0066 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0067 | 0/0 | 5621 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0068 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0069 | 0/0 | 5622 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0070 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0071 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0072 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0001t0073 | 0/0 | 5619 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002t0001 | 0/0 | 5620 | 5 | 0 | 0 | 5 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002t0002 | 0/0 | 5619 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002t0003 | 0/0 | 5622 | 6 | 1 | 0 | 5 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002t0004 | 0/0 | 5619 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002t0005 | 0/0 | 5622 | 10 | 0 | 2 | 7 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002t0006 | 0/0 | 5620 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002t0007 | 0/0 | 5622 | 3 | 0 | 0 | 2 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002t0009 | 0/0 | 5622 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002t0010 | 0/0 | 5623 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002t0012 | 0/0 | 5622 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002t0016 | 0/0 | 5623 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002t0024 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002t0027 | 0/0 | 5619 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002t0029 | 0/0 | 5619 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002t0030 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0002t0037 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0004t0001 | 0/0 | 5620 | 2 | 0 | 0 | 2 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0005t0007 | 0/0 | 5622 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0001c0006t0001 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
a0002c0003t0012 | 0/0 | 5622 | 3 | 0 | 0 | 3 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | copy fasta | chr4 | 15773328 | 15858232 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0191 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0006g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0006g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0006g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0007g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0007g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0008g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0008g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0008g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0008g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0008g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0008g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0009g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0009g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0009g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0009g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0009g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0010g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0010g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0010g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0010g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0010g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0011g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0011g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0011g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0013g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0013g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0013g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0013g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0014g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0014g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0014g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0014g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0015g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0015g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0015g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0016g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0016g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0017g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0017g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0017g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0018g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0018g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0019g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0019g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0019g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0020g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0020g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0021g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0021g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0022g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0022g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0023g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0023g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0024g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0025g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0025g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0026g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0026g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0028g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0028g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0030g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0031g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0031g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0032g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0032g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0033g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0033g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0034g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0035g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0036g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0038g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0039g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0040g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0041g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0042g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0043g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0044g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0045g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0046g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0047g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0048g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0049g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0050g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0051g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0052g0231 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0053g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0054g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0055g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0056g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0057g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0058g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0059g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0060g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0061g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0062g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0063g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0064g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0065g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0066g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0067g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0068g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0069g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0070g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0071g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0072g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0001t0073g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0005g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0005g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0006g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0007g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0009g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0010g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0012g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0016g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0024g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0027g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0027g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0029g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0029g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0030g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0002t0037g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0004t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0005t0007g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0001c0006t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0002c0003t0012g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0002c0003t0012g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
a0002c0003t0012g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0313 | EUR | GBR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | GBR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0305 | EUR | GBR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | GBR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | FIN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0229 | EUR | FIN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00408 | hp2 | a0001 | c0002 | t0004 | g0080 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00423 | hp1 | a0001 | c0004 | t0001 | g0296 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00423 | hp2 | a0001 | c0002 | t0005 | g0087 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00438 | hp1 | a0001 | c0001 | t0032 | g0173 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00609 | hp1 | a0001 | c0004 | t0001 | g0297 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00621 | hp2 | a0001 | c0002 | t0007 | g0077 | EAS | CHS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00642 | hp1 | a0001 | c0001 | t0041 | g0306 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0323 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00733 | hp2 | a0001 | c0001 | t0018 | g0006 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00735 | hp1 | a0001 | c0001 | t0018 | g0205 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0272 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0277 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01069 | hp2 | a0001 | c0001 | t0018 | g0006 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0304 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01106 | hp2 | a0001 | c0002 | t0009 | g0076 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01168 | hp1 | a0001 | c0001 | t0007 | g0019 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01169 | hp1 | a0001 | c0001 | t0007 | g0033 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0308 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01192 | hp2 | a0001 | c0002 | t0016 | g0106 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0248 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01243 | hp2 | a0001 | c0001 | t0067 | g0058 | AMR | PUR | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01256 | hp1 | a0001 | c0005 | t0007 | g0022 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0316 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0317 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0330 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0309 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01358 | hp2 | a0001 | c0001 | t0038 | g0203 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01361 | hp2 | a0001 | c0001 | t0010 | g0312 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01433 | hp2 | a0001 | c0001 | t0026 | g0061 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0245 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01884 | hp2 | a0001 | c0001 | t0024 | g0197 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01891 | hp1 | a0001 | c0001 | t0011 | g0004 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01891 | hp2 | a0001 | c0001 | t0016 | g0063 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01928 | hp2 | a0001 | c0002 | t0005 | g0073 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0322 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02027 | hp1 | a0001 | c0001 | t0007 | g0051 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02055 | hp2 | a0001 | c0001 | t0032 | g0326 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0307 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02074 | hp1 | a0001 | c0001 | t0008 | g0129 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02074 | hp2 | a0001 | c0002 | t0003 | g0154 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02083 | hp1 | a0001 | c0002 | t0003 | g0079 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02083 | hp2 | a0001 | c0001 | t0010 | g0314 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02135 | hp1 | a0001 | c0001 | t0008 | g0125 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02135 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02145 | hp1 | a0001 | c0001 | t0014 | g0214 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02145 | hp2 | a0001 | c0001 | t0057 | g0302 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02148 | hp1 | a0001 | c0002 | t0005 | g0094 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0218 | EAS | CDX | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02165 | hp2 | a0001 | c0001 | t0014 | g0175 | EAS | CDX | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02257 | hp1 | a0001 | c0001 | t0047 | g0185 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02257 | hp2 | a0001 | c0001 | t0030 | g0031 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02280 | hp1 | a0001 | c0001 | t0045 | g0187 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0115 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02293 | hp1 | a0001 | c0001 | t0028 | g0213 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02451 | hp2 | a0001 | c0001 | t0023 | g0043 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02523 | hp1 | a0001 | c0001 | t0007 | g0170 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02572 | hp1 | a0001 | c0001 | t0015 | g0070 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02572 | hp2 | a0001 | c0001 | t0042 | g0102 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02622 | hp1 | a0001 | c0001 | t0019 | g0184 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02622 | hp2 | a0001 | c0001 | t0069 | g0037 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0182 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02630 | hp2 | a0001 | c0001 | t0064 | g0029 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02647 | hp1 | a0001 | c0001 | t0011 | g0041 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02647 | hp2 | a0001 | c0001 | t0019 | g0156 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0303 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02735 | hp2 | a0001 | c0001 | t0009 | g0142 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02738 | hp1 | a0001 | c0001 | t0014 | g0174 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02738 | hp2 | a0001 | c0001 | t0010 | g0315 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02809 | hp2 | a0001 | c0002 | t0024 | g0075 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02818 | hp1 | a0001 | c0002 | t0037 | g0081 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02818 | hp2 | a0001 | c0001 | t0056 | g0049 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02895 | hp2 | a0001 | c0001 | t0011 | g0042 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02896 | hp1 | a0001 | c0001 | t0028 | g0059 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0064 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02922 | hp1 | a0001 | c0001 | t0071 | g0180 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02922 | hp2 | a0001 | c0001 | t0062 | g0108 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02965 | hp1 | a0001 | c0001 | t0034 | g0110 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02965 | hp2 | a0001 | c0001 | t0039 | g0159 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02970 | hp1 | a0001 | c0001 | t0063 | g0054 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02970 | hp2 | a0001 | c0001 | t0023 | g0069 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02976 | hp1 | a0001 | c0001 | t0061 | g0046 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02976 | hp2 | a0001 | c0001 | t0070 | g0030 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03017 | hp1 | a0001 | c0001 | t0040 | g0204 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03041 | hp2 | a0001 | c0001 | t0017 | g0186 | AFR | GWD | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03098 | hp1 | a0001 | c0002 | t0030 | g0062 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03098 | hp2 | a0001 | c0001 | t0022 | g0045 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03130 | hp1 | a0001 | c0001 | t0058 | g0301 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03130 | hp2 | a0001 | c0001 | t0049 | g0065 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03139 | hp1 | a0001 | c0001 | t0035 | g0158 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03139 | hp2 | a0001 | c0002 | t0003 | g0074 | AFR | ESN | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03209 | hp1 | a0001 | c0001 | t0060 | g0047 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03209 | hp2 | a0001 | c0001 | t0011 | g0038 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03453 | hp1 | a0001 | c0001 | t0015 | g0193 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03453 | hp2 | a0001 | c0001 | t0017 | g0068 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03486 | hp1 | a0001 | c0001 | t0011 | g0004 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03486 | hp2 | a0001 | c0001 | t0036 | g0160 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03491 | hp2 | a0001 | c0002 | t0007 | g0098 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0267 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0321 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0324 | SAS | STU | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | STU | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03831 | hp2 | a0001 | c0002 | t0010 | g0078 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03834 | hp1 | a0001 | c0001 | t0014 | g0148 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03834 | hp2 | a0001 | c0002 | t0005 | g0100 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03942 | hp1 | a0001 | c0001 | t0013 | g0291 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03942 | hp2 | a0001 | c0002 | t0006 | g0099 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | STU | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0255 | SAS | STU | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0172 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | BEB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | STU | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG04228 | hp1 | a0001 | c0001 | t0021 | g0234 | SAS | STU | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | STU | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18522 | hp1 | a0001 | c0001 | t0019 | g0150 | AFR | YRI | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | YRI | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18906 | hp1 | a0001 | c0002 | t0029 | g0163 | AFR | YRI | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18906 | hp2 | a0001 | c0001 | t0020 | g0179 | AFR | YRI | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18942 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18943 | hp1 | a0001 | c0002 | t0005 | g0088 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18944 | hp1 | a0001 | c0002 | t0007 | g0086 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18944 | hp2 | a0001 | c0001 | t0013 | g0281 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18945 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18945 | hp2 | a0001 | c0001 | t0006 | g0285 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18947 | hp1 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18950 | hp1 | a0002 | c0003 | t0012 | g0104 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18950 | hp2 | a0001 | c0001 | t0044 | g0253 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18951 | hp1 | a0002 | c0003 | t0012 | g0105 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18952 | hp2 | a0001 | c0001 | t0005 | g0319 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18953 | hp2 | a0001 | c0001 | t0008 | g0167 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18960 | hp2 | a0001 | c0001 | t0053 | g0293 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18965 | hp2 | a0001 | c0001 | t0059 | g0113 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18968 | hp2 | a0001 | c0001 | t0055 | g0147 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18969 | hp1 | a0001 | c0001 | t0010 | g0320 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18970 | hp1 | a0001 | c0001 | t0006 | g0132 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18972 | hp2 | a0001 | c0001 | t0051 | g0128 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18974 | hp1 | a0001 | c0001 | t0025 | g0282 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18974 | hp2 | a0001 | c0001 | t0006 | g0133 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18978 | hp1 | a0002 | c0003 | t0012 | g0103 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18979 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18980 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18981 | hp1 | a0001 | c0002 | t0005 | g0084 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18981 | hp2 | a0001 | c0001 | t0031 | g0146 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18982 | hp1 | a0001 | c0001 | t0009 | g0279 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18982 | hp2 | a0001 | c0001 | t0005 | g0138 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18984 | hp1 | a0001 | c0002 | t0012 | g0082 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18984 | hp2 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18986 | hp1 | a0001 | c0001 | t0054 | g0244 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18989 | hp1 | a0001 | c0001 | t0006 | g0276 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18993 | hp2 | a0001 | c0002 | t0005 | g0085 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18995 | hp1 | a0001 | c0001 | t0006 | g0286 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18995 | hp2 | a0001 | c0001 | t0008 | g0152 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA18999 | hp2 | a0001 | c0001 | t0025 | g0048 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19000 | hp1 | a0001 | c0002 | t0005 | g0089 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19000 | hp2 | a0001 | c0001 | t0013 | g0325 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19002 | hp1 | a0001 | c0001 | t0005 | g0137 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19003 | hp1 | a0001 | c0001 | t0006 | g0284 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19006 | hp1 | a0001 | c0001 | t0006 | g0121 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19006 | hp2 | a0001 | c0001 | t0009 | g0329 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19009 | hp2 | a0001 | c0002 | t0005 | g0093 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19011 | hp2 | a0001 | c0001 | t0010 | g0299 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19012 | hp2 | a0001 | c0001 | t0008 | g0136 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19030 | hp1 | a0001 | c0001 | t0020 | g0157 | AFR | LWK | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19030 | hp2 | a0001 | c0001 | t0016 | g0067 | AFR | LWK | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19043 | hp1 | a0001 | c0001 | t0009 | g0178 | AFR | LWK | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19043 | hp2 | a0001 | c0001 | t0026 | g0060 | AFR | LWK | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19054 | hp2 | a0001 | c0001 | t0006 | g0288 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19057 | hp2 | a0001 | c0001 | t0006 | g0036 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19060 | hp2 | a0001 | c0001 | t0006 | g0119 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19062 | hp1 | a0001 | c0001 | t0073 | g0195 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19062 | hp2 | a0001 | c0001 | t0022 | g0241 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19064 | hp1 | a0001 | c0002 | t0005 | g0095 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19067 | hp1 | a0001 | c0001 | t0006 | g0131 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19070 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19072 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19074 | hp1 | a0001 | c0001 | t0015 | g0010 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19074 | hp2 | a0001 | c0002 | t0004 | g0071 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19075 | hp2 | a0001 | c0001 | t0006 | g0151 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19077 | hp2 | a0001 | c0002 | t0027 | g0097 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19080 | hp1 | a0001 | c0001 | t0013 | g0290 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19080 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19081 | hp1 | a0001 | c0006 | t0001 | g0011 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19081 | hp2 | a0001 | c0001 | t0031 | g0145 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19083 | hp1 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19084 | hp2 | a0001 | c0001 | t0008 | g0166 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19087 | hp1 | a0001 | c0001 | t0006 | g0116 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19087 | hp2 | a0001 | c0001 | t0021 | g0055 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19088 | hp1 | a0001 | c0002 | t0027 | g0072 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19091 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19240 | hp1 | a0001 | c0001 | t0046 | g0044 | AFR | YRI | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA19240 | hp2 | a0001 | c0001 | t0066 | g0114 | AFR | YRI | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA20129 | hp1 | a0001 | c0001 | t0033 | g0194 | AFR | ASW | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA20129 | hp2 | a0001 | c0001 | t0033 | g0028 | AFR | ASW | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0181 | EUR | TSI | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | TSI | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02109 | hp2 | a0001 | c0001 | t0050 | g0221 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02486 | hp2 | a0001 | c0001 | t0048 | g0040 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02559 | hp1 | a0001 | c0001 | t0011 | g0039 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG02559 | hp2 | a0001 | c0001 | t0065 | g0101 | AFR | ACB | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03471 | hp1 | a0001 | c0002 | t0029 | g0164 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG03471 | hp2 | a0001 | c0001 | t0017 | g0053 | AFR | MSL | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG06807 | hp1 | a0001 | c0001 | t0072 | g0183 | AFR | USA | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | USA | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA21309 | hp1 | a0001 | c0001 | t0068 | g0196 | AFR | LWK | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
NA21309 | hp2 | a0001 | c0001 | t0043 | g0107 | AFR | LWK | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0191 | REF | REF | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0052 | g0231 | REF | REF | CD38_chr4_15773328_15858232 | CD38 | chr4 | 15773328 | 15858232 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:15824935
|
C | T | 1 | a0002 | 3 | NA18950.hp1 NA18951.hp1 NA18978.hp1 |
missense_variant | MODERATE | c.418C>T | p.Arg140Trp | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/8 | 505/5620 | 418/903 | 140/300 | chr4 | 15824935 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:15778483
|
A | G | 1 | a0001c0006 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.69A>G | p.Gln23Gln | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/8 | 156/5620 | 69/903 | 23/300 | chr4 | 15778483 | ||
chr4:15816625
|
C | T | 1 | a0001c0004 | 2 | HG00423.hp1 HG00609.hp1 |
synonymous_variant | LOW | c.348C>T | p.Thr116Thr | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/8 | 435/5620 | 348/903 | 116/300 | chr4 | 15816625 | ||
chr4:15834221
|
A | C | 2 | a0001c0002a0002c0003 | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
synonymous_variant | LOW | c.504A>C | p.Ile168Ile | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/8 | 591/5620 | 504/903 | 168/300 | chr4 | 15834221 | ||
chr4:15840107
|
A | G | 1 | a0001c0005 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.741A>G | p.Arg247Arg | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 6/8 | 828/5620 | 741/903 | 247/300 | chr4 | 15840107 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:15778329
|
C | A | 1 | a0001c0001t0034 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-86C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/8 | 86 | chr4 | 15778329 | |||||
chr4:15848707
|
T | G | 7 | a0001c0001t0020a0001c0001t0035a0001c0001t0036others(4): Show | 8 | HG01358.hp2 HG02818.hp1 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*105T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 105 | chr4 | 15848707 | |||||
chr4:15848740
|
T | C | 1 | a0001c0001t0041 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*138T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 138 | chr4 | 15848740 | |||||
chr4:15848759
|
A | G | 1 | a0001c0001t0073 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*157A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 157 | chr4 | 15848759 | |||||
chr4:15848790
|
T | C | 1 | a0001c0001t0042 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*188T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 188 | chr4 | 15848790 | |||||
chr4:15848936
|
C | G | 5 | a0001c0001t0033a0001c0001t0069a0001c0001t0070others(2): Show | 6 | HG02622.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*334C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 334 | chr4 | 15848936 | |||||
chr4:15849029
|
G | A | 1 | a0001c0001t0043 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*427G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 427 | chr4 | 15849029 | |||||
chr4:15849048
|
A | G | 1 | a0001c0001t0068 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*446A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 446 | chr4 | 15849048 | |||||
chr4:15849062
|
C | T | 47 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(44): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*460C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 460 | chr4 | 15849062 | |||||
chr4:15849196
|
A | T | 1 | a0001c0001t0067 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*594A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 594 | chr4 | 15849196 | |||||
chr4:15849526
|
C | T | 1 | a0001c0001t0054 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*924C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 924 | chr4 | 15849526 | |||||
chr4:15850345
|
G | A | 75 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(72): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*1743G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 1743 | chr4 | 15850345 | |||||
chr4:15850406
|
A | T | 2 | a0001c0001t0065a0001c0001t0066 | 2 | HG02559.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1804A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 1804 | chr4 | 15850406 | |||||
chr4:15850481
|
T | C | 18 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(15): Show | 64 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1879T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 1879 | chr4 | 15850481 | |||||
chr4:15850506
|
A | C | 2 | a0001c0001t0017a0001c0001t0049 | 4 | HG03041.hp2 HG03130.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1904A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 1904 | chr4 | 15850506 | |||||
chr4:15850692
|
C | T | 1 | a0001c0001t0053 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2090C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 2090 | chr4 | 15850692 | |||||
chr4:15850704
|
C | G | 2 | a0001c0001t0073a0001c0002t0027 | 3 | NA19062.hp1 NA19077.hp2 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2102C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 2102 | chr4 | 15850704 | |||||
chr4:15850841
|
G | A | 1 | a0001c0001t0057 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2239G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 2239 | chr4 | 15850841 | |||||
chr4:15851012
|
T | C | 1 | a0001c0001t0020 | 2 | NA18906.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2410T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 2410 | chr4 | 15851012 | |||||
chr4:15851174
|
G | C | 1 | a0001c0001t0034 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2572G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 2572 | chr4 | 15851174 | |||||
chr4:15851235
|
C | T | 6 | a0001c0001t0026a0001c0001t0062a0001c0001t0063others(3): Show | 7 | HG01243.hp2 HG01433.hp2 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2633C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 2633 | chr4 | 15851235 | |||||
chr4:15851261
|
C | T | 2 | a0001c0001t0060a0001c0001t0061 | 2 | HG02976.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2659C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 2659 | chr4 | 15851261 | |||||
chr4:15851390
|
C | A | 15 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(12): Show | 60 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2788C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 2788 | chr4 | 15851390 | |||||
chr4:15851617
|
A | T | 1 | a0001c0001t0031 | 2 | NA18981.hp2 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3015A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3015 | chr4 | 15851617 | |||||
chr4:15851726
|
A | G | 3 | a0001c0001t0008a0001c0001t0025a0001c0001t0059 | 12 | HG02074.hp1 HG02135.hp1 NA18942.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3124A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3124 | chr4 | 15851726 | |||||
chr4:15851759
|
G | A | 1 | a0001c0001t0050 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3157G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3157 | chr4 | 15851759 | |||||
chr4:15851854
|
A | T | 1 | a0001c0001t0049 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3252A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3252 | chr4 | 15851854 | |||||
chr4:15851948
|
GTATCTAA others(3): Show |
G | 2 | a0001c0001t0062a0001c0001t0072 | 2 | HG02922.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3359_*3368delTCTA others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3359 | INFO_REALIGN_3_PRIME | chr4 | 15851948 | ||||
chr4:15852061
|
T | C | 22 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(19): Show | 118 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*3459T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3459 | chr4 | 15852061 | |||||
chr4:15852343
|
G | C | 1 | a0001c0001t0020 | 2 | NA18906.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3741G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3741 | chr4 | 15852343 | |||||
chr4:15852484
|
T | C | 1 | a0001c0001t0070 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3882T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3882 | chr4 | 15852484 | |||||
chr4:15852594
|
C | A | 1 | a0001c0001t0065 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3992C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 3992 | chr4 | 15852594 | |||||
chr4:15852607
|
C | T | 2 | a0001c0001t0024a0001c0002t0024 | 2 | HG01884.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4005C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4005 | chr4 | 15852607 | |||||
chr4:15852797
|
G | A | 37 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(34): Show | 145 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*4195G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4195 | chr4 | 15852797 | |||||
chr4:15852809
|
C | CT | 14 | a0001c0001t0013a0001c0001t0015a0001c0001t0024others(11): Show | 20 | HG00438.hp1 HG01243.hp2 HG01884.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4225dupT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4226 | INFO_REALIGN_3_PRIME | chr4 | 15852809 | ||||
chr4:15852809
|
C | CTT | 17 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(14): Show | 73 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*4224_*4225dupTT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4226 | INFO_REALIGN_3_PRIME | chr4 | 15852809 | ||||
chr4:15852809
|
C | CTTT | 8 | a0001c0001t0010a0001c0001t0014a0001c0001t0016others(5): Show | 16 | HG01192.hp2 HG01361.hp2 HG01891.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4223_*4225dupTTT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4226 | INFO_REALIGN_3_PRIME | chr4 | 15852809 | ||||
chr4:15852809
|
CT | C | 29 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(26): Show | 135 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*4225delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4225 | INFO_REALIGN_3_PRIME | chr4 | 15852809 | ||||
chr4:15852829
|
G | T | 88 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(85): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
3_prime_UTR_variant | MODIFIER | c.*4227G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4227 | chr4 | 15852829 | |||||
chr4:15852843
|
G | A | 1 | a0001c0001t0044 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4241G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4241 | chr4 | 15852843 | |||||
chr4:15852901
|
C | G | 1 | a0001c0002t0037 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4299C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4299 | chr4 | 15852901 | |||||
chr4:15852905
|
G | T | 2 | a0001c0001t0046a0001c0002t0029 | 3 | HG03471.hp1 NA18906.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4303G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4303 | chr4 | 15852905 | |||||
chr4:15852955
|
C | T | 1 | a0001c0001t0064 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4353C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4353 | chr4 | 15852955 | |||||
chr4:15853011
|
C | T | 4 | a0001c0001t0044a0001c0001t0055a0001c0002t0012others(1): Show | 6 | NA18950.hp1 NA18950.hp2 NA18951.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4409C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4409 | chr4 | 15853011 | |||||
chr4:15853102
|
G | A | 36 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(33): Show | 139 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*4500G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4500 | chr4 | 15853102 | |||||
chr4:15853202
|
A | G | 1 | a0001c0001t0026 | 2 | HG01433.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4600A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 8/8 | 4600 | chr4 | 15853202 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:15778735
|
G | A | 26 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 27 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.233+88G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15778735 | ||||||
chr4:15778820
|
T | G | 212 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(209): Show | 221 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.233+173T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15778820 | ||||||
chr4:15778830
|
C | G | 37 | a0001c0001t0002g0008a0001c0001t0002g0181a0001c0001t0002g0188others(34): Show | 38 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.233+183C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15778830 | ||||||
chr4:15778862
|
C | CG | 88 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0140others(85): Show | 93 | HG00408.hp1 HG00733.hp1 HG00733.hp2 others(90): Show |
intron_variant | MODIFIER | c.233+224dupG | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15778862 | |||||
chr4:15778862
|
C | CGG | 21 | a0001c0001t0001g0176a0001c0001t0002g0032a0001c0001t0002g0165others(18): Show | 21 | HG00438.hp1 HG01169.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.233+223_233+224dup others(2): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15778862 | |||||
chr4:15778916
|
C | T | 66 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(63): Show | 68 | HG00099.hp2 HG00408.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.233+269C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15778916 | ||||||
chr4:15778962
|
G | A | 2 | a0001c0001t0003g0216a0001c0001t0003g0217 | 2 | NA19079.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.233+315G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15778962 | ||||||
chr4:15779012
|
C | T | 2 | a0001c0001t0002g0161a0001c0001t0002g0162 | 2 | NA18956.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.233+365C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779012 | ||||||
chr4:15779106
|
G | A | 9 | a0001c0001t0011g0004a0001c0001t0011g0038a0001c0001t0011g0039others(6): Show | 10 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+459G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779106 | ||||||
chr4:15779107
|
G | C | 9 | a0001c0001t0011g0004a0001c0001t0011g0038a0001c0001t0011g0039others(6): Show | 10 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+460G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779107 | ||||||
chr4:15779110
|
AC | A | 9 | a0001c0001t0011g0004a0001c0001t0011g0038a0001c0001t0011g0039others(6): Show | 10 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+464delC | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779110 | ||||||
chr4:15779463
|
G | A | 2 | a0001c0001t0002g0109a0001c0001t0002g0165 | 2 | HG02055.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.233+816G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779463 | ||||||
chr4:15779555
|
C | T | 1 | a0001c0001t0028g0213 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.233+908C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779555 | ||||||
chr4:15779701
|
T | C | 2 | a0001c0001t0060g0047a0001c0001t0061g0046 | 2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+1054T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779701 | ||||||
chr4:15779791
|
C | T | 1 | a0001c0001t0043g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.233+1144C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779791 | ||||||
chr4:15779963
|
A | G | 1 | a0001c0002t0016g0106 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.233+1316A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15779963 | ||||||
chr4:15780042
|
G | A | 1 | a0001c0001t0071g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.233+1395G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780042 | ||||||
chr4:15780264
|
A | G | 2 | a0001c0001t0003g0012a0001c0001t0003g0322 | 3 | HG00738.hp2 HG01099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.233+1617A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780264 | ||||||
chr4:15780298
|
A | G | 46 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0020g0157others(43): Show | 48 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.233+1651A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780298 | ||||||
chr4:15780302
|
C | G | 16 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(13): Show | 16 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.233+1655C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780302 | ||||||
chr4:15780413
|
A | G | 1 | a0001c0001t0004g0321 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.233+1766A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780413 | ||||||
chr4:15780518
|
T | TCA | 7 | a0001c0001t0001g0009a0001c0001t0001g0220a0001c0001t0001g0222others(4): Show | 8 | HG00280.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+1920_233+1921d others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | |||||
chr4:15780518
|
T | TCACACAC others(11): Show |
4 | a0001c0001t0015g0070a0001c0001t0017g0068a0001c0001t0023g0069others(1): Show | 4 | HG02572.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+1882_233+1883i others(20): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | |||||
chr4:15780518
|
T | TCACACAC others(15): Show |
4 | a0001c0001t0004g0064a0001c0001t0004g0066a0001c0001t0016g0063others(1): Show | 4 | HG01891.hp2 HG02896.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+1882_233+1883i others(24): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | |||||
chr4:15780518
|
T | TCACACAC others(17): Show |
4 | a0001c0001t0016g0067a0001c0001t0026g0060a0001c0001t0026g0061others(1): Show | 4 | HG01433.hp2 HG03098.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+1882_233+1883i others(26): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | |||||
chr4:15780518
|
T | TCACACAC others(21): Show |
3 | a0001c0001t0002g0057a0001c0001t0028g0059a0001c0001t0067g0058 | 3 | HG01243.hp2 HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.233+1882_233+1883i others(30): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | |||||
chr4:15780518
|
TCA | T | 107 | a0001c0001t0001g0140a0001c0001t0001g0233a0001c0001t0001g0235others(104): Show | 112 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.233+1920_233+1921d others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | |||||
chr4:15780518
|
TCACA | T | 91 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0176others(88): Show | 93 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.233+1918_233+1921d others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | |||||
chr4:15780518
|
TCACACA | T | 36 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0153others(33): Show | 36 | HG00741.hp1 HG01192.hp1 HG02622.hp2 others(33): Show |
intron_variant | MODIFIER | c.233+1916_233+1921d others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | |||||
chr4:15780518
|
TCACACAC others(1): Show |
T | 9 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0001g0295others(6): Show | 9 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(6): Show |
intron_variant | MODIFIER | c.233+1914_233+1921d others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | |||||
chr4:15780518
|
TCACACAC others(13): Show |
T | 1 | a0001c0001t0001g0300 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.233+1902_233+1921d others(22): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780518 | |||||
chr4:15780524
|
A | ACACACG | 3 | a0001c0002t0004g0071a0001c0002t0005g0073a0001c0002t0027g0072 | 3 | HG01928.hp2 NA19074.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.233+1882_233+1883i others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780524 | |||||
chr4:15780524
|
A | T | 2 | a0001c0001t0005g0319a0001c0001t0021g0055 | 2 | NA18952.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.233+1877A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780524 | ||||||
chr4:15780526
|
A | ACACG | 26 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(23): Show | 28 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.233+1882_233+1883i others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780526 | |||||
chr4:15780526
|
A | T | 3 | a0001c0001t0001g0011a0001c0001t0010g0320a0001c0006t0001g0011 | 3 | NA18969.hp1 NA18970.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.233+1879A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780526 | ||||||
chr4:15780528
|
A | ACG | 11 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(8): Show | 12 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.233+1882_233+1883i others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780528 | |||||
chr4:15780528
|
A | ACGCACAC others(25): Show |
1 | a0001c0001t0004g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.233+1882_233+1883i others(34): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780528 | |||||
chr4:15780528
|
A | ACGCG | 3 | a0002c0003t0012g0103a0002c0003t0012g0104a0002c0003t0012g0105 | 3 | NA18950.hp1 NA18951.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.233+1882_233+1883i others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15780528 | |||||
chr4:15780530
|
A | G | 13 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0181others(10): Show | 13 | HG02145.hp2 HG02559.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+1883A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780530 | ||||||
chr4:15780532
|
A | G | 100 | a0001c0001t0001g0140a0001c0001t0001g0310a0001c0001t0002g0005others(97): Show | 105 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.233+1885A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780532 | ||||||
chr4:15780534
|
A | G | 117 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0140others(114): Show | 123 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.233+1887A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780534 | ||||||
chr4:15780536
|
A | G | 29 | a0001c0001t0001g0015a0001c0001t0001g0153a0001c0001t0001g0176others(26): Show | 29 | HG01361.hp1 HG01891.hp2 HG02165.hp2 others(26): Show |
intron_variant | MODIFIER | c.233+1889A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780536 | ||||||
chr4:15780538
|
A | G | 6 | a0001c0001t0001g0153a0001c0001t0017g0053a0001c0001t0034g0110others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+1891A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780538 | ||||||
chr4:15780540
|
A | G | 1 | a0001c0001t0063g0054 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.233+1893A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780540 | ||||||
chr4:15780563
|
C | T | 10 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(7): Show | 11 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+1916C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780563 | ||||||
chr4:15780918
|
G | A | 2 | a0001c0001t0007g0115a0001c0001t0066g0114 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.233+2271G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15780918 | ||||||
chr4:15781070
|
G | T | 4 | a0001c0001t0030g0031a0001c0001t0064g0029a0001c0001t0069g0037others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+2423G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15781070 | ||||||
chr4:15781270
|
T | C | 1 | a0001c0001t0019g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.233+2623T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15781270 | ||||||
chr4:15781339
|
T | C | 1 | a0001c0001t0015g0193 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.233+2692T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15781339 | ||||||
chr4:15781358
|
G | C | 16 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(13): Show | 16 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.233+2711G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15781358 | ||||||
chr4:15781595
|
T | C | 1 | a0001c0001t0016g0063 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.233+2948T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15781595 | ||||||
chr4:15782043
|
G | A | 1 | a0001c0001t0056g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.233+3396G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15782043 | ||||||
chr4:15782364
|
T | A | 1 | a0001c0001t0009g0245 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.233+3717T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15782364 | ||||||
chr4:15782595
|
G | A | 1 | a0001c0002t0003g0074 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.233+3948G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15782595 | ||||||
chr4:15782600
|
G | A | 5 | a0001c0001t0020g0157a0001c0001t0020g0179a0001c0001t0035g0158others(2): Show | 5 | HG02965.hp2 HG03139.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+3953G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15782600 | ||||||
chr4:15782639
|
C | T | 1 | a0001c0001t0013g0291 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.233+3992C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15782639 | ||||||
chr4:15782764
|
T | C | 2 | a0001c0001t0057g0302a0001c0001t0058g0301 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.233+4117T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15782764 | ||||||
chr4:15782975
|
T | C | 54 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(51): Show | 56 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.233+4328T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15782975 | ||||||
chr4:15783256
|
G | A | 1 | a0001c0002t0007g0098 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.233+4609G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15783256 | ||||||
chr4:15783278
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.233+4631G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15783278 | ||||||
chr4:15783393
|
G | C | 54 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(51): Show | 56 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.233+4746G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15783393 | ||||||
chr4:15783404
|
T | C | 1 | a0001c0002t0024g0075 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.233+4757T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15783404 | ||||||
chr4:15783528
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.233+4881T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15783528 | ||||||
chr4:15783578
|
C | T | 144 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(141): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.233+4931C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15783578 | ||||||
chr4:15783698
|
G | A | 22 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(19): Show | 23 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.233+5051G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15783698 | ||||||
chr4:15783715
|
T | C | 2 | a0001c0001t0026g0060a0001c0001t0026g0061 | 2 | HG01433.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.233+5068T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15783715 | ||||||
chr4:15784036
|
C | T | 20 | a0001c0001t0001g0310a0001c0001t0003g0012a0001c0001t0003g0303others(17): Show | 21 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.233+5389C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784036 | ||||||
chr4:15784063
|
C | T | 2 | a0001c0001t0009g0178a0001c0001t0010g0314 | 2 | HG02083.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.233+5416C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784063 | ||||||
chr4:15784288
|
G | A | 16 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(13): Show | 16 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.233+5641G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784288 | ||||||
chr4:15784379
|
C | A | 68 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0001g0176others(65): Show | 72 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.233+5732C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784379 | ||||||
chr4:15784452
|
C | T | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.233+5805C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784452 | ||||||
chr4:15784525
|
G | C | 211 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(208): Show | 220 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.233+5878G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784525 | ||||||
chr4:15784532
|
C | T | 1 | a0001c0001t0059g0113 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.233+5885C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784532 | ||||||
chr4:15784605
|
A | G | 1 | a0001c0001t0054g0244 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.233+5958A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784605 | ||||||
chr4:15784661
|
A | G | 1 | a0001c0001t0006g0151 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.233+6014A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784661 | ||||||
chr4:15784701
|
T | C | 143 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(140): Show | 148 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.233+6054T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784701 | ||||||
chr4:15784785
|
C | T | 37 | a0001c0001t0002g0008a0001c0001t0002g0181a0001c0001t0002g0188others(34): Show | 38 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.233+6138C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784785 | ||||||
chr4:15784884
|
C | T | 54 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(51): Show | 56 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.233+6237C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784884 | ||||||
chr4:15784885
|
G | A | 29 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(26): Show | 30 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.233+6238G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784885 | ||||||
chr4:15784900
|
A | T | 36 | a0001c0001t0002g0008a0001c0001t0002g0181a0001c0001t0002g0188others(33): Show | 37 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.233+6253A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784900 | ||||||
chr4:15784970
|
C | T | 54 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(51): Show | 56 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.233+6323C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784970 | ||||||
chr4:15784998
|
A | G | 143 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(140): Show | 148 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.233+6351A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15784998 | ||||||
chr4:15785055
|
T | TA | 194 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(191): Show | 203 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.233+6420dupA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15785055 | |||||
chr4:15785055
|
T | TAA | 6 | a0001c0001t0004g0064a0001c0001t0007g0182a0001c0001t0017g0053others(3): Show | 6 | HG02630.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+6419_233+6420d others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15785055 | |||||
chr4:15785093
|
A | G | 10 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(7): Show | 11 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+6446A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785093 | ||||||
chr4:15785148
|
T | C | 3 | a0001c0001t0020g0157a0001c0001t0020g0179a0001c0001t0036g0160 | 3 | HG03486.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.233+6501T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785148 | ||||||
chr4:15785157
|
A | T | 143 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(140): Show | 148 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.233+6510A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785157 | ||||||
chr4:15785191
|
T | C | 1 | a0001c0001t0004g0064 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.233+6544T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785191 | ||||||
chr4:15785208
|
T | C | 1 | a0001c0001t0002g0117 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.233+6561T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785208 | ||||||
chr4:15785257
|
G | C | 2 | a0001c0001t0026g0060a0001c0001t0026g0061 | 2 | HG01433.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.233+6610G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785257 | ||||||
chr4:15785403
|
C | T | 1 | a0001c0001t0034g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+6756C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785403 | ||||||
chr4:15785459
|
A | G | 143 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(140): Show | 148 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.233+6812A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785459 | ||||||
chr4:15785463
|
C | A | 10 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(7): Show | 11 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+6816C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785463 | ||||||
chr4:15785539
|
C | CTTTCTT | 109 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(106): Show | 113 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.233+6895_233+6896i others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15785539 | |||||
chr4:15785539
|
C | CTTTCTTT | 21 | a0001c0001t0002g0057a0001c0001t0002g0212a0001c0001t0004g0056others(18): Show | 21 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.233+6895_233+6896i others(9): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15785539 | |||||
chr4:15785543
|
T | C | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.233+6896T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785543 | ||||||
chr4:15785591
|
T | C | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+6944T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785591 | ||||||
chr4:15785651
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.233+7004G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785651 | ||||||
chr4:15785750
|
T | C | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+7103T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785750 | ||||||
chr4:15785819
|
T | C | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+7172T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785819 | ||||||
chr4:15785853
|
A | G | 1 | a0001c0001t0002g0144 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.233+7206A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785853 | ||||||
chr4:15785897
|
C | T | 1 | a0001c0001t0043g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.233+7250C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785897 | ||||||
chr4:15785905
|
C | T | 13 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(10): Show | 14 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+7258C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785905 | ||||||
chr4:15785991
|
G | A | 2 | a0001c0001t0019g0156a0001c0001t0042g0102 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.233+7344G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785991 | ||||||
chr4:15785993
|
G | A | 1 | a0001c0001t0002g0323 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.233+7346G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15785993 | ||||||
chr4:15785993
|
GTCTGGAG others(16): Show |
G | 4 | a0001c0001t0001g0243a0001c0001t0003g0216a0001c0001t0003g0217others(1): Show | 4 | HG03927.hp2 NA19079.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+7368_233+7390d others(25): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15785993 | |||||
chr4:15786007
|
G | C | 18 | a0001c0001t0001g0310a0001c0001t0003g0012a0001c0001t0003g0303others(15): Show | 19 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.233+7360G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786007 | ||||||
chr4:15786061
|
G | C | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+7414G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786061 | ||||||
chr4:15786088
|
T | C | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+7441T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786088 | ||||||
chr4:15786175
|
T | A | 129 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(126): Show | 133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+7528T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786175 | ||||||
chr4:15786203
|
G | A | 1 | a0001c0001t0043g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.233+7556G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786203 | ||||||
chr4:15786284
|
C | A | 2 | a0001c0001t0014g0214a0001c0001t0072g0183 | 2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.233+7637C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786284 | ||||||
chr4:15786284
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.233+7637C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786284 | ||||||
chr4:15786332
|
C | T | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.233+7685C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786332 | ||||||
chr4:15786367
|
C | T | 1 | a0001c0001t0002g0003 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.233+7720C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786367 | ||||||
chr4:15786557
|
C | G | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+7910C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786557 | ||||||
chr4:15786633
|
C | T | 1 | a0001c0001t0033g0194 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.233+7986C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786633 | ||||||
chr4:15786700
|
C | G | 2 | a0001c0001t0057g0302a0001c0001t0058g0301 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.233+8053C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786700 | ||||||
chr4:15786700
|
C | T | 17 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(14): Show | 17 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.233+8053C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786700 | ||||||
chr4:15786733
|
G | A | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.233+8086G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786733 | ||||||
chr4:15786756
|
G | T | 1 | a0001c0002t0005g0095 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.233+8109G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786756 | ||||||
chr4:15786780
|
G | A | 1 | a0001c0001t0034g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+8133G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786780 | ||||||
chr4:15786781
|
C | T | 38 | a0001c0001t0002g0008a0001c0001t0002g0181a0001c0001t0002g0188others(35): Show | 39 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.233+8134C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786781 | ||||||
chr4:15786782
|
G | A | 2 | a0001c0001t0008g0152a0001c0001t0008g0166 | 2 | NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.233+8135G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786782 | ||||||
chr4:15786848
|
C | T | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+8201C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786848 | ||||||
chr4:15786860
|
C | T | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+8213C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786860 | ||||||
chr4:15786889
|
C | T | 1 | a0001c0001t0013g0290 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.233+8242C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786889 | ||||||
chr4:15786916
|
G | A | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.233+8269G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786916 | ||||||
chr4:15786968
|
G | C | 1 | a0001c0001t0034g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+8321G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786968 | ||||||
chr4:15786985
|
G | A | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+8338G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786985 | ||||||
chr4:15786999
|
G | A | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.233+8352G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15786999 | ||||||
chr4:15787018
|
GGCCGCTC others(1): Show |
G | 10 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(7): Show | 11 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+8373_233+8380d others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15787018 | |||||
chr4:15787028
|
A | T | 10 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(7): Show | 11 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+8381A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787028 | ||||||
chr4:15787030
|
T | A | 10 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(7): Show | 11 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+8383T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787030 | ||||||
chr4:15787096
|
C | A | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+8449C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787096 | ||||||
chr4:15787102
|
T | G | 231 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(228): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.233+8455T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787102 | ||||||
chr4:15787202
|
G | A | 56 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0002g0005others(53): Show | 60 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.233+8555G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787202 | ||||||
chr4:15787251
|
G | T | 1 | a0001c0001t0034g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+8604G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787251 | ||||||
chr4:15787262
|
T | C | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+8615T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787262 | ||||||
chr4:15787364
|
G | A | 10 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(7): Show | 11 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+8717G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787364 | ||||||
chr4:15787436
|
C | G | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+8789C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787436 | ||||||
chr4:15787508
|
C | T | 2 | a0001c0001t0004g0027a0001c0001t0033g0028 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.233+8861C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787508 | ||||||
chr4:15787665
|
T | C | 7 | a0001c0001t0003g0304a0001c0001t0003g0305a0001c0001t0003g0316others(4): Show | 7 | HG00140.hp1 HG00642.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+9018T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787665 | ||||||
chr4:15787694
|
C | T | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+9047C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787694 | ||||||
chr4:15787767
|
G | T | 1 | a0001c0001t0046g0044 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.233+9120G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787767 | ||||||
chr4:15787792
|
A | G | 210 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(207): Show | 219 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.233+9145A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787792 | ||||||
chr4:15787837
|
G | A | 11 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(8): Show | 11 | HG01243.hp2 HG01891.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.233+9190G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787837 | ||||||
chr4:15787857
|
G | A | 326 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0015others(323): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.233+9210G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787857 | ||||||
chr4:15787992
|
C | T | 2 | a0001c0001t0003g0313a0001c0001t0010g0312 | 2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.233+9345C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15787992 | ||||||
chr4:15788132
|
C | T | 1 | a0001c0001t0014g0175 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.233+9485C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15788132 | ||||||
chr4:15788485
|
CCAAA | C | 26 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 27 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.233+9841_233+9844d others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15788485 | |||||
chr4:15788530
|
A | C | 1 | a0001c0001t0002g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.233+9883A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15788530 | ||||||
chr4:15788530
|
A | G | 1 | a0001c0001t0034g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+9883A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15788530 | ||||||
chr4:15788715
|
A | T | 1 | a0001c0002t0005g0073 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.233+10068A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15788715 | ||||||
chr4:15788746
|
G | A | 1 | a0001c0002t0009g0076 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.233+10099G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15788746 | ||||||
chr4:15788823
|
A | G | 1 | a0001c0001t0034g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+10176A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15788823 | ||||||
chr4:15788970
|
A | G | 5 | a0001c0001t0020g0157a0001c0001t0020g0179a0001c0001t0035g0158others(2): Show | 5 | HG02965.hp2 HG03139.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+10323A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15788970 | ||||||
chr4:15788991
|
C | A | 134 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(131): Show | 138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.233+10344C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15788991 | ||||||
chr4:15789022
|
G | A | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+10375G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15789022 | ||||||
chr4:15789064
|
G | A | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+10417G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15789064 | ||||||
chr4:15789151
|
A | C | 1 | a0001c0001t0009g0245 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.233+10504A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15789151 | ||||||
chr4:15789151
|
A | G | 142 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(139): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.233+10504A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15789151 | ||||||
chr4:15789252
|
A | G | 13 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(10): Show | 14 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+10605A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15789252 | ||||||
chr4:15789376
|
A | C | 14 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(11): Show | 14 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+10729A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15789376 | ||||||
chr4:15789798
|
CCT | C | 28 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(25): Show | 29 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.233+11152_233+1115 others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15789798 | ||||||
chr4:15789841
|
G | T | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.233+11194G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15789841 | ||||||
chr4:15790103
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.233+11456C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790103 | ||||||
chr4:15790104
|
G | GCTCTCC | 6 | a0001c0001t0001g0243a0001c0001t0001g0310a0001c0001t0002g0118others(3): Show | 6 | HG00621.hp1 HG01081.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+11507_233+1151 others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790104 | |||||
chr4:15790104
|
GCTCTCC | G | 9 | a0001c0001t0001g0233a0001c0001t0001g0235a0001c0001t0001g0292others(6): Show | 9 | HG01261.hp2 HG01978.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.233+11507_233+1151 others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790104 | |||||
chr4:15790104
|
GCTCTCCC others(5): Show |
G | 1 | a0001c0001t0003g0304 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.233+11501_233+1151 others(16): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790104 | |||||
chr4:15790104
|
GCTCTCCC others(23): Show |
G | 1 | a0001c0001t0014g0214 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.233+11483_233+1151 others(34): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790104 | |||||
chr4:15790118
|
TCTCCCTC others(47): Show |
T | 4 | a0001c0001t0017g0053a0001c0001t0060g0047a0001c0001t0061g0046others(1): Show | 4 | HG02970.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+11477_233+1153 others(58): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790118 | |||||
chr4:15790124
|
TCTCCCTC others(41): Show |
T | 122 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(119): Show | 126 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.233+11483_233+1153 others(52): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790124 | |||||
chr4:15790125
|
C | CTCCCTT | 61 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0001g0176others(58): Show | 63 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.233+11483_233+1148 others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790125 | |||||
chr4:15790125
|
C | T | 2 | a0001c0001t0002g0143a0001c0001t0006g0151 | 2 | NA19054.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.233+11478C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790125 | ||||||
chr4:15790127
|
CCCTCTCC others(40): Show |
C | 2 | a0001c0001t0002g0013a0001c0001t0005g0014 | 2 | HG03927.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.233+11483_233+1152 others(51): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790127 | |||||
chr4:15790131
|
C | T | 4 | a0001c0001t0006g0116a0001c0001t0006g0119a0001c0001t0008g0002others(1): Show | 6 | NA18942.hp1 NA18945.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.233+11484C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790131 | ||||||
chr4:15790140
|
CCTCTCCC others(17): Show |
C | 13 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(10): Show | 14 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+11495_233+1151 others(28): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790140 | |||||
chr4:15790142
|
TCTCCCTC others(17): Show |
T | 1 | a0001c0001t0034g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+11501_233+1152 others(28): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790142 | |||||
chr4:15790154
|
TCTCCCCC others(11): Show |
T | 1 | a0001c0001t0014g0214 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.233+11517_233+1153 others(22): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790154 | |||||
chr4:15790178
|
C | T | 1 | a0001c0001t0034g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+11531C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790178 | ||||||
chr4:15790194
|
T | C | 13 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(10): Show | 14 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+11547T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790194 | ||||||
chr4:15790214
|
G | A | 1 | a0001c0001t0073g0195 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.233+11567G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790214 | ||||||
chr4:15790244
|
A | G | 25 | a0001c0001t0002g0008a0001c0001t0002g0181a0001c0001t0002g0188others(22): Show | 26 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.233+11597A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790244 | ||||||
chr4:15790293
|
C | T | 1 | a0001c0001t0033g0194 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.233+11646C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790293 | ||||||
chr4:15790308
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.233+11661G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790308 | ||||||
chr4:15790312
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.233+11665G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790312 | ||||||
chr4:15790325
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+11678G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790325 | ||||||
chr4:15790345
|
G | GT | 29 | a0001c0001t0001g0235a0001c0001t0001g0273a0001c0001t0001g0287others(26): Show | 30 | HG00438.hp1 HG01192.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.233+11710dupT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790345 | |||||
chr4:15790359
|
G | A | 1 | a0001c0001t0033g0194 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.233+11712G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790359 | ||||||
chr4:15790421
|
G | C | 37 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(34): Show | 39 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.233+11774G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790421 | ||||||
chr4:15790424
|
G | A | 16 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(13): Show | 16 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.233+11777G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790424 | ||||||
chr4:15790430
|
G | A | 1 | a0001c0001t0003g0198 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.233+11783G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790430 | ||||||
chr4:15790466
|
G | A | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.233+11819G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790466 | ||||||
chr4:15790493
|
G | A | 1 | a0001c0001t0034g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+11846G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790493 | ||||||
chr4:15790508
|
C | T | 1 | a0001c0001t0056g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.233+11861C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790508 | ||||||
chr4:15790553
|
T | C | 1 | a0001c0001t0034g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+11906T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790553 | ||||||
chr4:15790560
|
C | G | 37 | a0001c0001t0002g0008a0001c0001t0002g0181a0001c0001t0002g0188others(34): Show | 38 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.233+11913C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790560 | ||||||
chr4:15790596
|
A | AC | 5 | a0001c0001t0001g0300a0001c0001t0002g0122a0001c0001t0002g0168others(2): Show | 5 | HG01243.hp1 HG01952.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+11953dupC | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15790596 | |||||
chr4:15790600
|
C | T | 12 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(9): Show | 13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+11953C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790600 | ||||||
chr4:15790640
|
G | C | 1 | a0001c0001t0001g0224 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.233+11993G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790640 | ||||||
chr4:15790690
|
G | C | 2 | a0001c0001t0002g0005a0001c0001t0002g0177 | 3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.233+12043G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790690 | ||||||
chr4:15790734
|
C | G | 1 | a0001c0001t0034g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+12087C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790734 | ||||||
chr4:15790745
|
C | T | 2 | a0001c0001t0019g0156a0001c0001t0042g0102 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.233+12098C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790745 | ||||||
chr4:15790748
|
C | T | 1 | a0001c0001t0034g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+12101C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790748 | ||||||
chr4:15790814
|
A | G | 143 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(140): Show | 148 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.233+12167A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790814 | ||||||
chr4:15790844
|
G | A | 1 | a0001c0002t0004g0071 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.233+12197G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790844 | ||||||
chr4:15790890
|
T | C | 143 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(140): Show | 148 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.233+12243T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790890 | ||||||
chr4:15790909
|
C | T | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.233+12262C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790909 | ||||||
chr4:15790977
|
C | T | 1 | a0001c0001t0056g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.233+12330C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790977 | ||||||
chr4:15790981
|
G | A | 65 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0001g0176others(62): Show | 69 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.233+12334G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15790981 | ||||||
chr4:15791013
|
C | T | 37 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(34): Show | 39 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.233+12366C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791013 | ||||||
chr4:15791014
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.233+12367G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791014 | ||||||
chr4:15791018
|
G | A | 2 | a0001c0001t0004g0307a0001c0001t0010g0314 | 2 | HG02071.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.233+12371G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791018 | ||||||
chr4:15791038
|
G | A | 1 | a0001c0001t0016g0067 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.233+12391G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791038 | ||||||
chr4:15791044
|
T | TG | 40 | a0001c0001t0001g0015a0001c0001t0001g0176a0001c0001t0001g0250others(37): Show | 41 | HG00408.hp1 HG00621.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.233+12406dupG | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791044 | |||||
chr4:15791051
|
G | A | 1 | a0001c0001t0003g0303 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.233+12404G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791051 | ||||||
chr4:15791051
|
G | T | 2 | a0001c0001t0021g0055a0001c0001t0025g0048 | 2 | NA18999.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.233+12404G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791051 | ||||||
chr4:15791075
|
T | C | 94 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(91): Show | 97 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.233+12428T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791075 | ||||||
chr4:15791108
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.233+12461C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791108 | ||||||
chr4:15791159
|
G | A | 3 | a0001c0002t0003g0001a0001c0002t0003g0079a0001c0002t0010g0078 | 5 | HG02083.hp1 HG02135.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+12512G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791159 | ||||||
chr4:15791177
|
GGGGTCAG others(620): Show |
G | 1 | a0001c0001t0002g0199 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.233+12560_233+1318 others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791177 | |||||
chr4:15791194
|
C | T | 16 | a0001c0001t0002g0057a0001c0001t0004g0064a0001c0001t0004g0066others(13): Show | 16 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.233+12547C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791194 | ||||||
chr4:15791207
|
A | C | 1 | a0001c0001t0004g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.233+12560A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791207 | ||||||
chr4:15791207
|
A | T | 35 | a0001c0001t0002g0008a0001c0001t0002g0181a0001c0001t0002g0188others(32): Show | 36 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.233+12560A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791207 | ||||||
chr4:15791207
|
AGTCCGGG others(71): Show |
A | 88 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(85): Show | 91 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.233+12571_233+1264 others(82): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791207 | |||||
chr4:15791208
|
G | A | 35 | a0001c0001t0002g0008a0001c0001t0002g0181a0001c0001t0002g0188others(32): Show | 36 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.233+12561G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791208 | ||||||
chr4:15791211
|
C | CGGGA | 3 | a0001c0001t0060g0047a0001c0001t0061g0046a0001c0001t0063g0054 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12567_233+1257 others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791211 | |||||
chr4:15791212
|
G | A | 35 | a0001c0001t0002g0008a0001c0001t0002g0181a0001c0001t0002g0188others(32): Show | 36 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.233+12565G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791212 | ||||||
chr4:15791217
|
GT | G | 4 | a0001c0001t0002g0016a0001c0001t0004g0056a0001c0001t0017g0053others(1): Show | 4 | HG00408.hp1 HG03041.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+12571delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791217 | ||||||
chr4:15791220
|
A | G | 3 | a0001c0001t0060g0047a0001c0001t0061g0046a0001c0001t0063g0054 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12573A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791220 | ||||||
chr4:15791223
|
G | T | 4 | a0001c0001t0002g0016a0001c0001t0004g0056a0001c0001t0017g0053others(1): Show | 4 | HG00408.hp1 HG03041.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+12576G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791223 | ||||||
chr4:15791224
|
GCGCCTCT others(17): Show |
G | 3 | a0001c0001t0004g0056a0001c0001t0017g0053a0002c0003t0012g0103 | 3 | HG03041.hp1 HG03471.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.233+12578_233+1260 others(28): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791224 | ||||||
chr4:15791224
|
GCGCCTCT others(69): Show |
G | 1 | a0001c0001t0002g0016 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.233+12578_233+1265 others(80): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791224 | ||||||
chr4:15791226
|
G | C | 3 | a0001c0001t0060g0047a0001c0001t0061g0046a0001c0001t0063g0054 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12579G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791226 | ||||||
chr4:15791228
|
C | G | 3 | a0001c0001t0060g0047a0001c0001t0061g0046a0001c0001t0063g0054 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12581C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791228 | ||||||
chr4:15791229
|
T | C | 3 | a0001c0001t0060g0047a0001c0001t0061g0046a0001c0001t0063g0054 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12582T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791229 | ||||||
chr4:15791232
|
G | C | 1 | a0001c0001t0004g0127 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.233+12585G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791232 | ||||||
chr4:15791233
|
C | G | 3 | a0001c0001t0060g0047a0001c0001t0061g0046a0001c0001t0063g0054 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12586C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791233 | ||||||
chr4:15791236
|
G | A | 3 | a0001c0001t0060g0047a0001c0001t0061g0046a0001c0001t0063g0054 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12589G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791236 | ||||||
chr4:15791238
|
C | G | 3 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0212 | 3 | NA18943.hp2 NA18966.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.233+12591C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791238 | ||||||
chr4:15791243
|
C | CA | 3 | a0001c0001t0060g0047a0001c0001t0061g0046a0001c0001t0063g0054 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12596_233+1259 others(5): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791243 | ||||||
chr4:15791244
|
G | C | 236 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0140others(233): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.233+12597G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791244 | ||||||
chr4:15791246
|
A | C | 3 | a0001c0001t0060g0047a0001c0001t0061g0046a0001c0001t0063g0054 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12599A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791246 | ||||||
chr4:15791247
|
C | CGGG | 3 | a0001c0001t0060g0047a0001c0001t0061g0046a0001c0001t0063g0054 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12600_233+1260 others(7): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791247 | ||||||
chr4:15791248
|
T | A | 3 | a0001c0001t0060g0047a0001c0001t0061g0046a0001c0001t0063g0054 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12601T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791248 | ||||||
chr4:15791252
|
A | G | 3 | a0001c0001t0004g0056a0001c0001t0017g0053a0002c0003t0012g0103 | 3 | HG03041.hp1 HG03471.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.233+12605A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791252 | ||||||
chr4:15791253
|
A | G | 6 | a0001c0001t0004g0056a0001c0001t0017g0053a0001c0001t0060g0047others(3): Show | 6 | HG02970.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+12606A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791253 | ||||||
chr4:15791256
|
G | C | 3 | a0001c0001t0004g0056a0001c0001t0017g0053a0002c0003t0012g0103 | 3 | HG03041.hp1 HG03471.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.233+12609G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791256 | ||||||
chr4:15791257
|
A | G | 3 | a0001c0001t0060g0047a0001c0001t0061g0046a0001c0001t0063g0054 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12610A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791257 | ||||||
chr4:15791258
|
GGAGC | G | 3 | a0001c0001t0004g0056a0001c0001t0017g0053a0002c0003t0012g0103 | 3 | HG03041.hp1 HG03471.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.233+12612_233+1261 others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791258 | ||||||
chr4:15791262
|
CCCCTCTG others(493): Show |
C | 35 | a0001c0001t0002g0008a0001c0001t0002g0181a0001c0001t0002g0188others(32): Show | 36 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.233+12634_233+1313 others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791262 | |||||
chr4:15791265
|
CT | C | 3 | a0001c0001t0060g0047a0001c0001t0061g0046a0001c0001t0063g0054 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12619delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791265 | ||||||
chr4:15791266
|
T | C | 3 | a0001c0001t0004g0056a0001c0001t0017g0053a0002c0003t0012g0103 | 3 | HG03041.hp1 HG03471.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.233+12619T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791266 | ||||||
chr4:15791268
|
T | C | 6 | a0001c0001t0004g0056a0001c0001t0017g0053a0001c0001t0060g0047others(3): Show | 6 | HG02970.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+12621T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791268 | ||||||
chr4:15791272
|
C | T | 2 | a0001c0001t0057g0302a0001c0001t0058g0301 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.233+12625C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791272 | ||||||
chr4:15791273
|
G | T | 3 | a0001c0001t0002g0112a0001c0001t0002g0149a0001c0001t0019g0150 | 3 | HG02451.hp1 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.233+12626G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791273 | ||||||
chr4:15791281
|
A | G | 6 | a0001c0001t0004g0056a0001c0001t0017g0053a0001c0001t0060g0047others(3): Show | 6 | HG02970.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+12634A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791281 | ||||||
chr4:15791285
|
C | A | 2 | a0001c0001t0017g0053a0002c0003t0012g0103 | 2 | HG03471.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.233+12638C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791285 | ||||||
chr4:15791297
|
G | A | 93 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(90): Show | 96 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.233+12650G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791297 | ||||||
chr4:15791299
|
G | T | 1 | a0001c0001t0004g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.233+12652G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791299 | ||||||
chr4:15791300
|
A | G | 2 | a0001c0001t0001g0223a0001c0001t0004g0056 | 2 | HG01975.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.233+12653A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791300 | ||||||
chr4:15791300
|
A | T | 93 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(90): Show | 96 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.233+12653A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791300 | ||||||
chr4:15791304
|
G | T | 1 | a0001c0001t0054g0244 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.233+12657G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791304 | ||||||
chr4:15791307
|
G | A | 1 | a0002c0003t0012g0103 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.233+12660G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791307 | ||||||
chr4:15791317
|
T | C | 95 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(92): Show | 98 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.233+12670T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791317 | ||||||
chr4:15791321
|
C | T | 14 | a0001c0001t0004g0027a0001c0001t0020g0157a0001c0001t0020g0179others(11): Show | 14 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+12674C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791321 | ||||||
chr4:15791332
|
C | T | 1 | a0001c0005t0007g0022 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.233+12685C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791332 | ||||||
chr4:15791334
|
C | A | 89 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(86): Show | 92 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.233+12687C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791334 | ||||||
chr4:15791334
|
C | T | 1 | a0001c0001t0004g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.233+12687C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791334 | ||||||
chr4:15791335
|
G | A | 1 | a0001c0001t0003g0275 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.233+12688G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791335 | ||||||
chr4:15791344
|
G | A | 5 | a0001c0001t0020g0157a0001c0001t0020g0179a0001c0001t0035g0158others(2): Show | 5 | HG02965.hp2 HG03139.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+12697G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791344 | ||||||
chr4:15791351
|
GT | G | 93 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0002g0003others(90): Show | 96 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.233+12705delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791351 | ||||||
chr4:15791352
|
T | G | 2 | a0001c0001t0001g0023a0002c0003t0012g0103 | 2 | HG03831.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.233+12705T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791352 | ||||||
chr4:15791357
|
G | A | 54 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(51): Show | 56 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.233+12710G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791357 | ||||||
chr4:15791366
|
CCGCCCGG others(69): Show |
C | 1 | a0001c0001t0002g0016 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.233+12721_233+1279 others(80): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791366 | |||||
chr4:15791367
|
CGCCCGGC others(70): Show |
C | 21 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(18): Show | 22 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.233+12729_233+1280 others(81): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791367 | |||||
chr4:15791371
|
C | T | 2 | a0001c0001t0004g0056a0001c0001t0063g0054 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.233+12724C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791371 | ||||||
chr4:15791376
|
G | A | 85 | a0001c0001t0002g0057a0001c0001t0004g0027a0001c0001t0004g0050others(82): Show | 88 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.233+12729G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791376 | ||||||
chr4:15791382
|
C | T | 1 | a0001c0001t0004g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.233+12735C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791382 | ||||||
chr4:15791384
|
C | A | 9 | a0001c0001t0004g0027a0001c0001t0030g0031a0001c0001t0033g0028others(6): Show | 9 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.233+12737C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791384 | ||||||
chr4:15791389
|
G | A | 1 | a0001c0001t0033g0194 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.233+12742G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791389 | ||||||
chr4:15791394
|
GT | G | 72 | a0001c0001t0002g0057a0001c0001t0004g0027a0001c0001t0004g0064others(69): Show | 74 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.233+12748delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791394 | ||||||
chr4:15791400
|
G | T | 72 | a0001c0001t0002g0057a0001c0001t0004g0027a0001c0001t0004g0064others(69): Show | 74 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.233+12753G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791400 | ||||||
chr4:15791401
|
GCGCCTCT others(17): Show |
G | 72 | a0001c0001t0002g0057a0001c0001t0004g0027a0001c0001t0004g0064others(69): Show | 74 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.233+12755_233+1277 others(28): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791401 | ||||||
chr4:15791414
|
T | G | 202 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0140others(199): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.233+12767T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791414 | ||||||
chr4:15791421
|
G | C | 202 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0140others(199): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.233+12774G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791421 | ||||||
chr4:15791425
|
T | C | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.233+12778T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791425 | ||||||
chr4:15791429
|
A | G | 72 | a0001c0001t0002g0057a0001c0001t0004g0027a0001c0001t0004g0064others(69): Show | 74 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.233+12782A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791429 | ||||||
chr4:15791430
|
A | G | 72 | a0001c0001t0002g0057a0001c0001t0004g0027a0001c0001t0004g0064others(69): Show | 74 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.233+12783A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791430 | ||||||
chr4:15791433
|
G | C | 72 | a0001c0001t0002g0057a0001c0001t0004g0027a0001c0001t0004g0064others(69): Show | 74 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.233+12786G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791433 | ||||||
chr4:15791435
|
GGAC | G | 72 | a0001c0001t0002g0057a0001c0001t0004g0027a0001c0001t0004g0064others(69): Show | 74 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.233+12789_233+1279 others(7): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791435 | ||||||
chr4:15791438
|
C | T | 1 | a0001c0001t0004g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.233+12791C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791438 | ||||||
chr4:15791439
|
C | T | 1 | a0001c0001t0006g0116 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.233+12792C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791439 | ||||||
chr4:15791442
|
T | C | 72 | a0001c0001t0002g0057a0001c0001t0004g0027a0001c0001t0004g0064others(69): Show | 74 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.233+12795T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791442 | ||||||
chr4:15791444
|
T | C | 73 | a0001c0001t0002g0016a0001c0001t0002g0057a0001c0001t0004g0027others(70): Show | 75 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.233+12797T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791444 | ||||||
chr4:15791461
|
C | A | 1 | a0001c0001t0017g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.233+12814C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791461 | ||||||
chr4:15791462
|
G | A | 22 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(19): Show | 23 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.233+12815G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791462 | ||||||
chr4:15791465
|
C | A | 3 | a0001c0001t0031g0145a0001c0001t0031g0146a0001c0001t0032g0173 | 3 | HG00438.hp1 NA18981.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.233+12818C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791465 | ||||||
chr4:15791476
|
T | C | 1 | a0001c0001t0005g0319 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.233+12829T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791476 | ||||||
chr4:15791476
|
T | TG | 20 | a0001c0001t0001g0232a0001c0001t0001g0236a0001c0001t0001g0246others(17): Show | 20 | HG01099.hp1 HG01192.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.233+12838dupG | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791476 | |||||
chr4:15791476
|
TG | T | 82 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(79): Show | 85 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.233+12838delG | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791476 | |||||
chr4:15791483
|
GGGTCAGC others(191): Show |
G | 1 | a0001c0001t0004g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.233+12837_233+1303 others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791483 | ||||||
chr4:15791499
|
C | T | 2 | a0001c0001t0019g0156a0001c0001t0042g0102 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.233+12852C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791499 | ||||||
chr4:15791500
|
G | A | 1 | a0001c0001t0009g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.233+12853G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791500 | ||||||
chr4:15791512
|
A | C | 6 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0042g0102others(3): Show | 6 | HG02572.hp2 HG02647.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+12865A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791512 | ||||||
chr4:15791512
|
A | T | 90 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(87): Show | 93 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.233+12865A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791512 | ||||||
chr4:15791534
|
A | G | 4 | a0001c0001t0017g0053a0001c0001t0060g0047a0001c0001t0061g0046others(1): Show | 4 | HG02970.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+12887A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791534 | ||||||
chr4:15791548
|
C | T | 91 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(88): Show | 94 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.233+12901C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791548 | ||||||
chr4:15791559
|
C | T | 90 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(87): Show | 93 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.233+12912C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791559 | ||||||
chr4:15791561
|
C | T | 3 | a0001c0001t0060g0047a0001c0001t0061g0046a0001c0001t0063g0054 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12914C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791561 | ||||||
chr4:15791565
|
CGGGA | C | 92 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(89): Show | 95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12925_233+1292 others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791565 | |||||
chr4:15791578
|
G | A | 92 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(89): Show | 95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12931G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791578 | ||||||
chr4:15791582
|
GGTCA | G | 91 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(88): Show | 94 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.233+12937_233+1294 others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791582 | |||||
chr4:15791583
|
G | A | 13 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(10): Show | 14 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+12936G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791583 | ||||||
chr4:15791587
|
G | C | 91 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(88): Show | 94 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.233+12940G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791587 | ||||||
chr4:15791588
|
C | G | 91 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(88): Show | 94 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.233+12941C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791588 | ||||||
chr4:15791589
|
C | G | 1 | a0001c0001t0042g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.233+12942C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791589 | ||||||
chr4:15791591
|
C | T | 91 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(88): Show | 94 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.233+12944C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791591 | ||||||
chr4:15791592
|
C | T | 1 | a0001c0001t0042g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.233+12945C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791592 | ||||||
chr4:15791593
|
C | T | 91 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(88): Show | 94 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.233+12946C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791593 | ||||||
chr4:15791594
|
G | T | 1 | a0001c0001t0042g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.233+12947G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791594 | ||||||
chr4:15791595
|
C | G | 1 | a0001c0001t0042g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.233+12948C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791595 | ||||||
chr4:15791597
|
C | T | 3 | a0001c0001t0060g0047a0001c0001t0061g0046a0001c0001t0063g0054 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12950C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791597 | ||||||
chr4:15791598
|
G | T | 1 | a0001c0001t0042g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.233+12951G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791598 | ||||||
chr4:15791598
|
GGCCA | G | 91 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(88): Show | 94 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.233+12955_233+1295 others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791598 | |||||
chr4:15791608
|
C | T | 3 | a0001c0001t0060g0047a0001c0001t0061g0046a0001c0001t0063g0054 | 3 | HG02970.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+12961C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791608 | ||||||
chr4:15791610
|
C | T | 1 | a0001c0001t0017g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.233+12963C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791610 | ||||||
chr4:15791611
|
G | GTCCGGGA others(70): Show |
1 | a0001c0001t0046g0044 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.233+12973_233+1297 others(81): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791611 | |||||
chr4:15791611
|
G | T | 92 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(89): Show | 95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12964G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791611 | ||||||
chr4:15791612
|
T | A | 92 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(89): Show | 95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12965T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791612 | ||||||
chr4:15791613
|
CCGGG | C | 92 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(89): Show | 95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12967_233+1297 others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791613 | ||||||
chr4:15791618
|
A | T | 92 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(89): Show | 95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12971A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791618 | ||||||
chr4:15791620
|
G | GT | 12 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(9): Show | 13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+12973_233+1297 others(5): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791620 | ||||||
chr4:15791623
|
G | A | 92 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(89): Show | 95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12976G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791623 | ||||||
chr4:15791625
|
T | G | 12 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(9): Show | 13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+12978T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791625 | ||||||
chr4:15791626
|
G | GCGCCTCT others(17): Show |
12 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(9): Show | 13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+12979_233+1298 others(28): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791626 | ||||||
chr4:15791627
|
G | A | 92 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(89): Show | 95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12980G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791627 | ||||||
chr4:15791629
|
GGGGTC | G | 92 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(89): Show | 95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12983_233+1298 others(9): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791629 | ||||||
chr4:15791630
|
G | A | 12 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(9): Show | 13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+12983G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791630 | ||||||
chr4:15791631
|
G | A | 12 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(9): Show | 13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+12984G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791631 | ||||||
chr4:15791632
|
G | A | 1 | a0001c0001t0017g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.233+12985G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791632 | ||||||
chr4:15791634
|
C | G | 12 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(9): Show | 13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+12987C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791634 | ||||||
chr4:15791636
|
G | GGAT | 12 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(9): Show | 13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+12989_233+1299 others(7): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791636 | ||||||
chr4:15791636
|
G | T | 92 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(89): Show | 95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+12989G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791636 | ||||||
chr4:15791640
|
C | CCCGCCTG others(70): Show |
1 | a0001c0001t0017g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.233+12994_233+1299 others(81): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791640 | |||||
chr4:15791640
|
C | T | 104 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(101): Show | 108 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.233+12993C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791640 | ||||||
chr4:15791642
|
T | C | 2 | a0001c0001t0001g0250a0001c0001t0003g0277 | 2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.233+12995T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791642 | ||||||
chr4:15791660
|
G | A | 12 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(9): Show | 13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+13013G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791660 | ||||||
chr4:15791681
|
A | G | 106 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(103): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.233+13034A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791681 | ||||||
chr4:15791692
|
G | A | 2 | a0001c0001t0002g0169a0001c0001t0018g0006 | 3 | HG00733.hp2 HG01069.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.233+13045G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791692 | ||||||
chr4:15791695
|
T | C | 107 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(104): Show | 111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.233+13048T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791695 | ||||||
chr4:15791703
|
C | A | 1 | a0001c0001t0063g0054 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.233+13056C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791703 | ||||||
chr4:15791708
|
C | T | 107 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(104): Show | 111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.233+13061C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791708 | ||||||
chr4:15791709
|
G | A | 107 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(104): Show | 111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.233+13062G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791709 | ||||||
chr4:15791713
|
G | A | 107 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(104): Show | 111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.233+13066G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791713 | ||||||
chr4:15791713
|
GGGAGGTG others(119): Show |
G | 1 | a0001c0001t0001g0223 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.233+13115_233+1324 others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791713 | |||||
chr4:15791727
|
G | A | 1 | a0001c0001t0034g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+13080G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791727 | ||||||
chr4:15791761
|
A | AG | 107 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(104): Show | 111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.233+13114_233+1311 others(5): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791761 | ||||||
chr4:15791762
|
T | C | 107 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(104): Show | 111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.233+13115T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791762 | ||||||
chr4:15791772
|
C | T | 142 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(139): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.233+13125C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791772 | ||||||
chr4:15791780
|
C | T | 12 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(9): Show | 13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+13133C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791780 | ||||||
chr4:15791785
|
C | T | 12 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(9): Show | 13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+13138C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791785 | ||||||
chr4:15791786
|
G | A | 129 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(126): Show | 133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.233+13139G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791786 | ||||||
chr4:15791789
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.233+13142C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791789 | ||||||
chr4:15791797
|
A | T | 142 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(139): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.233+13150A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791797 | ||||||
chr4:15791804
|
A | G | 142 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(139): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.233+13157A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791804 | ||||||
chr4:15791809
|
C | T | 142 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(139): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.233+13162C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791809 | ||||||
chr4:15791811
|
G | GC | 68 | a0001c0001t0001g0024a0001c0001t0001g0140a0001c0001t0001g0153others(65): Show | 72 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.233+13170dupC | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15791811 | |||||
chr4:15791834
|
T | C | 142 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(139): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.233+13187T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791834 | ||||||
chr4:15791839
|
A | G | 142 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(139): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.233+13192A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791839 | ||||||
chr4:15791855
|
C | T | 142 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(139): Show | 147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.233+13208C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791855 | ||||||
chr4:15791905
|
G | C | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13258G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791905 | ||||||
chr4:15791906
|
G | C | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13259G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791906 | ||||||
chr4:15791911
|
C | G | 12 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(9): Show | 13 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+13264C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791911 | ||||||
chr4:15791925
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13278G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791925 | ||||||
chr4:15791930
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13283G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791930 | ||||||
chr4:15791932
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13285G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791932 | ||||||
chr4:15791941
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13294G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791941 | ||||||
chr4:15791942
|
G | A | 2 | a0001c0001t0002g0005a0001c0001t0002g0177 | 3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.233+13295G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791942 | ||||||
chr4:15791943
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13296G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791943 | ||||||
chr4:15791945
|
T | C | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13298T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791945 | ||||||
chr4:15791985
|
C | G | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13338C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791985 | ||||||
chr4:15791991
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13344G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15791991 | ||||||
chr4:15792003
|
A | G | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13356A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792003 | ||||||
chr4:15792026
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13379G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792026 | ||||||
chr4:15792027
|
G | T | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13380G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792027 | ||||||
chr4:15792036
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13389G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792036 | ||||||
chr4:15792039
|
T | A | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13392T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792039 | ||||||
chr4:15792075
|
T | C | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+13428T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792075 | ||||||
chr4:15792131
|
C | T | 131 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(128): Show | 135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.233+13484C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792131 | ||||||
chr4:15792185
|
G | A | 6 | a0001c0001t0006g0116a0001c0001t0006g0119a0001c0001t0008g0002others(3): Show | 8 | NA18942.hp1 NA18945.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+13538G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792185 | ||||||
chr4:15792239
|
G | A | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.233+13592G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792239 | ||||||
chr4:15792284
|
C | G | 1 | a0001c0001t0001g0242 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.233+13637C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792284 | ||||||
chr4:15792339
|
G | C | 5 | a0001c0001t0020g0157a0001c0001t0020g0179a0001c0001t0035g0158others(2): Show | 5 | HG02965.hp2 HG03139.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+13692G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792339 | ||||||
chr4:15792358
|
C | G | 1 | a0001c0001t0056g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.233+13711C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792358 | ||||||
chr4:15792427
|
T | A | 210 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(207): Show | 219 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.233+13780T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792427 | ||||||
chr4:15792432
|
T | A | 1 | a0001c0001t0004g0127 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.233+13785T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792432 | ||||||
chr4:15792432
|
T | TA | 3 | a0001c0001t0030g0031a0001c0001t0034g0110a0001c0001t0064g0029 | 3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.233+13789dupA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15792432 | |||||
chr4:15792437
|
T | A | 230 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(227): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.233+13790T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792437 | ||||||
chr4:15792446
|
G | A | 289 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0023others(286): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.233+13799G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792446 | ||||||
chr4:15792458
|
G | GA | 7 | a0001c0001t0017g0053a0001c0001t0030g0031a0001c0001t0034g0110others(4): Show | 7 | HG02257.hp2 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+13820dupA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15792458 | |||||
chr4:15792463
|
A | G | 65 | a0001c0001t0001g0140a0001c0001t0001g0176a0001c0001t0002g0005others(62): Show | 69 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.233+13816A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792463 | ||||||
chr4:15792467
|
AG | A | 3 | a0001c0001t0006g0036a0001c0001t0009g0178a0001c0002t0005g0093 | 3 | NA19009.hp2 NA19043.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.233+13821delG | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792467 | ||||||
chr4:15792468
|
G | A | 140 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(137): Show | 145 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.233+13821G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792468 | ||||||
chr4:15792486
|
G | T | 2 | a0001c0001t0002g0192a0001c0001t0002g0208 | 2 | HG00642.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.233+13839G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792486 | ||||||
chr4:15792523
|
A | C | 1 | a0001c0001t0002g0021 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.233+13876A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792523 | ||||||
chr4:15792524
|
A | C | 1 | a0001c0001t0017g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.233+13877A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792524 | ||||||
chr4:15792663
|
G | A | 131 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(128): Show | 135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.233+14016G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792663 | ||||||
chr4:15792817
|
C | T | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.233+14170C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792817 | ||||||
chr4:15792912
|
G | T | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.233+14265G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792912 | ||||||
chr4:15792989
|
G | C | 2 | a0001c0001t0001g0015a0001c0001t0006g0036 | 2 | NA19057.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.233+14342G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15792989 | ||||||
chr4:15793323
|
A | T | 2 | a0001c0001t0003g0272a0001c0001t0004g0229 | 2 | HG00280.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.233+14676A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15793323 | ||||||
chr4:15793369
|
C | T | 3 | a0001c0001t0030g0031a0001c0001t0034g0110a0001c0001t0064g0029 | 3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.233+14722C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15793369 | ||||||
chr4:15793518
|
T | A | 1 | a0001c0001t0003g0248 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.233+14871T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15793518 | ||||||
chr4:15793746
|
A | T | 3 | a0001c0001t0020g0157a0001c0001t0020g0179a0001c0001t0036g0160 | 3 | HG03486.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.233+15099A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15793746 | ||||||
chr4:15793859
|
C | T | 64 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0001g0176others(61): Show | 68 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.233+15212C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15793859 | ||||||
chr4:15793937
|
G | A | 67 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0001g0176others(64): Show | 71 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.233+15290G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15793937 | ||||||
chr4:15793942
|
T | G | 1 | a0001c0001t0001g0226 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.233+15295T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15793942 | ||||||
chr4:15794020
|
T | C | 1 | a0001c0001t0002g0161 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.233+15373T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794020 | ||||||
chr4:15794140
|
G | T | 15 | a0001c0001t0004g0050a0001c0001t0009g0178a0001c0001t0011g0004others(12): Show | 16 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.233+15493G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794140 | ||||||
chr4:15794263
|
T | A | 37 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(34): Show | 39 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.233+15616T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794263 | ||||||
chr4:15794295
|
T | G | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.233+15648T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794295 | ||||||
chr4:15794345
|
C | A | 1 | a0001c0001t0017g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.233+15698C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794345 | ||||||
chr4:15794358
|
C | G | 26 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 27 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.233+15711C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794358 | ||||||
chr4:15794364
|
T | G | 2 | a0001c0001t0060g0047a0001c0001t0061g0046 | 2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.233+15717T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794364 | ||||||
chr4:15794403
|
A | G | 3 | a0001c0001t0030g0031a0001c0001t0034g0110a0001c0001t0064g0029 | 3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.233+15756A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794403 | ||||||
chr4:15794465
|
C | T | 18 | a0001c0001t0001g0310a0001c0001t0003g0012a0001c0001t0003g0303others(15): Show | 19 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.233+15818C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794465 | ||||||
chr4:15794570
|
C | G | 3 | a0001c0001t0030g0031a0001c0001t0034g0110a0001c0001t0064g0029 | 3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.233+15923C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794570 | ||||||
chr4:15794656
|
G | C | 1 | a0001c0001t0018g0006 | 2 | HG00733.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.233+16009G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794656 | ||||||
chr4:15794710
|
A | G | 231 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(228): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.233+16063A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15794710 | ||||||
chr4:15794775
|
GA | G | 71 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0001g0176others(68): Show | 75 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.233+16135delA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15794775 | |||||
chr4:15795070
|
C | A | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.233+16423C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15795070 | ||||||
chr4:15795218
|
C | CGT | 8 | a0001c0001t0002g0013a0001c0001t0006g0286a0001c0001t0009g0142others(5): Show | 8 | HG02145.hp2 HG02559.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+16588_233+1658 others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15795218 | |||||
chr4:15795572
|
A | G | 1 | a0001c0001t0034g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233+16925A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15795572 | ||||||
chr4:15795640
|
A | C | 26 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 27 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.233+16993A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15795640 | ||||||
chr4:15795712
|
A | G | 134 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(131): Show | 138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.233+17065A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15795712 | ||||||
chr4:15795739
|
A | G | 2 | a0001c0001t0057g0302a0001c0001t0058g0301 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.233+17092A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15795739 | ||||||
chr4:15796081
|
T | G | 134 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(131): Show | 138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.233+17434T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796081 | ||||||
chr4:15796146
|
A | C | 1 | a0001c0001t0041g0306 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.233+17499A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796146 | ||||||
chr4:15796212
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.233+17565C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796212 | ||||||
chr4:15796383
|
T | C | 134 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(131): Show | 138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.233+17736T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796383 | ||||||
chr4:15796399
|
A | G | 1 | a0001c0001t0028g0213 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.233+17752A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796399 | ||||||
chr4:15796448
|
T | C | 124 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(121): Show | 128 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.233+17801T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796448 | ||||||
chr4:15796641
|
A | G | 37 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(34): Show | 39 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.233+17994A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796641 | ||||||
chr4:15796645
|
T | C | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.233+17998T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796645 | ||||||
chr4:15796762
|
C | T | 128 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(125): Show | 132 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.233+18115C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15796762 | ||||||
chr4:15797064
|
T | C | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.233+18417T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797064 | ||||||
chr4:15797122
|
A | G | 128 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(125): Show | 132 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.233+18475A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797122 | ||||||
chr4:15797320
|
A | G | 128 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(125): Show | 132 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.233+18673A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797320 | ||||||
chr4:15797407
|
T | C | 2 | a0001c0001t0008g0152a0001c0001t0008g0166 | 2 | NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.233+18760T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797407 | ||||||
chr4:15797584
|
C | T | 131 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(128): Show | 135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.234-18927C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797584 | ||||||
chr4:15797585
|
G | A | 1 | a0001c0001t0056g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.234-18926G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797585 | ||||||
chr4:15797842
|
G | A | 1 | a0001c0001t0002g0318 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.234-18669G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797842 | ||||||
chr4:15797910
|
T | C | 1 | a0001c0001t0008g0129 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.234-18601T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797910 | ||||||
chr4:15797927
|
G | T | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-18584G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797927 | ||||||
chr4:15797963
|
G | T | 1 | a0001c0001t0024g0197 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.234-18548G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15797963 | ||||||
chr4:15798018
|
T | C | 1 | a0001c0001t0070g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.234-18493T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798018 | ||||||
chr4:15798070
|
A | C | 26 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 27 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.234-18441A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798070 | ||||||
chr4:15798087
|
G | C | 2 | a0001c0001t0002g0005a0001c0001t0002g0177 | 3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.234-18424G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798087 | ||||||
chr4:15798166
|
G | A | 2 | a0001c0001t0035g0158a0001c0001t0039g0159 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.234-18345G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798166 | ||||||
chr4:15798218
|
C | T | 2 | a0001c0004t0001g0296a0001c0004t0001g0297 | 2 | HG00423.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.234-18293C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798218 | ||||||
chr4:15798255
|
C | T | 22 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(19): Show | 23 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.234-18256C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798255 | ||||||
chr4:15798278
|
C | T | 64 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0001g0176others(61): Show | 68 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.234-18233C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798278 | ||||||
chr4:15798365
|
T | C | 1 | a0001c0001t0002g0130 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.234-18146T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798365 | ||||||
chr4:15798540
|
G | A | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.234-17971G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798540 | ||||||
chr4:15798645
|
G | A | 143 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(140): Show | 148 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.234-17866G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798645 | ||||||
chr4:15798731
|
C | T | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.234-17780C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798731 | ||||||
chr4:15798895
|
T | G | 1 | a0001c0001t0001g0220 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.234-17616T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798895 | ||||||
chr4:15798961
|
C | T | 3 | a0001c0001t0003g0316a0001c0001t0003g0317a0001c0001t0010g0315 | 3 | HG01256.hp2 HG01258.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.234-17550C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15798961 | ||||||
chr4:15799167
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.234-17344C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799167 | ||||||
chr4:15799231
|
T | C | 1 | a0001c0001t0003g0303 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.234-17280T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799231 | ||||||
chr4:15799267
|
A | T | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-17244A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799267 | ||||||
chr4:15799414
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.234-17097T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799414 | ||||||
chr4:15799588
|
A | ATTGGG | 5 | a0001c0001t0002g0207a0001c0001t0002g0209a0001c0001t0002g0210others(2): Show | 5 | NA18943.hp2 NA18954.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.234-16921_234-1691 others(9): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15799588 | |||||
chr4:15799678
|
G | T | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-16833G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799678 | ||||||
chr4:15799713
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.234-16798T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799713 | ||||||
chr4:15799869
|
C | G | 2 | a0001c0001t0035g0158a0001c0001t0039g0159 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.234-16642C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799869 | ||||||
chr4:15799888
|
G | A | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-16623G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799888 | ||||||
chr4:15799925
|
C | T | 1 | a0001c0001t0070g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.234-16586C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15799925 | ||||||
chr4:15800295
|
T | G | 62 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(59): Show | 64 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.234-16216T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15800295 | ||||||
chr4:15800311
|
G | T | 9 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(6): Show | 10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-16200G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15800311 | ||||||
chr4:15800333
|
A | T | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-16178A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15800333 | ||||||
chr4:15800359
|
A | G | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.234-16152A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15800359 | ||||||
chr4:15800590
|
T | C | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-15921T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15800590 | ||||||
chr4:15800681
|
T | C | 2 | a0001c0002t0029g0163a0001c0002t0029g0164 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.234-15830T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15800681 | ||||||
chr4:15800912
|
C | T | 2 | a0001c0001t0031g0145a0001c0001t0031g0146 | 2 | NA18981.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.234-15599C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15800912 | ||||||
chr4:15800921
|
C | T | 1 | a0001c0001t0054g0244 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.234-15590C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15800921 | ||||||
chr4:15801047
|
C | G | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.234-15464C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15801047 | ||||||
chr4:15801144
|
T | TA | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-15366dupA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15801144 | |||||
chr4:15801240
|
G | A | 67 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0001g0176others(64): Show | 71 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.234-15271G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15801240 | ||||||
chr4:15801642
|
T | C | 134 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(131): Show | 138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.234-14869T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15801642 | ||||||
chr4:15801664
|
A | G | 5 | a0001c0001t0004g0066a0001c0002t0001g0090a0001c0002t0001g0091others(2): Show | 5 | NA18522.hp2 NA18942.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.234-14847A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15801664 | ||||||
chr4:15801872
|
C | G | 1 | a0001c0001t0004g0229 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.234-14639C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15801872 | ||||||
chr4:15801880
|
T | C | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-14631T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15801880 | ||||||
chr4:15801915
|
G | C | 134 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(131): Show | 138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.234-14596G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15801915 | ||||||
chr4:15802038
|
C | T | 143 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(140): Show | 148 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.234-14473C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15802038 | ||||||
chr4:15802303
|
G | T | 1 | a0001c0001t0009g0329 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.234-14208G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15802303 | ||||||
chr4:15802491
|
G | GTTTTA | 69 | a0001c0001t0001g0011a0001c0001t0001g0153a0001c0001t0001g0225others(66): Show | 70 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.234-13961_234-1395 others(9): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | |||||
chr4:15802491
|
G | GTTTTATT others(3): Show |
33 | a0001c0001t0001g0224a0001c0001t0001g0226a0001c0001t0001g0242others(30): Show | 33 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.234-13966_234-1395 others(14): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | |||||
chr4:15802491
|
G | GTTTTATT others(8): Show |
15 | a0001c0001t0001g0140a0001c0001t0001g0235a0001c0001t0001g0250others(12): Show | 15 | HG00642.hp1 HG00741.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.234-13971_234-1395 others(19): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | |||||
chr4:15802491
|
G | GTTTTATT others(13): Show |
3 | a0001c0001t0001g0300a0001c0001t0004g0255a0001c0001t0053g0293 | 3 | HG02523.hp2 HG04115.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.234-13976_234-1395 others(24): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | |||||
chr4:15802491
|
G | GTTTTATT others(23): Show |
1 | a0001c0001t0002g0122 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.234-13986_234-1395 others(34): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | |||||
chr4:15802491
|
GTTTTA | G | 47 | a0001c0001t0001g0176a0001c0001t0002g0005a0001c0001t0002g0112others(44): Show | 50 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.234-13961_234-1395 others(9): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | |||||
chr4:15802491
|
GTTTTATT others(3): Show |
G | 26 | a0001c0001t0002g0008a0001c0001t0002g0191a0001c0001t0002g0201others(23): Show | 27 | HG00099.hp2 HG00735.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.234-13966_234-1395 others(14): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | |||||
chr4:15802491
|
GTTTTATT others(8): Show |
G | 42 | a0001c0001t0002g0020a0001c0001t0002g0181a0001c0001t0002g0188others(39): Show | 43 | HG00642.hp2 HG00741.hp2 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.234-13971_234-1395 others(19): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | |||||
chr4:15802491
|
GTTTTATT others(13): Show |
G | 33 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(30): Show | 34 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.234-13976_234-1395 others(24): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | |||||
chr4:15802491
|
GTTTTATT others(18): Show |
G | 7 | a0001c0001t0020g0157a0001c0001t0020g0179a0001c0001t0035g0158others(4): Show | 7 | HG02622.hp2 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.234-13981_234-1395 others(29): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | |||||
chr4:15802491
|
GTTTTATT others(33): Show |
G | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-13996_234-1395 others(44): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15802491 | |||||
chr4:15802774
|
A | T | 1 | a0001c0001t0013g0291 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.234-13737A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15802774 | ||||||
chr4:15802817
|
T | C | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-13694T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15802817 | ||||||
chr4:15802864
|
C | A | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-13647C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15802864 | ||||||
chr4:15803052
|
C | T | 22 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(19): Show | 23 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.234-13459C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803052 | ||||||
chr4:15803317
|
G | A | 1 | a0001c0001t0060g0047 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.234-13194G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803317 | ||||||
chr4:15803352
|
A | C | 3 | a0001c0001t0020g0157a0001c0001t0020g0179a0001c0001t0036g0160 | 3 | HG03486.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.234-13159A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803352 | ||||||
chr4:15803414
|
G | C | 3 | a0001c0001t0009g0178a0001c0001t0019g0156a0001c0001t0042g0102 | 3 | HG02572.hp2 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-13097G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803414 | ||||||
chr4:15803445
|
T | A | 1 | a0001c0001t0001g0247 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.234-13066T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803445 | ||||||
chr4:15803583
|
C | T | 4 | a0001c0001t0002g0005a0001c0001t0002g0118a0001c0001t0002g0168others(1): Show | 5 | HG01081.hp2 HG01361.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-12928C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803583 | ||||||
chr4:15803656
|
T | G | 1 | a0001c0001t0004g0267 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.234-12855T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803656 | ||||||
chr4:15803722
|
G | T | 1 | a0001c0001t0002g0016 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.234-12789G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803722 | ||||||
chr4:15803759
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.234-12752G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803759 | ||||||
chr4:15803901
|
T | C | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.234-12610T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15803901 | ||||||
chr4:15804011
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.234-12500T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15804011 | ||||||
chr4:15804025
|
A | G | 134 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(131): Show | 138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.234-12486A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15804025 | ||||||
chr4:15804259
|
TG | T | 26 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 27 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.234-12251delG | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15804259 | ||||||
chr4:15804451
|
T | C | 63 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(60): Show | 65 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.234-12060T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15804451 | ||||||
chr4:15804636
|
A | G | 1 | a0001c0001t0009g0329 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.234-11875A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15804636 | ||||||
chr4:15804717
|
G | T | 3 | a0001c0001t0030g0031a0001c0001t0034g0110a0001c0001t0064g0029 | 3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.234-11794G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15804717 | ||||||
chr4:15804848
|
A | G | 1 | a0001c0004t0001g0297 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.234-11663A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15804848 | ||||||
chr4:15804920
|
G | A | 1 | a0001c0001t0033g0194 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.234-11591G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15804920 | ||||||
chr4:15805097
|
G | A | 62 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(59): Show | 64 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.234-11414G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805097 | ||||||
chr4:15805101
|
C | T | 2 | a0001c0002t0029g0163a0001c0002t0029g0164 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.234-11410C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805101 | ||||||
chr4:15805148
|
A | C | 9 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(6): Show | 10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-11363A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805148 | ||||||
chr4:15805337
|
T | TC | 135 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(132): Show | 139 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.234-11172dupC | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15805337 | |||||
chr4:15805346
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.234-11165C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805346 | ||||||
chr4:15805410
|
C | T | 66 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0001g0176others(63): Show | 70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.234-11101C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805410 | ||||||
chr4:15805477
|
A | G | 62 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(59): Show | 64 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.234-11034A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805477 | ||||||
chr4:15805496
|
C | T | 135 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(132): Show | 139 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.234-11015C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805496 | ||||||
chr4:15805498
|
T | C | 1 | a0001c0001t0002g0168 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.234-11013T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805498 | ||||||
chr4:15805545
|
T | C | 2 | a0001c0001t0015g0070a0001c0001t0023g0069 | 2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.234-10966T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805545 | ||||||
chr4:15805555
|
G | A | 1 | a0001c0002t0030g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.234-10956G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805555 | ||||||
chr4:15805644
|
A | G | 1 | a0001c0001t0002g0021 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.234-10867A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805644 | ||||||
chr4:15805801
|
T | C | 1 | a0001c0001t0002g0168 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.234-10710T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805801 | ||||||
chr4:15805933
|
C | T | 12 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(9): Show | 13 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.234-10578C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805933 | ||||||
chr4:15805989
|
G | T | 1 | a0001c0001t0001g0265 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.234-10522G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805989 | ||||||
chr4:15805994
|
T | G | 1 | a0001c0001t0001g0265 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.234-10517T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15805994 | ||||||
chr4:15806133
|
C | A | 133 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(130): Show | 137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.234-10378C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806133 | ||||||
chr4:15806134
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.234-10377G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806134 | ||||||
chr4:15806224
|
C | G | 6 | a0001c0001t0002g0130a0001c0001t0002g0143a0001c0001t0008g0125others(3): Show | 6 | HG02074.hp1 HG02129.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.234-10287C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806224 | ||||||
chr4:15806469
|
G | C | 2 | a0001c0001t0002g0005a0001c0001t0002g0177 | 3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.234-10042G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806469 | ||||||
chr4:15806574
|
T | C | 1 | a0001c0001t0042g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.234-9937T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806574 | ||||||
chr4:15806817
|
G | A | 3 | a0001c0001t0002g0169a0001c0001t0003g0304a0001c0001t0009g0142 | 3 | HG01081.hp1 HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.234-9694G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806817 | ||||||
chr4:15806823
|
G | A | 2 | a0001c0001t0057g0302a0001c0001t0058g0301 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.234-9688G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806823 | ||||||
chr4:15806832
|
C | T | 1 | a0001c0001t0071g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.234-9679C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806832 | ||||||
chr4:15806971
|
C | A | 1 | a0001c0001t0039g0159 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.234-9540C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15806971 | ||||||
chr4:15807105
|
G | A | 135 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(132): Show | 139 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.234-9406G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15807105 | ||||||
chr4:15807113
|
T | G | 1 | a0001c0001t0009g0329 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.234-9398T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15807113 | ||||||
chr4:15807228
|
T | C | 3 | a0001c0001t0030g0031a0001c0001t0034g0110a0001c0001t0064g0029 | 3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.234-9283T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15807228 | ||||||
chr4:15807445
|
G | A | 50 | a0001c0001t0009g0178a0001c0001t0017g0053a0001c0001t0020g0157others(47): Show | 52 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.234-9066G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15807445 | ||||||
chr4:15807539
|
C | G | 48 | a0001c0001t0017g0053a0001c0001t0020g0157a0001c0001t0020g0179others(45): Show | 50 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.234-8972C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15807539 | ||||||
chr4:15807540
|
CTGAG | C | 48 | a0001c0001t0017g0053a0001c0001t0020g0157a0001c0001t0020g0179others(45): Show | 50 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.234-8968_234-8965d others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15807540 | |||||
chr4:15807551
|
G | A | 5 | a0001c0001t0020g0157a0001c0001t0020g0179a0001c0001t0035g0158others(2): Show | 5 | HG02965.hp2 HG03139.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.234-8960G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15807551 | ||||||
chr4:15807551
|
G | C | 85 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(82): Show | 87 | HG00099.hp2 HG00408.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.234-8960G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15807551 | ||||||
chr4:15807555
|
G | C | 1 | a0001c0001t0050g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.234-8956G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15807555 | ||||||
chr4:15808124
|
G | A | 2 | a0001c0001t0009g0178a0001c0001t0042g0102 | 2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.234-8387G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15808124 | ||||||
chr4:15808231
|
T | G | 50 | a0001c0001t0009g0178a0001c0001t0017g0053a0001c0001t0020g0157others(47): Show | 52 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.234-8280T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15808231 | ||||||
chr4:15808351
|
A | G | 135 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(132): Show | 139 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.234-8160A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15808351 | ||||||
chr4:15808399
|
T | C | 28 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(25): Show | 29 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.234-8112T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15808399 | ||||||
chr4:15808585
|
A | G | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.234-7926A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15808585 | ||||||
chr4:15808664
|
A | G | 1 | a0001c0001t0042g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.234-7847A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15808664 | ||||||
chr4:15808765
|
A | G | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.234-7746A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15808765 | ||||||
chr4:15808797
|
G | T | 6 | a0001c0001t0001g0015a0001c0001t0002g0013a0001c0001t0005g0014others(3): Show | 6 | HG02027.hp1 HG03927.hp1 NA19057.hp2 others(3): Show |
intron_variant | MODIFIER | c.234-7714G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15808797 | ||||||
chr4:15809004
|
T | G | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.234-7507T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809004 | ||||||
chr4:15809156
|
G | T | 50 | a0001c0001t0009g0178a0001c0001t0017g0053a0001c0001t0020g0157others(47): Show | 52 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.234-7355G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809156 | ||||||
chr4:15809272
|
A | G | 1 | a0001c0001t0055g0147 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.234-7239A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809272 | ||||||
chr4:15809368
|
C | T | 3 | a0001c0001t0020g0157a0001c0001t0020g0179a0001c0001t0036g0160 | 3 | HG03486.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.234-7143C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809368 | ||||||
chr4:15809545
|
G | T | 2 | a0001c0001t0007g0019a0001c0001t0007g0033 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.234-6966G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809545 | ||||||
chr4:15809653
|
C | A | 135 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(132): Show | 139 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.234-6858C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809653 | ||||||
chr4:15809734
|
C | T | 1 | a0001c0001t0002g0323 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.234-6777C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809734 | ||||||
chr4:15809750
|
T | C | 133 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(130): Show | 137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.234-6761T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809750 | ||||||
chr4:15809819
|
T | G | 50 | a0001c0001t0009g0178a0001c0001t0017g0053a0001c0001t0020g0157others(47): Show | 52 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.234-6692T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809819 | ||||||
chr4:15809909
|
C | T | 133 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(130): Show | 137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.234-6602C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15809909 | ||||||
chr4:15810124
|
T | C | 3 | a0001c0001t0001g0278a0001c0001t0009g0279a0001c0001t0009g0329 | 3 | NA18982.hp1 NA19006.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.234-6387T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810124 | ||||||
chr4:15810139
|
C | T | 13 | a0001c0001t0009g0178a0001c0001t0017g0053a0001c0001t0020g0157others(10): Show | 13 | HG02559.hp2 HG02572.hp2 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.234-6372C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810139 | ||||||
chr4:15810272
|
C | T | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.234-6239C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810272 | ||||||
chr4:15810333
|
G | A | 1 | a0001c0002t0030g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.234-6178G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810333 | ||||||
chr4:15810467
|
G | A | 2 | a0001c0001t0057g0302a0001c0001t0058g0301 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.234-6044G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810467 | ||||||
chr4:15810793
|
C | T | 9 | a0001c0001t0017g0053a0001c0001t0020g0157a0001c0001t0020g0179others(6): Show | 9 | HG02965.hp2 HG02970.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.234-5718C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810793 | ||||||
chr4:15810796
|
G | C | 2 | a0001c0001t0002g0057a0001c0001t0028g0059 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.234-5715G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810796 | ||||||
chr4:15810808
|
C | T | 1 | a0001c0001t0072g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.234-5703C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810808 | ||||||
chr4:15810834
|
G | T | 122 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(119): Show | 126 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.234-5677G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810834 | ||||||
chr4:15810995
|
C | G | 133 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(130): Show | 137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.234-5516C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15810995 | ||||||
chr4:15811044
|
G | A | 133 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(130): Show | 137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.234-5467G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15811044 | ||||||
chr4:15811232
|
C | T | 1 | a0001c0001t0070g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.234-5279C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15811232 | ||||||
chr4:15811254
|
C | T | 69 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0001g0176others(66): Show | 73 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.234-5257C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15811254 | ||||||
chr4:15811255
|
G | A | 11 | a0001c0001t0009g0178a0001c0001t0017g0053a0001c0001t0020g0157others(8): Show | 11 | HG02572.hp2 HG02965.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.234-5256G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15811255 | ||||||
chr4:15811266
|
AT | A | 83 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(80): Show | 85 | HG00099.hp2 HG00408.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.234-5241delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15811266 | |||||
chr4:15811336
|
A | G | 11 | a0001c0001t0009g0178a0001c0001t0017g0053a0001c0001t0020g0157others(8): Show | 11 | HG02572.hp2 HG02965.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.234-5175A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15811336 | ||||||
chr4:15811510
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.234-5001C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15811510 | ||||||
chr4:15811668
|
CAGAT | C | 121 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(118): Show | 125 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.234-4840_234-4837d others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15811668 | |||||
chr4:15811984
|
T | G | 176 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(173): Show | 184 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.234-4527T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15811984 | ||||||
chr4:15812008
|
A | T | 1 | a0001c0001t0004g0267 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.234-4503A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812008 | ||||||
chr4:15812087
|
A | G | 11 | a0001c0001t0009g0178a0001c0001t0017g0053a0001c0001t0019g0156others(8): Show | 11 | HG02647.hp2 HG02965.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.234-4424A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812087 | ||||||
chr4:15812100
|
T | A | 176 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(173): Show | 184 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.234-4411T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812100 | ||||||
chr4:15812322
|
C | T | 9 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(6): Show | 10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-4189C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812322 | ||||||
chr4:15812365
|
G | T | 6 | a0001c0001t0002g0130a0001c0001t0002g0143a0001c0001t0008g0125others(3): Show | 6 | HG02074.hp1 HG02129.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.234-4146G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812365 | ||||||
chr4:15812466
|
G | C | 86 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(83): Show | 89 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.234-4045G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812466 | ||||||
chr4:15812479
|
C | T | 3 | a0001c0001t0030g0031a0001c0001t0034g0110a0001c0001t0064g0029 | 3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.234-4032C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812479 | ||||||
chr4:15812525
|
G | A | 1 | a0001c0001t0009g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.234-3986G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812525 | ||||||
chr4:15812684
|
G | A | 1 | a0001c0001t0004g0267 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.234-3827G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812684 | ||||||
chr4:15812686
|
C | T | 11 | a0001c0001t0009g0178a0001c0001t0017g0053a0001c0001t0019g0156others(8): Show | 11 | HG02647.hp2 HG02965.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.234-3825C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812686 | ||||||
chr4:15812723
|
A | G | 32 | a0001c0001t0002g0008a0001c0001t0002g0181a0001c0001t0002g0188others(29): Show | 33 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.234-3788A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812723 | ||||||
chr4:15812795
|
T | A | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.234-3716T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812795 | ||||||
chr4:15812956
|
C | T | 97 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(94): Show | 100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.234-3555C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812956 | ||||||
chr4:15812965
|
T | G | 1 | a0001c0001t0031g0145 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.234-3546T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812965 | ||||||
chr4:15812970
|
C | T | 1 | a0001c0001t0043g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.234-3541C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812970 | ||||||
chr4:15812998
|
G | A | 66 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0002g0005others(63): Show | 70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.234-3513G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15812998 | ||||||
chr4:15813191
|
T | C | 83 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(80): Show | 86 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.234-3320T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813191 | ||||||
chr4:15813299
|
C | T | 97 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(94): Show | 100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.234-3212C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813299 | ||||||
chr4:15813308
|
G | GT | 86 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(83): Show | 89 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.234-3196dupT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15813308 | |||||
chr4:15813337
|
T | C | 9 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(6): Show | 10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-3174T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813337 | ||||||
chr4:15813439
|
T | A | 1 | a0001c0001t0026g0060 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.234-3072T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813439 | ||||||
chr4:15813440
|
A | T | 9 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(6): Show | 10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-3071A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813440 | ||||||
chr4:15813623
|
G | A | 15 | a0001c0001t0001g0140a0001c0001t0002g0052a0001c0001t0002g0122others(12): Show | 15 | HG01071.hp2 HG01433.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.234-2888G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813623 | ||||||
chr4:15813658
|
C | T | 5 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0022g0045others(2): Show | 5 | HG01243.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-2853C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813658 | ||||||
chr4:15813672
|
C | T | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.234-2839C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813672 | ||||||
chr4:15813690
|
G | C | 98 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(95): Show | 101 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.234-2821G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813690 | ||||||
chr4:15813791
|
T | C | 57 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(54): Show | 59 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.234-2720T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15813791 | ||||||
chr4:15814168
|
C | G | 2 | a0001c0001t0057g0302a0001c0001t0058g0301 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.234-2343C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15814168 | ||||||
chr4:15814258
|
A | G | 88 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(85): Show | 91 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.234-2253A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15814258 | ||||||
chr4:15814408
|
G | A | 88 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(85): Show | 91 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.234-2103G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15814408 | ||||||
chr4:15814618
|
T | C | 16 | a0001c0001t0002g0057a0001c0001t0004g0056a0001c0001t0004g0064others(13): Show | 16 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.234-1893T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15814618 | ||||||
chr4:15814785
|
GTTTTTGT | G | 83 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(80): Show | 86 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.234-1699_234-1693d others(9): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15814785 | |||||
chr4:15814812
|
GT | G | 10 | a0001c0001t0001g0266a0001c0001t0017g0053a0001c0001t0019g0156others(7): Show | 10 | HG02647.hp2 HG02735.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1687delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 15814812 | |||||
chr4:15814819
|
T | G | 11 | a0001c0001t0001g0250a0001c0001t0003g0277a0001c0001t0004g0050others(8): Show | 12 | HG00741.hp1 HG01106.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.234-1692T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15814819 | ||||||
chr4:15814838
|
G | A | 1 | a0001c0001t0033g0194 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.234-1673G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15814838 | ||||||
chr4:15814845
|
T | C | 86 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(83): Show | 89 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.234-1666T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15814845 | ||||||
chr4:15814876
|
G | A | 1 | a0001c0001t0009g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.234-1635G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15814876 | ||||||
chr4:15815047
|
T | C | 107 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(104): Show | 111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.234-1464T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815047 | ||||||
chr4:15815049
|
C | T | 86 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(83): Show | 89 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.234-1462C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815049 | ||||||
chr4:15815113
|
C | T | 1 | a0001c0001t0023g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.234-1398C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815113 | ||||||
chr4:15815181
|
A | G | 23 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(20): Show | 24 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.234-1330A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815181 | ||||||
chr4:15815232
|
A | T | 19 | a0001c0001t0001g0310a0001c0001t0003g0012a0001c0001t0003g0198others(16): Show | 20 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.234-1279A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815232 | ||||||
chr4:15815335
|
T | C | 1 | a0001c0001t0007g0051 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.234-1176T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815335 | ||||||
chr4:15815410
|
T | G | 5 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(2): Show | 5 | HG02647.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-1101T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815410 | ||||||
chr4:15815694
|
T | A | 1 | a0001c0001t0004g0324 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.234-817T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815694 | ||||||
chr4:15815701
|
A | G | 107 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(104): Show | 111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.234-810A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815701 | ||||||
chr4:15815806
|
C | T | 175 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(172): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.234-705C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815806 | ||||||
chr4:15815833
|
T | C | 1 | a0001c0001t0003g0258 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.234-678T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815833 | ||||||
chr4:15815889
|
G | T | 1 | a0001c0001t0015g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.234-622G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815889 | ||||||
chr4:15815940
|
C | T | 2 | a0001c0001t0057g0302a0001c0001t0058g0301 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.234-571C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15815940 | ||||||
chr4:15816273
|
C | T | 1 | a0001c0001t0001g0009 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.234-238C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15816273 | ||||||
chr4:15816278
|
T | A | 2 | a0001c0001t0001g0233a0001c0001t0003g0258 | 2 | NA19064.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.234-233T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15816278 | ||||||
chr4:15816299
|
C | T | 66 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0002g0005others(63): Show | 70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.234-212C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15816299 | ||||||
chr4:15816355
|
G | A | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.234-156G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15816355 | ||||||
chr4:15816382
|
G | A | 1 | a0001c0001t0033g0194 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.234-129G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 1/7 | chr4 | 15816382 | ||||||
chr4:15816719
|
A | G | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.363+79A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15816719 | ||||||
chr4:15816743
|
A | C | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.363+103A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15816743 | ||||||
chr4:15816768
|
G | A | 67 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0002g0005others(64): Show | 71 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.363+128G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15816768 | ||||||
chr4:15816925
|
G | A | 59 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(56): Show | 60 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.363+285G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15816925 | ||||||
chr4:15816962
|
C | A | 5 | a0001c0001t0020g0157a0001c0001t0020g0179a0001c0001t0035g0158others(2): Show | 5 | HG02965.hp2 HG03139.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+322C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15816962 | ||||||
chr4:15816973
|
C | T | 2 | a0001c0002t0029g0163a0001c0002t0029g0164 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.363+333C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15816973 | ||||||
chr4:15817101
|
T | A | 1 | a0001c0001t0002g0169 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.363+461T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817101 | ||||||
chr4:15817216
|
G | C | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.363+576G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817216 | ||||||
chr4:15817229
|
T | C | 1 | a0001c0001t0005g0319 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.363+589T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817229 | ||||||
chr4:15817240
|
C | T | 69 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0002g0005others(66): Show | 73 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.363+600C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817240 | ||||||
chr4:15817293
|
A | G | 68 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0002g0005others(65): Show | 72 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.363+653A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817293 | ||||||
chr4:15817365
|
C | T | 68 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0001t0002g0005others(65): Show | 72 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.363+725C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817365 | ||||||
chr4:15817510
|
A | G | 1 | a0001c0001t0041g0306 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.363+870A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817510 | ||||||
chr4:15817614
|
T | C | 1 | a0001c0001t0009g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.363+974T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817614 | ||||||
chr4:15817691
|
G | A | 1 | a0001c0001t0006g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.363+1051G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817691 | ||||||
chr4:15817697
|
A | T | 5 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(2): Show | 5 | HG02647.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+1057A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817697 | ||||||
chr4:15817742
|
C | A | 2 | a0001c0001t0014g0148a0001c0001t0014g0174 | 2 | HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.363+1102C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15817742 | ||||||
chr4:15818084
|
A | G | 41 | a0001c0001t0013g0290a0001c0001t0046g0044a0001c0001t0065g0101others(38): Show | 43 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.363+1444A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818084 | ||||||
chr4:15818103
|
G | T | 8 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(5): Show | 9 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.363+1463G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818103 | ||||||
chr4:15818155
|
G | C | 4 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(1): Show | 4 | NA18942.hp2 NA18947.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+1515G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818155 | ||||||
chr4:15818227
|
G | C | 5 | a0001c0001t0002g0057a0001c0001t0002g0112a0001c0001t0002g0149others(2): Show | 5 | HG02451.hp1 HG02809.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+1587G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818227 | ||||||
chr4:15818228
|
G | A | 47 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(44): Show | 49 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.363+1588G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818228 | ||||||
chr4:15818279
|
T | G | 1 | a0001c0001t0001g0252 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.363+1639T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818279 | ||||||
chr4:15818293
|
C | T | 14 | a0001c0001t0004g0056a0001c0001t0004g0064a0001c0001t0004g0066others(11): Show | 14 | HG01433.hp2 HG01891.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.363+1653C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818293 | ||||||
chr4:15818557
|
A | G | 174 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0002g0003others(171): Show | 182 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.363+1917A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818557 | ||||||
chr4:15818676
|
G | C | 1 | a0001c0002t0006g0099 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.363+2036G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818676 | ||||||
chr4:15818693
|
C | G | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.363+2053C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818693 | ||||||
chr4:15818697
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.363+2057A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818697 | ||||||
chr4:15818747
|
C | T | 9 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(6): Show | 10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+2107C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818747 | ||||||
chr4:15818987
|
T | C | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.363+2347T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15818987 | ||||||
chr4:15819035
|
A | G | 5 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(2): Show | 5 | HG02647.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+2395A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819035 | ||||||
chr4:15819051
|
C | T | 1 | a0001c0001t0013g0291 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.363+2411C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819051 | ||||||
chr4:15819109
|
TCTCA | T | 21 | a0001c0001t0002g0008a0001c0001t0002g0181a0001c0001t0002g0188others(18): Show | 22 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.363+2474_363+2477d others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 15819109 | |||||
chr4:15819118
|
T | C | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.363+2478T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819118 | ||||||
chr4:15819238
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.363+2598C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819238 | ||||||
chr4:15819305
|
A | C | 4 | a0001c0002t0003g0074a0001c0002t0009g0076a0001c0002t0016g0106others(1): Show | 4 | HG01106.hp2 HG01192.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+2665A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819305 | ||||||
chr4:15819482
|
G | A | 1 | a0001c0001t0013g0291 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.363+2842G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819482 | ||||||
chr4:15819520
|
T | A | 1 | a0001c0001t0003g0251 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.363+2880T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819520 | ||||||
chr4:15819870
|
A | G | 1 | a0001c0001t0036g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.363+3230A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819870 | ||||||
chr4:15819885
|
A | T | 1 | a0001c0001t0042g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.363+3245A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819885 | ||||||
chr4:15819927
|
C | T | 2 | a0001c0001t0065g0101a0001c0001t0067g0058 | 2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.363+3287C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15819927 | ||||||
chr4:15820008
|
C | A | 1 | a0001c0001t0007g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.363+3368C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15820008 | ||||||
chr4:15820155
|
G | A | 1 | a0001c0001t0002g0124 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.363+3515G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15820155 | ||||||
chr4:15820410
|
T | C | 7 | a0001c0001t0020g0157a0001c0001t0020g0179a0001c0001t0035g0158others(4): Show | 7 | HG01358.hp2 HG02965.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+3770T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15820410 | ||||||
chr4:15820675
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0191 | 3 | HG00099.hp2 HG01517.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.363+4035C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15820675 | ||||||
chr4:15820765
|
T | A | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.364-4116T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15820765 | ||||||
chr4:15820839
|
C | G | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.364-4042C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15820839 | ||||||
chr4:15820858
|
G | A | 1 | a0001c0001t0043g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.364-4023G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15820858 | ||||||
chr4:15820883
|
T | C | 9 | a0001c0001t0001g0225a0001c0001t0001g0232a0001c0001t0001g0256others(6): Show | 9 | HG02735.hp1 NA18951.hp2 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.364-3998T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15820883 | ||||||
chr4:15821005
|
C | T | 68 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(65): Show | 72 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.364-3876C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821005 | ||||||
chr4:15821049
|
G | A | 48 | a0001c0001t0001g0024a0001c0001t0002g0003a0001c0001t0002g0013others(45): Show | 49 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.364-3832G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821049 | ||||||
chr4:15821149
|
A | G | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.364-3732A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821149 | ||||||
chr4:15821220
|
G | A | 68 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(65): Show | 72 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.364-3661G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821220 | ||||||
chr4:15821365
|
C | A | 1 | a0001c0001t0001g0328 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.364-3516C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821365 | ||||||
chr4:15821380
|
C | CA | 16 | a0001c0001t0001g0009a0001c0001t0001g0236a0001c0001t0001g0237others(13): Show | 18 | HG00140.hp2 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.364-3492dupA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 15821380 | |||||
chr4:15821439
|
C | T | 1 | a0001c0001t0003g0272 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.364-3442C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821439 | ||||||
chr4:15821491
|
A | G | 41 | a0001c0001t0013g0290a0001c0002t0001g0090a0001c0002t0001g0091others(38): Show | 43 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.364-3390A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821491 | ||||||
chr4:15821635
|
T | C | 1 | a0001c0001t0002g0171 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.364-3246T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821635 | ||||||
chr4:15821689
|
C | T | 1 | a0001c0001t0067g0058 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.364-3192C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821689 | ||||||
chr4:15821694
|
CA | C | 75 | a0001c0001t0001g0024a0001c0001t0002g0003a0001c0001t0002g0013others(72): Show | 78 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.364-3169delA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 15821694 | |||||
chr4:15821694
|
CAA | C | 29 | a0001c0001t0004g0050a0001c0001t0004g0056a0001c0001t0004g0064others(26): Show | 30 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.364-3170_364-3169d others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 15821694 | |||||
chr4:15821698
|
A | C | 1 | a0001c0001t0039g0159 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.364-3183A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821698 | ||||||
chr4:15821717
|
A | G | 1 | a0001c0001t0067g0058 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.364-3164A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821717 | ||||||
chr4:15821800
|
T | C | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.364-3081T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821800 | ||||||
chr4:15821821
|
C | G | 1 | a0001c0001t0002g0139 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.364-3060C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15821821 | ||||||
chr4:15822270
|
T | G | 14 | a0001c0001t0004g0056a0001c0001t0004g0064a0001c0001t0004g0066others(11): Show | 14 | HG01433.hp2 HG01891.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.364-2611T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822270 | ||||||
chr4:15822341
|
G | A | 70 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(67): Show | 74 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.364-2540G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822341 | ||||||
chr4:15822444
|
G | C | 174 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0002g0003others(171): Show | 182 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.364-2437G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822444 | ||||||
chr4:15822479
|
G | A | 3 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0155 | 3 | NA18942.hp2 NA18947.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.364-2402G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822479 | ||||||
chr4:15822532
|
T | C | 2 | a0001c0001t0004g0064a0001c0001t0004g0066 | 2 | HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.364-2349T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822532 | ||||||
chr4:15822545
|
A | G | 2 | a0001c0002t0029g0163a0001c0002t0029g0164 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.364-2336A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822545 | ||||||
chr4:15822630
|
A | C | 25 | a0001c0001t0001g0024a0001c0001t0002g0003a0001c0001t0002g0013others(22): Show | 26 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.364-2251A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822630 | ||||||
chr4:15822725
|
G | A | 1 | a0001c0004t0001g0297 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.364-2156G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822725 | ||||||
chr4:15822973
|
C | T | 2 | a0001c0001t0002g0169a0001c0001t0009g0142 | 2 | HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.364-1908C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15822973 | ||||||
chr4:15823053
|
G | A | 165 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0002g0003others(162): Show | 172 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.364-1828G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823053 | ||||||
chr4:15823119
|
C | T | 5 | a0001c0001t0002g0181a0001c0001t0002g0188a0001c0001t0002g0189others(2): Show | 5 | HG01168.hp2 HG01257.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-1762C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823119 | ||||||
chr4:15823351
|
C | T | 68 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(65): Show | 72 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.364-1530C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823351 | ||||||
chr4:15823408
|
T | G | 1 | a0001c0005t0007g0022 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.364-1473T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823408 | ||||||
chr4:15823417
|
C | T | 21 | a0001c0001t0001g0024a0001c0001t0002g0003a0001c0001t0002g0013others(18): Show | 22 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.364-1464C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823417 | ||||||
chr4:15823612
|
A | T | 1 | a0001c0001t0001g0328 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.364-1269A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823612 | ||||||
chr4:15823737
|
T | C | 7 | a0001c0001t0020g0157a0001c0001t0020g0179a0001c0001t0035g0158others(4): Show | 7 | HG01358.hp2 HG02965.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-1144T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823737 | ||||||
chr4:15823787
|
G | A | 9 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(6): Show | 10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.364-1094G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823787 | ||||||
chr4:15823835
|
A | G | 1 | a0001c0001t0002g0139 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.364-1046A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823835 | ||||||
chr4:15823899
|
A | T | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.364-982A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15823899 | ||||||
chr4:15824005
|
A | T | 1 | a0001c0001t0009g0245 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.364-876A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824005 | ||||||
chr4:15824007
|
A | C | 1 | a0001c0001t0001g0328 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.364-874A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824007 | ||||||
chr4:15824143
|
G | A | 1 | a0001c0001t0035g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.364-738G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824143 | ||||||
chr4:15824228
|
G | A | 1 | a0001c0002t0005g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.364-653G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824228 | ||||||
chr4:15824421
|
A | T | 1 | a0001c0001t0046g0044 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.364-460A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824421 | ||||||
chr4:15824443
|
G | C | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.364-438G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824443 | ||||||
chr4:15824504
|
A | C | 1 | a0001c0001t0062g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.364-377A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824504 | ||||||
chr4:15824517
|
T | C | 1 | a0001c0001t0002g0013 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.364-364T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824517 | ||||||
chr4:15824549
|
C | G | 5 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(2): Show | 5 | HG02647.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-332C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824549 | ||||||
chr4:15824561
|
G | A | 4 | a0001c0001t0002g0003a0001c0001t0002g0017a0001c0001t0002g0020others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-320G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824561 | ||||||
chr4:15824681
|
A | AAC | 4 | a0001c0001t0014g0214a0001c0001t0047g0185a0001c0001t0057g0302others(1): Show | 4 | HG02145.hp1 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-181_364-180dup others(2): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 15824681 | |||||
chr4:15824681
|
AAC | A | 122 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(119): Show | 129 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.364-181_364-180del others(2): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 15824681 | |||||
chr4:15824681
|
AACAC | A | 48 | a0001c0001t0001g0024a0001c0001t0002g0003a0001c0001t0002g0013others(45): Show | 49 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.364-183_364-180del others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 15824681 | |||||
chr4:15824711
|
G | A | 1 | a0001c0002t0007g0098 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.364-170G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824711 | ||||||
chr4:15824739
|
A | T | 58 | a0001c0001t0001g0024a0001c0001t0002g0003a0001c0001t0002g0013others(55): Show | 60 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.364-142A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824739 | ||||||
chr4:15824750
|
A | C | 1 | a0001c0001t0008g0167 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.364-131A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824750 | ||||||
chr4:15824760
|
C | T | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.364-121C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824760 | ||||||
chr4:15824792
|
G | GT | 59 | a0001c0001t0001g0024a0001c0001t0002g0003a0001c0001t0002g0013others(56): Show | 61 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.364-79dupT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 15824792 | |||||
chr4:15824842
|
A | C | 1 | a0001c0001t0004g0307 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.364-39A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 2/7 | chr4 | 15824842 | ||||||
chr4:15825231
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.499+215G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15825231 | ||||||
chr4:15825264
|
A | G | 3 | a0001c0002t0005g0100a0001c0002t0006g0099a0001c0002t0007g0098 | 3 | HG03491.hp2 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.499+248A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15825264 | ||||||
chr4:15825561
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.499+545T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15825561 | ||||||
chr4:15825592
|
T | C | 1 | a0001c0005t0007g0022 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.499+576T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15825592 | ||||||
chr4:15825878
|
C | G | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.499+862C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15825878 | ||||||
chr4:15825993
|
T | C | 25 | a0001c0001t0001g0024a0001c0001t0002g0003a0001c0001t0002g0013others(22): Show | 26 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.499+977T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15825993 | ||||||
chr4:15826183
|
C | T | 1 | a0001c0001t0010g0314 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.499+1167C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826183 | ||||||
chr4:15826300
|
G | A | 19 | a0001c0001t0001g0024a0001c0001t0002g0003a0001c0001t0002g0013others(16): Show | 20 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.499+1284G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826300 | ||||||
chr4:15826307
|
T | C | 1 | a0001c0001t0042g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.499+1291T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826307 | ||||||
chr4:15826450
|
CTT | C | 71 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(68): Show | 75 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.499+1437_499+1438d others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826450 | |||||
chr4:15826453
|
T | G | 4 | a0001c0001t0002g0017a0001c0001t0002g0149a0001c0001t0014g0174others(1): Show | 4 | HG01123.hp2 HG02451.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+1437T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826453 | ||||||
chr4:15826456
|
T | C | 4 | a0001c0001t0002g0017a0001c0001t0002g0149a0001c0001t0014g0174others(1): Show | 4 | HG01123.hp2 HG02451.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+1440T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826456 | ||||||
chr4:15826456
|
T | TGCGCAC | 8 | a0001c0002t0001g0155a0001c0002t0004g0071a0001c0002t0005g0087others(5): Show | 8 | HG00423.hp2 HG01106.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.499+1441_499+1446d others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826456 | |||||
chr4:15826457
|
G | GCGCA | 8 | a0001c0001t0007g0051a0001c0001t0009g0178a0001c0001t0013g0290others(5): Show | 8 | HG02027.hp1 HG02622.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.499+1443_499+1446d others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826457 | |||||
chr4:15826459
|
G | A | 4 | a0001c0001t0002g0017a0001c0001t0002g0149a0001c0001t0014g0174others(1): Show | 4 | HG01123.hp2 HG02451.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+1443G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826459 | ||||||
chr4:15826459
|
G | GCA | 25 | a0001c0001t0002g0008a0001c0001t0002g0201a0001c0001t0002g0206others(22): Show | 26 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.499+1481_499+1482d others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | |||||
chr4:15826459
|
G | GCACA | 10 | a0001c0001t0002g0181a0001c0001t0002g0188a0001c0001t0002g0189others(7): Show | 10 | HG00609.hp2 HG00642.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.499+1479_499+1482d others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | |||||
chr4:15826459
|
G | GCACGCA | 20 | a0001c0001t0001g0024a0001c0001t0002g0003a0001c0001t0002g0013others(17): Show | 21 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.499+1446_499+1447i others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | |||||
chr4:15826459
|
G | GCACGCAC others(1): Show |
9 | a0001c0001t0002g0032a0001c0001t0004g0056a0001c0001t0007g0019others(6): Show | 9 | HG01168.hp1 HG01891.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.499+1446_499+1447i others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | |||||
chr4:15826459
|
G | GCACGCAC others(3): Show |
3 | a0001c0001t0002g0020a0001c0001t0004g0064a0001c0001t0022g0045 | 3 | HG01255.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.499+1446_499+1447i others(12): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | |||||
chr4:15826459
|
G | GCACGCAC others(5): Show |
1 | a0001c0001t0017g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.499+1446_499+1447i others(14): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | |||||
chr4:15826459
|
G | GCACGCGC others(1): Show |
16 | a0001c0002t0001g0096a0001c0002t0003g0001a0001c0002t0005g0084others(13): Show | 18 | HG00621.hp2 HG01192.hp2 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.499+1446_499+1447i others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | |||||
chr4:15826459
|
G | GCACGCGC others(3): Show |
8 | a0001c0002t0001g0092a0001c0002t0002g0083a0001c0002t0003g0079others(5): Show | 8 | HG02074.hp2 HG02083.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.499+1446_499+1447i others(12): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | |||||
chr4:15826459
|
G | GCACGCGC others(5): Show |
2 | a0001c0002t0004g0080a0001c0002t0012g0082 | 2 | HG00408.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.499+1446_499+1447i others(14): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | |||||
chr4:15826459
|
GCA | G | 28 | a0001c0001t0001g0236a0001c0001t0001g0266a0001c0001t0001g0271others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.499+1481_499+1482d others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | |||||
chr4:15826459
|
GCACA | G | 69 | a0001c0001t0001g0009a0001c0001t0001g0153a0001c0001t0001g0237others(66): Show | 74 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(71): Show |
intron_variant | MODIFIER | c.499+1479_499+1482d others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | |||||
chr4:15826459
|
GCACACA | G | 4 | a0001c0001t0030g0031a0001c0001t0034g0110a0001c0001t0064g0029others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+1477_499+1482d others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826459 | |||||
chr4:15826461
|
A | ACG | 10 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(7): Show | 11 | HG01433.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.499+1446_499+1447i others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826461 | |||||
chr4:15826461
|
A | ACGCG | 4 | a0001c0002t0001g0091a0001c0002t0003g0074a0001c0002t0005g0073others(1): Show | 4 | HG01928.hp2 HG03139.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+1446_499+1447i others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826461 | |||||
chr4:15826461
|
A | G | 4 | a0001c0001t0001g0273a0001c0001t0002g0149a0001c0001t0014g0174others(1): Show | 4 | HG02451.hp1 HG02738.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+1445A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826461 | ||||||
chr4:15826463
|
A | G | 12 | a0001c0001t0002g0057a0001c0001t0002g0111a0001c0001t0002g0112others(9): Show | 12 | HG00099.hp1 HG00438.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+1447A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826463 | ||||||
chr4:15826465
|
A | G | 5 | a0001c0001t0002g0144a0001c0001t0008g0136a0001c0001t0014g0148others(2): Show | 5 | HG01934.hp1 HG02922.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.499+1449A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826465 | ||||||
chr4:15826467
|
A | G | 57 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(54): Show | 61 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.499+1451A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826467 | ||||||
chr4:15826469
|
A | G | 4 | a0001c0001t0030g0031a0001c0001t0034g0110a0001c0001t0064g0029others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+1453A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826469 | ||||||
chr4:15826645
|
C | A | 1 | a0001c0001t0004g0229 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.499+1629C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826645 | ||||||
chr4:15826758
|
G | GA | 74 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(71): Show | 78 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.499+1751dupA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15826758 | |||||
chr4:15826918
|
G | T | 1 | a0001c0001t0033g0194 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.499+1902G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826918 | ||||||
chr4:15826946
|
G | T | 1 | a0001c0001t0004g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.499+1930G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15826946 | ||||||
chr4:15827069
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.499+2053C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15827069 | ||||||
chr4:15827303
|
C | T | 4 | a0001c0001t0007g0019a0001c0001t0007g0033a0001c0001t0011g0042others(1): Show | 4 | HG01168.hp1 HG01169.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+2287C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15827303 | ||||||
chr4:15827336
|
ATGCAGAA others(8): Show |
A | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.499+2323_499+2337d others(17): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15827336 | |||||
chr4:15827579
|
A | G | 1 | a0001c0002t0037g0081 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.499+2563A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15827579 | ||||||
chr4:15827582
|
T | G | 65 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(62): Show | 69 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.499+2566T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15827582 | ||||||
chr4:15827606
|
T | C | 1 | a0001c0001t0011g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.499+2590T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15827606 | ||||||
chr4:15827748
|
C | T | 1 | a0001c0001t0006g0135 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.499+2732C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15827748 | ||||||
chr4:15827989
|
A | G | 228 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0153others(225): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.499+2973A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15827989 | ||||||
chr4:15828164
|
G | A | 2 | a0001c0002t0029g0163a0001c0002t0029g0164 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.499+3148G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15828164 | ||||||
chr4:15828311
|
C | T | 38 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(35): Show | 40 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.499+3295C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15828311 | ||||||
chr4:15828375
|
A | G | 1 | a0001c0001t0007g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.499+3359A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15828375 | ||||||
chr4:15828692
|
T | C | 3 | a0001c0001t0030g0031a0001c0001t0034g0110a0001c0001t0064g0029 | 3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.499+3676T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15828692 | ||||||
chr4:15828771
|
A | G | 2 | a0001c0001t0026g0060a0001c0001t0026g0061 | 2 | HG01433.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.499+3755A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15828771 | ||||||
chr4:15828979
|
G | A | 1 | a0001c0002t0030g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.499+3963G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15828979 | ||||||
chr4:15829239
|
G | A | 2 | a0001c0001t0065g0101a0001c0001t0067g0058 | 2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.499+4223G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15829239 | ||||||
chr4:15829273
|
A | G | 40 | a0001c0001t0013g0290a0001c0002t0001g0090a0001c0002t0001g0091others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.499+4257A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15829273 | ||||||
chr4:15829400
|
C | T | 19 | a0001c0001t0001g0024a0001c0001t0002g0003a0001c0001t0002g0013others(16): Show | 20 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.499+4384C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15829400 | ||||||
chr4:15829412
|
A | G | 1 | a0001c0001t0008g0136 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.499+4396A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15829412 | ||||||
chr4:15829497
|
G | T | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.499+4481G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15829497 | ||||||
chr4:15829508
|
G | A | 1 | a0001c0001t0006g0276 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.499+4492G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15829508 | ||||||
chr4:15829705
|
T | C | 1 | a0001c0001t0002g0209 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.500-4512T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15829705 | ||||||
chr4:15829725
|
C | T | 1 | a0001c0001t0043g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.500-4492C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15829725 | ||||||
chr4:15830045
|
A | C | 1 | a0001c0001t0001g0270 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.500-4172A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830045 | ||||||
chr4:15830130
|
A | T | 1 | a0001c0001t0001g0270 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.500-4087A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830130 | ||||||
chr4:15830184
|
G | T | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.500-4033G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830184 | ||||||
chr4:15830349
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.500-3868T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830349 | ||||||
chr4:15830440
|
T | G | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.500-3777T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830440 | ||||||
chr4:15830523
|
T | C | 3 | a0001c0001t0030g0031a0001c0001t0034g0110a0001c0001t0064g0029 | 3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.500-3694T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830523 | ||||||
chr4:15830575
|
A | G | 41 | a0001c0001t0013g0290a0001c0002t0001g0090a0001c0002t0001g0091others(38): Show | 43 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.500-3642A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830575 | ||||||
chr4:15830870
|
C | T | 1 | a0001c0001t0071g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.500-3347C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830870 | ||||||
chr4:15830881
|
T | C | 1 | a0001c0001t0072g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.500-3336T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830881 | ||||||
chr4:15830948
|
T | G | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.500-3269T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15830948 | ||||||
chr4:15831299
|
C | A | 1 | a0001c0002t0005g0073 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.500-2918C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15831299 | ||||||
chr4:15831302
|
G | A | 1 | a0001c0001t0009g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.500-2915G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15831302 | ||||||
chr4:15831319
|
T | G | 1 | a0001c0001t0004g0240 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.500-2898T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15831319 | ||||||
chr4:15831568
|
CT | C | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.500-2639delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15831568 | |||||
chr4:15831611
|
C | G | 1 | a0001c0001t0001g0274 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.500-2606C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15831611 | ||||||
chr4:15831909
|
A | G | 228 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0153others(225): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.500-2308A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15831909 | ||||||
chr4:15832016
|
C | T | 1 | a0001c0001t0003g0313 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.500-2201C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832016 | ||||||
chr4:15832172
|
C | T | 41 | a0001c0001t0013g0290a0001c0002t0001g0090a0001c0002t0001g0091others(38): Show | 43 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.500-2045C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832172 | ||||||
chr4:15832229
|
T | C | 6 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(3): Show | 6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.500-1988T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832229 | ||||||
chr4:15832241
|
A | G | 4 | a0001c0002t0003g0074a0001c0002t0009g0076a0001c0002t0016g0106others(1): Show | 4 | HG01106.hp2 HG01192.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-1976A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832241 | ||||||
chr4:15832243
|
C | T | 1 | a0001c0001t0060g0047 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.500-1974C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832243 | ||||||
chr4:15832340
|
C | T | 41 | a0001c0001t0013g0290a0001c0002t0001g0090a0001c0002t0001g0091others(38): Show | 43 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.500-1877C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832340 | ||||||
chr4:15832380
|
CCTGTTTG others(2): Show |
C | 9 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(6): Show | 10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.500-1834_500-1826d others(11): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15832380 | |||||
chr4:15832435
|
T | A | 1 | a0001c0001t0025g0282 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.500-1782T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832435 | ||||||
chr4:15832472
|
A | C | 41 | a0001c0001t0013g0290a0001c0002t0001g0090a0001c0002t0001g0091others(38): Show | 43 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.500-1745A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832472 | ||||||
chr4:15832482
|
A | G | 1 | a0001c0001t0019g0150 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.500-1735A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832482 | ||||||
chr4:15832607
|
T | A | 2 | a0001c0001t0016g0063a0001c0001t0049g0065 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.500-1610T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832607 | ||||||
chr4:15832665
|
T | G | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.500-1552T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832665 | ||||||
chr4:15832737
|
T | A | 2 | a0001c0001t0065g0101a0001c0001t0067g0058 | 2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.500-1480T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832737 | ||||||
chr4:15832872
|
A | G | 1 | a0001c0001t0004g0255 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.500-1345A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832872 | ||||||
chr4:15832983
|
A | G | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.500-1234A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15832983 | ||||||
chr4:15833129
|
TC | T | 6 | a0001c0001t0006g0276a0001c0001t0006g0284a0001c0001t0006g0285others(3): Show | 6 | HG02055.hp2 NA18945.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.500-1084delC | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 15833129 | |||||
chr4:15833163
|
T | A | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.500-1054T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15833163 | ||||||
chr4:15833576
|
A | G | 1 | a0001c0001t0059g0113 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.500-641A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15833576 | ||||||
chr4:15833582
|
T | C | 1 | a0001c0001t0003g0311 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.500-635T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15833582 | ||||||
chr4:15833742
|
T | C | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.500-475T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15833742 | ||||||
chr4:15833831
|
A | T | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.500-386A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15833831 | ||||||
chr4:15833863
|
G | T | 66 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(63): Show | 70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.500-354G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15833863 | ||||||
chr4:15833912
|
C | T | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.500-305C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15833912 | ||||||
chr4:15834083
|
G | A | 5 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(2): Show | 5 | HG02647.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-134G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 3/7 | chr4 | 15834083 | ||||||
chr4:15834360
|
C | T | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+58C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834360 | ||||||
chr4:15834408
|
G | T | 2 | a0001c0001t0004g0027a0001c0001t0033g0028 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.585+106G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834408 | ||||||
chr4:15834449
|
T | C | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+147T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834449 | ||||||
chr4:15834512
|
G | A | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+210G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834512 | ||||||
chr4:15834542
|
A | C | 1 | a0001c0001t0001g0261 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.585+240A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834542 | ||||||
chr4:15834614
|
G | A | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+312G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834614 | ||||||
chr4:15834688
|
A | G | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+386A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834688 | ||||||
chr4:15834829
|
C | A | 1 | a0001c0001t0042g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.585+527C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834829 | ||||||
chr4:15834894
|
A | AT | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+600dupT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15834894 | |||||
chr4:15834902
|
T | A | 1 | a0001c0001t0002g0017 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.585+600T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834902 | ||||||
chr4:15834903
|
A | T | 44 | a0001c0001t0001g0233a0001c0001t0001g0252a0001c0001t0003g0258others(41): Show | 46 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.585+601A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834903 | ||||||
chr4:15834904
|
A | T | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+602A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15834904 | ||||||
chr4:15835260
|
T | C | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+958T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835260 | ||||||
chr4:15835268
|
T | G | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+966T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835268 | ||||||
chr4:15835290
|
A | G | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+988A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835290 | ||||||
chr4:15835363
|
CT | C | 98 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0222others(95): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.585+1093delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | |||||
chr4:15835363
|
CTT | C | 73 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0140others(70): Show | 74 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.585+1092_585+1093d others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | |||||
chr4:15835363
|
CTTT | C | 55 | a0001c0001t0001g0153a0001c0001t0001g0328a0001c0001t0002g0052others(52): Show | 58 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.585+1091_585+1093d others(5): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | |||||
chr4:15835363
|
CTTTTT | C | 15 | a0001c0002t0001g0096a0001c0002t0002g0083a0001c0002t0005g0073others(12): Show | 15 | HG00423.hp2 HG00621.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.585+1089_585+1093d others(7): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | |||||
chr4:15835363
|
CTTTTTT | C | 27 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(24): Show | 30 | HG00408.hp2 HG01891.hp1 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.585+1088_585+1093d others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | |||||
chr4:15835363
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0130 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.585+1081_585+1093d others(15): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | |||||
chr4:15835363
|
CTTTTTTT others(7): Show |
C | 16 | a0001c0001t0004g0056a0001c0001t0004g0064a0001c0001t0004g0066others(13): Show | 16 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.585+1080_585+1093d others(16): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | |||||
chr4:15835363
|
CTTTTTTT others(8): Show |
C | 5 | a0001c0001t0009g0178a0001c0001t0026g0060a0001c0001t0026g0061others(2): Show | 5 | HG01243.hp2 HG01433.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.585+1079_585+1093d others(17): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | |||||
chr4:15835363
|
CTTTTTTT others(9): Show |
C | 3 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0062g0108 | 3 | HG02647.hp2 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.585+1078_585+1093d others(18): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 15835363 | |||||
chr4:15835382
|
T | C | 9 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(6): Show | 10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.585+1080T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835382 | ||||||
chr4:15835444
|
C | T | 6 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(3): Show | 6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+1142C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835444 | ||||||
chr4:15835452
|
C | A | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1150C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835452 | ||||||
chr4:15835567
|
G | A | 3 | a0001c0001t0069g0037a0001c0001t0070g0030a0001c0001t0071g0180 | 3 | HG02622.hp2 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.585+1265G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835567 | ||||||
chr4:15835647
|
A | G | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1345A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835647 | ||||||
chr4:15835657
|
C | T | 2 | a0001c0001t0057g0302a0001c0001t0058g0301 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.585+1355C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835657 | ||||||
chr4:15835674
|
G | A | 1 | a0001c0002t0016g0106 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.585+1372G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835674 | ||||||
chr4:15835754
|
T | C | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1452T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835754 | ||||||
chr4:15835759
|
A | G | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1457A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835759 | ||||||
chr4:15835763
|
T | C | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1461T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835763 | ||||||
chr4:15835777
|
T | G | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1475T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835777 | ||||||
chr4:15835964
|
G | A | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1662G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835964 | ||||||
chr4:15835995
|
A | G | 1 | a0001c0001t0043g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.585+1693A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15835995 | ||||||
chr4:15836008
|
A | G | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1706A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836008 | ||||||
chr4:15836015
|
T | G | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.585+1713T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836015 | ||||||
chr4:15836110
|
T | C | 66 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(63): Show | 70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.585+1808T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836110 | ||||||
chr4:15836228
|
T | G | 6 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(3): Show | 6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-1864T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836228 | ||||||
chr4:15836250
|
T | C | 1 | a0001c0002t0007g0098 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.586-1842T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836250 | ||||||
chr4:15836296
|
G | C | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.586-1796G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836296 | ||||||
chr4:15836321
|
G | C | 1 | a0001c0002t0030g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.586-1771G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836321 | ||||||
chr4:15836915
|
T | C | 6 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(3): Show | 6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-1177T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836915 | ||||||
chr4:15836927
|
G | A | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.586-1165G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15836927 | ||||||
chr4:15837098
|
G | A | 1 | a0001c0001t0004g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.586-994G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15837098 | ||||||
chr4:15837186
|
A | C | 6 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(3): Show | 6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-906A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15837186 | ||||||
chr4:15837206
|
C | T | 1 | a0001c0001t0006g0151 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.586-886C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15837206 | ||||||
chr4:15837223
|
G | A | 1 | a0001c0001t0002g0177 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.586-869G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15837223 | ||||||
chr4:15837339
|
C | T | 68 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(65): Show | 72 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.586-753C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15837339 | ||||||
chr4:15837340
|
A | G | 163 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0002g0003others(160): Show | 170 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.586-752A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15837340 | ||||||
chr4:15837748
|
T | C | 6 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(3): Show | 6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-344T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15837748 | ||||||
chr4:15837846
|
C | T | 1 | a0001c0001t0067g0058 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.586-246C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15837846 | ||||||
chr4:15838021
|
G | T | 1 | a0001c0001t0003g0251 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.586-71G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 4/7 | chr4 | 15838021 | ||||||
chr4:15838170
|
A | G | 6 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(3): Show | 6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.659+5A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838170 | ||||||
chr4:15838185
|
C | A | 1 | a0001c0001t0001g0294 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.659+20C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838185 | ||||||
chr4:15838197
|
T | C | 2 | a0001c0001t0002g0008a0001c0001t0002g0191 | 3 | HG00099.hp2 HG01517.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.659+32T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838197 | ||||||
chr4:15838456
|
G | A | 1 | a0001c0001t0002g0318 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.659+291G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838456 | ||||||
chr4:15838568
|
C | T | 6 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(3): Show | 6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.659+403C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838568 | ||||||
chr4:15838620
|
A | G | 66 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(63): Show | 70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.659+455A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838620 | ||||||
chr4:15838644
|
A | C | 1 | a0001c0001t0071g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.659+479A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838644 | ||||||
chr4:15838659
|
T | C | 1 | a0001c0001t0042g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.659+494T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838659 | ||||||
chr4:15838808
|
G | C | 66 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(63): Show | 70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.659+643G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838808 | ||||||
chr4:15838821
|
T | G | 66 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(63): Show | 70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.659+656T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838821 | ||||||
chr4:15838856
|
T | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0289a0001c0006t0001g0011 | 3 | NA18969.hp2 NA18970.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.659+691T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838856 | ||||||
chr4:15838935
|
A | G | 1 | a0001c0001t0002g0191 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.659+770A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15838935 | ||||||
chr4:15839000
|
G | T | 5 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(2): Show | 5 | HG02647.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.659+835G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839000 | ||||||
chr4:15839158
|
G | A | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.660-868G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839158 | ||||||
chr4:15839216
|
A | G | 228 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0153others(225): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.660-810A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839216 | ||||||
chr4:15839244
|
G | A | 1 | a0001c0001t0059g0113 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.660-782G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839244 | ||||||
chr4:15839281
|
G | A | 1 | a0001c0001t0007g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.660-745G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839281 | ||||||
chr4:15839415
|
C | CT | 15 | a0001c0001t0001g0024a0001c0001t0001g0257a0001c0001t0001g0260others(12): Show | 15 | HG01261.hp2 HG02257.hp1 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.660-585dupT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 15839415 | |||||
chr4:15839415
|
CT | C | 51 | a0001c0001t0001g0023a0001c0001t0001g0223a0001c0001t0001g0252others(48): Show | 53 | HG00408.hp2 HG00423.hp2 HG01168.hp2 others(50): Show |
intron_variant | MODIFIER | c.660-585delT | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 15839415 | |||||
chr4:15839415
|
CTT | C | 9 | a0001c0001t0011g0004a0001c0001t0011g0038a0001c0001t0011g0039others(6): Show | 10 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.660-586_660-585del others(2): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 15839415 | |||||
chr4:15839415
|
CTTTTTTT | C | 64 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(61): Show | 68 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.660-591_660-585del others(7): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 15839415 | |||||
chr4:15839419
|
T | C | 1 | a0001c0001t0013g0291 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.660-607T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839419 | ||||||
chr4:15839450
|
G | A | 1 | a0001c0001t0056g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.660-576G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839450 | ||||||
chr4:15839524
|
C | T | 1 | a0001c0001t0047g0185 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.660-502C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839524 | ||||||
chr4:15839688
|
G | C | 1 | a0001c0001t0007g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.660-338G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 5/7 | chr4 | 15839688 | ||||||
chr4:15840164
|
C | T | 6 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(3): Show | 6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.752+46C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 6/7 | chr4 | 15840164 | ||||||
chr4:15840187
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.752+69A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 6/7 | chr4 | 15840187 | ||||||
chr4:15840224
|
C | G | 6 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(3): Show | 6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.752+106C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 6/7 | chr4 | 15840224 | ||||||
chr4:15840268
|
C | A | 17 | a0001c0001t0004g0056a0001c0001t0004g0064a0001c0001t0004g0066others(14): Show | 17 | HG01433.hp2 HG01891.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.752+150C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 6/7 | chr4 | 15840268 | ||||||
chr4:15840280
|
T | G | 1 | a0001c0001t0001g0250 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.752+162T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 6/7 | chr4 | 15840280 | ||||||
chr4:15840369
|
C | G | 1 | a0001c0001t0001g0273 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.753-83C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 6/7 | chr4 | 15840369 | ||||||
chr4:15840662
|
C | T | 5 | a0001c0001t0015g0193a0001c0001t0017g0186a0001c0001t0024g0197others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.839+124C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15840662 | ||||||
chr4:15840674
|
T | C | 3 | a0001c0001t0030g0031a0001c0001t0034g0110a0001c0001t0064g0029 | 3 | HG02257.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.839+136T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15840674 | ||||||
chr4:15841001
|
C | T | 1 | a0001c0001t0004g0066 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.839+463C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841001 | ||||||
chr4:15841242
|
G | A | 1 | a0001c0001t0067g0058 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.839+704G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841242 | ||||||
chr4:15841532
|
TAAAAGCA others(6080): Show |
T | 6 | a0001c0001t0017g0053a0001c0001t0019g0156a0001c0001t0060g0047others(3): Show | 6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.839+1009_840-906de others(1): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15841532 | |||||
chr4:15841584
|
G | A | 1 | a0001c0001t0005g0319 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.839+1046G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841584 | ||||||
chr4:15841620
|
G | C | 1 | a0001c0001t0001g0266 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.839+1082G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841620 | ||||||
chr4:15841621
|
G | A | 1 | a0001c0001t0002g0191 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.839+1083G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841621 | ||||||
chr4:15841650
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.839+1112G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841650 | ||||||
chr4:15841703
|
A | G | 5 | a0001c0001t0006g0121a0001c0001t0006g0131a0001c0001t0006g0132others(2): Show | 5 | HG00408.hp2 NA18970.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.839+1165A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841703 | ||||||
chr4:15841719
|
G | A | 39 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(36): Show | 41 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.839+1181G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841719 | ||||||
chr4:15841729
|
G | A | 1 | a0001c0001t0015g0193 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.839+1191G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841729 | ||||||
chr4:15841873
|
G | A | 164 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0002g0003others(161): Show | 172 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.839+1335G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841873 | ||||||
chr4:15841916
|
C | T | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.839+1378C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841916 | ||||||
chr4:15841917
|
G | T | 1 | a0001c0001t0010g0320 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.839+1379G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841917 | ||||||
chr4:15841966
|
G | A | 2 | a0001c0001t0008g0152a0001c0001t0008g0166 | 2 | NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.839+1428G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841966 | ||||||
chr4:15841972
|
G | A | 1 | a0001c0001t0002g0206 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.839+1434G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15841972 | ||||||
chr4:15842005
|
G | C | 1 | a0001c0001t0042g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.839+1467G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842005 | ||||||
chr4:15842030
|
A | G | 6 | a0001c0001t0002g0124a0001c0001t0002g0139a0001c0001t0002g0161others(3): Show | 6 | NA18956.hp2 NA18966.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.839+1492A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842030 | ||||||
chr4:15842062
|
C | G | 1 | a0001c0001t0002g0177 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.839+1524C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842062 | ||||||
chr4:15842204
|
T | G | 1 | a0001c0001t0002g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.839+1666T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842204 | ||||||
chr4:15842233
|
T | C | 149 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0002g0003others(146): Show | 156 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.839+1695T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842233 | ||||||
chr4:15842258
|
C | A | 2 | a0001c0001t0005g0014a0001c0001t0005g0035 | 2 | NA19068.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.839+1720C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842258 | ||||||
chr4:15842314
|
T | C | 1 | a0001c0001t0004g0229 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.839+1776T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842314 | ||||||
chr4:15842320
|
A | G | 1 | a0001c0001t0004g0229 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.839+1782A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842320 | ||||||
chr4:15842321
|
G | A | 1 | a0001c0001t0004g0229 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.839+1783G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842321 | ||||||
chr4:15842376
|
C | A | 1 | a0001c0001t0003g0311 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.839+1838C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842376 | ||||||
chr4:15842390
|
T | C | 1 | a0001c0001t0003g0311 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.839+1852T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842390 | ||||||
chr4:15842396
|
G | A | 1 | a0001c0001t0003g0311 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.839+1858G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842396 | ||||||
chr4:15842443
|
A | T | 1 | a0001c0001t0003g0311 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.839+1905A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842443 | ||||||
chr4:15842501
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.839+1963G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842501 | ||||||
chr4:15842522
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.839+1984C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842522 | ||||||
chr4:15842523
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.839+1985G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842523 | ||||||
chr4:15842542
|
A | G | 2 | a0001c0001t0003g0012a0001c0001t0003g0322 | 3 | HG00738.hp2 HG01099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.839+2004A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842542 | ||||||
chr4:15842572
|
C | T | 1 | a0001c0002t0030g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.839+2034C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842572 | ||||||
chr4:15842842
|
A | C | 1 | a0001c0001t0010g0312 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.839+2304A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842842 | ||||||
chr4:15842879
|
G | C | 1 | a0001c0001t0022g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.839+2341G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842879 | ||||||
chr4:15842899
|
A | G | 1 | a0001c0001t0033g0194 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.839+2361A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842899 | ||||||
chr4:15842917
|
A | G | 1 | a0001c0001t0022g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.839+2379A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842917 | ||||||
chr4:15842927
|
C | T | 66 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(63): Show | 70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.839+2389C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15842927 | ||||||
chr4:15843061
|
G | A | 20 | a0001c0001t0001g0310a0001c0001t0003g0012a0001c0001t0003g0198others(17): Show | 21 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.839+2523G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843061 | ||||||
chr4:15843078
|
C | T | 1 | a0001c0001t0067g0058 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.839+2540C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843078 | ||||||
chr4:15843080
|
A | G | 7 | a0001c0001t0020g0157a0001c0001t0020g0179a0001c0001t0035g0158others(4): Show | 7 | HG01358.hp2 HG02965.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.839+2542A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843080 | ||||||
chr4:15843101
|
A | G | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.839+2563A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843101 | ||||||
chr4:15843168
|
A | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0269 | 2 | HG00140.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.839+2630A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843168 | ||||||
chr4:15843184
|
A | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0269 | 2 | HG00140.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.839+2646A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843184 | ||||||
chr4:15843213
|
C | A | 1 | a0001c0002t0004g0080 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.839+2675C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843213 | ||||||
chr4:15843248
|
C | T | 1 | a0001c0002t0007g0098 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.839+2710C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843248 | ||||||
chr4:15843288
|
A | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0269 | 2 | HG00140.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.839+2750A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843288 | ||||||
chr4:15843295
|
A | C | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.839+2757A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843295 | ||||||
chr4:15843478
|
G | A | 1 | a0001c0001t0002g0206 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.839+2940G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843478 | ||||||
chr4:15843575
|
A | G | 1 | a0001c0001t0069g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.839+3037A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843575 | ||||||
chr4:15843627
|
A | C | 1 | a0001c0001t0007g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.839+3089A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843627 | ||||||
chr4:15843772
|
T | A | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.839+3234T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843772 | ||||||
chr4:15843818
|
C | A | 40 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(37): Show | 42 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.839+3280C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843818 | ||||||
chr4:15843919
|
C | G | 4 | a0001c0001t0031g0145a0001c0001t0031g0146a0001c0001t0032g0173others(1): Show | 4 | HG00438.hp1 NA18968.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.839+3381C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15843919 | ||||||
chr4:15844325
|
G | A | 66 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(63): Show | 70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.839+3787G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844325 | ||||||
chr4:15844660
|
G | A | 1 | a0001c0001t0067g0058 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.840-3879G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844660 | ||||||
chr4:15844684
|
A | G | 2 | a0001c0001t0003g0012a0001c0001t0003g0322 | 3 | HG00738.hp2 HG01099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.840-3855A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844684 | ||||||
chr4:15844737
|
C | T | 1 | a0001c0001t0003g0305 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.840-3802C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844737 | ||||||
chr4:15844739
|
G | A | 1 | a0001c0001t0042g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.840-3800G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844739 | ||||||
chr4:15844783
|
C | T | 23 | a0001c0001t0001g0024a0001c0001t0002g0003a0001c0001t0002g0013others(20): Show | 24 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.840-3756C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844783 | ||||||
chr4:15844813
|
A | G | 1 | a0001c0002t0001g0155 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.840-3726A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844813 | ||||||
chr4:15844824
|
C | A | 41 | a0001c0001t0065g0101a0001c0002t0001g0090a0001c0002t0001g0091others(38): Show | 43 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.840-3715C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844824 | ||||||
chr4:15844868
|
G | C | 1 | a0001c0001t0038g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.840-3671G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844868 | ||||||
chr4:15844883
|
A | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0236a0001c0001t0001g0237others(2): Show | 6 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.840-3656A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15844883 | ||||||
chr4:15845050
|
T | C | 2 | a0001c0001t0001g0250a0001c0001t0003g0277 | 2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.840-3489T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845050 | ||||||
chr4:15845160
|
T | C | 2 | a0001c0001t0002g0008a0001c0001t0002g0191 | 3 | HG00099.hp2 HG01517.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.840-3379T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845160 | ||||||
chr4:15845234
|
C | T | 66 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(63): Show | 70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.840-3305C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845234 | ||||||
chr4:15845261
|
C | T | 2 | a0001c0001t0030g0031a0001c0001t0064g0029 | 2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.840-3278C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845261 | ||||||
chr4:15845289
|
T | C | 2 | a0001c0001t0001g0250a0001c0001t0003g0277 | 2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.840-3250T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845289 | ||||||
chr4:15845333
|
G | T | 1 | a0001c0001t0001g0310 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.840-3206G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845333 | ||||||
chr4:15845360
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.840-3179C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845360 | ||||||
chr4:15845364
|
G | C | 161 | a0001c0001t0001g0024a0001c0001t0001g0140a0001c0001t0001g0153others(158): Show | 168 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.840-3175G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845364 | ||||||
chr4:15845365
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.840-3174C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845365 | ||||||
chr4:15845406
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.840-3133C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845406 | ||||||
chr4:15845407
|
G | A | 2 | a0001c0001t0001g0250a0001c0001t0003g0277 | 2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.840-3132G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845407 | ||||||
chr4:15845434
|
T | C | 66 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(63): Show | 70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.840-3105T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845434 | ||||||
chr4:15845448
|
C | G | 66 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(63): Show | 70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.840-3091C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845448 | ||||||
chr4:15845502
|
C | G | 66 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(63): Show | 70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.840-3037C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845502 | ||||||
chr4:15845575
|
G | A | 1 | a0001c0001t0071g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.840-2964G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845575 | ||||||
chr4:15845774
|
C | G | 9 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(6): Show | 10 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.840-2765C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845774 | ||||||
chr4:15845935
|
C | CATTCCA | 165 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0002g0003others(162): Show | 173 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.840-2604_840-2603i others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845935 | ||||||
chr4:15845954
|
A | T | 39 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(36): Show | 41 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.840-2585A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845954 | ||||||
chr4:15845963
|
G | A | 1 | a0001c0001t0002g0021 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.840-2576G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15845963 | ||||||
chr4:15846016
|
C | G | 1 | a0001c0001t0042g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.840-2523C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846016 | ||||||
chr4:15846076
|
C | T | 39 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(36): Show | 41 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.840-2463C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846076 | ||||||
chr4:15846090
|
G | A | 1 | a0001c0001t0008g0136 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.840-2449G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846090 | ||||||
chr4:15846094
|
T | C | 8 | a0001c0001t0011g0004a0001c0001t0011g0038a0001c0001t0011g0039others(5): Show | 9 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.840-2445T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846094 | ||||||
chr4:15846170
|
C | A | 219 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0153others(216): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.840-2369C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846170 | ||||||
chr4:15846197
|
T | C | 20 | a0001c0001t0001g0310a0001c0001t0003g0012a0001c0001t0003g0198others(17): Show | 21 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.840-2342T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846197 | ||||||
chr4:15846270
|
T | C | 1 | a0001c0001t0004g0066 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.840-2269T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846270 | ||||||
chr4:15846295
|
C | G | 1 | a0001c0001t0067g0058 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.840-2244C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846295 | ||||||
chr4:15846301
|
A | C | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.840-2238A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846301 | ||||||
chr4:15846305
|
G | A | 1 | a0001c0001t0071g0180 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.840-2234G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846305 | ||||||
chr4:15846394
|
T | C | 1 | a0001c0001t0003g0305 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.840-2145T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846394 | ||||||
chr4:15846413
|
T | G | 1 | a0001c0001t0002g0161 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.840-2126T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846413 | ||||||
chr4:15846456
|
T | C | 1 | a0001c0001t0043g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.840-2083T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846456 | ||||||
chr4:15846494
|
G | A | 20 | a0001c0001t0001g0024a0001c0001t0002g0003a0001c0001t0002g0013others(17): Show | 21 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.840-2045G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846494 | ||||||
chr4:15846510
|
T | C | 9 | a0001c0001t0004g0056a0001c0001t0004g0064a0001c0001t0004g0066others(6): Show | 9 | HG01891.hp2 HG02572.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.840-2029T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846510 | ||||||
chr4:15846578
|
A | G | 39 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(36): Show | 41 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.840-1961A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846578 | ||||||
chr4:15846629
|
A | G | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.840-1910A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846629 | ||||||
chr4:15846630
|
C | A | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.840-1909C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846630 | ||||||
chr4:15846640
|
A | C | 1 | a0001c0001t0006g0284 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.840-1899A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846640 | ||||||
chr4:15846646
|
C | T | 165 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0002g0003others(162): Show | 173 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.840-1893C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846646 | ||||||
chr4:15846740
|
T | C | 1 | a0001c0001t0010g0320 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.840-1799T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846740 | ||||||
chr4:15846887
|
A | G | 14 | a0001c0001t0004g0056a0001c0001t0004g0064a0001c0001t0004g0066others(11): Show | 14 | HG01433.hp2 HG01891.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.840-1652A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846887 | ||||||
chr4:15846928
|
C | T | 91 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0002g0003others(88): Show | 96 | HG00408.hp1 HG00438.hp1 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.840-1611C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846928 | ||||||
chr4:15846984
|
T | G | 2 | a0001c0001t0004g0056a0001c0001t0022g0045 | 2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.840-1555T>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15846984 | ||||||
chr4:15847066
|
A | C | 166 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0002g0003others(163): Show | 174 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.840-1473A>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847066 | ||||||
chr4:15847109
|
C | T | 1 | a0001c0001t0056g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.840-1430C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847109 | ||||||
chr4:15847122
|
C | A | 1 | a0001c0002t0003g0154 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.840-1417C>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847122 | ||||||
chr4:15847122
|
C | T | 3 | a0001c0001t0001g0278a0001c0001t0009g0279a0001c0001t0009g0329 | 3 | NA18982.hp1 NA19006.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.840-1417C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847122 | ||||||
chr4:15847123
|
G | A | 25 | a0001c0001t0001g0024a0001c0001t0002g0003a0001c0001t0002g0013others(22): Show | 26 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.840-1416G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847123 | ||||||
chr4:15847350
|
A | G | 1 | a0001c0001t0006g0286 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.840-1189A>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847350 | ||||||
chr4:15847560
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0067g0058 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.840-972_840-971ins others(16): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847560 | |||||
chr4:15847564
|
A | AAAAAAAT others(10): Show |
1 | a0001c0002t0006g0099 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.840-972_840-971ins others(17): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847564 | |||||
chr4:15847564
|
A | AAAAAATA others(3): Show |
3 | a0001c0001t0020g0157a0001c0001t0020g0179a0001c0001t0036g0160 | 3 | HG03486.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.840-972_840-971ins others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847564 | |||||
chr4:15847565
|
A | AAAAAATA others(9): Show |
33 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(30): Show | 35 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.840-972_840-971ins others(16): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847565 | |||||
chr4:15847565
|
A | AAAAATAA others(8): Show |
2 | a0001c0002t0003g0154a0001c0002t0030g0062 | 2 | HG02074.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.840-972_840-971ins others(15): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847565 | |||||
chr4:15847568
|
T | A | 41 | a0001c0001t0035g0158a0001c0001t0038g0203a0001c0001t0039g0159others(38): Show | 43 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.840-971T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847568 | ||||||
chr4:15847570
|
A | AAAAAT | 3 | a0001c0001t0020g0157a0001c0001t0020g0179a0001c0001t0036g0160 | 3 | HG03486.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.840-964_840-960dup others(5): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847570 | |||||
chr4:15847570
|
A | AATAAATA others(10): Show |
66 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(63): Show | 70 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.840-968_840-967ins others(17): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847570 | |||||
chr4:15847570
|
A | ATAAATAA others(9): Show |
4 | a0001c0001t0035g0158a0001c0001t0038g0203a0001c0001t0039g0159others(1): Show | 4 | HG01358.hp2 HG02965.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.840-969_840-968ins others(16): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847570 | ||||||
chr4:15847595
|
C | CA | 56 | a0001c0001t0001g0011a0001c0001t0001g0140a0001c0001t0001g0225others(53): Show | 56 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.840-916dupA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
C | CAA | 17 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0176others(14): Show | 18 | HG00423.hp1 HG01243.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.840-917_840-916dup others(2): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
C | CAAAA | 12 | a0001c0001t0001g0024a0001c0001t0002g0003a0001c0001t0002g0018others(9): Show | 13 | HG01069.hp1 HG01071.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.840-919_840-916dup others(4): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
C | CAAAAA | 10 | a0001c0001t0002g0013a0001c0001t0002g0016a0001c0001t0002g0017others(7): Show | 10 | HG00408.hp1 HG01109.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.840-920_840-916dup others(5): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
C | CAAAAAAA others(3): Show |
4 | a0001c0001t0004g0056a0001c0001t0015g0070a0001c0001t0022g0045others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.840-925_840-916dup others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
C | CAAAAAAA others(4): Show |
6 | a0001c0001t0009g0178a0001c0001t0026g0060a0001c0001t0026g0061others(3): Show | 6 | HG01433.hp2 HG02257.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.840-926_840-916dup others(11): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
C | CAAAAAAA others(5): Show |
11 | a0001c0001t0004g0066a0001c0001t0034g0110a0001c0002t0001g0090others(8): Show | 11 | HG00408.hp2 HG01928.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.840-927_840-916dup others(12): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
C | CAAAAAAA others(6): Show |
14 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0096others(11): Show | 16 | HG00423.hp2 HG00621.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.840-928_840-916dup others(13): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
C | CAAAAAAA others(7): Show |
5 | a0001c0002t0002g0083a0001c0002t0003g0079a0001c0002t0005g0085others(2): Show | 5 | HG02083.hp1 HG03491.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.840-929_840-916dup others(14): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
C | CAAAAAAA others(9): Show |
1 | a0001c0002t0005g0084 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.840-931_840-916dup others(16): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
C | CAAAAAAA others(11): Show |
1 | a0001c0002t0005g0093 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.840-933_840-916dup others(18): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
CA | C | 12 | a0001c0001t0002g0323a0001c0001t0003g0012a0001c0001t0003g0303others(9): Show | 13 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.840-916delA | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
CAAAAAA | C | 6 | a0001c0001t0016g0063a0001c0001t0017g0068a0001c0001t0020g0157others(3): Show | 6 | HG01891.hp2 HG03130.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.840-921_840-916del others(6): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
CAAAAAAA | C | 33 | a0001c0001t0001g0023a0001c0001t0002g0008a0001c0001t0002g0181others(30): Show | 34 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.840-922_840-916del others(7): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
CAAAAAAA others(1): Show |
C | 7 | a0001c0001t0002g0190a0001c0001t0004g0255a0001c0001t0006g0121others(4): Show | 7 | HG01168.hp2 HG01358.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.840-923_840-916del others(8): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
CAAAAAAA others(2): Show |
C | 8 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0003g0198others(5): Show | 10 | HG00438.hp1 HG03669.hp2 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.840-924_840-916del others(9): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
CAAAAAAA others(3): Show |
C | 56 | a0001c0001t0001g0153a0001c0001t0002g0005a0001c0001t0002g0052others(53): Show | 58 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.840-925_840-916del others(10): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0006g0151 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.840-926_840-916del others(11): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0003g0313 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.840-927_840-916del others(12): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847595
|
CAAAAAAA others(7): Show |
C | 13 | a0001c0001t0004g0050a0001c0001t0011g0004a0001c0001t0011g0038others(10): Show | 14 | HG01106.hp2 HG01192.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.840-929_840-916del others(14): Show |
CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 15847595 | |||||
chr4:15847645
|
G | C | 171 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0002g0003others(168): Show | 179 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.840-894G>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847645 | ||||||
chr4:15847685
|
G | A | 36 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(33): Show | 38 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.840-854G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847685 | ||||||
chr4:15847752
|
T | C | 36 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(33): Show | 38 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.840-787T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847752 | ||||||
chr4:15847763
|
G | A | 8 | a0001c0001t0011g0004a0001c0001t0011g0038a0001c0001t0011g0039others(5): Show | 9 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.840-776G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847763 | ||||||
chr4:15847798
|
A | T | 1 | a0001c0002t0037g0081 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.840-741A>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847798 | ||||||
chr4:15847965
|
C | G | 36 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(33): Show | 38 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.840-574C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847965 | ||||||
chr4:15847977
|
C | T | 2 | a0001c0001t0030g0031a0001c0001t0064g0029 | 2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.840-562C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15847977 | ||||||
chr4:15848106
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.840-433C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848106 | ||||||
chr4:15848140
|
T | A | 21 | a0001c0001t0004g0056a0001c0001t0004g0064a0001c0001t0004g0066others(18): Show | 21 | HG01433.hp2 HG01891.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.840-399T>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848140 | ||||||
chr4:15848178
|
T | C | 13 | a0001c0001t0004g0056a0001c0001t0004g0064a0001c0001t0004g0066others(10): Show | 13 | HG01433.hp2 HG01891.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.840-361T>C | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848178 | ||||||
chr4:15848248
|
C | G | 1 | a0001c0001t0002g0323 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.840-291C>G | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848248 | ||||||
chr4:15848363
|
G | T | 171 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0002g0003others(168): Show | 179 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.840-176G>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848363 | ||||||
chr4:15848367
|
G | A | 1 | a0001c0001t0004g0240 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.840-172G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848367 | ||||||
chr4:15848425
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.840-114C>T | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848425 | ||||||
chr4:15848487
|
G | A | 14 | a0001c0001t0004g0056a0001c0001t0004g0064a0001c0001t0004g0066others(11): Show | 14 | HG01433.hp2 HG01891.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.840-52G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848487 | ||||||
chr4:15848503
|
G | A | 1 | a0001c0001t0065g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.840-36G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848503 | ||||||
chr4:15848511
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.840-28G>A | CD38 | ENSG00000004468.13 | transcript | ENST00000226279.8 | protein_coding | 7/7 | chr4 | 15848511 |