geneid | 957 |
---|---|
ensemblid | ENSG00000187097.13 |
hgncid | 3367 |
symbol | ENTPD5 |
name | ectonucleoside triphosphate diphosphohydrolase 5 (inactive) |
refseq_nuc | NM_001249.5 |
refseq_prot | NP_001240.1 |
ensembl_nuc | ENST00000334696.11 |
ensembl_prot | ENSP00000335246.6 |
mane_status | MANE Select |
chr | chr14 |
start | 73963230 |
end | 74019288 |
strand | - |
ver | v1.2 |
region | chr14:73963230-74019288 |
region5000 | chr14:73958230-74024288 |
regionname0 | ENTPD5_chr14_73963230_74019288 |
regionname5000 | ENTPD5_chr14_73958230_74024288 |
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 | 428 | 371 | 83 | 68 | 154 | 16 | 48 | 120 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0002 | 0/0 | 428 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0003 | 0/0 | 428 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0004 | 0/0 | 428 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
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 | 1287 | 199 | 51 | 24 | 95 | 7 | 20 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
c0002 | 0/0 | 1287 | 168 | 31 | 44 | 57 | 9 | 27 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
c0003 | 0/0 | 1287 | 5 | 5 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
c0004 | 0/0 | 1287 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
c0005 | 0/0 | 1287 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
c0006 | 0/0 | 1287 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
c0007 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
c0008 | 0/0 | 1287 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
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 | 0/1 | 3976 | 62 | 1 | 9 | 43 | 2 | 6 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0002 | 0/0 | 3976 | 57 | 2 | 9 | 32 | 2 | 12 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0003 | 0/0 | 3975 | 44 | 10 | 6 | 15 | 4 | 9 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0004 | 0/0 | 3975 | 39 | 19 | 1 | 9 | 0 | 10 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0005 | 0/0 | 3976 | 36 | 0 | 18 | 10 | 2 | 6 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0006 | 1/0 | 3975 | 32 | 9 | 5 | 11 | 4 | 2 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0007 | 0/0 | 3975 | 24 | 0 | 0 | 24 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0008 | 0/0 | 3975 | 12 | 9 | 3 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0009 | 0/0 | 3972 | 10 | 9 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0010 | 0/0 | 3975 | 7 | 6 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0011 | 0/0 | 3965 | 6 | 6 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0012 | 0/0 | 3974 | 5 | 4 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0013 | 0/0 | 3975 | 4 | 0 | 0 | 4 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0014 | 0/0 | 3975 | 4 | 0 | 3 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0015 | 0/0 | 3975 | 4 | 1 | 3 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0016 | 0/0 | 3974 | 4 | 3 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0017 | 0/0 | 3975 | 4 | 0 | 3 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0018 | 0/0 | 3975 | 3 | 3 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0019 | 0/0 | 3975 | 3 | 2 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0020 | 0/0 | 3976 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0021 | 0/0 | 3975 | 2 | 1 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0022 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0023 | 0/0 | 3975 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0024 | 0/0 | 3975 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0025 | 0/0 | 3975 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0026 | 0/0 | 3974 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0027 | 0/0 | 3975 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0028 | 0/0 | 3975 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0029 | 0/0 | 3976 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0030 | 0/0 | 3975 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0031 | 0/0 | 3975 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0032 | 0/0 | 3975 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0033 | 0/0 | 3975 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0034 | 0/0 | 3976 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0035 | 0/0 | 3975 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0036 | 0/0 | 3975 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
t0037 | 0/0 | 3975 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
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 | 2 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0007 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
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 | 1287 | 199 | 51 | 24 | 95 | 7 | 20 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0002 | 0/0 | 1287 | 168 | 31 | 44 | 57 | 9 | 27 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0005 | 0/0 | 1287 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0007 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0008 | 0/0 | 1287 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0002c0003 | 0/0 | 1287 | 5 | 5 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0003c0004 | 0/0 | 1287 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0004c0006 | 0/0 | 1287 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5262 | 62 | 1 | 9 | 43 | 2 | 6 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0004 | 0/0 | 5261 | 37 | 17 | 1 | 9 | 0 | 10 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0005 | 0/0 | 5262 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0006 | 1/0 | 5261 | 30 | 7 | 5 | 11 | 4 | 2 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0007 | 0/0 | 5261 | 24 | 0 | 0 | 24 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0011 | 0/0 | 5251 | 6 | 6 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0012 | 0/0 | 5260 | 5 | 4 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0013 | 0/0 | 5261 | 4 | 0 | 0 | 4 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0014 | 0/0 | 5261 | 4 | 0 | 3 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0015 | 0/0 | 5261 | 4 | 1 | 3 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0016 | 0/0 | 5260 | 4 | 3 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0018 | 0/0 | 5261 | 3 | 3 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0019 | 0/0 | 5261 | 3 | 2 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0022 | 0/0 | 5251 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0023 | 0/0 | 5261 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0024 | 0/0 | 5261 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0025 | 0/0 | 5261 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0026 | 0/0 | 5260 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0028 | 0/0 | 5261 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0030 | 0/0 | 5261 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0031 | 0/0 | 5261 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0032 | 0/0 | 5261 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0033 | 0/0 | 5261 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0034 | 0/0 | 5262 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0001t0035 | 0/0 | 5261 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0002t0002 | 0/0 | 5262 | 54 | 2 | 9 | 30 | 2 | 11 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0002t0003 | 0/0 | 5261 | 44 | 10 | 6 | 15 | 4 | 9 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0002t0005 | 0/0 | 5262 | 35 | 0 | 18 | 9 | 2 | 6 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0002t0008 | 0/0 | 5261 | 12 | 9 | 3 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0002t0009 | 0/0 | 5258 | 4 | 3 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0002t0010 | 0/0 | 5261 | 7 | 6 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0002t0017 | 0/0 | 5261 | 4 | 0 | 3 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0002t0020 | 0/0 | 5262 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0002t0021 | 0/0 | 5261 | 2 | 1 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0002t0027 | 0/0 | 5261 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0002t0029 | 0/0 | 5262 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0002t0036 | 0/0 | 5261 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0002t0037 | 0/0 | 5261 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0005t0002 | 0/0 | 5262 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0007t0009 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0001c0008t0002 | 0/0 | 5262 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0002c0003t0009 | 0/0 | 5258 | 5 | 5 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0003c0004t0006 | 0/0 | 5261 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
a0004c0006t0004 | 0/0 | 5261 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | copy fasta | chr14 | 73958230 | 74024288 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0011g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0011g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0011g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0011g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0012g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0012g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0012g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0012g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0012g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0013g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0013g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0013g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0013g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0014g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0014g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0014g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0014g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0015g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0015g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0015g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0016g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0016g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0016g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0016g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0018g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0018g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0019g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0019g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0022g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0023g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0024g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0025g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0026g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0028g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0030g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0031g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0032g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0033g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0034g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0035g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0007 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0009g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0009g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0009g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0010g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0010g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0017g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0017g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0017g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0020g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0020g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0021g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0021g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0027g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0029g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0036g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0037g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0005t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0005t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0007t0009g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0008t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0002c0003t0009g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0002c0003t0009g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0002c0003t0009g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0002c0003t0009g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0003c0004t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0003c0004t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0004c0006t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0014 | g0258 | EUR | GBR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00099 | hp2 | a0001 | c0002 | t0003 | g0084 | EUR | GBR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00280 | hp1 | a0001 | c0002 | t0017 | g0006 | EUR | FIN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00280 | hp2 | a0001 | c0002 | t0005 | g0002 | EUR | FIN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00323 | hp1 | a0001 | c0002 | t0005 | g0031 | EUR | FIN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | FIN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0311 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0252 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0322 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00438 | hp1 | a0001 | c0001 | t0013 | g0247 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00438 | hp2 | a0001 | c0001 | t0007 | g0153 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00558 | hp2 | a0001 | c0002 | t0003 | g0096 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00639 | hp1 | a0001 | c0002 | t0003 | g0120 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00639 | hp2 | a0001 | c0002 | t0005 | g0003 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00642 | hp1 | a0001 | c0002 | t0003 | g0088 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0338 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0310 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0071 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0337 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00738 | hp1 | a0001 | c0002 | t0003 | g0074 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00738 | hp2 | a0001 | c0001 | t0014 | g0260 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00741 | hp1 | a0001 | c0002 | t0005 | g0046 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00741 | hp2 | a0001 | c0001 | t0014 | g0259 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0331 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01070 | hp1 | a0001 | c0002 | t0005 | g0019 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01070 | hp2 | a0001 | c0001 | t0006 | g0272 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01071 | hp2 | a0001 | c0002 | t0005 | g0002 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01074 | hp1 | a0001 | c0001 | t0015 | g0008 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0237 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01081 | hp1 | a0001 | c0001 | t0019 | g0209 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01099 | hp1 | a0001 | c0001 | t0015 | g0122 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01099 | hp2 | a0001 | c0002 | t0005 | g0025 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01106 | hp1 | a0001 | c0002 | t0005 | g0032 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0063 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01109 | hp1 | a0001 | c0002 | t0008 | g0344 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01109 | hp2 | a0001 | c0002 | t0009 | g0227 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01167 | hp1 | a0001 | c0002 | t0005 | g0024 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0303 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0294 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01168 | hp2 | a0001 | c0002 | t0005 | g0050 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01169 | hp1 | a0001 | c0002 | t0005 | g0035 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0315 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01175 | hp1 | a0001 | c0001 | t0014 | g0268 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01175 | hp2 | a0001 | c0001 | t0015 | g0121 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0274 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01243 | hp1 | a0001 | c0002 | t0008 | g0055 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01243 | hp2 | a0001 | c0002 | t0010 | g0220 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01255 | hp1 | a0001 | c0001 | t0006 | g0061 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01255 | hp2 | a0001 | c0002 | t0017 | g0006 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01256 | hp1 | a0001 | c0002 | t0029 | g0028 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01258 | hp1 | a0001 | c0002 | t0017 | g0090 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01261 | hp1 | a0001 | c0002 | t0005 | g0042 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01261 | hp2 | a0001 | c0002 | t0003 | g0225 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0308 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01346 | hp2 | a0001 | c0002 | t0005 | g0033 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0316 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01358 | hp2 | a0001 | c0002 | t0003 | g0079 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01433 | hp1 | a0001 | c0001 | t0035 | g0026 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01433 | hp2 | a0001 | c0002 | t0037 | g0097 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01496 | hp2 | a0001 | c0002 | t0008 | g0341 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0105 | EUR | IBS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0062 | EUR | IBS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01516 | hp1 | a0001 | c0002 | t0003 | g0007 | EUR | IBS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0321 | EUR | IBS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01517 | hp1 | a0001 | c0002 | t0003 | g0106 | EUR | IBS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01517 | hp2 | a0001 | c0001 | t0006 | g0058 | EUR | IBS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0217 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0211 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01891 | hp1 | a0003 | c0004 | t0006 | g0112 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01891 | hp2 | a0004 | c0006 | t0004 | g0013 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01928 | hp2 | a0001 | c0002 | t0005 | g0027 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01934 | hp1 | a0001 | c0002 | t0005 | g0029 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01934 | hp2 | a0001 | c0002 | t0003 | g0086 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01943 | hp2 | a0001 | c0002 | t0005 | g0052 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01978 | hp1 | a0001 | c0002 | t0005 | g0047 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01978 | hp2 | a0001 | c0002 | t0021 | g0073 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01981 | hp1 | a0001 | c0002 | t0005 | g0030 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0356 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02040 | hp1 | a0001 | c0002 | t0003 | g0081 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02040 | hp2 | a0001 | c0002 | t0005 | g0036 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0098 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02055 | hp2 | a0002 | c0003 | t0009 | g0067 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02071 | hp1 | a0001 | c0001 | t0007 | g0053 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02080 | hp1 | a0001 | c0001 | t0007 | g0161 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0312 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02129 | hp1 | a0001 | c0002 | t0005 | g0038 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02132 | hp2 | a0001 | c0002 | t0003 | g0082 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0336 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02145 | hp1 | a0001 | c0002 | t0008 | g0345 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02145 | hp2 | a0001 | c0002 | t0003 | g0358 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02148 | hp1 | a0001 | c0002 | t0005 | g0003 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02148 | hp2 | a0001 | c0002 | t0017 | g0069 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02155 | hp1 | a0001 | c0001 | t0006 | g0280 | EAS | CDX | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | CDX | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02165 | hp1 | a0001 | c0002 | t0005 | g0044 | EAS | CDX | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CDX | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02257 | hp1 | a0002 | c0003 | t0009 | g0066 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02257 | hp2 | a0001 | c0002 | t0003 | g0075 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0134 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0207 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02280 | hp1 | a0001 | c0001 | t0011 | g0136 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02280 | hp2 | a0001 | c0002 | t0003 | g0099 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02451 | hp1 | a0001 | c0002 | t0003 | g0095 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02523 | hp1 | a0001 | c0001 | t0007 | g0318 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0111 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02572 | hp2 | a0001 | c0001 | t0012 | g0128 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02602 | hp1 | a0001 | c0002 | t0005 | g0039 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0267 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02622 | hp1 | a0001 | c0001 | t0022 | g0137 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02622 | hp2 | a0001 | c0001 | t0012 | g0360 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0212 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02630 | hp2 | a0001 | c0002 | t0008 | g0340 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02647 | hp1 | a0001 | c0001 | t0012 | g0127 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02647 | hp2 | a0001 | c0001 | t0015 | g0008 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02683 | hp2 | a0001 | c0002 | t0003 | g0076 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0241 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02717 | hp2 | a0001 | c0001 | t0012 | g0361 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02723 | hp1 | a0002 | c0003 | t0009 | g0004 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02723 | hp2 | a0001 | c0002 | t0008 | g0056 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02735 | hp1 | a0001 | c0002 | t0005 | g0040 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02735 | hp2 | a0001 | c0001 | t0030 | g0118 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0332 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02738 | hp2 | a0001 | c0002 | t0005 | g0049 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02809 | hp1 | a0001 | c0002 | t0003 | g0215 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0219 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02818 | hp1 | a0001 | c0001 | t0026 | g0018 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02818 | hp2 | a0001 | c0001 | t0025 | g0130 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02886 | hp1 | a0002 | c0003 | t0009 | g0065 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02895 | hp1 | a0001 | c0002 | t0003 | g0083 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02895 | hp2 | a0001 | c0002 | t0010 | g0224 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02897 | hp1 | a0001 | c0002 | t0010 | g0222 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02897 | hp2 | a0001 | c0002 | t0003 | g0080 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02922 | hp1 | a0001 | c0001 | t0011 | g0132 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02922 | hp2 | a0001 | c0001 | t0018 | g0270 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02965 | hp1 | a0001 | c0001 | t0011 | g0131 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02965 | hp2 | a0001 | c0001 | t0023 | g0129 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02970 | hp1 | a0001 | c0001 | t0016 | g0068 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0228 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02976 | hp1 | a0001 | c0001 | t0018 | g0005 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02976 | hp2 | a0001 | c0002 | t0008 | g0339 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03017 | hp2 | a0001 | c0002 | t0003 | g0265 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03041 | hp1 | a0001 | c0002 | t0008 | g0054 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0214 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0124 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0213 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0208 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03139 | hp1 | a0001 | c0001 | t0028 | g0218 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03139 | hp2 | a0004 | c0006 | t0004 | g0013 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03195 | hp2 | a0001 | c0002 | t0009 | g0016 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03209 | hp2 | a0001 | c0002 | t0008 | g0342 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0298 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03239 | hp2 | a0001 | c0002 | t0003 | g0085 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03453 | hp1 | a0001 | c0001 | t0011 | g0135 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03453 | hp2 | a0001 | c0002 | t0009 | g0016 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03486 | hp2 | a0001 | c0002 | t0010 | g0223 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03490 | hp1 | a0001 | c0002 | t0003 | g0101 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0113 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0295 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03491 | hp2 | a0001 | c0002 | t0005 | g0034 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03492 | hp1 | a0001 | c0002 | t0005 | g0045 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03492 | hp2 | a0001 | c0002 | t0003 | g0102 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03540 | hp1 | a0001 | c0001 | t0019 | g0014 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03540 | hp2 | a0001 | c0002 | t0010 | g0015 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03579 | hp1 | a0001 | c0002 | t0008 | g0271 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03579 | hp2 | a0001 | c0001 | t0024 | g0285 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03654 | hp1 | a0001 | c0002 | t0003 | g0072 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03654 | hp2 | a0001 | c0002 | t0003 | g0070 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03669 | hp1 | a0001 | c0002 | t0003 | g0103 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0251 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0328 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0264 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03704 | hp1 | a0001 | c0002 | t0003 | g0266 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03704 | hp2 | a0001 | c0008 | t0002 | g0324 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0262 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0297 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0242 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03927 | hp1 | a0001 | c0002 | t0036 | g0037 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0288 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03942 | hp1 | a0001 | c0002 | t0005 | g0048 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0263 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0334 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0244 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04184 | hp1 | a0001 | c0001 | t0012 | g0138 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04184 | hp2 | a0001 | c0001 | t0006 | g0057 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0314 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0243 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0256 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0333 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04228 | hp1 | a0001 | c0001 | t0006 | g0059 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0249 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0238 | AFR | YRI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0210 | AFR | YRI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18612 | hp1 | a0001 | c0001 | t0006 | g0279 | EAS | CHB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18906 | hp1 | a0001 | c0002 | t0010 | g0015 | AFR | YRI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18906 | hp2 | a0001 | c0002 | t0009 | g0226 | AFR | YRI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0287 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18944 | hp1 | a0001 | c0001 | t0006 | g0282 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0351 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18946 | hp2 | a0001 | c0001 | t0007 | g0216 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18947 | hp1 | a0001 | c0002 | t0003 | g0116 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0352 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0323 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18948 | hp2 | a0001 | c0001 | t0007 | g0173 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0330 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18952 | hp1 | a0001 | c0002 | t0003 | g0078 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18952 | hp2 | a0001 | c0001 | t0006 | g0277 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18953 | hp1 | a0001 | c0005 | t0002 | g0347 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18953 | hp2 | a0001 | c0001 | t0007 | g0183 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0305 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0309 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18957 | hp2 | a0001 | c0002 | t0005 | g0141 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18959 | hp1 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18959 | hp2 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18960 | hp1 | a0001 | c0005 | t0002 | g0346 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18960 | hp2 | a0001 | c0001 | t0007 | g0199 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18961 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18961 | hp2 | a0001 | c0001 | t0007 | g0143 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18962 | hp1 | a0001 | c0002 | t0003 | g0100 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0353 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18967 | hp2 | a0001 | c0002 | t0005 | g0020 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18969 | hp2 | a0001 | c0001 | t0007 | g0201 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18971 | hp2 | a0001 | c0002 | t0020 | g0289 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18974 | hp1 | a0001 | c0001 | t0032 | g0166 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18974 | hp2 | a0001 | c0001 | t0013 | g0269 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18975 | hp1 | a0001 | c0001 | t0007 | g0313 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18981 | hp1 | a0001 | c0001 | t0013 | g0240 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0327 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18982 | hp2 | a0001 | c0001 | t0007 | g0010 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0350 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18984 | hp1 | a0001 | c0002 | t0003 | g0104 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18984 | hp2 | a0001 | c0001 | t0007 | g0197 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18985 | hp2 | a0001 | c0002 | t0002 | g0326 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18986 | hp2 | a0001 | c0001 | t0004 | g0348 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18988 | hp1 | a0001 | c0002 | t0003 | g0117 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0301 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18994 | hp1 | a0001 | c0002 | t0005 | g0051 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18994 | hp2 | a0001 | c0002 | t0027 | g0317 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19001 | hp1 | a0001 | c0001 | t0006 | g0283 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0319 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19002 | hp2 | a0001 | c0001 | t0007 | g0195 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19004 | hp1 | a0001 | c0002 | t0003 | g0093 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0307 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19007 | hp1 | a0001 | c0002 | t0020 | g0290 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19007 | hp2 | a0001 | c0002 | t0003 | g0094 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19010 | hp1 | a0001 | c0002 | t0005 | g0022 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19010 | hp2 | a0001 | c0001 | t0006 | g0276 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0354 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19030 | hp1 | a0001 | c0001 | t0016 | g0114 | AFR | LWK | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19030 | hp2 | a0001 | c0002 | t0008 | g0362 | AFR | LWK | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19043 | hp1 | a0001 | c0001 | t0016 | g0119 | AFR | LWK | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19043 | hp2 | a0001 | c0002 | t0003 | g0359 | AFR | LWK | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19054 | hp1 | a0001 | c0001 | t0007 | g0200 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0355 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19056 | hp2 | a0001 | c0002 | t0003 | g0092 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19057 | hp2 | a0001 | c0001 | t0006 | g0273 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19058 | hp2 | a0001 | c0001 | t0006 | g0281 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19063 | hp1 | a0001 | c0001 | t0031 | g0248 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19063 | hp2 | a0001 | c0001 | t0007 | g0147 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19065 | hp1 | a0001 | c0001 | t0007 | g0010 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0302 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19067 | hp1 | a0001 | c0001 | t0006 | g0278 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19067 | hp2 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19070 | hp1 | a0001 | c0002 | t0005 | g0021 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19070 | hp2 | a0001 | c0001 | t0007 | g0146 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19074 | hp1 | a0001 | c0001 | t0006 | g0275 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19074 | hp2 | a0001 | c0002 | t0003 | g0077 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19075 | hp2 | a0001 | c0002 | t0002 | g0349 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19077 | hp1 | a0001 | c0001 | t0006 | g0284 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19077 | hp2 | a0001 | c0001 | t0013 | g0246 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19078 | hp1 | a0001 | c0002 | t0002 | g0325 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19078 | hp2 | a0001 | c0001 | t0007 | g0175 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19079 | hp1 | a0001 | c0002 | t0003 | g0123 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0329 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19080 | hp2 | a0001 | c0001 | t0007 | g0188 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19081 | hp1 | a0001 | c0001 | t0034 | g0232 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19082 | hp2 | a0001 | c0002 | t0005 | g0023 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19084 | hp1 | a0001 | c0002 | t0003 | g0089 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19084 | hp2 | a0001 | c0001 | t0007 | g0159 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19085 | hp2 | a0001 | c0002 | t0003 | g0107 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19088 | hp1 | a0001 | c0001 | t0007 | g0291 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19091 | hp1 | a0001 | c0001 | t0007 | g0172 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0296 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19240 | hp1 | a0001 | c0001 | t0033 | g0108 | AFR | YRI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19240 | hp2 | a0001 | c0002 | t0008 | g0343 | AFR | YRI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA20129 | hp1 | a0002 | c0003 | t0009 | g0004 | AFR | ASW | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA20129 | hp2 | a0001 | c0002 | t0003 | g0007 | AFR | ASW | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | TSI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0148 | EUR | TSI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0306 | EUR | TSI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA20805 | hp2 | a0001 | c0002 | t0003 | g0091 | EUR | TSI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01123 | hp1 | a0001 | c0001 | t0016 | g0115 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01123 | hp2 | a0001 | c0002 | t0005 | g0043 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0236 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02486 | hp1 | a0001 | c0002 | t0010 | g0221 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02486 | hp2 | a0001 | c0007 | t0009 | g0064 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02559 | hp2 | a0001 | c0001 | t0018 | g0005 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03471 | hp1 | a0001 | c0001 | t0019 | g0014 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG06807 | hp1 | a0001 | c0002 | t0003 | g0357 | AFR | USA | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG06807 | hp2 | a0001 | c0001 | t0011 | g0133 | AFR | USA | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA20300 | hp1 | a0001 | c0002 | t0021 | g0087 | AFR | USA | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0109 | AFR | USA | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA21309 | hp1 | a0003 | c0004 | t0006 | g0110 | AFR | LWK | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0300 | AFR | LWK | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0179 | REF | REF | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0060 | REF | REF | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73972970
|
T | C | 1 | a0002 | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp1 others(2): Show |
missense_variant | MODERATE | c.941A>G | p.Lys314Arg | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/16 | 1217/5261 | 941/1287 | 314/428 | chr14 | 73972970 | ||
chr14:73987972
|
C | G | 1 | a0003 | 2 | HG01891.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.131G>C | p.Ser44Thr | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/16 | 407/5261 | 131/1287 | 44/428 | chr14 | 73987972 | ||
chr14:73987978
|
T | C | 1 | a0004 | 2 | HG01891.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.125A>G | p.Asn42Ser | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/16 | 401/5261 | 125/1287 | 42/428 | chr14 | 73987978 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73972936
|
G | A | 1 | a0001c0008 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.975C>T | p.Ser325Ser | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/16 | 1251/5261 | 975/1287 | 325/428 | chr14 | 73972936 | ||
chr14:73972990
|
C | G | 2 | a0001c0007a0002c0003 | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
synonymous_variant | LOW | c.921G>C | p.Val307Val | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/16 | 1197/5261 | 921/1287 | 307/428 | chr14 | 73972990 | ||
chr14:73974981
|
G | A | 5 | a0001c0002a0001c0005a0001c0007others(2): Show | 177 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
synonymous_variant | LOW | c.727C>T | p.Leu243Leu | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/16 | 1003/5261 | 727/1287 | 243/428 | chr14 | 73974981 | ||
chr14:73983150
|
G | A | 1 | a0001c0005 | 2 | NA18953.hp1 NA18960.hp1 |
synonymous_variant | LOW | c.309C>T | p.Thr103Thr | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/16 | 585/5261 | 309/1287 | 103/428 | chr14 | 73983150 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73963280
|
C | T | 1 | a0001c0002t0010 | 7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3648G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 3648 | chr14 | 73963280 | |||||
chr14:73963436
|
G | A | 1 | a0001c0001t0033 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3492C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 3492 | chr14 | 73963436 | |||||
chr14:73963583
|
C | T | 1 | a0001c0001t0015 | 4 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3345G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 3345 | chr14 | 73963583 | |||||
chr14:73963744
|
C | T | 11 | a0001c0002t0002a0001c0002t0003a0001c0002t0008others(8): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*3184G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 3184 | chr14 | 73963744 | |||||
chr14:73964185
|
T | C | 1 | a0001c0001t0031 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2743A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2743 | chr14 | 73964185 | |||||
chr14:73964214
|
CAAT | C | 2 | a0001c0001t0011a0001c0001t0022 | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2711_*2713delATT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2711 | chr14 | 73964214 | |||||
chr14:73964250
|
A | G | 2 | a0001c0001t0013a0001c0001t0031 | 5 | HG00438.hp1 NA18974.hp2 NA18981.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2678T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2678 | chr14 | 73964250 | |||||
chr14:73964297
|
T | G | 1 | a0001c0002t0017 | 4 | HG00280.hp1 HG01255.hp2 HG01258.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2631A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2631 | chr14 | 73964297 | |||||
chr14:73964299
|
T | G | 1 | a0001c0001t0032 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2629A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2629 | chr14 | 73964299 | |||||
chr14:73964488
|
A | G | 18 | a0001c0001t0005a0001c0002t0002a0001c0002t0003others(15): Show | 178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*2440T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2440 | chr14 | 73964488 | |||||
chr14:73964725
|
G | A | 2 | a0001c0001t0007a0001c0001t0032 | 25 | HG00438.hp2 HG02071.hp1 HG02080.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2203C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2203 | chr14 | 73964725 | |||||
chr14:73964788
|
ATTT | A | 3 | a0001c0002t0009a0001c0007t0009a0002c0003t0009 | 10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2137_*2139delAAA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2137 | chr14 | 73964788 | |||||
chr14:73964860
|
A | AT | 3 | a0001c0001t0001a0001c0001t0034a0001c0001t0035 | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2067dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2067 | chr14 | 73964860 | |||||
chr14:73964905
|
A | G | 2 | a0001c0002t0036a0001c0002t0037 | 2 | HG01433.hp2 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2023T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2023 | chr14 | 73964905 | |||||
chr14:73965192
|
C | T | 1 | a0001c0001t0030 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1736G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1736 | chr14 | 73965192 | |||||
chr14:73965268
|
AGAGGATG | A | 2 | a0001c0001t0011a0001c0001t0022 | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1653_*1659delCATC others(3): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1653 | chr14 | 73965268 | |||||
chr14:73965363
|
C | T | 1 | a0001c0001t0023 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1565G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1565 | chr14 | 73965363 | |||||
chr14:73965415
|
G | A | 1 | a0001c0001t0012 | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1513C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1513 | chr14 | 73965415 | |||||
chr14:73965415
|
G | C | 1 | a0001c0001t0014 | 4 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1513C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1513 | chr14 | 73965415 | |||||
chr14:73965455
|
G | A | 5 | a0001c0002t0002a0001c0002t0020a0001c0002t0027others(2): Show | 60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1473C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1473 | chr14 | 73965455 | |||||
chr14:73965459
|
T | C | 10 | a0001c0002t0002a0001c0002t0003a0001c0002t0017others(7): Show | 112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1469A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1469 | chr14 | 73965459 | |||||
chr14:73965505
|
T | C | 1 | a0001c0002t0037 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1423A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1423 | chr14 | 73965505 | |||||
chr14:73965527
|
A | G | 1 | a0001c0001t0034 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1401T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1401 | chr14 | 73965527 | |||||
chr14:73965562
|
C | A | 11 | a0001c0002t0002a0001c0002t0003a0001c0002t0008others(8): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1366G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1366 | chr14 | 73965562 | |||||
chr14:73965720
|
C | CA | 4 | a0001c0002t0002a0001c0002t0020a0001c0005t0002others(1): Show | 59 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1207dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1207 | chr14 | 73965720 | |||||
chr14:73965727
|
A | G | 5 | a0001c0002t0003a0001c0002t0017a0001c0002t0021others(2): Show | 52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1201T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1201 | chr14 | 73965727 | |||||
chr14:73965892
|
G | A | 1 | a0001c0002t0029 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1036C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1036 | chr14 | 73965892 | |||||
chr14:73966282
|
C | G | 2 | a0001c0001t0023a0001c0001t0024 | 2 | HG02965.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*646G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 646 | chr14 | 73966282 | |||||
chr14:73966299
|
T | G | 1 | a0001c0001t0019 | 3 | HG01081.hp1 HG03471.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*629A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 629 | chr14 | 73966299 | |||||
chr14:73966300
|
T | C | 1 | a0001c0001t0019 | 3 | HG01081.hp1 HG03471.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*628A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 628 | chr14 | 73966300 | |||||
chr14:73966409
|
A | G | 1 | a0001c0002t0020 | 2 | NA18971.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*519T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 519 | chr14 | 73966409 | |||||
chr14:73966422
|
T | C | 1 | a0001c0002t0021 | 2 | HG01978.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*506A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 506 | chr14 | 73966422 | |||||
chr14:73966426
|
C | A | 3 | a0001c0001t0001a0001c0001t0034a0001c0001t0035 | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*502G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 502 | chr14 | 73966426 | |||||
chr14:73966435
|
C | T | 26 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(23): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*493G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 493 | chr14 | 73966435 | |||||
chr14:73966438
|
T | C | 7 | a0001c0001t0005a0001c0002t0005a0001c0002t0009others(4): Show | 54 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*490A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 490 | chr14 | 73966438 | |||||
chr14:73966468
|
G | GT | 3 | a0001c0001t0005a0001c0002t0005a0001c0002t0029 | 37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*459dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 459 | chr14 | 73966468 | |||||
chr14:73966468
|
GT | G | 4 | a0001c0001t0012a0001c0001t0016a0001c0001t0026others(1): Show | 11 | HG01123.hp1 HG01433.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*459delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 459 | chr14 | 73966468 | |||||
chr14:73966646
|
C | T | 1 | a0001c0001t0028 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*282G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 282 | chr14 | 73966646 | |||||
chr14:73966849
|
A | T | 11 | a0001c0002t0002a0001c0002t0003a0001c0002t0008others(8): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*79T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 79 | chr14 | 73966849 | |||||
chr14:73966861
|
A | G | 1 | a0001c0001t0012 | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*67T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 67 | chr14 | 73966861 | |||||
chr14:73966881
|
C | T | 1 | a0001c0001t0022 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*47G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 47 | chr14 | 73966881 | |||||
chr14:73966903
|
C | G | 1 | a0001c0001t0026 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*25G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 25 | chr14 | 73966903 | |||||
chr14:73966908
|
C | T | 3 | a0001c0001t0023a0001c0001t0024a0001c0001t0025 | 3 | HG02818.hp2 HG02965.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*20G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 20 | chr14 | 73966908 | |||||
chr14:73988110
|
C | A | 3 | a0001c0001t0001a0001c0001t0034a0001c0001t0035 | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(61): Show |
5_prime_UTR_variant | MODIFIER | c.-8G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/16 | 8 | chr14 | 73988110 | |||||
chr14:73988116
|
T | A | 5 | a0001c0002t0003a0001c0002t0017a0001c0002t0021others(2): Show | 52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
5_prime_UTR_variant | MODIFIER | c.-14A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/16 | 14 | chr14 | 73988116 | |||||
chr14:74015893
|
A | C | 1 | a0001c0001t0018 | 3 | HG02559.hp2 HG02922.hp2 HG02976.hp1 |
5_prime_UTR_variant | MODIFIER | c.-200T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/16 | 27791 | chr14 | 74015893 | |||||
chr14:74015895
|
A | G | 2 | a0001c0001t0011a0001c0001t0022 | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-202T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/16 | 27793 | chr14 | 74015895 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73967156
|
T | C | 122 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1201-142A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967156 | ||||||
chr14:73967183
|
C | T | 2 | a0001c0002t0008g0054a0001c0002t0008g0055 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1201-169G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967183 | ||||||
chr14:73967760
|
A | C | 1 | a0001c0001t0001g0180 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1201-746T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967760 | ||||||
chr14:73967799
|
CA | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(222): Show | 236 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.1201-786delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967799 | ||||||
chr14:73967799
|
CAA | C | 51 | a0001c0001t0007g0201a0001c0002t0003g0007a0001c0002t0003g0070others(48): Show | 53 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.1201-787_1201-786d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967799 | ||||||
chr14:73967799
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0002t0002g0287a0001c0002t0002g0329a0001c0002t0002g0330 | 3 | NA18941.hp2 NA18950.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1201-795_1201-786d others(12): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967799 | ||||||
chr14:73967813
|
A | G | 1 | a0001c0002t0002g0332 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1201-799T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967813 | ||||||
chr14:73967817
|
A | G | 12 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1201-803T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967817 | ||||||
chr14:73967818
|
G | A | 12 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1201-804C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967818 | ||||||
chr14:73967832
|
C | T | 12 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1201-818G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967832 | ||||||
chr14:73967911
|
G | A | 1 | a0001c0001t0011g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1201-897C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967911 | ||||||
chr14:73967920
|
T | A | 122 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1201-906A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967920 | ||||||
chr14:73968325
|
G | A | 49 | a0001c0001t0005g0041a0001c0002t0005g0002a0001c0002t0005g0003others(46): Show | 54 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1201-1311C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968325 | ||||||
chr14:73968425
|
CT | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(191): Show | 207 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1201-1412delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968425 | ||||||
chr14:73968425
|
CTT | C | 118 | a0001c0001t0001g0157a0001c0002t0002g0098a0001c0002t0002g0113others(115): Show | 120 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1201-1413_1201-141 others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968425 | ||||||
chr14:73968667
|
C | T | 35 | a0001c0001t0005g0041a0001c0002t0005g0002a0001c0002t0005g0003others(32): Show | 37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1200+1343G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968667 | ||||||
chr14:73968674
|
C | G | 2 | a0001c0001t0004g0125a0001c0001t0004g0126 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1200+1336G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968674 | ||||||
chr14:73968705
|
C | T | 1 | a0001c0001t0011g0132 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1200+1305G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968705 | ||||||
chr14:73968765
|
A | G | 1 | a0001c0001t0006g0279 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1200+1245T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968765 | ||||||
chr14:73968780
|
A | G | 35 | a0001c0001t0005g0041a0001c0002t0005g0002a0001c0002t0005g0003others(32): Show | 37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1200+1230T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968780 | ||||||
chr14:73968816
|
C | T | 1 | a0001c0001t0030g0118 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1200+1194G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968816 | ||||||
chr14:73968820
|
A | C | 1 | a0001c0001t0028g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1200+1190T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968820 | ||||||
chr14:73968912
|
G | C | 68 | a0001c0001t0004g0017a0001c0001t0004g0125a0001c0001t0004g0126others(65): Show | 71 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1200+1098C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968912 | ||||||
chr14:73969156
|
T | C | 25 | a0001c0001t0006g0105a0001c0001t0006g0109a0001c0001t0006g0124others(22): Show | 27 | HG01070.hp2 HG01074.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.1200+854A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969156 | ||||||
chr14:73969211
|
C | T | 6 | a0001c0002t0010g0015a0001c0002t0010g0220a0001c0002t0010g0221others(3): Show | 7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+799G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969211 | ||||||
chr14:73969255
|
G | C | 5 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200+755C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969255 | ||||||
chr14:73969261
|
C | A | 5 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200+749G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969261 | ||||||
chr14:73969332
|
G | A | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1200+678C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969332 | ||||||
chr14:73969440
|
C | G | 2 | a0001c0001t0004g0017a0001c0001t0004g0228 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1200+570G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969440 | ||||||
chr14:73969528
|
C | A | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1200+482G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969528 | ||||||
chr14:73969532
|
T | C | 8 | a0001c0002t0008g0056a0001c0002t0008g0339a0001c0002t0008g0340others(5): Show | 8 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1200+478A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969532 | ||||||
chr14:73969654
|
A | G | 10 | a0001c0002t0003g0077a0001c0002t0003g0089a0001c0002t0003g0092others(7): Show | 10 | NA18947.hp1 NA18962.hp1 NA18984.hp1 others(7): Show |
intron_variant | MODIFIER | c.1200+356T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969654 | ||||||
chr14:73969712
|
T | A | 3 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227 | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+298A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969712 | ||||||
chr14:73969715
|
T | TAATA | 49 | a0001c0001t0005g0041a0001c0002t0005g0002a0001c0002t0005g0003others(46): Show | 54 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1200+291_1200+294d others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969715 | ||||||
chr14:73969715
|
T | TAATAAAT others(1): Show |
119 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(116): Show | 121 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1200+287_1200+294d others(10): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969715 | ||||||
chr14:73969715
|
T | TAATAAAT others(5): Show |
3 | a0001c0002t0002g0298a0001c0002t0003g0358a0001c0002t0008g0362 | 3 | HG02145.hp2 HG03239.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1200+283_1200+294d others(14): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969715 | ||||||
chr14:73969718
|
T | A | 8 | a0001c0001t0001g0140a0001c0001t0001g0192a0001c0001t0001g0194others(5): Show | 8 | HG02015.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200+292A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969718 | ||||||
chr14:73969799
|
G | A | 190 | a0001c0001t0004g0017a0001c0001t0004g0125a0001c0001t0004g0126others(187): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1200+211C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969799 | ||||||
chr14:73969996
|
G | A | 8 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227others(5): Show | 10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1200+14C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969996 | ||||||
chr14:73970366
|
G | A | 54 | a0001c0001t0004g0241a0001c0001t0004g0243a0001c0001t0004g0244others(51): Show | 55 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1085-241C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970366 | ||||||
chr14:73970429
|
T | C | 12 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1085-304A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970429 | ||||||
chr14:73970510
|
G | A | 9 | a0001c0002t0008g0056a0001c0002t0008g0271a0001c0002t0008g0339others(6): Show | 9 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1085-385C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970510 | ||||||
chr14:73970541
|
C | T | 1 | a0001c0002t0003g0072 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1085-416G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970541 | ||||||
chr14:73970545
|
G | T | 3 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0249 | 3 | HG04115.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1085-420C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970545 | ||||||
chr14:73970742
|
A | G | 1 | a0001c0002t0010g0220 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1085-617T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970742 | ||||||
chr14:73970842
|
T | C | 5 | a0001c0002t0010g0015a0001c0002t0010g0220a0001c0002t0010g0222others(2): Show | 6 | HG01243.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1085-717A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970842 | ||||||
chr14:73970928
|
C | A | 12 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1085-803G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970928 | ||||||
chr14:73970947
|
TC | T | 3 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227 | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-823delG | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970947 | ||||||
chr14:73970975
|
C | A | 1 | a0001c0001t0006g0217 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1085-850G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970975 | ||||||
chr14:73970990
|
C | A | 4 | a0001c0002t0008g0056a0001c0002t0008g0341a0001c0002t0008g0342others(1): Show | 4 | HG01496.hp2 HG02145.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+862G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970990 | ||||||
chr14:73971131
|
C | T | 122 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1084+721G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971131 | ||||||
chr14:73971136
|
T | G | 1 | a0001c0002t0005g0052 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1084+716A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971136 | ||||||
chr14:73971162
|
GT | G | 120 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(117): Show | 122 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1084+689delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971162 | ||||||
chr14:73971253
|
G | A | 68 | a0001c0001t0004g0017a0001c0001t0004g0125a0001c0001t0004g0126others(65): Show | 71 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1084+599C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971253 | ||||||
chr14:73971261
|
G | A | 68 | a0001c0001t0004g0017a0001c0001t0004g0125a0001c0001t0004g0126others(65): Show | 71 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1084+591C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971261 | ||||||
chr14:73971270
|
A | G | 2 | a0001c0001t0012g0360a0001c0001t0012g0361 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1084+582T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971270 | ||||||
chr14:73971304
|
C | T | 1 | a0001c0002t0017g0069 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1084+548G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971304 | ||||||
chr14:73971364
|
G | A | 2 | a0001c0002t0002g0303a0001c0002t0002g0315 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1084+488C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971364 | ||||||
chr14:73971447
|
G | A | 5 | a0001c0001t0006g0210a0001c0001t0006g0211a0001c0001t0006g0212others(2): Show | 6 | HG01081.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1084+405C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971447 | ||||||
chr14:73971564
|
C | T | 3 | a0001c0002t0010g0015a0001c0002t0010g0223a0001c0002t0010g0224 | 4 | HG02895.hp2 HG03486.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+288G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971564 | ||||||
chr14:73971774
|
GCTTTAGG others(3): Show |
G | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1084+68_1084+77del others(10): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971774 | ||||||
chr14:73971789
|
A | G | 1 | a0001c0001t0007g0291 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1084+63T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971789 | ||||||
chr14:73972101
|
G | A | 1 | a0001c0002t0002g0286 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1028-193C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/15 | chr14 | 73972101 | ||||||
chr14:73972142
|
GC | G | 12 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1028-235delG | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/15 | chr14 | 73972142 | ||||||
chr14:73972144
|
C | T | 1 | a0001c0001t0004g0237 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1028-236G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/15 | chr14 | 73972144 | ||||||
chr14:73972160
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1028-252G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/15 | chr14 | 73972160 | ||||||
chr14:73972260
|
G | T | 1 | a0001c0002t0003g0107 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1028-352C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/15 | chr14 | 73972260 | ||||||
chr14:73972679
|
TA | T | 249 | a0001c0001t0004g0017a0001c0001t0004g0125a0001c0001t0004g0126others(246): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1027+204delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/15 | chr14 | 73972679 | ||||||
chr14:73972792
|
G | A | 190 | a0001c0001t0004g0017a0001c0001t0004g0125a0001c0001t0004g0126others(187): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1027+92C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/15 | chr14 | 73972792 | ||||||
chr14:73973168
|
G | A | 1 | a0001c0002t0005g0024 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.887-144C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973168 | ||||||
chr14:73973177
|
A | C | 2 | a0001c0001t0004g0017a0001c0001t0004g0228 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.887-153T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973177 | ||||||
chr14:73973192
|
C | T | 60 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.887-168G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973192 | ||||||
chr14:73973248
|
C | T | 5 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.887-224G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973248 | ||||||
chr14:73973299
|
T | C | 8 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227others(5): Show | 10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.887-275A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973299 | ||||||
chr14:73973416
|
A | G | 60 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.887-392T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973416 | ||||||
chr14:73973427
|
A | G | 1 | a0001c0002t0008g0271 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.887-403T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973427 | ||||||
chr14:73973458
|
C | G | 122 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.886+419G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973458 | ||||||
chr14:73973655
|
A | C | 1 | a0001c0001t0006g0284 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.886+222T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973655 | ||||||
chr14:73973738
|
T | C | 4 | a0001c0002t0003g0007a0001c0002t0003g0106a0001c0002t0003g0120others(1): Show | 5 | HG00639.hp1 HG01261.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.886+139A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973738 | ||||||
chr14:73973762
|
A | G | 2 | a0001c0001t0004g0017a0001c0001t0004g0228 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.886+115T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973762 | ||||||
chr14:73974017
|
T | G | 5 | a0001c0002t0010g0015a0001c0002t0010g0220a0001c0002t0010g0222others(2): Show | 6 | HG01243.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.785-39A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974017 | ||||||
chr14:73974150
|
A | G | 8 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227others(5): Show | 10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.785-172T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974150 | ||||||
chr14:73974256
|
A | T | 10 | a0001c0002t0008g0056a0001c0002t0008g0271a0001c0002t0008g0339others(7): Show | 10 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.785-278T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974256 | ||||||
chr14:73974286
|
C | T | 1 | a0001c0002t0003g0072 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.785-308G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974286 | ||||||
chr14:73974338
|
A | G | 1 | a0001c0001t0011g0135 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.785-360T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974338 | ||||||
chr14:73974473
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(53): Show | 61 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.784+451A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974473 | ||||||
chr14:73974541
|
T | C | 12 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.784+383A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974541 | ||||||
chr14:73974590
|
G | A | 1 | a0001c0001t0004g0237 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.784+334C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974590 | ||||||
chr14:73974642
|
G | T | 170 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(167): Show | 177 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.784+282C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974642 | ||||||
chr14:73974834
|
T | C | 253 | a0001c0001t0004g0017a0001c0001t0004g0125a0001c0001t0004g0126others(250): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.784+90A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974834 | ||||||
chr14:73975050
|
T | C | 1 | a0001c0001t0035g0026 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.723-65A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975050 | ||||||
chr14:73975403
|
CT | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(204): Show | 220 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.723-419delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975403 | ||||||
chr14:73975403
|
CTT | C | 105 | a0001c0001t0004g0219a0001c0001t0006g0283a0001c0001t0015g0122others(102): Show | 107 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.723-420_723-419del others(2): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975403 | ||||||
chr14:73975448
|
C | T | 122 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.723-463G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975448 | ||||||
chr14:73975483
|
C | A | 1 | a0001c0001t0023g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.722+453G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975483 | ||||||
chr14:73975507
|
T | C | 1 | a0001c0002t0008g0271 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.722+429A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975507 | ||||||
chr14:73975549
|
T | A | 50 | a0001c0002t0003g0007a0001c0002t0003g0070a0001c0002t0003g0072others(47): Show | 52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.722+387A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975549 | ||||||
chr14:73975554
|
G | A | 1 | a0001c0002t0003g0074 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.722+382C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975554 | ||||||
chr14:73975663
|
C | G | 1 | a0001c0002t0008g0271 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.722+273G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975663 | ||||||
chr14:73975797
|
G | C | 6 | a0001c0002t0010g0015a0001c0002t0010g0220a0001c0002t0010g0221others(3): Show | 7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.722+139C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975797 | ||||||
chr14:73975896
|
TACA | T | 5 | a0001c0002t0005g0025a0001c0002t0005g0027a0001c0002t0005g0030others(2): Show | 5 | HG01099.hp2 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.722+37_722+39delTG others(1): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975896 | ||||||
chr14:73975928
|
G | A | 5 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.722+8C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975928 | ||||||
chr14:73976018
|
G | A | 1 | a0001c0002t0002g0113 | 1 | HG03490.hp2 | splice_region_variant&intron_variant | LOW | c.643-3C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 9/15 | chr14 | 73976018 | ||||||
chr14:73976022
|
A | G | 2 | a0001c0002t0002g0327a0001c0002t0027g0317 | 2 | NA18981.hp2 NA18994.hp2 |
splice_region_variant&intron_variant | LOW | c.643-7T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 9/15 | chr14 | 73976022 | ||||||
chr14:73976154
|
G | A | 34 | a0001c0002t0005g0002a0001c0002t0005g0003a0001c0002t0005g0019others(31): Show | 36 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.643-139C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 9/15 | chr14 | 73976154 | ||||||
chr14:73976225
|
C | T | 1 | a0001c0002t0003g0359 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.642+99G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 9/15 | chr14 | 73976225 | ||||||
chr14:73976444
|
C | T | 2 | a0001c0002t0008g0343a0001c0002t0008g0344 | 2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.554-32G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976444 | ||||||
chr14:73976447
|
C | T | 5 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.554-35G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976447 | ||||||
chr14:73976523
|
C | T | 1 | a0001c0002t0003g0078 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.554-111G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976523 | ||||||
chr14:73976595
|
G | GT | 28 | a0001c0001t0001g0156a0001c0001t0001g0167a0001c0001t0001g0184others(25): Show | 28 | HG01175.hp1 HG01433.hp1 HG01928.hp1 others(25): Show |
intron_variant | MODIFIER | c.554-184dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976595 | ||||||
chr14:73976596
|
T | C | 1 | a0001c0001t0005g0041 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.554-184A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976596 | ||||||
chr14:73976651
|
C | G | 122 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.554-239G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976651 | ||||||
chr14:73976795
|
G | A | 49 | a0001c0001t0005g0041a0001c0002t0005g0002a0001c0002t0005g0003others(46): Show | 54 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.553+229C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976795 | ||||||
chr14:73976926
|
A | C | 1 | a0001c0002t0008g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.553+98T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976926 | ||||||
chr14:73976996
|
T | G | 2 | a0001c0001t0012g0127a0001c0001t0012g0128 | 2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.553+28A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976996 | ||||||
chr14:73977095
|
G | T | 1 | a0001c0001t0001g0150 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.518-36C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 7/15 | chr14 | 73977095 | ||||||
chr14:73977137
|
T | C | 9 | a0001c0001t0006g0109a0001c0001t0006g0124a0001c0001t0015g0008others(6): Show | 11 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.518-78A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 7/15 | chr14 | 73977137 | ||||||
chr14:73977380
|
G | T | 12 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.442-6C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73977380 | ||||||
chr14:73977387
|
G | GA | 62 | a0001c0001t0001g0155a0001c0001t0001g0205a0001c0001t0004g0219others(59): Show | 64 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.442-14dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73977387 | ||||||
chr14:73977535
|
C | T | 12 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-161G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73977535 | ||||||
chr14:73977736
|
G | C | 1 | a0001c0002t0003g0084 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.442-362C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73977736 | ||||||
chr14:73977922
|
C | A | 251 | a0001c0001t0004g0017a0001c0001t0004g0125a0001c0001t0004g0126others(248): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.442-548G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73977922 | ||||||
chr14:73977951
|
T | C | 1 | a0001c0001t0032g0166 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.442-577A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73977951 | ||||||
chr14:73978026
|
A | G | 5 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0179others(2): Show | 5 | HG00323.hp2 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-652T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978026 | ||||||
chr14:73978075
|
G | T | 50 | a0001c0002t0003g0007a0001c0002t0003g0070a0001c0002t0003g0072others(47): Show | 52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.442-701C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978075 | ||||||
chr14:73978270
|
T | TAAAAATG others(309): Show |
5 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-897_442-896ins others(316): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978270 | ||||||
chr14:73978270
|
T | TAAAAATG others(310): Show |
2 | a0001c0001t0011g0135a0001c0001t0011g0136 | 2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.442-897_442-896ins others(317): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978270 | ||||||
chr14:73978283
|
C | A | 1 | a0001c0002t0005g0040 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.442-909G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978283 | ||||||
chr14:73978285
|
A | G | 3 | a0001c0001t0023g0129a0001c0001t0024g0285a0001c0001t0025g0130 | 3 | HG02818.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.442-911T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978285 | ||||||
chr14:73978336
|
G | C | 8 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227others(5): Show | 10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-962C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978336 | ||||||
chr14:73978369
|
C | T | 1 | a0001c0001t0025g0130 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.442-995G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978369 | ||||||
chr14:73978429
|
C | T | 1 | a0001c0002t0002g0296 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.442-1055G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978429 | ||||||
chr14:73978468
|
G | A | 1 | a0001c0001t0004g0235 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.442-1094C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978468 | ||||||
chr14:73978549
|
C | T | 1 | a0001c0002t0005g0025 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.442-1175G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978549 | ||||||
chr14:73978558
|
G | A | 5 | a0001c0001t0006g0210a0001c0001t0006g0211a0001c0001t0006g0212others(2): Show | 6 | HG01081.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-1184C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978558 | ||||||
chr14:73978601
|
C | CAAACA | 124 | a0001c0001t0004g0017a0001c0001t0004g0228a0001c0002t0002g0098others(121): Show | 127 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.442-1232_442-1228d others(7): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978601 | ||||||
chr14:73978687
|
G | C | 50 | a0001c0002t0003g0007a0001c0002t0003g0070a0001c0002t0003g0072others(47): Show | 52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.442-1313C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978687 | ||||||
chr14:73978766
|
C | G | 4 | a0002c0003t0009g0004a0002c0003t0009g0065a0002c0003t0009g0066others(1): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-1392G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978766 | ||||||
chr14:73978915
|
AG | A | 4 | a0001c0001t0007g0195a0001c0002t0003g0092a0001c0002t0005g0050others(1): Show | 4 | HG01168.hp2 NA18957.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-1542delC | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978915 | ||||||
chr14:73978916
|
G | A | 235 | a0001c0001t0004g0017a0001c0001t0004g0125a0001c0001t0004g0126others(232): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.442-1542C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978916 | ||||||
chr14:73979027
|
C | T | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-1653G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979027 | ||||||
chr14:73979149
|
C | T | 8 | a0001c0002t0008g0056a0001c0002t0008g0339a0001c0002t0008g0340others(5): Show | 8 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-1775G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979149 | ||||||
chr14:73979173
|
C | T | 5 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-1799G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979173 | ||||||
chr14:73979179
|
G | A | 50 | a0001c0002t0003g0007a0001c0002t0003g0070a0001c0002t0003g0072others(47): Show | 52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.442-1805C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979179 | ||||||
chr14:73979200
|
T | C | 1 | a0001c0002t0008g0362 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442-1826A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979200 | ||||||
chr14:73979271
|
C | T | 4 | a0001c0001t0001g0151a0001c0001t0001g0165a0001c0001t0001g0176others(1): Show | 4 | HG02080.hp2 HG02129.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-1897G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979271 | ||||||
chr14:73979288
|
T | A | 1 | a0001c0002t0003g0088 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.442-1914A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979288 | ||||||
chr14:73979472
|
C | CT | 70 | a0001c0001t0001g0151a0001c0001t0001g0194a0001c0001t0004g0228others(67): Show | 72 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.442-2099dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979472 | ||||||
chr14:73979499
|
T | C | 1 | a0001c0002t0008g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.442-2125A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979499 | ||||||
chr14:73979572
|
C | T | 8 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227others(5): Show | 10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-2198G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979572 | ||||||
chr14:73979596
|
C | T | 1 | a0001c0002t0008g0362 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442-2222G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979596 | ||||||
chr14:73979621
|
A | G | 242 | a0001c0001t0004g0017a0001c0001t0004g0125a0001c0001t0004g0126others(239): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.442-2247T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979621 | ||||||
chr14:73979773
|
G | C | 1 | a0001c0001t0001g0255 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.442-2399C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979773 | ||||||
chr14:73979934
|
T | G | 1 | a0001c0002t0002g0242 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.442-2560A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979934 | ||||||
chr14:73979943
|
A | AT | 74 | a0001c0001t0001g0180a0001c0001t0004g0125a0001c0001t0004g0126others(71): Show | 77 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.442-2570dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979943 | ||||||
chr14:73979943
|
A | ATT | 65 | a0001c0001t0004g0234a0001c0001t0004g0235a0001c0001t0004g0243others(62): Show | 65 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.442-2571_442-2570d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979943 | ||||||
chr14:73979943
|
A | ATTT | 8 | a0001c0002t0002g0293a0001c0002t0002g0308a0001c0002t0002g0325others(5): Show | 8 | HG00735.hp2 HG01346.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-2572_442-2570d others(5): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979943 | ||||||
chr14:73979943
|
AT | A | 14 | a0001c0001t0001g0168a0001c0001t0001g0203a0001c0001t0012g0127others(11): Show | 15 | HG00099.hp2 HG01243.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.442-2570delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979943 | ||||||
chr14:73979943
|
ATT | A | 10 | a0001c0002t0008g0056a0001c0002t0008g0271a0001c0002t0008g0339others(7): Show | 10 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-2571_442-2570d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979943 | ||||||
chr14:73980105
|
C | T | 1 | a0001c0001t0026g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.442-2731G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980105 | ||||||
chr14:73980136
|
A | T | 1 | a0001c0001t0013g0246 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.442-2762T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980136 | ||||||
chr14:73980194
|
G | A | 1 | a0001c0002t0005g0043 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.442-2820C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980194 | ||||||
chr14:73980200
|
G | A | 1 | a0001c0002t0002g0299 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.441+2818C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980200 | ||||||
chr14:73980269
|
C | CT | 15 | a0001c0002t0003g0092a0001c0002t0008g0056a0001c0002t0008g0339others(12): Show | 16 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.441+2748dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980269 | ||||||
chr14:73980333
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.441+2685G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980333 | ||||||
chr14:73980343
|
C | T | 2 | a0001c0001t0006g0217a0001c0001t0028g0218 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.441+2675G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980343 | ||||||
chr14:73980366
|
G | C | 1 | a0001c0001t0006g0217 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.441+2652C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980366 | ||||||
chr14:73980369
|
A | G | 2 | a0001c0001t0006g0276a0001c0001t0006g0277 | 2 | NA18952.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.441+2649T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980369 | ||||||
chr14:73980409
|
G | A | 50 | a0001c0002t0003g0007a0001c0002t0003g0070a0001c0002t0003g0072others(47): Show | 52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.441+2609C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980409 | ||||||
chr14:73980479
|
G | T | 1 | a0001c0002t0003g0107 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.441+2539C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980479 | ||||||
chr14:73980495
|
C | T | 8 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227others(5): Show | 10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+2523G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980495 | ||||||
chr14:73980554
|
A | G | 122 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.441+2464T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980554 | ||||||
chr14:73980680
|
G | C | 60 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.441+2338C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980680 | ||||||
chr14:73980690
|
C | T | 122 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.441+2328G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980690 | ||||||
chr14:73980704
|
T | C | 6 | a0001c0002t0010g0015a0001c0002t0010g0220a0001c0002t0010g0221others(3): Show | 7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+2314A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980704 | ||||||
chr14:73981082
|
G | C | 60 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.441+1936C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981082 | ||||||
chr14:73981103
|
A | AAAAT | 3 | a0001c0001t0001g0192a0001c0001t0004g0213a0001c0001t0004g0214 | 3 | HG02015.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.441+1911_441+1914d others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981103 | ||||||
chr14:73981266
|
C | T | 5 | a0001c0001t0013g0240a0001c0001t0013g0246a0001c0001t0013g0247others(2): Show | 5 | HG00438.hp1 NA18974.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+1752G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981266 | ||||||
chr14:73981267
|
G | A | 2 | a0001c0002t0005g0044a0001c0002t0005g0141 | 2 | HG02165.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.441+1751C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981267 | ||||||
chr14:73981285
|
G | A | 4 | a0001c0001t0006g0057a0001c0001t0006g0059a0001c0001t0006g0063others(1): Show | 4 | HG00735.hp1 HG01106.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+1733C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981285 | ||||||
chr14:73981494
|
G | GTA | 68 | a0001c0001t0004g0125a0001c0001t0004g0126a0001c0001t0004g0207others(65): Show | 70 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.441+1522_441+1523d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981494 | ||||||
chr14:73981507
|
T | C | 1 | a0001c0002t0003g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.441+1511A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981507 | ||||||
chr14:73981807
|
C | CA | 8 | a0001c0001t0001g0180a0001c0001t0004g0252a0001c0001t0004g0267others(5): Show | 8 | HG00408.hp2 HG02602.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.441+1210dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981807 | ||||||
chr14:73981807
|
CA | C | 127 | a0001c0001t0001g0151a0001c0001t0006g0211a0001c0001t0007g0143others(124): Show | 130 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.441+1210delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981807 | ||||||
chr14:73981807
|
CAA | C | 42 | a0001c0001t0005g0041a0001c0002t0005g0002a0001c0002t0005g0003others(39): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.441+1209_441+1210d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981807 | ||||||
chr14:73981869
|
G | A | 8 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227others(5): Show | 10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+1149C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981869 | ||||||
chr14:73981922
|
T | C | 122 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.441+1096A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981922 | ||||||
chr14:73981948
|
T | C | 1 | a0001c0001t0001g0335 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.441+1070A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981948 | ||||||
chr14:73982213
|
T | C | 1 | a0001c0001t0012g0138 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.441+805A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982213 | ||||||
chr14:73982224
|
G | A | 1 | a0001c0001t0006g0071 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.441+794C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982224 | ||||||
chr14:73982385
|
A | G | 12 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+633T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982385 | ||||||
chr14:73982416
|
A | C | 12 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+602T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982416 | ||||||
chr14:73982430
|
C | T | 1 | a0001c0002t0008g0362 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.441+588G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982430 | ||||||
chr14:73982538
|
C | T | 2 | a0001c0001t0004g0017a0001c0001t0004g0228 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.441+480G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982538 | ||||||
chr14:73982781
|
A | G | 3 | a0001c0001t0023g0129a0001c0001t0024g0285a0001c0001t0025g0130 | 3 | HG02818.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.441+237T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982781 | ||||||
chr14:73982826
|
A | G | 1 | a0001c0001t0006g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.441+192T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982826 | ||||||
chr14:73982961
|
A | G | 50 | a0001c0002t0003g0007a0001c0002t0003g0070a0001c0002t0003g0072others(47): Show | 52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.441+57T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982961 | ||||||
chr14:73983437
|
A | G | 4 | a0002c0003t0009g0004a0002c0003t0009g0065a0002c0003t0009g0066others(1): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-276T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983437 | ||||||
chr14:73983605
|
C | T | 2 | a0001c0001t0004g0348a0001c0001t0004g0353 | 2 | NA18964.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.298-444G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983605 | ||||||
chr14:73983619
|
A | G | 239 | a0001c0001t0004g0017a0001c0001t0004g0125a0001c0001t0004g0126others(236): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.298-458T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983619 | ||||||
chr14:73983623
|
C | CA | 162 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(159): Show | 170 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.298-463dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983623 | ||||||
chr14:73983623
|
C | CAA | 61 | a0001c0001t0013g0240a0001c0002t0002g0098a0001c0002t0002g0113others(58): Show | 61 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.298-464_298-463dup others(2): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983623 | ||||||
chr14:73983623
|
CA | C | 8 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227others(5): Show | 10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-463delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983623 | ||||||
chr14:73983675
|
AATTATT | A | 2 | a0001c0001t0004g0017a0001c0001t0004g0228 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.298-520_298-515del others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983675 | ||||||
chr14:73983689
|
TTA | T | 59 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(56): Show | 59 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.298-530_298-529del others(2): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983689 | ||||||
chr14:73983690
|
TA | T | 60 | a0001c0002t0003g0007a0001c0002t0003g0070a0001c0002t0003g0072others(57): Show | 62 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.298-530delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983690 | ||||||
chr14:73983691
|
ATTATTT | A | 66 | a0001c0001t0004g0125a0001c0001t0004g0126a0001c0001t0004g0207others(63): Show | 68 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.298-536_298-531del others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983691 | ||||||
chr14:73983694
|
A | T | 121 | a0001c0001t0001g0151a0001c0001t0004g0219a0001c0002t0002g0098others(118): Show | 123 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.298-533T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983694 | ||||||
chr14:73983697
|
T | A | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.298-536A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983697 | ||||||
chr14:73983702
|
T | G | 36 | a0001c0001t0001g0171a0001c0001t0005g0041a0001c0002t0005g0002others(33): Show | 38 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.298-541A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983702 | ||||||
chr14:73983704
|
G | A | 122 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.298-543C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983704 | ||||||
chr14:73983752
|
G | C | 1 | a0001c0001t0001g0198 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.298-591C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983752 | ||||||
chr14:73983778
|
C | T | 1 | a0001c0002t0003g0082 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.298-617G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983778 | ||||||
chr14:73983910
|
C | T | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.298-749G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983910 | ||||||
chr14:73984030
|
C | A | 8 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227others(5): Show | 10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-869G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984030 | ||||||
chr14:73984049
|
C | T | 35 | a0001c0001t0005g0041a0001c0002t0005g0002a0001c0002t0005g0003others(32): Show | 37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.298-888G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984049 | ||||||
chr14:73984061
|
CTT | C | 60 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.298-902_298-901del others(2): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984061 | ||||||
chr14:73984260
|
G | C | 2 | a0001c0001t0012g0127a0001c0001t0012g0128 | 2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.298-1099C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984260 | ||||||
chr14:73984329
|
T | G | 1 | a0001c0001t0001g0193 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.298-1168A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984329 | ||||||
chr14:73984451
|
A | G | 1 | a0001c0001t0004g0256 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.298-1290T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984451 | ||||||
chr14:73984468
|
T | C | 315 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(312): Show | 330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.298-1307A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984468 | ||||||
chr14:73984523
|
A | G | 1 | a0001c0002t0003g0358 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.298-1362T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984523 | ||||||
chr14:73984601
|
C | T | 1 | a0001c0001t0006g0280 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.298-1440G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984601 | ||||||
chr14:73984612
|
C | T | 49 | a0001c0001t0005g0041a0001c0002t0005g0002a0001c0002t0005g0003others(46): Show | 54 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.298-1451G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984612 | ||||||
chr14:73984684
|
TTTAA | T | 3 | a0001c0001t0006g0210a0001c0001t0006g0211a0001c0001t0006g0212 | 3 | HG01884.hp2 HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.298-1527_298-1524d others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984684 | ||||||
chr14:73984831
|
G | A | 1 | a0001c0002t0036g0037 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.298-1670C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984831 | ||||||
chr14:73984896
|
T | C | 171 | a0001c0001t0005g0041a0001c0002t0002g0098a0001c0002t0002g0113others(168): Show | 178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.298-1735A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984896 | ||||||
chr14:73984912
|
C | T | 12 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-1751G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984912 | ||||||
chr14:73984918
|
G | C | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1757C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984918 | ||||||
chr14:73984919
|
C | CACCTCAT others(9): Show |
1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1759_298-1758i others(18): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984919 | ||||||
chr14:73984923
|
G | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1762C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984923 | ||||||
chr14:73984924
|
G | C | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1763C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984924 | ||||||
chr14:73984926
|
G | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1765C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984926 | ||||||
chr14:73984934
|
T | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1773A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984934 | ||||||
chr14:73984935
|
T | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1774A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984935 | ||||||
chr14:73984939
|
C | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1778G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984939 | ||||||
chr14:73984940
|
A | T | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1779T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984940 | ||||||
chr14:73984963
|
T | C | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1802A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984963 | ||||||
chr14:73984964
|
C | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1803G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984964 | ||||||
chr14:73984979
|
G | T | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1818C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984979 | ||||||
chr14:73984984
|
T | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1823A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984984 | ||||||
chr14:73984985
|
G | C | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1824C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984985 | ||||||
chr14:73984987
|
G | C | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1826C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984987 | ||||||
chr14:73984988
|
G | C | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1826C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984988 | ||||||
chr14:73984990
|
G | T | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1824C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984990 | ||||||
chr14:73984991
|
T | C | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1823A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984991 | ||||||
chr14:73984992
|
T | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1822A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984992 | ||||||
chr14:73984994
|
G | C | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1820C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984994 | ||||||
chr14:73984996
|
T | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1818A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984996 | ||||||
chr14:73984997
|
T | C | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1817A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984997 | ||||||
chr14:73985000
|
C | G | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1814G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985000 | ||||||
chr14:73985001
|
T | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1813A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985001 | ||||||
chr14:73985002
|
G | T | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1812C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985002 | ||||||
chr14:73985003
|
T | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1811A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985003 | ||||||
chr14:73985004
|
T | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1810A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985004 | ||||||
chr14:73985006
|
T | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1808A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985006 | ||||||
chr14:73985009
|
C | G | 1 | a0001c0002t0002g0322 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.297+1805G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985009 | ||||||
chr14:73985010
|
G | A | 2 | a0001c0001t0006g0217a0001c0001t0028g0218 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.297+1804C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985010 | ||||||
chr14:73985011
|
A | T | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1803T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985011 | ||||||
chr14:73985023
|
G | T | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1791C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985023 | ||||||
chr14:73985024
|
A | T | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1790T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985024 | ||||||
chr14:73985027
|
G | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1787C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985027 | ||||||
chr14:73985031
|
G | T | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1783C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985031 | ||||||
chr14:73985034
|
T | C | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1780A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985034 | ||||||
chr14:73985036
|
C | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1778G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985036 | ||||||
chr14:73985040
|
T | G | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1774A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985040 | ||||||
chr14:73985041
|
T | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1773A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985041 | ||||||
chr14:73985049
|
G | T | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1765C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985049 | ||||||
chr14:73985060
|
G | C | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1754C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985060 | ||||||
chr14:73985061
|
G | T | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1753C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985061 | ||||||
chr14:73985160
|
G | A | 1 | a0001c0002t0003g0091 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.297+1654C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985160 | ||||||
chr14:73985235
|
A | G | 60 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.297+1579T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985235 | ||||||
chr14:73985249
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.297+1565T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985249 | ||||||
chr14:73985252
|
T | A | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1562A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985252 | ||||||
chr14:73985256
|
G | C | 1 | a0001c0002t0027g0317 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.297+1558C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985256 | ||||||
chr14:73985258
|
G | A | 3 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227 | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+1556C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985258 | ||||||
chr14:73985258
|
G | C | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1556C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985258 | ||||||
chr14:73985259
|
T | C | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1555A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985259 | ||||||
chr14:73985273
|
G | GAACCCAA others(4): Show |
1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1540_297+1541i others(13): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985273 | ||||||
chr14:73985274
|
G | C | 1 | a0001c0002t0020g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1540C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985274 | ||||||
chr14:73985302
|
T | C | 1 | a0001c0002t0008g0345 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.297+1512A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985302 | ||||||
chr14:73985350
|
T | C | 1 | a0001c0001t0004g0219 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.297+1464A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985350 | ||||||
chr14:73985488
|
G | A | 1 | a0001c0002t0008g0054 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.297+1326C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985488 | ||||||
chr14:73985491
|
A | G | 1 | a0001c0001t0006g0071 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.297+1323T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985491 | ||||||
chr14:73985497
|
G | C | 1 | a0001c0002t0008g0054 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.297+1317C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985497 | ||||||
chr14:73985631
|
C | A | 2 | a0001c0001t0006g0058a0001c0001t0006g0062 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.297+1183G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985631 | ||||||
chr14:73985726
|
G | A | 5 | a0001c0002t0005g0034a0001c0002t0005g0038a0001c0002t0005g0039others(2): Show | 5 | HG02129.hp1 HG02602.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+1088C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985726 | ||||||
chr14:73985762
|
C | T | 50 | a0001c0002t0003g0007a0001c0002t0003g0070a0001c0002t0003g0072others(47): Show | 52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.297+1052G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985762 | ||||||
chr14:73985792
|
G | C | 60 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.297+1022C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985792 | ||||||
chr14:73985996
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.297+818G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985996 | ||||||
chr14:73985998
|
C | T | 1 | a0001c0001t0006g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.297+816G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985998 | ||||||
chr14:73986069
|
C | CA | 62 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(59): Show | 62 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.297+744dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73986069 | ||||||
chr14:73986069
|
CA | C | 69 | a0001c0001t0001g0162a0001c0001t0004g0017a0001c0001t0004g0125others(66): Show | 72 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.297+744delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73986069 | ||||||
chr14:73986081
|
A | G | 8 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227others(5): Show | 10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.297+733T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73986081 | ||||||
chr14:73986505
|
G | A | 12 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.297+309C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73986505 | ||||||
chr14:73986510
|
C | T | 2 | a0001c0002t0008g0054a0001c0002t0008g0055 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.297+304G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73986510 | ||||||
chr14:73986562
|
A | G | 1 | a0001c0002t0002g0332 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.297+252T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73986562 | ||||||
chr14:73986644
|
G | A | 1 | a0001c0001t0026g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.297+170C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73986644 | ||||||
chr14:73987003
|
AT | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(56): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.218-111delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987003 | ||||||
chr14:73987008
|
A | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(56): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.218-115T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987008 | ||||||
chr14:73987014
|
T | A | 2 | a0001c0001t0004g0213a0001c0001t0004g0214 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.218-121A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987014 | ||||||
chr14:73987114
|
T | C | 3 | a0001c0001t0004g0213a0001c0001t0004g0214a0001c0001t0004g0219 | 3 | HG02809.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.218-221A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987114 | ||||||
chr14:73987162
|
G | A | 4 | a0001c0001t0004g0236a0001c0001t0004g0237a0001c0001t0004g0238others(1): Show | 4 | HG01074.hp2 HG02109.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-269C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987162 | ||||||
chr14:73987260
|
T | A | 1 | a0001c0001t0004g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.218-367A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987260 | ||||||
chr14:73987284
|
G | A | 5 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.218-391C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987284 | ||||||
chr14:73987398
|
T | G | 1 | a0001c0002t0008g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.217+488A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987398 | ||||||
chr14:73987404
|
G | C | 3 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227 | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+482C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987404 | ||||||
chr14:73987492
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(52): Show | 60 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.217+394G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987492 | ||||||
chr14:73987815
|
A | G | 1 | a0001c0002t0003g0265 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.217+71T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987815 | ||||||
chr14:73987847
|
G | T | 10 | a0001c0002t0002g0287a0001c0002t0002g0292a0001c0002t0002g0299others(7): Show | 10 | NA18941.hp2 NA18950.hp1 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.217+39C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987847 | ||||||
chr14:73988493
|
T | G | 8 | a0001c0002t0008g0056a0001c0002t0008g0339a0001c0002t0008g0340others(5): Show | 8 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-70-321A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73988493 | ||||||
chr14:73988516
|
G | C | 60 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-70-344C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73988516 | ||||||
chr14:73988651
|
A | G | 1 | a0001c0001t0004g0254 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-70-479T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73988651 | ||||||
chr14:73988686
|
C | T | 122 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-70-514G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73988686 | ||||||
chr14:73988769
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-70-597C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73988769 | ||||||
chr14:73988791
|
C | T | 1 | a0001c0002t0003g0078 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-70-619G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73988791 | ||||||
chr14:73989008
|
C | G | 314 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(311): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.-70-836G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989008 | ||||||
chr14:73989069
|
G | A | 60 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-70-897C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989069 | ||||||
chr14:73989113
|
C | T | 5 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70-941G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989113 | ||||||
chr14:73989114
|
G | T | 1 | a0001c0001t0006g0217 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-70-942C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989114 | ||||||
chr14:73989237
|
T | G | 1 | a0001c0001t0023g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-70-1065A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989237 | ||||||
chr14:73989276
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(56): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.-70-1104G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989276 | ||||||
chr14:73989344
|
GTGAGGTC others(129): Show |
G | 4 | a0001c0002t0003g0072a0001c0002t0003g0101a0001c0002t0003g0102others(1): Show | 4 | HG03490.hp1 HG03492.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70-1308_-70-1173d others(2): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989344 | ||||||
chr14:73989388
|
C | G | 1 | a0001c0001t0013g0269 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-70-1216G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989388 | ||||||
chr14:73989423
|
C | T | 71 | a0001c0001t0004g0017a0001c0001t0004g0125a0001c0001t0004g0126others(68): Show | 74 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-70-1251G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989423 | ||||||
chr14:73989425
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(56): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.-70-1253G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989425 | ||||||
chr14:73989469
|
G | A | 42 | a0001c0002t0003g0007a0001c0002t0003g0070a0001c0002t0003g0074others(39): Show | 44 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.-70-1297C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989469 | ||||||
chr14:73989563
|
G | T | 60 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-70-1391C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989563 | ||||||
chr14:73989609
|
G | A | 51 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138others(48): Show | 53 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-70-1437C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989609 | ||||||
chr14:73989631
|
C | T | 1 | a0001c0001t0028g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-70-1459G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989631 | ||||||
chr14:73989632
|
A | G | 1 | a0001c0001t0028g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-70-1460T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989632 | ||||||
chr14:73989777
|
G | A | 2 | a0001c0002t0017g0006a0001c0002t0017g0069 | 3 | HG00280.hp1 HG01255.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.-70-1605C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989777 | ||||||
chr14:73989782
|
G | A | 7 | a0001c0002t0002g0287a0001c0002t0002g0302a0001c0002t0002g0307others(4): Show | 7 | NA18941.hp2 NA18950.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70-1610C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989782 | ||||||
chr14:73989832
|
C | CA | 13 | a0001c0001t0001g0164a0001c0001t0004g0017a0001c0001t0004g0228others(10): Show | 14 | HG01175.hp2 HG02055.hp1 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.-70-1661dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989832 | ||||||
chr14:73989832
|
C | CAA | 117 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(114): Show | 124 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-70-1662_-70-1661d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989832 | ||||||
chr14:73989832
|
C | CAAA | 49 | a0001c0001t0001g0139a0001c0001t0001g0189a0001c0001t0001g0190others(46): Show | 51 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-70-1663_-70-1661d others(5): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989832 | ||||||
chr14:73989832
|
C | CAAAA | 10 | a0001c0001t0012g0128a0001c0001t0012g0138a0001c0002t0005g0022others(7): Show | 11 | HG01099.hp2 HG01109.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.-70-1664_-70-1661d others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989832 | ||||||
chr14:73989832
|
C | CAAAAA | 6 | a0001c0002t0009g0226a0001c0002t0010g0221a0001c0002t0010g0222others(3): Show | 7 | HG02257.hp1 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70-1665_-70-1661d others(7): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989832 | ||||||
chr14:73989832
|
CA | C | 53 | a0001c0001t0006g0057a0001c0002t0002g0242a0001c0002t0002g0287others(50): Show | 53 | HG00423.hp2 HG00642.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-70-1661delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989832 | ||||||
chr14:73989970
|
A | G | 1 | a0001c0002t0005g0042 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-70-1798T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989970 | ||||||
chr14:73990176
|
C | T | 12 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-70-2004G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990176 | ||||||
chr14:73990293
|
C | G | 60 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-70-2121G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990293 | ||||||
chr14:73990313
|
C | T | 1 | a0001c0001t0004g0261 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-70-2141G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990313 | ||||||
chr14:73990381
|
C | CTGGAG | 50 | a0001c0002t0003g0007a0001c0002t0003g0070a0001c0002t0003g0072others(47): Show | 52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.-70-2214_-70-2210d others(7): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990381 | ||||||
chr14:73990390
|
A | G | 41 | a0001c0001t0005g0041a0001c0002t0005g0002a0001c0002t0005g0003others(38): Show | 44 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-70-2218T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990390 | ||||||
chr14:73990418
|
A | G | 35 | a0001c0001t0005g0041a0001c0002t0005g0002a0001c0002t0005g0003others(32): Show | 37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-70-2246T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990418 | ||||||
chr14:73990459
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(91): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.-70-2287G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990459 | ||||||
chr14:73990489
|
C | T | 3 | a0001c0001t0023g0129a0001c0001t0024g0285a0001c0001t0025g0130 | 3 | HG02818.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-70-2317G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990489 | ||||||
chr14:73990511
|
T | C | 60 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-70-2339A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990511 | ||||||
chr14:73990525
|
G | C | 68 | a0001c0001t0004g0017a0001c0001t0004g0125a0001c0001t0004g0126others(65): Show | 71 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.-70-2353C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990525 | ||||||
chr14:73990775
|
T | G | 35 | a0001c0001t0005g0041a0001c0002t0005g0002a0001c0002t0005g0003others(32): Show | 37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-70-2603A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990775 | ||||||
chr14:73991026
|
C | T | 3 | a0001c0001t0004g0207a0001c0001t0004g0208a0004c0006t0004g0013 | 4 | HG01891.hp2 HG02258.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70-2854G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991026 | ||||||
chr14:73991241
|
C | T | 110 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(107): Show | 112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-70-3069G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991241 | ||||||
chr14:73991288
|
G | A | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70-3116C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991288 | ||||||
chr14:73991293
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-70-3121C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991293 | ||||||
chr14:73991363
|
G | A | 1 | a0001c0002t0008g0345 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-70-3191C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991363 | ||||||
chr14:73991376
|
T | G | 4 | a0001c0001t0004g0017a0001c0001t0004g0228a0001c0002t0008g0054others(1): Show | 5 | HG01243.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70-3204A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991376 | ||||||
chr14:73991587
|
T | TA | 59 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(56): Show | 59 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-70-3416dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991587 | ||||||
chr14:73991587
|
TA | T | 36 | a0001c0001t0005g0041a0001c0001t0006g0275a0001c0002t0005g0002others(33): Show | 38 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-70-3416delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991587 | ||||||
chr14:73991601
|
C | A | 1 | a0001c0001t0006g0210 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-70-3429G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991601 | ||||||
chr14:73991608
|
C | CA | 16 | a0001c0001t0005g0041a0001c0001t0007g0143a0001c0001t0011g0132others(13): Show | 17 | HG00438.hp1 HG01243.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-70-3437dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991608 | ||||||
chr14:73991608
|
CA | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(56): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.-70-3437delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991608 | ||||||
chr14:73991620
|
A | C | 3 | a0001c0001t0023g0129a0001c0001t0024g0285a0001c0001t0025g0130 | 3 | HG02818.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-70-3448T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991620 | ||||||
chr14:73991625
|
A | AAAAAG | 38 | a0001c0002t0003g0007a0001c0002t0003g0070a0001c0002t0003g0074others(35): Show | 40 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.-70-3454_-70-3453i others(7): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991625 | ||||||
chr14:73991625
|
A | AAAAG | 73 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-70-3454_-70-3453i others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991625 | ||||||
chr14:73991625
|
A | AAAG | 9 | a0001c0001t0004g0017a0001c0001t0004g0228a0001c0002t0002g0310others(6): Show | 10 | HG00673.hp1 HG01243.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-70-3454_-70-3453i others(5): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991625 | ||||||
chr14:73991705
|
T | G | 1 | a0001c0002t0002g0352 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-70-3533A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991705 | ||||||
chr14:73991858
|
T | A | 122 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-70-3686A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991858 | ||||||
chr14:73991915
|
C | G | 2 | a0001c0001t0012g0360a0001c0001t0012g0361 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-70-3743G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991915 | ||||||
chr14:73991960
|
T | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(56): Show | 64 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.-70-3788A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991960 | ||||||
chr14:73992011
|
G | GTA | 61 | a0001c0001t0001g0335a0001c0002t0002g0098a0001c0002t0002g0113others(58): Show | 61 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.-70-3841_-70-3840d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992011 | ||||||
chr14:73992026
|
A | T | 60 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-70-3854T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992026 | ||||||
chr14:73992058
|
G | A | 1 | a0001c0002t0003g0078 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-70-3886C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992058 | ||||||
chr14:73992551
|
G | T | 6 | a0001c0002t0010g0015a0001c0002t0010g0220a0001c0002t0010g0221others(3): Show | 7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70-4379C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992551 | ||||||
chr14:73992674
|
A | C | 1 | a0001c0002t0008g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-70-4502T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992674 | ||||||
chr14:73992683
|
C | CA | 24 | a0001c0001t0001g0151a0001c0001t0001g0170a0001c0001t0001g0178others(21): Show | 25 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.-70-4512dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992683 | ||||||
chr14:73992683
|
CAAAAAAA others(1): Show |
C | 58 | a0001c0002t0002g0113a0001c0002t0002g0242a0001c0002t0002g0286others(55): Show | 58 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-70-4519_-70-4512d others(10): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992683 | ||||||
chr14:73992737
|
G | A | 9 | a0001c0002t0008g0056a0001c0002t0008g0271a0001c0002t0008g0339others(6): Show | 9 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-70-4565C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992737 | ||||||
chr14:73992833
|
T | C | 1 | a0001c0001t0004g0233 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-70-4661A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992833 | ||||||
chr14:73992914
|
A | C | 3 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227 | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70-4742T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992914 | ||||||
chr14:73992917
|
C | T | 35 | a0001c0001t0005g0041a0001c0002t0005g0002a0001c0002t0005g0003others(32): Show | 37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-70-4745G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992917 | ||||||
chr14:73992976
|
A | G | 124 | a0001c0001t0004g0017a0001c0001t0004g0228a0001c0002t0002g0098others(121): Show | 127 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-70-4804T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992976 | ||||||
chr14:73992986
|
G | C | 12 | a0001c0002t0003g0077a0001c0002t0003g0078a0001c0002t0003g0079others(9): Show | 12 | HG01358.hp2 NA18947.hp1 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-70-4814C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992986 | ||||||
chr14:73993012
|
A | C | 1 | a0001c0001t0004g0256 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-70-4840T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993012 | ||||||
chr14:73993392
|
C | T | 122 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-70-5220G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993392 | ||||||
chr14:73993423
|
C | T | 171 | a0001c0001t0005g0041a0001c0002t0002g0098a0001c0002t0002g0113others(168): Show | 178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.-70-5251G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993423 | ||||||
chr14:73993590
|
C | T | 8 | a0001c0002t0008g0056a0001c0002t0008g0339a0001c0002t0008g0340others(5): Show | 8 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-70-5418G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993590 | ||||||
chr14:73993608
|
T | A | 1 | a0001c0001t0001g0192 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-70-5436A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993608 | ||||||
chr14:73993735
|
CAGCAGCT others(8807): Show |
C | 1 | a0004c0006t0004g0013 | 2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-71+8542_-70-5564d others(2): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993735 | ||||||
chr14:73993785
|
A | T | 122 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-70-5613T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993785 | ||||||
chr14:73993921
|
C | CA | 4 | a0001c0001t0001g0171a0001c0001t0012g0360a0001c0001t0012g0361others(1): Show | 4 | HG02083.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70-5750dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993921 | ||||||
chr14:73993921
|
C | CAA | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70-5751_-70-5750d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993921 | ||||||
chr14:73993921
|
CA | C | 64 | a0001c0001t0004g0125a0001c0001t0004g0126a0001c0001t0004g0207others(61): Show | 65 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.-70-5750delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993921 | ||||||
chr14:73993924
|
AC | A | 50 | a0001c0001t0004g0213a0001c0001t0004g0214a0001c0001t0004g0219others(47): Show | 55 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.-70-5753delG | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993924 | ||||||
chr14:73993925
|
C | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(68): Show | 76 | HG00323.hp2 HG00558.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.-70-5753G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993925 | ||||||
chr14:73993928
|
A | C | 1 | a0001c0001t0012g0138 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-70-5756T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993928 | ||||||
chr14:73993929
|
A | C | 4 | a0001c0001t0006g0059a0001c0002t0005g0033a0001c0002t0005g0048others(1): Show | 4 | HG01346.hp2 HG02738.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70-5757T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993929 | ||||||
chr14:73993933
|
AAC | A | 109 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(106): Show | 111 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.-70-5763_-70-5762d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993933 | ||||||
chr14:73993934
|
AC | A | 5 | a0001c0001t0004g0017a0001c0001t0004g0228a0001c0002t0008g0054others(2): Show | 6 | HG01243.hp1 HG02451.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70-5763delG | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993934 | ||||||
chr14:73993935
|
C | A | 10 | a0001c0002t0008g0056a0001c0002t0008g0271a0001c0002t0008g0339others(7): Show | 10 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-70-5763G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993935 | ||||||
chr14:73993938
|
A | C | 50 | a0001c0002t0003g0007a0001c0002t0003g0070a0001c0002t0003g0072others(47): Show | 52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.-70-5766T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993938 | ||||||
chr14:73993971
|
A | C | 1 | a0001c0002t0009g0227 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-70-5799T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993971 | ||||||
chr14:73993988
|
T | C | 2 | a0001c0001t0004g0213a0001c0001t0004g0214 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-70-5816A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993988 | ||||||
chr14:73994271
|
G | A | 1 | a0001c0002t0003g0358 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-70-6099C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994271 | ||||||
chr14:73994414
|
T | A | 72 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(69): Show | 72 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.-70-6242A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994414 | ||||||
chr14:73994418
|
C | T | 72 | a0001c0002t0002g0098a0001c0002t0002g0113a0001c0002t0002g0242others(69): Show | 72 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.-70-6246G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994418 | ||||||
chr14:73994500
|
C | T | 1 | a0001c0002t0002g0310 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-70-6328G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994500 | ||||||
chr14:73994607
|
C | T | 1 | a0001c0002t0003g0079 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-70-6435G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994607 | ||||||
chr14:73994710
|
G | A | 1 | a0001c0002t0002g0329 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-70-6538C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994710 | ||||||
chr14:73994730
|
C | CA | 50 | a0001c0002t0003g0007a0001c0002t0003g0070a0001c0002t0003g0072others(47): Show | 52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.-70-6559dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994730 | ||||||
chr14:73994768
|
T | A | 12 | a0001c0001t0007g0313a0001c0001t0007g0318a0001c0002t0002g0286others(9): Show | 12 | HG00408.hp1 HG02083.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.-70-6596A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994768 | ||||||
chr14:73994879
|
T | A | 1 | a0001c0001t0031g0248 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-70-6707A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994879 | ||||||
chr14:73994895
|
C | G | 3 | a0001c0001t0004g0125a0001c0001t0004g0126a0001c0002t0008g0054 | 3 | HG03041.hp1 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-70-6723G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994895 | ||||||
chr14:73994927
|
T | C | 46 | a0001c0001t0001g0009a0001c0001t0001g0152a0001c0001t0001g0160others(43): Show | 50 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.-70-6755A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994927 | ||||||
chr14:73995048
|
A | AT | 45 | a0001c0002t0002g0098a0001c0002t0003g0007a0001c0002t0003g0070others(42): Show | 47 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.-70-6877dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995048 | ||||||
chr14:73995048
|
AT | A | 95 | a0001c0001t0001g0150a0001c0001t0001g0162a0001c0001t0001g0255others(92): Show | 99 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-70-6877delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995048 | ||||||
chr14:73995048
|
ATT | A | 45 | a0001c0001t0001g0193a0001c0001t0004g0017a0001c0001t0004g0228others(42): Show | 48 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-70-6878_-70-6877d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995048 | ||||||
chr14:73995066
|
A | T | 1 | a0001c0002t0008g0271 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-70-6894T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995066 | ||||||
chr14:73995079
|
T | C | 1 | a0001c0001t0007g0188 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-70-6907A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995079 | ||||||
chr14:73995359
|
A | G | 1 | a0001c0001t0013g0269 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-70-7187T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995359 | ||||||
chr14:73995406
|
G | T | 1 | a0001c0001t0013g0269 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-70-7234C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995406 | ||||||
chr14:73995501
|
T | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(77): Show | 86 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-70-7329A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995501 | ||||||
chr14:73995510
|
A | G | 315 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(312): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.-70-7338T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995510 | ||||||
chr14:73995513
|
G | A | 1 | a0001c0002t0008g0271 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-70-7341C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995513 | ||||||
chr14:73995585
|
A | AAAT | 45 | a0001c0001t0001g0165a0001c0001t0001g0205a0001c0001t0004g0208others(42): Show | 45 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.-70-7416_-70-7414d others(5): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995585 | ||||||
chr14:73995585
|
A | AAATAAT | 45 | a0001c0001t0001g0151a0001c0001t0001g0255a0001c0001t0004g0207others(42): Show | 47 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-70-7419_-70-7414d others(8): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995585 | ||||||
chr14:73995585
|
A | AAATAATA others(2): Show |
18 | a0001c0001t0004g0213a0001c0001t0004g0214a0001c0001t0004g0233others(15): Show | 19 | HG01069.hp2 HG01168.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.-70-7422_-70-7414d others(11): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995585 | ||||||
chr14:73995585
|
A | AAATAATA others(5): Show |
55 | a0001c0001t0007g0313a0001c0001t0011g0131a0001c0001t0011g0132others(52): Show | 57 | HG00423.hp2 HG00642.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.-70-7425_-70-7414d others(14): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995585 | ||||||
chr14:73995585
|
A | AAATAATA others(8): Show |
9 | a0001c0002t0002g0242a0001c0002t0002g0287a0001c0002t0002g0298others(6): Show | 9 | HG02486.hp2 HG03239.hp1 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.-70-7428_-70-7414d others(17): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995585 | ||||||
chr14:73995585
|
A | AAATAATA others(11): Show |
1 | a0001c0002t0002g0311 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-70-7431_-70-7414d others(20): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995585 | ||||||
chr14:73995585
|
A | T | 1 | a0001c0001t0001g0176 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-70-7413T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995585 | ||||||
chr14:73995585
|
AAAT | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(121): Show | 134 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.-70-7416_-70-7414d others(5): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995585 | ||||||
chr14:73995729
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-70-7557A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995729 | ||||||
chr14:73995769
|
G | A | 1 | a0001c0001t0006g0057 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-70-7597C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995769 | ||||||
chr14:73995861
|
T | A | 1 | a0001c0002t0005g0038 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-70-7689A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995861 | ||||||
chr14:73995898
|
T | A | 1 | a0001c0002t0017g0069 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-70-7726A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995898 | ||||||
chr14:73995987
|
G | C | 234 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0207others(231): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-70-7815C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995987 | ||||||
chr14:73996007
|
A | G | 1 | a0001c0001t0006g0280 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-70-7835T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996007 | ||||||
chr14:73996020
|
C | T | 1 | a0001c0002t0002g0295 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-70-7848G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996020 | ||||||
chr14:73996056
|
A | C | 5 | a0001c0001t0006g0217a0001c0001t0023g0129a0001c0001t0024g0285others(2): Show | 5 | HG01884.hp1 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70-7884T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996056 | ||||||
chr14:73996165
|
C | T | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-70-7993G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996165 | ||||||
chr14:73996186
|
T | C | 2 | a0001c0001t0018g0005a0001c0001t0018g0270 | 3 | HG02559.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-70-8014A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996186 | ||||||
chr14:73996231
|
T | C | 1 | a0001c0002t0003g0266 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-70-8059A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996231 | ||||||
chr14:73996369
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-70-8197G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996369 | ||||||
chr14:73996504
|
T | TA | 36 | a0001c0001t0004g0254a0001c0001t0005g0041a0001c0001t0006g0211others(33): Show | 38 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.-70-8333dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996504 | ||||||
chr14:73996504
|
TA | T | 78 | a0001c0001t0001g0158a0001c0001t0001g0164a0001c0001t0004g0348others(75): Show | 78 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-70-8333delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996504 | ||||||
chr14:73996857
|
C | T | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-70-8685G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996857 | ||||||
chr14:73996979
|
C | A | 11 | a0001c0001t0004g0125a0001c0001t0004g0126a0001c0001t0006g0109others(8): Show | 13 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-70-8807G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996979 | ||||||
chr14:73997020
|
C | T | 1 | a0001c0001t0007g0175 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-70-8848G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73997020 | ||||||
chr14:73997147
|
C | A | 9 | a0001c0002t0003g0077a0001c0002t0003g0092a0001c0002t0003g0093others(6): Show | 9 | NA18947.hp1 NA18962.hp1 NA18984.hp1 others(6): Show |
intron_variant | MODIFIER | c.-70-8975G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73997147 | ||||||
chr14:73997283
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-70-9111C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73997283 | ||||||
chr14:73997305
|
T | C | 3 | a0001c0001t0023g0129a0001c0001t0024g0285a0001c0001t0025g0130 | 3 | HG02818.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-70-9133A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73997305 | ||||||
chr14:73997368
|
T | C | 5 | a0001c0002t0005g0020a0001c0002t0005g0021a0001c0002t0005g0022others(2): Show | 5 | NA18967.hp2 NA18994.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70-9196A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73997368 | ||||||
chr14:73997632
|
C | T | 1 | a0001c0002t0002g0297 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-70-9460G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73997632 | ||||||
chr14:73997862
|
C | T | 1 | a0001c0001t0028g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-70-9690G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73997862 | ||||||
chr14:73998197
|
G | A | 2 | a0001c0002t0003g0265a0001c0002t0003g0266 | 2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-70-10025C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998197 | ||||||
chr14:73998288
|
C | G | 5 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70-10116G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998288 | ||||||
chr14:73998405
|
C | G | 1 | a0001c0002t0003g0078 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-70-10233G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998405 | ||||||
chr14:73998412
|
TTTTGTC | T | 9 | a0001c0001t0004g0125a0001c0001t0004g0126a0001c0001t0006g0109others(6): Show | 10 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.-70-10246_-70-1024 others(10): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998412 | ||||||
chr14:73998582
|
GA | G | 58 | a0001c0001t0005g0041a0001c0001t0007g0053a0001c0001t0011g0131others(55): Show | 63 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.-70-10411delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998582 | ||||||
chr14:73998587
|
A | G | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-70-10415T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998587 | ||||||
chr14:73998702
|
G | A | 1 | a0001c0001t0004g0229 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-70-10530C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998702 | ||||||
chr14:73998742
|
A | G | 8 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227others(5): Show | 10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-70-10570T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998742 | ||||||
chr14:73998908
|
G | C | 1 | a0001c0002t0003g0095 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-70-10736C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998908 | ||||||
chr14:73998959
|
T | C | 52 | a0001c0001t0030g0118a0001c0002t0002g0098a0001c0002t0003g0007others(49): Show | 54 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-70-10787A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998959 | ||||||
chr14:73999038
|
A | T | 104 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0207others(101): Show | 107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.-70-10866T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999038 | ||||||
chr14:73999053
|
T | A | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-70-10881A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999053 | ||||||
chr14:73999122
|
T | TTCA | 41 | a0001c0001t0001g0255a0001c0001t0004g0207a0001c0001t0004g0208others(38): Show | 41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-70-10953_-70-1095 others(7): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999122 | ||||||
chr14:73999256
|
A | G | 235 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0207others(232): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-70-11084T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999256 | ||||||
chr14:73999275
|
G | C | 1 | a0001c0001t0007g0173 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-70-11103C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999275 | ||||||
chr14:73999360
|
C | T | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70-11188G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999360 | ||||||
chr14:73999460
|
C | A | 1 | a0001c0002t0008g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-70-11288G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999460 | ||||||
chr14:73999496
|
C | A | 1 | a0001c0002t0008g0054 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-70-11324G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999496 | ||||||
chr14:73999496
|
C | CA | 38 | a0001c0001t0001g0255a0001c0001t0004g0207a0001c0001t0004g0208others(35): Show | 38 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.-70-11325_-70-1132 others(5): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999496 | ||||||
chr14:73999497
|
C | A | 155 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0207others(152): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-70-11325G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999497 | ||||||
chr14:73999524
|
G | A | 1 | a0001c0002t0008g0362 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-70-11352C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999524 | ||||||
chr14:73999550
|
C | T | 2 | a0001c0001t0004g0017a0001c0001t0004g0228 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-70-11378G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999550 | ||||||
chr14:73999591
|
T | C | 226 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0207others(223): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.-70-11419A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999591 | ||||||
chr14:73999591
|
T | G | 4 | a0002c0003t0009g0004a0002c0003t0009g0065a0002c0003t0009g0066others(1): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70-11419A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999591 | ||||||
chr14:73999653
|
G | A | 9 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138others(6): Show | 9 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-71+11438C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999653 | ||||||
chr14:73999653
|
GC | G | 3 | a0001c0001t0023g0129a0001c0001t0024g0285a0001c0001t0025g0130 | 3 | HG02818.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-71+11437delG | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999653 | ||||||
chr14:73999660
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-71+11431G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999660 | ||||||
chr14:73999791
|
C | CA | 5 | a0001c0001t0006g0210a0001c0001t0006g0211a0001c0001t0006g0212others(2): Show | 6 | HG01081.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71+11299dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999791 | ||||||
chr14:73999812
|
G | A | 5 | a0001c0001t0007g0313a0001c0002t0002g0311a0001c0002t0002g0312others(2): Show | 5 | HG00408.hp1 HG02083.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71+11279C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999812 | ||||||
chr14:73999860
|
C | T | 1 | a0001c0008t0002g0324 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-71+11231G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999860 | ||||||
chr14:73999948
|
C | T | 7 | a0001c0002t0005g0025a0001c0002t0005g0027a0001c0002t0005g0030others(4): Show | 7 | HG01099.hp2 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+11143G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999948 | ||||||
chr14:74000087
|
C | CA | 13 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(10): Show | 14 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-71+11003dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000087 | ||||||
chr14:74000087
|
CA | C | 41 | a0001c0001t0001g0203a0001c0001t0001g0230a0001c0001t0004g0219others(38): Show | 43 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.-71+11003delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000087 | ||||||
chr14:74000195
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-71+10896C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000195 | ||||||
chr14:74000235
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(75): Show | 84 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-71+10856A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000235 | ||||||
chr14:74000255
|
G | A | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+10836C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000255 | ||||||
chr14:74000378
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0145a0001c0001t0001g0187others(2): Show | 6 | HG02015.hp1 NA18956.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71+10713C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000378 | ||||||
chr14:74000378
|
G | C | 3 | a0001c0002t0003g0101a0001c0002t0003g0102a0001c0002t0003g0103 | 3 | HG03490.hp1 HG03492.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-71+10713C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000378 | ||||||
chr14:74000469
|
A | T | 5 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71+10622T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000469 | ||||||
chr14:74000519
|
G | A | 62 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(59): Show | 62 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.-71+10572C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000519 | ||||||
chr14:74000547
|
G | A | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+10544C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000547 | ||||||
chr14:74000651
|
T | A | 6 | a0001c0002t0010g0015a0001c0002t0010g0220a0001c0002t0010g0221others(3): Show | 7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+10440A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000651 | ||||||
chr14:74000698
|
G | A | 1 | a0001c0001t0004g0233 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-71+10393C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000698 | ||||||
chr14:74000746
|
C | A | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+10345G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000746 | ||||||
chr14:74000769
|
A | C | 235 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0207others(232): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-71+10322T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000769 | ||||||
chr14:74000828
|
G | A | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+10263C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000828 | ||||||
chr14:74000943
|
A | G | 3 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056 | 3 | HG01243.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-71+10148T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000943 | ||||||
chr14:74001054
|
G | A | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+10037C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001054 | ||||||
chr14:74001112
|
C | T | 3 | a0001c0001t0015g0008a0001c0001t0015g0121a0001c0001t0015g0122 | 4 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71+9979G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001112 | ||||||
chr14:74001136
|
T | C | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+9955A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001136 | ||||||
chr14:74001176
|
A | G | 235 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0207others(232): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-71+9915T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001176 | ||||||
chr14:74001284
|
C | T | 41 | a0001c0001t0001g0255a0001c0001t0004g0207a0001c0001t0004g0208others(38): Show | 41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-71+9807G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001284 | ||||||
chr14:74001362
|
T | A | 2 | a0001c0001t0004g0017a0001c0001t0004g0228 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-71+9729A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001362 | ||||||
chr14:74001371
|
G | C | 7 | a0001c0002t0008g0339a0001c0002t0008g0340a0001c0002t0008g0341others(4): Show | 7 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+9720C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001371 | ||||||
chr14:74001415
|
T | C | 1 | a0001c0002t0008g0344 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-71+9676A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001415 | ||||||
chr14:74001427
|
G | A | 1 | a0001c0002t0003g0096 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-71+9664C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001427 | ||||||
chr14:74001432
|
G | A | 1 | a0001c0002t0003g0358 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-71+9659C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001432 | ||||||
chr14:74001450
|
C | T | 2 | a0001c0001t0006g0217a0001c0001t0028g0218 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-71+9641G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001450 | ||||||
chr14:74001496
|
C | T | 1 | a0001c0002t0002g0336 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-71+9595G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001496 | ||||||
chr14:74001502
|
A | C | 6 | a0001c0001t0001g0194a0001c0001t0006g0210a0001c0001t0006g0211others(3): Show | 7 | HG01081.hp1 HG01884.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+9589T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001502 | ||||||
chr14:74001526
|
G | C | 2 | a0001c0001t0006g0217a0001c0001t0028g0218 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-71+9565C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001526 | ||||||
chr14:74001536
|
C | T | 1 | a0001c0001t0006g0217 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-71+9555G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001536 | ||||||
chr14:74001542
|
C | T | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+9549G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001542 | ||||||
chr14:74001552
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | NA18954.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-71+9539C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001552 | ||||||
chr14:74001632
|
C | T | 41 | a0001c0001t0001g0255a0001c0001t0004g0207a0001c0001t0004g0208others(38): Show | 41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-71+9459G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001632 | ||||||
chr14:74001666
|
C | CA | 10 | a0001c0001t0006g0063a0001c0001t0006g0109a0001c0001t0006g0111others(7): Show | 10 | HG01106.hp2 HG01123.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.-71+9424dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | ||||||
chr14:74001666
|
C | CAAAAA | 31 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0145others(28): Show | 35 | HG00323.hp2 HG01256.hp2 HG01258.hp2 others(32): Show |
intron_variant | MODIFIER | c.-71+9420_-71+9424d others(7): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | ||||||
chr14:74001666
|
C | CAAAAAA | 18 | a0001c0001t0001g0139a0001c0001t0001g0149a0001c0001t0001g0155others(15): Show | 18 | HG00438.hp2 HG00673.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.-71+9419_-71+9424d others(8): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | ||||||
chr14:74001666
|
C | CAAAAAAA | 14 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0150others(11): Show | 16 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-71+9418_-71+9424d others(9): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | ||||||
chr14:74001666
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0144 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-71+9415_-71+9424d others(12): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | ||||||
chr14:74001666
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0186 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-71+9414_-71+9424d others(13): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | ||||||
chr14:74001666
|
CAAAAAAA others(1): Show |
C | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+9417_-71+9424d others(10): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | ||||||
chr14:74001666
|
CAAAAAAA others(2): Show |
C | 7 | a0001c0002t0005g0003a0001c0002t0005g0022a0001c0002t0005g0023others(4): Show | 8 | HG00639.hp2 HG00741.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.-71+9416_-71+9424d others(11): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | ||||||
chr14:74001666
|
CAAAAAAA others(3): Show |
C | 46 | a0001c0001t0001g0158a0001c0001t0005g0041a0001c0001t0007g0053others(43): Show | 49 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.-71+9415_-71+9424d others(12): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | ||||||
chr14:74001666
|
CAAAAAAA others(4): Show |
C | 77 | a0001c0001t0004g0241a0001c0001t0004g0256a0001c0001t0004g0257others(74): Show | 78 | HG00408.hp1 HG00642.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.-71+9414_-71+9424d others(13): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | ||||||
chr14:74001666
|
CAAAAAAA others(5): Show |
C | 91 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0207others(88): Show | 94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-71+9413_-71+9424d others(14): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | ||||||
chr14:74001666
|
CAAAAAAA others(6): Show |
C | 8 | a0001c0001t0023g0129a0001c0001t0024g0285a0001c0001t0025g0130others(5): Show | 8 | HG01517.hp1 HG02818.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-71+9412_-71+9424d others(15): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | ||||||
chr14:74001666
|
CAAAAAAA others(9): Show |
C | 5 | a0001c0001t0001g0140a0001c0001t0001g0192a0001c0001t0001g0194others(2): Show | 5 | HG01070.hp2 HG01192.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71+9409_-71+9424d others(18): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | ||||||
chr14:74001745
|
G | C | 1 | a0001c0001t0006g0279 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-71+9346C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001745 | ||||||
chr14:74001829
|
T | G | 235 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0207others(232): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-71+9262A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001829 | ||||||
chr14:74001910
|
C | T | 162 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0207others(159): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.-71+9181G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001910 | ||||||
chr14:74001940
|
T | C | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+9151A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001940 | ||||||
chr14:74002034
|
G | A | 1 | a0001c0002t0002g0316 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-71+9057C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002034 | ||||||
chr14:74002194
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-71+8897G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002194 | ||||||
chr14:74002195
|
G | A | 51 | a0001c0001t0030g0118a0001c0002t0002g0098a0001c0002t0003g0007others(48): Show | 53 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-71+8896C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002195 | ||||||
chr14:74002263
|
T | C | 1 | a0003c0004t0006g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-71+8828A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002263 | ||||||
chr14:74002485
|
T | C | 37 | a0001c0001t0005g0041a0001c0001t0007g0053a0001c0002t0005g0002others(34): Show | 39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-71+8606A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002485 | ||||||
chr14:74002513
|
A | G | 1 | a0001c0002t0008g0271 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-71+8578T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002513 | ||||||
chr14:74002567
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-71+8524T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002567 | ||||||
chr14:74002744
|
TCTCCTTT others(5): Show |
T | 1 | a0001c0002t0003g0106 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-71+8335_-71+8346d others(14): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002744 | ||||||
chr14:74002777
|
A | T | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+8314T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002777 | ||||||
chr14:74002824
|
C | T | 5 | a0001c0001t0013g0240a0001c0001t0013g0246a0001c0001t0013g0247others(2): Show | 5 | HG00438.hp1 NA18974.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71+8267G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002824 | ||||||
chr14:74002856
|
T | C | 51 | a0001c0001t0030g0118a0001c0002t0002g0098a0001c0002t0003g0007others(48): Show | 53 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-71+8235A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002856 | ||||||
chr14:74002924
|
C | G | 28 | a0001c0001t0004g0125a0001c0001t0004g0126a0001c0001t0006g0071others(25): Show | 30 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.-71+8167G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002924 | ||||||
chr14:74002950
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | NA18990.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.-71+8141G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002950 | ||||||
chr14:74003212
|
G | T | 236 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0207others(233): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-71+7879C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003212 | ||||||
chr14:74003238
|
T | C | 8 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227others(5): Show | 10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-71+7853A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003238 | ||||||
chr14:74003305
|
C | A | 2 | a0001c0001t0004g0017a0001c0001t0004g0228 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-71+7786G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003305 | ||||||
chr14:74003305
|
C | T | 4 | a0002c0003t0009g0004a0002c0003t0009g0065a0002c0003t0009g0066others(1): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71+7786G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003305 | ||||||
chr14:74003360
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(75): Show | 84 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-71+7731G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003360 | ||||||
chr14:74003361
|
A | G | 315 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(312): Show | 330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.-71+7730T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003361 | ||||||
chr14:74003597
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | NA18954.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-71+7494T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003597 | ||||||
chr14:74003617
|
T | G | 1 | a0001c0002t0005g0141 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-71+7474A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003617 | ||||||
chr14:74003789
|
A | G | 3 | a0001c0001t0006g0105a0001c0001t0006g0148a0001c0001t0026g0018 | 3 | HG01515.hp1 HG02818.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-71+7302T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003789 | ||||||
chr14:74003840
|
T | C | 5 | a0001c0001t0001g0012a0001c0001t0001g0145a0001c0001t0001g0187others(2): Show | 6 | HG02015.hp1 NA18956.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71+7251A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003840 | ||||||
chr14:74003870
|
GAGGATCA others(136): Show |
G | 2 | a0001c0001t0012g0360a0001c0001t0012g0361 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-71+7078_-71+7220d others(2): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003870 | ||||||
chr14:74003929
|
A | T | 3 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138 | 3 | HG02572.hp2 HG02647.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-71+7162T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003929 | ||||||
chr14:74003936
|
A | T | 5 | a0001c0001t0006g0105a0001c0001t0006g0148a0001c0001t0018g0005others(2): Show | 6 | HG01515.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71+7155T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003936 | ||||||
chr14:74003960
|
C | A | 1 | a0001c0001t0007g0291 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-71+7131G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003960 | ||||||
chr14:74003963
|
G | A | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+7128C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003963 | ||||||
chr14:74004078
|
A | C | 236 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0207others(233): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-71+7013T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004078 | ||||||
chr14:74004119
|
T | A | 1 | a0001c0002t0003g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-71+6972A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004119 | ||||||
chr14:74004119
|
T | G | 62 | a0001c0001t0004g0017a0001c0001t0004g0228a0001c0001t0006g0217others(59): Show | 65 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.-71+6972A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004119 | ||||||
chr14:74004178
|
A | T | 1 | a0001c0001t0016g0115 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-71+6913T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004178 | ||||||
chr14:74004190
|
CAG | C | 42 | a0001c0001t0001g0255a0001c0001t0004g0207a0001c0001t0004g0208others(39): Show | 43 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.-71+6899_-71+6900d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004190 | ||||||
chr14:74004204
|
A | G | 236 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0207others(233): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-71+6887T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004204 | ||||||
chr14:74004313
|
A | G | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+6778T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004313 | ||||||
chr14:74004356
|
C | A | 2 | a0001c0001t0004g0017a0001c0001t0004g0228 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-71+6735G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004356 | ||||||
chr14:74004371
|
T | C | 1 | a0001c0002t0003g0099 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-71+6720A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004371 | ||||||
chr14:74004376
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-71+6715G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004376 | ||||||
chr14:74004500
|
G | T | 1 | a0001c0001t0004g0213 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-71+6591C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004500 | ||||||
chr14:74004513
|
G | A | 1 | a0001c0001t0028g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-71+6578C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004513 | ||||||
chr14:74004559
|
G | A | 8 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227others(5): Show | 10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-71+6532C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004559 | ||||||
chr14:74004564
|
T | C | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+6527A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004564 | ||||||
chr14:74004674
|
C | T | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+6417G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004674 | ||||||
chr14:74004689
|
T | C | 58 | a0001c0001t0005g0041a0001c0001t0007g0053a0001c0001t0011g0131others(55): Show | 63 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.-71+6402A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004689 | ||||||
chr14:74004969
|
T | G | 6 | a0001c0002t0010g0015a0001c0002t0010g0220a0001c0002t0010g0221others(3): Show | 7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+6122A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004969 | ||||||
chr14:74005068
|
G | C | 1 | a0001c0002t0005g0141 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-71+6023C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005068 | ||||||
chr14:74005134
|
G | A | 3 | a0001c0002t0010g0015a0001c0002t0010g0223a0001c0002t0010g0224 | 4 | HG02895.hp2 HG03486.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71+5957C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005134 | ||||||
chr14:74005159
|
G | A | 5 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71+5932C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005159 | ||||||
chr14:74005161
|
G | A | 8 | a0001c0002t0008g0339a0001c0002t0008g0340a0001c0002t0008g0341others(5): Show | 8 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-71+5930C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005161 | ||||||
chr14:74005192
|
G | A | 6 | a0001c0002t0010g0015a0001c0002t0010g0220a0001c0002t0010g0221others(3): Show | 7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+5899C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005192 | ||||||
chr14:74005234
|
C | A | 3 | a0001c0002t0005g0033a0001c0002t0005g0048a0001c0002t0005g0049 | 3 | HG01346.hp2 HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-71+5857G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005234 | ||||||
chr14:74005265
|
C | CA | 41 | a0001c0001t0001g0191a0001c0001t0001g0203a0001c0001t0001g0335others(38): Show | 43 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.-71+5825dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005265 | ||||||
chr14:74005272
|
AAAAAAAA others(11): Show |
A | 1 | a0001c0002t0002g0349 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-71+5801_-71+5818d others(20): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005272 | ||||||
chr14:74005273
|
AAAAAAAA others(10): Show |
A | 67 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(64): Show | 67 | HG00408.hp1 HG00642.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.-71+5801_-71+5817d others(19): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005273 | ||||||
chr14:74005274
|
AAAAAAAA others(1): Show |
A | 7 | a0001c0001t0023g0129a0001c0002t0010g0015a0001c0002t0010g0220others(4): Show | 8 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-71+5809_-71+5816d others(10): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005274 | ||||||
chr14:74005274
|
AAAAAAAA others(9): Show |
A | 3 | a0001c0001t0016g0115a0001c0002t0002g0322a0001c0002t0008g0362 | 3 | HG00423.hp2 HG01123.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-71+5801_-71+5816d others(18): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005274 | ||||||
chr14:74005290
|
G | A | 2 | a0001c0001t0023g0129a0001c0001t0024g0285 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-71+5801C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005290 | ||||||
chr14:74005320
|
G | GT | 37 | a0001c0001t0005g0041a0001c0001t0007g0053a0001c0002t0005g0002others(34): Show | 39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-71+5770dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005320 | ||||||
chr14:74005350
|
G | A | 1 | a0001c0002t0008g0271 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-71+5741C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005350 | ||||||
chr14:74005364
|
C | CAAAA | 61 | a0001c0001t0004g0017a0001c0001t0004g0228a0001c0001t0006g0217others(58): Show | 64 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-71+5723_-71+5726d others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005364 | ||||||
chr14:74005364
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0011g0132a0001c0002t0005g0031 | 2 | HG00323.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-71+5726_-71+5727i others(15): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005364 | ||||||
chr14:74005364
|
C | CAAAAAAA others(7): Show |
55 | a0001c0001t0001g0145a0001c0001t0001g0202a0001c0001t0001g0204others(52): Show | 59 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.-71+5726_-71+5727i others(16): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005364 | ||||||
chr14:74005364
|
C | CAAAAAAA others(8): Show |
173 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(170): Show | 180 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.-71+5726_-71+5727i others(17): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005364 | ||||||
chr14:74005364
|
C | CAAAAAAA others(9): Show |
14 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(11): Show | 14 | HG00099.hp1 HG00423.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-71+5726_-71+5727i others(18): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005364 | ||||||
chr14:74005364
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0014g0260 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-71+5726_-71+5727i others(19): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005364 | ||||||
chr14:74005364
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0004g0261 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-71+5726_-71+5727i others(20): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005364 | ||||||
chr14:74005369
|
A | AAAAAAAA others(7): Show |
6 | a0001c0002t0010g0015a0001c0002t0010g0220a0001c0002t0010g0221others(3): Show | 7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+5721_-71+5722i others(16): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005369 | ||||||
chr14:74005403
|
G | GT | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+5687dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005403 | ||||||
chr14:74005460
|
A | G | 1 | a0001c0001t0035g0026 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-71+5631T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005460 | ||||||
chr14:74005494
|
C | A | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+5597G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005494 | ||||||
chr14:74005497
|
C | T | 1 | a0001c0002t0002g0294 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-71+5594G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005497 | ||||||
chr14:74005523
|
A | G | 63 | a0001c0001t0004g0017a0001c0001t0004g0228a0001c0001t0006g0217others(60): Show | 66 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.-71+5568T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005523 | ||||||
chr14:74005529
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-71+5562G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005529 | ||||||
chr14:74005611
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-71+5480G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005611 | ||||||
chr14:74005615
|
C | G | 1 | a0001c0002t0005g0027 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-71+5476G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005615 | ||||||
chr14:74005827
|
A | C | 1 | a0001c0001t0007g0153 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-71+5264T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005827 | ||||||
chr14:74006145
|
A | C | 236 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0207others(233): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-71+4946T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006145 | ||||||
chr14:74006146
|
G | A | 1 | a0001c0005t0002g0347 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-71+4945C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006146 | ||||||
chr14:74006178
|
A | G | 353 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(350): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.-71+4913T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006178 | ||||||
chr14:74006225
|
T | A | 3 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227 | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71+4866A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006225 | ||||||
chr14:74006276
|
C | T | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+4815G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006276 | ||||||
chr14:74006284
|
C | CT | 77 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0196others(74): Show | 80 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-71+4806dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006284 | ||||||
chr14:74006298
|
T | TC | 3 | a0001c0002t0003g0101a0001c0002t0003g0102a0001c0002t0003g0103 | 3 | HG03490.hp1 HG03492.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-71+4792_-71+4793i others(3): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006298 | ||||||
chr14:74006314
|
C | T | 47 | a0001c0001t0030g0118a0001c0002t0002g0098a0001c0002t0003g0007others(44): Show | 49 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.-71+4777G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006314 | ||||||
chr14:74006352
|
C | T | 37 | a0001c0001t0005g0041a0001c0001t0007g0053a0001c0002t0005g0002others(34): Show | 39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-71+4739G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006352 | ||||||
chr14:74006369
|
C | T | 5 | a0001c0001t0006g0210a0001c0001t0006g0211a0001c0001t0006g0212others(2): Show | 6 | HG01081.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71+4722G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006369 | ||||||
chr14:74006427
|
G | C | 42 | a0001c0001t0001g0255a0001c0001t0004g0207a0001c0001t0004g0208others(39): Show | 43 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.-71+4664C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006427 | ||||||
chr14:74006432
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | NA18954.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-71+4659G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006432 | ||||||
chr14:74006436
|
G | T | 53 | a0001c0001t0004g0017a0001c0001t0004g0228a0001c0001t0030g0118others(50): Show | 56 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-71+4655C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006436 | ||||||
chr14:74006467
|
C | T | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+4624G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006467 | ||||||
chr14:74006534
|
C | T | 1 | a0001c0001t0033g0108 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-71+4557G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006534 | ||||||
chr14:74006589
|
T | C | 1 | a0001c0002t0008g0271 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-71+4502A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006589 | ||||||
chr14:74006600
|
A | T | 6 | a0001c0002t0010g0015a0001c0002t0010g0220a0001c0002t0010g0221others(3): Show | 7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+4491T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006600 | ||||||
chr14:74006650
|
G | A | 230 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0207others(227): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.-71+4441C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006650 | ||||||
chr14:74006692
|
C | T | 42 | a0001c0001t0001g0255a0001c0001t0004g0207a0001c0001t0004g0208others(39): Show | 43 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.-71+4399G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006692 | ||||||
chr14:74006710
|
T | C | 73 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+4381A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006710 | ||||||
chr14:74006722
|
C | T | 4 | a0001c0001t0007g0143a0001c0001t0007g0199a0001c0001t0007g0200others(1): Show | 4 | NA18960.hp2 NA18961.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71+4369G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006722 | ||||||
chr14:74006731
|
T | C | 53 | a0001c0001t0004g0017a0001c0001t0004g0228a0001c0001t0030g0118others(50): Show | 56 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-71+4360A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006731 | ||||||
chr14:74006759
|
A | AT | 47 | a0001c0001t0030g0118a0001c0002t0002g0098a0001c0002t0003g0007others(44): Show | 49 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.-71+4331dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006759 | ||||||
chr14:74006844
|
C | T | 2 | a0001c0002t0008g0339a0001c0002t0008g0340 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-71+4247G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006844 | ||||||
chr14:74006875
|
C | A | 71 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0313others(68): Show | 71 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-71+4216G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006875 | ||||||
chr14:74006892
|
AAAAGTCA others(3): Show |
A | 1 | a0001c0001t0004g0236 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-71+4189_-71+4198d others(12): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006892 | ||||||
chr14:74006904
|
T | C | 43 | a0001c0001t0005g0041a0001c0001t0007g0053a0001c0002t0005g0002others(40): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-71+4187A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006904 | ||||||
chr14:74006961
|
A | G | 1 | a0001c0002t0008g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-71+4130T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006961 | ||||||
chr14:74007122
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(75): Show | 83 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.-71+3969C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007122 | ||||||
chr14:74007184
|
C | G | 29 | a0001c0001t0001g0255a0001c0001t0004g0233a0001c0001t0004g0241others(26): Show | 29 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.-71+3907G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007184 | ||||||
chr14:74007238
|
A | G | 40 | a0001c0001t0005g0041a0001c0001t0007g0053a0001c0002t0002g0331others(37): Show | 42 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-71+3853T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007238 | ||||||
chr14:74007249
|
C | T | 1 | a0001c0002t0003g0107 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-71+3842G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007249 | ||||||
chr14:74007314
|
A | G | 1 | a0001c0002t0008g0362 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-71+3777T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007314 | ||||||
chr14:74007318
|
A | G | 1 | a0001c0002t0008g0362 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-71+3773T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007318 | ||||||
chr14:74007329
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-71+3762C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007329 | ||||||
chr14:74007332
|
T | C | 2 | a0001c0002t0008g0055a0001c0002t0008g0056 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-71+3759A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007332 | ||||||
chr14:74007333
|
A | G | 12 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0013g0240others(9): Show | 14 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-71+3758T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007333 | ||||||
chr14:74007338
|
G | A | 1 | a0001c0001t0013g0240 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-71+3753C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007338 | ||||||
chr14:74007365
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-71+3726A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007365 | ||||||
chr14:74007365
|
T | TA | 38 | a0001c0001t0001g0193a0001c0001t0005g0041a0001c0001t0007g0053others(35): Show | 40 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-71+3725dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007365 | ||||||
chr14:74007377
|
T | C | 1 | a0001c0002t0010g0220 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-71+3714A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007377 | ||||||
chr14:74007382
|
A | G | 2 | a0001c0001t0024g0285a0001c0002t0010g0220 | 2 | HG01243.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-71+3709T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007382 | ||||||
chr14:74007479
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0194 | 2 | NA18966.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-71+3612C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007479 | ||||||
chr14:74007693
|
T | C | 65 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(62): Show | 65 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.-71+3398A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007693 | ||||||
chr14:74007733
|
A | T | 9 | a0001c0001t0024g0285a0001c0002t0008g0339a0001c0002t0008g0340others(6): Show | 9 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-71+3358T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007733 | ||||||
chr14:74007831
|
AAT | A | 41 | a0001c0001t0001g0255a0001c0001t0004g0213a0001c0001t0004g0214others(38): Show | 41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-71+3258_-71+3259d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007831 | ||||||
chr14:74007832
|
AT | A | 9 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0006g0105others(6): Show | 10 | HG01168.hp2 HG01515.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.-71+3258delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007832 | ||||||
chr14:74007834
|
T | A | 1 | a0001c0002t0003g0106 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-71+3257A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007834 | ||||||
chr14:74007853
|
T | TG | 5 | a0001c0001t0012g0360a0001c0001t0012g0361a0001c0002t0003g0357others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71+3237dupC | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007853 | ||||||
chr14:74007873
|
G | C | 1 | a0001c0002t0002g0322 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-71+3218C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007873 | ||||||
chr14:74007967
|
A | AT | 5 | a0001c0001t0012g0360a0001c0001t0012g0361a0001c0002t0003g0357others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71+3123dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007967 | ||||||
chr14:74007993
|
G | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(76): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-71+3098C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007993 | ||||||
chr14:74008147
|
A | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(208): Show | 221 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.-71+2944T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008147 | ||||||
chr14:74008153
|
T | A | 73 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+2938A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008153 | ||||||
chr14:74008339
|
C | T | 1 | a0001c0001t0006g0281 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-71+2752G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008339 | ||||||
chr14:74008340
|
G | A | 5 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0229others(2): Show | 6 | HG01891.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71+2751C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008340 | ||||||
chr14:74008379
|
A | C | 1 | a0001c0002t0008g0339 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-71+2712T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008379 | ||||||
chr14:74008394
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-71+2697A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008394 | ||||||
chr14:74008439
|
A | G | 54 | a0001c0001t0005g0041a0001c0001t0007g0053a0001c0001t0011g0131others(51): Show | 58 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-71+2652T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008439 | ||||||
chr14:74008439
|
A | T | 5 | a0001c0001t0012g0360a0001c0001t0012g0361a0001c0002t0003g0357others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71+2652T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008439 | ||||||
chr14:74008464
|
C | T | 1 | a0001c0002t0008g0362 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-71+2627G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008464 | ||||||
chr14:74008481
|
C | T | 1 | a0001c0001t0007g0147 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-71+2610G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008481 | ||||||
chr14:74008510
|
CA | C | 5 | a0001c0001t0006g0210a0001c0001t0006g0211a0001c0001t0006g0212others(2): Show | 6 | HG01081.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71+2580delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008510 | ||||||
chr14:74008540
|
C | T | 1 | a0001c0002t0005g0025 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-71+2551G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008540 | ||||||
chr14:74008586
|
G | A | 5 | a0001c0001t0006g0210a0001c0001t0006g0211a0001c0001t0006g0212others(2): Show | 6 | HG01081.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71+2505C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008586 | ||||||
chr14:74008617
|
G | A | 2 | a0001c0002t0008g0055a0001c0002t0008g0056 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-71+2474C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008617 | ||||||
chr14:74008739
|
C | A | 1 | a0001c0002t0003g0116 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-71+2352G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008739 | ||||||
chr14:74008740
|
A | G | 1 | a0001c0002t0003g0116 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-71+2351T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008740 | ||||||
chr14:74008866
|
T | C | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+2225A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008866 | ||||||
chr14:74009093
|
T | C | 266 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(263): Show | 278 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.-71+1998A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009093 | ||||||
chr14:74009125
|
C | G | 1 | a0001c0002t0021g0073 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-71+1966G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009125 | ||||||
chr14:74009153
|
CAGA | C | 73 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+1935_-71+1937d others(5): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009153 | ||||||
chr14:74009243
|
T | C | 5 | a0001c0001t0012g0360a0001c0001t0012g0361a0001c0002t0003g0357others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71+1848A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009243 | ||||||
chr14:74009321
|
A | T | 37 | a0001c0001t0001g0255a0001c0001t0004g0233a0001c0001t0004g0234others(34): Show | 37 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.-71+1770T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009321 | ||||||
chr14:74009464
|
G | A | 1 | a0001c0002t0003g0072 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-71+1627C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009464 | ||||||
chr14:74009556
|
G | A | 3 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227 | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71+1535C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009556 | ||||||
chr14:74009591
|
TCCTTCTA others(4): Show |
T | 2 | a0001c0001t0023g0129a0001c0001t0025g0130 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-71+1489_-71+1499d others(13): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009591 | ||||||
chr14:74009595
|
T | C | 1 | a0001c0002t0003g0107 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-71+1496A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009595 | ||||||
chr14:74009696
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(76): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-71+1395G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009696 | ||||||
chr14:74009697
|
G | C | 5 | a0001c0001t0012g0360a0001c0001t0012g0361a0001c0002t0003g0357others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71+1394C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009697 | ||||||
chr14:74009791
|
C | CG | 3 | a0001c0001t0006g0071a0001c0002t0003g0070a0001c0002t0003g0072 | 3 | HG00735.hp1 HG03654.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-71+1299dupC | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009791 | ||||||
chr14:74009792
|
G | T | 1 | a0001c0001t0016g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-71+1299C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009792 | ||||||
chr14:74009793
|
A | AT | 54 | a0001c0001t0005g0041a0001c0001t0007g0053a0001c0001t0007g0146others(51): Show | 58 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-71+1297dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009793 | ||||||
chr14:74009793
|
A | G | 44 | a0001c0001t0006g0105a0001c0001t0030g0118a0001c0002t0002g0098others(41): Show | 46 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.-71+1298T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009793 | ||||||
chr14:74009793
|
A | T | 3 | a0001c0001t0006g0071a0001c0002t0003g0070a0001c0002t0003g0072 | 3 | HG00735.hp1 HG03654.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-71+1298T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009793 | ||||||
chr14:74009831
|
A | G | 11 | a0001c0001t0004g0017a0001c0001t0004g0228a0001c0001t0006g0217others(8): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-71+1260T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009831 | ||||||
chr14:74009849
|
T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(73): Show | 82 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-71+1242A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009849 | ||||||
chr14:74009860
|
C | T | 2 | a0001c0002t0017g0006a0001c0002t0017g0069 | 3 | HG00280.hp1 HG01255.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.-71+1231G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009860 | ||||||
chr14:74009920
|
T | C | 64 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(61): Show | 64 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.-71+1171A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009920 | ||||||
chr14:74009924
|
A | G | 2 | a0001c0001t0006g0217a0001c0001t0028g0218 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-71+1167T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009924 | ||||||
chr14:74010041
|
C | T | 2 | a0001c0001t0006g0217a0001c0001t0028g0218 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-71+1050G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010041 | ||||||
chr14:74010163
|
A | G | 78 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(75): Show | 78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-71+928T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010163 | ||||||
chr14:74010231
|
C | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(73): Show | 82 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-71+860G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010231 | ||||||
chr14:74010292
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-71+799G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010292 | ||||||
chr14:74010469
|
G | A | 1 | a0001c0002t0008g0362 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-71+622C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010469 | ||||||
chr14:74010497
|
T | G | 41 | a0001c0001t0001g0255a0001c0001t0004g0213a0001c0001t0004g0214others(38): Show | 41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-71+594A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010497 | ||||||
chr14:74010503
|
G | A | 54 | a0001c0001t0005g0041a0001c0001t0007g0053a0001c0001t0011g0131others(51): Show | 58 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-71+588C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010503 | ||||||
chr14:74010554
|
C | CA | 43 | a0001c0001t0001g0255a0001c0001t0004g0213a0001c0001t0004g0214others(40): Show | 43 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.-71+536dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010554 | ||||||
chr14:74010567
|
T | A | 1 | a0001c0002t0002g0288 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-71+524A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010567 | ||||||
chr14:74010581
|
A | G | 73 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+510T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010581 | ||||||
chr14:74010611
|
A | T | 266 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(263): Show | 278 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.-71+480T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010611 | ||||||
chr14:74010633
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(208): Show | 221 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.-71+458T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010633 | ||||||
chr14:74010705
|
C | T | 6 | a0001c0002t0010g0015a0001c0002t0010g0220a0001c0002t0010g0221others(3): Show | 7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+386G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010705 | ||||||
chr14:74010785
|
A | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(154): Show | 163 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.-71+306T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010785 | ||||||
chr14:74010804
|
C | T | 5 | a0001c0001t0012g0360a0001c0001t0012g0361a0001c0002t0003g0357others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71+287G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010804 | ||||||
chr14:74010870
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-71+221T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010870 | ||||||
chr14:74010944
|
T | C | 5 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0229others(2): Show | 6 | HG01891.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71+147A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010944 | ||||||
chr14:74010979
|
C | A | 3 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056 | 3 | HG01243.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-71+112G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010979 | ||||||
chr14:74011167
|
T | G | 2 | a0001c0002t0008g0339a0001c0002t0008g0340 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-130-17A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74011167 | ||||||
chr14:74011200
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-130-50G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74011200 | ||||||
chr14:74011735
|
T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(73): Show | 82 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-130-585A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74011735 | ||||||
chr14:74011779
|
T | C | 78 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(75): Show | 78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-130-629A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74011779 | ||||||
chr14:74011881
|
T | C | 78 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(75): Show | 78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-130-731A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74011881 | ||||||
chr14:74011958
|
T | C | 5 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0229others(2): Show | 6 | HG01891.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-130-808A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74011958 | ||||||
chr14:74012133
|
C | T | 1 | a0001c0002t0002g0242 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-130-983G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012133 | ||||||
chr14:74012156
|
G | C | 1 | a0001c0001t0004g0219 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-130-1006C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012156 | ||||||
chr14:74012290
|
GA | G | 4 | a0001c0001t0004g0213a0001c0001t0004g0214a0001c0002t0003g0215others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-130-1141delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012290 | ||||||
chr14:74012291
|
A | G | 1 | a0001c0001t0016g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-130-1141T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012291 | ||||||
chr14:74012291
|
AG | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(76): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-130-1142delC | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012291 | ||||||
chr14:74012291
|
AGG | A | 78 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(75): Show | 78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-130-1143_-130-114 others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012291 | ||||||
chr14:74012292
|
G | A | 1 | a0001c0001t0006g0280 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-130-1142C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012292 | ||||||
chr14:74012294
|
G | C | 9 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227others(6): Show | 11 | HG01109.hp2 HG01243.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-130-1144C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012294 | ||||||
chr14:74012362
|
C | A | 1 | a0001c0001t0030g0118 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-130-1212G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012362 | ||||||
chr14:74012487
|
A | G | 2 | a0001c0001t0004g0125a0001c0001t0004g0126 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-130-1337T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012487 | ||||||
chr14:74012514
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(76): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-130-1364G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012514 | ||||||
chr14:74012583
|
C | A | 1 | a0001c0001t0016g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-130-1433G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012583 | ||||||
chr14:74012660
|
G | T | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-130-1510C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012660 | ||||||
chr14:74012668
|
C | T | 1 | a0001c0002t0005g0024 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-130-1518G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012668 | ||||||
chr14:74012718
|
G | GGAAT | 41 | a0001c0001t0001g0255a0001c0001t0004g0213a0001c0001t0004g0214others(38): Show | 41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-130-1572_-130-156 others(8): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012718 | ||||||
chr14:74013043
|
T | G | 9 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227others(6): Show | 11 | HG01109.hp2 HG01243.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-130-1893A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013043 | ||||||
chr14:74013059
|
C | T | 1 | a0001c0002t0008g0362 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-130-1909G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013059 | ||||||
chr14:74013114
|
G | C | 4 | a0001c0001t0004g0262a0001c0001t0004g0263a0001c0001t0004g0264others(1): Show | 4 | HG02602.hp2 HG03688.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-130-1964C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013114 | ||||||
chr14:74013181
|
T | C | 1 | a0001c0001t0023g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-130-2031A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013181 | ||||||
chr14:74013329
|
C | T | 4 | a0001c0002t0005g0020a0001c0002t0005g0021a0001c0002t0005g0022others(1): Show | 4 | NA18967.hp2 NA19010.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.-130-2179G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013329 | ||||||
chr14:74013367
|
C | A | 64 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(61): Show | 64 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.-130-2217G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013367 | ||||||
chr14:74013381
|
G | A | 2 | a0001c0001t0023g0129a0001c0001t0025g0130 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-130-2231C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013381 | ||||||
chr14:74013418
|
T | C | 3 | a0001c0001t0006g0281a0001c0001t0006g0282a0001c0001t0006g0284 | 3 | NA18944.hp1 NA19058.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-130-2268A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013418 | ||||||
chr14:74013431
|
G | A | 2 | a0001c0001t0006g0217a0001c0001t0028g0218 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-130-2281C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013431 | ||||||
chr14:74013433
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(154): Show | 163 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.-130-2283A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013433 | ||||||
chr14:74013497
|
AT | A | 10 | a0001c0002t0005g0052a0001c0002t0009g0016a0001c0002t0009g0226others(7): Show | 12 | HG01109.hp2 HG01243.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.-131+2326delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013497 | ||||||
chr14:74013577
|
T | C | 1 | a0001c0002t0003g0120 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-131+2247A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013577 | ||||||
chr14:74013601
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(208): Show | 221 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.-131+2223T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013601 | ||||||
chr14:74013816
|
T | C | 1 | a0001c0001t0006g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-131+2008A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013816 | ||||||
chr14:74013910
|
T | C | 3 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138 | 3 | HG02572.hp2 HG02647.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-131+1914A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013910 | ||||||
chr14:74013956
|
C | G | 9 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227others(6): Show | 11 | HG01109.hp2 HG01243.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-131+1868G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013956 | ||||||
chr14:74014091
|
G | C | 38 | a0001c0001t0005g0041a0001c0001t0007g0053a0001c0001t0035g0026others(35): Show | 40 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-131+1733C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014091 | ||||||
chr14:74014099
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(76): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-131+1725T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014099 | ||||||
chr14:74014121
|
T | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(76): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-131+1703A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014121 | ||||||
chr14:74014171
|
C | T | 31 | a0001c0001t0001g0255a0001c0001t0004g0233a0001c0001t0004g0241others(28): Show | 31 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.-131+1653G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014171 | ||||||
chr14:74014234
|
G | A | 5 | a0001c0007t0009g0064a0002c0003t0009g0004a0002c0003t0009g0065others(2): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-131+1590C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014234 | ||||||
chr14:74014365
|
A | G | 73 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-131+1459T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014365 | ||||||
chr14:74014368
|
T | A | 2 | a0001c0002t0003g0265a0001c0002t0003g0266 | 2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-131+1456A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014368 | ||||||
chr14:74014380
|
TCC | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(73): Show | 82 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-131+1442_-131+144 others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014380 | ||||||
chr14:74014385
|
C | A | 3 | a0001c0002t0002g0287a0001c0002t0002g0329a0001c0002t0002g0330 | 3 | NA18941.hp2 NA18950.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-131+1439G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014385 | ||||||
chr14:74014385
|
C | T | 1 | a0001c0002t0003g0358 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-131+1439G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014385 | ||||||
chr14:74014386
|
C | G | 5 | a0001c0001t0012g0360a0001c0001t0012g0361a0001c0002t0003g0357others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131+1438G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014386 | ||||||
chr14:74014387
|
C | CA | 7 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0011g0133others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-131+1436_-131+143 others(5): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014387 | ||||||
chr14:74014387
|
C | G | 6 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0229others(3): Show | 7 | HG01891.hp2 HG02135.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-131+1437G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014387 | ||||||
chr14:74014388
|
C | A | 3 | a0001c0001t0015g0008a0001c0001t0015g0121a0001c0001t0015g0122 | 4 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-131+1436G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014388 | ||||||
chr14:74014389
|
C | G | 3 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227 | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-131+1435G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014389 | ||||||
chr14:74014390
|
CA | C | 74 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(71): Show | 74 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.-131+1433delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014390 | ||||||
chr14:74014391
|
A | C | 3 | a0001c0002t0002g0326a0001c0002t0002g0327a0001c0002t0002g0328 | 3 | HG03688.hp1 NA18981.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.-131+1433T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014391 | ||||||
chr14:74014537
|
T | G | 2 | a0001c0001t0012g0127a0001c0001t0012g0128 | 2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-131+1287A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014537 | ||||||
chr14:74014566
|
T | C | 4 | a0001c0001t0004g0213a0001c0001t0004g0214a0001c0001t0004g0219others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-131+1258A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014566 | ||||||
chr14:74014650
|
T | A | 4 | a0001c0001t0007g0143a0001c0001t0007g0199a0001c0001t0007g0200others(1): Show | 4 | NA18960.hp2 NA18961.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-131+1174A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014650 | ||||||
chr14:74014781
|
G | A | 2 | a0001c0001t0004g0017a0001c0001t0004g0228 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-131+1043C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014781 | ||||||
chr14:74014834
|
C | T | 1 | a0001c0001t0011g0131 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-131+990G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014834 | ||||||
chr14:74014953
|
G | T | 2 | a0001c0002t0020g0289a0001c0002t0020g0290 | 2 | NA18971.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-131+871C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014953 | ||||||
chr14:74014975
|
G | A | 1 | a0001c0001t0006g0284 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-131+849C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014975 | ||||||
chr14:74015080
|
CA | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(180): Show | 194 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-131+743delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015080 | ||||||
chr14:74015080
|
CAA | C | 76 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(73): Show | 76 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.-131+742_-131+743d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015080 | ||||||
chr14:74015214
|
T | C | 3 | a0001c0001t0004g0213a0001c0001t0004g0214a0001c0002t0003g0215 | 3 | HG02809.hp1 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-131+610A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015214 | ||||||
chr14:74015250
|
G | A | 78 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(75): Show | 78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-131+574C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015250 | ||||||
chr14:74015260
|
C | T | 2 | a0001c0001t0004g0017a0001c0001t0004g0228 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-131+564G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015260 | ||||||
chr14:74015276
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(76): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-131+548C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015276 | ||||||
chr14:74015336
|
A | G | 78 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(75): Show | 78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-131+488T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015336 | ||||||
chr14:74015359
|
G | C | 2 | a0001c0002t0002g0336a0001c0002t0002g0349 | 2 | HG02135.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-131+465C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015359 | ||||||
chr14:74015359
|
G | GC | 21 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0335others(18): Show | 21 | HG00642.hp2 HG01069.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.-131+464dupG | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015359 | ||||||
chr14:74015360
|
C | T | 1 | a0001c0001t0023g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-131+464G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015360 | ||||||
chr14:74015504
|
C | T | 1 | a0001c0001t0006g0057 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-131+320G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015504 | ||||||
chr14:74015534
|
G | A | 1 | a0001c0002t0008g0054 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-131+290C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015534 | ||||||
chr14:74015596
|
G | A | 3 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138 | 3 | HG02572.hp2 HG02647.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-131+228C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015596 | ||||||
chr14:74015608
|
C | T | 3 | a0001c0001t0012g0127a0001c0001t0012g0128a0001c0001t0012g0138 | 3 | HG02572.hp2 HG02647.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-131+216G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015608 | ||||||
chr14:74015699
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-131+125A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015699 | ||||||
chr14:74015717
|
T | C | 1 | a0001c0002t0008g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-131+107A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015717 | ||||||
chr14:74015747
|
A | C | 2 | a0001c0002t0008g0339a0001c0002t0008g0340 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-131+77T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015747 | ||||||
chr14:74015931
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18966.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.-237-1G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74015931 | ||||||
chr14:74015932
|
T | C | 2 | a0001c0002t0002g0337a0001c0002t0002g0338 | 2 | HG00642.hp2 HG00735.hp2 |
splice_acceptor_variant&intron_variant | HIGH | c.-237-2A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74015932 | ||||||
chr14:74016066
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-237-136C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016066 | ||||||
chr14:74016222
|
T | G | 2 | a0001c0001t0012g0360a0001c0001t0012g0361 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-237-292A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016222 | ||||||
chr14:74016245
|
A | G | 64 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(61): Show | 64 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.-237-315T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016245 | ||||||
chr14:74016281
|
C | T | 5 | a0001c0007t0009g0064a0002c0003t0009g0004a0002c0003t0009g0065others(2): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-237-351G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016281 | ||||||
chr14:74016468
|
C | G | 6 | a0001c0002t0010g0015a0001c0002t0010g0220a0001c0002t0010g0221others(3): Show | 7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-237-538G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016468 | ||||||
chr14:74016489
|
A | T | 3 | a0001c0002t0009g0016a0001c0002t0009g0226a0001c0002t0009g0227 | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-237-559T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016489 | ||||||
chr14:74016495
|
G | A | 2 | a0001c0005t0002g0346a0001c0005t0002g0347 | 2 | NA18953.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-237-565C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016495 | ||||||
chr14:74016640
|
A | G | 1 | a0001c0002t0002g0288 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-237-710T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016640 | ||||||
chr14:74016641
|
C | A | 37 | a0001c0001t0001g0255a0001c0001t0004g0233a0001c0001t0004g0234others(34): Show | 37 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.-237-711G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016641 | ||||||
chr14:74016700
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0004g0233 | 2 | HG00673.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-237-770G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016700 | ||||||
chr14:74016745
|
C | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(208): Show | 221 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.-237-815G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016745 | ||||||
chr14:74016839
|
C | A | 1 | a0001c0001t0012g0138 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-237-909G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016839 | ||||||
chr14:74016865
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(74): Show | 83 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.-237-935A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016865 | ||||||
chr14:74016912
|
C | T | 73 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-237-982G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016912 | ||||||
chr14:74017045
|
G | A | 5 | a0001c0001t0004g0125a0001c0001t0004g0126a0001c0002t0009g0016others(2): Show | 6 | HG01109.hp2 HG03098.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-237-1115C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017045 | ||||||
chr14:74017102
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-237-1172A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017102 | ||||||
chr14:74017116
|
C | T | 1 | a0001c0001t0004g0241 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-237-1186G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017116 | ||||||
chr14:74017185
|
G | A | 5 | a0001c0007t0009g0064a0002c0003t0009g0004a0002c0003t0009g0065others(2): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-237-1255C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017185 | ||||||
chr14:74017211
|
G | A | 1 | a0001c0001t0004g0229 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-237-1281C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017211 | ||||||
chr14:74017242
|
T | C | 78 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(75): Show | 78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-237-1312A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017242 | ||||||
chr14:74017258
|
C | T | 78 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(75): Show | 78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-237-1328G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017258 | ||||||
chr14:74017272
|
C | T | 73 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-237-1342G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017272 | ||||||
chr14:74017326
|
AAG | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(262): Show | 277 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.-237-1398_-237-139 others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017326 | ||||||
chr14:74017327
|
AG | A | 10 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0229others(7): Show | 12 | HG01081.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-237-1398delC | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017327 | ||||||
chr14:74017328
|
G | A | 1 | a0001c0002t0002g0349 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-237-1398C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017328 | ||||||
chr14:74017408
|
T | C | 37 | a0001c0001t0005g0041a0001c0001t0007g0053a0001c0001t0035g0026others(34): Show | 39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-237-1478A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017408 | ||||||
chr14:74017450
|
G | C | 13 | a0001c0001t0006g0272a0001c0001t0006g0273a0001c0001t0006g0274others(10): Show | 13 | HG01070.hp2 HG01192.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-237-1520C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017450 | ||||||
chr14:74017569
|
ACT | A | 73 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-237-1641_-237-164 others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017569 | ||||||
chr14:74017578
|
CA | C | 14 | a0001c0001t0004g0229a0001c0001t0004g0348a0001c0001t0006g0272others(11): Show | 15 | HG01070.hp2 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-237-1649delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017578 | ||||||
chr14:74017607
|
G | A | 41 | a0001c0001t0001g0255a0001c0001t0004g0213a0001c0001t0004g0214others(38): Show | 41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-238+1643C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017607 | ||||||
chr14:74017613
|
G | A | 9 | a0001c0001t0004g0348a0001c0001t0004g0353a0001c0001t0007g0216others(6): Show | 9 | NA18944.hp2 NA18946.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.-238+1637C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017613 | ||||||
chr14:74017657
|
G | A | 2 | a0001c0001t0006g0217a0001c0001t0028g0218 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-238+1593C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017657 | ||||||
chr14:74017698
|
T | C | 355 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(352): Show | 373 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.-238+1552A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017698 | ||||||
chr14:74017806
|
C | T | 3 | a0001c0002t0008g0054a0001c0002t0008g0055a0001c0002t0008g0056 | 3 | HG01243.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-238+1444G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017806 | ||||||
chr14:74017905
|
G | A | 1 | a0001c0001t0004g0219 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-238+1345C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017905 | ||||||
chr14:74017967
|
A | G | 73 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-238+1283T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017967 | ||||||
chr14:74018096
|
C | G | 1 | a0001c0001t0024g0285 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-238+1154G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018096 | ||||||
chr14:74018146
|
A | T | 6 | a0001c0002t0010g0015a0001c0002t0010g0220a0001c0002t0010g0221others(3): Show | 7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-238+1104T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018146 | ||||||
chr14:74018179
|
G | GA | 79 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0228others(76): Show | 84 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-238+1070dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018179 | ||||||
chr14:74018240
|
G | A | 2 | a0001c0001t0004g0017a0001c0001t0004g0228 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-238+1010C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018240 | ||||||
chr14:74018356
|
T | C | 1 | a0001c0001t0004g0229 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-238+894A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018356 | ||||||
chr14:74018430
|
C | T | 37 | a0001c0001t0005g0041a0001c0001t0007g0053a0001c0001t0035g0026others(34): Show | 39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-238+820G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018430 | ||||||
chr14:74018436
|
G | C | 3 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0034g0232 | 3 | NA19057.hp1 NA19081.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-238+814C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018436 | ||||||
chr14:74018544
|
G | T | 1 | a0001c0001t0026g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-238+706C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018544 | ||||||
chr14:74018661
|
G | A | 13 | a0001c0001t0006g0272a0001c0001t0006g0273a0001c0001t0006g0274others(10): Show | 13 | HG01070.hp2 HG01192.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-238+589C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018661 | ||||||
chr14:74018679
|
C | T | 73 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-238+571G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018679 | ||||||
chr14:74018820
|
G | A | 78 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(75): Show | 78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-238+430C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018820 | ||||||
chr14:74018889
|
G | A | 37 | a0001c0001t0001g0255a0001c0001t0004g0233a0001c0001t0004g0234others(34): Show | 37 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.-238+361C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018889 | ||||||
chr14:74018959
|
G | C | 1 | a0001c0001t0018g0270 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-238+291C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018959 | ||||||
chr14:74019030
|
G | A | 1 | a0001c0002t0008g0362 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-238+220C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74019030 | ||||||
chr14:74019078
|
T | C | 78 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(75): Show | 78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-238+172A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74019078 | ||||||
chr14:74019158
|
G | A | 1 | a0001c0002t0008g0271 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-238+92C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74019158 | ||||||
chr14:74019171
|
G | A | 13 | a0001c0001t0006g0272a0001c0001t0006g0273a0001c0001t0006g0274others(10): Show | 13 | HG01070.hp2 HG01192.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-238+79C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74019171 | ||||||
chr14:74019223
|
C | A | 78 | a0001c0001t0001g0320a0001c0001t0001g0335a0001c0001t0004g0348others(75): Show | 78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-238+27G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74019223 |