geneid | 79612 |
---|---|
ensemblid | ENSG00000172766.19 |
hgncid | 26164 |
symbol | NAA16 |
name | N-alpha-acetyltransferase 16, NatA auxiliary subunit |
refseq_nuc | NM_024561.5 |
refseq_prot | NP_078837.3 |
ensembl_nuc | ENST00000379406.8 |
ensembl_prot | ENSP00000368716.3 |
mane_status | MANE Select |
chr | chr13 |
start | 41311267 |
end | 41377030 |
strand | + |
ver | v1.2 |
region | chr13:41311267-41377030 |
region5000 | chr13:41306267-41382030 |
regionname0 | NAA16_chr13_41311267_41377030 |
regionname5000 | NAA16_chr13_41306267_41382030 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 864 | 328 | 63 | 60 | 163 | 11 | 31 | 124 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0002 | 0/0 | 864 | 17 | 15 | 2 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0003 | 0/0 | 864 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0004 | 0/0 | 864 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0005 | 0/0 | 864 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0006 | 0/0 | 864 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0007 | 0/0 | 676 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0008 | 0/0 | 864 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0009 | 0/0 | 864 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0010 | 0/0 | 864 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2595 | 301 | 55 | 57 | 149 | 11 | 29 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0002 | 0/0 | 2595 | 21 | 5 | 3 | 12 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0003 | 0/0 | 2595 | 16 | 14 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0004 | 0/0 | 2595 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0005 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0006 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0007 | 0/0 | 2595 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0008 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0009 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0010 | 0/0 | 2595 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0011 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0012 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0013 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0014 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0015 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0016 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0017 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
c0018 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1691 | 91 | 10 | 26 | 43 | 2 | 10 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0002 | 0/0 | 1691 | 70 | 10 | 9 | 35 | 5 | 11 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0003 | 0/0 | 1691 | 55 | 1 | 12 | 38 | 2 | 2 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0004 | 0/0 | 1691 | 47 | 7 | 5 | 27 | 1 | 7 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0005 | 0/0 | 1691 | 17 | 15 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0006 | 0/0 | 1691 | 14 | 11 | 3 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0007 | 0/0 | 1691 | 12 | 0 | 0 | 12 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0008 | 0/0 | 1691 | 11 | 10 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0009 | 0/0 | 1691 | 9 | 5 | 3 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0010 | 0/0 | 1691 | 5 | 5 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0011 | 0/0 | 1691 | 4 | 0 | 0 | 4 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0012 | 0/0 | 1694 | 3 | 0 | 0 | 3 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0013 | 0/0 | 1691 | 3 | 0 | 2 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0014 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0015 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0016 | 0/0 | 1691 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0017 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0018 | 0/0 | 1691 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0019 | 0/0 | 1691 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0020 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0021 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0022 | 0/0 | 1691 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0023 | 0/0 | 1691 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0024 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0025 | 0/0 | 1691 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
t0026 | 0/0 | 1691 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
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 | 7 | 2 | 1 | 4 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0003 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0009 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2595 | 301 | 55 | 57 | 149 | 11 | 29 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0002 | 0/0 | 2595 | 21 | 5 | 3 | 12 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0005 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0006 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0009 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0011 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0013 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0017 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0002c0003 | 0/0 | 2595 | 16 | 14 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0002c0014 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0003c0004 | 0/0 | 2595 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0004c0018 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0005c0007 | 0/0 | 2595 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0006c0010 | 0/0 | 2595 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0007c0008 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0008c0016 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0009c0012 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0010c0015 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4285 | 88 | 9 | 26 | 42 | 2 | 9 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0002 | 0/0 | 4285 | 68 | 10 | 8 | 34 | 5 | 11 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0003 | 0/0 | 4285 | 51 | 1 | 11 | 36 | 1 | 2 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0004 | 0/0 | 4285 | 47 | 7 | 5 | 27 | 1 | 7 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0006 | 0/0 | 4285 | 13 | 10 | 3 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0008 | 0/0 | 4285 | 10 | 9 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0010 | 0/0 | 4285 | 5 | 5 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0011 | 0/0 | 4285 | 4 | 0 | 0 | 4 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0012 | 0/0 | 4288 | 3 | 0 | 0 | 3 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0013 | 0/0 | 4285 | 3 | 0 | 2 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0017 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0018 | 0/0 | 4285 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0019 | 0/0 | 4285 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0020 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0021 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0022 | 0/0 | 4285 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0023 | 0/0 | 4285 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0024 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0001t0025 | 0/0 | 4285 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0002t0007 | 0/0 | 4285 | 12 | 0 | 0 | 12 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0002t0009 | 0/0 | 4285 | 9 | 5 | 3 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0005t0001 | 0/0 | 4285 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0006t0001 | 0/0 | 4285 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0009t0002 | 0/0 | 4285 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0011t0014 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0013t0015 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0001c0017t0006 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0002c0003t0005 | 0/0 | 4285 | 16 | 14 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0002c0014t0005 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0003c0004t0003 | 0/0 | 4285 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0004c0018t0008 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0005c0007t0003 | 0/0 | 4285 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0006c0010t0002 | 0/0 | 4285 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0007c0008t0026 | 0/0 | 4258 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0008c0016t0016 | 0/0 | 4285 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0009c0012t0001 | 0/0 | 4285 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
a0010c0015t0003 | 0/0 | 4285 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | copy fasta | chr13 | 41306267 | 41382030 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0001 | 0/0 | 7 | 2 | 1 | 4 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0006g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0006g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0008g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0008g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0010g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0010g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0010g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0011g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0011g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0011g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0011g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0012g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0012g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0012g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0013g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0013g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0013g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0017g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0018g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0019g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0020g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0021g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0022g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0023g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0024g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0001t0025g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0002t0007g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0002t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0002t0007g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0002t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0002t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0002t0007g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0002t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0002t0009g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0002t0009g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0002t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0002t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0002t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0002t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0002t0009g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0002t0009g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0005t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0006t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0009t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0011t0014g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0013t0015g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0001c0017t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0003t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0003t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0003t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0003t0005g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0003t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0003t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0003t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0003t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0003t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0003t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0003t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0003t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0003t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0003t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0003t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0003t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0002c0014t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0003c0004t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0003c0004t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0004c0018t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0005c0007t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0006c0010t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0007c0008t0026g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0008c0016t0016g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0009c0012t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
a0010c0015t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0256 | EUR | GBR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | GBR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0022 | EUR | GBR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00140 | hp2 | a0010 | c0015 | t0003 | g0147 | EUR | GBR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0219 | EUR | FIN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | FIN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00423 | hp1 | a0001 | c0002 | t0007 | g0157 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00597 | hp2 | a0001 | c0001 | t0025 | g0270 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00639 | hp1 | a0005 | c0007 | t0003 | g0003 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00673 | hp1 | a0003 | c0004 | t0003 | g0094 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | CHS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0067 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01069 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01071 | hp1 | a0001 | c0001 | t0022 | g0009 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01071 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01109 | hp2 | a0002 | c0003 | t0005 | g0038 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01167 | hp2 | a0006 | c0010 | t0002 | g0232 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01175 | hp1 | a0001 | c0002 | t0009 | g0169 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0028 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01243 | hp1 | a0001 | c0001 | t0013 | g0258 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01243 | hp2 | a0002 | c0003 | t0005 | g0036 | AMR | PUR | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0115 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0069 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01361 | hp2 | a0001 | c0002 | t0009 | g0016 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0171 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0132 | AMR | CLM | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0055 | EUR | IBS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0257 | EUR | IBS | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01884 | hp2 | a0001 | c0002 | t0009 | g0168 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01891 | hp1 | a0002 | c0003 | t0005 | g0045 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0027 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0060 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01981 | hp2 | a0001 | c0001 | t0008 | g0144 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG01993 | hp2 | a0001 | c0002 | t0009 | g0016 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02027 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02055 | hp1 | a0001 | c0002 | t0009 | g0312 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0076 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02129 | hp1 | a0001 | c0009 | t0002 | g0284 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02129 | hp2 | a0001 | c0006 | t0001 | g0205 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02135 | hp2 | a0001 | c0002 | t0007 | g0159 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02145 | hp1 | a0001 | c0001 | t0008 | g0141 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02145 | hp2 | a0002 | c0003 | t0005 | g0034 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0072 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CDX | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CDX | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | CDX | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02280 | hp1 | a0002 | c0003 | t0005 | g0041 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02300 | hp2 | a0001 | c0001 | t0013 | g0182 | AMR | PEL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0086 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02451 | hp2 | a0001 | c0001 | t0010 | g0136 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | KHV | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02572 | hp1 | a0001 | c0001 | t0008 | g0091 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0073 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02622 | hp2 | a0002 | c0003 | t0005 | g0047 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0133 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0071 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02717 | hp2 | a0001 | c0001 | t0017 | g0214 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02723 | hp1 | a0002 | c0003 | t0005 | g0046 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0083 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02809 | hp1 | a0001 | c0002 | t0009 | g0166 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02809 | hp2 | a0002 | c0003 | t0005 | g0043 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02818 | hp1 | a0002 | c0003 | t0005 | g0042 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02886 | hp1 | a0001 | c0001 | t0008 | g0085 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02886 | hp2 | a0002 | c0003 | t0005 | g0049 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02897 | hp2 | a0001 | c0001 | t0008 | g0142 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02922 | hp1 | a0002 | c0003 | t0005 | g0039 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02965 | hp1 | a0002 | c0014 | t0005 | g0037 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02970 | hp1 | a0001 | c0017 | t0006 | g0090 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02970 | hp2 | a0002 | c0003 | t0005 | g0048 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0013 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03041 | hp1 | a0001 | c0001 | t0010 | g0137 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03041 | hp2 | a0001 | c0013 | t0015 | g0153 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03098 | hp1 | a0001 | c0001 | t0008 | g0089 | AFR | MSL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03098 | hp2 | a0001 | c0011 | t0014 | g0154 | AFR | MSL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03139 | hp2 | a0001 | c0001 | t0020 | g0139 | AFR | ESN | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | MSL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03453 | hp2 | a0002 | c0003 | t0005 | g0050 | AFR | MSL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03486 | hp1 | a0001 | c0002 | t0009 | g0165 | AFR | MSL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | MSL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0105 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0307 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03540 | hp1 | a0002 | c0003 | t0005 | g0044 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03540 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | GWD | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0075 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03688 | hp2 | a0007 | c0008 | t0026 | g0078 | SAS | STU | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0306 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03831 | hp1 | a0001 | c0005 | t0001 | g0248 | SAS | BEB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0151 | SAS | BEB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03927 | hp1 | a0001 | c0002 | t0009 | g0164 | SAS | BEB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0308 | SAS | BEB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | BEB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0068 | SAS | BEB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | STU | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0013 | SAS | STU | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0032 | AFR | YRI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18522 | hp2 | a0002 | c0003 | t0005 | g0040 | AFR | YRI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | CHB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | YRI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18906 | hp2 | a0001 | c0001 | t0008 | g0087 | AFR | YRI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18944 | hp2 | a0001 | c0001 | t0012 | g0109 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18948 | hp1 | a0001 | c0001 | t0011 | g0103 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18957 | hp2 | a0001 | c0001 | t0019 | g0268 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18964 | hp1 | a0001 | c0001 | t0012 | g0014 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18965 | hp1 | a0001 | c0001 | t0012 | g0003 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18965 | hp2 | a0001 | c0002 | t0007 | g0161 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18967 | hp1 | a0001 | c0002 | t0007 | g0163 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18970 | hp2 | a0001 | c0001 | t0023 | g0265 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18971 | hp1 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18977 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18984 | hp1 | a0001 | c0001 | t0011 | g0117 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18987 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18990 | hp1 | a0001 | c0001 | t0011 | g0118 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18990 | hp2 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18992 | hp2 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19000 | hp2 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19002 | hp2 | a0001 | c0002 | t0007 | g0158 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19010 | hp2 | a0001 | c0002 | t0007 | g0162 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19030 | hp1 | a0001 | c0001 | t0006 | g0033 | AFR | LWK | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19030 | hp2 | a0001 | c0001 | t0021 | g0299 | AFR | LWK | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19043 | hp1 | a0001 | c0001 | t0010 | g0152 | AFR | LWK | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19043 | hp2 | a0001 | c0001 | t0010 | g0134 | AFR | LWK | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19055 | hp1 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19059 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19059 | hp2 | a0008 | c0016 | t0016 | g0160 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19067 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19078 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19080 | hp1 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19081 | hp1 | a0003 | c0004 | t0003 | g0097 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19083 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19085 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19086 | hp2 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19091 | hp2 | a0001 | c0001 | t0011 | g0104 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19240 | hp1 | a0001 | c0001 | t0024 | g0140 | AFR | YRI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | YRI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA20129 | hp1 | a0001 | c0001 | t0010 | g0135 | AFR | ASW | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ASW | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA20752 | hp1 | a0001 | c0001 | t0013 | g0019 | EUR | TSI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0022 | EUR | TSI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA20805 | hp2 | a0001 | c0001 | t0018 | g0128 | EUR | TSI | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02109 | hp2 | a0004 | c0018 | t0008 | g0088 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02486 | hp1 | a0001 | c0001 | t0008 | g0143 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02486 | hp2 | a0001 | c0002 | t0009 | g0167 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02559 | hp1 | a0002 | c0003 | t0005 | g0035 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG02559 | hp2 | a0001 | c0001 | t0008 | g0084 | AFR | ACB | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | MSL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG03471 | hp2 | a0009 | c0012 | t0001 | g0243 | AFR | MSL | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0293 | AFR | USA | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | USA | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA21309 | hp1 | a0001 | c0001 | t0006 | g0148 | AFR | LWK | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | LWK | NAA16_chr13_41306267_41382030 | NAA16 | chr13 | 41306267 | 41382030 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:41325779
|
C | G | 1 | a0004 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.619C>G | p.Gln207Glu | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/20 | 881/4285 | 619/2595 | 207/864 | chr13 | 41325779 | ||
chr13:41336653
|
A | G | 1 | a0010 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.911A>G | p.Glu304Gly | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/20 | 1173/4285 | 911/2595 | 304/864 | chr13 | 41336653 | ||
chr13:41355160
|
A | G | 1 | a0002 | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
missense_variant | MODERATE | c.1031A>G | p.Glu344Gly | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/20 | 1293/4285 | 1031/2595 | 344/864 | chr13 | 41355160 | ||
chr13:41358909
|
C | G | 1 | a0009 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.1357C>G | p.Leu453Val | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/20 | 1619/4285 | 1357/2595 | 453/864 | chr13 | 41358909 | ||
chr13:41367506
|
G | A | 1 | a0005 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.1607G>A | p.Arg536His | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/20 | 1869/4285 | 1607/2595 | 536/864 | chr13 | 41367506 | ||
chr13:41367565
|
A | G | 1 | a0006 | 1 | HG01167.hp2 | missense_variant | MODERATE | c.1666A>G | p.Lys556Glu | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/20 | 1928/4285 | 1666/2595 | 556/864 | chr13 | 41367565 | ||
chr13:41372284
|
TTAGCATT others(24): Show |
T | 1 | a0007 | 1 | HG03688.hp2 | frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.2032_2056+6delGCAT others(27): Show |
p.Ala678fs | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 16/20 | 2294/4285 | 2032/2595 | 678/864 | INFO_REALIGN_3_PRIME | chr13 | 41372284 | |
chr13:41373693
|
C | A | 1 | a0003 | 2 | HG00673.hp1 NA19081.hp1 |
missense_variant | MODERATE | c.2212C>A | p.Gln738Lys | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/20 | 2474/4285 | 2212/2595 | 738/864 | chr13 | 41373693 | ||
chr13:41375446
|
T | G | 1 | a0008 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.2439T>G | p.Phe813Leu | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2701/4285 | 2439/2595 | 813/864 | chr13 | 41375446 | ||
chr13:41375561
|
A | C | 1 | a0007 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2554A>C | p.Asn852His | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2816/4285 | 2554/2595 | 852/864 | chr13 | 41375561 | ||
chr13:41375575
|
T | G | 1 | a0007 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2568T>G | p.Asn856Lys | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2830/4285 | 2568/2595 | 856/864 | chr13 | 41375575 | ||
chr13:41375583
|
T | A | 1 | a0007 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2576T>A | p.Val859Asp | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2838/4285 | 2576/2595 | 859/864 | chr13 | 41375583 | ||
chr13:41375585
|
T | A | 1 | a0007 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2578T>A | p.Leu860Met | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2840/4285 | 2578/2595 | 860/864 | chr13 | 41375585 | ||
chr13:41375595
|
A | C | 1 | a0007 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2588A>C | p.Glu863Ala | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2850/4285 | 2588/2595 | 863/864 | chr13 | 41375595 | ||
chr13:41375598
|
T | C | 1 | a0007 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2591T>C | p.Ile864Thr | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2853/4285 | 2591/2595 | 864/864 | chr13 | 41375598 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:41325802
|
A | G | 1 | a0001c0017 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.642A>G | p.Glu214Glu | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/20 | 904/4285 | 642/2595 | 214/864 | chr13 | 41325802 | ||
chr13:41328803
|
T | C | 16 | a0001c0001a0001c0005a0001c0006others(13): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
synonymous_variant | LOW | c.771T>C | p.Asn257Asn | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/20 | 1033/4285 | 771/2595 | 257/864 | chr13 | 41328803 | ||
chr13:41331317
|
G | A | 1 | a0001c0005 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.855G>A | p.Lys285Lys | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/20 | 1117/4285 | 855/2595 | 285/864 | chr13 | 41331317 | ||
chr13:41355191
|
A | G | 1 | a0001c0013 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.1062A>G | p.Lys354Lys | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/20 | 1324/4285 | 1062/2595 | 354/864 | chr13 | 41355191 | ||
chr13:41358435
|
C | T | 1 | a0002c0014 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.1219C>T | p.Leu407Leu | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 11/20 | 1481/4285 | 1219/2595 | 407/864 | chr13 | 41358435 | ||
chr13:41362060
|
T | C | 1 | a0001c0006 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.1440T>C | p.Asn480Asn | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/20 | 1702/4285 | 1440/2595 | 480/864 | chr13 | 41362060 | ||
chr13:41367465
|
A | G | 2 | a0001c0011a0001c0013 | 2 | HG03041.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.1566A>G | p.Gln522Gln | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/20 | 1828/4285 | 1566/2595 | 522/864 | chr13 | 41367465 | ||
chr13:41367633
|
A | G | 1 | a0001c0009 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.1734A>G | p.Lys578Lys | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/20 | 1996/4285 | 1734/2595 | 578/864 | chr13 | 41367633 | ||
chr13:41375557
|
A | T | 1 | a0007c0008 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.2550A>T | p.Ala850Ala | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2812/4285 | 2550/2595 | 850/864 | chr13 | 41375557 | ||
chr13:41375578
|
T | C | 1 | a0007c0008 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.2571T>C | p.Tyr857Tyr | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2833/4285 | 2571/2595 | 857/864 | chr13 | 41375578 | ||
chr13:41375584
|
C | G | 1 | a0007c0008 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.2577C>G | p.Val859Val | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2839/4285 | 2577/2595 | 859/864 | chr13 | 41375584 | ||
chr13:41375587
|
G | A | 1 | a0007c0008 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.2580G>A | p.Leu860Leu | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2842/4285 | 2580/2595 | 860/864 | chr13 | 41375587 | ||
chr13:41375590
|
A | C | 1 | a0007c0008 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.2583A>C | p.Ala861Ala | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 2845/4285 | 2583/2595 | 861/864 | chr13 | 41375590 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:41311280
|
A | ACCG | 1 | a0001c0001t0012 | 3 | NA18944.hp2 NA18964.hp1 NA18965.hp1 |
5_prime_UTR_variant | MODIFIER | c.-235_-233dupCGC | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/20 | 232 | INFO_REALIGN_3_PRIME | chr13 | 41311280 | ||||
chr13:41311329
|
C | T | 1 | a0001c0001t0013 | 3 | HG01243.hp1 HG02300.hp2 NA20752.hp1 |
5_prime_UTR_variant | MODIFIER | c.-200C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/20 | 200 | chr13 | 41311329 | |||||
chr13:41311365
|
T | C | 2 | a0001c0011t0014a0001c0013t0015 | 2 | HG03041.hp2 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-164T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/20 | 164 | chr13 | 41311365 | |||||
chr13:41375603
|
A | T | 1 | a0007c0008t0026 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 1 | chr13 | 41375603 | |||||
chr13:41375611
|
A | C | 1 | a0007c0008t0026 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 9 | chr13 | 41375611 | |||||
chr13:41375618
|
A | C | 1 | a0007c0008t0026 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 16 | chr13 | 41375618 | |||||
chr13:41375620
|
A | C | 1 | a0001c0001t0025 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*18A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 18 | chr13 | 41375620 | |||||
chr13:41375627
|
T | G | 1 | a0007c0008t0026 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*25T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 25 | chr13 | 41375627 | |||||
chr13:41375668
|
G | T | 34 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
3_prime_UTR_variant | MODIFIER | c.*66G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 66 | chr13 | 41375668 | |||||
chr13:41375689
|
A | C | 1 | a0001c0001t0024 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*87A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 87 | chr13 | 41375689 | |||||
chr13:41375717
|
A | G | 1 | a0001c0001t0023 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*115A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 115 | chr13 | 41375717 | |||||
chr13:41375743
|
T | G | 1 | a0008c0016t0016 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*141T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 141 | chr13 | 41375743 | |||||
chr13:41375785
|
T | G | 1 | a0008c0016t0016 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*183T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 183 | chr13 | 41375785 | |||||
chr13:41375823
|
A | T | 1 | a0008c0016t0016 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*221A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 221 | chr13 | 41375823 | |||||
chr13:41375825
|
C | T | 2 | a0001c0001t0004a0007c0008t0026 | 48 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*223C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 223 | chr13 | 41375825 | |||||
chr13:41375826
|
G | A | 1 | a0001c0001t0011 | 4 | NA18948.hp1 NA18984.hp1 NA18990.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*224G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 224 | chr13 | 41375826 | |||||
chr13:41375968
|
C | T | 2 | a0002c0003t0005a0002c0014t0005 | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*366C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 366 | chr13 | 41375968 | |||||
chr13:41375990
|
A | G | 1 | a0001c0001t0022 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*388A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 388 | chr13 | 41375990 | |||||
chr13:41376016
|
G | A | 1 | a0001c0001t0017 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*414G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 414 | chr13 | 41376016 | |||||
chr13:41376087
|
C | T | 1 | a0001c0001t0021 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*485C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 485 | chr13 | 41376087 | |||||
chr13:41376089
|
A | T | 1 | a0008c0016t0016 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*487A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 487 | chr13 | 41376089 | |||||
chr13:41376142
|
T | C | 9 | a0001c0001t0003a0001c0001t0006a0001c0001t0011others(6): Show | 77 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*540T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 540 | chr13 | 41376142 | |||||
chr13:41376317
|
T | C | 1 | a0001c0011t0014 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*715T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 715 | chr13 | 41376317 | |||||
chr13:41376395
|
T | C | 1 | a0001c0001t0010 | 5 | HG02451.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*793T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 793 | chr13 | 41376395 | |||||
chr13:41376402
|
G | C | 14 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(11): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*800G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 800 | chr13 | 41376402 | |||||
chr13:41376403
|
G | T | 7 | a0001c0001t0003a0001c0001t0011a0001c0001t0012others(4): Show | 63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*801G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 801 | chr13 | 41376403 | |||||
chr13:41376424
|
G | A | 1 | a0001c0001t0020 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 822 | chr13 | 41376424 | |||||
chr13:41376426
|
A | G | 34 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
3_prime_UTR_variant | MODIFIER | c.*824A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 824 | chr13 | 41376426 | |||||
chr13:41376507
|
A | C | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(33): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
3_prime_UTR_variant | MODIFIER | c.*905A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 905 | chr13 | 41376507 | |||||
chr13:41376660
|
A | G | 1 | a0001c0001t0018 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1058A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 1058 | chr13 | 41376660 | |||||
chr13:41376786
|
T | C | 1 | a0001c0001t0019 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1184T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 1184 | chr13 | 41376786 | |||||
chr13:41376877
|
G | C | 8 | a0001c0001t0001a0001c0001t0019a0001c0001t0022others(5): Show | 95 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*1275G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 20/20 | 1275 | chr13 | 41376877 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:41311618
|
C | T | 1 | a0001c0002t0009g0312 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.54+36C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41311618 | ||||||
chr13:41311622
|
G | A | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.54+40G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41311622 | ||||||
chr13:41311714
|
G | T | 158 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(155): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.54+132G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41311714 | ||||||
chr13:41311779
|
G | T | 1 | a0001c0001t0002g0311 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.54+197G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41311779 | ||||||
chr13:41311783
|
C | T | 16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+201C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41311783 | ||||||
chr13:41311933
|
G | T | 2 | a0001c0001t0003g0155a0001c0001t0003g0156 | 2 | HG00544.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.54+351G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41311933 | ||||||
chr13:41311967
|
C | T | 1 | a0001c0001t0001g0310 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.54+385C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41311967 | ||||||
chr13:41312016
|
G | C | 16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+434G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312016 | ||||||
chr13:41312031
|
C | T | 2 | a0001c0011t0014g0154a0001c0013t0015g0153 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.54+449C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312031 | ||||||
chr13:41312067
|
G | C | 10 | a0001c0001t0006g0010a0001c0001t0006g0025a0001c0001t0006g0026others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.54+485G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312067 | ||||||
chr13:41312105
|
T | C | 16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+523T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312105 | ||||||
chr13:41312119
|
C | T | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.54+537C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312119 | ||||||
chr13:41312144
|
A | G | 1 | a0001c0001t0004g0151 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.54+562A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312144 | ||||||
chr13:41312207
|
G | A | 16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+625G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312207 | ||||||
chr13:41312403
|
C | T | 8 | a0001c0002t0009g0016a0001c0002t0009g0164a0001c0002t0009g0165others(5): Show | 9 | HG01175.hp1 HG01361.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.54+821C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312403 | ||||||
chr13:41312432
|
A | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(152): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.54+850A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312432 | ||||||
chr13:41312484
|
T | TC | 3 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0002g0176 | 3 | HG01255.hp1 NA19055.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.54+904dupC | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | 41312484 | |||||
chr13:41312558
|
A | C | 1 | a0001c0001t0006g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.54+976A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312558 | ||||||
chr13:41312570
|
T | C | 1 | a0001c0001t0002g0178 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.54+988T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312570 | ||||||
chr13:41312745
|
A | G | 10 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(7): Show | 10 | HG00621.hp1 HG03492.hp1 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.54+1163A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312745 | ||||||
chr13:41312785
|
G | A | 16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+1203G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312785 | ||||||
chr13:41312922
|
C | T | 5 | a0001c0002t0007g0002a0001c0002t0007g0161a0001c0002t0007g0162others(2): Show | 10 | NA18965.hp2 NA18967.hp1 NA18971.hp1 others(7): Show |
intron_variant | MODIFIER | c.54+1340C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41312922 | ||||||
chr13:41313233
|
C | A | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.54+1651C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41313233 | ||||||
chr13:41313279
|
C | G | 9 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0002g0022others(6): Show | 11 | HG00140.hp1 HG01192.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.54+1697C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41313279 | ||||||
chr13:41313290
|
C | G | 1 | a0001c0001t0002g0295 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.54+1708C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41313290 | ||||||
chr13:41313653
|
C | G | 16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+2071C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41313653 | ||||||
chr13:41313755
|
G | A | 38 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(35): Show | 47 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.54+2173G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41313755 | ||||||
chr13:41313865
|
C | CT | 202 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(199): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.54+2297dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | 41313865 | |||||
chr13:41313960
|
G | C | 1 | a0001c0001t0004g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.54+2378G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41313960 | ||||||
chr13:41313962
|
TTC | T | 5 | a0001c0002t0007g0002a0001c0002t0007g0161a0001c0002t0007g0162others(2): Show | 10 | NA18965.hp2 NA18967.hp1 NA18971.hp1 others(7): Show |
intron_variant | MODIFIER | c.54+2383_54+2384del others(2): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | 41313962 | |||||
chr13:41314168
|
GTAAA | G | 4 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(1): Show | 4 | HG02451.hp2 HG03041.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+2590_54+2593del others(4): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | 41314168 | |||||
chr13:41314272
|
T | G | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.55-2574T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41314272 | ||||||
chr13:41314475
|
C | G | 59 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(56): Show | 63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.55-2371C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41314475 | ||||||
chr13:41314481
|
G | GCAGAATC others(16): Show |
16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.55-2360_55-2338dup others(23): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | 41314481 | |||||
chr13:41314536
|
T | C | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.55-2310T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41314536 | ||||||
chr13:41314644
|
T | C | 1 | a0001c0001t0001g0017 | 2 | NA18747.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.55-2202T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41314644 | ||||||
chr13:41314729
|
G | T | 155 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(152): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.55-2117G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41314729 | ||||||
chr13:41314759
|
G | A | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.55-2087G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41314759 | ||||||
chr13:41314797
|
C | CCAACATA others(1): Show |
16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.55-2048_55-2041dup others(8): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | 41314797 | |||||
chr13:41314846
|
A | T | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG01496.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.55-2000A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41314846 | ||||||
chr13:41315023
|
A | T | 1 | a0001c0001t0002g0294 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.55-1823A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41315023 | ||||||
chr13:41315191
|
G | A | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.55-1655G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41315191 | ||||||
chr13:41315347
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.55-1499A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41315347 | ||||||
chr13:41315361
|
A | G | 199 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(196): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.55-1485A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41315361 | ||||||
chr13:41315534
|
C | T | 1 | a0001c0001t0002g0293 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.55-1312C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41315534 | ||||||
chr13:41315660
|
T | TTG | 10 | a0001c0001t0006g0010a0001c0001t0006g0025a0001c0001t0006g0026others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.55-1172_55-1171dup others(2): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | 41315660 | |||||
chr13:41315880
|
C | A | 2 | a0001c0001t0008g0084a0001c0001t0008g0085 | 2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.55-966C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41315880 | ||||||
chr13:41316105
|
G | A | 1 | a0001c0001t0006g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.55-741G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316105 | ||||||
chr13:41316305
|
A | AT | 65 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(62): Show | 69 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.55-522dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | 41316305 | |||||
chr13:41316324
|
T | G | 1 | a0001c0001t0013g0182 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.55-522T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316324 | ||||||
chr13:41316346
|
T | G | 16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.55-500T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316346 | ||||||
chr13:41316402
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.55-444G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316402 | ||||||
chr13:41316412
|
T | G | 1 | a0001c0001t0004g0052 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.55-434T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316412 | ||||||
chr13:41316453
|
C | T | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.55-393C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316453 | ||||||
chr13:41316495
|
C | T | 1 | a0001c0001t0002g0309 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.55-351C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316495 | ||||||
chr13:41316543
|
G | A | 6 | a0001c0001t0006g0148a0001c0001t0008g0086a0001c0001t0008g0087others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-303G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316543 | ||||||
chr13:41316787
|
G | A | 16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.55-59G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 1/19 | chr13 | 41316787 | ||||||
chr13:41317034
|
C | T | 38 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(35): Show | 47 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.139+104C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317034 | ||||||
chr13:41317036
|
A | G | 16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.139+106A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317036 | ||||||
chr13:41317115
|
T | C | 3 | a0001c0001t0002g0022a0001c0001t0002g0296a0001c0001t0002g0297 | 4 | HG00140.hp1 HG01192.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+185T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317115 | ||||||
chr13:41317135
|
G | A | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.139+205G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317135 | ||||||
chr13:41317143
|
C | T | 1 | a0001c0001t0004g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.139+213C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317143 | ||||||
chr13:41317220
|
A | G | 1 | a0001c0001t0003g0131 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.139+290A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317220 | ||||||
chr13:41317338
|
TG | T | 9 | a0001c0001t0006g0025a0001c0001t0006g0026a0001c0001t0006g0027others(6): Show | 9 | HG01192.hp1 HG01891.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.139+409delG | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317338 | ||||||
chr13:41317368
|
A | G | 2 | a0001c0011t0014g0154a0001c0013t0015g0153 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.139+438A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317368 | ||||||
chr13:41317518
|
C | T | 16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.139+588C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317518 | ||||||
chr13:41317883
|
T | G | 6 | a0001c0001t0008g0141a0001c0001t0008g0142a0001c0001t0008g0143others(3): Show | 6 | HG01981.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.140-923T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317883 | ||||||
chr13:41317905
|
C | G | 2 | a0001c0001t0002g0286a0001c0001t0002g0287 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.140-901C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317905 | ||||||
chr13:41317939
|
G | A | 1 | a0002c0003t0005g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.140-867G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41317939 | ||||||
chr13:41318001
|
C | T | 201 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(198): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.140-805C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318001 | ||||||
chr13:41318040
|
A | G | 3 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308 | 3 | HG03492.hp1 HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.140-766A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318040 | ||||||
chr13:41318196
|
T | C | 1 | a0001c0002t0007g0157 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.140-610T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318196 | ||||||
chr13:41318205
|
AT | A | 32 | a0001c0001t0001g0177a0001c0001t0002g0185a0001c0001t0002g0311others(29): Show | 32 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.140-584delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr13 | 41318205 | |||||
chr13:41318390
|
C | T | 8 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0280others(5): Show | 11 | HG02129.hp1 NA18942.hp1 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.140-416C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318390 | ||||||
chr13:41318421
|
C | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0278a0001c0001t0001g0279 | 4 | HG02071.hp1 HG02080.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.140-385C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318421 | ||||||
chr13:41318438
|
A | G | 16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.140-368A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318438 | ||||||
chr13:41318443
|
C | G | 8 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0280others(5): Show | 11 | HG02129.hp1 NA18942.hp1 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.140-363C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318443 | ||||||
chr13:41318459
|
C | T | 1 | a0001c0001t0021g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.140-347C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318459 | ||||||
chr13:41318480
|
G | T | 6 | a0001c0001t0008g0141a0001c0001t0008g0142a0001c0001t0008g0143others(3): Show | 6 | HG01981.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.140-326G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318480 | ||||||
chr13:41318495
|
C | T | 44 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(41): Show | 53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.140-311C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318495 | ||||||
chr13:41318529
|
A | T | 1 | a0001c0001t0002g0297 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.140-277A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318529 | ||||||
chr13:41318543
|
T | A | 1 | a0001c0001t0001g0186 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.140-263T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318543 | ||||||
chr13:41318571
|
T | C | 10 | a0001c0001t0006g0010a0001c0001t0006g0025a0001c0001t0006g0026others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.140-235T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318571 | ||||||
chr13:41318711
|
G | A | 1 | a0001c0001t0002g0309 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.140-95G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 2/19 | chr13 | 41318711 | ||||||
chr13:41318969
|
T | G | 200 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.244+59T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41318969 | ||||||
chr13:41318984
|
G | A | 5 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0089others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+74G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41318984 | ||||||
chr13:41319000
|
C | T | 1 | a0001c0001t0002g0277 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.244+90C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319000 | ||||||
chr13:41319044
|
C | G | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.244+134C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319044 | ||||||
chr13:41319397
|
A | G | 1 | a0001c0001t0006g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.244+487A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319397 | ||||||
chr13:41319437
|
A | G | 1 | a0001c0001t0003g0174 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.244+527A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319437 | ||||||
chr13:41319516
|
T | A | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0187 | 3 | HG00099.hp2 HG00735.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.244+606T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319516 | ||||||
chr13:41319620
|
G | A | 3 | a0001c0002t0009g0016a0001c0002t0009g0164a0001c0002t0009g0169 | 4 | HG01175.hp1 HG01361.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+710G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319620 | ||||||
chr13:41319677
|
T | C | 16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.244+767T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319677 | ||||||
chr13:41319784
|
T | G | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.244+874T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319784 | ||||||
chr13:41319847
|
A | G | 1 | a0001c0001t0008g0144 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.245-820A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41319847 | ||||||
chr13:41319863
|
A | AT | 6 | a0001c0001t0001g0020a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 7 | HG00738.hp2 HG01346.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-791dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr13 | 41319863 | |||||
chr13:41319863
|
AT | A | 17 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(14): Show | 23 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.245-791delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr13 | 41319863 | |||||
chr13:41320080
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.245-587A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41320080 | ||||||
chr13:41320130
|
C | T | 4 | a0001c0001t0008g0087a0001c0001t0008g0089a0001c0001t0008g0091others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-537C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41320130 | ||||||
chr13:41320155
|
A | G | 6 | a0001c0001t0006g0148a0001c0001t0008g0086a0001c0001t0008g0087others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-512A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41320155 | ||||||
chr13:41320203
|
AT | A | 6 | a0001c0001t0006g0148a0001c0001t0008g0086a0001c0001t0008g0087others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-462delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr13 | 41320203 | |||||
chr13:41320296
|
G | A | 2 | a0001c0001t0004g0055a0001c0001t0004g0151 | 2 | HG01515.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.245-371G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41320296 | ||||||
chr13:41320461
|
C | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0181others(9): Show | 15 | HG00597.hp2 HG02015.hp2 NA18747.hp1 others(12): Show |
intron_variant | MODIFIER | c.245-206C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41320461 | ||||||
chr13:41320501
|
C | G | 1 | a0001c0001t0001g0264 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.245-166C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41320501 | ||||||
chr13:41320618
|
A | G | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.245-49A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 3/19 | chr13 | 41320618 | ||||||
chr13:41320951
|
C | T | 1 | a0001c0001t0002g0263 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.402+127C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41320951 | ||||||
chr13:41321023
|
G | C | 1 | a0001c0001t0003g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.402+199G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321023 | ||||||
chr13:41321024
|
G | T | 16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.402+200G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321024 | ||||||
chr13:41321030
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.402+206T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321030 | ||||||
chr13:41321041
|
T | G | 203 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(200): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.402+217T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321041 | ||||||
chr13:41321084
|
G | C | 1 | a0001c0001t0002g0178 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.402+260G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321084 | ||||||
chr13:41321124
|
G | C | 1 | a0002c0003t0005g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.402+300G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321124 | ||||||
chr13:41321130
|
G | T | 16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.402+306G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321130 | ||||||
chr13:41321468
|
C | T | 3 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0276 | 3 | HG02622.hp1 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.402+644C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321468 | ||||||
chr13:41321675
|
C | A | 2 | a0001c0001t0003g0092a0001c0001t0003g0102 | 2 | NA18951.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.402+851C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321675 | ||||||
chr13:41321717
|
A | G | 1 | a0001c0001t0002g0260 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.402+893A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321717 | ||||||
chr13:41321769
|
TCTTA | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.402+954_402+957del others(4): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr13 | 41321769 | |||||
chr13:41321824
|
A | G | 1 | a0001c0001t0002g0259 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.402+1000A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321824 | ||||||
chr13:41321843
|
C | G | 5 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(2): Show | 5 | HG02451.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+1019C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321843 | ||||||
chr13:41321843
|
C | T | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.402+1019C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321843 | ||||||
chr13:41321852
|
T | C | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.402+1028T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321852 | ||||||
chr13:41321914
|
G | C | 1 | a0002c0003t0005g0035 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.402+1090G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41321914 | ||||||
chr13:41322017
|
C | T | 1 | a0001c0011t0014g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.403-1039C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41322017 | ||||||
chr13:41322119
|
C | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.403-937C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41322119 | ||||||
chr13:41322169
|
G | T | 1 | a0002c0003t0005g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.403-887G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41322169 | ||||||
chr13:41322226
|
AAGG | A | 59 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(56): Show | 63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.403-827_403-825del others(3): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr13 | 41322226 | |||||
chr13:41322316
|
T | G | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.403-740T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41322316 | ||||||
chr13:41322367
|
T | C | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.403-689T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41322367 | ||||||
chr13:41322636
|
GCTGTGTC others(4): Show |
G | 1 | a0001c0001t0011g0103 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.403-410_403-400del others(11): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr13 | 41322636 | |||||
chr13:41322739
|
A | T | 1 | a0001c0017t0006g0090 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.403-317A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 4/19 | chr13 | 41322739 | ||||||
chr13:41323353
|
C | CTT | 8 | a0001c0001t0002g0019a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG00099.hp1 HG00642.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.537+175_537+176dup others(2): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41323353 | |||||
chr13:41323412
|
A | G | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.537+222A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323412 | ||||||
chr13:41323424
|
T | C | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.537+234T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323424 | ||||||
chr13:41323425
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.537+235G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323425 | ||||||
chr13:41323431
|
A | G | 1 | a0001c0001t0002g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.537+241A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323431 | ||||||
chr13:41323526
|
A | G | 1 | a0001c0001t0004g0082 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.537+336A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323526 | ||||||
chr13:41323555
|
T | C | 52 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(49): Show | 60 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.537+365T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323555 | ||||||
chr13:41323566
|
A | G | 3 | a0001c0001t0003g0095a0001c0001t0003g0129a0001c0001t0018g0128 | 3 | HG00733.hp1 HG01106.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.537+376A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323566 | ||||||
chr13:41323594
|
C | T | 3 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0002g0255 | 3 | HG02109.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.537+404C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323594 | ||||||
chr13:41323635
|
A | T | 1 | a0001c0001t0006g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.537+445A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323635 | ||||||
chr13:41323647
|
C | T | 6 | a0001c0001t0006g0148a0001c0001t0008g0086a0001c0001t0008g0087others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.537+457C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323647 | ||||||
chr13:41323674
|
G | A | 22 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(19): Show | 22 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.537+484G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41323674 | ||||||
chr13:41324009
|
T | C | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.537+819T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324009 | ||||||
chr13:41324011
|
T | G | 59 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(56): Show | 63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.537+821T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324011 | ||||||
chr13:41324038
|
T | C | 1 | a0001c0001t0020g0139 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.537+848T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324038 | ||||||
chr13:41324204
|
G | T | 4 | a0001c0001t0004g0054a0001c0001t0004g0080a0001c0001t0004g0081others(1): Show | 4 | NA18977.hp1 NA19043.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.537+1014G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324204 | ||||||
chr13:41324255
|
A | G | 1 | a0001c0013t0015g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.537+1065A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324255 | ||||||
chr13:41324269
|
A | G | 58 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(55): Show | 62 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.537+1079A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324269 | ||||||
chr13:41324321
|
C | G | 1 | a0001c0011t0014g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.537+1131C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324321 | ||||||
chr13:41324322
|
A | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | NA18963.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.537+1132A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324322 | ||||||
chr13:41324363
|
CTTTT | C | 6 | a0001c0001t0006g0148a0001c0001t0008g0086a0001c0001t0008g0087others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.537+1200_537+1203d others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41324363 | |||||
chr13:41324363
|
CTTTTT | C | 15 | a0001c0001t0001g0252a0001c0001t0001g0271a0001c0001t0001g0279others(12): Show | 15 | HG01069.hp1 HG01175.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.537+1199_537+1203d others(7): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41324363 | |||||
chr13:41324363
|
CTTTTTT | C | 181 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(178): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.537+1198_537+1203d others(8): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41324363 | |||||
chr13:41324363
|
CTTTTTTT | C | 96 | a0001c0001t0001g0190a0001c0001t0001g0213a0001c0001t0003g0003others(93): Show | 109 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.537+1197_537+1203d others(9): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41324363 | |||||
chr13:41324367
|
T | C | 2 | a0001c0001t0008g0084a0001c0002t0009g0312 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.537+1177T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324367 | ||||||
chr13:41324374
|
T | C | 2 | a0001c0001t0004g0056a0001c0001t0004g0057 | 2 | NA18964.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.537+1184T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324374 | ||||||
chr13:41324377
|
T | C | 1 | a0001c0011t0014g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.537+1187T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324377 | ||||||
chr13:41324415
|
G | T | 1 | a0001c0001t0003g0125 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.537+1225G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324415 | ||||||
chr13:41324433
|
T | C | 1 | a0001c0001t0002g0296 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.537+1243T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324433 | ||||||
chr13:41324564
|
C | T | 1 | a0001c0002t0009g0169 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.538-1134C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324564 | ||||||
chr13:41324664
|
G | A | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.538-1034G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324664 | ||||||
chr13:41324870
|
C | T | 3 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308 | 3 | HG03492.hp1 HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.538-828C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324870 | ||||||
chr13:41324879
|
G | GT | 13 | a0001c0001t0001g0210a0001c0001t0006g0025a0001c0001t0006g0026others(10): Show | 13 | HG01192.hp1 HG01891.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.538-807dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41324879 | |||||
chr13:41324881
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.538-817T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41324881 | ||||||
chr13:41324957
|
G | GT | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(242): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.538-723dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41324957 | |||||
chr13:41324957
|
G | GTT | 46 | a0001c0001t0001g0250a0001c0001t0001g0264a0001c0001t0001g0288others(43): Show | 55 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.538-724_538-723dup others(2): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41324957 | |||||
chr13:41324957
|
GT | G | 16 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(13): Show | 22 | HG00423.hp1 HG01175.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.538-723delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr13 | 41324957 | |||||
chr13:41325060
|
C | T | 2 | a0001c0001t0004g0073a0001c0001t0004g0083 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.538-638C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41325060 | ||||||
chr13:41325139
|
A | G | 1 | a0001c0001t0004g0072 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.538-559A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41325139 | ||||||
chr13:41325236
|
T | C | 1 | a0001c0001t0002g0218 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.538-462T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41325236 | ||||||
chr13:41325267
|
A | G | 11 | a0001c0001t0006g0010a0001c0001t0006g0024a0001c0001t0006g0025others(8): Show | 12 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.538-431A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41325267 | ||||||
chr13:41325286
|
AATT | A | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.538-411_538-409del others(3): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41325286 | ||||||
chr13:41325399
|
A | T | 1 | a0001c0001t0001g0278 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.538-299A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41325399 | ||||||
chr13:41325584
|
G | A | 1 | a0001c0001t0002g0219 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.538-114G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 5/19 | chr13 | 41325584 | ||||||
chr13:41325934
|
A | T | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.691+83A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41325934 | ||||||
chr13:41325951
|
G | A | 1 | a0001c0001t0004g0060 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.691+100G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41325951 | ||||||
chr13:41326013
|
A | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.691+162A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326013 | ||||||
chr13:41326033
|
A | G | 1 | a0001c0002t0007g0159 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.691+182A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326033 | ||||||
chr13:41326154
|
T | C | 1 | a0001c0001t0006g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.691+303T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326154 | ||||||
chr13:41326164
|
G | A | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.691+313G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326164 | ||||||
chr13:41326337
|
C | T | 1 | a0001c0001t0006g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.691+486C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326337 | ||||||
chr13:41326375
|
A | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.691+524A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326375 | ||||||
chr13:41326429
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.691+578C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326429 | ||||||
chr13:41326436
|
A | G | 156 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(153): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.691+585A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326436 | ||||||
chr13:41326589
|
T | TA | 6 | a0001c0001t0006g0148a0001c0001t0008g0086a0001c0001t0008g0087others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+739dupA | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41326589 | |||||
chr13:41326793
|
T | C | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.691+942T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326793 | ||||||
chr13:41326803
|
C | T | 1 | a0001c0001t0013g0182 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.691+952C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326803 | ||||||
chr13:41326933
|
A | G | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.691+1082A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41326933 | ||||||
chr13:41327134
|
G | A | 1 | a0001c0001t0023g0265 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.691+1283G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41327134 | ||||||
chr13:41327160
|
T | C | 1 | a0001c0001t0002g0218 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.691+1309T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41327160 | ||||||
chr13:41327250
|
ATAAT | A | 16 | a0001c0001t0002g0293a0002c0003t0005g0035a0002c0003t0005g0036others(13): Show | 16 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.691+1403_691+1406d others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327250 | |||||
chr13:41327458
|
T | TA | 265 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(262): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.692-1255dupA | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327458 | |||||
chr13:41327718
|
C | T | 3 | a0001c0001t0003g0099a0001c0001t0003g0121a0001c0001t0003g0124 | 3 | NA18977.hp2 NA18987.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.692-1006C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41327718 | ||||||
chr13:41327719
|
A | G | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.692-1005A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41327719 | ||||||
chr13:41327735
|
T | TGTTTAAA others(304): Show |
1 | a0002c0014t0005g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.692-977_692-976ins others(311): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | |||||
chr13:41327735
|
T | TGTTTAAA others(321): Show |
1 | a0002c0003t0005g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.692-977_692-976ins others(328): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | |||||
chr13:41327735
|
T | TGTTTAAA others(322): Show |
3 | a0002c0003t0005g0039a0002c0003t0005g0040a0002c0003t0005g0041 | 3 | HG02280.hp1 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.692-977_692-976ins others(329): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | |||||
chr13:41327735
|
T | TGTTTAAA others(323): Show |
4 | a0002c0003t0005g0042a0002c0003t0005g0043a0002c0003t0005g0044others(1): Show | 4 | HG01891.hp1 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.692-977_692-976ins others(330): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | |||||
chr13:41327735
|
T | TGTTTAAA others(324): Show |
2 | a0002c0003t0005g0036a0002c0003t0005g0048 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.692-977_692-976ins others(331): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | |||||
chr13:41327735
|
T | TGTTTAAA others(327): Show |
2 | a0002c0003t0005g0034a0002c0003t0005g0046 | 2 | HG02145.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.692-977_692-976ins others(334): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | |||||
chr13:41327735
|
T | TGTTTAAA others(329): Show |
1 | a0002c0003t0005g0049 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.692-977_692-976ins others(336): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | |||||
chr13:41327735
|
T | TGTTTAAA others(331): Show |
1 | a0002c0003t0005g0035 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.692-977_692-976ins others(338): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | |||||
chr13:41327735
|
T | TGTTTAAA others(337): Show |
1 | a0002c0003t0005g0050 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.692-977_692-976ins others(344): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | |||||
chr13:41327735
|
T | TGTTTAAA others(346): Show |
1 | a0002c0003t0005g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.692-977_692-976ins others(353): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr13 | 41327735 | |||||
chr13:41327807
|
C | G | 2 | a0001c0011t0014g0154a0001c0013t0015g0153 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.692-917C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41327807 | ||||||
chr13:41327811
|
C | A | 2 | a0001c0001t0002g0179a0001c0001t0002g0251 | 2 | NA18940.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.692-913C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41327811 | ||||||
chr13:41327937
|
T | C | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.692-787T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41327937 | ||||||
chr13:41328012
|
T | G | 1 | a0001c0001t0006g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.692-712T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41328012 | ||||||
chr13:41328104
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.692-620C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41328104 | ||||||
chr13:41328157
|
G | T | 2 | a0001c0011t0014g0154a0001c0013t0015g0153 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.692-567G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41328157 | ||||||
chr13:41328528
|
A | G | 6 | a0001c0001t0008g0141a0001c0001t0008g0142a0001c0001t0008g0143others(3): Show | 6 | HG01981.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.692-196A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41328528 | ||||||
chr13:41328543
|
A | G | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.692-181A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41328543 | ||||||
chr13:41328590
|
C | A | 2 | a0001c0011t0014g0154a0001c0013t0015g0153 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.692-134C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41328590 | ||||||
chr13:41328617
|
A | G | 1 | a0001c0013t0015g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.692-107A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41328617 | ||||||
chr13:41328647
|
A | T | 1 | a0001c0001t0006g0032 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.692-77A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 6/19 | chr13 | 41328647 | ||||||
chr13:41328911
|
A | C | 1 | a0001c0001t0010g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.811+68A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41328911 | ||||||
chr13:41329259
|
T | C | 1 | a0001c0001t0010g0137 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.811+416T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41329259 | ||||||
chr13:41329278
|
G | T | 1 | a0001c0001t0004g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.811+435G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41329278 | ||||||
chr13:41329506
|
AT | A | 28 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0220others(25): Show | 28 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.811+681delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr13 | 41329506 | |||||
chr13:41329555
|
T | C | 1 | a0001c0001t0008g0144 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.811+712T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41329555 | ||||||
chr13:41329556
|
A | G | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.811+713A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41329556 | ||||||
chr13:41329573
|
C | T | 44 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(41): Show | 53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.811+730C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41329573 | ||||||
chr13:41329593
|
A | G | 1 | a0001c0001t0008g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.811+750A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41329593 | ||||||
chr13:41329722
|
A | G | 1 | a0001c0001t0008g0084 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.811+879A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41329722 | ||||||
chr13:41329919
|
T | C | 10 | a0001c0001t0006g0010a0001c0001t0006g0025a0001c0001t0006g0026others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.811+1076T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41329919 | ||||||
chr13:41330026
|
AT | A | 302 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(299): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.811+1194delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr13 | 41330026 | |||||
chr13:41330133
|
T | G | 157 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(154): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.812-1141T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41330133 | ||||||
chr13:41330173
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0192others(3): Show | 9 | HG01109.hp1 HG01167.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.812-1101G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41330173 | ||||||
chr13:41330286
|
G | A | 6 | a0001c0001t0006g0148a0001c0001t0008g0086a0001c0001t0008g0087others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.812-988G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41330286 | ||||||
chr13:41330480
|
T | C | 1 | a0001c0001t0003g0107 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.812-794T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41330480 | ||||||
chr13:41330928
|
C | T | 1 | a0001c0001t0006g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.812-346C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41330928 | ||||||
chr13:41331103
|
T | G | 1 | a0001c0001t0001g0196 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.812-171T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41331103 | ||||||
chr13:41331177
|
C | T | 1 | a0001c0001t0010g0135 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.812-97C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 7/19 | chr13 | 41331177 | ||||||
chr13:41331571
|
A | G | 2 | a0001c0001t0010g0134a0001c0001t0010g0136 | 2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.907+202A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41331571 | ||||||
chr13:41331583
|
A | C | 6 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0216others(3): Show | 6 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.907+214A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41331583 | ||||||
chr13:41331726
|
T | G | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.907+357T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41331726 | ||||||
chr13:41331766
|
A | G | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.907+397A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41331766 | ||||||
chr13:41331804
|
G | A | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.907+435G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41331804 | ||||||
chr13:41331872
|
G | T | 2 | a0001c0001t0003g0098a0001c0001t0003g0120 | 2 | NA18963.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.907+503G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41331872 | ||||||
chr13:41331953
|
A | T | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.907+584A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41331953 | ||||||
chr13:41332014
|
A | G | 6 | a0001c0001t0008g0141a0001c0001t0008g0142a0001c0001t0008g0143others(3): Show | 6 | HG01981.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.907+645A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41332014 | ||||||
chr13:41332132
|
A | G | 1 | a0001c0001t0001g0290 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.907+763A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41332132 | ||||||
chr13:41332797
|
TTGAC | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.907+1434_907+1437d others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr13 | 41332797 | |||||
chr13:41332880
|
A | G | 2 | a0001c0001t0010g0134a0001c0001t0010g0136 | 2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.907+1511A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41332880 | ||||||
chr13:41333247
|
T | C | 83 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(80): Show | 93 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.907+1878T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41333247 | ||||||
chr13:41333336
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.907+1967A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41333336 | ||||||
chr13:41333502
|
G | C | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.907+2133G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41333502 | ||||||
chr13:41333643
|
GCTT | G | 6 | a0001c0001t0002g0230a0001c0001t0002g0253a0001c0001t0002g0254others(3): Show | 6 | HG02109.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.907+2278_907+2280d others(5): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr13 | 41333643 | |||||
chr13:41333690
|
A | G | 61 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(58): Show | 65 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.907+2321A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41333690 | ||||||
chr13:41333714
|
C | T | 18 | a0001c0001t0008g0085a0002c0003t0005g0034a0002c0003t0005g0035others(15): Show | 18 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.907+2345C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41333714 | ||||||
chr13:41333879
|
G | A | 1 | a0001c0001t0008g0084 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.907+2510G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41333879 | ||||||
chr13:41333957
|
G | A | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.907+2588G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41333957 | ||||||
chr13:41333994
|
G | A | 5 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0089others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.907+2625G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41333994 | ||||||
chr13:41334586
|
C | G | 1 | a0001c0001t0010g0135 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.908-2064C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41334586 | ||||||
chr13:41334622
|
T | C | 1 | a0001c0017t0006g0090 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.908-2028T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41334622 | ||||||
chr13:41334751
|
A | C | 3 | a0001c0001t0001g0213a0001c0001t0001g0244a0009c0012t0001g0243 | 3 | HG02895.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.908-1899A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41334751 | ||||||
chr13:41334906
|
AC | A | 302 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(299): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.908-1736delC | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr13 | 41334906 | |||||
chr13:41335064
|
C | T | 2 | a0001c0001t0004g0055a0001c0001t0004g0151 | 2 | HG01515.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.908-1586C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335064 | ||||||
chr13:41335161
|
G | A | 10 | a0001c0001t0006g0010a0001c0001t0006g0025a0001c0001t0006g0026others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.908-1489G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335161 | ||||||
chr13:41335225
|
G | GAAGAT | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.908-1421_908-1420i others(7): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr13 | 41335225 | |||||
chr13:41335306
|
T | C | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.908-1344T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335306 | ||||||
chr13:41335435
|
G | A | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.908-1215G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335435 | ||||||
chr13:41335533
|
G | A | 1 | a0001c0001t0003g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.908-1117G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335533 | ||||||
chr13:41335613
|
T | G | 1 | a0001c0001t0006g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.908-1037T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335613 | ||||||
chr13:41335683
|
A | G | 3 | a0001c0001t0001g0193a0001c0001t0001g0209a0001c0001t0001g0289 | 3 | NA18956.hp2 NA18993.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.908-967A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335683 | ||||||
chr13:41335817
|
C | T | 5 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(2): Show | 5 | HG02451.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.908-833C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335817 | ||||||
chr13:41335859
|
GT | G | 241 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(238): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.908-778delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr13 | 41335859 | |||||
chr13:41335859
|
GTT | G | 60 | a0001c0001t0002g0230a0001c0001t0003g0003a0001c0001t0003g0006others(57): Show | 64 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.908-779_908-778del others(2): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr13 | 41335859 | |||||
chr13:41335872
|
T | C | 47 | a0001c0001t0002g0242a0001c0001t0002g0263a0001c0001t0004g0001others(44): Show | 56 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.908-778T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335872 | ||||||
chr13:41335922
|
T | A | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.908-728T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41335922 | ||||||
chr13:41336041
|
G | A | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.908-609G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41336041 | ||||||
chr13:41336103
|
A | G | 1 | a0001c0011t0014g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.908-547A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41336103 | ||||||
chr13:41336162
|
TA | T | 20 | a0001c0001t0001g0266a0001c0001t0004g0052a0001c0001t0008g0142others(17): Show | 20 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.908-479delA | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr13 | 41336162 | |||||
chr13:41336169
|
A | T | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.908-481A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41336169 | ||||||
chr13:41336171
|
A | T | 289 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(286): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.908-479A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41336171 | ||||||
chr13:41336351
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.908-299T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41336351 | ||||||
chr13:41336373
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.908-277G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41336373 | ||||||
chr13:41336495
|
T | C | 8 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0001g0231others(5): Show | 10 | HG00140.hp1 HG01192.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.908-155T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41336495 | ||||||
chr13:41336556
|
A | G | 18 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0180others(15): Show | 20 | HG00280.hp2 HG00738.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.908-94A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 8/19 | chr13 | 41336556 | ||||||
chr13:41336932
|
G | T | 1 | a0001c0001t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1014+176G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41336932 | ||||||
chr13:41337034
|
T | C | 2 | a0001c0001t0008g0084a0001c0001t0008g0085 | 2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1014+278T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337034 | ||||||
chr13:41337044
|
T | G | 1 | a0001c0001t0003g0099 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1014+288T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337044 | ||||||
chr13:41337096
|
A | G | 2 | a0001c0001t0008g0084a0001c0001t0008g0085 | 2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1014+340A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337096 | ||||||
chr13:41337357
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1014+601C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337357 | ||||||
chr13:41337415
|
C | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+659C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337415 | ||||||
chr13:41337491
|
C | T | 5 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(2): Show | 5 | HG02451.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+735C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337491 | ||||||
chr13:41337497
|
C | T | 3 | a0001c0001t0002g0189a0001c0001t0002g0241a0001c0001t0002g0263 | 3 | HG01358.hp2 HG02280.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1014+741C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337497 | ||||||
chr13:41337530
|
G | A | 1 | a0001c0001t0006g0032 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1014+774G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337530 | ||||||
chr13:41337542
|
C | CA | 283 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(280): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1014+803dupA | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41337542 | |||||
chr13:41337542
|
C | CAA | 12 | a0001c0001t0001g0288a0001c0001t0001g0290a0001c0001t0002g0221others(9): Show | 12 | HG00621.hp2 HG00735.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1014+802_1014+803d others(4): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41337542 | |||||
chr13:41337600
|
A | G | 1 | a0001c0001t0003g0116 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1014+844A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337600 | ||||||
chr13:41337676
|
GT | G | 22 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(19): Show | 22 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1014+922delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41337676 | |||||
chr13:41337787
|
A | G | 2 | a0001c0001t0008g0084a0001c0001t0008g0085 | 2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1014+1031A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337787 | ||||||
chr13:41337809
|
G | A | 1 | a0001c0001t0010g0135 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1014+1053G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337809 | ||||||
chr13:41337854
|
A | G | 11 | a0001c0001t0001g0021a0001c0001t0001g0193a0001c0001t0001g0206others(8): Show | 12 | HG00609.hp1 HG02056.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1014+1098A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337854 | ||||||
chr13:41337934
|
A | AG | 155 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(152): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1014+1179dupG | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41337934 | |||||
chr13:41337955
|
T | TA | 6 | a0001c0001t0002g0260a0001c0001t0008g0086a0001c0001t0008g0087others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+1207dupA | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41337955 | |||||
chr13:41337964
|
C | T | 1 | a0001c0001t0002g0292 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1014+1208C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337964 | ||||||
chr13:41337974
|
C | T | 1 | a0001c0011t0014g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1014+1218C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41337974 | ||||||
chr13:41338054
|
T | G | 72 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(69): Show | 77 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1014+1298T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338054 | ||||||
chr13:41338111
|
T | G | 1 | a0001c0001t0012g0109 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1014+1355T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338111 | ||||||
chr13:41338204
|
T | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(79): Show | 92 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.1014+1448T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338204 | ||||||
chr13:41338244
|
G | A | 16 | a0002c0003t0005g0035a0002c0003t0005g0036a0002c0003t0005g0038others(13): Show | 16 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1014+1488G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338244 | ||||||
chr13:41338268
|
T | C | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1014+1512T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338268 | ||||||
chr13:41338359
|
A | G | 2 | a0001c0011t0014g0154a0001c0013t0015g0153 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1014+1603A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338359 | ||||||
chr13:41338519
|
A | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+1763A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338519 | ||||||
chr13:41338724
|
A | T | 10 | a0001c0001t0006g0010a0001c0001t0006g0025a0001c0001t0006g0026others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014+1968A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338724 | ||||||
chr13:41338758
|
A | T | 2 | a0001c0001t0004g0075a0007c0008t0026g0078 | 2 | HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1014+2002A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338758 | ||||||
chr13:41338838
|
C | G | 1 | a0001c0001t0002g0305 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1014+2082C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338838 | ||||||
chr13:41338878
|
T | C | 155 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(152): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1014+2122T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338878 | ||||||
chr13:41338995
|
C | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+2239C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41338995 | ||||||
chr13:41339120
|
T | TTTG | 233 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(230): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1014+2376_1014+237 others(7): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41339120 | |||||
chr13:41339132
|
GT | G | 65 | a0001c0001t0001g0208a0001c0001t0003g0003a0001c0001t0003g0006others(62): Show | 69 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1014+2379delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41339132 | |||||
chr13:41339193
|
T | C | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+2437T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41339193 | ||||||
chr13:41339429
|
G | A | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1014+2673G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41339429 | ||||||
chr13:41339441
|
A | G | 1 | a0001c0001t0001g0250 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1014+2685A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41339441 | ||||||
chr13:41339455
|
A | C | 1 | a0001c0017t0006g0090 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1014+2699A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41339455 | ||||||
chr13:41339481
|
G | A | 2 | a0001c0001t0002g0179a0001c0001t0002g0251 | 2 | NA18940.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1014+2725G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41339481 | ||||||
chr13:41339531
|
A | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0244 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1014+2775A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41339531 | ||||||
chr13:41339618
|
T | C | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+2862T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41339618 | ||||||
chr13:41339870
|
G | A | 5 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0089others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+3114G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41339870 | ||||||
chr13:41340052
|
T | C | 2 | a0001c0001t0003g0096a0001c0001t0003g0110 | 2 | HG02523.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1014+3296T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340052 | ||||||
chr13:41340447
|
G | C | 202 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(199): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1014+3691G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340447 | ||||||
chr13:41340495
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0181others(8): Show | 14 | HG00597.hp2 HG02015.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.1014+3739T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340495 | ||||||
chr13:41340539
|
C | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+3783C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340539 | ||||||
chr13:41340647
|
G | GTTTTTTT others(5): Show |
1 | a0001c0002t0009g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1014+3924_1014+393 others(16): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | |||||
chr13:41340647
|
GTTTT | G | 4 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0159others(1): Show | 9 | HG00423.hp1 HG02135.hp2 NA18967.hp1 others(6): Show |
intron_variant | MODIFIER | c.1014+3932_1014+393 others(8): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | |||||
chr13:41340647
|
GTTTTTTT others(6): Show |
G | 2 | a0001c0001t0004g0075a0007c0008t0026g0078 | 2 | HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1014+3923_1014+393 others(17): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | |||||
chr13:41340647
|
GTTTTTTT others(7): Show |
G | 9 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0271others(6): Show | 9 | HG01981.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1014+3922_1014+393 others(18): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | |||||
chr13:41340647
|
GTTTTTTT others(8): Show |
G | 84 | a0001c0001t0001g0017a0001c0001t0001g0175a0001c0001t0001g0212others(81): Show | 89 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1014+3921_1014+393 others(19): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | |||||
chr13:41340647
|
GTTTTTTT others(9): Show |
G | 176 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(173): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1014+3920_1014+393 others(20): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | |||||
chr13:41340647
|
GTTTTTTT others(10): Show |
G | 31 | a0001c0001t0001g0180a0001c0001t0001g0220a0001c0001t0001g0222others(28): Show | 31 | HG00280.hp2 HG00738.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1014+3919_1014+393 others(21): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | |||||
chr13:41340647
|
GTTTTTTT others(11): Show |
G | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1014+3918_1014+393 others(22): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | |||||
chr13:41340647
|
GTTTTTTT others(14): Show |
G | 1 | a0002c0003t0005g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1014+3915_1014+393 others(25): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41340647 | |||||
chr13:41340671
|
T | G | 2 | a0001c0001t0006g0026a0001c0001t0006g0027 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1014+3915T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340671 | ||||||
chr13:41340674
|
T | G | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1014+3918T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340674 | ||||||
chr13:41340690
|
T | C | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1014+3934T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340690 | ||||||
chr13:41340691
|
T | C | 37 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0276others(34): Show | 38 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1014+3935T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340691 | ||||||
chr13:41340778
|
G | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+4022G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340778 | ||||||
chr13:41340822
|
G | A | 10 | a0001c0001t0006g0010a0001c0001t0006g0025a0001c0001t0006g0026others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014+4066G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340822 | ||||||
chr13:41340831
|
C | T | 1 | a0001c0001t0004g0057 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1014+4075C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340831 | ||||||
chr13:41340837
|
C | T | 71 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(68): Show | 76 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1014+4081C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340837 | ||||||
chr13:41340853
|
T | C | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1014+4097T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340853 | ||||||
chr13:41340880
|
C | T | 1 | a0001c0001t0004g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1014+4124C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340880 | ||||||
chr13:41340928
|
A | G | 38 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(35): Show | 47 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1014+4172A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41340928 | ||||||
chr13:41341267
|
A | G | 44 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(41): Show | 53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1014+4511A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41341267 | ||||||
chr13:41341788
|
A | G | 1 | a0001c0011t0014g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1014+5032A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41341788 | ||||||
chr13:41341820
|
T | C | 1 | a0001c0001t0008g0086 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1014+5064T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41341820 | ||||||
chr13:41341836
|
C | CT | 279 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(276): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1014+5093dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41341836 | |||||
chr13:41341836
|
C | CTT | 21 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(18): Show | 21 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1014+5092_1014+509 others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41341836 | |||||
chr13:41341980
|
C | T | 4 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(1): Show | 4 | HG02451.hp2 HG03041.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014+5224C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41341980 | ||||||
chr13:41341984
|
A | G | 1 | a0001c0001t0010g0135 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1014+5228A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41341984 | ||||||
chr13:41341988
|
T | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0181others(9): Show | 15 | HG00597.hp2 HG02015.hp2 NA18747.hp1 others(12): Show |
intron_variant | MODIFIER | c.1014+5232T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41341988 | ||||||
chr13:41341998
|
A | C | 1 | a0001c0001t0002g0298 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1014+5242A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41341998 | ||||||
chr13:41342010
|
T | C | 4 | a0001c0001t0011g0103a0001c0001t0011g0104a0001c0001t0011g0117others(1): Show | 4 | NA18948.hp1 NA18984.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1014+5254T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342010 | ||||||
chr13:41342067
|
C | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+5311C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342067 | ||||||
chr13:41342074
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1014+5318C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342074 | ||||||
chr13:41342130
|
CCTCT | C | 3 | a0001c0001t0008g0141a0001c0001t0008g0144a0001c0001t0024g0140 | 3 | HG01981.hp2 HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1014+5385_1014+538 others(8): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41342130 | |||||
chr13:41342143
|
C | CT | 7 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0280others(4): Show | 10 | NA18942.hp1 NA18943.hp1 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.1014+5399dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41342143 | |||||
chr13:41342177
|
G | A | 1 | a0001c0001t0010g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1014+5421G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342177 | ||||||
chr13:41342323
|
A | G | 2 | a0001c0001t0003g0114a0001c0001t0003g0115 | 2 | HG01255.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1014+5567A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342323 | ||||||
chr13:41342378
|
T | A | 1 | a0001c0002t0009g0164 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1014+5622T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342378 | ||||||
chr13:41342557
|
G | A | 3 | a0001c0001t0008g0142a0001c0001t0008g0143a0001c0001t0020g0139 | 3 | HG02486.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1014+5801G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342557 | ||||||
chr13:41342769
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1014+6013T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342769 | ||||||
chr13:41342815
|
A | T | 1 | a0001c0001t0001g0204 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1014+6059A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41342815 | ||||||
chr13:41343001
|
CAG | C | 71 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(68): Show | 76 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1014+6248_1014+624 others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41343001 | |||||
chr13:41343043
|
A | G | 1 | a0001c0001t0003g0105 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1014+6287A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343043 | ||||||
chr13:41343169
|
A | G | 2 | a0001c0001t0001g0250a0001c0001t0002g0238 | 2 | HG00597.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1014+6413A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343169 | ||||||
chr13:41343171
|
C | T | 1 | a0001c0001t0003g0113 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1014+6415C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343171 | ||||||
chr13:41343229
|
T | TGAGTA | 44 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(41): Show | 53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1014+6476_1014+648 others(9): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41343229 | |||||
chr13:41343432
|
A | G | 202 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(199): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1014+6676A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343432 | ||||||
chr13:41343461
|
C | A | 155 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(152): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1014+6705C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343461 | ||||||
chr13:41343511
|
A | T | 5 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(2): Show | 5 | HG02451.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+6755A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343511 | ||||||
chr13:41343637
|
C | G | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+6881C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343637 | ||||||
chr13:41343653
|
C | T | 5 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0089others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+6897C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343653 | ||||||
chr13:41343667
|
C | G | 2 | a0002c0003t0005g0035a0002c0003t0005g0049 | 2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1014+6911C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41343667 | ||||||
chr13:41344074
|
T | C | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1014+7318T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344074 | ||||||
chr13:41344082
|
GTTA | G | 7 | a0002c0003t0005g0036a0002c0003t0005g0039a0002c0003t0005g0041others(4): Show | 7 | HG01243.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1014+7333_1014+733 others(7): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41344082 | |||||
chr13:41344088
|
A | G | 1 | a0001c0001t0010g0137 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1014+7332A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344088 | ||||||
chr13:41344167
|
A | G | 1 | a0002c0003t0005g0049 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1014+7411A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344167 | ||||||
chr13:41344257
|
T | C | 1 | a0001c0001t0002g0256 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1014+7501T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344257 | ||||||
chr13:41344344
|
G | A | 60 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(57): Show | 64 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1014+7588G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344344 | ||||||
chr13:41344421
|
C | T | 5 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0089others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+7665C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344421 | ||||||
chr13:41344426
|
T | C | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1014+7670T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344426 | ||||||
chr13:41344507
|
G | C | 1 | a0001c0001t0006g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1014+7751G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344507 | ||||||
chr13:41344544
|
G | A | 10 | a0001c0001t0006g0010a0001c0001t0006g0025a0001c0001t0006g0026others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014+7788G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344544 | ||||||
chr13:41344666
|
T | C | 6 | a0001c0001t0006g0148a0001c0001t0008g0086a0001c0001t0008g0087others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+7910T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344666 | ||||||
chr13:41344774
|
A | G | 1 | a0002c0003t0005g0048 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1014+8018A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344774 | ||||||
chr13:41344793
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1014+8037A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344793 | ||||||
chr13:41344828
|
A | G | 11 | a0001c0001t0006g0010a0001c0001t0006g0024a0001c0001t0006g0025others(8): Show | 12 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.1014+8072A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41344828 | ||||||
chr13:41345025
|
T | C | 5 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(2): Show | 5 | HG02451.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+8269T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345025 | ||||||
chr13:41345068
|
G | A | 1 | a0001c0001t0003g0107 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1014+8312G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345068 | ||||||
chr13:41345235
|
T | G | 4 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(1): Show | 4 | HG02451.hp2 HG03041.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014+8479T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345235 | ||||||
chr13:41345450
|
G | A | 1 | a0003c0004t0003g0094 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1014+8694G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345450 | ||||||
chr13:41345530
|
T | C | 1 | a0001c0001t0006g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1014+8774T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345530 | ||||||
chr13:41345562
|
G | T | 1 | a0001c0001t0006g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1014+8806G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345562 | ||||||
chr13:41345692
|
C | T | 1 | a0001c0001t0006g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1014+8936C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345692 | ||||||
chr13:41345739
|
T | A | 59 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(56): Show | 63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1014+8983T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345739 | ||||||
chr13:41345763
|
C | G | 8 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0280others(5): Show | 11 | HG02129.hp1 NA18942.hp1 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014+9007C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345763 | ||||||
chr13:41345784
|
G | A | 4 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(1): Show | 4 | HG02451.hp2 HG03041.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014+9028G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345784 | ||||||
chr13:41345789
|
G | T | 8 | a0001c0001t0003g0006a0001c0001t0003g0015a0001c0001t0003g0130others(5): Show | 11 | HG00642.hp2 HG01074.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014+9033G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345789 | ||||||
chr13:41345853
|
C | T | 38 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(35): Show | 47 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1014+9097C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345853 | ||||||
chr13:41345920
|
A | G | 8 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(5): Show | 13 | HG00423.hp1 HG02135.hp2 NA18965.hp2 others(10): Show |
intron_variant | MODIFIER | c.1014+9164A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41345920 | ||||||
chr13:41346120
|
A | G | 8 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(5): Show | 13 | HG00423.hp1 HG02135.hp2 NA18965.hp2 others(10): Show |
intron_variant | MODIFIER | c.1015-9024A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346120 | ||||||
chr13:41346206
|
C | T | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1015-8938C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346206 | ||||||
chr13:41346237
|
C | G | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-8907C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346237 | ||||||
chr13:41346296
|
G | T | 2 | a0001c0001t0003g0132a0001c0001t0003g0133 | 2 | HG01496.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1015-8848G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346296 | ||||||
chr13:41346389
|
G | T | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1015-8755G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346389 | ||||||
chr13:41346538
|
A | G | 1 | a0001c0001t0004g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1015-8606A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346538 | ||||||
chr13:41346898
|
A | C | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1015-8246A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346898 | ||||||
chr13:41346900
|
T | C | 1 | a0001c0001t0004g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1015-8244T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346900 | ||||||
chr13:41346941
|
G | A | 1 | a0001c0001t0023g0265 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1015-8203G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41346941 | ||||||
chr13:41347067
|
A | C | 1 | a0001c0001t0004g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1015-8077A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347067 | ||||||
chr13:41347202
|
G | A | 1 | a0001c0001t0003g0113 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1015-7942G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347202 | ||||||
chr13:41347210
|
G | A | 7 | a0001c0001t0004g0011a0001c0001t0004g0052a0001c0001t0004g0056others(4): Show | 8 | HG00621.hp2 HG02080.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.1015-7934G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347210 | ||||||
chr13:41347222
|
AAAAAAC | A | 160 | a0001c0001t0001g0213a0001c0001t0001g0244a0001c0001t0002g0219others(157): Show | 174 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1015-7904_1015-789 others(10): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41347222 | |||||
chr13:41347223
|
AAAAAC | A | 6 | a0001c0001t0002g0221a0001c0001t0003g0105a0001c0001t0003g0127others(3): Show | 6 | HG00621.hp2 HG01192.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1015-7916_1015-791 others(9): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41347223 | |||||
chr13:41347224
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1015-7920A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347224 | ||||||
chr13:41347225
|
A | C | 53 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(50): Show | 61 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1015-7919A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347225 | ||||||
chr13:41347227
|
ACAAAAAC | A | 134 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(131): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1015-7916_1015-791 others(11): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347227 | ||||||
chr13:41347234
|
C | A | 18 | a0001c0001t0001g0213a0001c0001t0001g0244a0001c0001t0002g0219others(15): Show | 18 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.1015-7910C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347234 | ||||||
chr13:41347240
|
C | A | 9 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0001g0231others(6): Show | 11 | HG00140.hp1 HG01192.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1015-7904C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347240 | ||||||
chr13:41347320
|
T | A | 1 | a0001c0001t0010g0135 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1015-7824T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347320 | ||||||
chr13:41347321
|
A | C | 1 | a0001c0001t0010g0135 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1015-7823A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347321 | ||||||
chr13:41347359
|
TTTTAGGA others(16): Show |
T | 1 | a0001c0001t0003g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-7783_1015-776 others(27): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41347359 | |||||
chr13:41347750
|
T | C | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1015-7394T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347750 | ||||||
chr13:41347752
|
C | A | 1 | a0002c0003t0005g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1015-7392C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347752 | ||||||
chr13:41347752
|
C | G | 16 | a0002c0003t0005g0035a0002c0003t0005g0036a0002c0003t0005g0038others(13): Show | 16 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1015-7392C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347752 | ||||||
chr13:41347792
|
A | G | 38 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(35): Show | 47 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1015-7352A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347792 | ||||||
chr13:41347797
|
G | A | 155 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(152): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1015-7347G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41347797 | ||||||
chr13:41348043
|
G | A | 5 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0089others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1015-7101G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348043 | ||||||
chr13:41348108
|
T | A | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1015-7036T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348108 | ||||||
chr13:41348109
|
T | A | 145 | a0001c0001t0001g0204a0001c0001t0003g0003a0001c0001t0003g0006others(142): Show | 159 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.1015-7035T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348109 | ||||||
chr13:41348174
|
AT | A | 10 | a0001c0001t0006g0010a0001c0001t0006g0025a0001c0001t0006g0026others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1015-6960delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41348174 | |||||
chr13:41348231
|
A | G | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-6913A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348231 | ||||||
chr13:41348248
|
A | G | 1 | a0001c0001t0001g0021 | 2 | HG02080.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1015-6896A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348248 | ||||||
chr13:41348558
|
T | G | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-6586T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348558 | ||||||
chr13:41348563
|
A | C | 15 | a0002c0003t0005g0035a0002c0003t0005g0036a0002c0003t0005g0038others(12): Show | 15 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1015-6581A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348563 | ||||||
chr13:41348588
|
A | T | 1 | a0001c0001t0002g0302 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1015-6556A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348588 | ||||||
chr13:41348680
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1015-6464C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348680 | ||||||
chr13:41348693
|
G | A | 2 | a0001c0001t0003g0145a0010c0015t0003g0147 | 2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1015-6451G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348693 | ||||||
chr13:41348694
|
G | A | 18 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0180others(15): Show | 20 | HG00280.hp2 HG00738.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1015-6450G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348694 | ||||||
chr13:41348805
|
T | C | 10 | a0001c0001t0006g0010a0001c0001t0006g0025a0001c0001t0006g0026others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1015-6339T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348805 | ||||||
chr13:41348811
|
T | A | 2 | a0001c0001t0003g0119a0001c0001t0004g0065 | 2 | NA19010.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1015-6333T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348811 | ||||||
chr13:41348932
|
C | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-6212C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348932 | ||||||
chr13:41348983
|
T | C | 311 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(308): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1015-6161T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41348983 | ||||||
chr13:41349100
|
C | T | 1 | a0001c0001t0004g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1015-6044C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349100 | ||||||
chr13:41349190
|
T | A | 5 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0089others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1015-5954T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349190 | ||||||
chr13:41349277
|
T | C | 2 | a0001c0001t0001g0222a0001c0001t0001g0264 | 2 | HG01433.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1015-5867T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349277 | ||||||
chr13:41349325
|
A | G | 59 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(56): Show | 63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1015-5819A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349325 | ||||||
chr13:41349336
|
C | T | 1 | a0001c0001t0004g0082 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1015-5808C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349336 | ||||||
chr13:41349463
|
C | G | 2 | a0001c0011t0014g0154a0001c0013t0015g0153 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1015-5681C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349463 | ||||||
chr13:41349486
|
C | CT | 302 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(299): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1015-5649dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41349486 | |||||
chr13:41349629
|
A | T | 1 | a0001c0001t0003g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-5515A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349629 | ||||||
chr13:41349631
|
T | A | 1 | a0001c0001t0003g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-5513T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349631 | ||||||
chr13:41349680
|
C | T | 1 | a0001c0001t0004g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1015-5464C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349680 | ||||||
chr13:41349689
|
G | C | 1 | a0001c0001t0004g0082 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1015-5455G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349689 | ||||||
chr13:41349702
|
C | T | 201 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(198): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1015-5442C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349702 | ||||||
chr13:41349767
|
C | A | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1015-5377C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349767 | ||||||
chr13:41349835
|
G | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-5309G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349835 | ||||||
chr13:41349845
|
C | A | 1 | a0001c0001t0003g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-5299C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349845 | ||||||
chr13:41349869
|
G | A | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-5275G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349869 | ||||||
chr13:41349888
|
G | A | 2 | a0001c0001t0004g0055a0001c0001t0004g0151 | 2 | HG01515.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1015-5256G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349888 | ||||||
chr13:41349888
|
G | T | 1 | a0001c0001t0003g0127 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1015-5256G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349888 | ||||||
chr13:41349927
|
T | C | 1 | a0001c0001t0004g0055 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1015-5217T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349927 | ||||||
chr13:41349959
|
T | C | 1 | a0001c0001t0003g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-5185T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349959 | ||||||
chr13:41349960
|
C | T | 1 | a0001c0001t0003g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-5184C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349960 | ||||||
chr13:41349960
|
CA | C | 294 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(291): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1015-5168delA | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41349960 | |||||
chr13:41349961
|
A | C | 1 | a0001c0001t0003g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-5183A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349961 | ||||||
chr13:41349968
|
A | T | 1 | a0001c0001t0003g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-5176A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41349968 | ||||||
chr13:41350203
|
C | A | 2 | a0001c0001t0008g0084a0001c0001t0008g0085 | 2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1015-4941C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350203 | ||||||
chr13:41350297
|
GT | G | 298 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(295): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1015-4833delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41350297 | |||||
chr13:41350300
|
T | G | 1 | a0001c0001t0003g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-4844T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350300 | ||||||
chr13:41350368
|
A | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-4776A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350368 | ||||||
chr13:41350471
|
A | G | 1 | a0001c0001t0004g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1015-4673A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350471 | ||||||
chr13:41350532
|
A | G | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-4612A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350532 | ||||||
chr13:41350566
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1015-4578G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350566 | ||||||
chr13:41350603
|
TTTTG | T | 6 | a0001c0001t0006g0027a0001c0001t0006g0028a0001c0001t0006g0029others(3): Show | 6 | HG01192.hp1 HG01891.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1015-4537_1015-453 others(8): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41350603 | |||||
chr13:41350604
|
TTTGTTTT others(9): Show |
T | 1 | a0001c0001t0001g0290 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1015-4537_1015-452 others(20): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41350604 | |||||
chr13:41350607
|
G | T | 4 | a0001c0001t0006g0010a0001c0001t0006g0025a0001c0001t0006g0026others(1): Show | 5 | HG01069.hp2 HG01071.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1015-4537G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350607 | ||||||
chr13:41350611
|
T | G | 1 | a0001c0001t0003g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-4533T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350611 | ||||||
chr13:41350611
|
TTTTTTTT others(10): Show |
T | 57 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0266others(54): Show | 66 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1015-4524_1015-450 others(21): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41350611 | |||||
chr13:41350612
|
TTTTTTTT others(9): Show |
T | 1 | a0001c0001t0004g0056 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1015-4524_1015-450 others(20): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41350612 | |||||
chr13:41350618
|
TTG | T | 207 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(204): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1015-4524_1015-452 others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41350618 | |||||
chr13:41350619
|
TG | T | 18 | a0001c0001t0001g0177a0001c0001t0001g0194a0001c0001t0001g0207others(15): Show | 18 | HG01175.hp2 HG01496.hp2 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.1015-4524delG | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350619 | ||||||
chr13:41350619
|
TGTTTG | T | 3 | a0001c0001t0006g0025a0001c0001t0006g0026a0001c0001t0006g0032 | 3 | HG02895.hp2 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1015-4524_1015-452 others(9): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350619 | ||||||
chr13:41350620
|
G | T | 10 | a0001c0001t0003g0127a0001c0001t0006g0010a0001c0001t0006g0027others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1015-4524G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350620 | ||||||
chr13:41350622
|
T | G | 1 | a0001c0001t0001g0290 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1015-4522T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350622 | ||||||
chr13:41350623
|
T | G | 4 | a0001c0001t0001g0177a0001c0001t0001g0194a0001c0001t0001g0229others(1): Show | 4 | HG01981.hp1 HG03688.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-4521T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350623 | ||||||
chr13:41350624
|
G | T | 19 | a0001c0001t0001g0177a0001c0001t0001g0194a0001c0001t0001g0229others(16): Show | 20 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1015-4520G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350624 | ||||||
chr13:41350628
|
G | T | 242 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(239): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1015-4516G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350628 | ||||||
chr13:41350656
|
C | T | 60 | a0001c0001t0001g0250a0001c0001t0001g0283a0001c0001t0002g0005others(57): Show | 63 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.1015-4488C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350656 | ||||||
chr13:41350755
|
G | T | 1 | a0001c0001t0003g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-4389G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350755 | ||||||
chr13:41350883
|
C | T | 1 | a0001c0001t0008g0085 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1015-4261C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350883 | ||||||
chr13:41350981
|
A | G | 3 | a0001c0001t0001g0196a0001c0001t0001g0203a0001c0001t0001g0208 | 3 | NA18987.hp1 NA19011.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1015-4163A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41350981 | ||||||
chr13:41351049
|
C | T | 1 | a0001c0001t0021g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1015-4095C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351049 | ||||||
chr13:41351061
|
C | T | 38 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(35): Show | 47 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1015-4083C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351061 | ||||||
chr13:41351123
|
G | A | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1015-4021G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351123 | ||||||
chr13:41351148
|
A | G | 9 | a0001c0001t0006g0025a0001c0001t0006g0026a0001c0001t0006g0027others(6): Show | 9 | HG01192.hp1 HG01891.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1015-3996A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351148 | ||||||
chr13:41351175
|
C | T | 9 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0001g0231others(6): Show | 11 | HG00140.hp1 HG01192.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1015-3969C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351175 | ||||||
chr13:41351189
|
G | A | 2 | a0001c0001t0004g0073a0001c0001t0004g0083 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1015-3955G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351189 | ||||||
chr13:41351258
|
C | T | 1 | a0001c0001t0003g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-3886C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351258 | ||||||
chr13:41351288
|
C | T | 1 | a0001c0001t0003g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1015-3856C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351288 | ||||||
chr13:41351569
|
G | A | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-3575G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351569 | ||||||
chr13:41351632
|
T | C | 1 | a0001c0001t0002g0263 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1015-3512T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41351632 | ||||||
chr13:41351777
|
TG | T | 302 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(299): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1015-3363delG | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41351777 | |||||
chr13:41352064
|
A | G | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-3080A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352064 | ||||||
chr13:41352127
|
C | T | 155 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(152): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1015-3017C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352127 | ||||||
chr13:41352215
|
G | T | 301 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(298): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1015-2929G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352215 | ||||||
chr13:41352257
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0190others(7): Show | 13 | HG01109.hp1 HG01167.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1015-2887G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352257 | ||||||
chr13:41352366
|
A | G | 38 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(35): Show | 47 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1015-2778A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352366 | ||||||
chr13:41352426
|
G | A | 10 | a0001c0001t0006g0010a0001c0001t0006g0025a0001c0001t0006g0026others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1015-2718G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352426 | ||||||
chr13:41352475
|
C | T | 5 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(2): Show | 5 | HG02451.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1015-2669C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352475 | ||||||
chr13:41352511
|
C | T | 1 | a0001c0001t0002g0178 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1015-2633C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352511 | ||||||
chr13:41352624
|
C | T | 2 | a0001c0001t0002g0285a0001c0009t0002g0284 | 2 | HG02129.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1015-2520C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352624 | ||||||
chr13:41352713
|
G | A | 5 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0089others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1015-2431G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352713 | ||||||
chr13:41352717
|
C | T | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1015-2427C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352717 | ||||||
chr13:41352949
|
T | C | 1 | a0001c0001t0004g0074 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1015-2195T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352949 | ||||||
chr13:41352955
|
A | G | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1015-2189A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352955 | ||||||
chr13:41352973
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1015-2171C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41352973 | ||||||
chr13:41353113
|
T | TCAAAA | 224 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(221): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1015-2008_1015-200 others(9): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353113 | |||||
chr13:41353113
|
T | TCAAAACA others(3): Show |
14 | a0001c0001t0001g0272a0001c0001t0008g0086a0001c0001t0008g0087others(11): Show | 19 | HG02040.hp2 HG02109.hp2 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.1015-2013_1015-200 others(14): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353113 | |||||
chr13:41353113
|
T | TCAAAACA others(8): Show |
10 | a0001c0001t0006g0010a0001c0001t0006g0025a0001c0001t0006g0026others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1015-2018_1015-200 others(19): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353113 | |||||
chr13:41353113
|
T | TCAAAACA others(13): Show |
3 | a0001c0001t0003g0146a0001c0001t0003g0171a0001c0017t0006g0090 | 3 | HG01496.hp1 HG02970.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.1015-2023_1015-200 others(24): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353113 | |||||
chr13:41353113
|
T | TCAAAACA others(18): Show |
1 | a0001c0001t0006g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1015-2028_1015-200 others(29): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353113 | |||||
chr13:41353113
|
T | TCAAAACA others(13): Show |
55 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(52): Show | 59 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1015-2021_1015-202 others(24): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353113 | |||||
chr13:41353113
|
T | TCAAAACA others(18): Show |
1 | a0001c0001t0003g0130 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1015-2021_1015-202 others(29): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353113 | |||||
chr13:41353113
|
T | TCAAAACA others(23): Show |
1 | a0001c0001t0003g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1015-2021_1015-202 others(34): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353113 | |||||
chr13:41353149
|
A | C | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-1995A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41353149 | ||||||
chr13:41353482
|
A | G | 44 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(41): Show | 53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1015-1662A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41353482 | ||||||
chr13:41353542
|
A | G | 1 | a0001c0001t0002g0293 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1015-1602A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41353542 | ||||||
chr13:41353600
|
TAA | T | 285 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(282): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1015-1528_1015-152 others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353600 | |||||
chr13:41353600
|
TAAA | T | 17 | a0001c0001t0001g0208a0001c0001t0001g0226a0001c0001t0001g0266others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1015-1529_1015-152 others(7): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353600 | |||||
chr13:41353727
|
A | G | 2 | a0001c0001t0010g0134a0001c0001t0010g0136 | 2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1015-1417A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41353727 | ||||||
chr13:41353768
|
T | TAC | 4 | a0001c0001t0001g0215a0001c0001t0003g0112a0001c0001t0003g0119others(1): Show | 4 | HG02922.hp2 NA18947.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-1343_1015-134 others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353768 | |||||
chr13:41353768
|
T | TACAC | 3 | a0001c0001t0003g0107a0001c0001t0003g0130a0001c0001t0003g0145 | 3 | HG01433.hp1 HG03017.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1015-1345_1015-134 others(8): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353768 | |||||
chr13:41353768
|
TAC | T | 92 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(89): Show | 105 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1015-1343_1015-134 others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353768 | |||||
chr13:41353768
|
TACAC | T | 91 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0001g0213others(88): Show | 95 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.1015-1345_1015-134 others(8): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353768 | |||||
chr13:41353768
|
TACACAC | T | 8 | a0001c0001t0002g0176a0001c0001t0002g0233a0001c0001t0002g0235others(5): Show | 8 | HG02015.hp1 HG02027.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.1015-1347_1015-134 others(10): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353768 | |||||
chr13:41353768
|
TACACACA others(1): Show |
T | 9 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069others(6): Show | 9 | HG00738.hp1 HG01261.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1015-1349_1015-134 others(12): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353768 | |||||
chr13:41353768
|
TACACACA others(3): Show |
T | 40 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(37): Show | 49 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1015-1351_1015-134 others(14): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353768 | |||||
chr13:41353768
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0004g0072 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1015-1355_1015-134 others(18): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41353768 | |||||
chr13:41353801
|
A | C | 6 | a0001c0001t0001g0225a0001c0001t0010g0134a0001c0001t0010g0135others(3): Show | 6 | HG00280.hp2 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1015-1343A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41353801 | ||||||
chr13:41353806
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1015-1338A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41353806 | ||||||
chr13:41353978
|
C | T | 1 | a0009c0012t0001g0243 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1015-1166C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41353978 | ||||||
chr13:41354054
|
A | C | 1 | a0001c0001t0004g0070 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1015-1090A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354054 | ||||||
chr13:41354163
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1015-981G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354163 | ||||||
chr13:41354178
|
A | G | 78 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(75): Show | 82 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.1015-966A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354178 | ||||||
chr13:41354339
|
T | G | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1015-805T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354339 | ||||||
chr13:41354355
|
C | T | 1 | a0001c0001t0004g0059 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1015-789C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354355 | ||||||
chr13:41354391
|
A | T | 8 | a0001c0002t0007g0002a0001c0002t0007g0157a0001c0002t0007g0158others(5): Show | 13 | HG00423.hp1 HG02135.hp2 NA18965.hp2 others(10): Show |
intron_variant | MODIFIER | c.1015-753A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354391 | ||||||
chr13:41354457
|
T | A | 59 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(56): Show | 63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1015-687T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354457 | ||||||
chr13:41354468
|
G | A | 201 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(198): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1015-676G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354468 | ||||||
chr13:41354603
|
C | T | 2 | a0001c0011t0014g0154a0001c0013t0015g0153 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1015-541C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354603 | ||||||
chr13:41354612
|
A | C | 2 | a0002c0003t0005g0035a0002c0003t0005g0049 | 2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1015-532A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | chr13 | 41354612 | ||||||
chr13:41354668
|
A | ATTTTGTA others(47): Show |
1 | a0002c0003t0005g0049 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1015-474_1015-421d others(56): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41354668 | |||||
chr13:41354886
|
A | AT | 22 | a0001c0001t0001g0226a0001c0001t0001g0278a0001c0001t0002g0183others(19): Show | 27 | HG00423.hp1 HG01074.hp2 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.1015-239dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41354886 | |||||
chr13:41354886
|
A | ATT | 173 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(170): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1015-240_1015-239d others(4): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41354886 | |||||
chr13:41354886
|
A | ATTT | 109 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0194others(106): Show | 122 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1015-241_1015-239d others(5): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41354886 | |||||
chr13:41354886
|
A | ATTTT | 6 | a0001c0001t0001g0262a0001c0001t0003g0105a0001c0001t0003g0127others(3): Show | 6 | HG02630.hp2 HG03491.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1015-242_1015-239d others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41354886 | |||||
chr13:41354886
|
AT | A | 5 | a0001c0002t0009g0016a0001c0002t0009g0164a0001c0002t0009g0167others(2): Show | 6 | HG01175.hp1 HG01361.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1015-239delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr13 | 41354886 | |||||
chr13:41355394
|
C | G | 1 | a0001c0001t0003g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1087+178C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41355394 | ||||||
chr13:41355422
|
T | G | 1 | a0001c0001t0006g0029 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1087+206T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41355422 | ||||||
chr13:41355574
|
C | T | 5 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0089others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1087+358C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41355574 | ||||||
chr13:41355696
|
G | A | 1 | a0001c0001t0002g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1087+480G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41355696 | ||||||
chr13:41355976
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1087+760G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41355976 | ||||||
chr13:41356005
|
T | C | 1 | a0001c0001t0010g0135 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1087+789T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41356005 | ||||||
chr13:41356174
|
T | C | 311 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(308): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1087+958T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41356174 | ||||||
chr13:41356188
|
C | CG | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1087+977dupG | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr13 | 41356188 | |||||
chr13:41356214
|
G | C | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1087+998G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41356214 | ||||||
chr13:41356272
|
C | T | 1 | a0002c0003t0005g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1087+1056C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41356272 | ||||||
chr13:41356373
|
TATCTTAG others(88): Show |
T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1087+1253_1087+134 others(99): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr13 | 41356373 | |||||
chr13:41356711
|
A | G | 10 | a0001c0001t0006g0010a0001c0001t0006g0025a0001c0001t0006g0026others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1087+1495A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41356711 | ||||||
chr13:41356922
|
G | A | 1 | a0001c0001t0006g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1088-1382G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41356922 | ||||||
chr13:41357002
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1088-1302G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357002 | ||||||
chr13:41357004
|
C | T | 2 | a0001c0001t0004g0073a0001c0001t0004g0083 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1088-1300C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357004 | ||||||
chr13:41357045
|
C | T | 1 | a0001c0001t0002g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1088-1259C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357045 | ||||||
chr13:41357153
|
C | T | 311 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(308): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1088-1151C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357153 | ||||||
chr13:41357371
|
T | A | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1088-933T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357371 | ||||||
chr13:41357379
|
T | TTTC | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1088-923_1088-921d others(5): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr13 | 41357379 | |||||
chr13:41357474
|
G | A | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1088-830G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357474 | ||||||
chr13:41357550
|
A | G | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1088-754A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357550 | ||||||
chr13:41357727
|
A | G | 38 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(35): Show | 47 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1088-577A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357727 | ||||||
chr13:41357902
|
A | G | 2 | a0001c0001t0008g0084a0001c0001t0008g0085 | 2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1088-402A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41357902 | ||||||
chr13:41358197
|
T | C | 1 | a0001c0011t0014g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1088-107T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 10/19 | chr13 | 41358197 | ||||||
chr13:41358584
|
C | A | 1 | a0001c0001t0001g0149 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1257+111C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 11/19 | chr13 | 41358584 | ||||||
chr13:41358701
|
G | A | 1 | a0001c0005t0001g0248 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1258-109G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 11/19 | chr13 | 41358701 | ||||||
chr13:41359091
|
TA | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1410+133delA | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr13 | 41359091 | |||||
chr13:41359328
|
T | C | 59 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(56): Show | 63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1410+366T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41359328 | ||||||
chr13:41359501
|
A | G | 61 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(58): Show | 65 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1410+539A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41359501 | ||||||
chr13:41359610
|
G | T | 2 | a0001c0001t0002g0179a0001c0001t0002g0251 | 2 | NA18940.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1410+648G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41359610 | ||||||
chr13:41359612
|
T | C | 3 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136 | 3 | HG02451.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1410+650T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41359612 | ||||||
chr13:41359731
|
T | C | 1 | a0001c0001t0004g0059 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1410+769T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41359731 | ||||||
chr13:41359736
|
GA | G | 10 | a0001c0001t0006g0010a0001c0001t0006g0025a0001c0001t0006g0026others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1410+778delA | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr13 | 41359736 | |||||
chr13:41359786
|
A | G | 1 | a0001c0001t0002g0230 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1410+824A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41359786 | ||||||
chr13:41359807
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1410+845G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41359807 | ||||||
chr13:41360041
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1410+1079A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41360041 | ||||||
chr13:41360107
|
A | G | 1 | a0001c0001t0010g0135 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1410+1145A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41360107 | ||||||
chr13:41360458
|
C | G | 4 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(1): Show | 4 | HG02451.hp2 HG03041.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1410+1496C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41360458 | ||||||
chr13:41360476
|
G | A | 2 | a0001c0001t0002g0263a0001c0001t0006g0024 | 2 | HG01358.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1410+1514G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41360476 | ||||||
chr13:41360631
|
T | C | 1 | a0001c0001t0004g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1411-1400T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41360631 | ||||||
chr13:41360684
|
A | G | 1 | a0001c0001t0004g0013 | 2 | HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1411-1347A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41360684 | ||||||
chr13:41360751
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1411-1280A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41360751 | ||||||
chr13:41360795
|
A | G | 4 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(1): Show | 4 | HG02451.hp2 HG03041.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411-1236A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41360795 | ||||||
chr13:41360971
|
ATAAC | A | 5 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0089others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1411-1057_1411-105 others(8): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr13 | 41360971 | |||||
chr13:41361006
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0192 | 4 | HG01109.hp1 HG01167.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411-1025A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41361006 | ||||||
chr13:41361114
|
C | A | 61 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(58): Show | 65 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1411-917C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41361114 | ||||||
chr13:41361124
|
GTGACAAA others(3): Show |
G | 1 | a0001c0001t0010g0135 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1411-903_1411-894d others(12): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr13 | 41361124 | |||||
chr13:41361158
|
C | T | 2 | a0001c0001t0002g0176a0001c0001t0002g0237 | 2 | HG02015.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1411-873C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41361158 | ||||||
chr13:41361704
|
C | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1411-327C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41361704 | ||||||
chr13:41361770
|
C | T | 1 | a0001c0001t0006g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1411-261C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41361770 | ||||||
chr13:41361771
|
G | A | 5 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0089others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1411-260G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41361771 | ||||||
chr13:41361833
|
T | G | 44 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(41): Show | 53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1411-198T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41361833 | ||||||
chr13:41361904
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0267 | 2 | HG02015.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1411-127A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 12/19 | chr13 | 41361904 | ||||||
chr13:41362277
|
T | C | 2 | a0001c0001t0008g0142a0001c0001t0008g0143 | 2 | HG02486.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1539+118T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41362277 | ||||||
chr13:41362357
|
A | C | 1 | a0001c0001t0004g0069 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1539+198A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41362357 | ||||||
chr13:41362367
|
A | G | 1 | a0004c0018t0008g0088 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1539+208A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41362367 | ||||||
chr13:41362449
|
C | A | 1 | a0003c0004t0003g0094 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1539+290C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41362449 | ||||||
chr13:41362921
|
C | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1539+762C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41362921 | ||||||
chr13:41363226
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1539+1067T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41363226 | ||||||
chr13:41363394
|
C | T | 1 | a0001c0001t0002g0305 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1539+1235C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41363394 | ||||||
chr13:41363409
|
G | C | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1539+1250G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41363409 | ||||||
chr13:41363449
|
C | G | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1539+1290C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41363449 | ||||||
chr13:41363654
|
T | C | 72 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(69): Show | 77 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1539+1495T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41363654 | ||||||
chr13:41364051
|
TTAA | T | 44 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(41): Show | 53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1539+1894_1539+189 others(7): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr13 | 41364051 | |||||
chr13:41364067
|
A | G | 5 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(2): Show | 5 | HG02451.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+1908A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41364067 | ||||||
chr13:41364148
|
T | C | 59 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(56): Show | 63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1539+1989T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41364148 | ||||||
chr13:41364163
|
G | A | 1 | a0001c0001t0006g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1539+2004G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41364163 | ||||||
chr13:41364324
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1539+2165T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41364324 | ||||||
chr13:41364657
|
A | G | 5 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0089others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+2498A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41364657 | ||||||
chr13:41364684
|
CTT | C | 44 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(41): Show | 53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1539+2527_1539+252 others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr13 | 41364684 | |||||
chr13:41365148
|
CTAACTT | C | 6 | a0001c0001t0008g0141a0001c0001t0008g0142a0001c0001t0008g0143others(3): Show | 6 | HG01981.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-2288_1540-228 others(10): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr13 | 41365148 | |||||
chr13:41365360
|
T | C | 1 | a0001c0001t0002g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1540-2079T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41365360 | ||||||
chr13:41365464
|
C | G | 22 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(19): Show | 22 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1540-1975C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41365464 | ||||||
chr13:41365586
|
A | G | 2 | a0001c0011t0014g0154a0001c0013t0015g0153 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1540-1853A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41365586 | ||||||
chr13:41365713
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1540-1726C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41365713 | ||||||
chr13:41366055
|
C | CT | 5 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0089others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1540-1381dupT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr13 | 41366055 | |||||
chr13:41366342
|
T | G | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1540-1097T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41366342 | ||||||
chr13:41366411
|
A | G | 2 | a0001c0011t0014g0154a0001c0013t0015g0153 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1540-1028A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41366411 | ||||||
chr13:41366441
|
A | G | 1 | a0001c0001t0002g0254 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1540-998A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41366441 | ||||||
chr13:41366461
|
A | G | 61 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(58): Show | 65 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1540-978A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41366461 | ||||||
chr13:41366812
|
TTGGC | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1540-624_1540-621d others(6): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr13 | 41366812 | |||||
chr13:41366990
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1540-449T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41366990 | ||||||
chr13:41367005
|
T | G | 1 | a0001c0001t0002g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1540-434T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41367005 | ||||||
chr13:41367028
|
A | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1540-411A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41367028 | ||||||
chr13:41367192
|
T | C | 1 | a0006c0010t0002g0232 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1540-247T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41367192 | ||||||
chr13:41367280
|
T | A | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1540-159T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 13/19 | chr13 | 41367280 | ||||||
chr13:41367687
|
A | G | 1 | a0001c0013t0015g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1753+35A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41367687 | ||||||
chr13:41367777
|
C | T | 1 | a0001c0001t0002g0254 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1753+125C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41367777 | ||||||
chr13:41367853
|
A | C | 3 | a0001c0001t0008g0142a0001c0001t0008g0143a0001c0001t0020g0139 | 3 | HG02486.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1753+201A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41367853 | ||||||
chr13:41368098
|
C | G | 3 | a0001c0001t0008g0142a0001c0001t0008g0143a0001c0001t0020g0139 | 3 | HG02486.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1753+446C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368098 | ||||||
chr13:41368104
|
T | A | 6 | a0001c0001t0003g0099a0001c0001t0003g0113a0001c0001t0003g0121others(3): Show | 6 | NA18957.hp1 NA18977.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.1753+452T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368104 | ||||||
chr13:41368173
|
C | A | 1 | a0001c0001t0003g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1753+521C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368173 | ||||||
chr13:41368225
|
T | G | 1 | a0001c0001t0002g0238 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1753+573T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368225 | ||||||
chr13:41368291
|
A | G | 1 | a0001c0017t0006g0090 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1753+639A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368291 | ||||||
chr13:41368333
|
A | G | 1 | a0001c0001t0010g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1753+681A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368333 | ||||||
chr13:41368406
|
CAA | C | 3 | a0001c0001t0008g0142a0001c0001t0008g0143a0001c0001t0020g0139 | 3 | HG02486.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1754-682_1754-681d others(4): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr13 | 41368406 | |||||
chr13:41368443
|
G | C | 11 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0220others(8): Show | 13 | HG00280.hp2 HG00738.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1754-647G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368443 | ||||||
chr13:41368576
|
C | A | 1 | a0001c0001t0002g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1754-514C>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368576 | ||||||
chr13:41368608
|
A | G | 11 | a0001c0001t0006g0010a0001c0001t0006g0024a0001c0001t0006g0025others(8): Show | 12 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.1754-482A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368608 | ||||||
chr13:41368744
|
G | A | 7 | a0001c0001t0001g0220a0001c0001t0001g0228a0001c0001t0008g0086others(4): Show | 7 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1754-346G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368744 | ||||||
chr13:41368916
|
A | T | 61 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(58): Show | 65 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1754-174A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368916 | ||||||
chr13:41368929
|
A | G | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1754-161A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368929 | ||||||
chr13:41368969
|
G | A | 2 | a0001c0011t0014g0154a0001c0013t0015g0153 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1754-121G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41368969 | ||||||
chr13:41369003
|
A | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1754-87A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41369003 | ||||||
chr13:41369011
|
A | G | 1 | a0001c0001t0004g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1754-79A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41369011 | ||||||
chr13:41369013
|
T | G | 1 | a0001c0013t0015g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1754-77T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41369013 | ||||||
chr13:41369050
|
A | C | 1 | a0001c0001t0002g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1754-40A>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 14/19 | chr13 | 41369050 | ||||||
chr13:41369508
|
G | A | 22 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(19): Show | 22 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1947+225G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41369508 | ||||||
chr13:41369562
|
G | A | 1 | a0001c0001t0002g0277 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1947+279G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41369562 | ||||||
chr13:41369755
|
G | T | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1947+472G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41369755 | ||||||
chr13:41369763
|
A | G | 1 | a0001c0001t0004g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1947+480A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41369763 | ||||||
chr13:41369822
|
C | T | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1947+539C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41369822 | ||||||
chr13:41370008
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1947+725G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41370008 | ||||||
chr13:41370311
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1947+1028G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41370311 | ||||||
chr13:41370392
|
A | G | 1 | a0001c0001t0002g0242 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1947+1109A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41370392 | ||||||
chr13:41370483
|
T | C | 1 | a0001c0001t0002g0277 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1947+1200T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41370483 | ||||||
chr13:41370778
|
A | G | 1 | a0001c0001t0004g0076 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1948-1425A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41370778 | ||||||
chr13:41370847
|
A | G | 3 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136 | 3 | HG02451.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1948-1356A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41370847 | ||||||
chr13:41370848
|
C | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0187others(1): Show | 4 | HG00099.hp2 HG00735.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1948-1355C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41370848 | ||||||
chr13:41371033
|
TAAAAG | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0190others(8): Show | 14 | HG01109.hp1 HG01167.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1948-1168_1948-116 others(9): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr13 | 41371033 | |||||
chr13:41371113
|
C | G | 1 | a0001c0001t0002g0304 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1948-1090C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371113 | ||||||
chr13:41371153
|
G | T | 1 | a0001c0001t0004g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1948-1050G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371153 | ||||||
chr13:41371312
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0225 | 3 | HG00280.hp2 HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1948-891A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371312 | ||||||
chr13:41371407
|
C | G | 1 | a0002c0003t0005g0048 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1948-796C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371407 | ||||||
chr13:41371418
|
A | G | 1 | a0001c0001t0004g0082 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1948-785A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371418 | ||||||
chr13:41371470
|
A | G | 1 | a0002c0003t0005g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1948-733A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371470 | ||||||
chr13:41371591
|
G | A | 311 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(308): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1948-612G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371591 | ||||||
chr13:41371614
|
T | C | 2 | a0001c0001t0002g0286a0001c0001t0002g0287 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1948-589T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371614 | ||||||
chr13:41371620
|
A | G | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1948-583A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371620 | ||||||
chr13:41371953
|
T | C | 2 | a0001c0011t0014g0154a0001c0013t0015g0153 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1948-250T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371953 | ||||||
chr13:41371983
|
T | A | 1 | a0001c0001t0006g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1948-220T>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 15/19 | chr13 | 41371983 | ||||||
chr13:41372340
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2056+29A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 16/19 | chr13 | 41372340 | ||||||
chr13:41372458
|
G | A | 1 | a0001c0001t0004g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2056+147G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 16/19 | chr13 | 41372458 | ||||||
chr13:41372462
|
G | T | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2056+151G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 16/19 | chr13 | 41372462 | ||||||
chr13:41372502
|
T | C | 11 | a0001c0001t0003g0006a0001c0001t0003g0015a0001c0001t0003g0106others(8): Show | 14 | HG00642.hp2 HG01074.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.2056+191T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 16/19 | chr13 | 41372502 | ||||||
chr13:41373084
|
AAAT | A | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.2155+264_2155+266d others(5): Show |
NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr13 | 41373084 | |||||
chr13:41373297
|
G | T | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2156-340G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 17/19 | chr13 | 41373297 | ||||||
chr13:41373344
|
A | T | 17 | a0002c0003t0005g0034a0002c0003t0005g0035a0002c0003t0005g0036others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2156-293A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 17/19 | chr13 | 41373344 | ||||||
chr13:41373418
|
C | T | 44 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(41): Show | 53 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2156-219C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 17/19 | chr13 | 41373418 | ||||||
chr13:41373801
|
G | A | 1 | a0001c0002t0007g0158 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2299+21G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41373801 | ||||||
chr13:41373915
|
G | C | 155 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(152): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.2299+135G>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41373915 | ||||||
chr13:41373955
|
G | A | 1 | a0001c0001t0011g0117 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2299+175G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41373955 | ||||||
chr13:41373989
|
A | G | 59 | a0001c0001t0003g0003a0001c0001t0003g0006a0001c0001t0003g0014others(56): Show | 63 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.2299+209A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41373989 | ||||||
chr13:41374015
|
T | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(152): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.2299+235T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374015 | ||||||
chr13:41374038
|
G | T | 1 | a0001c0001t0010g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2299+258G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374038 | ||||||
chr13:41374041
|
C | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.2299+261C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374041 | ||||||
chr13:41374114
|
T | G | 1 | a0008c0016t0016g0160 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.2299+334T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374114 | ||||||
chr13:41374141
|
CT | C | 39 | a0001c0001t0004g0001a0001c0001t0004g0011a0001c0001t0004g0012others(36): Show | 48 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.2299+375delT | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr13 | 41374141 | |||||
chr13:41374145
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2299+365T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374145 | ||||||
chr13:41374233
|
T | G | 1 | a0008c0016t0016g0160 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.2299+453T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374233 | ||||||
chr13:41374249
|
A | T | 2 | a0001c0001t0008g0084a0001c0001t0008g0085 | 2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2299+469A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374249 | ||||||
chr13:41374271
|
G | GC | 12 | a0002c0003t0005g0035a0002c0003t0005g0036a0002c0003t0005g0038others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2300-470dupC | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr13 | 41374271 | |||||
chr13:41374350
|
A | G | 1 | a0001c0001t0008g0085 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2300-392A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374350 | ||||||
chr13:41374457
|
C | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.2300-285C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374457 | ||||||
chr13:41374548
|
C | T | 1 | a0001c0001t0003g0133 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2300-194C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374548 | ||||||
chr13:41374636
|
C | T | 1 | a0001c0001t0003g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2300-106C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374636 | ||||||
chr13:41374683
|
T | C | 22 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(19): Show | 22 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2300-59T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374683 | ||||||
chr13:41374686
|
C | G | 1 | a0001c0001t0002g0293 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2300-56C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 18/19 | chr13 | 41374686 | ||||||
chr13:41374843
|
A | G | 1 | a0008c0016t0016g0160 | 1 | NA19059.hp2 | splice_region_variant&intron_variant | LOW | c.2397+4A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41374843 | ||||||
chr13:41374844
|
G | T | 1 | a0008c0016t0016g0160 | 1 | NA19059.hp2 | splice_region_variant&intron_variant | LOW | c.2397+5G>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41374844 | ||||||
chr13:41374882
|
C | T | 1 | a0001c0001t0013g0182 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2397+43C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41374882 | ||||||
chr13:41374903
|
G | A | 1 | a0001c0001t0004g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2397+64G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41374903 | ||||||
chr13:41374955
|
C | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2397+116C>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41374955 | ||||||
chr13:41374973
|
G | A | 1 | a0001c0001t0006g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2397+134G>A | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41374973 | ||||||
chr13:41374980
|
T | C | 5 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0089others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397+141T>C | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41374980 | ||||||
chr13:41375085
|
C | T | 1 | a0001c0001t0006g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2397+246C>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41375085 | ||||||
chr13:41375126
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2398-279A>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41375126 | ||||||
chr13:41375235
|
A | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.2398-170A>T | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41375235 | ||||||
chr13:41375312
|
T | G | 1 | a0008c0016t0016g0160 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.2398-93T>G | NAA16 | ENSG00000172766.19 | transcript | ENST00000379406.8 | protein_coding | 19/19 | chr13 | 41375312 |