geneid | 51314 |
---|---|
ensemblid | ENSG00000086288.12 |
hgncid | 16473 |
symbol | NME8 |
name | NME/NM23 family member 8 |
refseq_nuc | NM_016616.5 |
refseq_prot | NP_057700.3 |
ensembl_nuc | ENST00000199447.9 |
ensembl_prot | ENSP00000199447.4 |
mane_status | MANE Select |
chr | chr7 |
start | 37848597 |
end | 37900397 |
strand | + |
ver | v1.2 |
region | chr7:37848597-37900397 |
region5000 | chr7:37843597-37905397 |
regionname0 | NME8_chr7_37848597_37900397 |
regionname5000 | NME8_chr7_37843597_37905397 |
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 | 588 | 158 | 34 | 28 | 68 | 7 | 21 | 52 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0002 | 0/0 | 588 | 74 | 5 | 5 | 54 | 1 | 9 | 44 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0003 | 0/0 | 588 | 51 | 38 | 3 | 8 | 1 | 1 | 5 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0004 | 0/0 | 588 | 32 | 1 | 11 | 15 | 1 | 4 | 13 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0005 | 0/0 | 588 | 30 | 0 | 8 | 18 | 3 | 1 | 13 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0006 | 0/0 | 588 | 12 | 0 | 4 | 5 | 1 | 2 | 5 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0007 | 0/0 | 588 | 8 | 1 | 1 | 6 | 0 | 0 | 5 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0008 | 0/0 | 588 | 6 | 0 | 2 | 0 | 2 | 2 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0009 | 0/0 | 588 | 3 | 1 | 0 | 1 | 0 | 1 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0010 | 0/0 | 588 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0011 | 0/0 | 588 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0012 | 0/0 | 588 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0013 | 0/0 | 588 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0014 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0015 | 0/0 | 545 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0016 | 0/0 | 264 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0017 | 0/0 | 151 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0018 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0019 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
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 | 1767 | 109 | 25 | 23 | 48 | 3 | 10 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0002 | 0/0 | 1767 | 37 | 5 | 2 | 26 | 0 | 4 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0003 | 0/0 | 1767 | 31 | 22 | 3 | 4 | 1 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0004 | 0/0 | 1767 | 30 | 4 | 4 | 13 | 4 | 5 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0005 | 0/0 | 1767 | 25 | 1 | 11 | 8 | 1 | 4 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0006 | 0/0 | 1767 | 18 | 0 | 4 | 12 | 2 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0007 | 0/0 | 1767 | 17 | 5 | 1 | 6 | 0 | 5 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0008 | 0/0 | 1767 | 17 | 0 | 1 | 14 | 0 | 2 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0009 | 0/0 | 1767 | 17 | 0 | 1 | 12 | 1 | 3 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0010 | 0/0 | 1767 | 14 | 10 | 0 | 4 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0011 | 0/0 | 1767 | 8 | 0 | 2 | 4 | 1 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0012 | 0/0 | 1767 | 7 | 0 | 0 | 7 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0013 | 0/0 | 1767 | 6 | 0 | 2 | 0 | 2 | 2 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0014 | 0/0 | 1767 | 5 | 0 | 0 | 4 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0015 | 0/0 | 1767 | 4 | 4 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0016 | 0/0 | 1767 | 4 | 0 | 2 | 1 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0017 | 0/0 | 1767 | 4 | 1 | 1 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0018 | 0/0 | 1767 | 4 | 0 | 0 | 4 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0019 | 0/0 | 1767 | 3 | 0 | 3 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0020 | 0/0 | 1767 | 3 | 0 | 1 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0021 | 0/0 | 1767 | 2 | 1 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0022 | 0/0 | 1767 | 2 | 1 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0023 | 0/0 | 1767 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0024 | 0/0 | 1767 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0025 | 0/0 | 1767 | 2 | 0 | 1 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0026 | 0/0 | 1767 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0027 | 0/0 | 1767 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0028 | 0/0 | 1767 | 2 | 0 | 0 | 1 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0029 | 0/0 | 1767 | 2 | 1 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0030 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0031 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0032 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0033 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0034 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0035 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
c0036 | 0/0 | 1767 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
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 | 542 | 212 | 41 | 28 | 112 | 5 | 26 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
t0002 | 0/0 | 542 | 88 | 34 | 18 | 23 | 7 | 6 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
t0003 | 0/0 | 542 | 51 | 2 | 12 | 26 | 3 | 8 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
t0004 | 0/0 | 542 | 28 | 0 | 8 | 17 | 1 | 2 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
t0005 | 0/0 | 542 | 4 | 4 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
t0006 | 0/0 | 542 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
t0007 | 0/0 | 542 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
t0008 | 0/0 | 542 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
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 | 5 | 0 | 0 | 5 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0005 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
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 | 1767 | 109 | 25 | 23 | 48 | 3 | 10 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0004 | 0/0 | 1767 | 30 | 4 | 4 | 13 | 4 | 5 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0007 | 0/0 | 1767 | 17 | 5 | 1 | 6 | 0 | 5 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0028 | 0/0 | 1767 | 2 | 0 | 0 | 1 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0002c0002 | 0/0 | 1767 | 37 | 5 | 2 | 26 | 0 | 4 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0002c0008 | 0/0 | 1767 | 17 | 0 | 1 | 14 | 0 | 2 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0002c0009 | 0/0 | 1767 | 17 | 0 | 1 | 12 | 1 | 3 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0002c0020 | 0/0 | 1767 | 3 | 0 | 1 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0003c0003 | 0/0 | 1767 | 31 | 22 | 3 | 4 | 1 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0003c0010 | 0/0 | 1767 | 14 | 10 | 0 | 4 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0003c0015 | 0/0 | 1767 | 4 | 4 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0003c0023 | 0/0 | 1767 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0004c0005 | 0/0 | 1767 | 25 | 1 | 11 | 8 | 1 | 4 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0004c0012 | 0/0 | 1767 | 7 | 0 | 0 | 7 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0005c0006 | 0/0 | 1767 | 18 | 0 | 4 | 12 | 2 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0005c0014 | 0/0 | 1767 | 5 | 0 | 0 | 4 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0005c0019 | 0/0 | 1767 | 3 | 0 | 3 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0005c0024 | 0/0 | 1767 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0005c0025 | 0/0 | 1767 | 2 | 0 | 1 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0006c0011 | 0/0 | 1767 | 8 | 0 | 2 | 4 | 1 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0006c0016 | 0/0 | 1767 | 4 | 0 | 2 | 1 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0007c0017 | 0/0 | 1767 | 4 | 1 | 1 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0007c0018 | 0/0 | 1767 | 4 | 0 | 0 | 4 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0008c0013 | 0/0 | 1767 | 6 | 0 | 2 | 0 | 2 | 2 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0009c0022 | 0/0 | 1767 | 2 | 1 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0009c0031 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0010c0021 | 0/0 | 1767 | 2 | 1 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0011c0029 | 0/0 | 1767 | 2 | 1 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0012c0027 | 0/0 | 1767 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0013c0026 | 0/0 | 1767 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0014c0033 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0015c0032 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0016c0030 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0017c0036 | 0/0 | 1767 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0018c0035 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0019c0034 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2308 | 55 | 20 | 10 | 18 | 2 | 5 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0001t0003 | 0/0 | 2308 | 28 | 1 | 7 | 16 | 1 | 3 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0001t0004 | 0/0 | 2308 | 22 | 0 | 6 | 14 | 0 | 2 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0001t0005 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0001t0006 | 0/0 | 2308 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0001t0007 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0004t0001 | 0/0 | 2308 | 14 | 2 | 1 | 7 | 1 | 3 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0004t0003 | 0/0 | 2308 | 12 | 0 | 2 | 6 | 2 | 2 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0004t0004 | 0/0 | 2308 | 2 | 0 | 1 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0004t0005 | 0/0 | 2308 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0007t0001 | 0/0 | 2308 | 14 | 4 | 1 | 6 | 0 | 3 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0007t0003 | 0/0 | 2308 | 2 | 0 | 0 | 0 | 0 | 2 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0007t0007 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0028t0001 | 0/0 | 2308 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0001c0028t0003 | 0/0 | 2308 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0002c0002t0001 | 0/0 | 2308 | 37 | 5 | 2 | 26 | 0 | 4 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0002c0008t0001 | 0/0 | 2308 | 17 | 0 | 1 | 14 | 0 | 2 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0002c0009t0001 | 0/0 | 2308 | 17 | 0 | 1 | 12 | 1 | 3 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0002c0020t0001 | 0/0 | 2308 | 3 | 0 | 1 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0003c0003t0001 | 0/0 | 2308 | 7 | 2 | 0 | 4 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0003c0003t0002 | 0/0 | 2308 | 23 | 19 | 3 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0003c0003t0008 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0003c0010t0001 | 0/0 | 2308 | 5 | 1 | 0 | 4 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0003c0010t0002 | 0/0 | 2308 | 9 | 9 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0003c0015t0001 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0003c0015t0002 | 0/0 | 2308 | 3 | 3 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0003c0023t0001 | 0/0 | 2308 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0004c0005t0001 | 0/0 | 2308 | 17 | 0 | 9 | 3 | 1 | 4 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0004c0005t0003 | 0/0 | 2308 | 7 | 1 | 2 | 4 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0004c0005t0004 | 0/0 | 2308 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0004c0012t0001 | 0/0 | 2308 | 5 | 0 | 0 | 5 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0004c0012t0004 | 0/0 | 2308 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0005c0006t0002 | 0/0 | 2308 | 18 | 0 | 4 | 12 | 2 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0005c0014t0002 | 0/0 | 2308 | 5 | 0 | 0 | 4 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0005c0019t0002 | 0/0 | 2308 | 3 | 0 | 3 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0005c0024t0002 | 0/0 | 2308 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0005c0025t0002 | 0/0 | 2308 | 2 | 0 | 1 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0006c0011t0002 | 0/0 | 2308 | 8 | 0 | 2 | 4 | 1 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0006c0016t0002 | 0/0 | 2308 | 4 | 0 | 2 | 1 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0007c0017t0001 | 0/0 | 2308 | 4 | 1 | 1 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0007c0018t0001 | 0/0 | 2308 | 4 | 0 | 0 | 4 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0008c0013t0002 | 0/0 | 2308 | 6 | 0 | 2 | 0 | 2 | 2 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0009c0022t0002 | 0/0 | 2308 | 2 | 1 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0009c0031t0001 | 0/0 | 2308 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0010c0021t0002 | 0/0 | 2308 | 2 | 1 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0011c0029t0001 | 0/0 | 2308 | 2 | 1 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0012c0027t0001 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0012c0027t0005 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0013c0026t0003 | 0/0 | 2308 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0013c0026t0004 | 0/0 | 2308 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0014c0033t0002 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0015c0032t0001 | 0/0 | 2308 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0016c0030t0001 | 0/0 | 2308 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0017c0036t0001 | 0/0 | 2308 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0018c0035t0001 | 0/0 | 2308 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
a0019c0034t0001 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | copy fasta | chr7 | 37843597 | 37905397 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0005 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0028t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0028t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0020t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0020t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0020t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0008g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0015t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0015t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0015t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0015t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0023t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0023t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0012t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0012t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0012t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0012t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0012t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0014t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0014t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0014t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0014t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0014t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0019t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0019t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0019t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0024t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0024t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0025t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0025t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0011t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0011t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0011t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0011t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0011t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0011t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0011t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0011t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0016t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0016t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0016t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0016t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0007c0017t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0007c0017t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0007c0017t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0007c0017t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0007c0018t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0007c0018t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0007c0018t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0007c0018t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0008c0013t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0008c0013t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0008c0013t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0008c0013t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0009c0022t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0009c0022t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0009c0031t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0010c0021t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0010c0021t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0011c0029t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0012c0027t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0012c0027t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0013c0026t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0013c0026t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0014c0033t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0015c0032t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0016c0030t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0017c0036t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0018c0035t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0019c0034t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0005 | c0006 | t0002 | g0286 | EUR | GBR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00099 | hp2 | a0004 | c0005 | t0001 | g0178 | EUR | GBR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00140 | hp1 | a0005 | c0006 | t0002 | g0275 | EUR | GBR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00280 | hp1 | a0002 | c0009 | t0001 | g0186 | EUR | FIN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00280 | hp2 | a0001 | c0004 | t0004 | g0259 | EUR | FIN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00323 | hp1 | a0001 | c0004 | t0003 | g0096 | EUR | FIN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | FIN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00423 | hp1 | a0001 | c0004 | t0003 | g0100 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00423 | hp2 | a0004 | c0012 | t0004 | g0241 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00544 | hp1 | a0007 | c0018 | t0001 | g0204 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00558 | hp1 | a0001 | c0004 | t0003 | g0050 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00558 | hp2 | a0005 | c0014 | t0002 | g0295 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00597 | hp1 | a0005 | c0006 | t0002 | g0293 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00609 | hp2 | a0001 | c0007 | t0001 | g0067 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00621 | hp1 | a0005 | c0024 | t0002 | g0297 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0260 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00639 | hp2 | a0013 | c0026 | t0004 | g0251 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00673 | hp1 | a0015 | c0032 | t0001 | g0131 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00673 | hp2 | a0001 | c0004 | t0001 | g0080 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00733 | hp2 | a0003 | c0003 | t0002 | g0329 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0213 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00735 | hp2 | a0001 | c0004 | t0003 | g0095 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00738 | hp1 | a0003 | c0003 | t0002 | g0025 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00738 | hp2 | a0006 | c0011 | t0002 | g0310 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00741 | hp2 | a0008 | c0013 | t0002 | g0023 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01069 | hp2 | a0005 | c0006 | t0002 | g0349 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0254 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0121 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01071 | hp1 | a0005 | c0006 | t0002 | g0350 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01074 | hp1 | a0001 | c0007 | t0001 | g0061 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01074 | hp2 | a0013 | c0026 | t0003 | g0075 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01081 | hp1 | a0006 | c0011 | t0002 | g0301 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01106 | hp1 | a0004 | c0005 | t0001 | g0008 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01109 | hp1 | a0002 | c0020 | t0001 | g0196 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01169 | hp2 | a0004 | c0005 | t0001 | g0008 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01175 | hp1 | a0005 | c0006 | t0002 | g0309 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01192 | hp1 | a0004 | c0005 | t0001 | g0059 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01192 | hp2 | a0005 | c0019 | t0002 | g0305 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01243 | hp1 | a0004 | c0005 | t0001 | g0168 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0235 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01256 | hp1 | a0005 | c0006 | t0002 | g0348 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01256 | hp2 | a0001 | c0004 | t0003 | g0082 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01261 | hp1 | a0002 | c0009 | t0001 | g0231 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01261 | hp2 | a0007 | c0017 | t0001 | g0197 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01358 | hp1 | a0011 | c0029 | t0001 | g0017 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01358 | hp2 | a0005 | c0025 | t0002 | g0312 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01433 | hp1 | a0010 | c0021 | t0002 | g0347 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01496 | hp1 | a0003 | c0003 | t0002 | g0025 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01496 | hp2 | a0004 | c0005 | t0003 | g0030 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01515 | hp1 | a0008 | c0013 | t0002 | g0022 | EUR | IBS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01515 | hp2 | a0001 | c0004 | t0003 | g0108 | EUR | IBS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01517 | hp1 | a0005 | c0025 | t0002 | g0308 | EUR | IBS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01517 | hp2 | a0008 | c0013 | t0002 | g0022 | EUR | IBS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01884 | hp1 | a0003 | c0003 | t0002 | g0342 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01884 | hp2 | a0010 | c0021 | t0002 | g0346 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01928 | hp1 | a0005 | c0019 | t0002 | g0304 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01928 | hp2 | a0001 | c0004 | t0001 | g0091 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01934 | hp2 | a0004 | c0005 | t0001 | g0071 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01943 | hp1 | a0006 | c0016 | t0002 | g0282 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01943 | hp2 | a0004 | c0005 | t0001 | g0041 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01975 | hp1 | a0004 | c0005 | t0001 | g0102 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0177 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01981 | hp1 | a0008 | c0013 | t0002 | g0023 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02040 | hp1 | a0002 | c0009 | t0001 | g0215 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02055 | hp1 | a0003 | c0003 | t0002 | g0343 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02056 | hp1 | a0001 | c0004 | t0001 | g0092 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0243 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02071 | hp1 | a0002 | c0008 | t0001 | g0272 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02080 | hp2 | a0005 | c0006 | t0002 | g0284 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02083 | hp2 | a0004 | c0012 | t0004 | g0252 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02135 | hp1 | a0002 | c0009 | t0001 | g0194 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02135 | hp2 | a0005 | c0006 | t0002 | g0287 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0151 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02148 | hp1 | a0004 | c0005 | t0001 | g0042 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02155 | hp1 | a0002 | c0008 | t0001 | g0273 | EAS | CDX | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | CDX | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02165 | hp1 | a0002 | c0008 | t0001 | g0179 | EAS | CDX | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02165 | hp2 | a0003 | c0010 | t0001 | g0129 | EAS | CDX | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02258 | hp2 | a0003 | c0010 | t0002 | g0317 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02273 | hp1 | a0004 | c0005 | t0001 | g0043 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02273 | hp2 | a0005 | c0019 | t0002 | g0276 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02280 | hp1 | a0003 | c0010 | t0001 | g0247 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0140 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02293 | hp1 | a0006 | c0016 | t0002 | g0307 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02293 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02300 | hp1 | a0004 | c0005 | t0003 | g0099 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02300 | hp2 | a0002 | c0008 | t0001 | g0233 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02451 | hp1 | a0003 | c0003 | t0002 | g0336 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02451 | hp2 | a0003 | c0003 | t0002 | g0316 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02523 | hp1 | a0003 | c0010 | t0001 | g0122 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02523 | hp2 | a0003 | c0003 | t0001 | g0128 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02572 | hp1 | a0001 | c0004 | t0001 | g0119 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02615 | hp1 | a0012 | c0027 | t0001 | g0146 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02615 | hp2 | a0001 | c0007 | t0001 | g0191 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02622 | hp1 | a0014 | c0033 | t0002 | g0318 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02622 | hp2 | a0001 | c0004 | t0001 | g0148 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0238 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02647 | hp2 | a0004 | c0005 | t0003 | g0090 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02683 | hp1 | a0003 | c0003 | t0001 | g0127 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02683 | hp2 | a0001 | c0004 | t0003 | g0084 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02717 | hp1 | a0003 | c0003 | t0001 | g0250 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02717 | hp2 | a0001 | c0007 | t0007 | g0078 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02723 | hp1 | a0003 | c0010 | t0002 | g0321 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02723 | hp2 | a0003 | c0023 | t0001 | g0246 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02735 | hp1 | a0017 | c0036 | t0001 | g0218 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0264 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0180 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02809 | hp1 | a0003 | c0010 | t0002 | g0335 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02809 | hp2 | a0003 | c0003 | t0002 | g0324 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02818 | hp1 | a0003 | c0003 | t0002 | g0341 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02818 | hp2 | a0009 | c0022 | t0002 | g0274 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02886 | hp1 | a0003 | c0003 | t0002 | g0345 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02886 | hp2 | a0001 | c0004 | t0005 | g0270 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02895 | hp1 | a0012 | c0027 | t0005 | g0271 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02895 | hp2 | a0003 | c0010 | t0002 | g0333 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02896 | hp1 | a0003 | c0003 | t0002 | g0322 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02896 | hp2 | a0003 | c0003 | t0002 | g0026 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02897 | hp1 | a0003 | c0003 | t0002 | g0026 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02897 | hp2 | a0003 | c0010 | t0002 | g0334 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02965 | hp1 | a0003 | c0003 | t0002 | g0325 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02970 | hp1 | a0003 | c0003 | t0002 | g0340 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02970 | hp2 | a0003 | c0010 | t0002 | g0332 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02976 | hp1 | a0003 | c0015 | t0002 | g0352 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02976 | hp2 | a0001 | c0007 | t0001 | g0187 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03017 | hp1 | a0002 | c0009 | t0001 | g0135 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0269 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03041 | hp2 | a0003 | c0015 | t0001 | g0249 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03130 | hp2 | a0003 | c0010 | t0002 | g0328 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03195 | hp1 | a0001 | c0007 | t0001 | g0190 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03195 | hp2 | a0003 | c0003 | t0002 | g0339 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03209 | hp1 | a0019 | c0034 | t0001 | g0112 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03225 | hp2 | a0003 | c0003 | t0002 | g0326 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03239 | hp1 | a0005 | c0014 | t0002 | g0303 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0265 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03453 | hp1 | a0003 | c0003 | t0001 | g0248 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03453 | hp2 | a0003 | c0003 | t0002 | g0280 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03486 | hp1 | a0001 | c0004 | t0005 | g0268 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03486 | hp2 | a0003 | c0023 | t0001 | g0245 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03490 | hp1 | a0004 | c0005 | t0001 | g0010 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03490 | hp2 | a0008 | c0013 | t0002 | g0313 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03491 | hp1 | a0001 | c0007 | t0001 | g0013 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03491 | hp2 | a0001 | c0004 | t0003 | g0103 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03492 | hp1 | a0001 | c0007 | t0001 | g0013 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03492 | hp2 | a0004 | c0005 | t0001 | g0010 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03654 | hp1 | a0006 | c0016 | t0002 | g0306 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03654 | hp2 | a0001 | c0007 | t0003 | g0097 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03669 | hp1 | a0001 | c0004 | t0001 | g0152 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03688 | hp1 | a0006 | c0011 | t0002 | g0283 | SAS | STU | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | STU | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03710 | hp1 | a0001 | c0004 | t0001 | g0170 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03710 | hp2 | a0001 | c0004 | t0001 | g0105 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03831 | hp1 | a0001 | c0007 | t0001 | g0033 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03831 | hp2 | a0002 | c0009 | t0001 | g0195 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03834 | hp1 | a0004 | c0005 | t0001 | g0155 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03834 | hp2 | a0002 | c0008 | t0001 | g0047 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03927 | hp2 | a0009 | c0022 | t0002 | g0331 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0134 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03942 | hp2 | a0001 | c0028 | t0003 | g0101 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG04115 | hp1 | a0008 | c0013 | t0002 | g0314 | SAS | STU | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG04115 | hp2 | a0002 | c0008 | t0001 | g0214 | SAS | STU | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG04184 | hp1 | a0001 | c0007 | t0003 | g0106 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG04199 | hp1 | a0002 | c0009 | t0001 | g0225 | SAS | STU | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0185 | SAS | STU | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0094 | SAS | STU | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG04204 | hp2 | a0004 | c0005 | t0001 | g0169 | SAS | STU | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | YRI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18522 | hp2 | a0003 | c0003 | t0008 | g0320 | AFR | YRI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18612 | hp1 | a0001 | c0007 | t0001 | g0160 | EAS | CHB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18612 | hp2 | a0002 | c0009 | t0001 | g0203 | EAS | CHB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18747 | hp1 | a0002 | c0008 | t0001 | g0018 | EAS | CHB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18747 | hp2 | a0002 | c0008 | t0001 | g0237 | EAS | CHB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18906 | hp2 | a0003 | c0003 | t0002 | g0337 | AFR | YRI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18940 | hp1 | a0003 | c0003 | t0001 | g0123 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18942 | hp2 | a0007 | c0017 | t0001 | g0137 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18944 | hp1 | a0005 | c0006 | t0002 | g0279 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18944 | hp2 | a0004 | c0005 | t0003 | g0009 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18945 | hp1 | a0007 | c0018 | t0001 | g0192 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18945 | hp2 | a0005 | c0006 | t0002 | g0288 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18947 | hp1 | a0007 | c0018 | t0001 | g0036 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18949 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18949 | hp2 | a0005 | c0006 | t0002 | g0289 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18950 | hp2 | a0001 | c0004 | t0003 | g0049 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18951 | hp1 | a0004 | c0005 | t0001 | g0037 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18951 | hp2 | a0002 | c0020 | t0001 | g0201 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18952 | hp1 | a0003 | c0003 | t0001 | g0126 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18952 | hp2 | a0005 | c0006 | t0002 | g0292 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18953 | hp1 | a0006 | c0016 | t0002 | g0296 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18953 | hp2 | a0002 | c0008 | t0001 | g0045 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18954 | hp1 | a0002 | c0009 | t0001 | g0001 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18954 | hp2 | a0003 | c0010 | t0001 | g0124 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18956 | hp1 | a0002 | c0008 | t0001 | g0210 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18957 | hp2 | a0001 | c0004 | t0003 | g0069 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18960 | hp1 | a0003 | c0010 | t0001 | g0130 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18960 | hp2 | a0001 | c0004 | t0001 | g0110 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18963 | hp2 | a0004 | c0005 | t0004 | g0261 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18966 | hp2 | a0005 | c0024 | t0002 | g0277 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18969 | hp1 | a0007 | c0018 | t0001 | g0193 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18969 | hp2 | a0002 | c0009 | t0001 | g0001 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18970 | hp1 | a0018 | c0035 | t0001 | g0182 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18970 | hp2 | a0004 | c0012 | t0001 | g0004 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18971 | hp2 | a0002 | c0008 | t0001 | g0209 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18973 | hp1 | a0016 | c0030 | t0001 | g0133 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18974 | hp1 | a0001 | c0004 | t0001 | g0165 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18975 | hp2 | a0005 | c0014 | t0002 | g0281 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18977 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18977 | hp2 | a0004 | c0005 | t0001 | g0083 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18978 | hp2 | a0001 | c0004 | t0001 | g0226 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18980 | hp2 | a0003 | c0003 | t0001 | g0132 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18983 | hp2 | a0002 | c0008 | t0001 | g0007 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18984 | hp1 | a0002 | c0008 | t0001 | g0018 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18984 | hp2 | a0006 | c0011 | t0002 | g0298 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18985 | hp2 | a0005 | c0006 | t0002 | g0024 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18986 | hp2 | a0002 | c0008 | t0001 | g0239 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18988 | hp1 | a0005 | c0014 | t0002 | g0290 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18988 | hp2 | a0002 | c0009 | t0001 | g0001 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18990 | hp1 | a0005 | c0014 | t0002 | g0294 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18990 | hp2 | a0004 | c0005 | t0001 | g0098 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18991 | hp1 | a0006 | c0011 | t0002 | g0302 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18991 | hp2 | a0004 | c0012 | t0001 | g0004 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18994 | hp1 | a0009 | c0031 | t0001 | g0125 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18994 | hp2 | a0002 | c0008 | t0001 | g0211 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18998 | hp1 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19001 | hp1 | a0002 | c0008 | t0001 | g0115 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19001 | hp2 | a0001 | c0007 | t0001 | g0039 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19004 | hp2 | a0002 | c0009 | t0001 | g0001 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19005 | hp2 | a0001 | c0007 | t0001 | g0171 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19010 | hp1 | a0004 | c0005 | t0003 | g0009 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19010 | hp2 | a0002 | c0009 | t0001 | g0001 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0136 | AFR | LWK | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19030 | hp2 | a0003 | c0010 | t0002 | g0327 | AFR | LWK | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19054 | hp2 | a0006 | c0011 | t0002 | g0299 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19056 | hp2 | a0005 | c0006 | t0002 | g0291 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19057 | hp1 | a0001 | c0004 | t0001 | g0118 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19058 | hp1 | a0004 | c0012 | t0001 | g0004 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19060 | hp1 | a0005 | c0006 | t0002 | g0024 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19065 | hp1 | a0007 | c0017 | t0001 | g0229 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19065 | hp2 | a0001 | c0028 | t0001 | g0038 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19068 | hp1 | a0001 | c0004 | t0003 | g0089 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19070 | hp1 | a0001 | c0007 | t0001 | g0120 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19070 | hp2 | a0002 | c0008 | t0001 | g0007 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19072 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19072 | hp2 | a0002 | c0020 | t0001 | g0202 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19076 | hp1 | a0004 | c0005 | t0003 | g0104 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19076 | hp2 | a0002 | c0009 | t0001 | g0244 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19078 | hp1 | a0004 | c0012 | t0001 | g0066 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19079 | hp1 | a0001 | c0004 | t0003 | g0117 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19080 | hp1 | a0006 | c0011 | t0002 | g0278 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19081 | hp1 | a0001 | c0004 | t0001 | g0223 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19082 | hp1 | a0004 | c0012 | t0001 | g0065 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19082 | hp2 | a0005 | c0006 | t0002 | g0311 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19084 | hp1 | a0002 | c0009 | t0001 | g0230 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19084 | hp2 | a0005 | c0006 | t0002 | g0285 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19085 | hp2 | a0002 | c0009 | t0001 | g0216 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19088 | hp2 | a0001 | c0007 | t0001 | g0068 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19091 | hp1 | a0002 | c0009 | t0001 | g0234 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19240 | hp1 | a0011 | c0029 | t0001 | g0017 | AFR | YRI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0005 | EUR | TSI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA20752 | hp2 | a0003 | c0003 | t0002 | g0330 | EUR | TSI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA20805 | hp1 | a0006 | c0011 | t0002 | g0300 | EUR | TSI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA20805 | hp2 | a0001 | c0004 | t0001 | g0157 | EUR | TSI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0220 | SAS | GIH | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0081 | SAS | GIH | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01123 | hp2 | a0001 | c0004 | t0004 | g0267 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02109 | hp2 | a0003 | c0003 | t0002 | g0338 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02486 | hp1 | a0003 | c0003 | t0002 | g0315 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02559 | hp1 | a0003 | c0010 | t0002 | g0319 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03471 | hp1 | a0001 | c0007 | t0001 | g0188 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03471 | hp2 | a0003 | c0015 | t0002 | g0351 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG06807 | hp1 | a0003 | c0015 | t0002 | g0323 | AFR | USA | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18955 | hp1 | a0004 | c0005 | t0003 | g0088 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA20300 | hp1 | a0007 | c0017 | t0001 | g0232 | AFR | USA | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | USA | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA21309 | hp1 | a0003 | c0003 | t0002 | g0344 | AFR | LWK | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:37850665
|
G | A | 9 | a0003a0005a0006others(6): Show | 107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
missense_variant | MODERATE | c.128G>A | p.Arg43Lys | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/18 | 500/2308 | 128/1767 | 43/588 | chr7 | 37850665 | ||
chr7:37863462
|
C | T | 1 | a0017 | 1 | HG02735.hp1 | stop_gained&splice_region_variant | HIGH | c.454C>T | p.Gln152* | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/18 | 826/2308 | 454/1767 | 152/588 | chr7 | 37863462 | ||
chr7:37865528
|
A | G | 1 | a0014 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.532A>G | p.Thr178Ala | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/18 | 904/2308 | 532/1767 | 178/588 | chr7 | 37865528 | ||
chr7:37867702
|
T | C | 11 | a0001a0003a0004others(8): Show | 254 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(251): Show |
missense_variant&splice_region_variant | MODERATE | c.622T>C | p.Cys208Arg | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/18 | 994/2308 | 622/1767 | 208/588 | chr7 | 37867702 | ||
chr7:37867730
|
T | C | 1 | a0016 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.650T>C | p.Met217Thr | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/18 | 1022/2308 | 650/1767 | 217/588 | chr7 | 37867730 | ||
chr7:37867819
|
G | A | 1 | a0010 | 2 | HG01433.hp1 HG01884.hp2 |
missense_variant | MODERATE | c.739G>A | p.Glu247Lys | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/18 | 1111/2308 | 739/1767 | 247/588 | chr7 | 37867819 | ||
chr7:37867873
|
G | T | 1 | a0016 | 1 | NA18973.hp1 | stop_gained | HIGH | c.793G>T | p.Gly265* | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/18 | 1165/2308 | 793/1767 | 265/588 | chr7 | 37867873 | ||
chr7:37884315
|
G | A | 2 | a0011a0012 | 4 | HG01358.hp1 HG02615.hp1 HG02895.hp1 others(1): Show |
missense_variant | MODERATE | c.1007G>A | p.Arg336His | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 13/18 | 1379/2308 | 1007/1767 | 336/588 | chr7 | 37884315 | ||
chr7:37884321
|
T | C | 2 | a0008a0013 | 8 | HG00639.hp2 HG00741.hp2 HG01074.hp2 others(5): Show |
missense_variant | MODERATE | c.1013T>C | p.Ile338Thr | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 13/18 | 1385/2308 | 1013/1767 | 338/588 | chr7 | 37884321 | ||
chr7:37894471
|
A | C | 1 | a0019 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.1405A>C | p.Ile469Leu | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/18 | 1777/2308 | 1405/1767 | 469/588 | chr7 | 37894471 | ||
chr7:37894544
|
T | C | 4 | a0004a0006a0007others(1): Show | 55 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(52): Show |
missense_variant | MODERATE | c.1478T>C | p.Ile493Thr | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/18 | 1850/2308 | 1478/1767 | 493/588 | chr7 | 37894544 | ||
chr7:37896962
|
T | A | 1 | a0015 | 1 | HG00673.hp1 | stop_gained | HIGH | c.1637T>A | p.Leu546* | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/18 | 2009/2308 | 1637/1767 | 546/588 | chr7 | 37896962 | ||
chr7:37897079
|
C | T | 1 | a0018 | 1 | NA18970.hp1 | missense_variant | MODERATE | c.1754C>T | p.Pro585Leu | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/18 | 2126/2308 | 1754/1767 | 585/588 | chr7 | 37897079 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:37850714
|
C | T | 18 | a0003c0003a0003c0010a0003c0015others(15): Show | 107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
synonymous_variant | LOW | c.177C>T | p.Asp59Asp | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/18 | 549/2308 | 177/1767 | 59/588 | chr7 | 37850714 | ||
chr7:37857294
|
G | A | 5 | a0005c0006a0005c0014a0005c0019others(2): Show | 40 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(37): Show |
synonymous_variant | LOW | c.219G>A | p.Val73Val | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/18 | 591/2308 | 219/1767 | 73/588 | chr7 | 37857294 | ||
chr7:37876853
|
A | G | 13 | a0001c0007a0001c0028a0002c0009others(10): Show | 74 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
synonymous_variant | LOW | c.840A>G | p.Arg280Arg | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/18 | 1212/2308 | 840/1767 | 280/588 | chr7 | 37876853 | ||
chr7:37894545
|
A | T | 8 | a0004c0005a0004c0012a0006c0011others(5): Show | 55 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(52): Show |
synonymous_variant | LOW | c.1479A>T | p.Ile493Ile | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/18 | 1851/2308 | 1479/1767 | 493/588 | chr7 | 37894545 | ||
chr7:37896928
|
T | C | 9 | a0001c0004a0001c0028a0002c0008others(6): Show | 67 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(64): Show |
synonymous_variant | LOW | c.1603T>C | p.Leu535Leu | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/18 | 1975/2308 | 1603/1767 | 535/588 | chr7 | 37896928 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:37848880
|
G | A | 3 | a0001c0001t0005a0001c0004t0005a0012c0027t0005 | 4 | HG02886.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-184G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/18 | 1387 | chr7 | 37848880 | |||||
chr7:37848884
|
G | A | 1 | a0001c0001t0006 | 2 | HG02145.hp1 HG03130.hp1 |
5_prime_UTR_variant | MODIFIER | c.-180G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/18 | 1383 | chr7 | 37848884 | |||||
chr7:37848886
|
G | T | 15 | a0003c0003t0002a0003c0003t0008a0003c0010t0002others(12): Show | 89 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(86): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-178G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/18 | chr7 | 37848886 | ||||||
chr7:37848972
|
C | T | 8 | a0001c0001t0004a0001c0001t0005a0001c0004t0004others(5): Show | 32 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(29): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-92C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/18 | chr7 | 37848972 | ||||||
chr7:37849025
|
C | T | 6 | a0001c0001t0003a0001c0004t0003a0001c0007t0003others(3): Show | 51 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(48): Show |
5_prime_UTR_variant | MODIFIER | c.-39C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/18 | 1242 | chr7 | 37849025 | |||||
chr7:37900382
|
A | G | 3 | a0001c0001t0007a0001c0007t0007a0003c0003t0008 | 3 | HG02280.hp2 HG02717.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*154A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 18/18 | 3290 | chr7 | 37900382 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:37848752
|
G | A | 101 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0035others(98): Show | 109 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-241+24G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 1/17 | chr7 | 37848752 | ||||||
chr7:37848758
|
G | A | 12 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(9): Show | 12 | HG00673.hp1 HG02165.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.-241+30G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 1/17 | chr7 | 37848758 | ||||||
chr7:37849181
|
T | C | 2 | a0002c0002t0001g0134a0002c0009t0001g0135 | 2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-8+125T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849181 | ||||||
chr7:37849205
|
A | G | 84 | a0003c0003t0002g0025a0003c0003t0002g0026a0003c0003t0002g0280others(81): Show | 89 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-8+149A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849205 | ||||||
chr7:37849215
|
G | A | 1 | a0002c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-8+159G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849215 | ||||||
chr7:37849232
|
A | C | 2 | a0003c0003t0002g0026a0003c0015t0002g0352 | 3 | HG02896.hp2 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-8+176A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849232 | ||||||
chr7:37849252
|
G | T | 1 | a0003c0015t0002g0351 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-8+196G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849252 | ||||||
chr7:37849318
|
T | A | 84 | a0003c0003t0002g0025a0003c0003t0002g0026a0003c0003t0002g0280others(81): Show | 89 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-8+262T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849318 | ||||||
chr7:37849410
|
C | T | 2 | a0002c0008t0001g0272a0002c0008t0001g0273 | 2 | HG02071.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-8+354C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849410 | ||||||
chr7:37849482
|
A | G | 3 | a0005c0006t0002g0348a0005c0006t0002g0349a0005c0006t0002g0350 | 3 | HG01069.hp2 HG01071.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-8+426A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849482 | ||||||
chr7:37849652
|
C | T | 96 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(93): Show | 101 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.-8+596C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849652 | ||||||
chr7:37849786
|
G | A | 1 | a0007c0017t0001g0137 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-7-474G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849786 | ||||||
chr7:37849833
|
T | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(10): Show | 16 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-7-427T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849833 | ||||||
chr7:37849868
|
TC | T | 5 | a0001c0001t0001g0028a0001c0001t0003g0027a0001c0001t0003g0029others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-391delC | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849868 | ||||||
chr7:37849868
|
TCA | T | 127 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(124): Show | 140 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-7-391_-7-390delCA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849868 | ||||||
chr7:37849869
|
CA | C | 61 | a0001c0001t0001g0224a0001c0004t0001g0223a0001c0004t0001g0226others(58): Show | 70 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.-7-370delA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 37849869 | |||||
chr7:37849869
|
CAA | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(20): Show | 26 | HG00423.hp2 HG00741.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-7-371_-7-370delAA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 37849869 | |||||
chr7:37849869
|
CAAA | C | 23 | a0001c0001t0004g0003a0001c0001t0004g0006a0001c0001t0004g0253others(20): Show | 28 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7-372_-7-370delAA others(1): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 37849869 | |||||
chr7:37849880
|
A | AC | 95 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(92): Show | 100 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.-7-380_-7-379insC | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849880 | ||||||
chr7:37849886
|
A | C | 96 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(93): Show | 101 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.-7-374A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849886 | ||||||
chr7:37849994
|
T | C | 2 | a0001c0001t0006g0150a0001c0001t0006g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-7-266T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849994 | ||||||
chr7:37850011
|
A | G | 1 | a0001c0007t0001g0120 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-7-249A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37850011 | ||||||
chr7:37850184
|
A | G | 101 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0035others(98): Show | 109 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-7-76A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37850184 | ||||||
chr7:37850236
|
TTTTC | T | 102 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(99): Show | 107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.-7-16_-7-13delCTTT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 37850236 | |||||
chr7:37850450
|
C | T | 1 | a0002c0002t0001g0240 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.91+15C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 4/17 | chr7 | 37850450 | ||||||
chr7:37850479
|
G | A | 102 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(99): Show | 107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.91+44G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 4/17 | chr7 | 37850479 | ||||||
chr7:37850580
|
A | G | 1 | a0002c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.92-49A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 4/17 | chr7 | 37850580 | ||||||
chr7:37850599
|
T | A | 1 | a0001c0004t0001g0152 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.92-30T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 4/17 | chr7 | 37850599 | ||||||
chr7:37850846
|
AATAG | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0149 | 5 | HG02257.hp2 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+116_198+119del others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 37850846 | |||||
chr7:37850922
|
C | G | 6 | a0003c0003t0001g0248a0003c0003t0001g0250a0003c0010t0001g0247others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+187C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37850922 | ||||||
chr7:37850979
|
A | G | 102 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(99): Show | 107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.198+244A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37850979 | ||||||
chr7:37850987
|
A | G | 102 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(99): Show | 107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.198+252A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37850987 | ||||||
chr7:37851005
|
T | C | 27 | a0001c0001t0004g0003a0001c0001t0004g0006a0001c0001t0004g0177others(24): Show | 32 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.198+270T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851005 | ||||||
chr7:37851263
|
T | C | 84 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(81): Show | 88 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.198+528T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851263 | ||||||
chr7:37851481
|
A | G | 1 | a0016c0030t0001g0133 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.198+746A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851481 | ||||||
chr7:37851483
|
TA | T | 102 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(99): Show | 107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.198+750delA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 37851483 | |||||
chr7:37851492
|
G | A | 102 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(99): Show | 107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.198+757G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851492 | ||||||
chr7:37851508
|
A | G | 102 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(99): Show | 107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.198+773A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851508 | ||||||
chr7:37851513
|
C | CTT | 102 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(99): Show | 107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.198+778_198+779ins others(2): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851513 | ||||||
chr7:37851654
|
A | G | 2 | a0003c0003t0002g0336a0003c0003t0002g0337 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.198+919A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851654 | ||||||
chr7:37851723
|
A | G | 1 | a0002c0008t0001g0239 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.198+988A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851723 | ||||||
chr7:37851755
|
C | A | 1 | a0001c0001t0001g0153 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.198+1020C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851755 | ||||||
chr7:37851835
|
A | G | 6 | a0003c0003t0001g0248a0003c0003t0001g0250a0003c0010t0001g0247others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+1100A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851835 | ||||||
chr7:37851839
|
A | G | 1 | a0001c0004t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.198+1104A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851839 | ||||||
chr7:37851932
|
T | A | 1 | a0004c0005t0003g0030 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.198+1197T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851932 | ||||||
chr7:37851963
|
A | G | 1 | a0001c0004t0001g0118 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.198+1228A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851963 | ||||||
chr7:37852055
|
G | C | 132 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(129): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.198+1320G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852055 | ||||||
chr7:37852109
|
C | CT | 9 | a0001c0001t0001g0176a0001c0004t0003g0117a0002c0002t0001g0238others(6): Show | 9 | HG00323.hp2 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.198+1385dupT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 37852109 | |||||
chr7:37852109
|
CT | C | 56 | a0003c0003t0002g0026a0003c0003t0002g0280a0003c0003t0002g0338others(53): Show | 60 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.198+1385delT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 37852109 | |||||
chr7:37852188
|
A | T | 1 | a0002c0008t0001g0237 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.198+1453A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852188 | ||||||
chr7:37852190
|
G | T | 86 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(83): Show | 90 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.198+1455G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852190 | ||||||
chr7:37852318
|
G | A | 1 | a0005c0006t0002g0275 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.198+1583G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852318 | ||||||
chr7:37852325
|
C | T | 4 | a0003c0010t0002g0332a0003c0010t0002g0333a0003c0010t0002g0334others(1): Show | 4 | HG02809.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1590C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852325 | ||||||
chr7:37852359
|
A | G | 1 | a0008c0013t0002g0314 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.198+1624A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852359 | ||||||
chr7:37852365
|
C | T | 12 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(9): Show | 12 | HG00673.hp1 HG02165.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.198+1630C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852365 | ||||||
chr7:37852415
|
A | C | 6 | a0003c0003t0001g0248a0003c0003t0001g0250a0003c0010t0001g0247others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+1680A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852415 | ||||||
chr7:37852470
|
C | A | 1 | a0005c0019t0002g0276 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.198+1735C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852470 | ||||||
chr7:37852507
|
C | T | 1 | a0002c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.198+1772C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852507 | ||||||
chr7:37852531
|
CACCAATC others(8): Show |
C | 1 | a0001c0001t0001g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.198+1800_198+1814d others(17): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 37852531 | |||||
chr7:37852627
|
A | C | 4 | a0001c0001t0005g0269a0001c0004t0005g0268a0001c0004t0005g0270others(1): Show | 4 | HG02886.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+1892A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852627 | ||||||
chr7:37852640
|
C | T | 96 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(93): Show | 101 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.198+1905C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852640 | ||||||
chr7:37852653
|
A | G | 1 | a0001c0004t0004g0267 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.198+1918A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852653 | ||||||
chr7:37852777
|
G | A | 18 | a0001c0001t0004g0003a0001c0001t0004g0242a0001c0001t0004g0243others(15): Show | 21 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.198+2042G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852777 | ||||||
chr7:37852964
|
G | A | 2 | a0007c0018t0001g0192a0007c0018t0001g0193 | 2 | NA18945.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.198+2229G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852964 | ||||||
chr7:37853217
|
G | A | 64 | a0001c0001t0001g0224a0001c0004t0001g0223a0001c0004t0001g0226others(61): Show | 73 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.198+2482G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853217 | ||||||
chr7:37853276
|
G | C | 86 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(83): Show | 90 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.198+2541G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853276 | ||||||
chr7:37853281
|
T | C | 1 | a0001c0001t0003g0031 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.198+2546T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853281 | ||||||
chr7:37853315
|
G | A | 276 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(273): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.198+2580G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853315 | ||||||
chr7:37853508
|
A | T | 2 | a0010c0021t0002g0346a0010c0021t0002g0347 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.198+2773A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853508 | ||||||
chr7:37853617
|
A | G | 96 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(93): Show | 101 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.198+2882A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853617 | ||||||
chr7:37853673
|
T | A | 27 | a0001c0001t0004g0003a0001c0001t0004g0006a0001c0001t0004g0177others(24): Show | 32 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.198+2938T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853673 | ||||||
chr7:37853730
|
A | G | 1 | a0008c0013t0002g0313 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.198+2995A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853730 | ||||||
chr7:37853876
|
G | T | 261 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(258): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.198+3141G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853876 | ||||||
chr7:37853878
|
G | T | 96 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(93): Show | 101 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.198+3143G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853878 | ||||||
chr7:37853995
|
C | A | 96 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(93): Show | 101 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.198+3260C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853995 | ||||||
chr7:37854098
|
AG | A | 345 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(342): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.199-3175delG | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37854098 | ||||||
chr7:37854138
|
T | C | 2 | a0001c0001t0006g0150a0001c0001t0006g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.199-3136T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37854138 | ||||||
chr7:37854288
|
T | G | 96 | a0003c0003t0001g0123a0003c0003t0001g0126a0003c0003t0001g0127others(93): Show | 101 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.199-2986T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37854288 | ||||||
chr7:37854348
|
C | A | 278 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(275): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.199-2926C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37854348 | ||||||
chr7:37854536
|
C | T | 3 | a0001c0001t0004g0006a0001c0001t0004g0177a0001c0001t0004g0266 | 5 | HG01346.hp1 HG01975.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-2738C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37854536 | ||||||
chr7:37854690
|
G | A | 3 | a0001c0001t0001g0154a0003c0023t0001g0245a0003c0023t0001g0246 | 3 | HG02723.hp2 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.199-2584G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37854690 | ||||||
chr7:37854722
|
C | T | 281 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(278): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.199-2552C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37854722 | ||||||
chr7:37854804
|
A | AC | 169 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(166): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.199-2464dupC | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 37854804 | |||||
chr7:37854896
|
A | G | 169 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(166): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.199-2378A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37854896 | ||||||
chr7:37855089
|
C | T | 1 | a0001c0004t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.199-2185C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855089 | ||||||
chr7:37855303
|
A | G | 1 | a0005c0025t0002g0312 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.199-1971A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855303 | ||||||
chr7:37855311
|
T | C | 4 | a0001c0001t0005g0269a0001c0004t0005g0268a0001c0004t0005g0270others(1): Show | 4 | HG02886.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-1963T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855311 | ||||||
chr7:37855362
|
G | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(10): Show | 16 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.199-1912G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855362 | ||||||
chr7:37855372
|
A | G | 31 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(28): Show | 36 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.199-1902A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855372 | ||||||
chr7:37855443
|
T | C | 1 | a0001c0001t0003g0034 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.199-1831T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855443 | ||||||
chr7:37855455
|
A | G | 1 | a0003c0010t0002g0335 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.199-1819A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855455 | ||||||
chr7:37855499
|
C | T | 282 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(279): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.199-1775C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855499 | ||||||
chr7:37855529
|
G | GT | 282 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(279): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.199-1743dupT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 37855529 | |||||
chr7:37855551
|
T | C | 1 | a0001c0004t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.199-1723T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855551 | ||||||
chr7:37855555
|
A | G | 88 | a0001c0001t0004g0264a0001c0001t0004g0265a0003c0003t0001g0123others(85): Show | 92 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.199-1719A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855555 | ||||||
chr7:37855638
|
C | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0019c0034t0001g0112 | 3 | HG02145.hp2 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.199-1636C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855638 | ||||||
chr7:37855665
|
T | C | 24 | a0001c0001t0004g0003a0001c0001t0004g0242a0001c0001t0004g0243others(21): Show | 27 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.199-1609T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855665 | ||||||
chr7:37855845
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.199-1429T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855845 | ||||||
chr7:37855889
|
C | G | 2 | a0001c0007t0001g0190a0001c0007t0001g0191 | 2 | HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.199-1385C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855889 | ||||||
chr7:37855937
|
TA | T | 12 | a0003c0003t0002g0025a0003c0003t0002g0322a0003c0003t0002g0324others(9): Show | 13 | HG00733.hp2 HG00738.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.199-1326delA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 37855937 | |||||
chr7:37856082
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.199-1192G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856082 | ||||||
chr7:37856092
|
C | T | 2 | a0001c0001t0006g0150a0001c0001t0006g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.199-1182C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856092 | ||||||
chr7:37856128
|
T | C | 2 | a0002c0008t0001g0007a0007c0018t0001g0036 | 3 | NA18947.hp1 NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.199-1146T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856128 | ||||||
chr7:37856243
|
C | T | 88 | a0001c0001t0004g0264a0001c0001t0004g0265a0003c0003t0001g0123others(85): Show | 92 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.199-1031C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856243 | ||||||
chr7:37856407
|
G | A | 137 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(134): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.199-867G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856407 | ||||||
chr7:37856510
|
C | G | 2 | a0001c0001t0001g0111a0001c0004t0001g0110 | 2 | NA18960.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.199-764C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856510 | ||||||
chr7:37856544
|
C | A | 194 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(191): Show | 216 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.199-730C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856544 | ||||||
chr7:37856549
|
C | T | 1 | a0001c0001t0003g0109 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.199-725C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856549 | ||||||
chr7:37856656
|
A | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(191): Show | 216 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.199-618A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856656 | ||||||
chr7:37856688
|
A | C | 1 | a0005c0006t0002g0024 | 2 | NA18985.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.199-586A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856688 | ||||||
chr7:37856841
|
G | C | 70 | a0003c0003t0002g0025a0003c0003t0002g0280a0003c0003t0002g0315others(67): Show | 74 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.199-433G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856841 | ||||||
chr7:37856997
|
A | C | 88 | a0001c0001t0004g0264a0001c0001t0004g0265a0003c0003t0001g0123others(85): Show | 92 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.199-277A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856997 | ||||||
chr7:37857075
|
G | A | 1 | a0019c0034t0001g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-199G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37857075 | ||||||
chr7:37857099
|
G | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(10): Show | 16 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.199-175G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37857099 | ||||||
chr7:37857192
|
C | A | 1 | a0001c0004t0001g0110 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.199-82C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37857192 | ||||||
chr7:37857502
|
G | A | 1 | a0001c0001t0004g0266 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.270+157G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857502 | ||||||
chr7:37857510
|
G | C | 1 | a0002c0009t0001g0194 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.270+165G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857510 | ||||||
chr7:37857581
|
C | T | 88 | a0001c0001t0004g0264a0001c0001t0004g0265a0003c0003t0001g0123others(85): Show | 92 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.270+236C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857581 | ||||||
chr7:37857594
|
T | C | 88 | a0001c0001t0004g0264a0001c0001t0004g0265a0003c0003t0001g0123others(85): Show | 92 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.270+249T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857594 | ||||||
chr7:37857596
|
A | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(191): Show | 216 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.270+251A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857596 | ||||||
chr7:37857607
|
G | A | 70 | a0003c0003t0002g0025a0003c0003t0002g0280a0003c0003t0002g0315others(67): Show | 74 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.270+262G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857607 | ||||||
chr7:37857626
|
T | G | 1 | a0005c0024t0002g0277 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.270+281T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857626 | ||||||
chr7:37857706
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0019c0034t0001g0112 | 3 | HG02145.hp2 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.270+361A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857706 | ||||||
chr7:37857781
|
A | T | 1 | a0001c0001t0001g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.270+436A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857781 | ||||||
chr7:37857850
|
A | C | 1 | a0001c0001t0001g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.270+505A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857850 | ||||||
chr7:37857853
|
C | A | 1 | a0001c0001t0001g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.270+508C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857853 | ||||||
chr7:37857854
|
A | C | 1 | a0001c0001t0001g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.270+509A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857854 | ||||||
chr7:37857920
|
G | A | 16 | a0001c0001t0004g0264a0001c0001t0004g0265a0003c0003t0001g0123others(13): Show | 16 | HG00673.hp1 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.270+575G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857920 | ||||||
chr7:37857988
|
G | C | 23 | a0003c0003t0002g0025a0003c0003t0002g0315a0003c0003t0002g0316others(20): Show | 24 | HG00733.hp2 HG00738.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.270+643G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857988 | ||||||
chr7:37858021
|
A | C | 1 | a0002c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.270+676A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858021 | ||||||
chr7:37858117
|
A | T | 1 | a0005c0006t0002g0311 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.270+772A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858117 | ||||||
chr7:37858260
|
A | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0149 | 5 | HG02257.hp2 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+915A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858260 | ||||||
chr7:37858274
|
T | C | 14 | a0001c0001t0004g0264a0001c0001t0004g0265a0003c0003t0001g0123others(11): Show | 14 | HG00673.hp1 HG02165.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.270+929T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858274 | ||||||
chr7:37858300
|
T | A | 4 | a0001c0007t0001g0039a0001c0007t0001g0120a0001c0028t0001g0038others(1): Show | 4 | NA18951.hp1 NA19001.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+955T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858300 | ||||||
chr7:37858348
|
C | T | 282 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(279): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.270+1003C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858348 | ||||||
chr7:37858362
|
T | A | 1 | a0003c0003t0002g0338 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.270+1017T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858362 | ||||||
chr7:37858400
|
T | A | 1 | a0006c0011t0002g0278 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.270+1055T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858400 | ||||||
chr7:37858430
|
C | T | 18 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0183others(15): Show | 24 | HG00408.hp2 HG00621.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.270+1085C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858430 | ||||||
chr7:37858500
|
G | A | 16 | a0001c0001t0004g0264a0001c0001t0004g0265a0003c0003t0001g0123others(13): Show | 16 | HG00673.hp1 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.270+1155G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858500 | ||||||
chr7:37858650
|
AC | A | 16 | a0001c0001t0004g0264a0001c0001t0004g0265a0003c0003t0001g0123others(13): Show | 16 | HG00673.hp1 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.270+1306delC | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858650 | ||||||
chr7:37858673
|
C | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(10): Show | 16 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.270+1328C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858673 | ||||||
chr7:37858674
|
G | A | 1 | a0002c0008t0001g0179 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.270+1329G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858674 | ||||||
chr7:37858677
|
G | A | 31 | a0001c0001t0004g0003a0001c0001t0004g0006a0001c0001t0004g0177others(28): Show | 36 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+1332G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858677 | ||||||
chr7:37858740
|
G | A | 1 | a0001c0007t0001g0120 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.270+1395G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858740 | ||||||
chr7:37858913
|
A | G | 1 | a0009c0022t0002g0274 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.270+1568A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858913 | ||||||
chr7:37858972
|
C | G | 1 | a0002c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.270+1627C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858972 | ||||||
chr7:37859092
|
G | A | 1 | a0005c0006t0002g0279 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.270+1747G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859092 | ||||||
chr7:37859128
|
G | A | 282 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(279): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.270+1783G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859128 | ||||||
chr7:37859535
|
A | G | 1 | a0002c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.270+2190A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859535 | ||||||
chr7:37859693
|
C | T | 1 | a0001c0004t0001g0226 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.271-2335C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859693 | ||||||
chr7:37859812
|
A | G | 1 | a0002c0009t0001g0234 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.271-2216A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859812 | ||||||
chr7:37859825
|
T | G | 4 | a0002c0002t0001g0021a0002c0002t0001g0235a0002c0002t0001g0236others(1): Show | 5 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-2203T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859825 | ||||||
chr7:37859916
|
G | T | 1 | a0003c0003t0001g0132 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.271-2112G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859916 | ||||||
chr7:37859966
|
C | T | 16 | a0001c0001t0004g0264a0001c0001t0004g0265a0003c0003t0001g0123others(13): Show | 16 | HG00673.hp1 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.271-2062C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859966 | ||||||
chr7:37859992
|
C | T | 4 | a0001c0001t0005g0269a0001c0004t0005g0268a0001c0004t0005g0270others(1): Show | 4 | HG02886.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-2036C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859992 | ||||||
chr7:37860023
|
T | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(21): Show | 28 | HG00741.hp1 HG01884.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.271-2005T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860023 | ||||||
chr7:37860260
|
A | G | 2 | a0005c0006t0002g0309a0006c0011t0002g0310 | 2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.271-1768A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860260 | ||||||
chr7:37860269
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.271-1759G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860269 | ||||||
chr7:37860453
|
T | G | 2 | a0001c0001t0006g0150a0001c0001t0006g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.271-1575T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860453 | ||||||
chr7:37860612
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.271-1416C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860612 | ||||||
chr7:37860649
|
A | G | 72 | a0003c0003t0002g0025a0003c0003t0002g0280a0003c0003t0002g0315others(69): Show | 76 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.271-1379A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860649 | ||||||
chr7:37860788
|
A | G | 1 | a0002c0009t0001g0225 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.271-1240A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860788 | ||||||
chr7:37860889
|
A | G | 10 | a0003c0003t0002g0026a0003c0003t0002g0338a0003c0003t0002g0339others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.271-1139A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860889 | ||||||
chr7:37860981
|
A | C | 1 | a0012c0027t0005g0271 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.271-1047A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860981 | ||||||
chr7:37861040
|
T | A | 137 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(134): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.271-988T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861040 | ||||||
chr7:37861134
|
T | A | 170 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(167): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.271-894T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861134 | ||||||
chr7:37861379
|
G | A | 16 | a0001c0001t0004g0264a0001c0001t0004g0265a0003c0003t0001g0123others(13): Show | 16 | HG00673.hp1 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.271-649G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861379 | ||||||
chr7:37861400
|
G | A | 31 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(28): Show | 36 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.271-628G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861400 | ||||||
chr7:37861586
|
T | G | 258 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(255): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.271-442T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861586 | ||||||
chr7:37861616
|
T | C | 1 | a0002c0009t0001g0195 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.271-412T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861616 | ||||||
chr7:37861783
|
T | C | 31 | a0001c0001t0004g0003a0001c0001t0004g0006a0001c0001t0004g0177others(28): Show | 36 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.271-245T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861783 | ||||||
chr7:37861848
|
A | G | 1 | a0001c0001t0004g0263 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.271-180A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861848 | ||||||
chr7:37861888
|
C | T | 31 | a0001c0001t0004g0003a0001c0001t0004g0006a0001c0001t0004g0177others(28): Show | 36 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.271-140C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861888 | ||||||
chr7:37861899
|
A | G | 1 | a0002c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.271-129A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861899 | ||||||
chr7:37861979
|
G | A | 282 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(279): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.271-49G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861979 | ||||||
chr7:37862014
|
C | T | 6 | a0003c0003t0001g0248a0003c0003t0001g0250a0003c0010t0001g0247others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-14C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37862014 | ||||||
chr7:37862025
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA19006.hp2 | splice_region_variant&intron_variant | LOW | c.271-3T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37862025 | ||||||
chr7:37862348
|
C | T | 1 | a0005c0025t0002g0308 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.387+204C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37862348 | ||||||
chr7:37862430
|
G | A | 106 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0035others(103): Show | 114 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.387+286G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37862430 | ||||||
chr7:37862567
|
A | G | 170 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(167): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.387+423A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37862567 | ||||||
chr7:37862583
|
G | A | 1 | a0013c0026t0004g0251 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.387+439G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37862583 | ||||||
chr7:37862609
|
C | G | 1 | a0001c0004t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.387+465C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37862609 | ||||||
chr7:37862640
|
G | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(10): Show | 16 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.387+496G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37862640 | ||||||
chr7:37862645
|
A | AT | 270 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(267): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.387+511dupT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 37862645 | |||||
chr7:37862645
|
A | T | 14 | a0001c0001t0004g0264a0001c0001t0004g0265a0003c0003t0001g0123others(11): Show | 14 | HG00673.hp1 HG02165.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.387+501A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37862645 | ||||||
chr7:37862887
|
A | G | 218 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(215): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.388-509A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37862887 | ||||||
chr7:37863131
|
A | T | 59 | a0001c0001t0001g0224a0001c0004t0001g0223a0001c0004t0001g0226others(56): Show | 67 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.388-265A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37863131 | ||||||
chr7:37863153
|
G | A | 1 | a0004c0005t0001g0008 | 2 | HG01106.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.388-243G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37863153 | ||||||
chr7:37863181
|
T | C | 3 | a0004c0005t0001g0041a0004c0005t0001g0042a0004c0005t0001g0043 | 3 | HG01943.hp2 HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.388-215T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37863181 | ||||||
chr7:37863218
|
T | G | 9 | a0003c0003t0002g0026a0003c0003t0002g0339a0003c0003t0002g0340others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.388-178T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37863218 | ||||||
chr7:37863257
|
A | G | 1 | a0001c0001t0004g0262 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.388-139A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37863257 | ||||||
chr7:37863316
|
A | T | 1 | a0001c0004t0003g0108 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.388-80A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37863316 | ||||||
chr7:37863340
|
C | T | 14 | a0001c0001t0004g0264a0001c0001t0004g0265a0003c0003t0001g0123others(11): Show | 14 | HG00673.hp1 HG02165.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.388-56C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37863340 | ||||||
chr7:37863393
|
T | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0019c0034t0001g0112 | 3 | HG02145.hp2 HG02559.hp2 HG03209.hp1 |
splice_region_variant&intron_variant | LOW | c.388-3T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37863393 | ||||||
chr7:37863500
|
T | C | 1 | a0004c0005t0003g0009 | 2 | NA18944.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.454+38T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37863500 | ||||||
chr7:37863773
|
T | A | 2 | a0010c0021t0002g0346a0010c0021t0002g0347 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.454+311T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37863773 | ||||||
chr7:37863831
|
C | T | 1 | a0003c0015t0002g0351 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.454+369C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37863831 | ||||||
chr7:37863867
|
T | C | 1 | a0002c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.454+405T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37863867 | ||||||
chr7:37863955
|
G | A | 1 | a0003c0010t0001g0122 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.455-393G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37863955 | ||||||
chr7:37864244
|
T | C | 28 | a0003c0003t0002g0025a0003c0003t0002g0280a0003c0003t0002g0315others(25): Show | 29 | HG00733.hp2 HG00738.hp1 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.455-104T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37864244 | ||||||
chr7:37864251
|
A | T | 121 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(118): Show | 133 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.455-97A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37864251 | ||||||
chr7:37864302
|
C | T | 235 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(232): Show | 257 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.455-46C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37864302 | ||||||
chr7:37864303
|
G | A | 1 | a0002c0002t0001g0180 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.455-45G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37864303 | ||||||
chr7:37864432
|
T | C | 1 | a0007c0017t0001g0197 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.528+11T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864432 | ||||||
chr7:37864463
|
TAAC | T | 121 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(118): Show | 133 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.528+46_528+48delAA others(1): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 37864463 | |||||
chr7:37864464
|
A | T | 1 | a0003c0003t0008g0320 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.528+43A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864464 | ||||||
chr7:37864497
|
G | A | 121 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(118): Show | 133 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.528+76G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864497 | ||||||
chr7:37864615
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.528+194C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864615 | ||||||
chr7:37864659
|
C | T | 1 | a0007c0018t0001g0193 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.528+238C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864659 | ||||||
chr7:37864665
|
C | A | 55 | a0002c0002t0001g0044a0002c0002t0001g0046a0002c0008t0001g0007others(52): Show | 59 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.528+244C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864665 | ||||||
chr7:37864711
|
C | G | 1 | a0002c0002t0001g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.528+290C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864711 | ||||||
chr7:37864718
|
T | C | 2 | a0003c0003t0002g0315a0003c0003t0002g0316 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.528+297T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864718 | ||||||
chr7:37864772
|
G | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(10): Show | 16 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.528+351G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864772 | ||||||
chr7:37864945
|
A | G | 6 | a0003c0003t0001g0248a0003c0003t0001g0250a0003c0010t0001g0247others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.528+524A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864945 | ||||||
chr7:37865016
|
A | T | 55 | a0002c0002t0001g0044a0002c0002t0001g0046a0002c0008t0001g0007others(52): Show | 59 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.529-509A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37865016 | ||||||
chr7:37865079
|
T | C | 1 | a0005c0014t0002g0281 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.529-446T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37865079 | ||||||
chr7:37865082
|
C | G | 1 | a0002c0002t0001g0219 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.529-443C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37865082 | ||||||
chr7:37865094
|
A | G | 1 | a0002c0002t0001g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.529-431A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37865094 | ||||||
chr7:37865291
|
G | A | 1 | a0001c0004t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.529-234G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37865291 | ||||||
chr7:37865374
|
C | A | 4 | a0001c0001t0005g0269a0001c0004t0005g0268a0001c0004t0005g0270others(1): Show | 4 | HG02886.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-151C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37865374 | ||||||
chr7:37865491
|
G | A | 1 | a0009c0022t0002g0274 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.529-34G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37865491 | ||||||
chr7:37865665
|
G | T | 1 | a0001c0001t0001g0015 | 2 | HG00140.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.621+48G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37865665 | ||||||
chr7:37865681
|
A | C | 1 | a0005c0006t0002g0275 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.621+64A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37865681 | ||||||
chr7:37865683
|
T | A | 2 | a0001c0001t0006g0150a0001c0001t0006g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.621+66T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37865683 | ||||||
chr7:37865818
|
G | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(230): Show | 255 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.621+201G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37865818 | ||||||
chr7:37865856
|
G | A | 1 | a0002c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.621+239G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37865856 | ||||||
chr7:37865912
|
A | C | 4 | a0003c0003t0008g0320a0003c0010t0002g0317a0003c0010t0002g0319others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+295A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37865912 | ||||||
chr7:37866025
|
G | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(230): Show | 255 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.621+408G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866025 | ||||||
chr7:37866061
|
C | A | 31 | a0001c0001t0004g0003a0001c0001t0004g0006a0001c0001t0004g0177others(28): Show | 36 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.621+444C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866061 | ||||||
chr7:37866373
|
C | T | 3 | a0003c0003t0002g0025a0003c0003t0002g0330a0009c0022t0002g0331 | 4 | HG00738.hp1 HG01496.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+756C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866373 | ||||||
chr7:37866395
|
T | C | 350 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(347): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.621+778T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866395 | ||||||
chr7:37866551
|
C | T | 1 | a0002c0002t0001g0219 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.621+934C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866551 | ||||||
chr7:37866552
|
G | A | 1 | a0006c0016t0002g0282 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.621+935G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866552 | ||||||
chr7:37866602
|
T | TAAGATAA others(377): Show |
1 | a0001c0007t0003g0106 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.621+998_621+999ins others(384): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 37866602 | |||||
chr7:37866693
|
T | C | 41 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(38): Show | 44 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.622-1009T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866693 | ||||||
chr7:37866762
|
C | T | 2 | a0001c0007t0001g0033a0003c0010t0001g0130 | 2 | HG03831.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.622-940C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866762 | ||||||
chr7:37866813
|
G | A | 2 | a0001c0001t0001g0011a0004c0005t0001g0155 | 3 | HG01109.hp2 HG01175.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.622-889G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866813 | ||||||
chr7:37866875
|
C | T | 288 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(285): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.622-827C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866875 | ||||||
chr7:37866987
|
T | C | 232 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(229): Show | 254 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.622-715T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866987 | ||||||
chr7:37867127
|
G | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(229): Show | 254 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.622-575G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37867127 | ||||||
chr7:37867237
|
G | T | 1 | a0001c0001t0001g0147 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.622-465G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37867237 | ||||||
chr7:37867293
|
C | CT | 11 | a0001c0001t0006g0150a0001c0001t0006g0151a0003c0003t0002g0329others(8): Show | 11 | HG00733.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.622-397dupT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 37867293 | |||||
chr7:37867416
|
A | G | 31 | a0001c0001t0004g0003a0001c0001t0004g0006a0001c0001t0004g0177others(28): Show | 36 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.622-286A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37867416 | ||||||
chr7:37867445
|
T | G | 25 | a0003c0003t0002g0025a0003c0003t0002g0315a0003c0003t0002g0316others(22): Show | 26 | HG00733.hp2 HG00738.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.622-257T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37867445 | ||||||
chr7:37867631
|
G | T | 1 | a0002c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.622-71G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37867631 | ||||||
chr7:37867925
|
T | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(10): Show | 16 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.818+27T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37867925 | ||||||
chr7:37867954
|
C | T | 26 | a0001c0001t0003g0031a0001c0001t0003g0048a0001c0001t0003g0051others(23): Show | 26 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.818+56C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37867954 | ||||||
chr7:37868085
|
T | C | 1 | a0004c0005t0001g0059 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.818+187T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868085 | ||||||
chr7:37868198
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.818+300G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868198 | ||||||
chr7:37868215
|
G | C | 1 | a0001c0001t0003g0048 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.818+317G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868215 | ||||||
chr7:37868244
|
G | A | 1 | a0001c0007t0001g0061 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.818+346G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868244 | ||||||
chr7:37868388
|
C | T | 2 | a0002c0008t0001g0233a0007c0017t0001g0232 | 2 | HG02300.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.818+490C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868388 | ||||||
chr7:37868429
|
CT | C | 231 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(228): Show | 253 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.818+540delT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37868429 | |||||
chr7:37868481
|
A | C | 2 | a0001c0001t0006g0150a0001c0001t0006g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.818+583A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868481 | ||||||
chr7:37868776
|
G | A | 1 | a0004c0005t0001g0010 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.818+878G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868776 | ||||||
chr7:37868821
|
A | C | 1 | a0003c0010t0002g0327 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.818+923A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868821 | ||||||
chr7:37868852
|
T | TA | 6 | a0003c0003t0001g0248a0003c0003t0001g0250a0003c0010t0001g0247others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.818+958dupA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37868852 | |||||
chr7:37868903
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.818+1005G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868903 | ||||||
chr7:37868971
|
G | A | 2 | a0001c0001t0006g0150a0001c0001t0006g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.818+1073G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868971 | ||||||
chr7:37868993
|
G | A | 1 | a0002c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.818+1095G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868993 | ||||||
chr7:37869042
|
G | A | 12 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(9): Show | 15 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.818+1144G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869042 | ||||||
chr7:37869145
|
G | A | 1 | a0001c0004t0004g0267 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.818+1247G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869145 | ||||||
chr7:37869177
|
T | C | 116 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(113): Show | 125 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.818+1279T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869177 | ||||||
chr7:37869185
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.818+1287C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869185 | ||||||
chr7:37869204
|
G | T | 1 | a0001c0007t0003g0106 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.818+1306G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869204 | ||||||
chr7:37869235
|
C | T | 31 | a0001c0001t0004g0003a0001c0001t0004g0006a0001c0001t0004g0177others(28): Show | 36 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.818+1337C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869235 | ||||||
chr7:37869294
|
C | G | 1 | a0003c0003t0002g0326 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.818+1396C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869294 | ||||||
chr7:37869434
|
T | C | 235 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(232): Show | 258 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.818+1536T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869434 | ||||||
chr7:37869728
|
G | A | 1 | a0004c0012t0004g0252 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.818+1830G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869728 | ||||||
chr7:37869957
|
C | A | 1 | a0002c0008t0001g0115 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.818+2059C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869957 | ||||||
chr7:37869957
|
C | T | 1 | a0006c0016t0002g0307 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.818+2059C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869957 | ||||||
chr7:37870069
|
C | T | 1 | a0001c0004t0005g0270 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.818+2171C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870069 | ||||||
chr7:37870099
|
C | T | 1 | a0001c0004t0001g0152 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.818+2201C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870099 | ||||||
chr7:37870245
|
T | TA | 284 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(281): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.818+2360dupA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37870245 | |||||
chr7:37870245
|
T | TAA | 4 | a0001c0001t0004g0006a0001c0001t0004g0177a0001c0001t0004g0266others(1): Show | 6 | HG01346.hp1 HG01975.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.818+2359_818+2360d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37870245 | |||||
chr7:37870386
|
C | A | 2 | a0001c0001t0001g0158a0001c0004t0001g0157 | 2 | HG01934.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.818+2488C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870386 | ||||||
chr7:37870386
|
C | T | 1 | a0004c0005t0001g0043 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.818+2488C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870386 | ||||||
chr7:37870400
|
T | C | 58 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(55): Show | 64 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.818+2502T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870400 | ||||||
chr7:37870485
|
A | G | 1 | a0002c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.818+2587A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870485 | ||||||
chr7:37870504
|
G | A | 115 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(112): Show | 124 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.818+2606G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870504 | ||||||
chr7:37870519
|
G | A | 2 | a0010c0021t0002g0346a0010c0021t0002g0347 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.818+2621G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870519 | ||||||
chr7:37870588
|
CA | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0028others(227): Show | 257 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.818+2710delA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37870588 | |||||
chr7:37870588
|
CAA | C | 20 | a0001c0001t0001g0144a0001c0001t0001g0154a0001c0001t0001g0173others(17): Show | 20 | HG01975.hp1 HG02055.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.818+2709_818+2710d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37870588 | |||||
chr7:37870699
|
T | C | 4 | a0003c0003t0001g0248a0003c0010t0001g0247a0003c0023t0001g0245others(1): Show | 4 | HG02280.hp1 HG02723.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.818+2801T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870699 | ||||||
chr7:37870826
|
A | G | 1 | a0003c0010t0002g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.818+2928A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870826 | ||||||
chr7:37870923
|
T | C | 1 | a0001c0004t0003g0049 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.818+3025T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870923 | ||||||
chr7:37870938
|
A | G | 29 | a0001c0007t0001g0039a0001c0007t0001g0061a0001c0007t0001g0120others(26): Show | 34 | HG01074.hp1 HG01192.hp2 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.818+3040A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870938 | ||||||
chr7:37871122
|
T | C | 1 | a0005c0006t0002g0284 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.818+3224T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871122 | ||||||
chr7:37871131
|
G | T | 5 | a0003c0003t0002g0336a0003c0003t0002g0337a0010c0021t0002g0346others(2): Show | 5 | HG01433.hp1 HG01884.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.818+3233G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871131 | ||||||
chr7:37871153
|
G | C | 2 | a0003c0003t0002g0280a0012c0027t0001g0146 | 2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.818+3255G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871153 | ||||||
chr7:37871255
|
G | A | 1 | a0018c0035t0001g0182 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.818+3357G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871255 | ||||||
chr7:37871344
|
C | T | 1 | a0004c0005t0004g0261 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.818+3446C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871344 | ||||||
chr7:37871426
|
G | A | 1 | a0004c0005t0004g0261 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.818+3528G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871426 | ||||||
chr7:37871439
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.818+3541T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871439 | ||||||
chr7:37871562
|
T | G | 1 | a0002c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.818+3664T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871562 | ||||||
chr7:37871574
|
C | G | 78 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0063others(75): Show | 86 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.818+3676C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871574 | ||||||
chr7:37871666
|
T | G | 1 | a0002c0008t0001g0239 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.818+3768T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871666 | ||||||
chr7:37871701
|
A | G | 60 | a0001c0001t0001g0028a0001c0001t0001g0079a0001c0001t0001g0086others(57): Show | 61 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.818+3803A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871701 | ||||||
chr7:37871766
|
C | T | 7 | a0003c0010t0002g0317a0003c0010t0002g0319a0003c0010t0002g0332others(4): Show | 7 | HG02258.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.818+3868C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871766 | ||||||
chr7:37871939
|
C | G | 2 | a0001c0007t0007g0078a0003c0010t0002g0321 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.818+4041C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871939 | ||||||
chr7:37871949
|
C | T | 1 | a0001c0007t0001g0033 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.818+4051C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871949 | ||||||
chr7:37872002
|
A | G | 1 | a0002c0008t0001g0233 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.818+4104A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872002 | ||||||
chr7:37872385
|
C | A | 1 | a0003c0003t0001g0132 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.819-4447C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872385 | ||||||
chr7:37872419
|
C | A | 34 | a0001c0001t0006g0150a0001c0001t0006g0151a0001c0007t0001g0013others(31): Show | 37 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.819-4413C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872419 | ||||||
chr7:37872592
|
A | G | 224 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(221): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.819-4240A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872592 | ||||||
chr7:37872623
|
A | G | 4 | a0002c0002t0001g0021a0002c0002t0001g0235a0002c0002t0001g0236others(1): Show | 5 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.819-4209A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872623 | ||||||
chr7:37872656
|
T | G | 258 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(255): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.819-4176T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872656 | ||||||
chr7:37872684
|
G | A | 4 | a0002c0002t0001g0021a0002c0002t0001g0235a0002c0002t0001g0236others(1): Show | 5 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.819-4148G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872684 | ||||||
chr7:37872695
|
G | A | 223 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(220): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-4137G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872695 | ||||||
chr7:37872745
|
ACT | A | 223 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(220): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-4084_819-4083d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37872745 | |||||
chr7:37872752
|
A | T | 34 | a0001c0001t0006g0150a0001c0001t0006g0151a0001c0007t0001g0013others(31): Show | 37 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.819-4080A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872752 | ||||||
chr7:37872778
|
AACTC | A | 223 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(220): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-4052_819-4049d others(6): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37872778 | |||||
chr7:37872884
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.819-3948C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872884 | ||||||
chr7:37872901
|
G | A | 1 | a0008c0013t0002g0314 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.819-3931G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872901 | ||||||
chr7:37872921
|
A | T | 5 | a0001c0001t0006g0150a0001c0001t0006g0151a0002c0009t0001g0186others(2): Show | 5 | HG00280.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.819-3911A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872921 | ||||||
chr7:37872925
|
C | A | 1 | a0003c0010t0002g0317 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.819-3907C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872925 | ||||||
chr7:37872933
|
G | T | 223 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(220): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-3899G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872933 | ||||||
chr7:37872958
|
G | T | 3 | a0001c0001t0006g0150a0001c0001t0006g0151a0002c0009t0001g0186 | 3 | HG00280.hp1 HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.819-3874G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872958 | ||||||
chr7:37873027
|
T | A | 34 | a0001c0001t0006g0150a0001c0001t0006g0151a0001c0007t0001g0013others(31): Show | 37 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.819-3805T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873027 | ||||||
chr7:37873075
|
A | G | 223 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(220): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-3757A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873075 | ||||||
chr7:37873116
|
G | A | 1 | a0002c0002t0001g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.819-3716G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873116 | ||||||
chr7:37873129
|
G | A | 22 | a0001c0007t0001g0013a0001c0007t0001g0067a0001c0007t0001g0068others(19): Show | 25 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.819-3703G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873129 | ||||||
chr7:37873146
|
A | G | 257 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(254): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.819-3686A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873146 | ||||||
chr7:37873154
|
G | T | 223 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(220): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-3678G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873154 | ||||||
chr7:37873175
|
C | T | 2 | a0001c0001t0006g0150a0001c0001t0006g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.819-3657C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873175 | ||||||
chr7:37873317
|
G | A | 117 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0032others(114): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.819-3515G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873317 | ||||||
chr7:37873359
|
C | CAAA | 46 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0063others(43): Show | 49 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.819-3460_819-3458d others(5): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37873359 | |||||
chr7:37873359
|
C | CAAAA | 107 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0032others(104): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.819-3461_819-3458d others(6): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37873359 | |||||
chr7:37873359
|
C | CAAAAA | 9 | a0001c0001t0001g0172a0001c0001t0001g0175a0001c0001t0004g0253others(6): Show | 9 | HG01981.hp2 HG02738.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.819-3462_819-3458d others(7): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37873359 | |||||
chr7:37873359
|
CA | C | 6 | a0001c0001t0001g0107a0001c0004t0003g0096a0003c0003t0002g0026others(3): Show | 7 | HG00323.hp1 HG02572.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.819-3458delA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37873359 | |||||
chr7:37873370
|
A | AAAAAAAA others(3): Show |
3 | a0003c0010t0001g0247a0003c0023t0001g0245a0003c0023t0001g0246 | 3 | HG02280.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.819-3458_819-3457i others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37873370 | |||||
chr7:37873370
|
A | AAAAAAAA others(2): Show |
57 | a0001c0001t0001g0224a0001c0001t0003g0031a0001c0001t0003g0048others(54): Show | 64 | HG00544.hp2 HG00597.hp2 HG01074.hp1 others(61): Show |
intron_variant | MODIFIER | c.819-3458_819-3457i others(11): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37873370 | |||||
chr7:37873395
|
G | A | 225 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(222): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.819-3437G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873395 | ||||||
chr7:37873491
|
T | TAAACAAT others(40): Show |
5 | a0003c0003t0002g0280a0010c0021t0002g0346a0010c0021t0002g0347others(2): Show | 6 | HG01358.hp1 HG01433.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.819-3341_819-3340i others(49): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873491 | ||||||
chr7:37873492
|
T | A | 5 | a0003c0003t0002g0280a0010c0021t0002g0346a0010c0021t0002g0347others(2): Show | 6 | HG01358.hp1 HG01433.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.819-3340T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873492 | ||||||
chr7:37873509
|
T | A | 1 | a0001c0001t0003g0051 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.819-3323T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873509 | ||||||
chr7:37873591
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.819-3241A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873591 | ||||||
chr7:37873604
|
A | G | 1 | a0005c0006t0002g0311 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.819-3228A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873604 | ||||||
chr7:37873729
|
T | G | 2 | a0002c0008t0001g0045a0006c0016t0002g0296 | 2 | NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.819-3103T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873729 | ||||||
chr7:37873848
|
A | G | 1 | a0012c0027t0001g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.819-2984A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873848 | ||||||
chr7:37873887
|
C | G | 1 | a0003c0010t0002g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.819-2945C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873887 | ||||||
chr7:37873901
|
G | T | 223 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(220): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-2931G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873901 | ||||||
chr7:37873949
|
T | C | 225 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(222): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.819-2883T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873949 | ||||||
chr7:37873995
|
A | G | 223 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(220): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-2837A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873995 | ||||||
chr7:37874012
|
G | A | 260 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(257): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.819-2820G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874012 | ||||||
chr7:37874125
|
A | T | 223 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(220): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-2707A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874125 | ||||||
chr7:37874158
|
G | A | 1 | a0005c0024t0002g0297 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.819-2674G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874158 | ||||||
chr7:37874183
|
T | G | 160 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(157): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.819-2649T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874183 | ||||||
chr7:37874328
|
G | A | 224 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(221): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.819-2504G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874328 | ||||||
chr7:37874333
|
G | C | 223 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(220): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-2499G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874333 | ||||||
chr7:37874354
|
G | A | 34 | a0001c0001t0006g0150a0001c0001t0006g0151a0001c0007t0001g0013others(31): Show | 37 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.819-2478G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874354 | ||||||
chr7:37874481
|
G | A | 1 | a0002c0009t0001g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.819-2351G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874481 | ||||||
chr7:37874511
|
G | A | 223 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(220): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-2321G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874511 | ||||||
chr7:37874567
|
A | G | 5 | a0003c0003t0002g0280a0010c0021t0002g0346a0010c0021t0002g0347others(2): Show | 6 | HG01358.hp1 HG01433.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.819-2265A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874567 | ||||||
chr7:37874625
|
C | A | 2 | a0001c0004t0001g0223a0007c0017t0001g0137 | 2 | NA18942.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.819-2207C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874625 | ||||||
chr7:37874719
|
C | T | 1 | a0017c0036t0001g0218 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.819-2113C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874719 | ||||||
chr7:37874834
|
T | C | 3 | a0005c0006t0002g0286a0005c0006t0002g0309a0006c0011t0002g0310 | 3 | HG00099.hp1 HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.819-1998T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874834 | ||||||
chr7:37874862
|
A | G | 37 | a0001c0001t0006g0150a0001c0001t0006g0151a0001c0007t0001g0013others(34): Show | 40 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.819-1970A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874862 | ||||||
chr7:37874972
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0003g0005a0001c0001t0003g0027others(3): Show | 9 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.819-1860C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874972 | ||||||
chr7:37875015
|
A | G | 1 | a0001c0004t0001g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.819-1817A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875015 | ||||||
chr7:37875065
|
G | C | 257 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(254): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.819-1767G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875065 | ||||||
chr7:37875092
|
C | T | 1 | a0007c0017t0001g0137 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.819-1740C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875092 | ||||||
chr7:37875114
|
A | G | 28 | a0001c0001t0001g0224a0001c0001t0003g0031a0001c0001t0003g0048others(25): Show | 30 | HG00544.hp2 HG00597.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.819-1718A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875114 | ||||||
chr7:37875134
|
A | C | 257 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(254): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.819-1698A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875134 | ||||||
chr7:37875147
|
A | G | 44 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0063others(41): Show | 47 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.819-1685A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875147 | ||||||
chr7:37875176
|
G | A | 34 | a0001c0001t0006g0150a0001c0001t0006g0151a0001c0007t0001g0013others(31): Show | 37 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.819-1656G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875176 | ||||||
chr7:37875223
|
A | G | 39 | a0001c0001t0001g0012a0001c0001t0001g0159a0001c0001t0001g0175others(36): Show | 46 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.819-1609A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875223 | ||||||
chr7:37875358
|
T | A | 256 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(253): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.819-1474T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875358 | ||||||
chr7:37875401
|
G | GAC | 37 | a0001c0001t0001g0014a0001c0001t0001g0156a0001c0001t0001g0161others(34): Show | 41 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.819-1414_819-1413d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37875401 | |||||
chr7:37875420
|
C | A | 2 | a0001c0001t0001g0173a0001c0004t0001g0118 | 2 | NA19057.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.819-1412C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875420 | ||||||
chr7:37875471
|
CAGAG | C | 151 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(148): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.819-1357_819-1354d others(6): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37875471 | |||||
chr7:37875506
|
G | T | 1 | a0001c0007t0001g0033 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.819-1326G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875506 | ||||||
chr7:37875535
|
G | A | 3 | a0003c0003t0002g0026a0003c0003t0002g0339a0003c0015t0002g0352 | 4 | HG02896.hp2 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.819-1297G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875535 | ||||||
chr7:37875573
|
AT | A | 14 | a0001c0001t0001g0224a0001c0001t0003g0031a0001c0001t0003g0048others(11): Show | 14 | HG00597.hp2 HG02040.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.819-1252delT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37875573 | |||||
chr7:37875613
|
T | G | 1 | a0001c0001t0001g0167 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.819-1219T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875613 | ||||||
chr7:37875663
|
A | T | 2 | a0001c0001t0006g0150a0001c0001t0006g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.819-1169A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875663 | ||||||
chr7:37875669
|
A | C | 2 | a0012c0027t0001g0146a0012c0027t0005g0271 | 2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.819-1163A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875669 | ||||||
chr7:37875671
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(8): Show | 14 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.819-1161G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875671 | ||||||
chr7:37875872
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.819-960G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875872 | ||||||
chr7:37875973
|
C | T | 3 | a0003c0003t0002g0026a0003c0003t0002g0339a0003c0015t0002g0352 | 4 | HG02896.hp2 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.819-859C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875973 | ||||||
chr7:37875978
|
C | T | 151 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(148): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.819-854C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875978 | ||||||
chr7:37875993
|
G | A | 1 | a0003c0010t0002g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.819-839G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875993 | ||||||
chr7:37876042
|
C | T | 69 | a0001c0001t0006g0150a0001c0001t0006g0151a0001c0007t0001g0013others(66): Show | 76 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.819-790C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876042 | ||||||
chr7:37876074
|
G | T | 220 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(217): Show | 243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.819-758G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876074 | ||||||
chr7:37876108
|
C | CT | 220 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(217): Show | 243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.819-724_819-723ins others(1): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876108 | ||||||
chr7:37876124
|
C | T | 1 | a0005c0025t0002g0312 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.819-708C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876124 | ||||||
chr7:37876214
|
C | A | 69 | a0001c0001t0006g0150a0001c0001t0006g0151a0001c0007t0001g0013others(66): Show | 76 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.819-618C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876214 | ||||||
chr7:37876215
|
A | C | 1 | a0002c0009t0001g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.819-617A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876215 | ||||||
chr7:37876216
|
C | CTATA | 4 | a0001c0001t0004g0006a0001c0001t0004g0177a0002c0002t0001g0180others(1): Show | 6 | HG01346.hp1 HG01975.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.819-603_819-600dup others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876216 | |||||
chr7:37876216
|
CTATA | C | 3 | a0001c0007t0001g0187a0003c0010t0002g0319a0014c0033t0002g0318 | 3 | HG02559.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.819-603_819-600del others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876216 | |||||
chr7:37876225
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0015 | 2 | HG00140.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.819-603_819-592del others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876225 | |||||
chr7:37876229
|
T | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(42): Show | 51 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.819-603T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876229 | ||||||
chr7:37876229
|
T | TATAG | 8 | a0001c0001t0001g0142a0001c0001t0001g0154a0001c0001t0001g0173others(5): Show | 8 | HG00735.hp2 HG02809.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.819-575_819-572dup others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876229 | |||||
chr7:37876229
|
T | TATAGATA others(5): Show |
2 | a0001c0001t0001g0107a0003c0015t0002g0352 | 2 | HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.819-583_819-572dup others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876229 | |||||
chr7:37876229
|
T | TATATATA others(1): Show |
23 | a0001c0001t0001g0224a0001c0001t0003g0031a0001c0001t0003g0048others(20): Show | 23 | HG00544.hp2 HG00597.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.819-600_819-599ins others(8): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876229 | |||||
chr7:37876229
|
T | TATATATA others(5): Show |
1 | a0003c0003t0002g0339 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.819-600_819-599ins others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876229 | |||||
chr7:37876229
|
T | TATATATA others(9): Show |
1 | a0003c0003t0002g0026 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.819-600_819-599ins others(16): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876229 | |||||
chr7:37876229
|
TATAG | T | 31 | a0001c0001t0001g0163a0001c0001t0006g0150a0001c0001t0006g0151others(28): Show | 35 | HG00280.hp1 HG01074.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.819-575_819-572del others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876229 | |||||
chr7:37876229
|
TATAGATA others(1): Show |
T | 56 | a0001c0001t0001g0014a0001c0001t0001g0156a0001c0001t0001g0161others(53): Show | 64 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.819-579_819-572del others(8): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876229 | |||||
chr7:37876229
|
TATAGATA others(5): Show |
T | 39 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(36): Show | 41 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.819-583_819-572del others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876229 | |||||
chr7:37876231
|
TAG | T | 5 | a0002c0020t0001g0196a0003c0010t0001g0247a0003c0010t0002g0327others(2): Show | 5 | HG01109.hp1 HG02280.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.819-599_819-598del others(2): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876231 | |||||
chr7:37876231
|
TAGATAG | T | 25 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0040others(22): Show | 28 | HG00323.hp2 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.819-599_819-594del others(6): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876231 | |||||
chr7:37876231
|
TAGATAGA others(3): Show |
T | 1 | a0001c0001t0001g0167 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.819-599_819-590del others(10): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876231 | |||||
chr7:37876233
|
G | T | 5 | a0001c0001t0004g0266a0003c0003t0002g0280a0010c0021t0002g0346others(2): Show | 5 | HG01433.hp1 HG01884.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.819-599G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876233 | ||||||
chr7:37876235
|
T | A | 23 | a0001c0001t0001g0224a0001c0001t0003g0031a0001c0001t0003g0048others(20): Show | 23 | HG00544.hp2 HG00597.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.819-597T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876235 | ||||||
chr7:37876237
|
G | T | 4 | a0001c0001t0006g0150a0001c0001t0006g0151a0012c0027t0001g0146others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.819-595G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876237 | ||||||
chr7:37876372
|
C | T | 28 | a0001c0001t0001g0224a0001c0001t0003g0031a0001c0001t0003g0048others(25): Show | 30 | HG00544.hp2 HG00597.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.819-460C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876372 | ||||||
chr7:37876386
|
C | A | 32 | a0001c0007t0001g0013a0001c0007t0001g0067a0001c0007t0001g0068others(29): Show | 35 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.819-446C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876386 | ||||||
chr7:37876413
|
TAAAC | T | 69 | a0001c0001t0006g0150a0001c0001t0006g0151a0001c0007t0001g0013others(66): Show | 76 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.819-416_819-413del others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876413 | |||||
chr7:37876681
|
AT | A | 69 | a0001c0001t0006g0150a0001c0001t0006g0151a0001c0007t0001g0013others(66): Show | 76 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.819-150delT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876681 | ||||||
chr7:37876694
|
G | A | 2 | a0001c0007t0001g0013a0001c0007t0003g0106 | 3 | HG03491.hp1 HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.819-138G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876694 | ||||||
chr7:37876709
|
A | T | 151 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(148): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.819-123A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876709 | ||||||
chr7:37877026
|
A | G | 1 | a0011c0029t0001g0017 | 2 | HG01358.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.994+19A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877026 | ||||||
chr7:37877085
|
A | G | 1 | a0005c0006t0002g0292 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.994+78A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877085 | ||||||
chr7:37877197
|
A | G | 28 | a0001c0001t0001g0224a0001c0001t0003g0031a0001c0001t0003g0048others(25): Show | 30 | HG00544.hp2 HG00597.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.994+190A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877197 | ||||||
chr7:37877354
|
T | A | 1 | a0003c0003t0002g0025 | 2 | HG00738.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.994+347T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877354 | ||||||
chr7:37877472
|
A | G | 1 | a0006c0016t0002g0282 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.994+465A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877472 | ||||||
chr7:37877490
|
A | G | 151 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(148): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.994+483A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877490 | ||||||
chr7:37877687
|
G | A | 2 | a0003c0003t0002g0315a0003c0003t0002g0316 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.994+680G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877687 | ||||||
chr7:37877794
|
C | G | 2 | a0001c0001t0006g0150a0001c0001t0006g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.994+787C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877794 | ||||||
chr7:37877863
|
T | C | 220 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(217): Show | 243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.994+856T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877863 | ||||||
chr7:37877898
|
G | C | 1 | a0001c0001t0001g0189 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.994+891G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877898 | ||||||
chr7:37878002
|
A | G | 219 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(216): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.994+995A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878002 | ||||||
chr7:37878220
|
A | G | 220 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(217): Show | 243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.994+1213A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878220 | ||||||
chr7:37878286
|
A | G | 219 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(216): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.994+1279A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878286 | ||||||
chr7:37878343
|
T | A | 219 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(216): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.994+1336T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878343 | ||||||
chr7:37878394
|
G | C | 117 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0032others(114): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.994+1387G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878394 | ||||||
chr7:37878478
|
C | T | 1 | a0005c0025t0002g0312 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.994+1471C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878478 | ||||||
chr7:37878499
|
C | G | 31 | a0001c0007t0001g0013a0001c0007t0001g0067a0001c0007t0001g0068others(28): Show | 34 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.994+1492C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878499 | ||||||
chr7:37878563
|
A | T | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.994+1556A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878563 | ||||||
chr7:37878739
|
T | C | 3 | a0003c0003t0002g0026a0003c0003t0002g0339a0003c0015t0002g0352 | 4 | HG02896.hp2 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.994+1732T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878739 | ||||||
chr7:37878936
|
G | C | 1 | a0012c0027t0001g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.994+1929G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878936 | ||||||
chr7:37878989
|
G | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(10): Show | 16 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.994+1982G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878989 | ||||||
chr7:37879110
|
G | A | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.994+2103G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879110 | ||||||
chr7:37879126
|
T | TTA | 97 | a0001c0001t0001g0224a0001c0001t0003g0031a0001c0001t0003g0048others(94): Show | 106 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.994+2133_994+2134d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37879126 | |||||
chr7:37879211
|
T | C | 219 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(216): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.994+2204T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879211 | ||||||
chr7:37879263
|
C | A | 2 | a0002c0020t0001g0201a0002c0020t0001g0202 | 2 | NA18951.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.994+2256C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879263 | ||||||
chr7:37879283
|
T | G | 219 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(216): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.994+2276T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879283 | ||||||
chr7:37879559
|
A | G | 5 | a0002c0002t0001g0016a0002c0002t0001g0206a0002c0002t0001g0207others(2): Show | 6 | NA18962.hp1 NA18968.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.994+2552A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879559 | ||||||
chr7:37879767
|
G | C | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.994+2760G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879767 | ||||||
chr7:37879846
|
C | A | 65 | a0001c0001t0006g0150a0001c0001t0006g0151a0001c0007t0001g0013others(62): Show | 72 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.994+2839C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879846 | ||||||
chr7:37879901
|
A | G | 61 | a0001c0001t0001g0028a0001c0001t0001g0079a0001c0001t0001g0086others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.994+2894A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879901 | ||||||
chr7:37879943
|
T | A | 63 | a0001c0007t0001g0013a0001c0007t0001g0033a0001c0007t0001g0039others(60): Show | 70 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.994+2936T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879943 | ||||||
chr7:37879952
|
A | G | 1 | a0003c0010t0002g0328 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.994+2945A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879952 | ||||||
chr7:37879990
|
G | A | 185 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(182): Show | 206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.994+2983G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879990 | ||||||
chr7:37880085
|
TTG | T | 182 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(179): Show | 203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.994+3080_994+3081d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37880085 | |||||
chr7:37880086
|
TG | T | 3 | a0002c0002t0001g0183a0002c0009t0001g0230a0006c0011t0002g0302 | 3 | NA18985.hp1 NA18991.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.994+3080delG | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880086 | ||||||
chr7:37880087
|
G | T | 29 | a0001c0001t0001g0224a0001c0001t0003g0031a0001c0001t0003g0048others(26): Show | 31 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.994+3080G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880087 | ||||||
chr7:37880150
|
T | G | 3 | a0003c0003t0002g0026a0003c0003t0002g0339a0003c0015t0002g0352 | 4 | HG02896.hp2 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.994+3143T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880150 | ||||||
chr7:37880307
|
T | C | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.994+3300T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880307 | ||||||
chr7:37880355
|
C | T | 1 | a0009c0031t0001g0125 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.994+3348C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880355 | ||||||
chr7:37880392
|
G | A | 2 | a0001c0001t0006g0150a0001c0001t0006g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.994+3385G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880392 | ||||||
chr7:37880403
|
C | T | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.994+3396C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880403 | ||||||
chr7:37880411
|
A | G | 43 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0063others(40): Show | 46 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.994+3404A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880411 | ||||||
chr7:37880512
|
G | A | 63 | a0001c0007t0001g0013a0001c0007t0001g0033a0001c0007t0001g0039others(60): Show | 70 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.994+3505G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880512 | ||||||
chr7:37880569
|
G | A | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.994+3562G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880569 | ||||||
chr7:37880718
|
A | T | 3 | a0010c0021t0002g0346a0010c0021t0002g0347a0019c0034t0001g0112 | 3 | HG01433.hp1 HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.995-3585A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880718 | ||||||
chr7:37880757
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.995-3546G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880757 | ||||||
chr7:37880784
|
C | T | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-3519C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880784 | ||||||
chr7:37880802
|
AT | A | 215 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(212): Show | 238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.995-3493delT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37880802 | |||||
chr7:37880812
|
G | A | 4 | a0002c0009t0001g0001a0002c0009t0001g0230a0002c0009t0001g0234others(1): Show | 8 | NA18954.hp1 NA18969.hp2 NA18988.hp2 others(5): Show |
intron_variant | MODIFIER | c.995-3491G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880812 | ||||||
chr7:37880868
|
G | A | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-3435G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880868 | ||||||
chr7:37880882
|
T | A | 1 | a0001c0004t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.995-3421T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880882 | ||||||
chr7:37881030
|
T | C | 1 | a0003c0003t0002g0339 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.995-3273T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881030 | ||||||
chr7:37881073
|
T | C | 2 | a0001c0001t0006g0150a0001c0001t0006g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.995-3230T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881073 | ||||||
chr7:37881081
|
C | G | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-3222C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881081 | ||||||
chr7:37881265
|
T | C | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-3038T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881265 | ||||||
chr7:37881279
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0079 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.995-3024G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881279 | ||||||
chr7:37881520
|
T | C | 1 | a0003c0003t0001g0132 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.995-2783T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881520 | ||||||
chr7:37881525
|
T | C | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-2778T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881525 | ||||||
chr7:37881580
|
C | T | 4 | a0002c0002t0001g0021a0002c0002t0001g0235a0002c0002t0001g0236others(1): Show | 5 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-2723C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881580 | ||||||
chr7:37881650
|
T | C | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-2653T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881650 | ||||||
chr7:37881755
|
T | C | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-2548T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881755 | ||||||
chr7:37881941
|
T | G | 2 | a0001c0001t0001g0064a0009c0022t0002g0331 | 2 | HG00733.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.995-2362T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881941 | ||||||
chr7:37881972
|
C | T | 3 | a0004c0005t0001g0041a0004c0005t0001g0042a0004c0005t0001g0043 | 3 | HG01943.hp2 HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.995-2331C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881972 | ||||||
chr7:37882028
|
G | A | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-2275G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882028 | ||||||
chr7:37882098
|
T | C | 28 | a0001c0007t0001g0013a0001c0007t0001g0067a0001c0007t0001g0068others(25): Show | 31 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.995-2205T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882098 | ||||||
chr7:37882323
|
C | T | 1 | a0007c0017t0001g0197 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.995-1980C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882323 | ||||||
chr7:37882487
|
A | G | 2 | a0001c0001t0006g0150a0001c0001t0006g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.995-1816A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882487 | ||||||
chr7:37882546
|
G | GGAAAGAA others(5): Show |
1 | a0001c0004t0004g0267 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.995-1714_995-1703d others(14): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882546 | |||||
chr7:37882546
|
GGAAAGAA others(1): Show |
G | 3 | a0001c0001t0001g0142a0003c0003t0001g0250a0003c0015t0002g0351 | 3 | HG02717.hp1 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.995-1710_995-1703d others(10): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882546 | |||||
chr7:37882551
|
G | C | 3 | a0002c0009t0001g0186a0012c0027t0001g0146a0012c0027t0005g0271 | 3 | HG00280.hp1 HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.995-1752G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882551 | ||||||
chr7:37882552
|
A | G | 1 | a0002c0002t0001g0198 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.995-1751A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882552 | ||||||
chr7:37882555
|
GAAAGAAA others(3): Show |
G | 1 | a0003c0003t0002g0322 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.995-1746_995-1737d others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882555 | |||||
chr7:37882581
|
AAGAAAGA others(21): Show |
A | 1 | a0005c0006t0002g0291 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.995-1718_995-1691d others(30): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882581 | |||||
chr7:37882581
|
AAGAAAGA others(25): Show |
A | 2 | a0001c0001t0001g0164a0003c0003t0002g0340 | 2 | HG02970.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.995-1702_995-1671d others(34): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882581 | |||||
chr7:37882585
|
AAGAAAGA others(17): Show |
A | 10 | a0001c0001t0004g0253a0003c0003t0002g0025a0003c0003t0002g0330others(7): Show | 11 | HG00738.hp1 HG00738.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.995-1714_995-1691d others(26): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882585 | |||||
chr7:37882585
|
AAGAAAGA others(19): Show |
A | 1 | a0002c0002t0001g0180 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.995-1714_995-1689d others(28): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882585 | |||||
chr7:37882585
|
AAGAAAGA others(21): Show |
A | 9 | a0001c0001t0001g0035a0001c0001t0001g0161a0001c0001t0001g0166others(6): Show | 9 | HG01070.hp1 HG02818.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.995-1702_995-1675d others(30): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882585 | |||||
chr7:37882589
|
AAGAAAGA others(7): Show |
A | 12 | a0001c0001t0001g0175a0001c0001t0003g0005a0001c0001t0003g0027others(9): Show | 16 | HG00099.hp1 HG00639.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.995-1710_995-1697d others(16): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882589 | |||||
chr7:37882589
|
AAGAAAGA others(15): Show |
A | 6 | a0001c0001t0004g0006a0001c0001t0004g0266a0001c0007t0001g0160others(3): Show | 8 | HG01346.hp1 HG02135.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.995-1710_995-1689d others(24): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882589 | |||||
chr7:37882589
|
AAGAAAGA others(17): Show |
A | 16 | a0001c0001t0001g0064a0001c0001t0001g0070a0001c0001t0001g0172others(13): Show | 16 | HG00558.hp1 HG00621.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.995-1702_995-1679d others(26): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882589 | |||||
chr7:37882593
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.995-1710A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882593 | ||||||
chr7:37882593
|
AAGAAAGA others(3): Show |
A | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.995-1706_995-1697d others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882593 | |||||
chr7:37882593
|
AAGAAAGA others(7): Show |
A | 2 | a0001c0001t0006g0151a0012c0027t0001g0146 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.995-1706_995-1693d others(16): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882593 | |||||
chr7:37882593
|
AAGAAAGA others(11): Show |
A | 10 | a0001c0001t0001g0015a0001c0007t0001g0033a0001c0007t0001g0061others(7): Show | 11 | HG00140.hp2 HG01074.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.995-1706_995-1689d others(20): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882593 | |||||
chr7:37882593
|
AAGAAAGA others(13): Show |
A | 1 | a0001c0004t0003g0100 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.995-1702_995-1683d others(22): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882593 | |||||
chr7:37882597
|
A | AAGAAAGA others(3): Show |
3 | a0001c0004t0003g0084a0003c0003t0002g0336a0017c0036t0001g0218 | 3 | HG02451.hp1 HG02683.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.995-1703_995-1702i others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(7): Show |
4 | a0001c0001t0003g0029a0001c0004t0003g0082a0004c0005t0001g0083others(1): Show | 5 | HG01256.hp2 NA18943.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-1703_995-1702i others(16): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(17): Show |
1 | a0001c0004t0001g0080 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.995-1703_995-1702i others(26): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(13): Show |
1 | a0001c0001t0003g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.995-1703_995-1702i others(22): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(15): Show |
1 | a0001c0001t0003g0034 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.995-1703_995-1702i others(24): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(15): Show |
1 | a0001c0001t0001g0079 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.995-1703_995-1702i others(24): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(9): Show |
5 | a0001c0001t0001g0028a0001c0001t0003g0109a0003c0003t0002g0326others(2): Show | 5 | HG01123.hp1 HG01192.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-1703_995-1702i others(18): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(11): Show |
2 | a0001c0004t0001g0110a0001c0004t0003g0108 | 2 | HG01515.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.995-1703_995-1702i others(20): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(5): Show |
6 | a0001c0001t0003g0085a0001c0004t0003g0096a0002c0002t0001g0213others(3): Show | 6 | HG00323.hp1 HG00735.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.995-1703_995-1702i others(14): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(7): Show |
3 | a0001c0001t0001g0111a0005c0014t0002g0294a0005c0014t0002g0303 | 3 | HG03239.hp1 NA18990.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.995-1703_995-1702i others(16): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(9): Show |
1 | a0001c0001t0001g0113 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.995-1703_995-1702i others(18): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(11): Show |
1 | a0001c0001t0001g0086 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.995-1703_995-1702i others(20): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(4): Show |
1 | a0004c0005t0003g0030 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.995-1703_995-1702i others(13): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(6): Show |
1 | a0004c0005t0001g0042 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.995-1703_995-1702i others(15): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(1): Show |
6 | a0001c0004t0003g0089a0003c0003t0002g0337a0004c0005t0003g0090others(3): Show | 6 | HG00558.hp2 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.995-1703_995-1702i others(10): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(4): Show |
1 | a0003c0003t0002g0315 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.995-1703_995-1702i others(13): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(3): Show |
1 | a0003c0003t0002g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.995-1703_995-1702i others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(5): Show |
3 | a0001c0004t0001g0091a0001c0004t0001g0118a0003c0003t0001g0132 | 3 | HG01928.hp2 NA18980.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.995-1703_995-1702i others(14): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | AAGAAAGA others(9): Show |
1 | a0001c0004t0003g0095 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.995-1703_995-1702i others(18): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
A | G | 25 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0138others(22): Show | 30 | HG00140.hp1 HG00741.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.995-1706A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882597 | ||||||
chr7:37882597
|
AAG | A | 3 | a0002c0002t0001g0021a0002c0002t0001g0238a0002c0009t0001g0230 | 4 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.995-1688_995-1687d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
AAGAG | A | 3 | a0001c0001t0005g0269a0001c0004t0005g0270a0003c0003t0008g0320 | 3 | HG02886.hp2 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.995-1690_995-1687d others(6): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
AAGAGAG | A | 3 | a0001c0007t0001g0187a0002c0020t0001g0196a0003c0010t0001g0247 | 3 | HG01109.hp1 HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.995-1692_995-1687d others(8): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
AAGAGAGA others(1): Show |
A | 15 | a0001c0001t0001g0167a0001c0001t0001g0176a0001c0001t0003g0073others(12): Show | 15 | HG00323.hp2 HG01081.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.995-1694_995-1687d others(10): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
AAGAGAGA others(3): Show |
A | 12 | a0001c0001t0006g0150a0001c0007t0003g0097a0001c0028t0001g0038others(9): Show | 16 | HG00280.hp1 HG02040.hp1 HG02895.hp1 others(13): Show |
intron_variant | MODIFIER | c.995-1696_995-1687d others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
AAGAGAGA others(5): Show |
A | 14 | a0001c0001t0001g0040a0001c0004t0001g0226a0001c0007t0007g0078others(11): Show | 15 | HG01081.hp1 HG02717.hp2 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.995-1698_995-1687d others(14): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
AAGAGAGA others(7): Show |
A | 5 | a0001c0001t0004g0177a0001c0007t0001g0039a0001c0007t0001g0190others(2): Show | 5 | HG01928.hp1 HG01975.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-1700_995-1687d others(16): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882597
|
AAGAGAGA others(9): Show |
A | 56 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0032others(53): Show | 67 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.995-1702_995-1687d others(18): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | |||||
chr7:37882599
|
G | GAA | 22 | a0001c0001t0001g0224a0001c0001t0003g0031a0001c0001t0003g0048others(19): Show | 22 | HG00597.hp2 HG00673.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.995-1703_995-1702i others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882599 | |||||
chr7:37882599
|
G | GAAAGAA | 5 | a0001c0001t0003g0077a0001c0001t0004g0264a0001c0028t0003g0101others(2): Show | 5 | HG00544.hp2 HG02683.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-1703_995-1702i others(8): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882599 | |||||
chr7:37882599
|
GAGAGAGA others(27): Show |
G | 1 | a0002c0002t0001g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.995-1700_995-1667d others(36): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882599 | |||||
chr7:37882601
|
G | A | 43 | a0001c0001t0001g0153a0001c0001t0003g0074a0001c0001t0003g0087others(40): Show | 48 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.995-1702G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882601 | ||||||
chr7:37882603
|
G | A | 24 | a0001c0001t0001g0224a0001c0001t0003g0031a0001c0001t0003g0048others(21): Show | 25 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.995-1700G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882603 | ||||||
chr7:37882605
|
G | A | 41 | a0001c0001t0001g0153a0001c0001t0003g0051a0001c0001t0003g0056others(38): Show | 45 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.995-1698G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882605 | ||||||
chr7:37882605
|
GAGAGAGA others(9): Show |
G | 7 | a0001c0001t0001g0012a0005c0006t0002g0275a0005c0006t0002g0284others(4): Show | 9 | HG00140.hp1 HG01074.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.995-1694_995-1679d others(18): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882605 | |||||
chr7:37882607
|
G | A | 21 | a0001c0001t0003g0031a0001c0001t0003g0052a0001c0001t0003g0053others(18): Show | 22 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.995-1696G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882607 | ||||||
chr7:37882609
|
G | A | 63 | a0001c0001t0001g0153a0001c0001t0001g0167a0001c0001t0001g0176others(60): Show | 66 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.995-1694G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882609 | ||||||
chr7:37882609
|
GAGAGAGA others(5): Show |
G | 4 | a0002c0002t0001g0044a0002c0008t0001g0233a0003c0003t0002g0322others(1): Show | 4 | HG02300.hp2 HG02896.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-1690_995-1679d others(14): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882609 | |||||
chr7:37882611
|
G | A | 27 | a0001c0001t0003g0052a0001c0001t0003g0053a0001c0001t0003g0077others(24): Show | 32 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.995-1692G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882611 | ||||||
chr7:37882611
|
GAGAGAA | G | 4 | a0003c0010t0002g0333a0003c0010t0002g0334a0003c0010t0002g0335others(1): Show | 4 | HG01884.hp2 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-1688_995-1683d others(8): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882611 | |||||
chr7:37882611
|
GAGAGAAA others(3): Show |
G | 2 | a0002c0002t0001g0199a0002c0002t0001g0200 | 2 | NA18964.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.995-1688_995-1679d others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882611 | |||||
chr7:37882613
|
G | A | 92 | a0001c0001t0001g0040a0001c0001t0001g0113a0001c0001t0001g0138others(89): Show | 96 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.995-1690G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882613 | ||||||
chr7:37882613
|
G | GAA | 3 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0147 | 3 | HG00741.hp1 HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.995-1689_995-1688i others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882613 | |||||
chr7:37882613
|
G | GAGAA | 6 | a0001c0001t0001g0002a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 9 | HG02257.hp2 HG02280.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.995-1662_995-1659d others(6): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882613 | |||||
chr7:37882613
|
G | GAGAGAA | 3 | a0001c0001t0001g0143a0001c0001t0001g0149a0003c0003t0002g0324 | 3 | HG02630.hp1 HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.995-1687_995-1686i others(8): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882613 | |||||
chr7:37882613
|
G | GAGAGAGA others(1): Show |
4 | a0001c0001t0001g0114a0001c0001t0001g0154a0001c0001t0001g0189others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.995-1687_995-1686i others(10): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882613 | |||||
chr7:37882613
|
G | GAGAGAGA others(7): Show |
1 | a0003c0015t0002g0323 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.995-1687_995-1686i others(16): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882613 | |||||
chr7:37882613
|
GAGAA | G | 5 | a0003c0003t0002g0280a0003c0003t0002g0339a0005c0006t0002g0024others(2): Show | 6 | HG01433.hp1 HG03195.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.995-1662_995-1659d others(6): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882613 | |||||
chr7:37882613
|
GAGAAAGA others(1): Show |
G | 3 | a0001c0001t0001g0159a0005c0006t0002g0285a0006c0011t0002g0278 | 3 | HG03927.hp1 NA19080.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.995-1666_995-1659d others(10): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882613 | |||||
chr7:37882615
|
G | A | 1 | a0002c0009t0001g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.995-1688G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882615 | ||||||
chr7:37882615
|
GAAAGAA | G | 12 | a0001c0001t0001g0175a0001c0001t0003g0005a0001c0001t0003g0027others(9): Show | 15 | HG00099.hp1 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.995-1686_995-1681d others(8): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882615 | |||||
chr7:37882616
|
A | AG | 3 | a0001c0001t0003g0085a0001c0004t0004g0267a0002c0002t0001g0213 | 3 | HG00735.hp1 HG01123.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.995-1687_995-1686i others(3): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882616 | ||||||
chr7:37882617
|
A | G | 20 | a0001c0001t0001g0107a0001c0001t0003g0087a0001c0001t0004g0253others(17): Show | 23 | HG00738.hp1 HG00738.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.995-1686A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882617 | ||||||
chr7:37882617
|
AAG | A | 5 | a0001c0007t0001g0171a0002c0009t0001g0203a0004c0012t0001g0004others(2): Show | 7 | HG02083.hp2 NA18612.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.995-1684_995-1683d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882617 | |||||
chr7:37882621
|
A | AAG | 3 | a0002c0009t0001g0135a0003c0010t0001g0130a0004c0005t0001g0037 | 3 | HG03017.hp1 NA18951.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.995-1680_995-1679d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882621 | |||||
chr7:37882621
|
A | G | 12 | a0001c0001t0004g0253a0003c0003t0002g0025a0003c0003t0002g0330others(9): Show | 14 | HG00738.hp1 HG00738.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.995-1682A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882621 | ||||||
chr7:37882621
|
AAG | A | 10 | a0001c0007t0001g0013a0001c0007t0001g0067a0001c0007t0007g0078others(7): Show | 11 | HG00423.hp2 HG00609.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.995-1680_995-1679d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882621 | |||||
chr7:37882623
|
G | GAA | 4 | a0001c0007t0001g0068a0002c0020t0001g0202a0003c0010t0001g0122others(1): Show | 4 | HG02523.hp1 NA18945.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-1678_995-1677d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882623 | |||||
chr7:37882629
|
AAG | A | 4 | a0001c0001t0001g0153a0005c0024t0002g0297a0012c0027t0001g0146others(1): Show | 4 | HG00621.hp1 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.995-1672_995-1671d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882629 | |||||
chr7:37882631
|
GAA | G | 3 | a0001c0001t0004g0258a0001c0004t0003g0100a0002c0008t0001g0239 | 3 | HG00423.hp1 NA18986.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.995-1670_995-1669d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882631 | |||||
chr7:37882633
|
AAG | A | 40 | a0001c0001t0001g0063a0001c0001t0001g0116a0001c0001t0001g0156others(37): Show | 50 | HG00280.hp2 HG01106.hp1 HG01169.hp2 others(47): Show |
intron_variant | MODIFIER | c.995-1668_995-1667d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882633 | |||||
chr7:37882635
|
G | A | 1 | a0002c0002t0001g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.995-1668G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882635 | ||||||
chr7:37882639
|
G | A | 131 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(128): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.995-1664G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882639 | ||||||
chr7:37882641
|
A | AAAAG | 5 | a0001c0028t0003g0101a0007c0018t0001g0036a0007c0018t0001g0204others(2): Show | 5 | HG00544.hp1 HG03942.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.995-1661_995-1660i others(6): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882641 | |||||
chr7:37882641
|
A | G | 131 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(128): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.995-1662A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882641 | ||||||
chr7:37882641
|
AAG | A | 51 | a0001c0001t0001g0063a0001c0001t0001g0116a0001c0001t0001g0153others(48): Show | 61 | HG00280.hp2 HG00423.hp1 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.995-1658_995-1657d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882641 | |||||
chr7:37882641
|
AAGAGAAA others(9): Show |
A | 2 | a0002c0002t0001g0021a0002c0002t0001g0238 | 3 | HG02258.hp1 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.995-1658_995-1643d others(18): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882641 | |||||
chr7:37882643
|
G | A | 138 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 150 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.995-1660G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882643 | ||||||
chr7:37882643
|
G | GAAAGAAA others(55): Show |
1 | a0001c0001t0003g0052 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.995-1659_995-1658i others(64): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | |||||
chr7:37882643
|
G | GAAAGAAA others(59): Show |
1 | a0004c0005t0001g0037 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.995-1659_995-1658i others(68): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | |||||
chr7:37882643
|
G | GAAAGAAA others(47): Show |
1 | a0001c0001t0001g0224 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.995-1659_995-1658i others(56): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | |||||
chr7:37882643
|
G | GAAAGAAA others(51): Show |
1 | a0001c0001t0003g0031 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.995-1659_995-1658i others(60): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | |||||
chr7:37882643
|
G | GAAAGAAA others(47): Show |
3 | a0001c0001t0003g0053a0001c0001t0003g0054a0002c0002t0001g0217 | 3 | HG02071.hp2 NA18957.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.995-1659_995-1658i others(56): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | |||||
chr7:37882643
|
G | GAAAGAAA others(43): Show |
6 | a0001c0001t0003g0055a0001c0001t0003g0057a0001c0001t0003g0077others(3): Show | 6 | HG00544.hp2 HG00673.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.995-1659_995-1658i others(52): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | |||||
chr7:37882643
|
G | GAAAGAAA others(39): Show |
4 | a0001c0001t0003g0048a0001c0001t0003g0058a0001c0001t0004g0265others(1): Show | 4 | HG02683.hp1 HG03239.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.995-1659_995-1658i others(48): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | |||||
chr7:37882643
|
G | GAAAGAAA others(35): Show |
5 | a0001c0001t0003g0051a0002c0002t0001g0134a0002c0008t0001g0237others(2): Show | 5 | HG02523.hp2 HG03942.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-1659_995-1658i others(44): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | |||||
chr7:37882643
|
G | GAAAGAAA others(31): Show |
1 | a0001c0001t0003g0056 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.995-1659_995-1658i others(40): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | |||||
chr7:37882643
|
G | GAAAGAGA others(27): Show |
1 | a0002c0002t0001g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.995-1659_995-1658i others(36): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | |||||
chr7:37882655
|
A | G | 2 | a0012c0027t0001g0146a0012c0027t0005g0271 | 2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.995-1648A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882655 | ||||||
chr7:37882657
|
G | A | 2 | a0012c0027t0001g0146a0012c0027t0005g0271 | 2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.995-1646G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882657 | ||||||
chr7:37882724
|
G | T | 1 | a0001c0004t0001g0223 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.995-1579G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882724 | ||||||
chr7:37882931
|
A | C | 1 | a0007c0018t0001g0204 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.995-1372A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882931 | ||||||
chr7:37882942
|
G | A | 2 | a0001c0004t0001g0223a0007c0017t0001g0137 | 2 | NA18942.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.995-1361G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882942 | ||||||
chr7:37882987
|
G | A | 29 | a0001c0001t0001g0224a0001c0001t0003g0031a0001c0001t0003g0048others(26): Show | 31 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.995-1316G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882987 | ||||||
chr7:37883085
|
A | G | 4 | a0002c0002t0001g0021a0002c0002t0001g0235a0002c0002t0001g0236others(1): Show | 5 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-1218A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883085 | ||||||
chr7:37883199
|
G | A | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-1104G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883199 | ||||||
chr7:37883205
|
A | G | 1 | a0002c0009t0001g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.995-1098A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883205 | ||||||
chr7:37883284
|
T | G | 1 | a0001c0004t0001g0118 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.995-1019T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883284 | ||||||
chr7:37883330
|
T | A | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-973T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883330 | ||||||
chr7:37883376
|
T | G | 1 | a0001c0001t0003g0085 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.995-927T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883376 | ||||||
chr7:37883408
|
C | A | 1 | a0001c0001t0004g0265 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.995-895C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883408 | ||||||
chr7:37883438
|
A | C | 1 | a0001c0004t0001g0105 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.995-865A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883438 | ||||||
chr7:37883496
|
C | T | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-807C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883496 | ||||||
chr7:37883673
|
C | T | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-630C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883673 | ||||||
chr7:37883892
|
G | A | 3 | a0001c0007t0001g0039a0001c0007t0001g0120a0001c0028t0001g0038 | 3 | NA19001.hp2 NA19065.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.995-411G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883892 | ||||||
chr7:37883909
|
A | T | 29 | a0001c0007t0001g0033a0001c0007t0001g0039a0001c0007t0001g0061others(26): Show | 33 | HG01074.hp1 HG01109.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.995-394A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883909 | ||||||
chr7:37883917
|
C | T | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-386C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883917 | ||||||
chr7:37883962
|
T | TAC | 76 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0063others(73): Show | 81 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.995-318_995-317dup others(2): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37883962 | |||||
chr7:37883962
|
T | TACAC | 4 | a0001c0001t0001g0167a0002c0002t0001g0217a0002c0002t0001g0219others(1): Show | 4 | HG00280.hp1 HG01081.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-320_995-317dup others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37883962 | |||||
chr7:37883983
|
ACACC | A | 30 | a0001c0007t0001g0013a0001c0007t0001g0067a0001c0007t0001g0068others(27): Show | 34 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.995-316_995-313del others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37883983 | |||||
chr7:37883985
|
A | C | 1 | a0002c0008t0001g0214 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.995-318A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883985 | ||||||
chr7:37883985
|
ACC | A | 4 | a0003c0010t0002g0332a0003c0010t0002g0333a0003c0010t0002g0334others(1): Show | 4 | HG02809.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-316_995-315del others(2): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37883985 | |||||
chr7:37883987
|
C | A | 189 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(186): Show | 212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.995-316C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883987 | ||||||
chr7:37884247
|
G | A | 214 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(211): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.995-56G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37884247 | ||||||
chr7:37884739
|
G | A | 1 | a0003c0015t0002g0351 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1139+292G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 13/17 | chr7 | 37884739 | ||||||
chr7:37885053
|
T | C | 4 | a0002c0002t0001g0021a0002c0002t0001g0235a0002c0002t0001g0236others(1): Show | 5 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1140-92T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 13/17 | chr7 | 37885053 | ||||||
chr7:37885135
|
T | G | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1140-10T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 13/17 | chr7 | 37885135 | ||||||
chr7:37885277
|
A | G | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1247+25A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37885277 | ||||||
chr7:37885286
|
C | T | 32 | a0001c0007t0001g0013a0001c0007t0001g0067a0001c0007t0001g0068others(29): Show | 36 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1247+34C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37885286 | ||||||
chr7:37885339
|
C | G | 1 | a0003c0003t0002g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1247+87C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37885339 | ||||||
chr7:37885472
|
T | A | 1 | a0015c0032t0001g0131 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1247+220T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37885472 | ||||||
chr7:37885534
|
C | T | 1 | a0001c0004t0004g0267 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1247+282C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37885534 | ||||||
chr7:37885653
|
C | T | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1247+401C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37885653 | ||||||
chr7:37885836
|
T | C | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1247+584T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37885836 | ||||||
chr7:37885982
|
A | G | 2 | a0003c0010t0002g0333a0003c0010t0002g0334 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1247+730A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37885982 | ||||||
chr7:37886046
|
A | G | 32 | a0001c0007t0001g0033a0001c0007t0001g0039a0001c0007t0001g0061others(29): Show | 36 | HG01074.hp1 HG01109.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.1247+794A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37886046 | ||||||
chr7:37886328
|
C | T | 3 | a0003c0010t0001g0247a0003c0023t0001g0245a0003c0023t0001g0246 | 3 | HG02280.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1247+1076C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37886328 | ||||||
chr7:37886400
|
A | G | 1 | a0005c0006t0002g0287 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1247+1148A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37886400 | ||||||
chr7:37886491
|
C | T | 346 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(343): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.1247+1239C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37886491 | ||||||
chr7:37886709
|
G | A | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1247+1457G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37886709 | ||||||
chr7:37886862
|
C | CA | 124 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(121): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.1248-1405dupA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 37886862 | |||||
chr7:37886913
|
T | C | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1248-1364T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37886913 | ||||||
chr7:37887116
|
A | G | 1 | a0001c0001t0004g0263 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1248-1161A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887116 | ||||||
chr7:37887156
|
A | C | 119 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(116): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1248-1121A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887156 | ||||||
chr7:37887520
|
G | T | 1 | a0005c0006t0002g0286 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1248-757G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887520 | ||||||
chr7:37887657
|
G | C | 1 | a0001c0007t0007g0078 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1248-620G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887657 | ||||||
chr7:37887786
|
C | G | 1 | a0005c0019t0002g0304 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1248-491C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887786 | ||||||
chr7:37887887
|
A | G | 4 | a0003c0010t0002g0332a0003c0010t0002g0333a0003c0010t0002g0334others(1): Show | 4 | HG02809.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1248-390A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887887 | ||||||
chr7:37887946
|
A | G | 2 | a0004c0005t0001g0178a0006c0011t0002g0283 | 2 | HG00099.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1248-331A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887946 | ||||||
chr7:37887948
|
G | C | 52 | a0001c0001t0001g0028a0001c0001t0001g0079a0001c0001t0001g0093others(49): Show | 53 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1248-329G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887948 | ||||||
chr7:37887980
|
C | T | 41 | a0001c0001t0001g0012a0001c0001t0001g0159a0001c0001t0001g0175others(38): Show | 48 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1248-297C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887980 | ||||||
chr7:37887996
|
G | A | 1 | a0001c0001t0003g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1248-281G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887996 | ||||||
chr7:37888007
|
A | G | 1 | a0003c0010t0002g0328 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1248-270A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37888007 | ||||||
chr7:37888100
|
G | A | 185 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(182): Show | 206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1248-177G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37888100 | ||||||
chr7:37888138
|
T | C | 1 | a0006c0016t0002g0296 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1248-139T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37888138 | ||||||
chr7:37888177
|
T | G | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1248-100T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37888177 | ||||||
chr7:37888249
|
G | A | 1 | a0007c0017t0001g0137 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1248-28G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37888249 | ||||||
chr7:37888740
|
G | A | 1 | a0008c0013t0002g0313 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1399+312G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37888740 | ||||||
chr7:37888942
|
A | G | 5 | a0001c0001t0006g0150a0001c0001t0006g0151a0002c0009t0001g0186others(2): Show | 5 | HG00280.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1399+514A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37888942 | ||||||
chr7:37889102
|
C | T | 2 | a0003c0003t0002g0315a0003c0003t0002g0316 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1399+674C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889102 | ||||||
chr7:37889257
|
T | A | 1 | a0001c0001t0001g0149 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1399+829T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889257 | ||||||
chr7:37889346
|
C | G | 28 | a0001c0001t0001g0224a0001c0001t0003g0048a0001c0001t0003g0051others(25): Show | 30 | HG00544.hp2 HG00673.hp1 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.1399+918C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889346 | ||||||
chr7:37889371
|
G | A | 1 | a0003c0015t0002g0351 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1399+943G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889371 | ||||||
chr7:37889452
|
C | A | 215 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(212): Show | 238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1399+1024C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889452 | ||||||
chr7:37889685
|
AG | A | 8 | a0001c0001t0001g0012a0001c0001t0003g0005a0001c0001t0003g0027others(5): Show | 12 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1399+1258delG | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889685 | ||||||
chr7:37889717
|
G | T | 1 | a0002c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1399+1289G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889717 | ||||||
chr7:37889844
|
G | T | 2 | a0012c0027t0001g0146a0012c0027t0005g0271 | 2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1399+1416G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889844 | ||||||
chr7:37889948
|
AT | A | 73 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0035others(70): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1399+1524delT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 37889948 | |||||
chr7:37889966
|
T | G | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1399+1538T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889966 | ||||||
chr7:37890087
|
T | C | 1 | a0007c0018t0001g0204 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1399+1659T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890087 | ||||||
chr7:37890092
|
T | G | 24 | a0001c0001t0001g0015a0001c0007t0001g0033a0001c0007t0001g0039others(21): Show | 29 | HG00140.hp2 HG01074.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.1399+1664T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890092 | ||||||
chr7:37890250
|
A | G | 2 | a0003c0023t0001g0245a0003c0023t0001g0246 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1399+1822A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890250 | ||||||
chr7:37890298
|
G | A | 1 | a0003c0015t0002g0351 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1399+1870G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890298 | ||||||
chr7:37890491
|
C | T | 3 | a0001c0007t0001g0039a0001c0007t0001g0120a0001c0028t0001g0038 | 3 | NA19001.hp2 NA19065.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1399+2063C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890491 | ||||||
chr7:37890610
|
C | A | 66 | a0001c0001t0001g0015a0001c0007t0001g0013a0001c0007t0001g0033others(63): Show | 75 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.1399+2182C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890610 | ||||||
chr7:37890772
|
G | A | 41 | a0001c0001t0001g0012a0001c0001t0001g0159a0001c0001t0001g0175others(38): Show | 48 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1399+2344G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890772 | ||||||
chr7:37890802
|
A | G | 30 | a0001c0001t0001g0224a0001c0001t0003g0048a0001c0001t0003g0051others(27): Show | 32 | HG00544.hp2 HG00673.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1399+2374A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890802 | ||||||
chr7:37890839
|
A | G | 2 | a0001c0001t0006g0150a0001c0001t0006g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1399+2411A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890839 | ||||||
chr7:37890864
|
T | C | 1 | a0002c0009t0001g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1399+2436T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890864 | ||||||
chr7:37890938
|
A | G | 1 | a0002c0020t0001g0196 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1399+2510A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890938 | ||||||
chr7:37891027
|
T | G | 2 | a0001c0001t0006g0150a0001c0001t0006g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1399+2599T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891027 | ||||||
chr7:37891145
|
A | G | 1 | a0002c0002t0001g0206 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1399+2717A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891145 | ||||||
chr7:37891166
|
A | G | 1 | a0005c0014t0002g0303 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1399+2738A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891166 | ||||||
chr7:37891207
|
T | C | 1 | a0002c0002t0001g0205 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1399+2779T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891207 | ||||||
chr7:37891228
|
T | C | 5 | a0002c0009t0001g0001a0002c0009t0001g0215a0002c0009t0001g0230others(2): Show | 9 | HG02040.hp1 NA18954.hp1 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.1399+2800T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891228 | ||||||
chr7:37891323
|
A | T | 1 | a0001c0001t0001g0166 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1399+2895A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891323 | ||||||
chr7:37891405
|
C | T | 216 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1399+2977C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891405 | ||||||
chr7:37891493
|
C | G | 1 | a0002c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1400-2973C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891493 | ||||||
chr7:37891736
|
A | G | 3 | a0003c0010t0001g0247a0003c0023t0001g0245a0003c0023t0001g0246 | 3 | HG02280.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1400-2730A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891736 | ||||||
chr7:37891754
|
T | C | 289 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(286): Show | 315 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1400-2712T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891754 | ||||||
chr7:37891879
|
A | G | 30 | a0001c0001t0001g0224a0001c0001t0003g0048a0001c0001t0003g0051others(27): Show | 32 | HG00544.hp2 HG00673.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1400-2587A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891879 | ||||||
chr7:37891930
|
A | G | 2 | a0001c0001t0006g0150a0001c0001t0006g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1400-2536A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891930 | ||||||
chr7:37891934
|
TC | T | 33 | a0001c0001t0001g0015a0001c0007t0001g0033a0001c0007t0001g0039others(30): Show | 38 | HG00140.hp2 HG01074.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1400-2530delC | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 37891934 | |||||
chr7:37891959
|
T | A | 1 | a0005c0006t0002g0287 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1400-2507T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891959 | ||||||
chr7:37892184
|
T | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(13): Show | 19 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1400-2282T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892184 | ||||||
chr7:37892247
|
T | G | 214 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(211): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1400-2219T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892247 | ||||||
chr7:37892387
|
T | C | 1 | a0001c0001t0003g0109 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1400-2079T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892387 | ||||||
chr7:37892568
|
A | C | 1 | a0001c0001t0001g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1400-1898A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892568 | ||||||
chr7:37892593
|
T | A | 1 | a0007c0018t0001g0204 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1400-1873T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892593 | ||||||
chr7:37892653
|
T | G | 77 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0035others(74): Show | 86 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1400-1813T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892653 | ||||||
chr7:37892844
|
C | T | 1 | a0012c0027t0001g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1400-1622C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892844 | ||||||
chr7:37892845
|
G | A | 30 | a0001c0007t0001g0013a0001c0007t0001g0171a0001c0007t0003g0106others(27): Show | 34 | HG00423.hp2 HG00544.hp1 HG02083.hp2 others(31): Show |
intron_variant | MODIFIER | c.1400-1621G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892845 | ||||||
chr7:37892856
|
T | TG | 9 | a0001c0001t0001g0070a0001c0001t0003g0031a0001c0001t0004g0003others(6): Show | 12 | HG00597.hp2 HG02615.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.1400-1603dupG | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 37892856 | |||||
chr7:37892858
|
G | A | 1 | a0001c0001t0006g0151 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1400-1608G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892858 | ||||||
chr7:37892888
|
G | T | 206 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(203): Show | 228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1400-1578G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892888 | ||||||
chr7:37892942
|
G | A | 24 | a0001c0001t0001g0224a0001c0001t0003g0048a0001c0001t0003g0051others(21): Show | 26 | HG00280.hp1 HG01346.hp1 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.1400-1524G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892942 | ||||||
chr7:37893097
|
A | C | 41 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0064others(38): Show | 44 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1400-1369A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893097 | ||||||
chr7:37893140
|
T | C | 1 | a0007c0017t0001g0197 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1400-1326T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893140 | ||||||
chr7:37893221
|
G | C | 292 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(289): Show | 317 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.1400-1245G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893221 | ||||||
chr7:37893286
|
G | A | 210 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0032others(207): Show | 231 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1400-1180G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893286 | ||||||
chr7:37893388
|
A | G | 1 | a0001c0007t0007g0078 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1400-1078A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893388 | ||||||
chr7:37893420
|
A | G | 3 | a0003c0010t0002g0317a0003c0010t0002g0319a0014c0033t0002g0318 | 3 | HG02258.hp2 HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1400-1046A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893420 | ||||||
chr7:37893457
|
T | G | 116 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0028others(113): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1400-1009T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893457 | ||||||
chr7:37893551
|
C | A | 268 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(265): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1400-915C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893551 | ||||||
chr7:37893695
|
T | C | 2 | a0001c0001t0004g0177a0007c0017t0001g0232 | 2 | HG01975.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1400-771T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893695 | ||||||
chr7:37893895
|
G | A | 1 | a0003c0010t0002g0335 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1400-571G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893895 | ||||||
chr7:37893949
|
C | T | 2 | a0012c0027t0001g0146a0019c0034t0001g0112 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1400-517C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893949 | ||||||
chr7:37894005
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1400-461A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37894005 | ||||||
chr7:37894038
|
G | C | 40 | a0001c0001t0001g0063a0001c0001t0003g0081a0001c0001t0003g0085others(37): Show | 41 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1400-428G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37894038 | ||||||
chr7:37894065
|
C | T | 24 | a0001c0001t0001g0111a0001c0001t0001g0167a0001c0001t0001g0224others(21): Show | 24 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1400-401C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37894065 | ||||||
chr7:37894332
|
G | A | 1 | a0003c0003t0002g0322 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1400-134G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37894332 | ||||||
chr7:37894381
|
C | G | 241 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(238): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1400-85C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37894381 | ||||||
chr7:37894632
|
G | A | 237 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(234): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1544+22G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894632 | ||||||
chr7:37894718
|
A | C | 27 | a0001c0001t0001g0093a0001c0001t0001g0116a0001c0001t0003g0029others(24): Show | 31 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1544+108A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894718 | ||||||
chr7:37894730
|
T | G | 1 | a0009c0031t0001g0125 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1544+120T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894730 | ||||||
chr7:37894794
|
T | G | 6 | a0001c0001t0001g0012a0001c0001t0003g0005a0001c0001t0003g0027others(3): Show | 9 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1544+184T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894794 | ||||||
chr7:37894800
|
A | C | 342 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(339): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1544+190A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894800 | ||||||
chr7:37894855
|
T | C | 25 | a0001c0001t0001g0111a0001c0001t0001g0167a0001c0001t0001g0224others(22): Show | 26 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1544+245T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894855 | ||||||
chr7:37894863
|
T | C | 28 | a0001c0001t0001g0093a0001c0001t0001g0116a0001c0001t0003g0029others(25): Show | 32 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1544+253T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894863 | ||||||
chr7:37894863
|
TCCTTC | T | 3 | a0001c0007t0001g0187a0001c0007t0001g0188a0002c0009t0001g0135 | 3 | HG02976.hp2 HG03017.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1544+268_1544+272d others(7): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 37894863 | |||||
chr7:37894950
|
T | G | 1 | a0005c0006t0002g0285 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1544+340T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894950 | ||||||
chr7:37894980
|
C | T | 66 | a0001c0001t0001g0063a0001c0004t0001g0080a0001c0004t0001g0091others(63): Show | 68 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1544+370C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894980 | ||||||
chr7:37894987
|
A | G | 18 | a0001c0001t0001g0111a0001c0001t0001g0167a0001c0001t0001g0224others(15): Show | 18 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1544+377A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894987 | ||||||
chr7:37895071
|
A | G | 102 | a0001c0001t0001g0015a0001c0001t0001g0063a0001c0001t0001g0070others(99): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1544+461A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895071 | ||||||
chr7:37895190
|
A | G | 14 | a0004c0005t0001g0059a0004c0005t0001g0155a0004c0005t0001g0169others(11): Show | 16 | HG00099.hp2 HG00423.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1544+580A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895190 | ||||||
chr7:37895212
|
C | T | 1 | a0002c0002t0001g0227 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1544+602C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895212 | ||||||
chr7:37895294
|
A | C | 5 | a0001c0001t0001g0173a0001c0007t0001g0187a0001c0007t0001g0188others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1544+684A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895294 | ||||||
chr7:37895339
|
G | A | 18 | a0001c0001t0001g0111a0001c0001t0001g0167a0001c0001t0001g0224others(15): Show | 18 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1544+729G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895339 | ||||||
chr7:37895366
|
T | G | 67 | a0001c0001t0001g0063a0001c0004t0001g0080a0001c0004t0001g0091others(64): Show | 69 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1544+756T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895366 | ||||||
chr7:37895402
|
T | C | 4 | a0002c0002t0001g0021a0002c0002t0001g0235a0002c0002t0001g0236others(1): Show | 5 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1544+792T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895402 | ||||||
chr7:37895477
|
T | C | 1 | a0003c0003t0008g0320 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1544+867T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895477 | ||||||
chr7:37895504
|
C | A | 65 | a0001c0004t0001g0080a0001c0004t0001g0091a0001c0004t0001g0092others(62): Show | 67 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1544+894C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895504 | ||||||
chr7:37895548
|
G | A | 3 | a0001c0004t0003g0096a0001c0004t0003g0108a0001c0004t0004g0267 | 3 | HG00323.hp1 HG01123.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1544+938G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895548 | ||||||
chr7:37895572
|
A | G | 4 | a0002c0002t0001g0021a0002c0002t0001g0235a0002c0002t0001g0236others(1): Show | 5 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1544+962A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895572 | ||||||
chr7:37895610
|
A | G | 2 | a0010c0021t0002g0346a0010c0021t0002g0347 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1544+1000A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895610 | ||||||
chr7:37895646
|
C | T | 6 | a0001c0001t0004g0006a0001c0007t0001g0061a0002c0009t0001g0231others(3): Show | 8 | HG01074.hp1 HG01192.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1544+1036C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895646 | ||||||
chr7:37895681
|
C | T | 1 | a0001c0007t0001g0120 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1544+1071C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895681 | ||||||
chr7:37895875
|
C | T | 313 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(310): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1545-995C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895875 | ||||||
chr7:37895892
|
A | C | 1 | a0006c0011t0002g0301 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1545-978A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895892 | ||||||
chr7:37895909
|
G | C | 35 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0114others(32): Show | 42 | HG00140.hp2 HG00639.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1545-961G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895909 | ||||||
chr7:37895965
|
A | G | 313 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(310): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1545-905A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895965 | ||||||
chr7:37896052
|
CGT | C | 4 | a0001c0007t0001g0039a0003c0010t0001g0124a0003c0010t0001g0130others(1): Show | 4 | NA18952.hp2 NA18954.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1545-813_1545-812d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 37896052 | |||||
chr7:37896053
|
G | A | 23 | a0001c0001t0001g0093a0001c0001t0001g0116a0001c0001t0003g0029others(20): Show | 27 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.1545-817G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896053 | ||||||
chr7:37896068
|
G | A | 35 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0114others(32): Show | 42 | HG00140.hp2 HG00639.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1545-802G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896068 | ||||||
chr7:37896093
|
G | A | 313 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(310): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1545-777G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896093 | ||||||
chr7:37896095
|
C | T | 1 | a0001c0004t0001g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1545-775C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896095 | ||||||
chr7:37896128
|
T | G | 67 | a0001c0001t0001g0063a0001c0004t0001g0080a0001c0004t0001g0091others(64): Show | 69 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1545-742T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896128 | ||||||
chr7:37896188
|
G | T | 313 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(310): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1545-682G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896188 | ||||||
chr7:37896383
|
G | GAA | 179 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0040others(176): Show | 189 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1545-486_1545-485i others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 37896383 | |||||
chr7:37896447
|
G | A | 4 | a0003c0010t0002g0332a0003c0010t0002g0333a0003c0010t0002g0334others(1): Show | 4 | HG02809.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1545-423G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896447 | ||||||
chr7:37896499
|
G | T | 27 | a0001c0001t0001g0093a0001c0001t0001g0116a0001c0001t0003g0029others(24): Show | 31 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1545-371G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896499 | ||||||
chr7:37896684
|
C | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(309): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1545-186C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896684 | ||||||
chr7:37896687
|
C | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(309): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1545-183C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896687 | ||||||
chr7:37896782
|
T | C | 312 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(309): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1545-88T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896782 | ||||||
chr7:37897152
|
A | G | 2 | a0001c0001t0005g0269a0003c0003t0002g0338 | 2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.*15+45A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897152 | ||||||
chr7:37897246
|
A | G | 1 | a0001c0001t0003g0076 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.*15+139A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897246 | ||||||
chr7:37897298
|
C | T | 7 | a0001c0001t0001g0107a0001c0001t0001g0142a0003c0003t0001g0250others(4): Show | 8 | HG02572.hp2 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.*15+191C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897298 | ||||||
chr7:37897431
|
T | C | 65 | a0001c0004t0001g0080a0001c0004t0001g0091a0001c0004t0001g0092others(62): Show | 67 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.*15+324T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897431 | ||||||
chr7:37897512
|
C | T | 4 | a0001c0004t0001g0119a0001c0004t0001g0148a0003c0015t0001g0249others(1): Show | 4 | HG02572.hp1 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.*15+405C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897512 | ||||||
chr7:37897548
|
C | A | 59 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0001g0111others(56): Show | 65 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.*15+441C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897548 | ||||||
chr7:37897572
|
G | A | 226 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(223): Show | 253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.*15+465G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897572 | ||||||
chr7:37897687
|
C | T | 1 | a0019c0034t0001g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.*15+580C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897687 | ||||||
chr7:37897696
|
T | C | 345 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(342): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.*15+589T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897696 | ||||||
chr7:37897706
|
T | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(223): Show | 253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.*15+599T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897706 | ||||||
chr7:37897781
|
T | C | 27 | a0001c0001t0001g0111a0001c0001t0001g0141a0001c0001t0001g0167others(24): Show | 28 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.*15+674T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897781 | ||||||
chr7:37897821
|
T | C | 27 | a0001c0001t0001g0111a0001c0001t0001g0141a0001c0001t0001g0167others(24): Show | 28 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.*15+714T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897821 | ||||||
chr7:37897870
|
T | C | 1 | a0003c0010t0002g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.*15+763T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897870 | ||||||
chr7:37898033
|
A | G | 27 | a0001c0001t0001g0111a0001c0001t0001g0141a0001c0001t0001g0167others(24): Show | 28 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.*15+926A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898033 | ||||||
chr7:37898085
|
C | T | 27 | a0001c0001t0001g0111a0001c0001t0001g0141a0001c0001t0001g0167others(24): Show | 28 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.*15+978C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898085 | ||||||
chr7:37898409
|
A | G | 48 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0079others(45): Show | 55 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.*15+1302A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898409 | ||||||
chr7:37898633
|
A | G | 7 | a0001c0001t0003g0081a0001c0001t0004g0266a0001c0007t0001g0013others(4): Show | 8 | HG02735.hp1 HG02738.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.*15+1526A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898633 | ||||||
chr7:37898712
|
GGTGAAAT others(7): Show |
G | 1 | a0002c0009t0001g0225 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.*16-1531_*16-1518d others(16): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898712 | ||||||
chr7:37898752
|
C | T | 1 | a0002c0002t0001g0219 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.*16-1492C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898752 | ||||||
chr7:37898770
|
A | T | 1 | a0002c0009t0001g0225 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.*16-1474A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898770 | ||||||
chr7:37898820
|
A | G | 51 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(48): Show | 61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.*16-1424A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898820 | ||||||
chr7:37898836
|
T | C | 26 | a0001c0001t0001g0111a0001c0001t0001g0167a0001c0001t0001g0224others(23): Show | 27 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.*16-1408T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898836 | ||||||
chr7:37898855
|
G | A | 1 | a0003c0003t0001g0128 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.*16-1389G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898855 | ||||||
chr7:37898882
|
A | T | 26 | a0001c0001t0001g0111a0001c0001t0001g0167a0001c0001t0001g0224others(23): Show | 27 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.*16-1362A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898882 | ||||||
chr7:37898895
|
A | T | 1 | a0002c0008t0001g0272 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.*16-1349A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898895 | ||||||
chr7:37899008
|
G | A | 51 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(48): Show | 61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.*16-1236G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899008 | ||||||
chr7:37899035
|
T | G | 26 | a0001c0001t0001g0111a0001c0001t0001g0167a0001c0001t0001g0224others(23): Show | 27 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.*16-1209T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899035 | ||||||
chr7:37899169
|
A | C | 316 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(313): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.*16-1075A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899169 | ||||||
chr7:37899332
|
C | T | 1 | a0002c0009t0001g0194 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.*16-912C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899332 | ||||||
chr7:37899425
|
G | C | 1 | a0001c0001t0007g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.*16-819G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899425 | ||||||
chr7:37899495
|
TG | T | 25 | a0001c0001t0001g0111a0001c0001t0001g0167a0001c0001t0001g0224others(22): Show | 26 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.*16-743delG | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 37899495 | |||||
chr7:37899528
|
G | T | 1 | a0002c0009t0001g0225 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.*16-716G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899528 | ||||||
chr7:37899537
|
G | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0079 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.*16-707G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899537 | ||||||
chr7:37899637
|
A | G | 26 | a0001c0001t0001g0093a0001c0001t0001g0116a0001c0001t0003g0029others(23): Show | 30 | HG00544.hp2 HG00597.hp2 HG02083.hp1 others(27): Show |
intron_variant | MODIFIER | c.*16-607A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899637 | ||||||
chr7:37899763
|
G | A | 26 | a0001c0001t0001g0111a0001c0001t0001g0167a0001c0001t0001g0224others(23): Show | 27 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.*16-481G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899763 | ||||||
chr7:37899802
|
A | T | 1 | a0006c0016t0002g0296 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.*16-442A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899802 | ||||||
chr7:37899862
|
T | C | 26 | a0001c0001t0001g0111a0001c0001t0001g0167a0001c0001t0001g0224others(23): Show | 27 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.*16-382T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899862 | ||||||
chr7:37899990
|
G | A | 1 | a0001c0007t0001g0190 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.*16-254G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899990 | ||||||
chr7:37900102
|
G | T | 1 | a0019c0034t0001g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.*16-142G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37900102 | ||||||
chr7:37900126
|
C | T | 1 | a0019c0034t0001g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.*16-118C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37900126 | ||||||
chr7:37900128
|
C | T | 1 | a0002c0002t0001g0213 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.*16-116C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37900128 | ||||||
chr7:37900182
|
G | A | 26 | a0001c0001t0001g0111a0001c0001t0001g0167a0001c0001t0001g0224others(23): Show | 27 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.*16-62G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37900182 | ||||||
chr7:37900201
|
G | T | 4 | a0001c0004t0003g0050a0002c0008t0001g0018a0002c0008t0001g0272others(1): Show | 5 | HG00558.hp1 HG02071.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.*16-43G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37900201 | ||||||
chr7:37900212
|
T | A | 1 | a0009c0022t0002g0331 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*16-32T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37900212 | ||||||
chr7:37900238
|
T | C | 52 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(49): Show | 62 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(59): Show |
splice_region_variant&intron_variant | LOW | c.*16-6T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37900238 |