geneid | 728841 |
---|---|
ensemblid | ENSG00000270231.5 |
hgncid | 31990 |
symbol | NBPF8 |
name | NBPF member 8 |
refseq_nuc | NM_001037501.5 |
refseq_prot | NP_001032590.2 |
ensembl_nuc | ENST00000698216.1 |
ensembl_prot | ENSP00000513610.1 |
mane_status | MANE Select |
chr | chr1 |
start | 120415035 |
end | 120469676 |
strand | + |
ver | v1.2 |
region | chr1:120415035-120469676 |
region5000 | chr1:120410035-120474676 |
regionname0 | NBPF8_chr1_120415035_120469676 |
regionname5000 | NBPF8_chr1_120410035_120474676 |
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 | 59 | 87 | 44 | 21 | 8 | 5 | 9 | 6 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002 | 0/0 | 57 | 75 | 5 | 15 | 46 | 3 | 6 | 35 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0003 | 0/0 | 252 | 33 | 13 | 3 | 15 | 0 | 2 | 6 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0004 | 1/1 | 942 | 27 | 0 | 2 | 15 | 0 | 8 | 8 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0005 | 0/0 | 942 | 27 | 3 | 18 | 1 | 1 | 4 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0006 | 0/0 | 252 | 17 | 3 | 0 | 14 | 0 | 0 | 12 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0007 | 0/0 | 942 | 9 | 0 | 2 | 0 | 3 | 4 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0008 | 0/0 | 942 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0009 | 0/0 | 252 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0010 | 0/0 | 671 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0011 | 0/0 | 252 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0012 | 0/0 | 59 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0013 | 0/0 | 73 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0014 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0015 | 0/0 | 942 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0016 | 0/0 | 942 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0017 | 0/0 | 942 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0018 | 0/0 | 252 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0019 | 0/0 | 73 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
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 | 2144 | 56 | 0 | 12 | 36 | 3 | 5 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0002 | 0/0 | 2827 | 46 | 15 | 15 | 4 | 5 | 7 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0003 | 0/0 | 2710 | 28 | 10 | 1 | 15 | 0 | 2 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0004 | 0/0 | 2829 | 26 | 2 | 18 | 1 | 1 | 4 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0005 | 1/0 | 2829 | 25 | 0 | 1 | 15 | 0 | 8 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0006 | 0/0 | 2710 | 17 | 3 | 0 | 14 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0007 | 0/0 | 2708 | 11 | 2 | 5 | 3 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0008 | 0/0 | 2829 | 9 | 0 | 2 | 0 | 3 | 4 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0009 | 0/0 | 2144 | 8 | 0 | 0 | 8 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0010 | 0/0 | 2827 | 8 | 8 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0011 | 0/0 | 2827 | 6 | 6 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0012 | 0/0 | 2710 | 5 | 3 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0013 | 0/0 | 2144 | 4 | 4 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0014 | 0/0 | 2829 | 4 | 4 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0015 | 0/1 | 2829 | 2 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0016 | 0/0 | 2710 | 2 | 0 | 1 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0017 | 0/0 | 2016 | 2 | 0 | 0 | 0 | 0 | 2 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0018 | 0/0 | 2827 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0019 | 0/0 | 2708 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0020 | 0/0 | 2827 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0021 | 0/0 | 2708 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0022 | 0/0 | 2827 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0023 | 0/0 | 2710 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0024 | 0/0 | 2144 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0025 | 0/0 | 2144 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0026 | 0/0 | 2144 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0027 | 0/0 | 2144 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0028 | 0/0 | 2144 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0029 | 0/0 | 2144 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0030 | 0/0 | 2144 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0031 | 0/0 | 2829 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0032 | 0/0 | 2829 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0033 | 0/0 | 2829 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0034 | 0/0 | 2710 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0035 | 0/0 | 2829 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0036 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0037 | 0/0 | 2829 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0038 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0039 | 0/0 | 2827 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0040 | 0/0 | 2717 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0041 | 0/0 | 2827 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0042 | 0/0 | 2827 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0043 | 0/0 | 2708 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0044 | 0/0 | 2827 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
c0045 | 0/0 | 2827 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
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 | 4430 | 40 | 0 | 5 | 30 | 1 | 4 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0002 | 0/0 | 4428 | 34 | 5 | 13 | 2 | 6 | 8 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0003 | 1/1 | 4428 | 25 | 0 | 3 | 15 | 1 | 4 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0004 | 0/0 | 4428 | 23 | 2 | 14 | 1 | 1 | 5 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0005 | 0/0 | 4428 | 17 | 3 | 0 | 14 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0006 | 0/0 | 4430 | 10 | 1 | 1 | 6 | 0 | 2 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0007 | 0/0 | 4428 | 10 | 2 | 4 | 4 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0008 | 0/0 | 4428 | 9 | 8 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0009 | 0/0 | 4430 | 8 | 0 | 7 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0010 | 0/0 | 4430 | 7 | 0 | 0 | 7 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0011 | 0/0 | 4428 | 7 | 0 | 1 | 0 | 3 | 3 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0012 | 0/0 | 4430 | 7 | 0 | 0 | 7 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0013 | 0/0 | 4428 | 6 | 6 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0014 | 0/0 | 4428 | 5 | 5 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0015 | 0/0 | 4428 | 5 | 5 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0016 | 0/0 | 4428 | 5 | 0 | 0 | 0 | 0 | 5 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0017 | 0/0 | 4430 | 4 | 4 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0018 | 0/0 | 4430 | 4 | 4 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0019 | 0/0 | 4428 | 3 | 2 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0020 | 0/0 | 4430 | 2 | 0 | 0 | 1 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0021 | 0/0 | 4428 | 2 | 0 | 1 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0022 | 0/0 | 4432 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0023 | 0/0 | 4428 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0024 | 0/0 | 4428 | 2 | 0 | 0 | 0 | 0 | 2 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0025 | 0/0 | 4428 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0026 | 0/0 | 4430 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0027 | 0/0 | 4430 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0028 | 0/0 | 4428 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0029 | 0/0 | 4428 | 2 | 1 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0030 | 0/0 | 4430 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0031 | 0/0 | 4428 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0032 | 0/0 | 4428 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0033 | 0/0 | 4428 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0034 | 0/0 | 4428 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0035 | 0/0 | 4428 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0036 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0037 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0038 | 0/0 | 4428 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0039 | 0/0 | 4428 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0040 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0041 | 0/0 | 4430 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0042 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0043 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0044 | 0/0 | 4428 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0045 | 0/0 | 4428 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0046 | 0/0 | 4428 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0047 | 0/0 | 4428 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0048 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0049 | 0/0 | 4428 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0050 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0051 | 0/0 | 4432 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0052 | 0/0 | 4428 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0053 | 0/0 | 4428 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0054 | 0/0 | 4428 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0055 | 0/0 | 4428 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0056 | 0/0 | 4428 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0057 | 0/0 | 4428 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0058 | 0/0 | 4428 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0059 | 0/0 | 4428 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0060 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0061 | 0/0 | 4432 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0062 | 0/0 | 4428 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0063 | 0/0 | 4428 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0064 | 0/0 | 4430 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0065 | 0/0 | 4428 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0066 | 0/0 | 4428 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0067 | 0/0 | 4428 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0068 | 0/0 | 4428 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
t0069 | 0/0 | 4428 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
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 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0268 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0278 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 2827 | 46 | 15 | 15 | 4 | 5 | 7 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0007 | 0/0 | 2708 | 11 | 2 | 5 | 3 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0010 | 0/0 | 2827 | 8 | 8 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0011 | 0/0 | 2827 | 6 | 6 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0018 | 0/0 | 2827 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0019 | 0/0 | 2708 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0020 | 0/0 | 2827 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0021 | 0/0 | 2708 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0022 | 0/0 | 2827 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0040 | 0/0 | 2717 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0041 | 0/0 | 2827 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0042 | 0/0 | 2827 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0043 | 0/0 | 2708 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0044 | 0/0 | 2827 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0045 | 0/0 | 2827 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0001 | 0/0 | 2144 | 56 | 0 | 12 | 36 | 3 | 5 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0009 | 0/0 | 2144 | 8 | 0 | 0 | 8 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0013 | 0/0 | 2144 | 4 | 4 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0024 | 0/0 | 2144 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0025 | 0/0 | 2144 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0026 | 0/0 | 2144 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0027 | 0/0 | 2144 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0028 | 0/0 | 2144 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0029 | 0/0 | 2144 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0030 | 0/0 | 2144 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0003c0003 | 0/0 | 2710 | 28 | 10 | 1 | 15 | 0 | 2 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0003c0012 | 0/0 | 2710 | 5 | 3 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0004c0005 | 1/0 | 2829 | 25 | 0 | 1 | 15 | 0 | 8 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0004c0015 | 0/1 | 2829 | 2 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0005c0004 | 0/0 | 2829 | 26 | 2 | 18 | 1 | 1 | 4 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0005c0036 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0006c0006 | 0/0 | 2710 | 17 | 3 | 0 | 14 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0007c0008 | 0/0 | 2829 | 9 | 0 | 2 | 0 | 3 | 4 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0008c0014 | 0/0 | 2829 | 4 | 4 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0009c0016 | 0/0 | 2710 | 2 | 0 | 1 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0010c0017 | 0/0 | 2016 | 2 | 0 | 0 | 0 | 0 | 2 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0011c0023 | 0/0 | 2710 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0012c0039 | 0/0 | 2827 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0013c0037 | 0/0 | 2829 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0014c0033 | 0/0 | 2829 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0015c0032 | 0/0 | 2829 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0016c0031 | 0/0 | 2829 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0017c0035 | 0/0 | 2829 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0018c0034 | 0/0 | 2710 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0019c0038 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002 | 0/0 | 7254 | 30 | 4 | 12 | 2 | 5 | 7 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0002t0008 | 0/0 | 7254 | 8 | 7 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0002t0028 | 0/0 | 7254 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0002t0029 | 0/0 | 7254 | 2 | 1 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0002t0031 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0002t0052 | 0/0 | 7254 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0002t0053 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0002t0056 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0007t0007 | 0/0 | 7135 | 7 | 0 | 4 | 3 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0007t0019 | 0/0 | 7135 | 3 | 2 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0007t0057 | 0/0 | 7135 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0010t0032 | 0/0 | 7254 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0010t0058 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0010t0059 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0010t0060 | 0/0 | 7256 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0010t0061 | 0/0 | 7258 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0010t0062 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0010t0063 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0011t0008 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0011t0015 | 0/0 | 7254 | 5 | 5 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0018t0018 | 0/0 | 7256 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0019t0054 | 0/0 | 7135 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0019t0055 | 0/0 | 7135 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0020t0030 | 0/0 | 7256 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0021t0018 | 0/0 | 7137 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0022t0007 | 0/0 | 7254 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0040t0002 | 0/0 | 7144 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0041t0002 | 0/0 | 7254 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0042t0002 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0043t0007 | 0/0 | 7135 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0044t0031 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0001c0045t0065 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0001t0001 | 0/0 | 6573 | 30 | 0 | 4 | 22 | 1 | 3 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0001t0009 | 0/0 | 6573 | 7 | 0 | 6 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0001t0010 | 0/0 | 6573 | 5 | 0 | 0 | 5 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0001t0020 | 0/0 | 6573 | 2 | 0 | 0 | 1 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0001t0021 | 0/0 | 6571 | 2 | 0 | 1 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0001t0022 | 0/0 | 6575 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0001t0036 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0001t0038 | 0/0 | 6571 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0001t0039 | 0/0 | 6571 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0001t0040 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0001t0041 | 0/0 | 6573 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0001t0042 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0001t0043 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0001t0064 | 0/0 | 6573 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0009t0001 | 0/0 | 6573 | 7 | 0 | 0 | 7 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0009t0037 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0013t0014 | 0/0 | 6571 | 4 | 4 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0024t0044 | 0/0 | 6571 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0025t0001 | 0/0 | 6573 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0026t0001 | 0/0 | 6573 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0027t0001 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0028t0014 | 0/0 | 6571 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0029t0010 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0002c0030t0009 | 0/0 | 6573 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0003c0003t0006 | 0/0 | 7139 | 10 | 1 | 1 | 6 | 0 | 2 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0003c0003t0012 | 0/0 | 7139 | 7 | 0 | 0 | 7 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0003c0003t0013 | 0/0 | 7137 | 6 | 6 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0003c0003t0047 | 0/0 | 7137 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0003c0003t0048 | 0/0 | 7139 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0003c0003t0049 | 0/0 | 7137 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0003c0003t0050 | 0/0 | 7139 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0003c0003t0051 | 0/0 | 7141 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0003c0012t0026 | 0/0 | 7139 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0003c0012t0027 | 0/0 | 7139 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0003c0012t0046 | 0/0 | 7137 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0004c0005t0003 | 1/0 | 7256 | 17 | 0 | 1 | 13 | 0 | 2 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0004c0005t0016 | 0/0 | 7256 | 5 | 0 | 0 | 0 | 0 | 5 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0004c0005t0066 | 0/0 | 7256 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0004c0005t0067 | 0/0 | 7256 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0004c0005t0069 | 0/0 | 7256 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0004c0015t0003 | 0/1 | 7256 | 2 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0005c0004t0004 | 0/0 | 7256 | 20 | 2 | 14 | 1 | 1 | 2 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0005c0004t0011 | 0/0 | 7256 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0005c0004t0023 | 0/0 | 7256 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0005c0004t0024 | 0/0 | 7256 | 2 | 0 | 0 | 0 | 0 | 2 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0005c0004t0033 | 0/0 | 7256 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0005c0036t0005 | 0/0 | 7256 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0006c0006t0005 | 0/0 | 7137 | 16 | 2 | 0 | 14 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0006c0006t0035 | 0/0 | 7137 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0007c0008t0011 | 0/0 | 7256 | 6 | 0 | 0 | 0 | 3 | 3 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0007c0008t0025 | 0/0 | 7256 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0007c0008t0045 | 0/0 | 7256 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0008c0014t0017 | 0/0 | 7258 | 4 | 4 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0009c0016t0003 | 0/0 | 7137 | 2 | 0 | 1 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0010c0017t0004 | 0/0 | 6443 | 2 | 0 | 0 | 0 | 0 | 2 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0011c0023t0010 | 0/0 | 7139 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0012c0039t0002 | 0/0 | 7254 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0013c0037t0068 | 0/0 | 7256 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0014c0033t0003 | 0/0 | 7256 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0015c0032t0003 | 0/0 | 7256 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0016c0031t0003 | 0/0 | 7256 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0017c0035t0004 | 0/0 | 7256 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0018c0034t0034 | 0/0 | 7137 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
a0019c0038t0003 | 0/0 | 6600 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | copy fasta | chr1 | 120410035 | 120474676 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0008g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0008g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0008g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0008g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0028g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0028g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0029g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0029g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0031g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0052g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0053g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0002t0056g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0007t0007g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0007t0007g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0007t0007g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0007t0007g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0007t0007g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0007t0007g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0007t0019g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0007t0019g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0007t0019g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0007t0057g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0010t0032g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0010t0032g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0010t0058g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0010t0059g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0010t0060g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0010t0061g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0010t0062g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0010t0063g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0011t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0011t0015g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0011t0015g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0011t0015g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0011t0015g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0011t0015g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0018t0018g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0018t0018g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0019t0054g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0019t0055g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0020t0030g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0020t0030g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0021t0018g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0021t0018g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0022t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0022t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0040t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0041t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0042t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0043t0007g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0044t0031g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0001c0045t0065g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0009g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0009g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0009g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0009g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0009g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0009g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0010g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0010g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0010g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0010g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0010g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0020g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0020g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0021g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0021g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0022g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0022g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0036g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0038g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0039g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0040g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0041g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0042g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0043g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0001t0064g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0009t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0009t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0009t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0009t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0009t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0009t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0009t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0009t0037g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0013t0014g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0013t0014g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0013t0014g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0013t0014g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0024t0044g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0025t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0026t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0027t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0028t0014g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0029t0010g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0002c0030t0009g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0006g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0006g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0006g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0012g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0012g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0012g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0012g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0012g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0012g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0013g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0013g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0013g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0013g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0013g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0013g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0047g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0048g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0049g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0050g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0003t0051g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0012t0026g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0012t0026g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0012t0027g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0012t0027g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0003c0012t0046g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0003g0278 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0016g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0016g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0016g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0016g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0066g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0067g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0005t0069g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0015t0003g0268 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0004c0015t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0011g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0023g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0023g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0024g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0024g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0004t0033g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0005c0036t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0006c0006t0005g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0006c0006t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0006c0006t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0006c0006t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0006c0006t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0006c0006t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0006c0006t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0006c0006t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0006c0006t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0006c0006t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0006c0006t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0006c0006t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0006c0006t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0006c0006t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0006c0006t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0006c0006t0035g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0007c0008t0011g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0007c0008t0011g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0007c0008t0011g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0007c0008t0011g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0007c0008t0011g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0007c0008t0011g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0007c0008t0025g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0007c0008t0025g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0007c0008t0045g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0008c0014t0017g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0008c0014t0017g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0008c0014t0017g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0008c0014t0017g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0009c0016t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0009c0016t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0010c0017t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0010c0017t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0011c0023t0010g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0012c0039t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0013c0037t0068g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0014c0033t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0015c0032t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0016c0031t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0017c0035t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0018c0034t0034g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
a0019c0038t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0007 | c0008 | t0011 | g0239 | EUR | GBR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0029 | EUR | GBR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0026 | EUR | GBR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00140 | hp2 | a0016 | c0031 | t0003 | g0253 | EUR | GBR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0032 | EUR | FIN | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00280 | hp2 | a0002 | c0001 | t0064 | g0162 | EUR | FIN | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00323 | hp1 | a0005 | c0004 | t0004 | g0237 | EUR | FIN | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0047 | EUR | FIN | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00408 | hp1 | a0004 | c0005 | t0003 | g0271 | EAS | CHS | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00408 | hp2 | a0002 | c0001 | t0001 | g0171 | EAS | CHS | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | CHS | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00544 | hp2 | a0003 | c0003 | t0012 | g0189 | EAS | CHS | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00609 | hp1 | a0002 | c0001 | t0001 | g0167 | EAS | CHS | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | CHS | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00639 | hp1 | a0005 | c0004 | t0004 | g0282 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00639 | hp2 | a0005 | c0004 | t0004 | g0231 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00642 | hp1 | a0005 | c0004 | t0004 | g0233 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00642 | hp2 | a0001 | c0007 | t0007 | g0091 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00673 | hp1 | a0002 | c0001 | t0001 | g0150 | EAS | CHS | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00673 | hp2 | a0002 | c0029 | t0010 | g0149 | EAS | CHS | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00735 | hp1 | a0004 | c0005 | t0003 | g0256 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00738 | hp1 | a0002 | c0001 | t0001 | g0122 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0019 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00741 | hp1 | a0005 | c0004 | t0033 | g0240 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG00741 | hp2 | a0002 | c0001 | t0001 | g0168 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01069 | hp1 | a0001 | c0007 | t0007 | g0003 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01069 | hp2 | a0005 | c0004 | t0004 | g0008 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01070 | hp1 | a0001 | c0007 | t0007 | g0003 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01070 | hp2 | a0007 | c0008 | t0025 | g0236 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01071 | hp1 | a0005 | c0004 | t0004 | g0008 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01071 | hp2 | a0001 | c0007 | t0007 | g0093 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01074 | hp1 | a0007 | c0008 | t0025 | g0222 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01074 | hp2 | a0002 | c0001 | t0001 | g0155 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01099 | hp1 | a0005 | c0004 | t0023 | g0215 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0030 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01106 | hp1 | a0005 | c0004 | t0011 | g0130 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01109 | hp1 | a0002 | c0024 | t0044 | g0176 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01109 | hp2 | a0005 | c0004 | t0023 | g0216 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01167 | hp1 | a0001 | c0041 | t0002 | g0025 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01167 | hp2 | a0002 | c0001 | t0009 | g0009 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01169 | hp1 | a0002 | c0001 | t0009 | g0009 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01175 | hp1 | a0002 | c0001 | t0021 | g0152 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01175 | hp2 | a0001 | c0002 | t0008 | g0054 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0027 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01192 | hp2 | a0005 | c0004 | t0004 | g0007 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01243 | hp1 | a0002 | c0001 | t0009 | g0156 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01255 | hp1 | a0005 | c0004 | t0004 | g0241 | AMR | CLM | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01258 | hp1 | a0002 | c0001 | t0009 | g0120 | AMR | CLM | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01258 | hp2 | a0001 | c0002 | t0052 | g0018 | AMR | CLM | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0044 | AMR | CLM | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01261 | hp2 | a0005 | c0004 | t0004 | g0235 | AMR | CLM | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01346 | hp1 | a0002 | c0025 | t0001 | g0011 | AMR | CLM | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0028 | AMR | CLM | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01358 | hp1 | a0002 | c0001 | t0001 | g0154 | AMR | CLM | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01358 | hp2 | a0005 | c0004 | t0004 | g0232 | AMR | CLM | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01361 | hp1 | a0001 | c0002 | t0029 | g0015 | AMR | CLM | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01361 | hp2 | a0004 | c0015 | t0003 | g0269 | AMR | CLM | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01433 | hp1 | a0001 | c0007 | t0019 | g0089 | AMR | CLM | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01433 | hp2 | a0005 | c0004 | t0004 | g0234 | AMR | CLM | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01496 | hp1 | a0005 | c0004 | t0004 | g0230 | AMR | CLM | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01496 | hp2 | a0002 | c0001 | t0009 | g0246 | AMR | CLM | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0017 | EUR | IBS | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01516 | hp2 | a0007 | c0008 | t0011 | g0221 | EUR | IBS | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01517 | hp1 | a0007 | c0008 | t0011 | g0220 | EUR | IBS | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01517 | hp2 | a0012 | c0039 | t0002 | g0021 | EUR | IBS | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01891 | hp1 | a0001 | c0002 | t0053 | g0051 | AFR | ACB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01891 | hp2 | a0002 | c0013 | t0014 | g0209 | AFR | ACB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01928 | hp1 | a0003 | c0012 | t0027 | g0200 | AMR | PEL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01928 | hp2 | a0002 | c0001 | t0041 | g0245 | AMR | PEL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01934 | hp1 | a0003 | c0003 | t0006 | g0187 | AMR | PEL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PEL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01943 | hp1 | a0002 | c0030 | t0009 | g0244 | AMR | PEL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01943 | hp2 | a0005 | c0004 | t0004 | g0213 | AMR | PEL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01993 | hp1 | a0005 | c0004 | t0004 | g0007 | AMR | PEL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG01993 | hp2 | a0002 | c0001 | t0009 | g0243 | AMR | PEL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02004 | hp1 | a0005 | c0004 | t0004 | g0214 | AMR | PEL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0020 | AMR | PEL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02015 | hp1 | a0004 | c0005 | t0066 | g0257 | EAS | KHV | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02015 | hp2 | a0003 | c0003 | t0012 | g0188 | EAS | KHV | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02040 | hp1 | a0004 | c0005 | t0003 | g0262 | EAS | KHV | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02040 | hp2 | a0002 | c0001 | t0001 | g0138 | EAS | KHV | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02071 | hp1 | a0006 | c0006 | t0005 | g0004 | EAS | KHV | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02071 | hp2 | a0019 | c0038 | t0003 | g0260 | EAS | KHV | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02074 | hp1 | a0002 | c0027 | t0001 | g0135 | EAS | KHV | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02074 | hp2 | a0003 | c0003 | t0012 | g0186 | EAS | KHV | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02080 | hp1 | a0003 | c0003 | t0006 | g0197 | EAS | KHV | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02080 | hp2 | a0004 | c0005 | t0003 | g0255 | EAS | KHV | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02129 | hp1 | a0002 | c0001 | t0043 | g0247 | EAS | KHV | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02129 | hp2 | a0004 | c0005 | t0003 | g0261 | EAS | KHV | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02135 | hp1 | a0004 | c0005 | t0003 | g0273 | EAS | KHV | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02135 | hp2 | a0002 | c0001 | t0001 | g0139 | EAS | KHV | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02155 | hp1 | a0003 | c0003 | t0006 | g0195 | EAS | CDX | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02155 | hp2 | a0002 | c0001 | t0001 | g0170 | EAS | CDX | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02165 | hp1 | a0003 | c0003 | t0012 | g0190 | EAS | CDX | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02165 | hp2 | a0003 | c0003 | t0006 | g0193 | EAS | CDX | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02257 | hp1 | a0001 | c0020 | t0030 | g0068 | AFR | ACB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02257 | hp2 | a0001 | c0018 | t0018 | g0071 | AFR | ACB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02258 | hp1 | a0003 | c0003 | t0006 | g0211 | AFR | ACB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02258 | hp2 | a0001 | c0002 | t0008 | g0002 | AFR | ACB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02280 | hp1 | a0005 | c0036 | t0005 | g0114 | AFR | ACB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02280 | hp2 | a0001 | c0010 | t0032 | g0075 | AFR | ACB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02300 | hp1 | a0009 | c0016 | t0003 | g0251 | AMR | PEL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02300 | hp2 | a0003 | c0012 | t0027 | g0201 | AMR | PEL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02451 | hp1 | a0001 | c0010 | t0061 | g0073 | AFR | ACB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02451 | hp2 | a0001 | c0002 | t0029 | g0039 | AFR | ACB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02523 | hp1 | a0003 | c0003 | t0012 | g0192 | EAS | KHV | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02523 | hp2 | a0006 | c0006 | t0005 | g0103 | EAS | KHV | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02572 | hp1 | a0008 | c0014 | t0017 | g0098 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02572 | hp2 | a0001 | c0010 | t0032 | g0078 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02602 | hp1 | a0015 | c0032 | t0003 | g0270 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02602 | hp2 | a0005 | c0004 | t0024 | g0218 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02615 | hp1 | a0003 | c0012 | t0026 | g0206 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02615 | hp2 | a0001 | c0002 | t0008 | g0058 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02622 | hp1 | a0002 | c0028 | t0014 | g0128 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02622 | hp2 | a0001 | c0010 | t0058 | g0076 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02630 | hp1 | a0003 | c0003 | t0013 | g0184 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02630 | hp2 | a0001 | c0021 | t0018 | g0069 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02647 | hp1 | a0006 | c0006 | t0035 | g0107 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02647 | hp2 | a0001 | c0019 | t0055 | g0063 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02683 | hp1 | a0005 | c0004 | t0024 | g0217 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02683 | hp2 | a0003 | c0003 | t0006 | g0127 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02717 | hp1 | a0001 | c0020 | t0030 | g0067 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02717 | hp2 | a0001 | c0002 | t0008 | g0062 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02723 | hp1 | a0001 | c0021 | t0018 | g0070 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02723 | hp2 | a0005 | c0004 | t0004 | g0238 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02735 | hp2 | a0002 | c0001 | t0020 | g0133 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02809 | hp1 | a0002 | c0013 | t0014 | g0210 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02809 | hp2 | a0001 | c0011 | t0015 | g0057 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02818 | hp1 | a0001 | c0010 | t0059 | g0080 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02818 | hp2 | a0003 | c0003 | t0048 | g0183 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0042 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02895 | hp2 | a0003 | c0012 | t0026 | g0207 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02965 | hp1 | a0006 | c0006 | t0005 | g0113 | AFR | ESN | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02965 | hp2 | a0003 | c0003 | t0013 | g0205 | AFR | ESN | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02970 | hp1 | a0001 | c0018 | t0018 | g0072 | AFR | ESN | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02970 | hp2 | a0001 | c0011 | t0015 | g0059 | AFR | ESN | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02976 | hp1 | a0002 | c0013 | t0014 | g0094 | AFR | ESN | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02976 | hp2 | a0008 | c0014 | t0017 | g0095 | AFR | ESN | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03041 | hp1 | a0001 | c0022 | t0007 | g0082 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03041 | hp2 | a0003 | c0003 | t0013 | g0203 | AFR | GWD | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03130 | hp1 | a0008 | c0014 | t0017 | g0096 | AFR | ESN | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0043 | AFR | ESN | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03195 | hp1 | a0002 | c0013 | t0014 | g0208 | AFR | ESN | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03195 | hp2 | a0001 | c0010 | t0063 | g0077 | AFR | ESN | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03209 | hp1 | a0001 | c0002 | t0056 | g0048 | AFR | MSL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0031 | AFR | MSL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03225 | hp1 | a0001 | c0011 | t0015 | g0053 | AFR | MSL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03225 | hp2 | a0003 | c0003 | t0013 | g0204 | AFR | MSL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03239 | hp1 | a0009 | c0016 | t0003 | g0276 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0040 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03453 | hp1 | a0001 | c0042 | t0002 | g0050 | AFR | MSL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03453 | hp2 | a0008 | c0014 | t0017 | g0097 | AFR | MSL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03486 | hp1 | a0001 | c0007 | t0019 | g0086 | AFR | MSL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03486 | hp2 | a0001 | c0002 | t0008 | g0002 | AFR | MSL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03490 | hp1 | a0004 | c0005 | t0016 | g0010 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0041 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03491 | hp1 | a0001 | c0007 | t0057 | g0092 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03491 | hp2 | a0010 | c0017 | t0004 | g0226 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03492 | hp1 | a0010 | c0017 | t0004 | g0227 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03492 | hp2 | a0004 | c0005 | t0016 | g0010 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03516 | hp1 | a0001 | c0044 | t0031 | g0064 | AFR | ESN | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03516 | hp2 | a0003 | c0003 | t0049 | g0116 | AFR | ESN | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03579 | hp1 | a0001 | c0022 | t0007 | g0083 | AFR | MSL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03579 | hp2 | a0001 | c0002 | t0008 | g0060 | AFR | MSL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03654 | hp1 | a0003 | c0003 | t0006 | g0280 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03654 | hp2 | a0005 | c0004 | t0004 | g0242 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03669 | hp1 | a0002 | c0001 | t0001 | g0005 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03669 | hp2 | a0017 | c0035 | t0004 | g0219 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03704 | hp1 | a0005 | c0004 | t0004 | g0228 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03704 | hp2 | a0004 | c0005 | t0067 | g0249 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03710 | hp1 | a0007 | c0008 | t0011 | g0223 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03710 | hp2 | a0004 | c0005 | t0016 | g0254 | SAS | PJL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03831 | hp1 | a0004 | c0005 | t0016 | g0279 | SAS | BEB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03831 | hp2 | a0004 | c0005 | t0003 | g0250 | SAS | BEB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03834 | hp1 | a0007 | c0008 | t0011 | g0229 | SAS | BEB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03834 | hp2 | a0002 | c0001 | t0001 | g0146 | SAS | BEB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG04115 | hp1 | a0007 | c0008 | t0011 | g0129 | SAS | STU | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0024 | SAS | STU | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG04184 | hp1 | a0002 | c0001 | t0001 | g0144 | SAS | BEB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0012 | SAS | BEB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG04199 | hp1 | a0002 | c0001 | t0009 | g0145 | SAS | STU | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG04199 | hp2 | a0004 | c0005 | t0016 | g0258 | SAS | STU | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG04204 | hp1 | a0007 | c0008 | t0045 | g0224 | SAS | STU | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0036 | SAS | STU | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0046 | SAS | STU | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG04228 | hp2 | a0004 | c0005 | t0003 | g0264 | SAS | STU | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18522 | hp1 | a0001 | c0010 | t0062 | g0079 | AFR | YRI | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18522 | hp2 | a0003 | c0003 | t0013 | g0202 | AFR | YRI | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18612 | hp1 | a0002 | c0001 | t0010 | g0134 | EAS | CHB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18612 | hp2 | a0004 | c0005 | t0003 | g0263 | EAS | CHB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18747 | hp1 | a0002 | c0001 | t0001 | g0172 | EAS | CHB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18747 | hp2 | a0003 | c0003 | t0050 | g0117 | EAS | CHB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18906 | hp1 | a0003 | c0003 | t0047 | g0212 | AFR | YRI | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18906 | hp2 | a0001 | c0010 | t0060 | g0081 | AFR | YRI | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18941 | hp1 | a0004 | c0005 | t0003 | g0274 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18941 | hp2 | a0006 | c0006 | t0005 | g0100 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18942 | hp1 | a0002 | c0001 | t0001 | g0143 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18942 | hp2 | a0002 | c0009 | t0001 | g0158 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18947 | hp1 | a0001 | c0043 | t0007 | g0088 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18947 | hp2 | a0002 | c0001 | t0001 | g0141 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18952 | hp1 | a0002 | c0001 | t0036 | g0148 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18952 | hp2 | a0004 | c0005 | t0003 | g0259 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18954 | hp1 | a0002 | c0001 | t0038 | g0132 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18954 | hp2 | a0004 | c0005 | t0003 | g0252 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18961 | hp1 | a0002 | c0001 | t0001 | g0178 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18961 | hp2 | a0006 | c0006 | t0005 | g0004 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18962 | hp1 | a0001 | c0002 | t0028 | g0035 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18962 | hp2 | a0002 | c0001 | t0042 | g0005 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18964 | hp1 | a0006 | c0006 | t0005 | g0105 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18964 | hp2 | a0002 | c0001 | t0022 | g0126 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18965 | hp1 | a0006 | c0006 | t0005 | g0102 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18965 | hp2 | a0002 | c0001 | t0001 | g0153 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18966 | hp1 | a0004 | c0005 | t0003 | g0267 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18966 | hp2 | a0002 | c0009 | t0001 | g0125 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18970 | hp1 | a0006 | c0006 | t0005 | g0106 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18970 | hp2 | a0002 | c0009 | t0001 | g0173 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18972 | hp1 | a0006 | c0006 | t0005 | g0101 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18972 | hp2 | a0002 | c0009 | t0001 | g0165 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18975 | hp1 | a0002 | c0001 | t0039 | g0169 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18975 | hp2 | a0001 | c0007 | t0007 | g0087 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18977 | hp1 | a0001 | c0007 | t0007 | g0085 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18977 | hp2 | a0002 | c0001 | t0010 | g0166 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18978 | hp1 | a0005 | c0004 | t0004 | g0131 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18978 | hp2 | a0004 | c0005 | t0003 | g0248 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18979 | hp1 | a0001 | c0002 | t0028 | g0037 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18979 | hp2 | a0011 | c0023 | t0010 | g0151 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18983 | hp1 | a0014 | c0033 | t0003 | g0275 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18983 | hp2 | a0002 | c0001 | t0022 | g0118 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18985 | hp1 | a0006 | c0006 | t0005 | g0104 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18985 | hp2 | a0002 | c0001 | t0001 | g0140 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18987 | hp1 | a0004 | c0005 | t0003 | g0277 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18987 | hp2 | a0002 | c0001 | t0001 | g0142 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18988 | hp1 | a0006 | c0006 | t0005 | g0109 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18988 | hp2 | a0002 | c0001 | t0020 | g0175 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18989 | hp1 | a0003 | c0003 | t0006 | g0194 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18989 | hp2 | a0002 | c0001 | t0010 | g0124 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18992 | hp1 | a0002 | c0001 | t0001 | g0177 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18992 | hp2 | a0002 | c0009 | t0037 | g0159 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18998 | hp1 | a0002 | c0001 | t0001 | g0181 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA18998 | hp2 | a0002 | c0009 | t0001 | g0174 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19002 | hp1 | a0003 | c0003 | t0012 | g0006 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19002 | hp2 | a0002 | c0001 | t0001 | g0281 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19010 | hp1 | a0002 | c0009 | t0001 | g0123 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19010 | hp2 | a0013 | c0037 | t0068 | g0266 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19011 | hp1 | a0003 | c0003 | t0006 | g0199 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19011 | hp2 | a0002 | c0001 | t0010 | g0163 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19043 | hp1 | a0001 | c0011 | t0015 | g0056 | AFR | LWK | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19043 | hp2 | a0006 | c0006 | t0005 | g0115 | AFR | LWK | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19058 | hp1 | a0004 | c0005 | t0069 | g0272 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19058 | hp2 | a0002 | c0001 | t0010 | g0161 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19060 | hp1 | a0002 | c0001 | t0001 | g0137 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19060 | hp2 | a0003 | c0003 | t0006 | g0196 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19062 | hp1 | a0006 | c0006 | t0005 | g0110 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19062 | hp2 | a0002 | c0001 | t0040 | g0179 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19064 | hp1 | a0006 | c0006 | t0005 | g0108 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19064 | hp2 | a0002 | c0001 | t0001 | g0147 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19065 | hp1 | a0006 | c0006 | t0005 | g0112 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19065 | hp2 | a0002 | c0001 | t0001 | g0157 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19083 | hp1 | a0003 | c0003 | t0012 | g0006 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19083 | hp2 | a0002 | c0001 | t0001 | g0119 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19084 | hp1 | a0003 | c0003 | t0051 | g0198 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19084 | hp2 | a0002 | c0001 | t0001 | g0180 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19085 | hp1 | a0018 | c0034 | t0034 | g0111 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19085 | hp2 | a0004 | c0005 | t0003 | g0265 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19086 | hp1 | a0002 | c0009 | t0001 | g0160 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19086 | hp2 | a0006 | c0006 | t0005 | g0099 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19090 | hp1 | a0001 | c0007 | t0007 | g0084 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA19090 | hp2 | a0002 | c0001 | t0001 | g0121 | EAS | JPT | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | ASW | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA20129 | hp2 | a0003 | c0003 | t0013 | g0185 | AFR | ASW | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA20752 | hp1 | a0002 | c0001 | t0001 | g0164 | EUR | TSI | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA20752 | hp2 | a0002 | c0001 | t0021 | g0182 | EUR | TSI | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA20905 | hp1 | a0001 | c0040 | t0002 | g0033 | SAS | GIH | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA20905 | hp2 | a0002 | c0026 | t0001 | g0136 | SAS | GIH | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02109 | hp1 | a0001 | c0011 | t0015 | g0052 | AFR | ACB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02109 | hp2 | a0001 | c0045 | t0065 | g0074 | AFR | ACB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02486 | hp1 | a0001 | c0011 | t0008 | g0049 | AFR | ACB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02486 | hp2 | a0001 | c0002 | t0031 | g0065 | AFR | ACB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02559 | hp1 | a0005 | c0004 | t0004 | g0225 | AFR | ACB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG02559 | hp2 | a0001 | c0002 | t0008 | g0055 | AFR | ACB | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03471 | hp1 | a0001 | c0002 | t0008 | g0061 | AFR | MSL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
HG03471 | hp2 | a0001 | c0007 | t0019 | g0090 | AFR | MSL | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA20300 | hp1 | a0003 | c0012 | t0046 | g0191 | AFR | USA | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
NA20300 | hp2 | a0001 | c0019 | t0054 | g0066 | AFR | USA | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
homoSapiens_chm13v2 | hp1 | a0004 | c0015 | t0003 | g0268 | REF | REF | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
homoSapiens_grch38 | hp1 | a0004 | c0005 | t0003 | g0278 | REF | REF | NBPF8_chr1_120410035_120474676 | NBPF8 | chr1 | 120410035 | 120474676 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:120436234
|
G | A | 1 | a0004 | 1 | HG03704.hp2 | splice_region_variant | LOW | c.-289G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | chr1 | 120436234 | ||||||
chr1:120436234
|
G | C | 2 | a0001a0012 | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
splice_region_variant | LOW | c.-289G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | chr1 | 120436234 | ||||||
chr1:120436530
|
T | G | 3 | a0002a0003a0011 | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
missense_variant | MODERATE | c.8T>G | p.Val3Gly | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | 980/7256 | 8/2829 | 3/942 | chr1 | 120436530 | ||
chr1:120436551
|
G | A | 1 | a0007 | 9 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(6): Show |
missense_variant | MODERATE | c.29G>A | p.Ser10Asn | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | 1001/7256 | 29/2829 | 10/942 | chr1 | 120436551 | ||
chr1:120436615
|
CAAACAGC others(6346): Show |
C | 1 | a0002 | 75 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(72): Show |
exon_loss_variant | HIGH | c.122_778+1507del | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/23 | 1094/7256 | INFO_REALIGN_3_PRIME | chr1 | 120436615 | ||||
chr1:120436638
|
AAG | A | 2 | a0001a0012 | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
frameshift_variant | HIGH | c.122_123delGA | p.Arg41fs | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | 1094/7256 | 122/2829 | 41/942 | INFO_REALIGN_3_PRIME | chr1 | 120436638 | |
chr1:120436644
|
G | A | 1 | a0011 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.122G>A | p.Arg41Lys | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | 1094/7256 | 122/2829 | 41/942 | chr1 | 120436644 | ||
chr1:120436644
|
GATGTTTT others(6346): Show |
G | 1 | a0019 | 1 | HG02071.hp2 | exon_loss_variant | HIGH | c.493+102_779-3049de others(1): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr1 | 120436644 | |||||
chr1:120436667
|
G | A | 1 | a0012 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.145G>A | p.Gly49Ser | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | 1117/7256 | 145/2829 | 49/942 | chr1 | 120436667 | ||
chr1:120436677
|
C | T | 1 | a0001 | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
missense_variant | MODERATE | c.155C>T | p.Ala52Val | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | 1127/7256 | 155/2829 | 52/942 | chr1 | 120436677 | ||
chr1:120438573
|
T | C | 1 | a0003 | 33 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(30): Show |
missense_variant | MODERATE | c.205T>C | p.Phe69Leu | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/23 | 1177/7256 | 205/2829 | 69/942 | chr1 | 120438573 | ||
chr1:120438586
|
A | T | 1 | a0013 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.218A>T | p.Asn73Ile | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/23 | 1190/7256 | 218/2829 | 73/942 | chr1 | 120438586 | ||
chr1:120438587
|
T | A | 1 | a0013 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.219T>A | p.Asn73Lys | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/23 | 1191/7256 | 219/2829 | 73/942 | chr1 | 120438587 | ||
chr1:120438588
|
G | T | 1 | a0013 | 1 | NA19010.hp2 | stop_gained | HIGH | c.220G>T | p.Glu74* | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/23 | 1192/7256 | 220/2829 | 74/942 | chr1 | 120438588 | ||
chr1:120438645
|
A | G | 2 | a0003a0011 | 34 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(31): Show |
missense_variant&splice_region_variant | MODERATE | c.277A>G | p.Arg93Gly | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/23 | 1249/7256 | 277/2829 | 93/942 | chr1 | 120438645 | ||
chr1:120439538
|
A | G | 11 | a0001a0003a0005others(8): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
missense_variant | MODERATE | c.341A>G | p.Gln114Arg | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/23 | 1313/7256 | 341/2829 | 114/942 | chr1 | 120439538 | ||
chr1:120439595
|
T | C | 1 | a0018 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.398T>C | p.Leu133Pro | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/23 | 1370/7256 | 398/2829 | 133/942 | chr1 | 120439595 | ||
chr1:120440166
|
ATGCTTTT others(12626): Show |
A | 1 | a0010 | 2 | HG03491.hp2 HG03492.hp1 |
exon_loss_variant | HIGH | c.493+483_1306+474de others(1): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr1 | 120440166 | |||||
chr1:120441298
|
A | T | 2 | a0001a0012 | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
missense_variant | MODERATE | c.587A>T | p.Glu196Val | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/23 | 1559/7256 | 587/2829 | 196/942 | chr1 | 120441298 | ||
chr1:120441370
|
CCAACCAG others(6345): Show |
C | 6 | a0001a0003a0006others(3): Show | 70 | HG00544.hp2 HG00642.hp2 HG01069.hp1 others(67): Show |
frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.778+1492_918del | p.Val260fs | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/23 | 779/2829 | 260/942 | INFO_REALIGN_3_PRIME | chr1 | 120441370 | ||
chr1:120441486
|
T | C | 3 | a0001a0008a0012 | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
missense_variant | MODERATE | c.775T>C | p.Ser259Pro | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/23 | 1747/7256 | 775/2829 | 259/942 | chr1 | 120441486 | ||
chr1:120442949
|
ACCCCCAG others(6346): Show |
A | 1 | a0001 | 1 | NA20905.hp1 | splice_acceptor_variant&disruptive_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.778+1465_892del | p.Val260_Gln298delin others(4): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/23 | 779/2829 | 260/942 | INFO_REALIGN_3_PRIME | chr1 | 120442949 | ||
chr1:120449372
|
G | A | 1 | a0008 | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
missense_variant | MODERATE | c.958G>A | p.Gly320Ser | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/23 | 1930/7256 | 958/2829 | 320/942 | chr1 | 120449372 | ||
chr1:120449382
|
C | A | 1 | a0001 | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
missense_variant | MODERATE | c.968C>A | p.Ala323Asp | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/23 | 1940/7256 | 968/2829 | 323/942 | chr1 | 120449382 | ||
chr1:120449388
|
G | A | 11 | a0001a0002a0003others(8): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
missense_variant | MODERATE | c.974G>A | p.Arg325Gln | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/23 | 1946/7256 | 974/2829 | 325/942 | chr1 | 120449388 | ||
chr1:120451263
|
A | G | 1 | a0001 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.1072A>G | p.Lys358Glu | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 10/23 | 2044/7256 | 1072/2829 | 358/942 | chr1 | 120451263 | ||
chr1:120451275
|
G | T | 1 | a0014 | 1 | NA18983.hp1 | stop_gained | HIGH | c.1084G>T | p.Glu362* | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 10/23 | 2056/7256 | 1084/2829 | 362/942 | chr1 | 120451275 | ||
chr1:120452139
|
A | T | 1 | a0001 | 8 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(5): Show |
missense_variant | MODERATE | c.1114A>T | p.Thr372Ser | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/23 | 2086/7256 | 1114/2829 | 372/942 | chr1 | 120452139 | ||
chr1:120452200
|
T | G | 6 | a0001a0002a0003others(3): Show | 201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
missense_variant | MODERATE | c.1175T>G | p.Leu392Arg | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/23 | 2147/7256 | 1175/2829 | 392/942 | chr1 | 120452200 | ||
chr1:120452236
|
C | T | 1 | a0001 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.1211C>T | p.Pro404Leu | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/23 | 2183/7256 | 1211/2829 | 404/942 | chr1 | 120452236 | ||
chr1:120452245
|
C | T | 1 | a0003 | 5 | HG01928.hp1 HG02300.hp2 HG02615.hp1 others(2): Show |
missense_variant | MODERATE | c.1220C>T | p.Pro407Leu | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/23 | 2192/7256 | 1220/2829 | 407/942 | chr1 | 120452245 | ||
chr1:120452249
|
C | G | 1 | a0001 | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
missense_variant | MODERATE | c.1224C>G | p.Asp408Glu | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/23 | 2196/7256 | 1224/2829 | 408/942 | chr1 | 120452249 | ||
chr1:120452313
|
G | T | 1 | a0002 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.1288G>T | p.Val430Phe | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/23 | 2260/7256 | 1288/2829 | 430/942 | chr1 | 120452313 | ||
chr1:120453410
|
G | T | 1 | a0008 | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
missense_variant | MODERATE | c.1345G>T | p.Val449Leu | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 12/23 | 2317/7256 | 1345/2829 | 449/942 | chr1 | 120453410 | ||
chr1:120453419
|
A | G | 1 | a0015 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.1354A>G | p.Lys452Glu | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 12/23 | 2326/7256 | 1354/2829 | 452/942 | chr1 | 120453419 | ||
chr1:120460584
|
G | A | 2 | a0001a0012 | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
missense_variant | MODERATE | c.1813G>A | p.Asp605Asn | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/23 | 2785/7256 | 1813/2829 | 605/942 | chr1 | 120460584 | ||
chr1:120460587
|
C | G | 1 | a0002 | 8 | NA18942.hp2 NA18966.hp2 NA18970.hp2 others(5): Show |
missense_variant | MODERATE | c.1816C>G | p.Gln606Glu | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/23 | 2788/7256 | 1816/2829 | 606/942 | chr1 | 120460587 | ||
chr1:120460607
|
A | C | 1 | a0016 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.1836A>C | p.Gln612His | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/23 | 2808/7256 | 1836/2829 | 612/942 | chr1 | 120460607 | ||
chr1:120460621
|
C | A | 3 | a0002a0003a0011 | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
missense_variant | MODERATE | c.1850C>A | p.Pro617His | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/23 | 2822/7256 | 1850/2829 | 617/942 | chr1 | 120460621 | ||
chr1:120461348
|
A | T | 1 | a0008 | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
missense_variant | MODERATE | c.1948A>T | p.Thr650Ser | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/23 | 2920/7256 | 1948/2829 | 650/942 | chr1 | 120461348 | ||
chr1:120461384
|
A | G | 1 | a0016 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.1984A>G | p.Ile662Val | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/23 | 2956/7256 | 1984/2829 | 662/942 | chr1 | 120461384 | ||
chr1:120462850
|
A | G | 1 | a0002 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.2135A>G | p.Asp712Gly | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/23 | 3107/7256 | 2135/2829 | 712/942 | chr1 | 120462850 | ||
chr1:120462952
|
C | T | 3 | a0002a0003a0011 | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
missense_variant | MODERATE | c.2237C>T | p.Ala746Val | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/23 | 3209/7256 | 2237/2829 | 746/942 | chr1 | 120462952 | ||
chr1:120464486
|
C | T | 1 | a0001 | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
missense_variant | MODERATE | c.2414C>T | p.Pro805Leu | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 21/23 | 3386/7256 | 2414/2829 | 805/942 | chr1 | 120464486 | ||
chr1:120464515
|
G | A | 1 | a0017 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.2443G>A | p.Glu815Lys | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 21/23 | 3415/7256 | 2443/2829 | 815/942 | chr1 | 120464515 | ||
chr1:120465985
|
A | G | 1 | a0003 | 33 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(30): Show |
missense_variant | MODERATE | c.2593A>G | p.Ser865Gly | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 3565/7256 | 2593/2829 | 865/942 | chr1 | 120465985 | ||
chr1:120466058
|
T | A | 1 | a0008 | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
missense_variant | MODERATE | c.2666T>A | p.Met889Lys | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 3638/7256 | 2666/2829 | 889/942 | chr1 | 120466058 | ||
chr1:120466107
|
C | G | 2 | a0001a0012 | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
stop_gained | HIGH | c.2715C>G | p.Tyr905* | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 3687/7256 | 2715/2829 | 905/942 | chr1 | 120466107 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:120436552
|
C | T | 2 | a0001c0010a0001c0045 | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
synonymous_variant | LOW | c.30C>T | p.Ser10Ser | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | 1002/7256 | 30/2829 | 10/942 | chr1 | 120436552 | ||
chr1:120436585
|
C | T | 2 | a0001c0044a0002c0030 | 2 | HG01943.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.63C>T | p.Asn21Asn | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | 1035/7256 | 63/2829 | 21/942 | chr1 | 120436585 | ||
chr1:120439611
|
G | A | 1 | a0001c0018 | 2 | HG02257.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.414G>A | p.Lys138Lys | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/23 | 1386/7256 | 414/2829 | 138/942 | chr1 | 120439611 | ||
chr1:120440749
|
C | T | 6 | a0001c0018a0001c0020a0001c0021others(3): Show | 40 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(37): Show |
synonymous_variant | LOW | c.501C>T | p.Asp167Asp | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 7/23 | 1473/7256 | 501/2829 | 167/942 | chr1 | 120440749 | ||
chr1:120440794
|
G | A | 1 | a0008c0014 | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
synonymous_variant | LOW | c.546G>A | p.Val182Val | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 7/23 | 1518/7256 | 546/2829 | 182/942 | chr1 | 120440794 | ||
chr1:120441404
|
T | C | 4 | a0004c0015a0005c0004a0007c0008others(1): Show | 38 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(35): Show |
synonymous_variant | LOW | c.693T>C | p.Phe231Phe | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/23 | 1665/7256 | 693/2829 | 231/942 | chr1 | 120441404 | ||
chr1:120441449
|
C | T | 1 | a0001c0042 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.738C>T | p.Ser246Ser | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/23 | 1710/7256 | 738/2829 | 246/942 | chr1 | 120441449 | ||
chr1:120449389
|
A | G | 36 | a0001c0002a0001c0007a0001c0010others(33): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
synonymous_variant | LOW | c.975A>G | p.Arg325Arg | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/23 | 1947/7256 | 975/2829 | 325/942 | chr1 | 120449389 | ||
chr1:120449392
|
G | A | 1 | a0002c0024 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.978G>A | p.Gln326Gln | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/23 | 1950/7256 | 978/2829 | 326/942 | chr1 | 120449392 | ||
chr1:120455446
|
A | G | 37 | a0001c0002a0001c0007a0001c0010others(34): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
synonymous_variant | LOW | c.1623A>G | p.Gly541Gly | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/23 | 2595/7256 | 1623/2829 | 541/942 | chr1 | 120455446 | ||
chr1:120459454
|
G | A | 1 | a0016c0031 | 1 | HG00140.hp2 | synonymous_variant | LOW | c.1725G>A | p.Leu575Leu | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/23 | 2697/7256 | 1725/2829 | 575/942 | chr1 | 120459454 | ||
chr1:120461263
|
G | A | 10 | a0002c0001a0002c0009a0002c0024others(7): Show | 72 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(69): Show |
synonymous_variant | LOW | c.1863G>A | p.Arg621Arg | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/23 | 2835/7256 | 1863/2829 | 621/942 | chr1 | 120461263 | ||
chr1:120461338
|
C | T | 1 | a0016c0031 | 1 | HG00140.hp2 | synonymous_variant | LOW | c.1938C>T | p.Cys646Cys | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/23 | 2910/7256 | 1938/2829 | 646/942 | chr1 | 120461338 | ||
chr1:120461365
|
C | T | 1 | a0002c0027 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.1965C>T | p.Pro655Pro | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/23 | 2937/7256 | 1965/2829 | 655/942 | chr1 | 120461365 | ||
chr1:120461377
|
G | C | 34 | a0001c0002a0001c0007a0001c0010others(31): Show | 221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
synonymous_variant | LOW | c.1977G>C | p.Ala659Ala | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/23 | 2949/7256 | 1977/2829 | 659/942 | chr1 | 120461377 | ||
chr1:120462956
|
T | C | 1 | a0002c0025 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.2241T>C | p.Leu747Leu | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/23 | 3213/7256 | 2241/2829 | 747/942 | chr1 | 120462956 | ||
chr1:120464487
|
G | C | 1 | a0002c0028 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.2415G>C | p.Pro805Pro | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 21/23 | 3387/7256 | 2415/2829 | 805/942 | chr1 | 120464487 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:120415062
|
T | G | 84 | a0001c0002t0002a0001c0002t0008a0001c0002t0028others(81): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
5_prime_UTR_variant | MODIFIER | c.-945T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/23 | 21461 | chr1 | 120415062 | |||||
chr1:120415071
|
G | A | 1 | a0004c0005t0066 | 1 | HG02015.hp1 | 5_prime_UTR_variant | MODIFIER | c.-936G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/23 | 21452 | chr1 | 120415071 | |||||
chr1:120415110
|
G | T | 1 | a0001c0045t0065 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-897G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/23 | 21413 | chr1 | 120415110 | |||||
chr1:120415133
|
C | T | 1 | a0002c0001t0064 | 1 | HG00280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-874C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/23 | 21390 | chr1 | 120415133 | |||||
chr1:120415211
|
G | A | 1 | a0005c0004t0033 | 1 | HG00741.hp1 | 5_prime_UTR_variant | MODIFIER | c.-796G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/23 | 21312 | chr1 | 120415211 | |||||
chr1:120415216
|
A | G | 8 | a0001c0010t0032a0001c0010t0058a0001c0010t0059others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-791A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/23 | 21307 | chr1 | 120415216 | |||||
chr1:120415225
|
A | G | 33 | a0001c0002t0002a0001c0002t0008a0001c0002t0028others(30): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
5_prime_UTR_variant | MODIFIER | c.-782A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/23 | 21298 | chr1 | 120415225 | |||||
chr1:120415231
|
A | T | 11 | a0003c0003t0006a0003c0003t0012a0003c0003t0013others(8): Show | 33 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(30): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-776A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/23 | chr1 | 120415231 | ||||||
chr1:120415262
|
C | A | 1 | a0001c0007t0019 | 3 | HG01433.hp1 HG03471.hp2 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-745C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/23 | 21261 | chr1 | 120415262 | |||||
chr1:120415279
|
A | G | 2 | a0001c0002t0031a0001c0044t0031 | 2 | HG02486.hp2 HG03516.hp1 |
5_prime_UTR_variant | MODIFIER | c.-728A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/23 | 21244 | chr1 | 120415279 | |||||
chr1:120415287
|
G | A | 4 | a0005c0036t0005a0006c0006t0005a0006c0006t0035others(1): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-720G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/23 | 21236 | chr1 | 120415287 | |||||
chr1:120415296
|
C | T | 8 | a0001c0010t0032a0001c0010t0058a0001c0010t0059others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-711C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/23 | chr1 | 120415296 | ||||||
chr1:120419964
|
T | G | 1 | a0008c0014t0017 | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-588T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/23 | 16559 | chr1 | 120419964 | |||||
chr1:120419987
|
G | T | 5 | a0001c0007t0007a0001c0007t0019a0001c0007t0057others(2): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-565G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/23 | chr1 | 120419987 | ||||||
chr1:120420024
|
C | A | 1 | a0001c0010t0058 | 1 | HG02622.hp2 | 5_prime_UTR_variant | MODIFIER | c.-528C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/23 | 16499 | chr1 | 120420024 | |||||
chr1:120420029
|
C | T | 4 | a0005c0036t0005a0006c0006t0005a0006c0006t0035others(1): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-523C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/23 | chr1 | 120420029 | ||||||
chr1:120420064
|
A | C | 4 | a0005c0004t0011a0007c0008t0011a0007c0008t0025others(1): Show | 10 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-488A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/23 | 16459 | chr1 | 120420064 | |||||
chr1:120420106
|
C | T | 1 | a0001c0002t0056 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-446C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/23 | 16417 | chr1 | 120420106 | |||||
chr1:120427799
|
G | A | 1 | a0002c0001t0036 | 1 | NA18952.hp1 | 5_prime_UTR_variant | MODIFIER | c.-340G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/23 | 8724 | chr1 | 120427799 | |||||
chr1:120436246
|
C | T | 1 | a0001c0019t0055 | 1 | HG02647.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-277C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | chr1 | 120436246 | ||||||
chr1:120436298
|
T | C | 11 | a0003c0003t0006a0003c0003t0012a0003c0003t0013others(8): Show | 33 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-225T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | 225 | chr1 | 120436298 | |||||
chr1:120436303
|
G | A | 1 | a0001c0002t0056 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-220G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | 220 | chr1 | 120436303 | |||||
chr1:120436303
|
G | C | 1 | a0018c0034t0034 | 1 | NA19085.hp1 | 5_prime_UTR_variant | MODIFIER | c.-220G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | 220 | chr1 | 120436303 | |||||
chr1:120436307
|
T | G | 1 | a0002c0009t0037 | 1 | NA18992.hp2 | 5_prime_UTR_variant | MODIFIER | c.-216T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | 216 | chr1 | 120436307 | |||||
chr1:120436436
|
T | C | 1 | a0003c0012t0026 | 2 | HG02615.hp1 HG02895.hp2 |
5_prime_UTR_variant | MODIFIER | c.-87T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | 87 | chr1 | 120436436 | |||||
chr1:120436472
|
G | A | 16 | a0001c0002t0002a0001c0002t0008a0001c0002t0028others(13): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
5_prime_UTR_variant | MODIFIER | c.-51G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/23 | 51 | chr1 | 120436472 | |||||
chr1:120466236
|
G | A | 1 | a0006c0006t0035 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 15 | chr1 | 120466236 | |||||
chr1:120466462
|
G | A | 2 | a0002c0013t0014a0002c0028t0014 | 5 | HG01891.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*241G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 241 | chr1 | 120466462 | |||||
chr1:120466571
|
C | G | 1 | a0002c0024t0044 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*350C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 350 | chr1 | 120466571 | |||||
chr1:120466654
|
T | C | 1 | a0002c0001t0038 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*433T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 433 | chr1 | 120466654 | |||||
chr1:120466869
|
T | C | 1 | a0001c0002t0052 | 1 | HG01258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*648T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 648 | chr1 | 120466869 | |||||
chr1:120466913
|
C | T | 15 | a0001c0002t0002a0001c0002t0008a0001c0002t0028others(12): Show | 57 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*692C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 692 | chr1 | 120466913 | |||||
chr1:120467028
|
C | A | 1 | a0001c0007t0057 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*807C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 807 | chr1 | 120467028 | |||||
chr1:120467086
|
A | G | 4 | a0001c0010t0032a0001c0010t0058a0001c0010t0062others(1): Show | 5 | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*865A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 865 | chr1 | 120467086 | |||||
chr1:120467197
|
G | A | 3 | a0003c0012t0026a0003c0012t0027a0003c0012t0046 | 5 | HG01928.hp1 HG02300.hp2 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*976G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 976 | chr1 | 120467197 | |||||
chr1:120467311
|
G | A | 1 | a0004c0005t0016 | 5 | HG03490.hp1 HG03492.hp2 HG03710.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1090G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1090 | chr1 | 120467311 | |||||
chr1:120467356
|
T | C | 1 | a0007c0008t0025 | 2 | HG01070.hp2 HG01074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1135T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1135 | chr1 | 120467356 | |||||
chr1:120467418
|
T | C | 1 | a0001c0010t0062 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1197T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1197 | chr1 | 120467418 | |||||
chr1:120467480
|
G | A | 1 | a0002c0024t0044 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1259G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1259 | chr1 | 120467480 | |||||
chr1:120467487
|
A | G | 20 | a0003c0003t0006a0003c0003t0012a0003c0003t0049others(17): Show | 79 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1266A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1266 | chr1 | 120467487 | |||||
chr1:120467530
|
C | T | 5 | a0001c0007t0007a0001c0007t0019a0001c0007t0057others(2): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1309C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1309 | chr1 | 120467530 | |||||
chr1:120467777
|
T | A | 1 | a0007c0008t0045 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1556T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1556 | chr1 | 120467777 | |||||
chr1:120467833
|
A | T | 4 | a0005c0036t0005a0006c0006t0005a0006c0006t0035others(1): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1612A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1612 | chr1 | 120467833 | |||||
chr1:120467855
|
G | C | 5 | a0001c0018t0018a0001c0020t0030a0001c0021t0018others(2): Show | 10 | HG02257.hp1 HG02257.hp2 HG02615.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1634G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1634 | chr1 | 120467855 | |||||
chr1:120467949
|
A | T | 1 | a0001c0002t0029 | 2 | HG01361.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1728A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1728 | chr1 | 120467949 | |||||
chr1:120467951
|
A | AGT | 29 | a0001c0010t0060a0001c0018t0018a0001c0020t0030others(26): Show | 98 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1740_*1741dupTG | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1742 | INFO_REALIGN_3_PRIME | chr1 | 120467951 | ||||
chr1:120467951
|
A | AGTGT | 3 | a0001c0010t0061a0002c0001t0022a0003c0003t0051 | 4 | HG02451.hp1 NA18964.hp2 NA18983.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1738_*1741dupTGTG | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1742 | INFO_REALIGN_3_PRIME | chr1 | 120467951 | ||||
chr1:120467963
|
C | T | 71 | a0001c0002t0002a0001c0002t0008a0001c0002t0028others(68): Show | 217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*1742C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1742 | chr1 | 120467963 | |||||
chr1:120468027
|
C | G | 1 | a0002c0001t0043 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1806C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1806 | chr1 | 120468027 | |||||
chr1:120468085
|
G | T | 1 | a0003c0003t0047 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1864G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1864 | chr1 | 120468085 | |||||
chr1:120468103
|
A | G | 1 | a0002c0001t0042 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1882A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1882 | chr1 | 120468103 | |||||
chr1:120468104
|
T | C | 5 | a0001c0007t0007a0001c0007t0019a0001c0007t0057others(2): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1883T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1883 | chr1 | 120468104 | |||||
chr1:120468135
|
A | C | 1 | a0002c0001t0041 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1914A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1914 | chr1 | 120468135 | |||||
chr1:120468163
|
C | T | 62 | a0001c0002t0008a0001c0002t0053a0001c0002t0056others(59): Show | 193 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*1942C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 1942 | chr1 | 120468163 | |||||
chr1:120468244
|
C | A | 1 | a0001c0002t0028 | 2 | NA18962.hp1 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2023C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 2023 | chr1 | 120468244 | |||||
chr1:120468452
|
G | T | 1 | a0004c0005t0069 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2231G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 2231 | chr1 | 120468452 | |||||
chr1:120468489
|
T | C | 4 | a0005c0036t0005a0006c0006t0005a0006c0006t0035others(1): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2268T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 2268 | chr1 | 120468489 | |||||
chr1:120468496
|
C | T | 73 | a0001c0002t0002a0001c0002t0008a0001c0002t0028others(70): Show | 213 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*2275C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 2275 | chr1 | 120468496 | |||||
chr1:120468520
|
A | G | 2 | a0003c0003t0013a0003c0003t0049 | 7 | HG02630.hp1 HG02965.hp2 HG03041.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2299A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 2299 | chr1 | 120468520 | |||||
chr1:120468534
|
G | A | 2 | a0001c0010t0060a0001c0010t0061 | 2 | HG02451.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2313G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 2313 | chr1 | 120468534 | |||||
chr1:120468540
|
G | A | 5 | a0002c0001t0010a0002c0001t0039a0002c0001t0042others(2): Show | 9 | HG00673.hp2 NA18612.hp1 NA18962.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2319G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 2319 | chr1 | 120468540 | |||||
chr1:120468651
|
T | C | 32 | a0001c0002t0002a0001c0002t0008a0001c0002t0028others(29): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2430T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 2430 | chr1 | 120468651 | |||||
chr1:120468770
|
C | T | 13 | a0001c0007t0007a0001c0007t0019a0001c0007t0057others(10): Show | 23 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2549C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 2549 | chr1 | 120468770 | |||||
chr1:120468787
|
G | A | 3 | a0001c0018t0018a0001c0020t0030a0001c0021t0018 | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2566G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 2566 | chr1 | 120468787 | |||||
chr1:120468823
|
C | T | 13 | a0001c0007t0007a0001c0007t0019a0001c0007t0057others(10): Show | 23 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2602C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 2602 | chr1 | 120468823 | |||||
chr1:120468871
|
C | T | 1 | a0004c0005t0069 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2650C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 2650 | chr1 | 120468871 | |||||
chr1:120468872
|
G | A | 31 | a0001c0002t0002a0001c0002t0008a0001c0002t0028others(28): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2651G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 2651 | chr1 | 120468872 | |||||
chr1:120469016
|
T | G | 6 | a0001c0007t0007a0001c0007t0019a0001c0007t0057others(3): Show | 16 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2795T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 2795 | chr1 | 120469016 | |||||
chr1:120469152
|
G | A | 84 | a0001c0002t0002a0001c0002t0008a0001c0002t0028others(81): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*2931G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 2931 | chr1 | 120469152 | |||||
chr1:120469154
|
G | T | 2 | a0003c0003t0013a0003c0003t0049 | 7 | HG02630.hp1 HG02965.hp2 HG03041.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2933G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 2933 | chr1 | 120469154 | |||||
chr1:120469355
|
C | T | 1 | a0013c0037t0068 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3134C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 3134 | chr1 | 120469355 | |||||
chr1:120469446
|
T | C | 1 | a0001c0019t0054 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3225T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 3225 | chr1 | 120469446 | |||||
chr1:120469511
|
C | T | 15 | a0001c0002t0002a0001c0002t0008a0001c0002t0028others(12): Show | 57 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*3290C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 3290 | chr1 | 120469511 | |||||
chr1:120469609
|
A | G | 1 | a0002c0001t0040 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3388A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 3388 | chr1 | 120469609 | |||||
chr1:120469631
|
T | G | 1 | a0005c0004t0024 | 2 | HG02602.hp2 HG02683.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3410T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 23/23 | 3410 | chr1 | 120469631 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:120415369
|
G | A | 1 | a0002c0025t0001g0011 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-703+65G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120415369 | ||||||
chr1:120415407
|
G | A | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-703+103G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120415407 | ||||||
chr1:120415426
|
G | A | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.-703+122G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120415426 | ||||||
chr1:120415437
|
C | A | 1 | a0002c0013t0014g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-703+133C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120415437 | ||||||
chr1:120415565
|
C | A | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-703+261C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120415565 | ||||||
chr1:120415694
|
G | A | 18 | a0005c0036t0005g0114a0006c0006t0005g0004a0006c0006t0005g0099others(15): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.-703+390G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120415694 | ||||||
chr1:120415699
|
C | T | 1 | a0005c0004t0004g0282 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-703+395C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120415699 | ||||||
chr1:120415732
|
G | A | 18 | a0005c0036t0005g0114a0006c0006t0005g0004a0006c0006t0005g0099others(15): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.-703+428G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120415732 | ||||||
chr1:120415746
|
A | T | 1 | a0002c0001t0001g0281 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-703+442A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120415746 | ||||||
chr1:120415819
|
T | TCCGG | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-703+516_-703+519d others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 120415819 | |||||
chr1:120415822
|
G | A | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.-703+518G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120415822 | ||||||
chr1:120415833
|
T | C | 1 | a0001c0002t0002g0012 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-703+529T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120415833 | ||||||
chr1:120415965
|
C | T | 1 | a0004c0005t0016g0010 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-703+661C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120415965 | ||||||
chr1:120415972
|
C | T | 1 | a0003c0003t0006g0280 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-703+668C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120415972 | ||||||
chr1:120416067
|
C | T | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-703+763C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120416067 | ||||||
chr1:120416068
|
G | A | 1 | a0003c0003t0049g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-703+764G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120416068 | ||||||
chr1:120416376
|
G | A | 2 | a0001c0022t0007g0082a0001c0022t0007g0083 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-703+1072G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120416376 | ||||||
chr1:120416416
|
G | A | 1 | a0003c0003t0050g0117 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-703+1112G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120416416 | ||||||
chr1:120416575
|
C | T | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-703+1271C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120416575 | ||||||
chr1:120416576
|
T | G | 250 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(247): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-703+1272T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120416576 | ||||||
chr1:120416605
|
C | CA | 21 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0016others(18): Show | 22 | HG00735.hp2 HG00738.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.-703+1326dupA | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 120416605 | |||||
chr1:120416605
|
CA | C | 25 | a0001c0002t0008g0002a0001c0002t0008g0054a0001c0002t0008g0055others(22): Show | 26 | HG01175.hp2 HG01433.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.-703+1326delA | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 120416605 | |||||
chr1:120416605
|
CAA | C | 17 | a0001c0002t0031g0065a0001c0007t0007g0003a0001c0007t0007g0091others(14): Show | 18 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.-703+1325_-703+132 others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 120416605 | |||||
chr1:120416605
|
CAAAAAAA others(5): Show |
C | 5 | a0002c0001t0043g0247a0008c0014t0017g0095a0008c0014t0017g0096others(2): Show | 5 | HG02129.hp1 HG02572.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-703+1315_-703+132 others(16): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 120416605 | |||||
chr1:120416637
|
G | A | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.-703+1333G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120416637 | ||||||
chr1:120416778
|
C | T | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-703+1474C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120416778 | ||||||
chr1:120416786
|
G | T | 6 | a0002c0001t0009g0009a0002c0001t0009g0243a0002c0001t0009g0246others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-703+1482G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120416786 | ||||||
chr1:120416838
|
C | T | 36 | a0005c0004t0004g0007a0005c0004t0004g0008a0005c0004t0004g0131others(33): Show | 38 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.-703+1534C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120416838 | ||||||
chr1:120417010
|
G | T | 250 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(247): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-703+1706G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417010 | ||||||
chr1:120417059
|
G | A | 70 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(67): Show | 71 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-703+1755G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417059 | ||||||
chr1:120417073
|
G | A | 1 | a0003c0003t0048g0183 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-703+1769G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417073 | ||||||
chr1:120417110
|
C | T | 3 | a0003c0003t0006g0211a0003c0003t0047g0212a0003c0003t0048g0183 | 3 | HG02258.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-703+1806C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417110 | ||||||
chr1:120417283
|
G | A | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-703+1979G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417283 | ||||||
chr1:120417347
|
G | A | 8 | a0006c0006t0005g0004a0006c0006t0005g0099a0006c0006t0005g0100others(5): Show | 9 | HG02071.hp1 HG02523.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.-703+2043G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417347 | ||||||
chr1:120417401
|
C | T | 2 | a0001c0022t0007g0082a0001c0022t0007g0083 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-703+2097C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417401 | ||||||
chr1:120417542
|
C | T | 36 | a0005c0004t0004g0007a0005c0004t0004g0008a0005c0004t0004g0131others(33): Show | 38 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.-703+2238C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417542 | ||||||
chr1:120417581
|
G | A | 56 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(53): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.-702-2269G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417581 | ||||||
chr1:120417607
|
C | CT | 28 | a0001c0002t0002g0017a0001c0007t0007g0003a0001c0007t0007g0084others(25): Show | 29 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.-702-2232dupT | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 120417607 | |||||
chr1:120417607
|
C | CTT | 56 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(53): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.-702-2233_-702-223 others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 120417607 | |||||
chr1:120417655
|
C | T | 1 | a0002c0001t0021g0182 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-702-2195C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417655 | ||||||
chr1:120417657
|
G | A | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-702-2193G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417657 | ||||||
chr1:120417736
|
A | G | 5 | a0002c0013t0014g0094a0002c0013t0014g0208a0002c0013t0014g0209others(2): Show | 5 | HG01891.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-702-2114A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417736 | ||||||
chr1:120417752
|
A | C | 3 | a0001c0007t0019g0086a0001c0007t0019g0089a0001c0007t0019g0090 | 3 | HG01433.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-702-2098A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417752 | ||||||
chr1:120417854
|
G | T | 2 | a0003c0012t0026g0206a0003c0012t0026g0207 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-702-1996G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417854 | ||||||
chr1:120417865
|
T | C | 5 | a0002c0013t0014g0094a0002c0013t0014g0208a0002c0013t0014g0209others(2): Show | 5 | HG01891.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-702-1985T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417865 | ||||||
chr1:120417970
|
T | C | 5 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-702-1880T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417970 | ||||||
chr1:120417977
|
T | G | 232 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(229): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-702-1873T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120417977 | ||||||
chr1:120418005
|
T | C | 232 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(229): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-702-1845T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418005 | ||||||
chr1:120418013
|
T | G | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-702-1837T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418013 | ||||||
chr1:120418146
|
G | A | 1 | a0001c0011t0008g0049 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-702-1704G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418146 | ||||||
chr1:120418210
|
G | A | 1 | a0001c0018t0018g0071 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-702-1640G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418210 | ||||||
chr1:120418292
|
G | A | 1 | a0001c0010t0032g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-702-1558G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418292 | ||||||
chr1:120418337
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-702-1513A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418337 | ||||||
chr1:120418460
|
G | A | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-702-1390G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418460 | ||||||
chr1:120418472
|
G | A | 1 | a0001c0010t0059g0080 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-702-1378G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418472 | ||||||
chr1:120418491
|
G | A | 1 | a0006c0006t0005g0106 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-702-1359G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418491 | ||||||
chr1:120418494
|
G | A | 1 | a0002c0001t0038g0132 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-702-1356G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418494 | ||||||
chr1:120418558
|
T | A | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-702-1292T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418558 | ||||||
chr1:120418603
|
T | A | 63 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(60): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.-702-1247T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418603 | ||||||
chr1:120418686
|
T | G | 214 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(211): Show | 220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.-702-1164T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418686 | ||||||
chr1:120418723
|
T | A | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-702-1127T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418723 | ||||||
chr1:120418736
|
T | C | 196 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(193): Show | 201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.-702-1114T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418736 | ||||||
chr1:120418740
|
G | A | 2 | a0004c0005t0003g0250a0004c0005t0067g0249 | 2 | HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-702-1110G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418740 | ||||||
chr1:120418840
|
C | T | 1 | a0001c0019t0055g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-702-1010C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120418840 | ||||||
chr1:120419113
|
A | G | 5 | a0003c0003t0013g0202a0003c0003t0013g0203a0003c0003t0013g0204others(2): Show | 5 | HG02965.hp2 HG03041.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-702-737A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120419113 | ||||||
chr1:120419236
|
T | A | 56 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(53): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.-702-614T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120419236 | ||||||
chr1:120419377
|
C | G | 1 | a0005c0004t0004g0242 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-702-473C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120419377 | ||||||
chr1:120419517
|
A | G | 15 | a0001c0002t0008g0002a0001c0002t0008g0054a0001c0002t0008g0055others(12): Show | 16 | HG01175.hp2 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-702-333A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120419517 | ||||||
chr1:120419626
|
T | A | 75 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(72): Show | 76 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.-702-224T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120419626 | ||||||
chr1:120419630
|
T | G | 2 | a0001c0010t0060g0081a0001c0010t0061g0073 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-702-220T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120419630 | ||||||
chr1:120419677
|
G | A | 1 | a0002c0001t0020g0133 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-702-173G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 1/22 | chr1 | 120419677 | ||||||
chr1:120420126
|
C | T | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.-434+8C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420126 | ||||||
chr1:120420205
|
G | T | 2 | a0001c0020t0030g0067a0001c0020t0030g0068 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-434+87G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420205 | ||||||
chr1:120420265
|
G | A | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.-434+147G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420265 | ||||||
chr1:120420288
|
G | A | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.-434+170G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420288 | ||||||
chr1:120420312
|
C | T | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-434+194C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420312 | ||||||
chr1:120420313
|
T | C | 18 | a0005c0036t0005g0114a0006c0006t0005g0004a0006c0006t0005g0099others(15): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.-434+195T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420313 | ||||||
chr1:120420389
|
A | G | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-434+271A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420389 | ||||||
chr1:120420419
|
C | A | 1 | a0001c0002t0052g0018 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-434+301C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420419 | ||||||
chr1:120420436
|
C | G | 1 | a0001c0002t0002g0047 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-434+318C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420436 | ||||||
chr1:120420455
|
C | T | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-434+337C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420455 | ||||||
chr1:120420464
|
G | A | 70 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(67): Show | 71 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-434+346G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420464 | ||||||
chr1:120420499
|
A | G | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-434+381A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420499 | ||||||
chr1:120420510
|
C | A | 7 | a0003c0003t0013g0184a0003c0003t0013g0185a0003c0003t0013g0202others(4): Show | 7 | HG02630.hp1 HG02965.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-434+392C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420510 | ||||||
chr1:120420586
|
G | C | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-434+468G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420586 | ||||||
chr1:120420629
|
G | A | 1 | a0006c0006t0035g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-434+511G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420629 | ||||||
chr1:120420631
|
C | T | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-434+513C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420631 | ||||||
chr1:120420670
|
G | A | 1 | a0002c0013t0014g0208 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-434+552G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420670 | ||||||
chr1:120420702
|
C | T | 1 | a0001c0045t0065g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-434+584C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420702 | ||||||
chr1:120420745
|
C | T | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-434+627C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420745 | ||||||
chr1:120420759
|
T | C | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-434+641T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420759 | ||||||
chr1:120420763
|
C | A | 1 | a0003c0003t0012g0006 | 2 | NA19002.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-434+645C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420763 | ||||||
chr1:120420900
|
G | C | 1 | a0002c0001t0010g0134 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-434+782G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420900 | ||||||
chr1:120420901
|
C | A | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-434+783C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420901 | ||||||
chr1:120420921
|
C | T | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-434+803C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420921 | ||||||
chr1:120420926
|
G | A | 22 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(19): Show | 23 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-434+808G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120420926 | ||||||
chr1:120421023
|
T | C | 250 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(247): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-434+905T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120421023 | ||||||
chr1:120421085
|
G | A | 1 | a0002c0013t0014g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-434+967G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120421085 | ||||||
chr1:120421182
|
T | A | 1 | a0002c0001t0022g0118 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-434+1064T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120421182 | ||||||
chr1:120421276
|
G | A | 1 | a0009c0016t0003g0251 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-434+1158G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120421276 | ||||||
chr1:120421483
|
T | C | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-434+1365T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120421483 | ||||||
chr1:120421498
|
C | T | 22 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(19): Show | 23 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-434+1380C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120421498 | ||||||
chr1:120421510
|
T | C | 1 | a0005c0004t0004g0282 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-434+1392T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120421510 | ||||||
chr1:120421526
|
C | T | 1 | a0004c0005t0016g0279 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-434+1408C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120421526 | ||||||
chr1:120421606
|
C | T | 1 | a0001c0042t0002g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-434+1488C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120421606 | ||||||
chr1:120421629
|
C | T | 39 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(36): Show | 40 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.-434+1511C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120421629 | ||||||
chr1:120421663
|
C | T | 2 | a0001c0010t0060g0081a0001c0010t0061g0073 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-434+1545C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120421663 | ||||||
chr1:120421714
|
C | T | 1 | a0002c0001t0001g0181 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-434+1596C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120421714 | ||||||
chr1:120421741
|
C | T | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-434+1623C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120421741 | ||||||
chr1:120421843
|
C | T | 1 | a0003c0003t0006g0127 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-434+1725C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120421843 | ||||||
chr1:120421853
|
A | T | 1 | a0002c0001t0001g0180 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-434+1735A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120421853 | ||||||
chr1:120422029
|
C | T | 5 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-434+1911C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120422029 | ||||||
chr1:120422034
|
C | G | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-434+1916C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120422034 | ||||||
chr1:120422203
|
C | T | 36 | a0005c0004t0004g0007a0005c0004t0004g0008a0005c0004t0004g0131others(33): Show | 38 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.-434+2085C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120422203 | ||||||
chr1:120422222
|
A | G | 1 | a0002c0001t0040g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-434+2104A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120422222 | ||||||
chr1:120422480
|
T | A | 1 | a0001c0002t0053g0051 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-434+2362T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120422480 | ||||||
chr1:120422483
|
C | T | 1 | a0005c0004t0004g0241 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-434+2365C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120422483 | ||||||
chr1:120422521
|
G | A | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-434+2403G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120422521 | ||||||
chr1:120422543
|
G | A | 10 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-434+2425G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120422543 | ||||||
chr1:120422684
|
CT | C | 14 | a0006c0006t0005g0004a0006c0006t0005g0099a0006c0006t0005g0100others(11): Show | 15 | HG02071.hp1 HG02523.hp2 NA18941.hp2 others(12): Show |
intron_variant | MODIFIER | c.-434+2567delT | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120422684 | ||||||
chr1:120422791
|
G | A | 1 | a0001c0007t0007g0087 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-434+2673G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120422791 | ||||||
chr1:120422855
|
C | CGTT | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-434+2738_-434+274 others(7): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 120422855 | |||||
chr1:120422959
|
CT | C | 45 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(42): Show | 46 | HG00140.hp2 HG00408.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.-434+2859delT | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 120422959 | |||||
chr1:120422959
|
CTT | C | 231 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(228): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-434+2858_-434+285 others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 120422959 | |||||
chr1:120423082
|
C | A | 1 | a0005c0004t0004g0213 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-434+2964C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120423082 | ||||||
chr1:120423144
|
A | AT | 28 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(25): Show | 29 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.-434+3034dupT | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 120423144 | |||||
chr1:120423271
|
G | A | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.-434+3153G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120423271 | ||||||
chr1:120423373
|
G | T | 1 | a0001c0019t0055g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-434+3255G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120423373 | ||||||
chr1:120423386
|
C | T | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-434+3268C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120423386 | ||||||
chr1:120423463
|
T | C | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-434+3345T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120423463 | ||||||
chr1:120423527
|
T | C | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-434+3409T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120423527 | ||||||
chr1:120423566
|
A | T | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-434+3448A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120423566 | ||||||
chr1:120423680
|
G | A | 17 | a0002c0001t0001g0119a0002c0001t0001g0137a0002c0001t0001g0138others(14): Show | 17 | HG01346.hp1 HG02040.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.-434+3562G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120423680 | ||||||
chr1:120423767
|
G | A | 1 | a0003c0003t0012g0186 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-434+3649G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120423767 | ||||||
chr1:120423854
|
G | A | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.-434+3736G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120423854 | ||||||
chr1:120423995
|
C | T | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-433-3711C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120423995 | ||||||
chr1:120424115
|
C | T | 39 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(36): Show | 40 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.-433-3591C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120424115 | ||||||
chr1:120424214
|
G | A | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-433-3492G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120424214 | ||||||
chr1:120424301
|
T | C | 1 | a0003c0012t0026g0206 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-433-3405T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120424301 | ||||||
chr1:120424393
|
G | A | 1 | a0001c0045t0065g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-433-3313G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120424393 | ||||||
chr1:120424505
|
C | T | 1 | a0003c0012t0027g0200 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-433-3201C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120424505 | ||||||
chr1:120424509
|
G | A | 63 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(60): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.-433-3197G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120424509 | ||||||
chr1:120424536
|
C | T | 8 | a0003c0003t0006g0193a0003c0003t0006g0194a0003c0003t0006g0195others(5): Show | 8 | HG02080.hp1 HG02155.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.-433-3170C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120424536 | ||||||
chr1:120424596
|
T | A | 1 | a0005c0004t0004g0214 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-433-3110T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120424596 | ||||||
chr1:120424694
|
TGCCTTG | T | 3 | a0001c0002t0002g0013a0001c0002t0002g0019a0001c0002t0002g0047 | 3 | HG00323.hp2 HG00738.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-433-3007_-433-300 others(10): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 120424694 | |||||
chr1:120424736
|
C | T | 1 | a0002c0024t0044g0176 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-433-2970C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120424736 | ||||||
chr1:120424776
|
A | T | 70 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(67): Show | 71 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-433-2930A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120424776 | ||||||
chr1:120424830
|
T | G | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.-433-2876T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120424830 | ||||||
chr1:120425081
|
G | A | 36 | a0005c0004t0004g0007a0005c0004t0004g0008a0005c0004t0004g0131others(33): Show | 38 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.-433-2625G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425081 | ||||||
chr1:120425130
|
G | A | 1 | a0002c0001t0009g0120 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-433-2576G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425130 | ||||||
chr1:120425141
|
G | A | 1 | a0001c0011t0015g0053 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-433-2565G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425141 | ||||||
chr1:120425167
|
C | A | 6 | a0001c0002t0002g0001a0001c0002t0002g0014a0001c0002t0002g0020others(3): Show | 7 | HG01106.hp2 HG01169.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.-433-2539C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425167 | ||||||
chr1:120425254
|
C | G | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-433-2452C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425254 | ||||||
chr1:120425293
|
G | A | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-433-2413G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425293 | ||||||
chr1:120425328
|
C | T | 2 | a0009c0016t0003g0251a0009c0016t0003g0276 | 2 | HG02300.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-433-2378C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425328 | ||||||
chr1:120425329
|
G | A | 71 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(68): Show | 72 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-433-2377G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425329 | ||||||
chr1:120425368
|
G | C | 1 | a0001c0019t0054g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-433-2338G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425368 | ||||||
chr1:120425398
|
A | T | 1 | a0014c0033t0003g0275 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-433-2308A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425398 | ||||||
chr1:120425440
|
T | A | 2 | a0005c0004t0023g0215a0005c0004t0023g0216 | 2 | HG01099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.-433-2266T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425440 | ||||||
chr1:120425481
|
G | C | 214 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(211): Show | 220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.-433-2225G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425481 | ||||||
chr1:120425490
|
A | G | 70 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(67): Show | 71 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-433-2216A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425490 | ||||||
chr1:120425539
|
G | A | 107 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(104): Show | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-433-2167G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425539 | ||||||
chr1:120425601
|
G | T | 2 | a0003c0012t0026g0206a0003c0012t0026g0207 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-433-2105G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425601 | ||||||
chr1:120425603
|
C | G | 1 | a0005c0004t0033g0240 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-433-2103C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425603 | ||||||
chr1:120425690
|
G | A | 2 | a0005c0004t0024g0217a0005c0004t0024g0218 | 2 | HG02602.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-433-2016G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425690 | ||||||
chr1:120425889
|
A | G | 2 | a0001c0010t0060g0081a0001c0010t0061g0073 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-433-1817A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120425889 | ||||||
chr1:120426080
|
G | A | 1 | a0001c0002t0002g0024 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-433-1626G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120426080 | ||||||
chr1:120426087
|
G | A | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-433-1619G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120426087 | ||||||
chr1:120426134
|
A | C | 2 | a0001c0020t0030g0067a0001c0020t0030g0068 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-433-1572A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120426134 | ||||||
chr1:120426173
|
G | A | 1 | a0003c0003t0013g0184 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-433-1533G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120426173 | ||||||
chr1:120426183
|
C | T | 2 | a0001c0002t0002g0044a0001c0002t0002g0045 | 2 | HG01261.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-433-1523C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120426183 | ||||||
chr1:120426199
|
G | A | 1 | a0001c0010t0059g0080 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-433-1507G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120426199 | ||||||
chr1:120426208
|
G | A | 32 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0193others(29): Show | 33 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.-433-1498G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120426208 | ||||||
chr1:120426250
|
T | TCCTTA | 5 | a0002c0001t0009g0009a0002c0001t0009g0243a0002c0001t0009g0246others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.-433-1452_-433-144 others(9): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 120426250 | |||||
chr1:120426289
|
C | T | 2 | a0001c0002t0002g0042a0001c0002t0002g0043 | 2 | HG02895.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-433-1417C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120426289 | ||||||
chr1:120426310
|
C | T | 2 | a0001c0010t0060g0081a0001c0010t0061g0073 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-433-1396C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120426310 | ||||||
chr1:120426345
|
C | T | 1 | a0002c0013t0014g0208 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-433-1361C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120426345 | ||||||
chr1:120426384
|
G | C | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-433-1322G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120426384 | ||||||
chr1:120426657
|
G | T | 2 | a0001c0021t0018g0069a0001c0021t0018g0070 | 2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-433-1049G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120426657 | ||||||
chr1:120426806
|
G | A | 8 | a0001c0002t0002g0026a0001c0002t0002g0027a0001c0002t0002g0028others(5): Show | 8 | HG00099.hp2 HG00140.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.-433-900G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120426806 | ||||||
chr1:120426935
|
T | A | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-433-771T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120426935 | ||||||
chr1:120427047
|
T | C | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-433-659T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120427047 | ||||||
chr1:120427057
|
C | A | 7 | a0003c0003t0013g0184a0003c0003t0013g0185a0003c0003t0013g0202others(4): Show | 7 | HG02630.hp1 HG02965.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-433-649C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120427057 | ||||||
chr1:120427088
|
C | T | 1 | a0002c0001t0001g0147 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-433-618C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120427088 | ||||||
chr1:120427113
|
T | G | 2 | a0001c0002t0031g0065a0001c0044t0031g0064 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-433-593T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120427113 | ||||||
chr1:120427235
|
G | A | 1 | a0004c0005t0016g0254 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-433-471G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120427235 | ||||||
chr1:120427420
|
A | G | 1 | a0006c0006t0005g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-433-286A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120427420 | ||||||
chr1:120427430
|
C | G | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-433-276C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120427430 | ||||||
chr1:120427531
|
A | G | 107 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(104): Show | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-433-175A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120427531 | ||||||
chr1:120427642
|
G | C | 1 | a0003c0003t0006g0187 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-433-64G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 2/22 | chr1 | 120427642 | ||||||
chr1:120428102
|
T | C | 1 | a0002c0024t0044g0176 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-292+255T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428102 | ||||||
chr1:120428125
|
G | A | 250 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(247): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-292+278G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428125 | ||||||
chr1:120428137
|
G | A | 32 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0193others(29): Show | 33 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.-292+290G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428137 | ||||||
chr1:120428155
|
C | T | 2 | a0009c0016t0003g0251a0009c0016t0003g0276 | 2 | HG02300.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-292+308C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428155 | ||||||
chr1:120428165
|
A | G | 1 | a0007c0008t0011g0239 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-292+318A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428165 | ||||||
chr1:120428315
|
G | A | 12 | a0002c0001t0001g0119a0002c0001t0001g0137a0002c0001t0001g0138others(9): Show | 12 | HG02040.hp2 HG02074.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.-292+468G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428315 | ||||||
chr1:120428330
|
C | T | 18 | a0005c0036t0005g0114a0006c0006t0005g0004a0006c0006t0005g0099others(15): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.-292+483C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428330 | ||||||
chr1:120428359
|
C | G | 1 | a0002c0001t0021g0182 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-292+512C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428359 | ||||||
chr1:120428402
|
A | T | 3 | a0001c0007t0007g0085a0001c0007t0007g0087a0001c0043t0007g0088 | 3 | NA18947.hp1 NA18975.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.-292+555A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428402 | ||||||
chr1:120428575
|
T | G | 1 | a0002c0001t0036g0148 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-292+728T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428575 | ||||||
chr1:120428643
|
C | T | 1 | a0001c0002t0002g0012 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-292+796C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428643 | ||||||
chr1:120428690
|
G | T | 1 | a0002c0001t0020g0175 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-292+843G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428690 | ||||||
chr1:120428724
|
G | A | 1 | a0008c0014t0017g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-292+877G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428724 | ||||||
chr1:120428738
|
T | G | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-292+891T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428738 | ||||||
chr1:120428754
|
C | T | 107 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(104): Show | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-292+907C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428754 | ||||||
chr1:120428767
|
C | T | 196 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(193): Show | 201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.-292+920C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428767 | ||||||
chr1:120428772
|
C | T | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-292+925C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428772 | ||||||
chr1:120428782
|
C | G | 3 | a0002c0001t0022g0118a0002c0001t0022g0126a0002c0001t0038g0132 | 3 | NA18954.hp1 NA18964.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-292+935C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428782 | ||||||
chr1:120428804
|
C | T | 1 | a0005c0004t0004g0282 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-292+957C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428804 | ||||||
chr1:120428839
|
A | G | 1 | a0001c0010t0059g0080 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-292+992A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428839 | ||||||
chr1:120428936
|
A | G | 250 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(247): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-292+1089A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428936 | ||||||
chr1:120428939
|
C | T | 1 | a0003c0003t0047g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-292+1092C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428939 | ||||||
chr1:120428975
|
G | A | 1 | a0006c0006t0005g0108 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-292+1128G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120428975 | ||||||
chr1:120429195
|
C | T | 1 | a0005c0004t0004g0241 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-292+1348C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120429195 | ||||||
chr1:120429222
|
C | T | 84 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(81): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.-292+1375C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120429222 | ||||||
chr1:120429233
|
T | C | 2 | a0003c0003t0006g0211a0003c0003t0048g0183 | 2 | HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-292+1386T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120429233 | ||||||
chr1:120429244
|
C | T | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-292+1397C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120429244 | ||||||
chr1:120429361
|
A | G | 1 | a0001c0002t0002g0041 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-292+1514A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120429361 | ||||||
chr1:120429391
|
G | A | 1 | a0002c0001t0009g0243 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-292+1544G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120429391 | ||||||
chr1:120429442
|
C | T | 1 | a0003c0003t0006g0211 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-292+1595C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120429442 | ||||||
chr1:120429751
|
G | A | 1 | a0006c0006t0005g0108 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-292+1904G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120429751 | ||||||
chr1:120429810
|
G | A | 1 | a0001c0019t0054g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-292+1963G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120429810 | ||||||
chr1:120429813
|
C | T | 2 | a0002c0001t0001g0181a0002c0001t0036g0148 | 2 | NA18952.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-292+1966C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120429813 | ||||||
chr1:120429846
|
C | T | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-292+1999C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120429846 | ||||||
chr1:120429847
|
G | A | 1 | a0001c0002t0029g0015 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-292+2000G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120429847 | ||||||
chr1:120429896
|
A | G | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.-292+2049A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120429896 | ||||||
chr1:120430151
|
G | A | 63 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(60): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.-292+2304G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120430151 | ||||||
chr1:120430182
|
G | C | 250 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(247): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-292+2335G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120430182 | ||||||
chr1:120430292
|
C | T | 1 | a0001c0019t0054g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-292+2445C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120430292 | ||||||
chr1:120430462
|
C | T | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-292+2615C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120430462 | ||||||
chr1:120430470
|
A | G | 3 | a0003c0003t0006g0197a0003c0003t0006g0199a0003c0003t0051g0198 | 3 | HG02080.hp1 NA19011.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-292+2623A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120430470 | ||||||
chr1:120430476
|
G | T | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-292+2629G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120430476 | ||||||
chr1:120430613
|
G | A | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-292+2766G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120430613 | ||||||
chr1:120430615
|
G | A | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-292+2768G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120430615 | ||||||
chr1:120430621
|
G | A | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-292+2774G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120430621 | ||||||
chr1:120430752
|
C | CA | 85 | a0001c0002t0002g0013a0001c0002t0002g0016a0001c0002t0002g0024others(82): Show | 86 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.-292+2927dupA | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120430752 | |||||
chr1:120430752
|
C | CAA | 7 | a0001c0010t0058g0076a0001c0010t0059g0080a0002c0001t0001g0121others(4): Show | 7 | HG00673.hp1 HG00673.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-292+2926_-292+292 others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120430752 | |||||
chr1:120430752
|
CA | C | 16 | a0001c0002t0002g0040a0001c0002t0002g0045a0001c0007t0007g0093others(13): Show | 16 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-292+2927delA | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120430752 | |||||
chr1:120430799
|
G | A | 1 | a0004c0005t0003g0255 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-292+2952G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120430799 | ||||||
chr1:120430854
|
A | G | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.-292+3007A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120430854 | ||||||
chr1:120430883
|
T | A | 14 | a0006c0006t0005g0004a0006c0006t0005g0099a0006c0006t0005g0100others(11): Show | 15 | HG02071.hp1 HG02523.hp2 NA18941.hp2 others(12): Show |
intron_variant | MODIFIER | c.-292+3036T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120430883 | ||||||
chr1:120431131
|
GA | G | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-292+3294delA | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431131 | |||||
chr1:120431218
|
C | CAT | 6 | a0002c0013t0014g0094a0002c0013t0014g0208a0002c0013t0014g0209others(3): Show | 6 | HG01891.hp2 HG01943.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-292+3380_-292+338 others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431218 | |||||
chr1:120431252
|
CGT | C | 131 | a0001c0002t0002g0013a0001c0002t0002g0019a0001c0002t0002g0040others(128): Show | 133 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.-292+3434_-292+343 others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431252 | |||||
chr1:120431252
|
CGTGT | C | 22 | a0003c0012t0026g0206a0005c0004t0023g0215a0005c0004t0023g0216others(19): Show | 23 | HG01099.hp1 HG01109.hp2 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-292+3432_-292+343 others(8): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431252 | |||||
chr1:120431252
|
CGTGTGT | C | 41 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(38): Show | 42 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.-292+3430_-292+343 others(10): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431252 | |||||
chr1:120431272
|
T | C | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-292+3425T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431272 | ||||||
chr1:120431277
|
G | C | 1 | a0002c0013t0014g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-292+3430G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431277 | ||||||
chr1:120431279
|
G | A | 3 | a0001c0019t0054g0066a0001c0020t0030g0067a0001c0020t0030g0068 | 3 | HG02257.hp1 HG02717.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-292+3432G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431279 | ||||||
chr1:120431280
|
T | C | 3 | a0001c0002t0002g0013a0001c0002t0002g0019a0001c0002t0002g0047 | 3 | HG00323.hp2 HG00738.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-292+3433T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431280 | ||||||
chr1:120431281
|
G | A | 83 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(80): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-292+3434G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431281 | ||||||
chr1:120431301
|
ATTATCAT others(31): Show |
A | 6 | a0001c0002t0002g0019a0001c0007t0007g0003a0001c0007t0007g0091others(3): Show | 7 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.-292+3493_-292+353 others(42): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431301 | |||||
chr1:120431321
|
AATATATA others(33): Show |
A | 3 | a0001c0002t0002g0041a0001c0002t0002g0042a0001c0002t0002g0043 | 3 | HG02895.hp1 HG03130.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.-292+3493_-292+353 others(44): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431321 | |||||
chr1:120431321
|
AATATATA others(35): Show |
A | 7 | a0001c0002t0002g0027a0001c0002t0002g0028a0001c0002t0002g0029others(4): Show | 7 | HG00099.hp2 HG00323.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-292+3493_-292+353 others(46): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431321 | |||||
chr1:120431321
|
AATATATA others(37): Show |
A | 10 | a0001c0002t0002g0012a0001c0002t0002g0017a0001c0002t0002g0022others(7): Show | 10 | HG00140.hp1 HG00609.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.-292+3493_-292+353 others(48): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431321 | |||||
chr1:120431321
|
AATATATA others(39): Show |
A | 12 | a0001c0002t0002g0016a0001c0002t0002g0031a0001c0002t0002g0032others(9): Show | 12 | HG00280.hp1 HG00544.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.-292+3493_-292+353 others(50): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431321 | |||||
chr1:120431321
|
AATATATA others(41): Show |
A | 15 | a0001c0002t0002g0001a0001c0002t0002g0014a0001c0002t0002g0020others(12): Show | 16 | HG01099.hp2 HG01106.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-292+3493_-292+354 others(52): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431321 | |||||
chr1:120431321
|
AATATATA others(43): Show |
A | 1 | a0001c0019t0055g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-292+3493_-292+354 others(54): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431321 | |||||
chr1:120431321
|
AATATATA others(45): Show |
A | 6 | a0001c0002t0008g0002a0001c0002t0008g0055a0001c0002t0008g0061others(3): Show | 7 | HG01891.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-292+3493_-292+354 others(56): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431321 | |||||
chr1:120431323
|
TATATATA others(29): Show |
T | 8 | a0001c0002t0002g0013a0001c0002t0029g0039a0001c0007t0019g0089others(5): Show | 8 | HG01243.hp2 HG01433.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-292+3493_-292+352 others(40): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431323 | |||||
chr1:120431325
|
TATATATA others(27): Show |
T | 1 | a0001c0010t0063g0077 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-292+3493_-292+352 others(38): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431325 | |||||
chr1:120431327
|
TATATATA others(25): Show |
T | 3 | a0001c0007t0007g0084a0001c0007t0007g0085a0001c0043t0007g0088 | 3 | NA18947.hp1 NA18977.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-292+3493_-292+352 others(36): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431327 | |||||
chr1:120431329
|
TATATATA others(23): Show |
T | 7 | a0001c0002t0002g0024a0001c0007t0007g0087a0001c0007t0019g0086others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-292+3493_-292+352 others(34): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431329 | |||||
chr1:120431331
|
TATATATA others(21): Show |
T | 2 | a0001c0010t0058g0076a0001c0020t0030g0067 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-292+3493_-292+352 others(32): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431331 | |||||
chr1:120431333
|
TATATATT others(19): Show |
T | 2 | a0001c0010t0062g0079a0001c0020t0030g0068 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-292+3493_-292+351 others(30): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431333 | |||||
chr1:120431335
|
TATATTTA others(17): Show |
T | 1 | a0001c0007t0019g0090 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-292+3493_-292+351 others(28): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431335 | |||||
chr1:120431337
|
TATTTATC others(15): Show |
T | 1 | a0001c0002t0031g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-292+3493_-292+351 others(26): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431337 | |||||
chr1:120431359
|
A | AAT | 9 | a0004c0005t0003g0248a0004c0005t0003g0250a0004c0005t0003g0256others(6): Show | 9 | HG00735.hp1 HG01943.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.-292+3554_-292+355 others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431359 | |||||
chr1:120431359
|
A | AATATATA others(5): Show |
1 | a0008c0014t0017g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-292+3544_-292+355 others(16): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431359 | |||||
chr1:120431359
|
AAT | A | 33 | a0002c0001t0001g0172a0002c0001t0001g0281a0002c0025t0001g0011others(30): Show | 35 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-292+3554_-292+355 others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431359 | |||||
chr1:120431359
|
AATAT | A | 13 | a0002c0001t0001g0178a0002c0001t0020g0133a0002c0001t0043g0247others(10): Show | 14 | HG01070.hp2 HG01074.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.-292+3552_-292+355 others(8): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431359 | |||||
chr1:120431359
|
AATATAT | A | 23 | a0002c0001t0001g0138a0002c0001t0001g0139a0002c0001t0001g0140others(20): Show | 23 | HG00099.hp1 HG00408.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.-292+3550_-292+355 others(10): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431359 | |||||
chr1:120431359
|
AATATATA others(1): Show |
A | 7 | a0002c0001t0001g0167a0002c0001t0001g0168a0002c0001t0010g0166others(4): Show | 7 | HG00609.hp1 HG00741.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-292+3548_-292+355 others(12): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431359 | |||||
chr1:120431359
|
AATATATA others(3): Show |
A | 36 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0137others(33): Show | 37 | HG00280.hp2 HG00673.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.-292+3546_-292+355 others(14): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431359 | |||||
chr1:120431359
|
AATATATA others(5): Show |
A | 10 | a0002c0001t0001g0122a0002c0001t0001g0153a0002c0001t0001g0154others(7): Show | 10 | HG00673.hp2 HG00738.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-292+3544_-292+355 others(16): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431359 | |||||
chr1:120431359
|
AATATATA others(7): Show |
A | 20 | a0002c0001t0022g0126a0003c0003t0006g0193a0003c0003t0006g0194others(17): Show | 21 | HG00544.hp2 HG01928.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.-292+3542_-292+355 others(18): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431359 | |||||
chr1:120431359
|
AATATATA others(9): Show |
A | 12 | a0002c0001t0021g0152a0002c0001t0021g0182a0003c0003t0006g0211others(9): Show | 12 | HG01175.hp1 HG02258.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-292+3540_-292+355 others(20): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431359 | |||||
chr1:120431359
|
AATATATA others(11): Show |
A | 18 | a0003c0003t0006g0197a0005c0036t0005g0114a0006c0006t0005g0004others(15): Show | 19 | HG02071.hp1 HG02080.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.-292+3538_-292+355 others(22): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431359 | |||||
chr1:120431398
|
A | C | 1 | a0003c0003t0006g0127 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-292+3551A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431398 | ||||||
chr1:120431401
|
T | C | 5 | a0003c0003t0013g0202a0003c0003t0013g0203a0003c0003t0013g0204others(2): Show | 5 | HG02965.hp2 HG03041.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-292+3554T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431401 | ||||||
chr1:120431419
|
C | CAT | 76 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(73): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.-292+3583_-292+358 others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431419 | |||||
chr1:120431419
|
C | T | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-292+3572C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431419 | ||||||
chr1:120431419
|
CAT | C | 36 | a0005c0004t0004g0007a0005c0004t0004g0008a0005c0004t0004g0131others(33): Show | 38 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.-292+3583_-292+358 others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120431419 | |||||
chr1:120431474
|
A | G | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-292+3627A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431474 | ||||||
chr1:120431501
|
A | T | 1 | a0003c0003t0006g0195 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-292+3654A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431501 | ||||||
chr1:120431525
|
G | T | 1 | a0004c0005t0069g0272 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-292+3678G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431525 | ||||||
chr1:120431590
|
A | G | 1 | a0001c0002t0002g0014 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-292+3743A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431590 | ||||||
chr1:120431695
|
G | A | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-292+3848G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431695 | ||||||
chr1:120431813
|
C | T | 4 | a0004c0005t0016g0010a0004c0005t0016g0254a0004c0005t0016g0258others(1): Show | 5 | HG03490.hp1 HG03492.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.-292+3966C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431813 | ||||||
chr1:120431830
|
G | A | 2 | a0001c0002t0002g0020a0012c0039t0002g0021 | 2 | HG01517.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.-292+3983G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431830 | ||||||
chr1:120431847
|
A | G | 195 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(192): Show | 201 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.-292+4000A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431847 | ||||||
chr1:120431859
|
C | T | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-292+4012C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120431859 | ||||||
chr1:120432023
|
C | T | 192 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(189): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-292+4176C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120432023 | ||||||
chr1:120432243
|
G | A | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-291-3989G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120432243 | ||||||
chr1:120432258
|
G | A | 2 | a0001c0018t0018g0071a0001c0018t0018g0072 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-291-3974G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120432258 | ||||||
chr1:120432374
|
CT | C | 184 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(181): Show | 189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.-291-3843delT | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120432374 | |||||
chr1:120432374
|
CTT | C | 6 | a0001c0002t0002g0045a0001c0019t0054g0066a0001c0020t0030g0067others(3): Show | 6 | HG01243.hp1 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-291-3844_-291-384 others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120432374 | |||||
chr1:120432392
|
T | C | 2 | a0001c0002t0031g0065a0001c0044t0031g0064 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-291-3840T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120432392 | ||||||
chr1:120432485
|
A | C | 1 | a0005c0004t0004g0008 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-291-3747A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120432485 | ||||||
chr1:120432573
|
C | T | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-291-3659C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120432573 | ||||||
chr1:120432766
|
G | C | 2 | a0001c0018t0018g0071a0001c0018t0018g0072 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-291-3466G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120432766 | ||||||
chr1:120432807
|
G | GT | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-291-3423dupT | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120432807 | |||||
chr1:120432890
|
G | A | 1 | a0005c0004t0004g0242 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-291-3342G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120432890 | ||||||
chr1:120432926
|
A | G | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-291-3306A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120432926 | ||||||
chr1:120433151
|
C | T | 6 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(3): Show | 6 | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-291-3081C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120433151 | ||||||
chr1:120433241
|
G | A | 36 | a0005c0004t0004g0007a0005c0004t0004g0008a0005c0004t0004g0131others(33): Show | 38 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.-291-2991G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120433241 | ||||||
chr1:120433243
|
A | C | 36 | a0005c0004t0004g0007a0005c0004t0004g0008a0005c0004t0004g0131others(33): Show | 38 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.-291-2989A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120433243 | ||||||
chr1:120433277
|
C | T | 32 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0193others(29): Show | 33 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.-291-2955C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120433277 | ||||||
chr1:120433665
|
C | T | 2 | a0001c0018t0018g0071a0001c0018t0018g0072 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-291-2567C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120433665 | ||||||
chr1:120433726
|
C | T | 1 | a0001c0002t0002g0046 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-291-2506C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120433726 | ||||||
chr1:120433730
|
G | A | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-291-2502G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120433730 | ||||||
chr1:120433749
|
G | A | 1 | a0003c0003t0006g0187 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-291-2483G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120433749 | ||||||
chr1:120433948
|
T | C | 107 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(104): Show | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-291-2284T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120433948 | ||||||
chr1:120434003
|
G | A | 56 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(53): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.-291-2229G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434003 | ||||||
chr1:120434037
|
G | A | 1 | a0001c0045t0065g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-291-2195G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434037 | ||||||
chr1:120434087
|
G | C | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-291-2145G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434087 | ||||||
chr1:120434090
|
C | T | 1 | a0001c0011t0008g0049 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-291-2142C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434090 | ||||||
chr1:120434101
|
G | A | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-291-2131G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434101 | ||||||
chr1:120434129
|
G | T | 2 | a0001c0010t0060g0081a0001c0010t0061g0073 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-291-2103G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434129 | ||||||
chr1:120434141
|
G | A | 2 | a0002c0001t0021g0152a0002c0001t0021g0182 | 2 | HG01175.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-291-2091G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434141 | ||||||
chr1:120434143
|
A | T | 1 | a0004c0005t0003g0248 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-291-2089A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434143 | ||||||
chr1:120434147
|
C | T | 1 | a0001c0010t0058g0076 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-291-2085C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434147 | ||||||
chr1:120434203
|
G | A | 1 | a0001c0002t0031g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-291-2029G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434203 | ||||||
chr1:120434228
|
AT | A | 8 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(5): Show | 8 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-291-2003delT | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434228 | ||||||
chr1:120434229
|
T | A | 8 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(5): Show | 8 | HG02109.hp2 HG02165.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-291-2003T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434229 | ||||||
chr1:120434231
|
T | A | 2 | a0001c0010t0060g0081a0001c0010t0061g0073 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-291-2001T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434231 | ||||||
chr1:120434289
|
TTA | T | 236 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(233): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-291-1932_-291-193 others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120434289 | |||||
chr1:120434318
|
C | T | 2 | a0001c0002t0029g0015a0001c0002t0029g0039 | 2 | HG01361.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-291-1914C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434318 | ||||||
chr1:120434319
|
G | A | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-291-1913G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434319 | ||||||
chr1:120434375
|
GTATATAT others(14): Show |
G | 1 | a0003c0003t0006g0193 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-291-1852_-291-183 others(25): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120434375 | |||||
chr1:120434415
|
T | TTA | 32 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0193others(29): Show | 33 | HG00544.hp2 HG01106.hp1 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.-291-1804_-291-180 others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr1 | 120434415 | |||||
chr1:120434457
|
A | C | 70 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(67): Show | 71 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-291-1775A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434457 | ||||||
chr1:120434475
|
T | G | 32 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0193others(29): Show | 33 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.-291-1757T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434475 | ||||||
chr1:120434572
|
G | A | 1 | a0005c0004t0004g0242 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-291-1660G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434572 | ||||||
chr1:120434575
|
C | A | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-291-1657C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434575 | ||||||
chr1:120434600
|
T | C | 1 | a0002c0001t0001g0144 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-291-1632T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434600 | ||||||
chr1:120434698
|
A | T | 1 | a0004c0005t0003g0248 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-291-1534A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434698 | ||||||
chr1:120434855
|
A | C | 1 | a0002c0001t0021g0152 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-291-1377A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434855 | ||||||
chr1:120434941
|
C | T | 3 | a0005c0036t0005g0114a0006c0006t0005g0113a0006c0006t0005g0115 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-291-1291C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120434941 | ||||||
chr1:120435034
|
C | T | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-291-1198C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435034 | ||||||
chr1:120435121
|
C | A | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-291-1111C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435121 | ||||||
chr1:120435292
|
T | C | 2 | a0001c0002t0031g0065a0001c0044t0031g0064 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-291-940T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435292 | ||||||
chr1:120435396
|
A | G | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-291-836A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435396 | ||||||
chr1:120435517
|
C | A | 1 | a0006c0006t0005g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-291-715C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435517 | ||||||
chr1:120435521
|
C | A | 18 | a0005c0036t0005g0114a0006c0006t0005g0004a0006c0006t0005g0099others(15): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.-291-711C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435521 | ||||||
chr1:120435541
|
A | C | 250 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(247): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-291-691A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435541 | ||||||
chr1:120435558
|
A | G | 1 | a0001c0002t0008g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-291-674A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435558 | ||||||
chr1:120435569
|
C | T | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-291-663C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435569 | ||||||
chr1:120435572
|
G | A | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-291-660G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435572 | ||||||
chr1:120435596
|
T | C | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-291-636T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435596 | ||||||
chr1:120435625
|
G | A | 3 | a0001c0010t0032g0078a0001c0010t0062g0079a0001c0010t0063g0077 | 3 | HG02572.hp2 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-291-607G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435625 | ||||||
chr1:120435642
|
A | G | 1 | a0007c0008t0011g0239 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-291-590A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435642 | ||||||
chr1:120435656
|
C | T | 1 | a0003c0003t0047g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-291-576C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435656 | ||||||
chr1:120435719
|
A | T | 18 | a0005c0036t0005g0114a0006c0006t0005g0004a0006c0006t0005g0099others(15): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.-291-513A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435719 | ||||||
chr1:120435726
|
C | T | 1 | a0001c0043t0007g0088 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-291-506C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435726 | ||||||
chr1:120435771
|
C | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-291-461C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435771 | ||||||
chr1:120435849
|
G | A | 8 | a0003c0003t0006g0193a0003c0003t0006g0194a0003c0003t0006g0195others(5): Show | 8 | HG02080.hp1 HG02155.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.-291-383G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435849 | ||||||
chr1:120435873
|
T | A | 84 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(81): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.-291-359T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120435873 | ||||||
chr1:120436057
|
T | A | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-291-175T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120436057 | ||||||
chr1:120436194
|
G | T | 1 | a0006c0006t0005g0108 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-291-38G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120436194 | ||||||
chr1:120436227
|
T | G | 1 | a0002c0025t0001g0011 | 1 | HG01346.hp1 | splice_region_variant&intron_variant | LOW | c.-291-5T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 3/22 | chr1 | 120436227 | ||||||
chr1:120436870
|
T | C | 4 | a0003c0003t0013g0202a0003c0003t0013g0203a0003c0003t0013g0205others(1): Show | 4 | HG02965.hp2 HG03041.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+173T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120436870 | ||||||
chr1:120436955
|
C | T | 2 | a0001c0002t0002g0016a0004c0005t0003g0259 | 2 | HG00735.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.175+258C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120436955 | ||||||
chr1:120436961
|
G | A | 1 | a0001c0019t0054g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.175+264G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120436961 | ||||||
chr1:120437153
|
C | G | 4 | a0006c0006t0005g0106a0006c0006t0005g0109a0006c0006t0005g0110others(1): Show | 4 | NA18970.hp1 NA18988.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+456C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120437153 | ||||||
chr1:120437173
|
G | T | 1 | a0001c0002t0008g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.175+476G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120437173 | ||||||
chr1:120437212
|
C | T | 32 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0193others(29): Show | 33 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.175+515C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120437212 | ||||||
chr1:120437309
|
A | G | 89 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(86): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.175+612A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120437309 | ||||||
chr1:120437384
|
G | A | 1 | a0001c0007t0007g0087 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.175+687G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120437384 | ||||||
chr1:120437386
|
A | G | 79 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(76): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.175+689A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120437386 | ||||||
chr1:120437418
|
G | A | 1 | a0001c0019t0054g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.175+721G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120437418 | ||||||
chr1:120437449
|
C | A | 1 | a0003c0012t0027g0201 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.175+752C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120437449 | ||||||
chr1:120437464
|
G | T | 32 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0193others(29): Show | 33 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.175+767G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120437464 | ||||||
chr1:120437519
|
G | A | 33 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0193others(30): Show | 34 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.175+822G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120437519 | ||||||
chr1:120437549
|
T | C | 1 | a0008c0014t0017g0097 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.175+852T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120437549 | ||||||
chr1:120437575
|
G | C | 1 | a0001c0002t0052g0018 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.175+878G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120437575 | ||||||
chr1:120437618
|
G | A | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+921G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120437618 | ||||||
chr1:120437909
|
A | C | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-635A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120437909 | ||||||
chr1:120438161
|
A | G | 1 | a0005c0004t0004g0282 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.176-383A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120438161 | ||||||
chr1:120438254
|
A | G | 63 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(60): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.176-290A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120438254 | ||||||
chr1:120438288
|
C | T | 1 | a0001c0019t0054g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.176-256C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120438288 | ||||||
chr1:120438315
|
C | A | 32 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0193others(29): Show | 33 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.176-229C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120438315 | ||||||
chr1:120438328
|
G | A | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.176-216G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120438328 | ||||||
chr1:120438354
|
C | T | 4 | a0001c0002t0002g0013a0001c0002t0002g0019a0001c0002t0002g0041others(1): Show | 4 | HG00323.hp2 HG00738.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-190C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120438354 | ||||||
chr1:120438356
|
TTAAATTT others(7): Show |
T | 1 | a0013c0037t0068g0266 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.176-186_176-173del others(14): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 120438356 | |||||
chr1:120438369
|
G | T | 25 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0193others(22): Show | 26 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.176-175G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120438369 | ||||||
chr1:120438513
|
C | A | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.176-31C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 4/22 | chr1 | 120438513 | ||||||
chr1:120438657
|
C | T | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+11C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/22 | chr1 | 120438657 | ||||||
chr1:120438713
|
C | T | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.278+67C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/22 | chr1 | 120438713 | ||||||
chr1:120438754
|
A | G | 1 | a0001c0002t0056g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.278+108A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/22 | chr1 | 120438754 | ||||||
chr1:120438826
|
A | G | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.278+180A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/22 | chr1 | 120438826 | ||||||
chr1:120438857
|
T | C | 1 | a0008c0014t0017g0097 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.278+211T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/22 | chr1 | 120438857 | ||||||
chr1:120438889
|
T | C | 1 | a0015c0032t0003g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.278+243T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/22 | chr1 | 120438889 | ||||||
chr1:120438935
|
G | A | 1 | a0001c0018t0018g0072 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.278+289G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/22 | chr1 | 120438935 | ||||||
chr1:120438981
|
A | G | 1 | a0013c0037t0068g0266 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.278+335A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/22 | chr1 | 120438981 | ||||||
chr1:120439167
|
T | C | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.279-309T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/22 | chr1 | 120439167 | ||||||
chr1:120439207
|
T | C | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.279-269T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/22 | chr1 | 120439207 | ||||||
chr1:120439226
|
A | C | 1 | a0005c0004t0004g0225 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.279-250A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/22 | chr1 | 120439226 | ||||||
chr1:120439279
|
G | A | 1 | a0003c0003t0006g0193 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.279-197G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/22 | chr1 | 120439279 | ||||||
chr1:120439425
|
G | A | 32 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0193others(29): Show | 33 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.279-51G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/22 | chr1 | 120439425 | ||||||
chr1:120439444
|
A | G | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.279-32A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/22 | chr1 | 120439444 | ||||||
chr1:120439445
|
C | G | 1 | a0001c0002t0052g0018 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.279-31C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/22 | chr1 | 120439445 | ||||||
chr1:120439464
|
A | G | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.279-12A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 5/22 | chr1 | 120439464 | ||||||
chr1:120439748
|
C | T | 79 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(76): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.493+58C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120439748 | ||||||
chr1:120439775
|
A | T | 1 | a0013c0037t0068g0266 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.493+85A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120439775 | ||||||
chr1:120439777
|
C | T | 1 | a0013c0037t0068g0266 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.493+87C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120439777 | ||||||
chr1:120439784
|
GT | G | 206 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(203): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.493+102delT | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr1 | 120439784 | |||||
chr1:120439789
|
T | G | 1 | a0013c0037t0068g0266 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.493+99T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120439789 | ||||||
chr1:120439791
|
T | A | 1 | a0013c0037t0068g0266 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.493+101T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120439791 | ||||||
chr1:120439999
|
T | C | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.493+309T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120439999 | ||||||
chr1:120440072
|
T | A | 3 | a0001c0007t0019g0086a0001c0007t0019g0089a0001c0007t0019g0090 | 3 | HG01433.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.493+382T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120440072 | ||||||
chr1:120440163
|
C | T | 1 | a0001c0002t0008g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.493+473C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120440163 | ||||||
chr1:120440230
|
G | T | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.494-512G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120440230 | ||||||
chr1:120440236
|
G | T | 32 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0193others(29): Show | 33 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.494-506G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120440236 | ||||||
chr1:120440265
|
C | A | 1 | a0004c0005t0003g0277 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.494-477C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120440265 | ||||||
chr1:120440266
|
T | C | 1 | a0004c0005t0003g0277 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.494-476T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120440266 | ||||||
chr1:120440270
|
C | A | 1 | a0004c0005t0003g0277 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.494-472C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120440270 | ||||||
chr1:120440329
|
C | T | 2 | a0004c0005t0003g0250a0004c0005t0067g0249 | 2 | HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.494-413C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120440329 | ||||||
chr1:120440334
|
C | T | 6 | a0001c0007t0057g0092a0001c0022t0007g0083a0008c0014t0017g0095others(3): Show | 6 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.494-408C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120440334 | ||||||
chr1:120440500
|
T | C | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-242T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120440500 | ||||||
chr1:120440578
|
G | A | 6 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(3): Show | 6 | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.494-164G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120440578 | ||||||
chr1:120440667
|
T | C | 1 | a0011c0023t0010g0151 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.494-75T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120440667 | ||||||
chr1:120440676
|
G | A | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-66G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120440676 | ||||||
chr1:120440699
|
A | C | 1 | a0013c0037t0068g0266 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.494-43A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120440699 | ||||||
chr1:120440713
|
A | G | 56 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(53): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.494-29A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120440713 | ||||||
chr1:120440741
|
A | G | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
splice_acceptor_variant&intron_variant | HIGH | c.494-1A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 6/22 | chr1 | 120440741 | ||||||
chr1:120440878
|
C | A | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.566+64C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 7/22 | chr1 | 120440878 | ||||||
chr1:120440944
|
C | T | 1 | a0001c0002t0008g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.566+130C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 7/22 | chr1 | 120440944 | ||||||
chr1:120440961
|
T | C | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.566+147T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 7/22 | chr1 | 120440961 | ||||||
chr1:120441001
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.566+187T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 7/22 | chr1 | 120441001 | ||||||
chr1:120441184
|
C | G | 1 | a0007c0008t0011g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.567-94C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 7/22 | chr1 | 120441184 | ||||||
chr1:120441193
|
A | G | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.567-85A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 7/22 | chr1 | 120441193 | ||||||
chr1:120441739
|
GGCAGGCA others(6359): Show |
G | 1 | a0005c0036t0005g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.778+254_779-1085de others(1): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr1 | 120441739 | |||||
chr1:120441780
|
G | C | 1 | a0001c0002t0002g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.778+291G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120441780 | ||||||
chr1:120441835
|
T | C | 2 | a0001c0018t0018g0071a0001c0018t0018g0072 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.778+346T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120441835 | ||||||
chr1:120441962
|
C | A | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.778+473C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120441962 | ||||||
chr1:120442018
|
C | CA | 38 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(35): Show | 40 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.778+545dupA | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr1 | 120442018 | |||||
chr1:120442018
|
C | CAAAAAAA others(6346): Show |
1 | a0004c0005t0069g0272 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.778+545_778+546ins others(6353): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr1 | 120442018 | |||||
chr1:120442018
|
C | CAAAAAAA others(6347): Show |
8 | a0004c0005t0003g0252a0004c0005t0003g0261a0004c0005t0003g0262others(5): Show | 8 | HG02040.hp1 HG02129.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.778+545_778+546ins others(6354): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr1 | 120442018 | |||||
chr1:120442018
|
C | CAAAAAAA others(6347): Show |
1 | a0004c0005t0016g0010 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.778+545_778+546ins others(6354): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr1 | 120442018 | |||||
chr1:120442018
|
CAAAAAAA others(6346): Show |
C | 39 | a0001c0022t0007g0082a0005c0004t0004g0007a0005c0004t0004g0008others(36): Show | 41 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.778+545_779-807del | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr1 | 120442018 | |||||
chr1:120442020
|
AAAAAAAA others(6343): Show |
A | 25 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0024others(22): Show | 25 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.778+546_779-809del | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr1 | 120442020 | |||||
chr1:120442021
|
AAAAAAAA others(6342): Show |
A | 1 | a0001c0002t0029g0015 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.778+546_779-810del | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr1 | 120442021 | |||||
chr1:120442057
|
G | A | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.778+568G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120442057 | ||||||
chr1:120442088
|
G | A | 1 | a0001c0040t0002g0033 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.778+599G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120442088 | ||||||
chr1:120442502
|
CAAAAAAG others(6346): Show |
C | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.778+1019_779-333de others(1): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr1 | 120442502 | |||||
chr1:120442981
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1492G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120442981 | ||||||
chr1:120442982
|
T | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1493T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120442982 | ||||||
chr1:120443036
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1547G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443036 | ||||||
chr1:120443037
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1548A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443037 | ||||||
chr1:120443043
|
G | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1554G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443043 | ||||||
chr1:120443061
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1572T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443061 | ||||||
chr1:120443071
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1582G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443071 | ||||||
chr1:120443092
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1603G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443092 | ||||||
chr1:120443194
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1705T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443194 | ||||||
chr1:120443243
|
G | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1754G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443243 | ||||||
chr1:120443251
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1762A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443251 | ||||||
chr1:120443276
|
C | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1787C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443276 | ||||||
chr1:120443277
|
A | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1788A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443277 | ||||||
chr1:120443280
|
G | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1791G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443280 | ||||||
chr1:120443293
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1804A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443293 | ||||||
chr1:120443308
|
C | T | 2 | a0001c0022t0007g0083a0002c0029t0010g0149 | 2 | HG00673.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.778+1819C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443308 | ||||||
chr1:120443333
|
A | G | 1 | a0002c0009t0001g0165 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.778+1844A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443333 | ||||||
chr1:120443336
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1847A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443336 | ||||||
chr1:120443337
|
T | C | 10 | a0002c0001t0001g0157a0002c0001t0040g0179a0002c0009t0001g0123others(7): Show | 10 | NA18942.hp2 NA18966.hp2 NA18970.hp2 others(7): Show |
intron_variant | MODIFIER | c.778+1848T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443337 | ||||||
chr1:120443389
|
G | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1900G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443389 | ||||||
chr1:120443412
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1923A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443412 | ||||||
chr1:120443413
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1924G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443413 | ||||||
chr1:120443461
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+1972G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443461 | ||||||
chr1:120443490
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2001G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443490 | ||||||
chr1:120443506
|
C | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2017C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443506 | ||||||
chr1:120443542
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2053G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443542 | ||||||
chr1:120443543
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2054C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443543 | ||||||
chr1:120443561
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2072C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443561 | ||||||
chr1:120443563
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2074A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443563 | ||||||
chr1:120443607
|
A | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2118A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443607 | ||||||
chr1:120443608
|
C | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2119C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443608 | ||||||
chr1:120443609
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2120A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443609 | ||||||
chr1:120443628
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2139T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443628 | ||||||
chr1:120443650
|
C | T | 1 | a0002c0001t0001g0122 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.778+2161C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443650 | ||||||
chr1:120443658
|
G | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2169G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443658 | ||||||
chr1:120443661
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2172C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443661 | ||||||
chr1:120443662
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2173A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443662 | ||||||
chr1:120443670
|
C | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2181C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443670 | ||||||
chr1:120443677
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2188A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443677 | ||||||
chr1:120443681
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2192T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443681 | ||||||
chr1:120443711
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2222C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443711 | ||||||
chr1:120443739
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2250A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443739 | ||||||
chr1:120443741
|
C | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2252C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443741 | ||||||
chr1:120443747
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2258G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443747 | ||||||
chr1:120443750
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2261C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443750 | ||||||
chr1:120443751
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2262A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443751 | ||||||
chr1:120443764
|
A | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2275A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443764 | ||||||
chr1:120443767
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2278A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443767 | ||||||
chr1:120443768
|
A | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2279A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443768 | ||||||
chr1:120443771
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2282G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443771 | ||||||
chr1:120443785
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2296G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443785 | ||||||
chr1:120443786
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2297A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443786 | ||||||
chr1:120443805
|
C | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2316C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443805 | ||||||
chr1:120443810
|
A | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2321A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443810 | ||||||
chr1:120443813
|
T | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2324T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443813 | ||||||
chr1:120443830
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2341A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443830 | ||||||
chr1:120443833
|
G | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2344G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443833 | ||||||
chr1:120443834
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2345C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443834 | ||||||
chr1:120443835
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2346A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443835 | ||||||
chr1:120443837
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2348T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443837 | ||||||
chr1:120443851
|
A | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2362A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443851 | ||||||
chr1:120443856
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2367T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443856 | ||||||
chr1:120443872
|
G | A | 74 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(71): Show | 75 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.778+2383G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443872 | ||||||
chr1:120443874
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2385C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443874 | ||||||
chr1:120443880
|
A | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2391A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443880 | ||||||
chr1:120443881
|
C | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2392C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443881 | ||||||
chr1:120443883
|
A | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2394A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443883 | ||||||
chr1:120443885
|
C | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2396C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443885 | ||||||
chr1:120443886
|
A | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2397A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443886 | ||||||
chr1:120443889
|
A | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2400A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443889 | ||||||
chr1:120443890
|
C | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2401C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443890 | ||||||
chr1:120443892
|
A | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2403A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443892 | ||||||
chr1:120443895
|
A | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2406A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443895 | ||||||
chr1:120443916
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2427A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443916 | ||||||
chr1:120443965
|
T | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2476T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443965 | ||||||
chr1:120443972
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2483G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443972 | ||||||
chr1:120443973
|
C | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2484C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443973 | ||||||
chr1:120443981
|
C | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2492C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120443981 | ||||||
chr1:120444001
|
A | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2512A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444001 | ||||||
chr1:120444020
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2531A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444020 | ||||||
chr1:120444021
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2532G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444021 | ||||||
chr1:120444022
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2533C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444022 | ||||||
chr1:120444036
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2547G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444036 | ||||||
chr1:120444039
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2550A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444039 | ||||||
chr1:120444050
|
C | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2561C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444050 | ||||||
chr1:120444052
|
C | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2563C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444052 | ||||||
chr1:120444053
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2564A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444053 | ||||||
chr1:120444055
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2566C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444055 | ||||||
chr1:120444068
|
C | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2579C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444068 | ||||||
chr1:120444081
|
C | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2592C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444081 | ||||||
chr1:120444111
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2622T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444111 | ||||||
chr1:120444159
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2670A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444159 | ||||||
chr1:120444173
|
G | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2684G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444173 | ||||||
chr1:120444174
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2685C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444174 | ||||||
chr1:120444180
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2691C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444180 | ||||||
chr1:120444186
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2697A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444186 | ||||||
chr1:120444193
|
T | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2704T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444193 | ||||||
chr1:120444201
|
A | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2712A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444201 | ||||||
chr1:120444211
|
G | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2722G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444211 | ||||||
chr1:120444212
|
T | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2723T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444212 | ||||||
chr1:120444243
|
A | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2754A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444243 | ||||||
chr1:120444273
|
TGCTGTTT others(50): Show |
T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2785_778+2841d others(59): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444273 | ||||||
chr1:120444331
|
A | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2842A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444331 | ||||||
chr1:120444334
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2845T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444334 | ||||||
chr1:120444364
|
T | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2875T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444364 | ||||||
chr1:120444367
|
C | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2878C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444367 | ||||||
chr1:120444374
|
C | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2885C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444374 | ||||||
chr1:120444408
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2919C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444408 | ||||||
chr1:120444413
|
T | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2924T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444413 | ||||||
chr1:120444419
|
T | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2930T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444419 | ||||||
chr1:120444434
|
G | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2945G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444434 | ||||||
chr1:120444438
|
T | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2949T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444438 | ||||||
chr1:120444444
|
T | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2955T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444444 | ||||||
chr1:120444448
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2959G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444448 | ||||||
chr1:120444451
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2962C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444451 | ||||||
chr1:120444454
|
G | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2965G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444454 | ||||||
chr1:120444455
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2966A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444455 | ||||||
chr1:120444460
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2971T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444460 | ||||||
chr1:120444474
|
A | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2985A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444474 | ||||||
chr1:120444481
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+2992A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444481 | ||||||
chr1:120444514
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3025A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444514 | ||||||
chr1:120444624
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3135G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444624 | ||||||
chr1:120444631
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3142G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444631 | ||||||
chr1:120444642
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3153G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444642 | ||||||
chr1:120444680
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3191C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444680 | ||||||
chr1:120444682
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3193C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444682 | ||||||
chr1:120444692
|
T | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3203T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444692 | ||||||
chr1:120444705
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3216G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444705 | ||||||
chr1:120444709
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3220T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444709 | ||||||
chr1:120444725
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3236C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444725 | ||||||
chr1:120444828
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3339C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444828 | ||||||
chr1:120444839
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3350G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444839 | ||||||
chr1:120444844
|
C | T | 1 | a0002c0001t0001g0164 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.778+3355C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444844 | ||||||
chr1:120444878
|
C | T | 1 | a0002c0001t0001g0143 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.778+3389C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444878 | ||||||
chr1:120444898
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3409G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444898 | ||||||
chr1:120444910
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3421T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444910 | ||||||
chr1:120444916
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3427C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444916 | ||||||
chr1:120444924
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3435G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444924 | ||||||
chr1:120444927
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3438T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444927 | ||||||
chr1:120444998
|
A | G | 74 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(71): Show | 75 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.778+3509A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120444998 | ||||||
chr1:120445009
|
A | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3520A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445009 | ||||||
chr1:120445013
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3524G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445013 | ||||||
chr1:120445015
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3526A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445015 | ||||||
chr1:120445017
|
G | C | 8 | a0002c0001t0001g0122a0002c0001t0001g0153a0002c0001t0001g0154others(5): Show | 8 | HG00609.hp1 HG00738.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.778+3528G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445017 | ||||||
chr1:120445020
|
G | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3531G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445020 | ||||||
chr1:120445028
|
C | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3539C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445028 | ||||||
chr1:120445032
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3543T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445032 | ||||||
chr1:120445042
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3553G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445042 | ||||||
chr1:120445066
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3577C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445066 | ||||||
chr1:120445074
|
A | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3585A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445074 | ||||||
chr1:120445081
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3592A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445081 | ||||||
chr1:120445082
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3593T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445082 | ||||||
chr1:120445083
|
G | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3594G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445083 | ||||||
chr1:120445107
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3618A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445107 | ||||||
chr1:120445126
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3637A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445126 | ||||||
chr1:120445127
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3638T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445127 | ||||||
chr1:120445128
|
G | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3639G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445128 | ||||||
chr1:120445128
|
GAC | G | 9 | a0002c0001t0001g0157a0002c0001t0040g0179a0002c0009t0001g0123others(6): Show | 9 | NA18942.hp2 NA18966.hp2 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.778+3645_778+3646d others(4): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr1 | 120445128 | |||||
chr1:120445152
|
C | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3663C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445152 | ||||||
chr1:120445153
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3664A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445153 | ||||||
chr1:120445160
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3671A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445160 | ||||||
chr1:120445164
|
T | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3675T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445164 | ||||||
chr1:120445167
|
G | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3678G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445167 | ||||||
chr1:120445168
|
T | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3679T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445168 | ||||||
chr1:120445170
|
C | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3681C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445170 | ||||||
chr1:120445173
|
T | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3684T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445173 | ||||||
chr1:120445189
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3700T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445189 | ||||||
chr1:120445229
|
G | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3740G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445229 | ||||||
chr1:120445254
|
C | A | 2 | a0001c0022t0007g0083a0004c0005t0003g0256 | 2 | HG00735.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.778+3765C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445254 | ||||||
chr1:120445267
|
G | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3778G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445267 | ||||||
chr1:120445275
|
C | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3786C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445275 | ||||||
chr1:120445275
|
C | G | 1 | a0002c0009t0001g0160 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.778+3786C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445275 | ||||||
chr1:120445293
|
A | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3804A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445293 | ||||||
chr1:120445308
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3819T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445308 | ||||||
chr1:120445312
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778+3823G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445312 | ||||||
chr1:120445344
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3849T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445344 | ||||||
chr1:120445358
|
T | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3835T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445358 | ||||||
chr1:120445394
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3799T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445394 | ||||||
chr1:120445420
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3773A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445420 | ||||||
chr1:120445467
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3726A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445467 | ||||||
chr1:120445517
|
A | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3676A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445517 | ||||||
chr1:120445631
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3562G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445631 | ||||||
chr1:120445636
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3557C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445636 | ||||||
chr1:120445641
|
C | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3552C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445641 | ||||||
chr1:120445650
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3543G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445650 | ||||||
chr1:120445652
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3541A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445652 | ||||||
chr1:120445662
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3531G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445662 | ||||||
chr1:120445673
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3520G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445673 | ||||||
chr1:120445723
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3470C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445723 | ||||||
chr1:120445726
|
G | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3467G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445726 | ||||||
chr1:120445739
|
T | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3454T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445739 | ||||||
chr1:120445741
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3452A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445741 | ||||||
chr1:120445756
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3437A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445756 | ||||||
chr1:120445776
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3417A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445776 | ||||||
chr1:120445796
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3397T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445796 | ||||||
chr1:120445817
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3376A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445817 | ||||||
chr1:120445879
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3314A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445879 | ||||||
chr1:120445891
|
A | G | 75 | a0001c0022t0007g0083a0002c0001t0001g0005a0002c0001t0001g0119others(72): Show | 76 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.779-3302A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120445891 | ||||||
chr1:120446101
|
C | T | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-3092C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120446101 | ||||||
chr1:120446582
|
G | A | 1 | a0002c0024t0044g0176 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.779-2611G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120446582 | ||||||
chr1:120446665
|
A | AGGGCCTG others(6345): Show |
1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.779-1472_779-1471i others(6354): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr1 | 120446665 | |||||
chr1:120446924
|
C | T | 1 | a0002c0001t0001g0164 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.779-2269C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120446924 | ||||||
chr1:120446933
|
C | G | 3 | a0002c0001t0001g0144a0002c0001t0001g0146a0002c0001t0009g0145 | 3 | HG03834.hp2 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.779-2260C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120446933 | ||||||
chr1:120447016
|
G | T | 1 | a0002c0009t0001g0125 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.779-2177G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120447016 | ||||||
chr1:120447019
|
T | C | 69 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(66): Show | 70 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.779-2174T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120447019 | ||||||
chr1:120447093
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-2100A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120447093 | ||||||
chr1:120447101
|
C | T | 74 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(71): Show | 75 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.779-2092C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120447101 | ||||||
chr1:120447216
|
G | A | 1 | a0002c0001t0001g0281 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.779-1977G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120447216 | ||||||
chr1:120447353
|
T | C | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.779-1840T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120447353 | ||||||
chr1:120447722
|
T | C | 76 | a0001c0022t0007g0083a0002c0001t0001g0005a0002c0001t0001g0119others(73): Show | 77 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.779-1471T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120447722 | ||||||
chr1:120447838
|
T | C | 123 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(120): Show | 126 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.779-1355T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120447838 | ||||||
chr1:120447858
|
T | C | 1 | a0006c0006t0005g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.779-1335T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120447858 | ||||||
chr1:120448255
|
G | A | 1 | a0002c0001t0001g0122 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.779-938G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120448255 | ||||||
chr1:120448370
|
C | CA | 8 | a0002c0001t0001g0147a0002c0013t0014g0094a0002c0013t0014g0208others(5): Show | 8 | HG01891.hp2 HG02080.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.779-807dupA | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr1 | 120448370 | |||||
chr1:120448396
|
C | T | 2 | a0001c0018t0018g0071a0001c0018t0018g0072 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.779-797C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120448396 | ||||||
chr1:120448399
|
G | A | 1 | a0001c0019t0055g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.779-794G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120448399 | ||||||
chr1:120448440
|
G | A | 62 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(59): Show | 64 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.779-753G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120448440 | ||||||
chr1:120448467
|
C | T | 2 | a0002c0013t0014g0094a0002c0013t0014g0209 | 2 | HG01891.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.779-726C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120448467 | ||||||
chr1:120448624
|
G | A | 1 | a0001c0002t0053g0051 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.779-569G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120448624 | ||||||
chr1:120448624
|
G | C | 1 | a0001c0019t0054g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.779-569G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120448624 | ||||||
chr1:120448699
|
G | T | 8 | a0006c0006t0005g0004a0006c0006t0005g0099a0006c0006t0005g0100others(5): Show | 9 | HG02071.hp1 HG02523.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.779-494G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120448699 | ||||||
chr1:120448800
|
C | T | 2 | a0001c0021t0018g0069a0001c0021t0018g0070 | 2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.779-393C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120448800 | ||||||
chr1:120448914
|
C | A | 1 | a0001c0002t0029g0039 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.779-279C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120448914 | ||||||
chr1:120449053
|
G | C | 107 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(104): Show | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.779-140G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120449053 | ||||||
chr1:120449143
|
T | C | 1 | a0002c0028t0014g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.779-50T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120449143 | ||||||
chr1:120449160
|
A | T | 1 | a0002c0001t0001g0146 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.779-33A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120449160 | ||||||
chr1:120449162
|
C | A | 1 | a0002c0001t0001g0146 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.779-31C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 8/22 | chr1 | 120449162 | ||||||
chr1:120449428
|
G | A | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.988+26G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120449428 | ||||||
chr1:120449451
|
C | G | 2 | a0002c0001t0001g0167a0002c0001t0001g0170 | 2 | HG00609.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.988+49C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120449451 | ||||||
chr1:120449595
|
T | G | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.988+193T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120449595 | ||||||
chr1:120449600
|
C | T | 1 | a0003c0012t0027g0200 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.988+198C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120449600 | ||||||
chr1:120449660
|
T | C | 1 | a0004c0005t0003g0273 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.988+258T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120449660 | ||||||
chr1:120449688
|
G | T | 34 | a0005c0004t0004g0007a0005c0004t0004g0008a0005c0004t0004g0131others(31): Show | 36 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.988+286G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120449688 | ||||||
chr1:120449708
|
T | C | 1 | a0002c0001t0001g0157 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.988+306T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120449708 | ||||||
chr1:120449739
|
C | G | 2 | a0002c0013t0014g0094a0002c0013t0014g0209 | 2 | HG01891.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.988+337C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120449739 | ||||||
chr1:120449879
|
C | A | 1 | a0001c0002t0053g0051 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.988+477C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120449879 | ||||||
chr1:120449910
|
C | T | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.988+508C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120449910 | ||||||
chr1:120449953
|
G | A | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.988+551G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120449953 | ||||||
chr1:120449984
|
T | A | 1 | a0001c0042t0002g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.988+582T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120449984 | ||||||
chr1:120450011
|
C | G | 248 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(245): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.988+609C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450011 | ||||||
chr1:120450099
|
T | A | 1 | a0001c0010t0061g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.988+697T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450099 | ||||||
chr1:120450134
|
G | A | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.988+732G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450134 | ||||||
chr1:120450173
|
G | A | 1 | a0004c0015t0003g0268 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.988+771G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450173 | ||||||
chr1:120450205
|
C | T | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.988+803C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450205 | ||||||
chr1:120450206
|
G | A | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.988+804G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450206 | ||||||
chr1:120450213
|
C | A | 5 | a0004c0005t0003g0248a0004c0005t0003g0259a0004c0005t0003g0267others(2): Show | 5 | NA18941.hp1 NA18952.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.988+811C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450213 | ||||||
chr1:120450279
|
C | T | 34 | a0005c0004t0004g0007a0005c0004t0004g0008a0005c0004t0004g0131others(31): Show | 36 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.988+877C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450279 | ||||||
chr1:120450299
|
G | A | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.989-881G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450299 | ||||||
chr1:120450300
|
C | G | 6 | a0001c0011t0008g0049a0001c0011t0015g0052a0001c0011t0015g0053others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.989-880C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450300 | ||||||
chr1:120450316
|
G | T | 56 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(53): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.989-864G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450316 | ||||||
chr1:120450344
|
C | G | 3 | a0001c0002t0008g0002a0001c0002t0008g0061a0001c0002t0008g0062 | 4 | HG02258.hp2 HG02717.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.989-836C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450344 | ||||||
chr1:120450347
|
C | T | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.989-833C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450347 | ||||||
chr1:120450398
|
C | T | 82 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(79): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.989-782C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450398 | ||||||
chr1:120450411
|
A | C | 3 | a0001c0002t0008g0002a0001c0002t0008g0061a0001c0002t0008g0062 | 4 | HG02258.hp2 HG02717.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.989-769A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450411 | ||||||
chr1:120450578
|
T | A | 70 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(67): Show | 71 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.989-602T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450578 | ||||||
chr1:120450579
|
C | A | 1 | a0005c0004t0033g0240 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.989-601C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450579 | ||||||
chr1:120450580
|
A | T | 70 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(67): Show | 71 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.989-600A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450580 | ||||||
chr1:120450644
|
A | G | 2 | a0001c0021t0018g0069a0001c0021t0018g0070 | 2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.989-536A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450644 | ||||||
chr1:120450739
|
C | A | 107 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(104): Show | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.989-441C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450739 | ||||||
chr1:120450843
|
T | C | 107 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(104): Show | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.989-337T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450843 | ||||||
chr1:120450872
|
G | T | 2 | a0001c0018t0018g0071a0001c0018t0018g0072 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.989-308G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450872 | ||||||
chr1:120450921
|
C | G | 1 | a0001c0002t0002g0017 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.989-259C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450921 | ||||||
chr1:120450993
|
T | C | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.989-187T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120450993 | ||||||
chr1:120451008
|
C | T | 248 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(245): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.989-172C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120451008 | ||||||
chr1:120451119
|
G | T | 1 | a0002c0001t0020g0133 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.989-61G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120451119 | ||||||
chr1:120451127
|
C | A | 1 | a0001c0020t0030g0067 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.989-53C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 9/22 | chr1 | 120451127 | ||||||
chr1:120451308
|
A | AG | 248 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(245): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1091+31dupG | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr1 | 120451308 | |||||
chr1:120451356
|
C | T | 248 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(245): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1091+74C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 10/22 | chr1 | 120451356 | ||||||
chr1:120451438
|
G | A | 1 | a0001c0019t0054g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1091+156G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 10/22 | chr1 | 120451438 | ||||||
chr1:120451480
|
C | G | 1 | a0006c0006t0005g0113 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1091+198C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 10/22 | chr1 | 120451480 | ||||||
chr1:120451558
|
C | A | 1 | a0001c0002t0002g0041 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1091+276C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 10/22 | chr1 | 120451558 | ||||||
chr1:120451667
|
A | C | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091+385A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 10/22 | chr1 | 120451667 | ||||||
chr1:120451668
|
A | T | 1 | a0002c0001t0001g0164 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1091+386A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 10/22 | chr1 | 120451668 | ||||||
chr1:120451680
|
C | T | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1091+398C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 10/22 | chr1 | 120451680 | ||||||
chr1:120451810
|
T | A | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092-307T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 10/22 | chr1 | 120451810 | ||||||
chr1:120451934
|
A | T | 1 | a0001c0002t0002g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1092-183A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 10/22 | chr1 | 120451934 | ||||||
chr1:120451939
|
G | A | 1 | a0001c0007t0007g0085 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1092-178G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 10/22 | chr1 | 120451939 | ||||||
chr1:120451988
|
T | C | 1 | a0002c0001t0009g0145 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1092-129T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 10/22 | chr1 | 120451988 | ||||||
chr1:120452339
|
G | T | 1 | a0002c0001t0001g0137 | 1 | NA19060.hp1 | splice_region_variant&intron_variant | LOW | c.1306+8G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452339 | ||||||
chr1:120452353
|
A | G | 1 | a0004c0005t0003g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1306+22A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452353 | ||||||
chr1:120452381
|
A | G | 2 | a0002c0001t0001g0157a0002c0001t0040g0179 | 2 | NA19062.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1306+50A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452381 | ||||||
chr1:120452437
|
TA | T | 32 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0193others(29): Show | 33 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.1306+108delA | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr1 | 120452437 | |||||
chr1:120452453
|
T | C | 70 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(67): Show | 71 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1306+122T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452453 | ||||||
chr1:120452456
|
C | T | 56 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(53): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1306+125C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452456 | ||||||
chr1:120452524
|
A | C | 1 | a0006c0006t0005g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1306+193A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452524 | ||||||
chr1:120452541
|
G | C | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1306+210G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452541 | ||||||
chr1:120452549
|
G | A | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1306+218G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452549 | ||||||
chr1:120452607
|
C | T | 39 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(36): Show | 40 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.1306+276C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452607 | ||||||
chr1:120452608
|
G | A | 1 | a0004c0005t0003g0265 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1306+277G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452608 | ||||||
chr1:120452615
|
G | A | 1 | a0005c0004t0004g0242 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1306+284G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452615 | ||||||
chr1:120452651
|
A | T | 1 | a0003c0003t0012g0192 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1306+320A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452651 | ||||||
chr1:120452673
|
T | C | 1 | a0001c0002t0002g0034 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1306+342T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452673 | ||||||
chr1:120452739
|
C | T | 56 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(53): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1306+408C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452739 | ||||||
chr1:120452746
|
G | C | 22 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(19): Show | 23 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1306+415G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452746 | ||||||
chr1:120452769
|
C | T | 18 | a0005c0036t0005g0114a0006c0006t0005g0004a0006c0006t0005g0099others(15): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.1306+438C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452769 | ||||||
chr1:120452789
|
A | G | 1 | a0001c0007t0057g0092 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1306+458A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452789 | ||||||
chr1:120452828
|
G | A | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306+497G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452828 | ||||||
chr1:120452897
|
G | A | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1307-475G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452897 | ||||||
chr1:120452985
|
A | T | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.1307-387A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120452985 | ||||||
chr1:120453026
|
A | G | 3 | a0003c0012t0027g0200a0003c0012t0027g0201a0003c0012t0046g0191 | 3 | HG01928.hp1 HG02300.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1307-346A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120453026 | ||||||
chr1:120453030
|
C | T | 3 | a0003c0012t0027g0200a0003c0012t0027g0201a0003c0012t0046g0191 | 3 | HG01928.hp1 HG02300.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1307-342C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120453030 | ||||||
chr1:120453114
|
C | G | 36 | a0005c0004t0004g0007a0005c0004t0004g0008a0005c0004t0004g0131others(33): Show | 38 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1307-258C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120453114 | ||||||
chr1:120453141
|
A | T | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307-231A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120453141 | ||||||
chr1:120453340
|
A | C | 14 | a0006c0006t0005g0004a0006c0006t0005g0099a0006c0006t0005g0100others(11): Show | 15 | HG02071.hp1 HG02523.hp2 NA18941.hp2 others(12): Show |
intron_variant | MODIFIER | c.1307-32A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 11/22 | chr1 | 120453340 | ||||||
chr1:120453533
|
CA | C | 36 | a0005c0004t0004g0007a0005c0004t0004g0008a0005c0004t0004g0131others(33): Show | 38 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1379+94delA | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr1 | 120453533 | |||||
chr1:120453547
|
T | C | 214 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(211): Show | 220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1379+103T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 12/22 | chr1 | 120453547 | ||||||
chr1:120453552
|
A | G | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1379+108A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 12/22 | chr1 | 120453552 | ||||||
chr1:120453558
|
A | G | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.1379+114A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 12/22 | chr1 | 120453558 | ||||||
chr1:120453698
|
A | G | 1 | a0002c0001t0022g0118 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1380-211A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 12/22 | chr1 | 120453698 | ||||||
chr1:120453755
|
G | T | 2 | a0007c0008t0011g0220a0007c0008t0011g0221 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1380-154G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 12/22 | chr1 | 120453755 | ||||||
chr1:120453824
|
G | A | 15 | a0001c0002t0008g0002a0001c0002t0008g0054a0001c0002t0008g0055others(12): Show | 16 | HG01175.hp2 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1380-85G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 12/22 | chr1 | 120453824 | ||||||
chr1:120453877
|
T | A | 107 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(104): Show | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.1380-32T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 12/22 | chr1 | 120453877 | ||||||
chr1:120454290
|
C | T | 2 | a0001c0010t0060g0081a0001c0010t0061g0073 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1585+176C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120454290 | ||||||
chr1:120454394
|
C | T | 2 | a0001c0022t0007g0082a0001c0022t0007g0083 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1585+280C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120454394 | ||||||
chr1:120454629
|
A | G | 2 | a0001c0002t0002g0042a0001c0002t0002g0043 | 2 | HG02895.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1585+515A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120454629 | ||||||
chr1:120454659
|
T | C | 1 | a0001c0007t0057g0092 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1585+545T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120454659 | ||||||
chr1:120454702
|
G | T | 1 | a0001c0007t0057g0092 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1585+588G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120454702 | ||||||
chr1:120454703
|
A | AT | 6 | a0004c0005t0003g0255a0004c0005t0003g0259a0004c0005t0003g0263others(3): Show | 6 | HG02080.hp2 HG02135.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1585+618dupT | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 120454703 | |||||
chr1:120454703
|
A | ATTTT | 7 | a0001c0007t0007g0003a0001c0007t0007g0085a0001c0007t0007g0093others(4): Show | 8 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1585+615_1585+618d others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 120454703 | |||||
chr1:120454703
|
A | ATTTTT | 13 | a0001c0002t0008g0060a0001c0007t0007g0084a0001c0007t0007g0087others(10): Show | 13 | HG00642.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1585+614_1585+618d others(7): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 120454703 | |||||
chr1:120454703
|
A | ATTTTTT | 21 | a0001c0002t0002g0013a0001c0002t0002g0017a0001c0002t0002g0020others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.1585+613_1585+618d others(8): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 120454703 | |||||
chr1:120454703
|
A | ATTTTTTT | 40 | a0001c0002t0002g0001a0001c0002t0002g0014a0001c0002t0002g0016others(37): Show | 42 | HG00140.hp1 HG00408.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1585+612_1585+618d others(9): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 120454703 | |||||
chr1:120454703
|
A | ATTTTTTT others(1): Show |
43 | a0001c0002t0002g0019a0001c0002t0002g0028a0001c0002t0002g0029others(40): Show | 44 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1585+611_1585+618d others(10): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 120454703 | |||||
chr1:120454703
|
A | ATTTTTTT others(2): Show |
13 | a0001c0002t0002g0012a0001c0002t0002g0044a0001c0011t0015g0053others(10): Show | 13 | HG01243.hp1 HG01261.hp1 HG02970.hp2 others(10): Show |
intron_variant | MODIFIER | c.1585+610_1585+618d others(11): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 120454703 | |||||
chr1:120454703
|
A | ATTTTTTT others(3): Show |
3 | a0002c0001t0001g0140a0002c0001t0001g0143a0002c0001t0001g0147 | 3 | NA18942.hp1 NA18985.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1585+609_1585+618d others(12): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 120454703 | |||||
chr1:120454703
|
A | ATTTTTTT others(4): Show |
1 | a0002c0024t0044g0176 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1585+608_1585+618d others(13): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 120454703 | |||||
chr1:120454703
|
A | ATTTTTTT others(6): Show |
1 | a0002c0001t0001g0141 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1585+606_1585+618d others(15): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 120454703 | |||||
chr1:120454703
|
A | ATTTTTTT others(7): Show |
1 | a0002c0001t0021g0152 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1585+605_1585+618d others(16): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 120454703 | |||||
chr1:120454703
|
A | T | 1 | a0001c0002t0002g0046 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1585+589A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120454703 | ||||||
chr1:120454703
|
AT | A | 33 | a0004c0005t0003g0265a0004c0005t0003g0267a0004c0005t0003g0274others(30): Show | 36 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.1585+618delT | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 120454703 | |||||
chr1:120454703
|
ATTTTTT | A | 20 | a0002c0001t0001g0153a0002c0001t0001g0154a0002c0001t0001g0155others(17): Show | 20 | HG01074.hp2 HG01358.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1585+613_1585+618d others(8): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 120454703 | |||||
chr1:120454703
|
ATTTTTTT | A | 12 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0195others(9): Show | 13 | HG00544.hp2 HG01934.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.1585+612_1585+618d others(9): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 120454703 | |||||
chr1:120454703
|
ATTTTTTT others(4): Show |
A | 7 | a0002c0013t0014g0094a0002c0013t0014g0208a0002c0013t0014g0209others(4): Show | 7 | HG01891.hp2 HG02622.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1585+608_1585+618d others(13): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 120454703 | |||||
chr1:120454703
|
ATTTTTTT others(5): Show |
A | 18 | a0001c0021t0018g0069a0001c0021t0018g0070a0005c0036t0005g0114others(15): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.1585+607_1585+618d others(14): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 120454703 | |||||
chr1:120454734
|
C | T | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1585+620C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120454734 | ||||||
chr1:120454797
|
C | G | 151 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(148): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1586-612C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120454797 | ||||||
chr1:120454917
|
G | A | 18 | a0005c0036t0005g0114a0006c0006t0005g0004a0006c0006t0005g0099others(15): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.1586-492G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120454917 | ||||||
chr1:120454943
|
G | T | 8 | a0006c0006t0005g0004a0006c0006t0005g0099a0006c0006t0005g0100others(5): Show | 9 | HG02071.hp1 HG02523.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.1586-466G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120454943 | ||||||
chr1:120454992
|
T | C | 2 | a0002c0001t0001g0141a0002c0001t0001g0147 | 2 | NA18947.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1586-417T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120454992 | ||||||
chr1:120454997
|
C | T | 1 | a0004c0005t0003g0255 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1586-412C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120454997 | ||||||
chr1:120455092
|
G | A | 1 | a0002c0001t0009g0156 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1586-317G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120455092 | ||||||
chr1:120455118
|
G | T | 82 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(79): Show | 85 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1586-291G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120455118 | ||||||
chr1:120455140
|
T | G | 18 | a0005c0036t0005g0114a0006c0006t0005g0004a0006c0006t0005g0099others(15): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.1586-269T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120455140 | ||||||
chr1:120455198
|
A | T | 2 | a0001c0002t0031g0065a0001c0044t0031g0064 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1586-211A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120455198 | ||||||
chr1:120455287
|
G | A | 1 | a0006c0006t0035g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1586-122G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 13/22 | chr1 | 120455287 | ||||||
chr1:120455613
|
C | T | 4 | a0001c0002t0008g0002a0001c0002t0008g0055a0001c0002t0008g0061others(1): Show | 5 | HG02258.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1637+153C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120455613 | ||||||
chr1:120455619
|
T | C | 6 | a0005c0004t0004g0214a0005c0004t0004g0228a0005c0004t0004g0237others(3): Show | 6 | HG00323.hp1 HG00741.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1637+159T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120455619 | ||||||
chr1:120455723
|
C | T | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1637+263C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120455723 | ||||||
chr1:120455942
|
G | A | 8 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(5): Show | 8 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1637+482G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120455942 | ||||||
chr1:120455967
|
T | C | 1 | a0001c0019t0054g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1637+507T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120455967 | ||||||
chr1:120455974
|
T | G | 1 | a0001c0022t0007g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1637+514T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120455974 | ||||||
chr1:120456074
|
C | T | 2 | a0006c0006t0005g0099a0006c0006t0005g0104 | 2 | NA18985.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1637+614C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456074 | ||||||
chr1:120456084
|
T | A | 1 | a0002c0001t0022g0126 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1637+624T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456084 | ||||||
chr1:120456135
|
T | C | 83 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(80): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1637+675T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456135 | ||||||
chr1:120456167
|
C | T | 1 | a0002c0028t0014g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1637+707C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456167 | ||||||
chr1:120456258
|
G | A | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1637+798G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456258 | ||||||
chr1:120456347
|
C | T | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1637+887C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456347 | ||||||
chr1:120456359
|
C | G | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1637+899C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456359 | ||||||
chr1:120456381
|
T | G | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1637+921T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456381 | ||||||
chr1:120456388
|
G | T | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1637+928G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456388 | ||||||
chr1:120456434
|
A | G | 214 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(211): Show | 220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1637+974A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456434 | ||||||
chr1:120456450
|
G | A | 7 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(4): Show | 8 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.1637+990G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456450 | ||||||
chr1:120456452
|
A | T | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1637+992A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456452 | ||||||
chr1:120456526
|
C | CT | 89 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(86): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.1637+1068dupT | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 120456526 | |||||
chr1:120456549
|
T | C | 32 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0193others(29): Show | 33 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.1637+1089T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456549 | ||||||
chr1:120456549
|
T | G | 164 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(161): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1637+1089T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456549 | ||||||
chr1:120456552
|
G | T | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1637+1092G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456552 | ||||||
chr1:120456576
|
G | A | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1637+1116G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456576 | ||||||
chr1:120456592
|
C | CT | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1637+1139dupT | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 120456592 | |||||
chr1:120456707
|
C | T | 2 | a0001c0002t0031g0065a0001c0044t0031g0064 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1637+1247C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456707 | ||||||
chr1:120456792
|
T | C | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1637+1332T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456792 | ||||||
chr1:120456826
|
C | T | 1 | a0001c0010t0059g0080 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1637+1366C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456826 | ||||||
chr1:120456844
|
A | G | 1 | a0004c0005t0003g0273 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1637+1384A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456844 | ||||||
chr1:120456904
|
G | A | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.1637+1444G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120456904 | ||||||
chr1:120457158
|
G | A | 2 | a0002c0001t0021g0152a0002c0001t0021g0182 | 2 | HG01175.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1637+1698G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457158 | ||||||
chr1:120457431
|
G | C | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1638-1936G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457431 | ||||||
chr1:120457439
|
A | T | 1 | a0003c0003t0047g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1638-1928A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457439 | ||||||
chr1:120457495
|
C | T | 32 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0193others(29): Show | 33 | HG00544.hp2 HG01928.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.1638-1872C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457495 | ||||||
chr1:120457558
|
C | T | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.1638-1809C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457558 | ||||||
chr1:120457587
|
G | T | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-1780G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457587 | ||||||
chr1:120457656
|
A | G | 107 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(104): Show | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.1638-1711A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457656 | ||||||
chr1:120457727
|
TAAA | T | 5 | a0002c0013t0014g0094a0002c0013t0014g0208a0002c0013t0014g0209others(2): Show | 5 | HG01891.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1638-1632_1638-163 others(7): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 120457727 | |||||
chr1:120457728
|
A | AT | 5 | a0001c0011t0015g0052a0001c0011t0015g0053a0001c0011t0015g0056others(2): Show | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1638-1639_1638-163 others(5): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457728 | ||||||
chr1:120457730
|
A | AATATATA others(19): Show |
1 | a0001c0010t0032g0078 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1638-1636_1638-163 others(30): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 120457730 | |||||
chr1:120457730
|
A | T | 5 | a0001c0011t0015g0052a0001c0011t0015g0053a0001c0011t0015g0056others(2): Show | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1638-1637A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457730 | ||||||
chr1:120457732
|
A | AT | 70 | a0001c0002t0002g0012a0001c0002t0002g0016a0001c0002t0002g0017others(67): Show | 73 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1638-1635_1638-163 others(5): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457732 | ||||||
chr1:120457732
|
A | ATAT | 88 | a0001c0002t0002g0001a0001c0002t0002g0013a0001c0002t0002g0014others(85): Show | 90 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1638-1635_1638-163 others(7): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457732 | ||||||
chr1:120457732
|
A | ATATAT | 13 | a0001c0002t0002g0024a0001c0002t0028g0035a0001c0019t0054g0066others(10): Show | 13 | HG02257.hp1 HG02717.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.1638-1635_1638-163 others(9): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457732 | ||||||
chr1:120457732
|
A | ATATATAT others(4): Show |
1 | a0002c0024t0044g0176 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1638-1635_1638-163 others(15): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457732 | ||||||
chr1:120457732
|
A | ATATATAT others(14): Show |
1 | a0001c0010t0059g0080 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1638-1635_1638-163 others(25): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457732 | ||||||
chr1:120457732
|
A | ATATATAT others(16): Show |
1 | a0001c0010t0060g0081 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1638-1635_1638-163 others(27): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457732 | ||||||
chr1:120457732
|
A | ATATATAT others(20): Show |
1 | a0001c0010t0058g0076 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1638-1635_1638-163 others(31): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457732 | ||||||
chr1:120457732
|
A | ATATATAT others(22): Show |
3 | a0001c0010t0032g0075a0001c0010t0061g0073a0001c0010t0063g0077 | 3 | HG02280.hp2 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1638-1635_1638-163 others(33): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457732 | ||||||
chr1:120457732
|
A | ATATATAT others(24): Show |
1 | a0001c0045t0065g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1638-1635_1638-163 others(35): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457732 | ||||||
chr1:120457732
|
A | T | 6 | a0001c0010t0032g0078a0001c0011t0015g0052a0001c0011t0015g0053others(3): Show | 6 | HG02109.hp1 HG02572.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1638-1635A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457732 | ||||||
chr1:120457734
|
A | AT | 4 | a0001c0002t0053g0051a0001c0007t0007g0087a0001c0011t0008g0049others(1): Show | 4 | HG01891.hp1 HG02486.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638-1633_1638-163 others(5): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457734 | ||||||
chr1:120457734
|
A | T | 187 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(184): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1638-1633A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457734 | ||||||
chr1:120457735
|
A | C | 5 | a0001c0011t0015g0052a0001c0011t0015g0053a0001c0011t0015g0056others(2): Show | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1638-1632A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457735 | ||||||
chr1:120457736
|
A | AT | 17 | a0005c0036t0005g0114a0006c0006t0005g0004a0006c0006t0005g0099others(14): Show | 18 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.1638-1631_1638-163 others(5): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457736 | ||||||
chr1:120457736
|
A | ATATATAT others(20): Show |
1 | a0001c0010t0062g0079 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1638-1631_1638-163 others(31): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457736 | ||||||
chr1:120457736
|
A | T | 228 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(225): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1638-1631A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457736 | ||||||
chr1:120457737
|
A | G | 5 | a0001c0011t0015g0052a0001c0011t0015g0053a0001c0011t0015g0056others(2): Show | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1638-1630A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457737 | ||||||
chr1:120457738
|
T | A | 4 | a0004c0005t0003g0267a0004c0005t0003g0274a0004c0005t0003g0277others(1): Show | 4 | HG03669.hp2 NA18941.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-1629T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457738 | ||||||
chr1:120457745
|
A | G | 5 | a0002c0013t0014g0094a0002c0013t0014g0208a0002c0013t0014g0209others(2): Show | 5 | HG01891.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1638-1622A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457745 | ||||||
chr1:120457774
|
A | C | 1 | a0002c0001t0001g0144 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1638-1593A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457774 | ||||||
chr1:120457778
|
A | T | 1 | a0001c0010t0062g0079 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1638-1589A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457778 | ||||||
chr1:120457793
|
GA | G | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.1638-1564delA | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 120457793 | |||||
chr1:120457808
|
G | A | 70 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(67): Show | 71 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1638-1559G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457808 | ||||||
chr1:120457908
|
C | T | 1 | a0002c0001t0021g0182 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1638-1459C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457908 | ||||||
chr1:120457963
|
TA | T | 107 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(104): Show | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.1638-1403delA | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457963 | ||||||
chr1:120457994
|
T | A | 1 | a0003c0003t0050g0117 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1638-1373T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120457994 | ||||||
chr1:120458112
|
C | T | 139 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(136): Show | 142 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.1638-1255C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120458112 | ||||||
chr1:120458113
|
G | T | 8 | a0002c0001t0001g0119a0002c0001t0001g0137a0002c0001t0001g0140others(5): Show | 8 | NA18942.hp1 NA18947.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.1638-1254G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120458113 | ||||||
chr1:120458137
|
C | T | 28 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(25): Show | 29 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1638-1230C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120458137 | ||||||
chr1:120458148
|
T | C | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1638-1219T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120458148 | ||||||
chr1:120458187
|
T | C | 1 | a0005c0004t0004g0008 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1638-1180T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120458187 | ||||||
chr1:120458319
|
C | T | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1638-1048C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120458319 | ||||||
chr1:120458334
|
A | T | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1638-1033A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120458334 | ||||||
chr1:120458415
|
G | C | 1 | a0002c0013t0014g0208 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1638-952G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120458415 | ||||||
chr1:120458540
|
C | T | 1 | a0019c0038t0003g0260 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1638-827C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120458540 | ||||||
chr1:120458852
|
G | A | 1 | a0001c0010t0061g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1638-515G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120458852 | ||||||
chr1:120458858
|
G | T | 1 | a0001c0019t0054g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1638-509G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120458858 | ||||||
chr1:120458931
|
G | A | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1638-436G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120458931 | ||||||
chr1:120459001
|
C | CAAGAACT others(315): Show |
1 | a0005c0004t0004g0225 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1638-351_1638-350i others(324): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 120459001 | |||||
chr1:120459001
|
C | CAAGAACT others(316): Show |
3 | a0005c0004t0004g0213a0005c0004t0004g0282a0007c0008t0011g0220 | 3 | HG00639.hp1 HG01517.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.1638-351_1638-350i others(325): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 120459001 | |||||
chr1:120459001
|
C | CAAGAACT others(317): Show |
21 | a0005c0004t0004g0007a0005c0004t0004g0008a0005c0004t0004g0228others(18): Show | 23 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.1638-351_1638-350i others(326): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 120459001 | |||||
chr1:120459001
|
C | CAAGAACT others(318): Show |
8 | a0005c0004t0004g0214a0005c0004t0004g0230a0005c0004t0004g0232others(5): Show | 8 | HG01106.hp1 HG01109.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1638-351_1638-350i others(327): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 120459001 | |||||
chr1:120459001
|
C | CAAGAACT others(319): Show |
1 | a0005c0004t0004g0131 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1638-351_1638-350i others(328): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 120459001 | |||||
chr1:120459001
|
C | CAAGAACT others(322): Show |
1 | a0005c0004t0004g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1638-351_1638-350i others(331): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 120459001 | |||||
chr1:120459001
|
C | CAAGAACT others(317): Show |
1 | a0005c0004t0004g0241 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1638-351_1638-350i others(326): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 120459001 | |||||
chr1:120459152
|
T | G | 1 | a0006c0006t0005g0106 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1638-215T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120459152 | ||||||
chr1:120459165
|
T | C | 75 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(72): Show | 76 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1638-202T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120459165 | ||||||
chr1:120459166
|
G | A | 6 | a0003c0003t0012g0006a0003c0003t0012g0186a0003c0003t0012g0188others(3): Show | 7 | HG00544.hp2 HG02015.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1638-201G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120459166 | ||||||
chr1:120459234
|
T | C | 6 | a0002c0001t0001g0144a0008c0014t0017g0095a0008c0014t0017g0096others(3): Show | 6 | HG00140.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1638-133T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120459234 | ||||||
chr1:120459318
|
T | A | 6 | a0002c0001t0001g0144a0008c0014t0017g0095a0008c0014t0017g0096others(3): Show | 6 | HG00140.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1638-49T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120459318 | ||||||
chr1:120459332
|
A | G | 2 | a0001c0002t0002g0030a0001c0002t0002g0032 | 2 | HG00280.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1638-35A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120459332 | ||||||
chr1:120459334
|
C | G | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1638-33C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120459334 | ||||||
chr1:120459339
|
A | G | 6 | a0002c0001t0001g0144a0008c0014t0017g0095a0008c0014t0017g0096others(3): Show | 6 | HG00140.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1638-28A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120459339 | ||||||
chr1:120459346
|
C | G | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.1638-21C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | 120459346 | ||||||
chr1:120459608
|
G | C | 86 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(83): Show | 89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.1801+78G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120459608 | ||||||
chr1:120459612
|
G | C | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1801+82G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120459612 | ||||||
chr1:120459615
|
G | A | 1 | a0002c0001t0001g0122 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1801+85G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120459615 | ||||||
chr1:120459692
|
G | A | 1 | a0007c0008t0011g0229 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1801+162G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120459692 | ||||||
chr1:120459740
|
C | G | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1801+210C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120459740 | ||||||
chr1:120459740
|
C | T | 107 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(104): Show | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.1801+210C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120459740 | ||||||
chr1:120459741
|
G | A | 2 | a0001c0002t0031g0065a0001c0044t0031g0064 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1801+211G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120459741 | ||||||
chr1:120459776
|
T | C | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1801+246T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120459776 | ||||||
chr1:120459789
|
G | A | 1 | a0001c0002t0008g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1801+259G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120459789 | ||||||
chr1:120459833
|
G | A | 107 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(104): Show | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.1801+303G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120459833 | ||||||
chr1:120459841
|
T | A | 1 | a0003c0003t0047g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1801+311T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120459841 | ||||||
chr1:120459996
|
G | A | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1801+466G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120459996 | ||||||
chr1:120460030
|
G | A | 15 | a0001c0002t0008g0002a0001c0002t0008g0054a0001c0002t0008g0055others(12): Show | 16 | HG01175.hp2 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1801+500G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120460030 | ||||||
chr1:120460035
|
C | T | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1801+505C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120460035 | ||||||
chr1:120460105
|
G | A | 2 | a0009c0016t0003g0251a0009c0016t0003g0276 | 2 | HG02300.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1802-468G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120460105 | ||||||
chr1:120460135
|
C | G | 1 | a0002c0001t0021g0182 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1802-438C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120460135 | ||||||
chr1:120460174
|
C | T | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1802-399C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120460174 | ||||||
chr1:120460175
|
C | T | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1802-398C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120460175 | ||||||
chr1:120460228
|
G | A | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1802-345G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120460228 | ||||||
chr1:120460235
|
G | A | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1802-338G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120460235 | ||||||
chr1:120460241
|
T | C | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1802-332T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120460241 | ||||||
chr1:120460305
|
A | T | 2 | a0001c0002t0031g0065a0001c0044t0031g0064 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1802-268A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120460305 | ||||||
chr1:120460347
|
G | A | 2 | a0001c0002t0031g0065a0001c0044t0031g0064 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1802-226G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120460347 | ||||||
chr1:120460365
|
T | A | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1802-208T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120460365 | ||||||
chr1:120460366
|
CAG | C | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1802-206_1802-205d others(4): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120460366 | ||||||
chr1:120460470
|
T | C | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1802-103T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120460470 | ||||||
chr1:120460492
|
G | C | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1802-81G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120460492 | ||||||
chr1:120460557
|
A | C | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1802-16A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 15/22 | chr1 | 120460557 | ||||||
chr1:120460742
|
C | T | 108 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(105): Show | 110 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1853+118C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120460742 | ||||||
chr1:120460781
|
G | C | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1853+157G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120460781 | ||||||
chr1:120460850
|
C | T | 107 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(104): Show | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.1853+226C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120460850 | ||||||
chr1:120460861
|
T | C | 2 | a0001c0020t0030g0067a0001c0020t0030g0068 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1853+237T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120460861 | ||||||
chr1:120460883
|
G | C | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1853+259G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120460883 | ||||||
chr1:120460893
|
T | C | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1853+269T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120460893 | ||||||
chr1:120460912
|
G | T | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1853+288G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120460912 | ||||||
chr1:120461002
|
T | G | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1854-252T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120461002 | ||||||
chr1:120461005
|
C | A | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1854-249C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120461005 | ||||||
chr1:120461014
|
A | C | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1854-240A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120461014 | ||||||
chr1:120461015
|
A | T | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1854-239A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120461015 | ||||||
chr1:120461016
|
C | CTG | 43 | a0001c0002t0002g0001a0001c0002t0002g0013a0001c0002t0002g0014others(40): Show | 45 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1854-190_1854-189d others(4): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 120461016 | |||||
chr1:120461016
|
C | CTGTG | 24 | a0001c0002t0002g0016a0001c0002t0002g0020a0001c0002t0002g0023others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.1854-192_1854-189d others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 120461016 | |||||
chr1:120461016
|
CTG | C | 20 | a0001c0002t0002g0012a0001c0021t0018g0069a0001c0021t0018g0070others(17): Show | 22 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.1854-190_1854-189d others(4): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 120461016 | |||||
chr1:120461016
|
CTGTG | C | 16 | a0001c0002t0008g0055a0001c0011t0015g0056a0001c0019t0055g0063others(13): Show | 16 | HG01099.hp1 HG01106.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1854-192_1854-189d others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 120461016 | |||||
chr1:120461016
|
CTGTGTG | C | 13 | a0001c0002t0031g0065a0001c0019t0054g0066a0001c0020t0030g0067others(10): Show | 13 | HG01070.hp2 HG01074.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1854-194_1854-189d others(8): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 120461016 | |||||
chr1:120461016
|
CTGTGTGT others(1): Show |
C | 14 | a0001c0002t0008g0002a0001c0002t0008g0061a0001c0002t0008g0062others(11): Show | 15 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1854-196_1854-189d others(10): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 120461016 | |||||
chr1:120461016
|
CTGTGTGT others(3): Show |
C | 1 | a0006c0006t0005g0105 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1854-198_1854-189d others(12): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 120461016 | |||||
chr1:120461016
|
CTGTGTGT others(7): Show |
C | 10 | a0001c0007t0057g0092a0001c0010t0032g0075a0001c0010t0032g0078others(7): Show | 10 | HG01109.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1854-202_1854-189d others(16): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 120461016 | |||||
chr1:120461016
|
CTGTGTGT others(9): Show |
C | 18 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(15): Show | 19 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.1854-204_1854-189d others(18): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 120461016 | |||||
chr1:120461016
|
CTGTGTGT others(11): Show |
C | 102 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(99): Show | 104 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1854-206_1854-189d others(20): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 120461016 | |||||
chr1:120461016
|
CTGTGTGT others(15): Show |
C | 1 | a0001c0002t0056g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1854-210_1854-189d others(24): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 120461016 | |||||
chr1:120461016
|
CTGTGTGT others(17): Show |
C | 5 | a0006c0006t0005g0004a0006c0006t0005g0099a0006c0006t0005g0100others(2): Show | 6 | HG02071.hp1 NA18941.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.1854-212_1854-189d others(26): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 120461016 | |||||
chr1:120461054
|
GTGTGTGT others(9): Show |
G | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1854-198_1854-183d others(18): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 120461054 | |||||
chr1:120461080
|
C | T | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1854-174C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120461080 | ||||||
chr1:120461097
|
A | G | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1854-157A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120461097 | ||||||
chr1:120461098
|
G | T | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1854-156G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120461098 | ||||||
chr1:120461109
|
C | T | 6 | a0005c0004t0004g0214a0005c0004t0004g0228a0005c0004t0004g0237others(3): Show | 6 | HG00323.hp1 HG00741.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1854-145C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120461109 | ||||||
chr1:120461124
|
T | C | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1854-130T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120461124 | ||||||
chr1:120461174
|
T | C | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1854-80T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120461174 | ||||||
chr1:120461175
|
G | A | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1854-79G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120461175 | ||||||
chr1:120461220
|
A | C | 156 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(153): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1854-34A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120461220 | ||||||
chr1:120461228
|
T | C | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1854-26T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120461228 | ||||||
chr1:120461246
|
T | C | 1 | a0003c0003t0013g0185 | 1 | NA20129.hp2 | splice_region_variant&intron_variant | LOW | c.1854-8T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | chr1 | 120461246 | ||||||
chr1:120461446
|
G | A | 1 | a0005c0004t0004g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2026+20G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/22 | chr1 | 120461446 | ||||||
chr1:120461492
|
T | A | 1 | a0007c0008t0011g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2026+66T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/22 | chr1 | 120461492 | ||||||
chr1:120461538
|
G | C | 1 | a0002c0001t0021g0182 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2026+112G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/22 | chr1 | 120461538 | ||||||
chr1:120461617
|
C | T | 22 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(19): Show | 23 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.2026+191C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/22 | chr1 | 120461617 | ||||||
chr1:120461649
|
G | A | 3 | a0001c0002t0002g0017a0001c0002t0002g0030a0016c0031t0003g0253 | 3 | HG00140.hp2 HG01099.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2026+223G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/22 | chr1 | 120461649 | ||||||
chr1:120461715
|
G | T | 1 | a0002c0001t0010g0166 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2026+289G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/22 | chr1 | 120461715 | ||||||
chr1:120461726
|
G | A | 2 | a0004c0015t0003g0268a0004c0015t0003g0269 | 2 | HG01361.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2026+300G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/22 | chr1 | 120461726 | ||||||
chr1:120461729
|
G | A | 1 | a0003c0003t0047g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2026+303G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/22 | chr1 | 120461729 | ||||||
chr1:120461765
|
G | A | 1 | a0001c0018t0018g0071 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2026+339G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/22 | chr1 | 120461765 | ||||||
chr1:120461778
|
G | A | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2026+352G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/22 | chr1 | 120461778 | ||||||
chr1:120461825
|
C | A | 1 | a0001c0019t0054g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2027-321C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/22 | chr1 | 120461825 | ||||||
chr1:120461853
|
G | A | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2027-293G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/22 | chr1 | 120461853 | ||||||
chr1:120461882
|
T | C | 1 | a0001c0019t0054g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2027-264T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/22 | chr1 | 120461882 | ||||||
chr1:120461925
|
C | T | 1 | a0016c0031t0003g0253 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2027-221C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/22 | chr1 | 120461925 | ||||||
chr1:120461956
|
A | G | 1 | a0001c0002t0002g0019 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2027-190A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/22 | chr1 | 120461956 | ||||||
chr1:120462072
|
G | A | 3 | a0001c0007t0019g0086a0001c0007t0019g0089a0001c0007t0019g0090 | 3 | HG01433.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2027-74G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 17/22 | chr1 | 120462072 | ||||||
chr1:120462252
|
G | C | 1 | a0002c0001t0010g0166 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2078+55G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 18/22 | chr1 | 120462252 | ||||||
chr1:120462305
|
A | T | 214 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(211): Show | 220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2078+108A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 18/22 | chr1 | 120462305 | ||||||
chr1:120462342
|
A | T | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2078+145A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 18/22 | chr1 | 120462342 | ||||||
chr1:120462418
|
G | A | 1 | a0001c0019t0054g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2078+221G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 18/22 | chr1 | 120462418 | ||||||
chr1:120462468
|
C | A | 1 | a0005c0004t0004g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2078+271C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 18/22 | chr1 | 120462468 | ||||||
chr1:120462503
|
C | T | 22 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(19): Show | 23 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.2079-291C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 18/22 | chr1 | 120462503 | ||||||
chr1:120462516
|
T | A | 1 | a0002c0001t0009g0246 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2079-278T>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 18/22 | chr1 | 120462516 | ||||||
chr1:120462543
|
G | A | 22 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(19): Show | 23 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.2079-251G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 18/22 | chr1 | 120462543 | ||||||
chr1:120462745
|
G | T | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2079-49G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 18/22 | chr1 | 120462745 | ||||||
chr1:120462760
|
C | T | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.2079-34C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 18/22 | chr1 | 120462760 | ||||||
chr1:120462981
|
A | G | 1 | a0001c0022t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2251+15A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/22 | chr1 | 120462981 | ||||||
chr1:120463052
|
C | A | 36 | a0005c0004t0004g0007a0005c0004t0004g0008a0005c0004t0004g0131others(33): Show | 38 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.2251+86C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/22 | chr1 | 120463052 | ||||||
chr1:120463138
|
G | A | 1 | a0001c0042t0002g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2251+172G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/22 | chr1 | 120463138 | ||||||
chr1:120463162
|
T | C | 10 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(7): Show | 10 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2251+196T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/22 | chr1 | 120463162 | ||||||
chr1:120463243
|
A | G | 1 | a0003c0003t0006g0127 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2251+277A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/22 | chr1 | 120463243 | ||||||
chr1:120463304
|
C | A | 1 | a0001c0002t0002g0028 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2251+338C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/22 | chr1 | 120463304 | ||||||
chr1:120463338
|
G | T | 67 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(64): Show | 68 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.2252-338G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/22 | chr1 | 120463338 | ||||||
chr1:120463350
|
C | T | 18 | a0005c0036t0005g0114a0006c0006t0005g0004a0006c0006t0005g0099others(15): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.2252-326C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/22 | chr1 | 120463350 | ||||||
chr1:120463469
|
C | T | 1 | a0001c0042t0002g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2252-207C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/22 | chr1 | 120463469 | ||||||
chr1:120463475
|
G | T | 196 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(193): Show | 201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.2252-201G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/22 | chr1 | 120463475 | ||||||
chr1:120463506
|
A | T | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2252-170A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/22 | chr1 | 120463506 | ||||||
chr1:120463580
|
G | A | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2252-96G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/22 | chr1 | 120463580 | ||||||
chr1:120463581
|
G | C | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2252-95G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/22 | chr1 | 120463581 | ||||||
chr1:120463667
|
G | T | 2 | a0001c0002t0002g0012a0001c0040t0002g0033 | 2 | HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2252-9G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 19/22 | chr1 | 120463667 | ||||||
chr1:120463799
|
G | A | 1 | a0001c0022t0007g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2303+72G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120463799 | ||||||
chr1:120463822
|
T | C | 1 | a0001c0002t0056g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2303+95T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120463822 | ||||||
chr1:120463834
|
C | G | 1 | a0002c0009t0037g0159 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2303+107C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120463834 | ||||||
chr1:120463931
|
G | T | 3 | a0001c0007t0007g0003a0001c0007t0007g0091a0001c0007t0007g0093 | 4 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.2303+204G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120463931 | ||||||
chr1:120463974
|
G | A | 18 | a0005c0036t0005g0114a0006c0006t0005g0004a0006c0006t0005g0099others(15): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.2303+247G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120463974 | ||||||
chr1:120464001
|
T | C | 6 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0020t0030g0067others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2303+274T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464001 | ||||||
chr1:120464017
|
T | G | 18 | a0005c0036t0005g0114a0006c0006t0005g0004a0006c0006t0005g0099others(15): Show | 19 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.2303+290T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464017 | ||||||
chr1:120464057
|
C | T | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2304-319C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464057 | ||||||
chr1:120464084
|
A | T | 22 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(19): Show | 23 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.2304-292A>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464084 | ||||||
chr1:120464113
|
C | T | 1 | a0002c0001t0009g0009 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2304-263C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464113 | ||||||
chr1:120464115
|
TTC | T | 42 | a0001c0010t0032g0075a0002c0001t0001g0005a0002c0001t0001g0119others(39): Show | 42 | HG00609.hp1 HG00673.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.2304-243_2304-242d others(4): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464115 | |||||
chr1:120464115
|
TTCTC | T | 13 | a0001c0010t0060g0081a0001c0010t0061g0073a0002c0001t0001g0121others(10): Show | 13 | HG00408.hp2 HG00673.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.2304-245_2304-242d others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464115 | |||||
chr1:120464115
|
TTCTCTC | T | 5 | a0001c0002t0002g0026a0001c0002t0002g0036a0001c0021t0018g0069others(2): Show | 5 | HG00140.hp1 HG01167.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2304-247_2304-242d others(8): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464115 | |||||
chr1:120464115
|
TTCTCTCT others(1): Show |
T | 8 | a0001c0002t0002g0017a0001c0002t0002g0041a0001c0002t0002g0047others(5): Show | 9 | HG00323.hp2 HG01516.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2304-249_2304-242d others(10): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464115 | |||||
chr1:120464115
|
TTCTCTCT others(3): Show |
T | 21 | a0001c0002t0002g0001a0001c0002t0002g0014a0001c0002t0002g0016others(18): Show | 22 | HG00280.hp1 HG00735.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.2304-251_2304-242d others(12): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464115 | |||||
chr1:120464115
|
TTCTCTCT others(5): Show |
T | 16 | a0001c0002t0002g0012a0001c0002t0002g0013a0001c0002t0002g0024others(13): Show | 16 | HG00099.hp2 HG00609.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.2304-253_2304-242d others(14): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464115 | |||||
chr1:120464115
|
TTCTCTCT others(9): Show |
T | 1 | a0001c0040t0002g0033 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2304-257_2304-242d others(18): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464115 | |||||
chr1:120464121
|
CTCTCTCT others(7): Show |
C | 3 | a0001c0002t0002g0019a0001c0002t0002g0031a0001c0002t0002g0034 | 3 | HG00544.hp1 HG00738.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2304-253_2304-240d others(16): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464121 | |||||
chr1:120464121
|
CTCTCTCT others(17): Show |
C | 1 | a0001c0002t0008g0054 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2304-253_2304-230d others(26): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464121 | |||||
chr1:120464123
|
CTCTCTCT others(5): Show |
C | 3 | a0001c0002t0002g0020a0001c0002t0002g0044a0012c0039t0002g0021 | 3 | HG01261.hp1 HG01517.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.2304-251_2304-240d others(14): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464123 | |||||
chr1:120464123
|
CTCTCTCT others(7): Show |
C | 1 | a0001c0002t0002g0023 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2304-251_2304-238d others(16): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464123 | |||||
chr1:120464127
|
CTCTCTCT others(5): Show |
C | 3 | a0001c0018t0018g0071a0001c0018t0018g0072a0001c0045t0065g0074 | 3 | HG02109.hp2 HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2304-247_2304-236d others(14): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464127 | |||||
chr1:120464129
|
C | G | 10 | a0001c0002t0002g0026a0001c0002t0002g0036a0001c0010t0032g0078others(7): Show | 10 | HG00140.hp1 HG01167.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2304-247C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464129 | ||||||
chr1:120464129
|
CTCTCTG | C | 12 | a0002c0001t0001g0142a0002c0001t0001g0144a0002c0001t0001g0154others(9): Show | 13 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.2304-245_2304-240d others(8): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464129 | |||||
chr1:120464131
|
C | G | 64 | a0001c0002t0002g0017a0001c0002t0002g0026a0001c0002t0002g0036others(61): Show | 66 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.2304-245C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464131 | ||||||
chr1:120464133
|
C | CTG | 6 | a0004c0005t0016g0254a0004c0005t0016g0258a0005c0004t0004g0242others(3): Show | 6 | HG00639.hp1 HG02300.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.2304-199_2304-198d others(4): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464133 | |||||
chr1:120464133
|
C | CTGTG | 3 | a0004c0005t0003g0262a0004c0005t0016g0010a0005c0004t0004g0008 | 5 | HG01069.hp2 HG01071.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.2304-201_2304-198d others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464133 | |||||
chr1:120464133
|
C | G | 120 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0026others(117): Show | 122 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.2304-243C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464133 | ||||||
chr1:120464133
|
CTG | C | 9 | a0004c0005t0003g0263a0004c0005t0003g0274a0004c0005t0016g0279others(6): Show | 9 | HG00323.hp1 HG01099.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2304-199_2304-198d others(4): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464133 | |||||
chr1:120464133
|
CTGTG | C | 9 | a0004c0005t0003g0250a0004c0005t0003g0264a0004c0005t0003g0265others(6): Show | 9 | HG02004.hp1 HG02683.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.2304-201_2304-198d others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464133 | |||||
chr1:120464133
|
CTGTGTG | C | 29 | a0004c0005t0003g0255a0004c0005t0003g0271a0005c0004t0011g0130others(26): Show | 30 | HG00099.hp1 HG00408.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.2304-203_2304-198d others(8): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464133 | |||||
chr1:120464133
|
CTGTGTGT others(1): Show |
C | 8 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(5): Show | 9 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.2304-205_2304-198d others(10): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464133 | |||||
chr1:120464133
|
CTGTGTGT others(5): Show |
C | 5 | a0001c0007t0019g0086a0001c0007t0019g0089a0001c0007t0019g0090others(2): Show | 5 | HG01433.hp1 HG03041.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2304-209_2304-198d others(14): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464133 | |||||
chr1:120464135
|
G | C | 1 | a0005c0004t0004g0213 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2304-241G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464135 | ||||||
chr1:120464137
|
G | C | 2 | a0005c0004t0023g0215a0005c0004t0023g0216 | 2 | HG01099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.2304-239G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464137 | ||||||
chr1:120464139
|
G | C | 1 | a0006c0006t0005g0105 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2304-237G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464139 | ||||||
chr1:120464141
|
G | C | 17 | a0005c0036t0005g0114a0006c0006t0005g0004a0006c0006t0005g0099others(14): Show | 18 | HG02071.hp1 HG02280.hp1 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.2304-235G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464141 | ||||||
chr1:120464147
|
G | C | 1 | a0001c0007t0019g0089 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2304-229G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464147 | ||||||
chr1:120464163
|
G | C | 5 | a0003c0003t0012g0006a0003c0003t0012g0186a0003c0003t0012g0188others(2): Show | 6 | HG02015.hp2 HG02074.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.2304-213G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464163 | ||||||
chr1:120464163
|
G | GTC | 6 | a0003c0003t0006g0127a0003c0003t0006g0211a0003c0003t0012g0189others(3): Show | 6 | HG00544.hp2 HG02258.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.2304-212_2304-211i others(4): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464163 | |||||
chr1:120464163
|
G | GTGTC | 8 | a0003c0003t0006g0187a0003c0003t0006g0193a0003c0003t0006g0194others(5): Show | 8 | HG01934.hp1 HG02080.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.2304-210_2304-209i others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464163 | |||||
chr1:120464167
|
G | C | 19 | a0003c0003t0006g0127a0003c0003t0006g0187a0003c0003t0006g0193others(16): Show | 20 | HG00544.hp2 HG01934.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.2304-209G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464167 | ||||||
chr1:120464167
|
G | GTCTGTC | 8 | a0003c0003t0013g0184a0003c0003t0013g0202a0003c0003t0013g0203others(5): Show | 8 | HG01928.hp1 HG02300.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2304-208_2304-207i others(8): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464167 | |||||
chr1:120464167
|
G | GTGTCTGT others(1): Show |
5 | a0003c0003t0013g0185a0003c0003t0013g0204a0003c0003t0013g0205others(2): Show | 5 | HG02965.hp2 HG03225.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2304-206_2304-205i others(10): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464167 | |||||
chr1:120464171
|
G | C | 97 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(94): Show | 99 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.2304-205G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464171 | ||||||
chr1:120464171
|
G | GTC | 3 | a0002c0001t0001g0178a0002c0001t0022g0126a0002c0001t0038g0132 | 3 | NA18954.hp1 NA18961.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.2304-204_2304-203i others(4): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 120464171 | |||||
chr1:120464175
|
G | C | 144 | a0001c0002t0008g0002a0001c0002t0008g0061a0001c0002t0008g0062others(141): Show | 149 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.2304-201G>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464175 | ||||||
chr1:120464179
|
C | G | 1 | a0001c0010t0059g0080 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2304-197C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464179 | ||||||
chr1:120464247
|
G | T | 1 | a0001c0011t0008g0049 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2304-129G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464247 | ||||||
chr1:120464314
|
T | G | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.2304-62T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464314 | ||||||
chr1:120464321
|
T | C | 214 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(211): Show | 220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2304-55T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464321 | ||||||
chr1:120464347
|
G | T | 18 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(15): Show | 19 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.2304-29G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464347 | ||||||
chr1:120464366
|
C | T | 107 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(104): Show | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.2304-10C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | chr1 | 120464366 | ||||||
chr1:120464607
|
G | A | 2 | a0001c0020t0030g0067a0001c0020t0030g0068 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2476+59G>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 21/22 | chr1 | 120464607 | ||||||
chr1:120464675
|
T | G | 9 | a0001c0010t0032g0075a0001c0010t0032g0078a0001c0010t0058g0076others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2476+127T>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 21/22 | chr1 | 120464675 | ||||||
chr1:120464677
|
T | C | 67 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(64): Show | 68 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.2476+129T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 21/22 | chr1 | 120464677 | ||||||
chr1:120464771
|
C | T | 14 | a0006c0006t0005g0004a0006c0006t0005g0099a0006c0006t0005g0100others(11): Show | 15 | HG02071.hp1 HG02523.hp2 NA18941.hp2 others(12): Show |
intron_variant | MODIFIER | c.2476+223C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 21/22 | chr1 | 120464771 | ||||||
chr1:120464990
|
G | T | 59 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(56): Show | 61 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.2477-273G>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 21/22 | chr1 | 120464990 | ||||||
chr1:120465109
|
T | C | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.2477-154T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 21/22 | chr1 | 120465109 | ||||||
chr1:120465160
|
A | G | 1 | a0001c0011t0015g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2477-103A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 21/22 | chr1 | 120465160 | ||||||
chr1:120465197
|
C | G | 4 | a0008c0014t0017g0095a0008c0014t0017g0096a0008c0014t0017g0097others(1): Show | 4 | HG02572.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2477-66C>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 21/22 | chr1 | 120465197 | ||||||
chr1:120465374
|
A | G | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
splice_region_variant&intron_variant | LOW | c.2585+3A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 22/22 | chr1 | 120465374 | ||||||
chr1:120465399
|
A | G | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.2585+28A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 22/22 | chr1 | 120465399 | ||||||
chr1:120465458
|
C | T | 58 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(55): Show | 60 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.2585+87C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 22/22 | chr1 | 120465458 | ||||||
chr1:120465472
|
A | G | 196 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(193): Show | 201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.2585+101A>G | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 22/22 | chr1 | 120465472 | ||||||
chr1:120465481
|
C | T | 1 | a0001c0019t0054g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2585+110C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 22/22 | chr1 | 120465481 | ||||||
chr1:120465486
|
A | C | 1 | a0002c0001t0036g0148 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2585+115A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 22/22 | chr1 | 120465486 | ||||||
chr1:120465555
|
C | A | 79 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(76): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.2585+184C>A | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 22/22 | chr1 | 120465555 | ||||||
chr1:120465567
|
T | C | 57 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(54): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.2585+196T>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 22/22 | chr1 | 120465567 | ||||||
chr1:120465731
|
A | C | 85 | a0001c0002t0002g0001a0001c0002t0002g0012a0001c0002t0002g0013others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.2586-247A>C | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 22/22 | chr1 | 120465731 | ||||||
chr1:120465742
|
C | T | 1 | a0001c0010t0032g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2586-236C>T | NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 22/22 | chr1 | 120465742 | ||||||
chr1:120465756
|
CTCTCTG | C | 107 | a0002c0001t0001g0005a0002c0001t0001g0119a0002c0001t0001g0121others(104): Show | 109 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.2586-204_2586-199d others(8): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr1 | 120465756 | |||||
chr1:120465784
|
CTCTG | C | 13 | a0001c0007t0007g0003a0001c0007t0007g0084a0001c0007t0007g0085others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.2586-190_2586-187d others(6): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr1 | 120465784 |