geneid | 87178 |
---|---|
ensemblid | ENSG00000138035.15 |
hgncid | 23166 |
symbol | PNPT1 |
name | polyribonucleotide nucleotidyltransferase 1 |
refseq_nuc | NM_033109.5 |
refseq_prot | NP_149100.2 |
ensembl_nuc | ENST00000447944.7 |
ensembl_prot | ENSP00000400646.2 |
mane_status | MANE Select |
chr | chr2 |
start | 55634061 |
end | 55693844 |
strand | - |
ver | v1.2 |
region | chr2:55634061-55693844 |
region5000 | chr2:55629061-55698844 |
regionname0 | PNPT1_chr2_55634061_55693844 |
regionname5000 | PNPT1_chr2_55629061_55698844 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 783 | 217 | 27 | 37 | 111 | 5 | 36 | 83 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002 | 0/0 | 783 | 122 | 36 | 30 | 42 | 5 | 9 | 38 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0003 | 0/1 | 783 | 44 | 28 | 5 | 8 | 0 | 2 | 7 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0004 | 0/0 | 783 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0005 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0006 | 0/0 | 783 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0007 | 0/0 | 783 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0008 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0009 | 0/0 | 783 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0010 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2352 | 202 | 26 | 31 | 111 | 5 | 28 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
c0002 | 0/0 | 2352 | 115 | 35 | 29 | 37 | 5 | 9 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
c0003 | 0/1 | 2352 | 44 | 28 | 5 | 8 | 0 | 2 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
c0004 | 0/0 | 2352 | 12 | 1 | 5 | 0 | 0 | 6 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
c0005 | 0/0 | 2352 | 5 | 0 | 1 | 4 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
c0006 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
c0007 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
c0008 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
c0009 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
c0010 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
c0011 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
c0012 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
c0013 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
c0014 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
c0015 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
c0016 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
c0017 | 0/0 | 2352 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
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 | 2198 | 101 | 13 | 22 | 52 | 4 | 10 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0002 | 0/0 | 2198 | 85 | 29 | 27 | 18 | 3 | 8 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0003 | 1/0 | 2198 | 70 | 0 | 6 | 56 | 0 | 7 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0004 | 0/1 | 2197 | 39 | 24 | 4 | 7 | 0 | 3 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0005 | 0/0 | 2200 | 11 | 0 | 0 | 10 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0006 | 0/0 | 2198 | 10 | 1 | 3 | 0 | 1 | 5 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0007 | 0/0 | 2198 | 10 | 0 | 5 | 0 | 0 | 5 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0008 | 0/0 | 2198 | 7 | 7 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0009 | 0/0 | 2199 | 5 | 0 | 1 | 3 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0010 | 0/0 | 2198 | 5 | 5 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0011 | 0/0 | 2198 | 3 | 0 | 0 | 3 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0012 | 0/0 | 2198 | 3 | 0 | 0 | 3 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0013 | 0/0 | 2199 | 2 | 0 | 1 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0014 | 0/0 | 2199 | 2 | 1 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0015 | 0/0 | 2198 | 2 | 0 | 0 | 2 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0016 | 0/0 | 2197 | 2 | 2 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0017 | 0/0 | 2198 | 2 | 0 | 0 | 2 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0018 | 0/0 | 2198 | 2 | 2 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0019 | 0/0 | 2197 | 2 | 2 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0020 | 0/0 | 2197 | 2 | 2 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0021 | 0/0 | 2198 | 2 | 1 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0022 | 0/0 | 2199 | 2 | 0 | 1 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0023 | 0/0 | 2198 | 2 | 0 | 0 | 0 | 2 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0024 | 0/0 | 2198 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0025 | 0/0 | 2199 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0026 | 0/0 | 2198 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0027 | 0/0 | 2198 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0028 | 0/0 | 2198 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0029 | 0/0 | 2198 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0030 | 0/0 | 2198 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0031 | 0/0 | 2198 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0032 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0033 | 0/0 | 2198 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0034 | 0/0 | 2197 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0035 | 0/0 | 2197 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0036 | 0/0 | 2205 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0037 | 0/0 | 2198 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0038 | 0/0 | 2198 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0039 | 0/0 | 2199 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0040 | 0/0 | 2200 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0041 | 0/0 | 2198 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
t0042 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
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 | 4 | 0 | 0 | 4 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0341 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0377 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2352 | 202 | 26 | 31 | 111 | 5 | 28 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0004 | 0/0 | 2352 | 12 | 1 | 5 | 0 | 0 | 6 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0009 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0010 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0017 | 0/0 | 2352 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0002 | 0/0 | 2352 | 115 | 35 | 29 | 37 | 5 | 9 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0005 | 0/0 | 2352 | 5 | 0 | 1 | 4 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0011 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0015 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0003c0003 | 0/1 | 2352 | 44 | 28 | 5 | 8 | 0 | 2 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0004c0016 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0005c0006 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0006c0008 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0007c0007 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0008c0013 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0009c0012 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0010c0014 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4549 | 84 | 13 | 20 | 38 | 4 | 9 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0002 | 0/0 | 4549 | 2 | 0 | 0 | 0 | 0 | 2 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0003 | 1/0 | 4549 | 68 | 0 | 6 | 55 | 0 | 6 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0006 | 0/0 | 4549 | 10 | 1 | 3 | 0 | 1 | 5 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0008 | 0/0 | 4549 | 7 | 7 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0009 | 0/0 | 4550 | 5 | 0 | 1 | 3 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0011 | 0/0 | 4549 | 3 | 0 | 0 | 3 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0012 | 0/0 | 4549 | 3 | 0 | 0 | 3 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0013 | 0/0 | 4550 | 2 | 0 | 1 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0014 | 0/0 | 4550 | 2 | 1 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0015 | 0/0 | 4549 | 2 | 0 | 0 | 2 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0017 | 0/0 | 4549 | 2 | 0 | 0 | 2 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0019 | 0/0 | 4548 | 2 | 2 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0024 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0025 | 0/0 | 4550 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0026 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0027 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0028 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0030 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0031 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0033 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0036 | 0/0 | 4556 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0001t0037 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0004t0004 | 0/0 | 4548 | 2 | 1 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0004t0007 | 0/0 | 4549 | 10 | 0 | 5 | 0 | 0 | 5 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0009t0029 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0010t0003 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0001c0017t0001 | 0/0 | 4549 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0002t0001 | 0/0 | 4549 | 12 | 0 | 0 | 12 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0002t0002 | 0/0 | 4549 | 77 | 28 | 27 | 13 | 3 | 6 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0002t0005 | 0/0 | 4551 | 11 | 0 | 0 | 10 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0002t0010 | 0/0 | 4549 | 4 | 4 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0002t0021 | 0/0 | 4549 | 2 | 1 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0002t0022 | 0/0 | 4550 | 2 | 0 | 1 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0002t0023 | 0/0 | 4549 | 2 | 0 | 0 | 0 | 2 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0002t0038 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0002t0039 | 0/0 | 4550 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0002t0040 | 0/0 | 4551 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0002t0041 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0002t0042 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0005t0001 | 0/0 | 4549 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0005t0002 | 0/0 | 4549 | 4 | 0 | 0 | 4 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0011t0001 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0002c0015t0002 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0003c0003t0004 | 0/1 | 4548 | 35 | 21 | 4 | 7 | 0 | 2 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0003c0003t0016 | 0/0 | 4548 | 2 | 2 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0003c0003t0018 | 0/0 | 4549 | 2 | 2 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0003c0003t0020 | 0/0 | 4548 | 2 | 2 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0003c0003t0032 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0003c0003t0034 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0003c0003t0035 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0004c0016t0001 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0005c0006t0004 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0006c0008t0001 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0007c0007t0003 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0008c0013t0004 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0009c0012t0002 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
a0010c0014t0010 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | copy fasta | chr2 | 55629061 | 55698844 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0341 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0008g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0008g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0008g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0009g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0009g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0009g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0009g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0009g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0011g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0011g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0011g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0012g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0012g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0012g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0013g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0013g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0014g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0014g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0015g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0015g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0017g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0017g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0019g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0019g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0024g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0025g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0026g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0027g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0028g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0030g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0031g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0033g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0036g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0037g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0004g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0007g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0007g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0007g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0007g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0007g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0007g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0007g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0007g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0009t0029g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0010t0003g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0017t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0377 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0005g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0005g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0010g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0010g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0010g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0010g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0021g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0021g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0022g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0022g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0023g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0023g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0038g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0039g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0040g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0041g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0042g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0005t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0005t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0005t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0005t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0005t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0011t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0015t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0016g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0016g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0018g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0018g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0020g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0020g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0032g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0034g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0035g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0004c0016t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0005c0006t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0006c0008t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0007c0007t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0008c0013t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0009c0012t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0010c0014t0010g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0023 | g0274 | EUR | GBR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00099 | hp2 | a0001 | c0001 | t0006 | g0118 | EUR | GBR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | GBR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0225 | EUR | GBR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0368 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0369 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0370 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0344 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0319 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00558 | hp2 | a0001 | c0001 | t0011 | g0134 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00621 | hp1 | a0001 | c0001 | t0036 | g0154 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00621 | hp2 | a0001 | c0001 | t0009 | g0336 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00642 | hp1 | a0002 | c0002 | t0022 | g0239 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0259 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0226 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0223 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0220 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0261 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01070 | hp2 | a0001 | c0004 | t0007 | g0065 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0221 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0263 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0374 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01074 | hp2 | a0001 | c0017 | t0001 | g0378 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01081 | hp1 | a0001 | c0004 | t0007 | g0005 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01099 | hp1 | a0001 | c0004 | t0007 | g0005 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0266 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0363 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0267 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0245 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0244 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01167 | hp1 | a0002 | c0002 | t0021 | g0286 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0373 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01168 | hp2 | a0003 | c0003 | t0004 | g0075 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01169 | hp1 | a0003 | c0003 | t0004 | g0074 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01175 | hp2 | a0003 | c0003 | t0004 | g0090 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01192 | hp1 | a0001 | c0004 | t0007 | g0060 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01243 | hp1 | a0003 | c0003 | t0034 | g0078 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01255 | hp1 | a0003 | c0003 | t0004 | g0095 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0288 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0276 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01261 | hp1 | a0001 | c0001 | t0006 | g0191 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0283 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01346 | hp2 | a0002 | c0005 | t0001 | g0175 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0348 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0262 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0230 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0218 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01433 | hp2 | a0001 | c0004 | t0007 | g0006 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0120 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0377 | EUR | IBS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | IBS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01884 | hp1 | a0001 | c0001 | t0008 | g0204 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0247 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01891 | hp1 | a0003 | c0003 | t0016 | g0070 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01891 | hp2 | a0002 | c0002 | t0002 | g0275 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0264 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0293 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01934 | hp1 | a0001 | c0001 | t0006 | g0162 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0298 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0273 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0295 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01978 | hp1 | a0001 | c0001 | t0013 | g0169 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01978 | hp2 | a0001 | c0001 | t0009 | g0297 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0365 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0234 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0335 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02056 | hp2 | a0001 | c0001 | t0031 | g0372 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02071 | hp1 | a0001 | c0001 | t0012 | g0153 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02071 | hp2 | a0002 | c0005 | t0002 | g0128 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02074 | hp1 | a0001 | c0001 | t0017 | g0329 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0315 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02083 | hp1 | a0001 | c0001 | t0011 | g0158 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0296 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0304 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02129 | hp2 | a0002 | c0011 | t0001 | g0029 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0237 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02145 | hp2 | a0003 | c0003 | t0018 | g0082 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CDX | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0334 | EAS | CDX | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0352 | EAS | CDX | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CDX | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02257 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0194 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0289 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02280 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02280 | hp2 | a0001 | c0001 | t0014 | g0171 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0265 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0258 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0375 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02451 | hp1 | a0003 | c0003 | t0020 | g0101 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02523 | hp1 | a0004 | c0016 | t0001 | g0042 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0361 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02572 | hp1 | a0002 | c0002 | t0042 | g0277 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02572 | hp2 | a0001 | c0001 | t0024 | g0193 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0243 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0328 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02615 | hp1 | a0003 | c0003 | t0020 | g0067 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02622 | hp1 | a0003 | c0003 | t0004 | g0080 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02622 | hp2 | a0003 | c0003 | t0004 | g0079 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02630 | hp1 | a0003 | c0003 | t0004 | g0072 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02630 | hp2 | a0002 | c0002 | t0002 | g0228 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02647 | hp1 | a0003 | c0003 | t0004 | g0069 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02683 | hp1 | a0001 | c0009 | t0029 | g0119 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02698 | hp1 | a0001 | c0001 | t0033 | g0345 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02698 | hp2 | a0001 | c0001 | t0006 | g0123 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02717 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02717 | hp2 | a0001 | c0001 | t0008 | g0195 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0232 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02723 | hp2 | a0003 | c0003 | t0004 | g0094 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0285 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0358 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0346 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0376 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02809 | hp1 | a0002 | c0002 | t0010 | g0280 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02809 | hp2 | a0001 | c0001 | t0008 | g0196 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02818 | hp2 | a0001 | c0001 | t0019 | g0216 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02886 | hp1 | a0002 | c0002 | t0002 | g0229 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02886 | hp2 | a0001 | c0001 | t0019 | g0215 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02895 | hp1 | a0003 | c0003 | t0004 | g0084 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02895 | hp2 | a0002 | c0002 | t0010 | g0112 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02897 | hp1 | a0002 | c0002 | t0010 | g0113 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02897 | hp2 | a0003 | c0003 | t0004 | g0110 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02922 | hp1 | a0003 | c0003 | t0035 | g0077 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02922 | hp2 | a0002 | c0002 | t0010 | g0279 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02965 | hp1 | a0003 | c0003 | t0004 | g0092 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02965 | hp2 | a0001 | c0001 | t0008 | g0205 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02970 | hp1 | a0001 | c0004 | t0004 | g0025 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02970 | hp2 | a0003 | c0003 | t0004 | g0066 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02976 | hp1 | a0003 | c0003 | t0004 | g0086 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03017 | hp1 | a0001 | c0004 | t0007 | g0063 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03017 | hp2 | a0001 | c0004 | t0004 | g0008 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03041 | hp1 | a0008 | c0013 | t0004 | g0013 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03041 | hp2 | a0002 | c0002 | t0002 | g0268 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0269 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0022 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03130 | hp2 | a0002 | c0002 | t0038 | g0024 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03139 | hp1 | a0003 | c0003 | t0004 | g0083 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03139 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03195 | hp1 | a0003 | c0003 | t0004 | g0076 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03195 | hp2 | a0003 | c0003 | t0004 | g0091 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03209 | hp2 | a0003 | c0003 | t0016 | g0071 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03225 | hp1 | a0002 | c0002 | t0002 | g0020 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03225 | hp2 | a0003 | c0003 | t0018 | g0100 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03239 | hp1 | a0001 | c0001 | t0006 | g0116 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03239 | hp2 | a0001 | c0001 | t0037 | g0178 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03453 | hp1 | a0002 | c0002 | t0002 | g0271 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03453 | hp2 | a0010 | c0014 | t0010 | g0281 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03486 | hp1 | a0002 | c0002 | t0002 | g0227 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03486 | hp2 | a0003 | c0003 | t0004 | g0099 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0356 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03491 | hp1 | a0001 | c0004 | t0007 | g0061 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0301 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03492 | hp1 | a0001 | c0004 | t0007 | g0006 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03516 | hp1 | a0003 | c0003 | t0004 | g0085 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03540 | hp1 | a0001 | c0001 | t0027 | g0172 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03540 | hp2 | a0002 | c0002 | t0002 | g0284 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03579 | hp1 | a0003 | c0003 | t0004 | g0088 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03579 | hp2 | a0002 | c0002 | t0002 | g0217 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0318 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03654 | hp2 | a0002 | c0002 | t0041 | g0272 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0224 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03669 | hp2 | a0006 | c0008 | t0001 | g0043 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03688 | hp2 | a0002 | c0002 | t0039 | g0260 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03704 | hp2 | a0003 | c0003 | t0004 | g0097 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0350 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03710 | hp2 | a0001 | c0001 | t0026 | g0130 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03834 | hp1 | a0001 | c0004 | t0007 | g0064 | SAS | BEB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03927 | hp2 | a0001 | c0001 | t0009 | g0360 | SAS | BEB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03942 | hp1 | a0001 | c0001 | t0025 | g0208 | SAS | BEB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0351 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04115 | hp2 | a0001 | c0004 | t0007 | g0062 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04184 | hp1 | a0003 | c0003 | t0004 | g0068 | SAS | BEB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0241 | SAS | BEB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0222 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04204 | hp1 | a0001 | c0001 | t0028 | g0111 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04204 | hp2 | a0002 | c0002 | t0005 | g0231 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04228 | hp1 | a0001 | c0001 | t0006 | g0114 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04228 | hp2 | a0001 | c0001 | t0006 | g0117 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0246 | AFR | YRI | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18612 | hp2 | a0003 | c0003 | t0004 | g0104 | EAS | CHB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0357 | EAS | CHB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18906 | hp1 | a0002 | c0015 | t0002 | g0018 | AFR | YRI | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18906 | hp2 | a0005 | c0006 | t0004 | g0106 | AFR | YRI | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18940 | hp2 | a0001 | c0001 | t0014 | g0176 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18942 | hp1 | a0001 | c0001 | t0030 | g0046 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0355 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18944 | hp2 | a0002 | c0005 | t0002 | g0136 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18946 | hp1 | a0002 | c0002 | t0022 | g0238 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18946 | hp2 | a0003 | c0003 | t0032 | g0109 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18947 | hp1 | a0002 | c0002 | t0040 | g0253 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0349 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18950 | hp2 | a0002 | c0005 | t0002 | g0124 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18952 | hp1 | a0002 | c0002 | t0005 | g0001 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0337 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18961 | hp1 | a0001 | c0001 | t0009 | g0359 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18963 | hp2 | a0002 | c0005 | t0002 | g0127 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18964 | hp1 | a0001 | c0001 | t0013 | g0141 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18973 | hp1 | a0002 | c0002 | t0005 | g0251 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18979 | hp1 | a0002 | c0002 | t0005 | g0278 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18979 | hp2 | a0003 | c0003 | t0004 | g0108 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0371 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18982 | hp2 | a0002 | c0002 | t0005 | g0255 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18983 | hp1 | a0002 | c0002 | t0005 | g0252 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18984 | hp1 | a0003 | c0003 | t0004 | g0103 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0364 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18986 | hp1 | a0001 | c0001 | t0017 | g0325 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0343 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0353 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18990 | hp2 | a0001 | c0001 | t0011 | g0148 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18998 | hp1 | a0002 | c0002 | t0005 | g0254 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19000 | hp1 | a0001 | c0001 | t0009 | g0308 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19001 | hp1 | a0002 | c0002 | t0005 | g0001 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19002 | hp2 | a0003 | c0003 | t0004 | g0096 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0367 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19003 | hp2 | a0002 | c0002 | t0005 | g0001 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19006 | hp2 | a0001 | c0001 | t0012 | g0146 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0333 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19007 | hp2 | a0002 | c0002 | t0005 | g0001 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19030 | hp1 | a0003 | c0003 | t0004 | g0073 | AFR | LWK | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19043 | hp1 | a0001 | c0001 | t0008 | g0203 | AFR | LWK | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19054 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19057 | hp1 | a0001 | c0001 | t0015 | g0050 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19057 | hp2 | a0009 | c0012 | t0002 | g0236 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0347 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19063 | hp1 | a0007 | c0007 | t0003 | g0306 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19074 | hp1 | a0002 | c0002 | t0005 | g0250 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0366 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19078 | hp2 | a0003 | c0003 | t0004 | g0105 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19080 | hp1 | a0001 | c0001 | t0012 | g0143 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19089 | hp2 | a0003 | c0003 | t0004 | g0107 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19090 | hp1 | a0001 | c0001 | t0015 | g0051 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0339 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19091 | hp2 | a0003 | c0003 | t0004 | g0102 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA20129 | hp1 | a0003 | c0003 | t0004 | g0093 | AFR | ASW | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | ASW | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA20752 | hp2 | a0002 | c0002 | t0023 | g0257 | EUR | TSI | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0270 | EUR | TSI | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA20905 | hp1 | a0001 | c0010 | t0003 | g0300 | SAS | GIH | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA20905 | hp2 | a0001 | c0001 | t0006 | g0115 | SAS | GIH | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02109 | hp2 | a0003 | c0003 | t0004 | g0081 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0282 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02486 | hp2 | a0001 | c0001 | t0006 | g0121 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02559 | hp1 | a0003 | c0003 | t0004 | g0089 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0021 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03471 | hp1 | a0002 | c0002 | t0002 | g0012 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03471 | hp2 | a0003 | c0003 | t0004 | g0087 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | USA | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG06807 | hp2 | a0002 | c0002 | t0021 | g0287 | AFR | USA | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0362 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0016 | AFR | LWK | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA21309 | hp2 | a0001 | c0001 | t0008 | g0202 | AFR | LWK | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0004 | g0098 | REF | REF | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0341 | REF | REF | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55645391
|
A | C | 1 | a0009 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.1780T>G | p.Ser594Ala | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/28 | 1801/4549 | 1780/2352 | 594/783 | chr2 | 55645391 | ||
chr2:55645403
|
T | C | 3 | a0003a0005a0008 | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
missense_variant | MODERATE | c.1768A>G | p.Asn590Asp | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/28 | 1789/4549 | 1768/2352 | 590/783 | chr2 | 55645403 | ||
chr2:55661972
|
C | T | 1 | a0006 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.1231G>A | p.Val411Ile | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/28 | 1252/4549 | 1231/2352 | 411/783 | chr2 | 55661972 | ||
chr2:55662008
|
A | T | 1 | a0007 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.1195T>A | p.Phe399Ile | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/28 | 1216/4549 | 1195/2352 | 399/783 | chr2 | 55662008 | ||
chr2:55667055
|
C | T | 1 | a0005 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.1112G>A | p.Ser371Asn | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/28 | 1133/4549 | 1112/2352 | 371/783 | chr2 | 55667055 | ||
chr2:55671351
|
T | C | 1 | a0010 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.944A>G | p.Lys315Arg | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/28 | 965/4549 | 944/2352 | 315/783 | chr2 | 55671351 | ||
chr2:55684985
|
T | C | 5 | a0002a0004a0008others(2): Show | 126 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(123): Show |
missense_variant | MODERATE | c.361A>G | p.Ile121Val | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/28 | 382/4549 | 361/2352 | 121/783 | chr2 | 55684985 | ||
chr2:55685034
|
T | A | 1 | a0004 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.312A>T | p.Gln104His | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/28 | 333/4549 | 312/2352 | 104/783 | chr2 | 55685034 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55646272
|
A | G | 1 | a0002c0011 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.1725T>C | p.Ile575Ile | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/28 | 1746/4549 | 1725/2352 | 575/783 | chr2 | 55646272 | ||
chr2:55656182
|
G | T | 7 | a0001c0004a0002c0002a0002c0011others(4): Show | 132 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(129): Show |
synonymous_variant | LOW | c.1390C>A | p.Arg464Arg | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/28 | 1411/4549 | 1390/2352 | 464/783 | chr2 | 55656182 | ||
chr2:55660190
|
C | T | 1 | a0001c0009 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.1251G>A | p.Gly417Gly | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/28 | 1272/4549 | 1251/2352 | 417/783 | chr2 | 55660190 | ||
chr2:55672007
|
G | A | 1 | a0002c0015 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.906C>T | p.Tyr302Tyr | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/28 | 927/4549 | 906/2352 | 302/783 | chr2 | 55672007 | ||
chr2:55672970
|
T | C | 1 | a0001c0010 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.789A>G | p.Val263Val | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 9/28 | 810/4549 | 789/2352 | 263/783 | chr2 | 55672970 | ||
chr2:55693722
|
T | C | 1 | a0001c0017 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.102A>G | p.Gln34Gln | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/28 | 123/4549 | 102/2352 | 34/783 | chr2 | 55693722 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55634260
|
C | CT | 5 | a0001c0001t0009a0001c0001t0014a0002c0002t0039others(2): Show | 11 | HG00621.hp2 HG01978.hp2 HG02145.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1976dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1976 | chr2 | 55634260 | |||||
chr2:55634260
|
C | CTT | 2 | a0002c0002t0005a0002c0002t0040 | 12 | HG04204.hp2 NA18947.hp1 NA18952.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1975_*1976dupAA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1976 | chr2 | 55634260 | |||||
chr2:55634318
|
A | G | 1 | a0002c0002t0038 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1919T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1919 | chr2 | 55634318 | |||||
chr2:55634343
|
C | T | 1 | a0002c0002t0023 | 2 | HG00099.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1894G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1894 | chr2 | 55634343 | |||||
chr2:55634367
|
T | G | 1 | a0002c0002t0040 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1870A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1870 | chr2 | 55634367 | |||||
chr2:55634407
|
G | T | 1 | a0003c0003t0034 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1830C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1830 | chr2 | 55634407 | |||||
chr2:55634462
|
G | A | 1 | a0001c0001t0017 | 2 | HG02074.hp1 NA18986.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1775C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1775 | chr2 | 55634462 | |||||
chr2:55634508
|
C | A | 1 | a0001c0009t0029 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1729G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1729 | chr2 | 55634508 | |||||
chr2:55634510
|
C | T | 18 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(15): Show | 125 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*1727G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1727 | chr2 | 55634510 | |||||
chr2:55634561
|
A | T | 3 | a0001c0001t0006a0001c0001t0028a0001c0009t0029 | 12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1676T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1676 | chr2 | 55634561 | |||||
chr2:55634602
|
C | T | 1 | a0001c0001t0019 | 2 | HG02818.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1635G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1635 | chr2 | 55634602 | |||||
chr2:55634619
|
G | A | 1 | a0002c0002t0041 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1618C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1618 | chr2 | 55634619 | |||||
chr2:55634802
|
C | T | 1 | a0001c0004t0007 | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1435G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1435 | chr2 | 55634802 | |||||
chr2:55634805
|
C | T | 1 | a0001c0001t0028 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1432G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1432 | chr2 | 55634805 | |||||
chr2:55634975
|
G | A | 1 | a0001c0001t0033 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1262C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1262 | chr2 | 55634975 | |||||
chr2:55635039
|
A | G | 1 | a0001c0001t0012 | 3 | HG02071.hp1 NA19006.hp2 NA19080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1198T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1198 | chr2 | 55635039 | |||||
chr2:55635136
|
G | A | 1 | a0001c0001t0030 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1101C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1101 | chr2 | 55635136 | |||||
chr2:55635220
|
A | T | 10 | a0001c0004t0004a0002c0002t0021a0003c0003t0004others(7): Show | 49 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1017T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1017 | chr2 | 55635220 | |||||
chr2:55635298
|
A | G | 1 | a0001c0001t0011 | 3 | HG00558.hp2 HG02083.hp1 NA18990.hp2 |
3_prime_UTR_variant | MODIFIER | c.*939T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 939 | chr2 | 55635298 | |||||
chr2:55635305
|
T | C | 50 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(47): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*932A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 932 | chr2 | 55635305 | |||||
chr2:55635315
|
AT | A | 47 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(44): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*921delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 921 | chr2 | 55635315 | |||||
chr2:55635336
|
C | T | 1 | a0001c0001t0027 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*901G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 901 | chr2 | 55635336 | |||||
chr2:55635383
|
C | T | 2 | a0001c0001t0025a0001c0001t0026 | 2 | HG03710.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*854G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 854 | chr2 | 55635383 | |||||
chr2:55635462
|
G | A | 1 | a0003c0003t0020 | 2 | HG02451.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*775C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 775 | chr2 | 55635462 | |||||
chr2:55635490
|
C | G | 1 | a0003c0003t0032 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*747G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 747 | chr2 | 55635490 | |||||
chr2:55635529
|
G | A | 1 | a0002c0002t0041 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*708C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 708 | chr2 | 55635529 | |||||
chr2:55635636
|
A | T | 1 | a0001c0001t0024 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*601T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 601 | chr2 | 55635636 | |||||
chr2:55635640
|
C | A | 15 | a0001c0001t0002a0002c0002t0002a0002c0002t0005others(12): Show | 110 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*597G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 597 | chr2 | 55635640 | |||||
chr2:55635666
|
T | C | 3 | a0002c0002t0010a0002c0002t0042a0010c0014t0010 | 6 | HG02572.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*571A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 571 | chr2 | 55635666 | |||||
chr2:55635669
|
T | TTTGGTAA | 22 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(19): Show | 138 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*561_*567dupTTACCA others(1): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 567 | chr2 | 55635669 | |||||
chr2:55635726
|
C | T | 1 | a0003c0003t0016 | 2 | HG01891.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*511G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 511 | chr2 | 55635726 | |||||
chr2:55635809
|
G | C | 1 | a0001c0001t0015 | 2 | NA19057.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*428C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 428 | chr2 | 55635809 | |||||
chr2:55635919
|
A | C | 1 | a0001c0001t0031 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*318T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 318 | chr2 | 55635919 | |||||
chr2:55635931
|
TTCTA | T | 21 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(18): Show | 137 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*302_*305delTAGA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 302 | chr2 | 55635931 | |||||
chr2:55635975
|
CTA | C | 21 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(18): Show | 137 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*260_*261delTA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 260 | chr2 | 55635975 | |||||
chr2:55636166
|
A | G | 1 | a0001c0001t0008 | 7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*71T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 71 | chr2 | 55636166 | |||||
chr2:55636225
|
T | TA | 18 | a0001c0001t0002a0001c0001t0037a0001c0004t0007others(15): Show | 123 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*11dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 11 | chr2 | 55636225 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55636656
|
G | A | 1 | a0001c0001t0003g0293 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2197-264C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55636656 | ||||||
chr2:55636733
|
T | C | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2197-341A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55636733 | ||||||
chr2:55636741
|
A | C | 14 | a0001c0001t0003g0289a0001c0001t0003g0290a0001c0001t0003g0293others(11): Show | 14 | HG01928.hp2 HG01934.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.2197-349T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55636741 | ||||||
chr2:55636871
|
A | AAAC | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2197-482_2197-480d others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55636871 | ||||||
chr2:55636871
|
AAACAAC | A | 102 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0007others(99): Show | 110 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.2197-485_2197-480d others(8): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55636871 | ||||||
chr2:55636871
|
AAACAACA others(2): Show |
A | 48 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0132others(45): Show | 48 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.2197-488_2197-480d others(11): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55636871 | ||||||
chr2:55636929
|
A | G | 48 | a0001c0004t0004g0008a0001c0004t0004g0025a0003c0003t0004g0066others(45): Show | 48 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(45): Show |
intron_variant | MODIFIER | c.2197-537T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55636929 | ||||||
chr2:55637237
|
A | G | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2196+315T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55637237 | ||||||
chr2:55637268
|
C | T | 6 | a0002c0002t0010g0112a0002c0002t0010g0113a0002c0002t0010g0279others(3): Show | 6 | HG02572.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2196+284G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55637268 | ||||||
chr2:55637298
|
T | C | 1 | a0002c0002t0002g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2196+254A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55637298 | ||||||
chr2:55637709
|
G | A | 1 | a0006c0008t0001g0043 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2149-110C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55637709 | ||||||
chr2:55637903
|
G | T | 7 | a0001c0001t0008g0194a0001c0001t0008g0195a0001c0001t0008g0196others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2149-304C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55637903 | ||||||
chr2:55637999
|
C | CA | 15 | a0001c0001t0001g0057a0001c0001t0001g0139a0001c0001t0001g0161others(12): Show | 15 | HG01109.hp2 HG01243.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.2149-401dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55637999 | ||||||
chr2:55638088
|
G | A | 1 | a0002c0015t0002g0018 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2149-489C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638088 | ||||||
chr2:55638100
|
G | A | 1 | a0001c0001t0003g0350 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2149-501C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638100 | ||||||
chr2:55638303
|
G | GA | 9 | a0001c0001t0001g0131a0001c0001t0003g0292a0001c0001t0003g0334others(6): Show | 9 | HG00621.hp2 HG01167.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.2149-705dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638303 | ||||||
chr2:55638303
|
GA | G | 242 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(239): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.2149-705delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638303 | ||||||
chr2:55638334
|
G | C | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.2149-735C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638334 | ||||||
chr2:55638394
|
G | A | 4 | a0001c0001t0003g0353a0001c0001t0003g0354a0001c0001t0017g0325others(1): Show | 4 | HG02074.hp1 NA18975.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149-795C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638394 | ||||||
chr2:55638449
|
C | T | 1 | a0001c0001t0008g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2149-850G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638449 | ||||||
chr2:55638514
|
C | T | 1 | a0001c0001t0026g0130 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2149-915G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638514 | ||||||
chr2:55638576
|
G | C | 1 | a0001c0001t0001g0182 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2149-977C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638576 | ||||||
chr2:55638817
|
C | T | 1 | a0001c0001t0003g0354 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2149-1218G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638817 | ||||||
chr2:55638916
|
A | C | 1 | a0002c0002t0002g0258 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2149-1317T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638916 | ||||||
chr2:55639318
|
A | G | 301 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(298): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.2148+1309T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639318 | ||||||
chr2:55639382
|
G | C | 2 | a0002c0002t0002g0223a0002c0002t0022g0239 | 2 | HG00642.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.2148+1245C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639382 | ||||||
chr2:55639470
|
C | G | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.2148+1157G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639470 | ||||||
chr2:55639589
|
G | C | 1 | a0001c0001t0003g0290 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2148+1038C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639589 | ||||||
chr2:55639592
|
C | G | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2148+1035G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639592 | ||||||
chr2:55639614
|
A | G | 4 | a0002c0002t0002g0261a0002c0002t0002g0263a0002c0002t0002g0270others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.2148+1013T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639614 | ||||||
chr2:55639838
|
T | G | 1 | a0001c0001t0003g0292 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2148+789A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639838 | ||||||
chr2:55639862
|
G | C | 1 | a0001c0001t0003g0290 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2148+765C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639862 | ||||||
chr2:55639877
|
C | A | 1 | a0010c0014t0010g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2148+750G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639877 | ||||||
chr2:55639892
|
A | C | 1 | a0002c0002t0001g0039 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2148+735T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639892 | ||||||
chr2:55639953
|
T | C | 1 | a0002c0002t0002g0244 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2148+674A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639953 | ||||||
chr2:55639962
|
C | A | 7 | a0001c0001t0008g0194a0001c0001t0008g0195a0001c0001t0008g0196others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2148+665G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639962 | ||||||
chr2:55640016
|
A | C | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2148+611T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640016 | ||||||
chr2:55640129
|
T | C | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2148+498A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640129 | ||||||
chr2:55640144
|
T | G | 1 | a0003c0003t0004g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2148+483A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640144 | ||||||
chr2:55640200
|
C | A | 1 | a0001c0001t0001g0213 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2148+427G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640200 | ||||||
chr2:55640249
|
G | A | 1 | a0003c0003t0004g0098 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2148+378C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640249 | ||||||
chr2:55640296
|
T | C | 1 | a0003c0003t0004g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2148+331A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640296 | ||||||
chr2:55640311
|
G | A | 7 | a0001c0001t0008g0194a0001c0001t0008g0195a0001c0001t0008g0196others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2148+316C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640311 | ||||||
chr2:55640313
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2148+314G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640313 | ||||||
chr2:55640339
|
A | T | 15 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0187others(12): Show | 15 | HG00438.hp1 HG03710.hp2 HG03942.hp1 others(12): Show |
intron_variant | MODIFIER | c.2148+288T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640339 | ||||||
chr2:55640399
|
G | A | 1 | a0002c0002t0010g0279 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2148+228C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640399 | ||||||
chr2:55640482
|
T | G | 4 | a0002c0002t0002g0007a0002c0002t0002g0240a0002c0002t0002g0242others(1): Show | 5 | NA18939.hp1 NA19004.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.2148+145A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640482 | ||||||
chr2:55640710
|
A | G | 1 | a0001c0001t0006g0121 | 1 | HG02486.hp2 | splice_region_variant&intron_variant | LOW | c.2070-5T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55640710 | ||||||
chr2:55640803
|
A | G | 142 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(139): Show | 142 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.2070-98T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55640803 | ||||||
chr2:55640871
|
C | T | 1 | a0006c0008t0001g0043 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2070-166G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55640871 | ||||||
chr2:55640889
|
G | C | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(1): Show | 4 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.2070-184C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55640889 | ||||||
chr2:55641018
|
G | A | 2 | a0003c0003t0004g0091a0003c0003t0004g0093 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2070-313C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641018 | ||||||
chr2:55641093
|
G | A | 2 | a0003c0003t0004g0107a0003c0003t0004g0108 | 2 | NA18979.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2070-388C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641093 | ||||||
chr2:55641094
|
C | T | 1 | a0002c0002t0002g0019 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2070-389G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641094 | ||||||
chr2:55641127
|
G | T | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2070-422C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641127 | ||||||
chr2:55641137
|
T | C | 1 | a0003c0003t0004g0090 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2070-432A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641137 | ||||||
chr2:55641262
|
C | T | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2070-557G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641262 | ||||||
chr2:55641283
|
A | AT | 11 | a0001c0001t0003g0294a0001c0001t0003g0302a0001c0001t0003g0305others(8): Show | 11 | HG00544.hp2 HG01358.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.2070-579dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641283 | ||||||
chr2:55641283
|
AT | A | 224 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(221): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.2070-579delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641283 | ||||||
chr2:55641283
|
ATT | A | 60 | a0001c0001t0001g0028a0001c0001t0001g0125a0001c0001t0001g0126others(57): Show | 60 | HG00140.hp1 HG00558.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.2070-580_2070-579d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641283 | ||||||
chr2:55641310
|
C | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0185 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2070-605G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641310 | ||||||
chr2:55641338
|
G | A | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(1): Show | 4 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.2070-633C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641338 | ||||||
chr2:55641467
|
C | T | 12 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0116others(9): Show | 12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.2070-762G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641467 | ||||||
chr2:55641550
|
G | A | 1 | a0001c0001t0026g0130 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2070-845C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641550 | ||||||
chr2:55641831
|
T | G | 112 | a0001c0001t0002g0346a0001c0001t0002g0356a0001c0004t0007g0005others(109): Show | 122 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.2070-1126A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641831 | ||||||
chr2:55641836
|
C | G | 30 | a0001c0001t0001g0028a0001c0001t0001g0049a0001c0001t0001g0053others(27): Show | 30 | HG00099.hp2 HG01261.hp1 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2070-1131G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641836 | ||||||
chr2:55641846
|
C | CT | 36 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(33): Show | 36 | HG00423.hp2 HG00735.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.2070-1142dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641846 | ||||||
chr2:55642066
|
C | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0055 | 2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2069+1092G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642066 | ||||||
chr2:55642344
|
A | C | 1 | a0002c0002t0002g0021 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2069+814T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642344 | ||||||
chr2:55642358
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2069+800C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642358 | ||||||
chr2:55642359
|
T | C | 1 | a0002c0002t0002g0224 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2069+799A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642359 | ||||||
chr2:55642377
|
G | C | 1 | a0002c0002t0002g0225 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2069+781C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642377 | ||||||
chr2:55642382
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2069+776C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642382 | ||||||
chr2:55642433
|
C | T | 98 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(95): Show | 98 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.2069+725G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642433 | ||||||
chr2:55642597
|
C | T | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2069+561G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642597 | ||||||
chr2:55642605
|
C | CA | 100 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(97): Show | 100 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.2069+552dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642605 | ||||||
chr2:55642605
|
C | CAA | 11 | a0001c0001t0001g0170a0001c0001t0001g0174a0001c0004t0004g0025others(8): Show | 11 | HG02145.hp2 HG02559.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.2069+551_2069+552d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642605 | ||||||
chr2:55642709
|
A | G | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.2069+449T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642709 | ||||||
chr2:55642829
|
A | T | 1 | a0001c0004t0007g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2069+329T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642829 | ||||||
chr2:55643036
|
C | T | 1 | a0001c0001t0003g0312 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2069+122G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55643036 | ||||||
chr2:55643504
|
G | T | 1 | a0001c0001t0003g0349 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1907-79C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 23/27 | chr2 | 55643504 | ||||||
chr2:55643562
|
T | C | 67 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0129others(64): Show | 67 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1907-137A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 23/27 | chr2 | 55643562 | ||||||
chr2:55643692
|
A | G | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.1907-267T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 23/27 | chr2 | 55643692 | ||||||
chr2:55643738
|
CA | C | 296 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(293): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1907-314delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 23/27 | chr2 | 55643738 | ||||||
chr2:55643790
|
T | C | 8 | a0001c0001t0003g0292a0001c0001t0003g0305a0001c0001t0003g0322others(5): Show | 8 | HG00544.hp2 HG02074.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.1907-365A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 23/27 | chr2 | 55643790 | ||||||
chr2:55644150
|
G | A | 297 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1906+487C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 23/27 | chr2 | 55644150 | ||||||
chr2:55644194
|
A | G | 13 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0116others(10): Show | 13 | HG00099.hp2 HG01167.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1906+443T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 23/27 | chr2 | 55644194 | ||||||
chr2:55644797
|
A | AT | 8 | a0001c0001t0001g0214a0001c0001t0003g0358a0002c0002t0010g0112others(5): Show | 8 | HG02572.hp1 HG02735.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1823-78dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55644797 | ||||||
chr2:55644857
|
G | C | 1 | a0001c0001t0003g0328 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1823-137C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55644857 | ||||||
chr2:55644941
|
G | A | 7 | a0001c0001t0008g0194a0001c0001t0008g0195a0001c0001t0008g0196others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1823-221C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55644941 | ||||||
chr2:55644946
|
G | A | 7 | a0001c0001t0008g0194a0001c0001t0008g0195a0001c0001t0008g0196others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1823-226C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55644946 | ||||||
chr2:55645009
|
C | T | 1 | a0001c0001t0006g0114 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1823-289G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55645009 | ||||||
chr2:55645022
|
A | AT | 19 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0157others(16): Show | 19 | HG00438.hp2 HG01175.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.1823-303dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55645022 | ||||||
chr2:55645022
|
AT | A | 8 | a0001c0001t0001g0058a0001c0001t0003g0321a0001c0001t0003g0358others(5): Show | 8 | HG01070.hp2 HG02451.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1823-303delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55645022 | ||||||
chr2:55645044
|
G | A | 1 | a0002c0002t0002g0019 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1822+305C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55645044 | ||||||
chr2:55645116
|
C | A | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1822+233G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55645116 | ||||||
chr2:55645124
|
T | C | 64 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0129others(61): Show | 64 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1822+225A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55645124 | ||||||
chr2:55645226
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1822+123C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55645226 | ||||||
chr2:55645246
|
G | A | 3 | a0001c0001t0003g0324a0003c0003t0004g0066a0003c0003t0004g0080 | 3 | HG02622.hp1 HG02970.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1822+103C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55645246 | ||||||
chr2:55645582
|
T | C | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1739-150A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55645582 | ||||||
chr2:55645834
|
ACTT | A | 98 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0007others(95): Show | 106 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.1739-405_1739-403d others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55645834 | ||||||
chr2:55645868
|
C | A | 31 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(28): Show | 31 | HG00423.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1738+391G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55645868 | ||||||
chr2:55645879
|
G | A | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738+380C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55645879 | ||||||
chr2:55645909
|
C | T | 1 | a0003c0003t0004g0092 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1738+350G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55645909 | ||||||
chr2:55645931
|
G | A | 6 | a0001c0001t0001g0125a0001c0001t0001g0129a0002c0005t0002g0124others(3): Show | 6 | HG02071.hp2 NA18944.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738+328C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55645931 | ||||||
chr2:55645988
|
C | T | 31 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(28): Show | 31 | HG00423.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1738+271G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55645988 | ||||||
chr2:55646080
|
G | A | 98 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0007others(95): Show | 106 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.1738+179C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55646080 | ||||||
chr2:55646166
|
T | A | 102 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0007others(99): Show | 110 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.1738+93A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55646166 | ||||||
chr2:55646222
|
G | C | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738+37C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55646222 | ||||||
chr2:55646250
|
C | G | 77 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(74): Show | 77 | HG00423.hp2 HG01168.hp2 HG01169.hp1 others(74): Show |
intron_variant | MODIFIER | c.1738+9G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55646250 | ||||||
chr2:55646773
|
TGTAA | T | 12 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0116others(9): Show | 12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603-291_1603-288d others(6): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 19/27 | chr2 | 55646773 | ||||||
chr2:55646863
|
C | T | 1 | a0003c0003t0020g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1603-377G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 19/27 | chr2 | 55646863 | ||||||
chr2:55646901
|
C | T | 10 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(7): Show | 12 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1603-415G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 19/27 | chr2 | 55646901 | ||||||
chr2:55647158
|
A | T | 7 | a0001c0001t0008g0194a0001c0001t0008g0195a0001c0001t0008g0196others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602+189T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 19/27 | chr2 | 55647158 | ||||||
chr2:55647197
|
T | C | 27 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(24): Show | 27 | HG00423.hp2 HG01192.hp2 HG02027.hp2 others(24): Show |
intron_variant | MODIFIER | c.1602+150A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 19/27 | chr2 | 55647197 | ||||||
chr2:55647333
|
G | A | 1 | a0001c0001t0003g0304 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1602+14C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 19/27 | chr2 | 55647333 | ||||||
chr2:55647676
|
C | T | 43 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(40): Show | 43 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.1496-223G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55647676 | ||||||
chr2:55647891
|
C | A | 1 | a0003c0003t0004g0068 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1496-438G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55647891 | ||||||
chr2:55648109
|
C | T | 1 | a0001c0001t0006g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1496-656G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648109 | ||||||
chr2:55648167
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1496-714G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648167 | ||||||
chr2:55648186
|
A | G | 3 | a0001c0001t0001g0142a0001c0001t0012g0143a0001c0001t0014g0176 | 3 | NA18940.hp2 NA19056.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1496-733T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648186 | ||||||
chr2:55648233
|
C | T | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.1496-780G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648233 | ||||||
chr2:55648371
|
T | C | 2 | a0001c0001t0003g0324a0001c0001t0003g0364 | 2 | NA18942.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1496-918A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648371 | ||||||
chr2:55648390
|
T | A | 17 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(14): Show | 17 | HG01192.hp2 HG01243.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1496-937A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648390 | ||||||
chr2:55648481
|
A | G | 1 | a0003c0003t0020g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1496-1028T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648481 | ||||||
chr2:55648520
|
CAATTT | C | 15 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0187others(12): Show | 15 | HG00438.hp1 HG03710.hp2 HG03942.hp1 others(12): Show |
intron_variant | MODIFIER | c.1496-1072_1496-106 others(9): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648520 | ||||||
chr2:55648539
|
T | C | 1 | a0002c0002t0038g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1496-1086A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648539 | ||||||
chr2:55648611
|
A | G | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.1496-1158T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648611 | ||||||
chr2:55648703
|
C | T | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1496-1250G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648703 | ||||||
chr2:55648939
|
T | C | 1 | a0008c0013t0004g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1496-1486A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648939 | ||||||
chr2:55649256
|
T | C | 2 | a0001c0001t0001g0190a0001c0001t0001g0340 | 2 | NA18971.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1496-1803A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649256 | ||||||
chr2:55649376
|
C | T | 11 | a0001c0001t0003g0004a0001c0001t0003g0316a0001c0001t0003g0321others(8): Show | 13 | NA18612.hp1 NA18943.hp1 NA18955.hp2 others(10): Show |
intron_variant | MODIFIER | c.1496-1923G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649376 | ||||||
chr2:55649412
|
C | G | 1 | a0001c0001t0001g0213 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1496-1959G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649412 | ||||||
chr2:55649421
|
T | C | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1496-1968A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649421 | ||||||
chr2:55649474
|
C | T | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1496-2021G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649474 | ||||||
chr2:55649550
|
T | C | 15 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(12): Show | 15 | HG00423.hp2 HG02027.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.1496-2097A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649550 | ||||||
chr2:55649794
|
G | C | 1 | a0001c0001t0001g0206 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1496-2341C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649794 | ||||||
chr2:55649874
|
C | G | 1 | a0001c0001t0003g0301 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1496-2421G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649874 | ||||||
chr2:55649978
|
C | T | 97 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0007others(94): Show | 105 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.1496-2525G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649978 | ||||||
chr2:55650036
|
G | C | 4 | a0001c0001t0003g0353a0001c0001t0003g0354a0001c0001t0017g0325others(1): Show | 4 | HG02074.hp1 NA18975.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1496-2583C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650036 | ||||||
chr2:55650079
|
G | A | 124 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(121): Show | 124 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.1496-2626C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650079 | ||||||
chr2:55650099
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1496-2646C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650099 | ||||||
chr2:55650111
|
A | T | 6 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(3): Show | 6 | HG01192.hp2 HG03490.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.1496-2658T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650111 | ||||||
chr2:55650141
|
C | CACCTCT | 69 | a0001c0001t0001g0188a0002c0002t0002g0002a0002c0002t0002g0003others(66): Show | 77 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1496-2694_1496-268 others(10): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650141 | ||||||
chr2:55650141
|
C | CACCTCTA others(5): Show |
6 | a0002c0002t0010g0112a0002c0002t0010g0113a0002c0002t0010g0279others(3): Show | 6 | HG02572.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1496-2700_1496-268 others(16): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650141 | ||||||
chr2:55650141
|
C | CACCTCTA others(11): Show |
8 | a0002c0002t0002g0217a0002c0002t0002g0226a0002c0002t0002g0227others(5): Show | 8 | HG00738.hp1 HG02630.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1496-2706_1496-268 others(22): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650141 | ||||||
chr2:55650141
|
CACCTCTA others(5): Show |
C | 1 | a0001c0001t0002g0346 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1496-2700_1496-268 others(16): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650141 | ||||||
chr2:55650167
|
C | T | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1496-2714G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650167 | ||||||
chr2:55650217
|
C | T | 123 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(120): Show | 123 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1496-2764G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650217 | ||||||
chr2:55650268
|
G | C | 1 | a0002c0002t0002g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1496-2815C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650268 | ||||||
chr2:55650281
|
T | C | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.1496-2828A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650281 | ||||||
chr2:55650287
|
C | T | 124 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(121): Show | 124 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.1496-2834G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650287 | ||||||
chr2:55650341
|
C | T | 7 | a0001c0001t0001g0028a0001c0001t0001g0170a0001c0001t0001g0173others(4): Show | 7 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1496-2888G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650341 | ||||||
chr2:55650351
|
G | T | 1 | a0001c0001t0003g0295 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1496-2898C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650351 | ||||||
chr2:55650387
|
C | T | 1 | a0003c0003t0004g0102 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1496-2934G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650387 | ||||||
chr2:55650563
|
A | AC | 6 | a0001c0001t0001g0132a0001c0001t0001g0168a0001c0001t0006g0191others(3): Show | 6 | HG01261.hp1 HG01952.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1496-3111dupG | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650563 | ||||||
chr2:55650585
|
C | T | 1 | a0001c0001t0003g0352 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1496-3132G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650585 | ||||||
chr2:55650639
|
C | T | 1 | a0008c0013t0004g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1496-3186G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650639 | ||||||
chr2:55650640
|
G | A | 2 | a0001c0001t0001g0370a0001c0001t0001g0371 | 2 | HG00438.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1496-3187C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650640 | ||||||
chr2:55650702
|
G | A | 2 | a0002c0002t0002g0258a0002c0002t0002g0273 | 2 | HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1496-3249C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650702 | ||||||
chr2:55650721
|
G | A | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1496-3268C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650721 | ||||||
chr2:55650755
|
C | T | 1 | a0001c0001t0003g0352 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1496-3302G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650755 | ||||||
chr2:55650837
|
C | T | 2 | a0002c0002t0021g0286a0002c0002t0021g0287 | 2 | HG01167.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1496-3384G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650837 | ||||||
chr2:55650849
|
AGTGAGGA others(131): Show |
A | 1 | a0001c0001t0003g0349 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1496-3534_1496-339 others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650849 | ||||||
chr2:55650884
|
C | G | 8 | a0002c0002t0002g0217a0002c0002t0002g0226a0002c0002t0002g0227others(5): Show | 8 | HG00738.hp1 HG02630.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1496-3431G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650884 | ||||||
chr2:55650893
|
G | A | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1496-3440C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650893 | ||||||
chr2:55650899
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1496-3446C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650899 | ||||||
chr2:55650902
|
G | GTCAGCCC others(42): Show |
6 | a0003c0003t0004g0098a0003c0003t0004g0102a0003c0003t0004g0103others(3): Show | 6 | NA18612.hp2 NA18946.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.1496-3498_1496-345 others(53): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650902 | ||||||
chr2:55650912
|
C | T | 9 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(6): Show | 11 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.1496-3459G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650912 | ||||||
chr2:55650916
|
C | T | 2 | a0001c0001t0011g0134a0001c0001t0011g0158 | 2 | HG00558.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1496-3463G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650916 | ||||||
chr2:55650930
|
G | T | 1 | a0001c0001t0001g0152 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1496-3477C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650930 | ||||||
chr2:55650959
|
C | T | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1496-3506G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650959 | ||||||
chr2:55650966
|
G | GGCCAGCC others(121): Show |
1 | a0002c0002t0002g0270 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1496-3641_1496-351 others(132): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650966 | ||||||
chr2:55651135
|
G | A | 2 | a0002c0002t0002g0220a0002c0002t0002g0221 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1496-3682C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651135 | ||||||
chr2:55651179
|
C | T | 2 | a0001c0001t0015g0050a0001c0001t0015g0051 | 2 | NA19057.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1495+3721G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651179 | ||||||
chr2:55651204
|
C | T | 116 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(113): Show | 124 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1495+3696G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651204 | ||||||
chr2:55651213
|
G | C | 2 | a0003c0003t0004g0107a0003c0003t0004g0108 | 2 | NA18979.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1495+3687C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651213 | ||||||
chr2:55651218
|
C | A | 2 | a0003c0003t0004g0107a0003c0003t0004g0108 | 2 | NA18979.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1495+3682G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651218 | ||||||
chr2:55651228
|
G | C | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1495+3672C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651228 | ||||||
chr2:55651250
|
G | C | 2 | a0002c0002t0010g0280a0010c0014t0010g0281 | 2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1495+3650C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651250 | ||||||
chr2:55651497
|
A | C | 3 | a0001c0001t0003g0366a0001c0001t0003g0367a0001c0001t0003g0368 | 3 | HG00423.hp1 NA19003.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1495+3403T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651497 | ||||||
chr2:55651510
|
C | G | 125 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1495+3390G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651510 | ||||||
chr2:55651542
|
A | G | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1495+3358T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651542 | ||||||
chr2:55651564
|
C | T | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1495+3336G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651564 | ||||||
chr2:55651645
|
C | T | 1 | a0002c0002t0022g0239 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1495+3255G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651645 | ||||||
chr2:55651773
|
TA | T | 179 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0129others(176): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1495+3126delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651773 | ||||||
chr2:55651774
|
A | T | 7 | a0001c0001t0001g0028a0001c0001t0001g0170a0001c0001t0001g0173others(4): Show | 7 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1495+3126T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651774 | ||||||
chr2:55651789
|
A | T | 1 | a0002c0002t0001g0030 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1495+3111T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651789 | ||||||
chr2:55651792
|
A | T | 124 | a0001c0001t0001g0173a0001c0004t0007g0005a0001c0004t0007g0006others(121): Show | 134 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1495+3108T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651792 | ||||||
chr2:55651828
|
T | C | 5 | a0002c0002t0002g0014a0002c0002t0002g0015a0002c0002t0002g0016others(2): Show | 5 | HG02257.hp1 HG03139.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495+3072A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651828 | ||||||
chr2:55651885
|
C | CA | 17 | a0001c0001t0003g0288a0001c0001t0003g0299a0001c0001t0003g0347others(14): Show | 17 | HG00099.hp1 HG01070.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.1495+3014dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651885 | ||||||
chr2:55651885
|
C | CAA | 97 | a0001c0004t0007g0061a0002c0002t0001g0030a0002c0002t0001g0031others(94): Show | 105 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.1495+3013_1495+301 others(6): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651885 | ||||||
chr2:55651885
|
C | CAAA | 12 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(9): Show | 14 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1495+3012_1495+301 others(7): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651885 | ||||||
chr2:55651885
|
CA | C | 102 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(99): Show | 102 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1495+3014delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651885 | ||||||
chr2:55651885
|
CAAA | C | 62 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0129others(59): Show | 62 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1495+3012_1495+301 others(7): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651885 | ||||||
chr2:55651989
|
T | C | 7 | a0001c0001t0008g0194a0001c0001t0008g0195a0001c0001t0008g0196others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1495+2911A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651989 | ||||||
chr2:55652181
|
TG | T | 124 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(121): Show | 134 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1495+2718delC | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55652181 | ||||||
chr2:55652321
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0055 | 3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1495+2579G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55652321 | ||||||
chr2:55652492
|
T | C | 1 | a0002c0002t0002g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1495+2408A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55652492 | ||||||
chr2:55652554
|
C | T | 2 | a0002c0002t0001g0047a0002c0002t0001g0054 | 2 | NA18962.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1495+2346G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55652554 | ||||||
chr2:55652587
|
G | C | 1 | a0004c0016t0001g0042 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1495+2313C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55652587 | ||||||
chr2:55652656
|
T | C | 7 | a0001c0001t0001g0028a0001c0001t0001g0170a0001c0001t0001g0173others(4): Show | 7 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1495+2244A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55652656 | ||||||
chr2:55652911
|
G | C | 12 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0116others(9): Show | 12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1495+1989C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55652911 | ||||||
chr2:55652963
|
T | A | 1 | a0001c0001t0026g0130 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1495+1937A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55652963 | ||||||
chr2:55653047
|
T | C | 116 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(113): Show | 124 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1495+1853A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55653047 | ||||||
chr2:55653173
|
A | G | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.1495+1727T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55653173 | ||||||
chr2:55653307
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0055 | 3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1495+1593G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55653307 | ||||||
chr2:55653431
|
C | T | 10 | a0001c0004t0004g0008a0001c0004t0004g0025a0001c0004t0007g0005others(7): Show | 12 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1495+1469G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55653431 | ||||||
chr2:55653544
|
T | A | 1 | a0009c0012t0002g0236 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1495+1356A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55653544 | ||||||
chr2:55653594
|
G | T | 2 | a0002c0002t0002g0285a0002c0002t0002g0363 | 2 | HG01106.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1495+1306C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55653594 | ||||||
chr2:55654041
|
G | A | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.1495+859C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654041 | ||||||
chr2:55654072
|
T | C | 1 | a0002c0002t0002g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1495+828A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654072 | ||||||
chr2:55654091
|
G | A | 6 | a0002c0002t0010g0112a0002c0002t0010g0113a0002c0002t0010g0279others(3): Show | 6 | HG02572.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495+809C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654091 | ||||||
chr2:55654122
|
T | C | 116 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(113): Show | 124 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1495+778A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654122 | ||||||
chr2:55654179
|
C | T | 6 | a0002c0002t0010g0112a0002c0002t0010g0113a0002c0002t0010g0279others(3): Show | 6 | HG02572.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495+721G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654179 | ||||||
chr2:55654192
|
G | A | 4 | a0001c0001t0003g0353a0001c0001t0003g0354a0001c0001t0017g0325others(1): Show | 4 | HG02074.hp1 NA18975.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495+708C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654192 | ||||||
chr2:55654194
|
T | A | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.1495+706A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654194 | ||||||
chr2:55654256
|
C | CA | 134 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0126others(131): Show | 142 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1495+643dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654256 | ||||||
chr2:55654256
|
C | CAA | 12 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(9): Show | 14 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1495+642_1495+643d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654256 | ||||||
chr2:55654345
|
G | A | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1495+555C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654345 | ||||||
chr2:55654357
|
T | C | 1 | a0003c0003t0032g0109 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1495+543A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654357 | ||||||
chr2:55654403
|
T | C | 116 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(113): Show | 124 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1495+497A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654403 | ||||||
chr2:55654681
|
C | T | 297 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1495+219G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654681 | ||||||
chr2:55654790
|
G | C | 1 | a0002c0002t0002g0283 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1495+110C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654790 | ||||||
chr2:55654819
|
TCCTGCCT others(19): Show |
T | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.1495+55_1495+80del others(26): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654819 | ||||||
chr2:55654997
|
T | A | 2 | a0001c0001t0003g0324a0001c0001t0003g0364 | 2 | NA18942.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1442-44A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55654997 | ||||||
chr2:55655112
|
A | T | 1 | a0003c0003t0004g0090 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1442-159T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655112 | ||||||
chr2:55655172
|
A | C | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1442-219T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655172 | ||||||
chr2:55655336
|
A | C | 124 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(121): Show | 134 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1442-383T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655336 | ||||||
chr2:55655336
|
A | T | 253 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(250): Show | 255 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.1442-383T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655336 | ||||||
chr2:55655356
|
A | G | 251 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(248): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1442-403T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655356 | ||||||
chr2:55655367
|
G | A | 2 | a0002c0002t0002g0220a0002c0002t0002g0221 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1442-414C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655367 | ||||||
chr2:55655430
|
A | C | 116 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(113): Show | 124 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1442-477T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655430 | ||||||
chr2:55655517
|
A | G | 10 | a0001c0001t0003g0307a0001c0001t0003g0313a0001c0001t0003g0314others(7): Show | 10 | HG00544.hp1 HG02080.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.1442-564T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655517 | ||||||
chr2:55655537
|
T | C | 297 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1442-584A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655537 | ||||||
chr2:55655594
|
A | T | 377 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(374): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.1441+537T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655594 | ||||||
chr2:55655634
|
G | A | 2 | a0002c0002t0021g0286a0002c0002t0021g0287 | 2 | HG01167.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1441+497C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655634 | ||||||
chr2:55655908
|
A | G | 1 | a0002c0002t0002g0373 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1441+223T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655908 | ||||||
chr2:55656405
|
A | T | 1 | a0001c0001t0001g0213 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1285-34T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55656405 | ||||||
chr2:55656430
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1285-59A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55656430 | ||||||
chr2:55656458
|
T | C | 1 | a0007c0007t0003g0306 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1285-87A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55656458 | ||||||
chr2:55656578
|
C | A | 297 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1285-207G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55656578 | ||||||
chr2:55656598
|
C | A | 99 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(96): Show | 99 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1285-227G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55656598 | ||||||
chr2:55656896
|
G | A | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.1285-525C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55656896 | ||||||
chr2:55656971
|
T | A | 130 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1285-600A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55656971 | ||||||
chr2:55657047
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1285-676C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657047 | ||||||
chr2:55657050
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0309 | 2 | NA19000.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1285-679G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657050 | ||||||
chr2:55657117
|
T | A | 122 | a0001c0004t0004g0008a0001c0004t0004g0025a0001c0004t0007g0005others(119): Show | 132 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.1285-746A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657117 | ||||||
chr2:55657174
|
G | A | 1 | a0002c0002t0001g0039 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1285-803C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657174 | ||||||
chr2:55657228
|
C | T | 106 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(103): Show | 116 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.1285-857G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657228 | ||||||
chr2:55657361
|
A | G | 1 | a0001c0001t0003g0342 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1285-990T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657361 | ||||||
chr2:55657474
|
T | C | 297 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1285-1103A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657474 | ||||||
chr2:55657593
|
T | C | 131 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(128): Show | 131 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1285-1222A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657593 | ||||||
chr2:55657729
|
G | A | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.1285-1358C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657729 | ||||||
chr2:55657856
|
C | CA | 16 | a0002c0002t0002g0003a0002c0002t0002g0235a0002c0002t0002g0248others(13): Show | 18 | HG00639.hp1 HG00735.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.1285-1486dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
C | CAA | 14 | a0001c0001t0001g0053a0002c0002t0002g0219a0002c0002t0002g0220others(11): Show | 14 | HG00140.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1285-1487_1285-148 others(6): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
C | CAAA | 8 | a0002c0002t0002g0014a0002c0002t0002g0223a0002c0002t0002g0285others(5): Show | 8 | HG00642.hp1 HG01069.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1285-1488_1285-148 others(7): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
C | CAAAAAAA others(3): Show |
1 | a0002c0002t0002g0241 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1285-1495_1285-148 others(14): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
C | CAAAAAAA others(5): Show |
2 | a0002c0002t0002g0266a0002c0002t0005g0231 | 2 | HG01099.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1285-1497_1285-148 others(16): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
C | CAAAAAAA others(6): Show |
1 | a0002c0002t0002g0267 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1285-1498_1285-148 others(17): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
C | CAAAAAAA others(8): Show |
1 | a0002c0002t0002g0244 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1285-1500_1285-148 others(19): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
C | CAAAAAAA others(17): Show |
1 | a0002c0002t0002g0243 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1285-1509_1285-148 others(28): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CA | C | 6 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0218others(3): Show | 6 | HG01433.hp1 HG01516.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1285-1486delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAA | C | 8 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0019others(5): Show | 8 | HG01074.hp1 HG01168.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1285-1487_1285-148 others(6): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAA | C | 10 | a0001c0001t0001g0028a0001c0001t0001g0173a0001c0001t0001g0174others(7): Show | 10 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1285-1491_1285-148 others(10): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA | C | 10 | a0001c0001t0001g0125a0001c0001t0001g0157a0001c0001t0001g0170others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1285-1492_1285-148 others(11): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0001g0126a0001c0001t0001g0142a0001c0001t0001g0144others(5): Show | 8 | HG01516.hp2 HG02027.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1285-1493_1285-148 others(12): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(2): Show |
C | 33 | a0001c0001t0001g0122a0001c0001t0001g0129a0001c0001t0001g0132others(30): Show | 33 | HG00558.hp2 HG00621.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1285-1494_1285-148 others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(3): Show |
C | 21 | a0001c0001t0001g0131a0001c0001t0001g0133a0001c0001t0001g0135others(18): Show | 21 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1285-1495_1285-148 others(14): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(5): Show |
C | 9 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0044others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285-1497_1285-148 others(16): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(6): Show |
C | 14 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0056others(11): Show | 17 | HG00423.hp2 HG01192.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.1285-1498_1285-148 others(17): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(7): Show |
C | 13 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(10): Show | 13 | HG01361.hp2 HG02129.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1285-1499_1285-148 others(18): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(8): Show |
C | 4 | a0001c0001t0001g0041a0001c0001t0008g0195a0002c0002t0002g0258others(1): Show | 4 | HG01952.hp2 HG02293.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285-1500_1285-148 others(19): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(9): Show |
C | 5 | a0001c0001t0008g0194a0001c0001t0008g0196a0001c0001t0008g0202others(2): Show | 5 | HG02258.hp1 HG02809.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1285-1501_1285-148 others(20): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(10): Show |
C | 1 | a0002c0002t0002g0222 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1285-1502_1285-148 others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(13): Show |
C | 2 | a0002c0002t0002g0022a0002c0002t0002g0023 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1285-1505_1285-148 others(24): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(14): Show |
C | 10 | a0003c0003t0004g0068a0003c0003t0004g0073a0003c0003t0004g0090others(7): Show | 10 | HG01175.hp2 HG02145.hp2 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1285-1506_1285-148 others(25): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(15): Show |
C | 49 | a0001c0001t0002g0346a0001c0001t0003g0292a0001c0001t0003g0294others(46): Show | 49 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.1285-1507_1285-148 others(26): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(16): Show |
C | 66 | a0001c0001t0002g0356a0001c0001t0003g0004a0001c0001t0003g0288others(63): Show | 68 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.1285-1508_1285-148 others(27): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(17): Show |
C | 1 | a0002c0002t0002g0017 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1285-1509_1285-148 others(28): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(18): Show |
C | 27 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0187others(24): Show | 27 | HG00438.hp1 HG00738.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1285-1510_1285-148 others(29): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(21): Show |
C | 1 | a0001c0004t0007g0062 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1285-1513_1285-148 others(32): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(22): Show |
C | 7 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(4): Show | 9 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285-1514_1285-148 others(33): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(26): Show |
C | 2 | a0002c0002t0021g0286a0002c0002t0021g0287 | 2 | HG01167.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1285-1518_1285-148 others(37): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657856
|
CAAAAAAA others(27): Show |
C | 1 | a0001c0010t0003g0300 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1285-1519_1285-148 others(38): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | ||||||
chr2:55657892
|
A | G | 1 | a0003c0003t0032g0109 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1285-1521T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657892 | ||||||
chr2:55657919
|
G | A | 126 | a0001c0001t0002g0346a0001c0001t0002g0356a0001c0001t0003g0004others(123): Show | 128 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1285-1548C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657919 | ||||||
chr2:55657950
|
A | G | 67 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0129others(64): Show | 67 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1285-1579T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657950 | ||||||
chr2:55658093
|
G | A | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1285-1722C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55658093 | ||||||
chr2:55658128
|
G | A | 2 | a0002c0002t0002g0009a0002c0002t0002g0011 | 2 | HG02280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1285-1757C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55658128 | ||||||
chr2:55658373
|
C | T | 15 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0187others(12): Show | 15 | HG00438.hp1 HG03710.hp2 HG03942.hp1 others(12): Show |
intron_variant | MODIFIER | c.1284+1784G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55658373 | ||||||
chr2:55658565
|
T | C | 1 | a0001c0001t0008g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1284+1592A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55658565 | ||||||
chr2:55658775
|
G | T | 1 | a0001c0001t0001g0059 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1284+1382C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55658775 | ||||||
chr2:55659079
|
C | T | 2 | a0002c0002t0021g0286a0002c0002t0021g0287 | 2 | HG01167.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1284+1078G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659079 | ||||||
chr2:55659387
|
T | C | 3 | a0001c0004t0007g0006a0001c0004t0007g0061a0001c0004t0007g0062 | 4 | HG01433.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284+770A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659387 | ||||||
chr2:55659467
|
T | C | 98 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0007others(95): Show | 106 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.1284+690A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659467 | ||||||
chr2:55659505
|
G | A | 1 | a0001c0001t0003g0292 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1284+652C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659505 | ||||||
chr2:55659521
|
CTT | C | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.1284+634_1284+635d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659521 | ||||||
chr2:55659543
|
C | T | 1 | a0002c0002t0002g0273 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1284+614G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659543 | ||||||
chr2:55659573
|
G | A | 1 | a0001c0001t0001g0370 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1284+584C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659573 | ||||||
chr2:55659641
|
A | G | 1 | a0001c0001t0033g0345 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1284+516T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659641 | ||||||
chr2:55659645
|
C | T | 142 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(139): Show | 142 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1284+512G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659645 | ||||||
chr2:55659658
|
C | T | 2 | a0002c0002t0005g0001a0002c0002t0005g0278 | 5 | NA18952.hp1 NA18979.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284+499G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659658 | ||||||
chr2:55659736
|
G | A | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.1284+421C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659736 | ||||||
chr2:55659867
|
C | T | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1284+290G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659867 | ||||||
chr2:55659940
|
A | G | 2 | a0002c0002t0002g0245a0002c0002t0002g0276 | 2 | HG01109.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1284+217T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659940 | ||||||
chr2:55660025
|
GC | G | 6 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(3): Show | 6 | HG01192.hp2 HG03490.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.1284+131delG | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55660025 | ||||||
chr2:55660041
|
T | C | 142 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(139): Show | 142 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1284+116A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55660041 | ||||||
chr2:55660057
|
C | A | 1 | a0001c0001t0006g0114 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1284+100G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55660057 | ||||||
chr2:55660401
|
T | C | 3 | a0001c0001t0003g0335a0001c0001t0003g0361a0001c0001t0009g0336 | 3 | HG00621.hp2 HG02056.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1248-208A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55660401 | ||||||
chr2:55660515
|
C | T | 1 | a0002c0002t0002g0247 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1248-322G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55660515 | ||||||
chr2:55660568
|
C | T | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1248-375G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55660568 | ||||||
chr2:55660614
|
T | G | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.1248-421A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55660614 | ||||||
chr2:55660679
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0055 | 3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1248-486C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55660679 | ||||||
chr2:55660815
|
G | C | 1 | a0003c0003t0020g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1248-622C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55660815 | ||||||
chr2:55661091
|
C | CT | 19 | a0001c0001t0001g0125a0001c0001t0001g0192a0001c0001t0001g0210others(16): Show | 19 | HG00423.hp1 HG01175.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.1247+864dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661091 | ||||||
chr2:55661091
|
CT | C | 142 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(139): Show | 150 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(147): Show |
intron_variant | MODIFIER | c.1247+864delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661091 | ||||||
chr2:55661091
|
CTT | C | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1247+863_1247+864d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661091 | ||||||
chr2:55661091
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0009g0336 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1247+854_1247+864d others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661091 | ||||||
chr2:55661110
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1247+846A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661110 | ||||||
chr2:55661240
|
C | T | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.1247+716G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661240 | ||||||
chr2:55661260
|
T | C | 7 | a0001c0001t0001g0028a0001c0001t0001g0170a0001c0001t0001g0173others(4): Show | 7 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1247+696A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661260 | ||||||
chr2:55661278
|
G | A | 315 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(312): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1247+678C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661278 | ||||||
chr2:55661288
|
T | A | 7 | a0001c0001t0008g0194a0001c0001t0008g0195a0001c0001t0008g0196others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1247+668A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661288 | ||||||
chr2:55661477
|
T | A | 188 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.1247+479A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661477 | ||||||
chr2:55661494
|
C | T | 1 | a0001c0001t0003g0318 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1247+462G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661494 | ||||||
chr2:55661740
|
T | A | 1 | a0007c0007t0003g0306 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1247+216A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661740 | ||||||
chr2:55661900
|
T | C | 1 | a0001c0001t0003g0288 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1247+56A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661900 | ||||||
chr2:55661927
|
G | A | 296 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(293): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1247+29C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661927 | ||||||
chr2:55662063
|
C | T | 2 | a0001c0001t0012g0146a0001c0001t0012g0153 | 2 | HG02071.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1177-37G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662063 | ||||||
chr2:55662158
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0055 | 3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1177-132G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662158 | ||||||
chr2:55662201
|
A | G | 7 | a0001c0001t0001g0028a0001c0001t0001g0170a0001c0001t0001g0173others(4): Show | 7 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1177-175T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662201 | ||||||
chr2:55662208
|
A | C | 3 | a0001c0001t0003g0299a0001c0001t0003g0319a0001c0001t0009g0308 | 3 | HG00558.hp1 NA19000.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1177-182T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662208 | ||||||
chr2:55662226
|
T | C | 1 | a0006c0008t0001g0043 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1177-200A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662226 | ||||||
chr2:55662295
|
G | C | 4 | a0001c0001t0003g0353a0001c0001t0003g0354a0001c0001t0017g0325others(1): Show | 4 | HG02074.hp1 NA18975.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177-269C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662295 | ||||||
chr2:55662319
|
G | A | 12 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0116others(9): Show | 12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177-293C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662319 | ||||||
chr2:55662331
|
G | A | 128 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(125): Show | 128 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1177-305C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662331 | ||||||
chr2:55662533
|
G | A | 128 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(125): Show | 128 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1177-507C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662533 | ||||||
chr2:55662566
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1177-540A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662566 | ||||||
chr2:55662567
|
T | C | 1 | a0002c0002t0038g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1177-541A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662567 | ||||||
chr2:55662741
|
G | A | 94 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(91): Show | 94 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1177-715C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662741 | ||||||
chr2:55662880
|
A | AT | 8 | a0001c0004t0007g0064a0002c0002t0001g0369a0002c0002t0002g0240others(5): Show | 8 | HG00423.hp2 HG01168.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.1177-855dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662880 | ||||||
chr2:55662880
|
AT | A | 34 | a0001c0001t0001g0131a0001c0001t0001g0137a0001c0001t0001g0138others(31): Show | 34 | HG00438.hp1 HG01261.hp1 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.1177-855delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662880 | ||||||
chr2:55662880
|
ATT | A | 93 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(90): Show | 93 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1177-856_1177-855d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662880 | ||||||
chr2:55662897
|
TG | T | 77 | a0001c0001t0001g0122a0001c0001t0002g0346a0001c0001t0002g0356others(74): Show | 79 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1177-872delC | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662897 | ||||||
chr2:55662898
|
G | T | 6 | a0001c0001t0003g0291a0001c0001t0003g0354a0001c0001t0003g0366others(3): Show | 6 | HG02970.hp1 HG03017.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1177-872C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662898 | ||||||
chr2:55662946
|
T | C | 1 | a0007c0007t0003g0306 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1177-920A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662946 | ||||||
chr2:55663175
|
C | T | 1 | a0001c0001t0006g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1177-1149G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55663175 | ||||||
chr2:55663468
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0055 | 3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1177-1442C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55663468 | ||||||
chr2:55663468
|
G | T | 46 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(43): Show | 46 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.1177-1442C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55663468 | ||||||
chr2:55663552
|
C | A | 2 | a0003c0003t0004g0091a0003c0003t0004g0093 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1177-1526G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55663552 | ||||||
chr2:55663678
|
G | A | 3 | a0001c0001t0003g0335a0001c0001t0003g0361a0001c0001t0009g0336 | 3 | HG00621.hp2 HG02056.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1177-1652C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55663678 | ||||||
chr2:55663893
|
G | C | 1 | a0002c0002t0002g0376 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1177-1867C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55663893 | ||||||
chr2:55663970
|
CAGA | C | 3 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0055 | 3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1177-1947_1177-194 others(7): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55663970 | ||||||
chr2:55664005
|
T | C | 45 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(42): Show | 45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1177-1979A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55664005 | ||||||
chr2:55664029
|
G | A | 1 | a0002c0002t0038g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1177-2003C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55664029 | ||||||
chr2:55664185
|
T | C | 134 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1177-2159A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55664185 | ||||||
chr2:55664234
|
T | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0151 | 2 | HG02080.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1177-2208A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55664234 | ||||||
chr2:55664483
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1177-2457C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55664483 | ||||||
chr2:55664602
|
C | G | 1 | a0003c0003t0004g0096 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1176+2389G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55664602 | ||||||
chr2:55664851
|
G | A | 1 | a0001c0001t0008g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1176+2140C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55664851 | ||||||
chr2:55665117
|
G | A | 1 | a0001c0001t0003g0349 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1176+1874C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665117 | ||||||
chr2:55665126
|
A | C | 118 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(115): Show | 126 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.1176+1865T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665126 | ||||||
chr2:55665173
|
G | T | 2 | a0001c0004t0007g0005a0001c0004t0007g0060 | 3 | HG01081.hp1 HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1176+1818C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665173 | ||||||
chr2:55665221
|
A | G | 118 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(115): Show | 126 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.1176+1770T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665221 | ||||||
chr2:55665243
|
C | T | 297 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1176+1748G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665243 | ||||||
chr2:55665375
|
T | G | 1 | a0001c0001t0001g0152 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1176+1616A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665375 | ||||||
chr2:55665594
|
A | C | 1 | a0001c0001t0003g0361 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1176+1397T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665594 | ||||||
chr2:55665628
|
CACAACTC others(6): Show |
C | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(1): Show | 4 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1176+1350_1176+136 others(17): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665628 | ||||||
chr2:55665672
|
G | A | 1 | a0002c0002t0002g0244 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1176+1319C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665672 | ||||||
chr2:55665805
|
T | C | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1176+1186A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665805 | ||||||
chr2:55665882
|
G | A | 7 | a0001c0001t0008g0194a0001c0001t0008g0195a0001c0001t0008g0196others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176+1109C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665882 | ||||||
chr2:55666130
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1176+861T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55666130 | ||||||
chr2:55666201
|
C | A | 295 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(292): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1176+790G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55666201 | ||||||
chr2:55666206
|
C | T | 1 | a0001c0001t0009g0308 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1176+785G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55666206 | ||||||
chr2:55666587
|
C | A | 1 | a0001c0001t0001g0213 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1176+404G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55666587 | ||||||
chr2:55666742
|
C | T | 1 | a0001c0001t0003g0318 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1176+249G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55666742 | ||||||
chr2:55666955
|
A | G | 62 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0129others(59): Show | 62 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1176+36T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55666955 | ||||||
chr2:55667097
|
T | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0055 | 3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
splice_region_variant&intron_variant | LOW | c.1074-4A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667097 | ||||||
chr2:55667108
|
G | A | 2 | a0002c0002t0002g0223a0002c0002t0022g0239 | 2 | HG00642.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1074-15C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667108 | ||||||
chr2:55667112
|
T | C | 118 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(115): Show | 126 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.1074-19A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667112 | ||||||
chr2:55667284
|
T | G | 1 | a0002c0002t0001g0052 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1074-191A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667284 | ||||||
chr2:55667293
|
G | A | 167 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.1074-200C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667293 | ||||||
chr2:55667311
|
T | C | 1 | a0002c0002t0002g0248 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1074-218A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667311 | ||||||
chr2:55667321
|
G | A | 18 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(15): Show | 18 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.1074-228C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667321 | ||||||
chr2:55667349
|
C | G | 2 | a0001c0001t0003g0291a0001c0001t0003g0312 | 2 | NA18994.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1074-256G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667349 | ||||||
chr2:55667410
|
C | T | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1074-317G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667410 | ||||||
chr2:55667510
|
C | T | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1073+352G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667510 | ||||||
chr2:55667530
|
C | T | 4 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073+332G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667530 | ||||||
chr2:55667558
|
C | T | 1 | a0003c0003t0020g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1073+304G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667558 | ||||||
chr2:55667585
|
CA | C | 177 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(174): Show | 179 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.1073+276delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667585 | ||||||
chr2:55667688
|
A | G | 4 | a0001c0001t0001g0044a0001c0001t0015g0050a0001c0001t0015g0051others(1): Show | 4 | NA18942.hp1 NA18955.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073+174T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667688 | ||||||
chr2:55668017
|
T | C | 1 | a0001c0001t0008g0196 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.977-59A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668017 | ||||||
chr2:55668170
|
T | C | 62 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0129others(59): Show | 62 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.977-212A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668170 | ||||||
chr2:55668186
|
T | C | 297 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.977-228A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668186 | ||||||
chr2:55668275
|
T | A | 2 | a0003c0003t0004g0092a0003c0003t0035g0077 | 2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.977-317A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668275 | ||||||
chr2:55668362
|
G | C | 1 | a0001c0001t0003g0361 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.977-404C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668362 | ||||||
chr2:55668439
|
T | A | 1 | a0001c0001t0003g0307 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.977-481A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668439 | ||||||
chr2:55668496
|
G | A | 7 | a0002c0002t0002g0220a0002c0002t0002g0221a0002c0002t0002g0373others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.977-538C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668496 | ||||||
chr2:55668518
|
G | A | 1 | a0001c0001t0003g0304 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.977-560C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668518 | ||||||
chr2:55668590
|
G | A | 1 | a0001c0001t0003g0307 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.977-632C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668590 | ||||||
chr2:55668707
|
C | T | 1 | a0001c0001t0003g0307 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.977-749G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668707 | ||||||
chr2:55668708
|
T | C | 1 | a0001c0001t0003g0307 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.977-750A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668708 | ||||||
chr2:55668709
|
C | T | 1 | a0001c0001t0003g0307 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.977-751G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668709 | ||||||
chr2:55668719
|
C | CCTCCCTA others(5): Show |
1 | a0001c0001t0003g0307 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.977-762_977-761ins others(12): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668719 | ||||||
chr2:55668816
|
G | A | 1 | a0002c0002t0002g0243 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.977-858C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668816 | ||||||
chr2:55668857
|
C | G | 7 | a0001c0001t0008g0194a0001c0001t0008g0195a0001c0001t0008g0196others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.977-899G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668857 | ||||||
chr2:55669161
|
G | C | 17 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0074others(14): Show | 17 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.977-1203C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669161 | ||||||
chr2:55669163
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.977-1205A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669163 | ||||||
chr2:55669177
|
A | T | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.977-1219T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669177 | ||||||
chr2:55669185
|
AC | A | 44 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(41): Show | 44 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.977-1228delG | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669185 | ||||||
chr2:55669248
|
A | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0055 | 3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.977-1290T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669248 | ||||||
chr2:55669270
|
T | G | 1 | a0002c0002t0022g0238 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.977-1312A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669270 | ||||||
chr2:55669457
|
A | G | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.977-1499T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669457 | ||||||
chr2:55669463
|
T | A | 1 | a0002c0002t0002g0246 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.977-1505A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669463 | ||||||
chr2:55669463
|
T | C | 137 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(134): Show | 137 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.977-1505A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669463 | ||||||
chr2:55669614
|
A | G | 2 | a0003c0003t0004g0066a0003c0003t0004g0080 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.977-1656T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669614 | ||||||
chr2:55669761
|
A | T | 1 | a0001c0001t0003g0351 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.976+1558T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669761 | ||||||
chr2:55669761
|
AC | A | 104 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0007others(101): Show | 112 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.976+1557delG | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669761 | ||||||
chr2:55669761
|
ACT | A | 128 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(125): Show | 130 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.976+1556_976+1557d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669761 | ||||||
chr2:55669761
|
ACTT | A | 64 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0129others(61): Show | 64 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.976+1555_976+1557d others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669761 | ||||||
chr2:55669762
|
CT | C | 14 | a0001c0001t0003g0292a0001c0001t0003g0296a0001c0001t0003g0305others(11): Show | 14 | HG00544.hp1 HG00544.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.976+1556delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669762 | ||||||
chr2:55669871
|
G | A | 1 | a0001c0001t0008g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.976+1448C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669871 | ||||||
chr2:55669887
|
T | C | 1 | a0002c0002t0002g0244 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.976+1432A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669887 | ||||||
chr2:55669905
|
C | A | 1 | a0002c0002t0002g0246 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.976+1414G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669905 | ||||||
chr2:55670052
|
C | T | 2 | a0003c0003t0004g0107a0003c0003t0004g0108 | 2 | NA18979.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.976+1267G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670052 | ||||||
chr2:55670095
|
A | G | 6 | a0001c0001t0006g0115a0001c0001t0006g0116a0001c0001t0006g0120others(3): Show | 6 | HG01261.hp1 HG01496.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.976+1224T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670095 | ||||||
chr2:55670217
|
C | T | 1 | a0001c0001t0006g0162 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.976+1102G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670217 | ||||||
chr2:55670287
|
C | T | 1 | a0001c0001t0003g0288 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.976+1032G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670287 | ||||||
chr2:55670307
|
C | A | 2 | a0001c0001t0003g0324a0001c0001t0003g0364 | 2 | NA18942.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.976+1012G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670307 | ||||||
chr2:55670337
|
C | A | 1 | a0002c0002t0002g0373 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.976+982G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670337 | ||||||
chr2:55670421
|
C | T | 6 | a0002c0002t0005g0250a0002c0002t0005g0251a0002c0002t0005g0252others(3): Show | 6 | NA18947.hp1 NA18973.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.976+898G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670421 | ||||||
chr2:55670430
|
T | C | 296 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(293): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.976+889A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670430 | ||||||
chr2:55670465
|
C | T | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.976+854G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670465 | ||||||
chr2:55670485
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0055 | 3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.976+834G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670485 | ||||||
chr2:55670565
|
T | C | 125 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(122): Show | 135 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.976+754A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670565 | ||||||
chr2:55670772
|
G | A | 1 | a0001c0001t0008g0196 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.976+547C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670772 | ||||||
chr2:55670861
|
T | C | 137 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(134): Show | 137 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.976+458A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670861 | ||||||
chr2:55670970
|
TAA | T | 284 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(281): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.976+347_976+348del others(2): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670970 | ||||||
chr2:55670970
|
TAAA | T | 11 | a0001c0001t0001g0041a0001c0001t0001g0179a0001c0001t0028g0111others(8): Show | 13 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.976+346_976+348del others(3): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670970 | ||||||
chr2:55670995
|
C | CT | 12 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0116others(9): Show | 12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.976+323dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670995 | ||||||
chr2:55671066
|
C | T | 1 | a0001c0001t0003g0291 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.976+253G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55671066 | ||||||
chr2:55671068
|
A | G | 117 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(114): Show | 125 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.976+251T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55671068 | ||||||
chr2:55671155
|
C | G | 113 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(110): Show | 121 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.976+164G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55671155 | ||||||
chr2:55671553
|
C | G | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0187others(11): Show | 14 | HG00438.hp1 HG03710.hp2 HG03942.hp1 others(11): Show |
intron_variant | MODIFIER | c.919-177G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/27 | chr2 | 55671553 | ||||||
chr2:55671598
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.919-222A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/27 | chr2 | 55671598 | ||||||
chr2:55671638
|
T | A | 1 | a0002c0002t0038g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.919-262A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/27 | chr2 | 55671638 | ||||||
chr2:55671748
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.918+247G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/27 | chr2 | 55671748 | ||||||
chr2:55671794
|
A | G | 296 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(293): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.918+201T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/27 | chr2 | 55671794 | ||||||
chr2:55671795
|
C | T | 101 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0007others(98): Show | 109 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.918+200G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/27 | chr2 | 55671795 | ||||||
chr2:55671827
|
AAAAAC | A | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.918+163_918+167del others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/27 | chr2 | 55671827 | ||||||
chr2:55671961
|
G | A | 1 | a0003c0003t0020g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.918+34C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/27 | chr2 | 55671961 | ||||||
chr2:55672093
|
A | T | 297 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.867-47T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 9/27 | chr2 | 55672093 | ||||||
chr2:55672110
|
T | C | 1 | a0002c0002t0002g0244 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.867-64A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 9/27 | chr2 | 55672110 | ||||||
chr2:55672290
|
T | C | 117 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(114): Show | 125 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.867-244A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 9/27 | chr2 | 55672290 | ||||||
chr2:55672638
|
G | C | 1 | a0001c0001t0033g0345 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.866+255C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 9/27 | chr2 | 55672638 | ||||||
chr2:55672661
|
T | C | 1 | a0003c0003t0004g0097 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.866+232A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 9/27 | chr2 | 55672661 | ||||||
chr2:55673096
|
G | GA | 13 | a0001c0001t0003g0292a0001c0001t0006g0114a0001c0001t0006g0115others(10): Show | 13 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.680-18dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673096 | ||||||
chr2:55673148
|
A | G | 117 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(114): Show | 125 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.680-69T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673148 | ||||||
chr2:55673274
|
A | G | 1 | a0001c0001t0033g0345 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.680-195T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673274 | ||||||
chr2:55673277
|
T | C | 1 | a0002c0002t0002g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.680-198A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673277 | ||||||
chr2:55673324
|
A | G | 117 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(114): Show | 125 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.680-245T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673324 | ||||||
chr2:55673355
|
C | G | 1 | a0002c0002t0002g0375 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.680-276G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673355 | ||||||
chr2:55673425
|
G | A | 12 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0116others(9): Show | 12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.680-346C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673425 | ||||||
chr2:55673493
|
C | T | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.680-414G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673493 | ||||||
chr2:55673664
|
G | A | 1 | a0002c0002t0002g0246 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.680-585C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673664 | ||||||
chr2:55673772
|
T | C | 1 | a0001c0001t0025g0208 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.680-693A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673772 | ||||||
chr2:55673803
|
A | C | 288 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(285): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.680-724T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673803 | ||||||
chr2:55673876
|
C | T | 2 | a0001c0001t0003g0316a0001c0001t0003g0327 | 2 | NA18981.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.680-797G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673876 | ||||||
chr2:55673879
|
C | T | 1 | a0002c0002t0002g0019 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.680-800G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673879 | ||||||
chr2:55674182
|
T | C | 288 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(285): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.680-1103A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674182 | ||||||
chr2:55674258
|
G | A | 1 | a0003c0003t0004g0099 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.680-1179C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674258 | ||||||
chr2:55674317
|
A | G | 296 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(293): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.680-1238T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674317 | ||||||
chr2:55674355
|
A | C | 1 | a0002c0002t0002g0226 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.680-1276T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674355 | ||||||
chr2:55674441
|
G | T | 1 | a0002c0002t0002g0259 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.680-1362C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674441 | ||||||
chr2:55674600
|
T | A | 1 | a0003c0003t0004g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.680-1521A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674600 | ||||||
chr2:55674906
|
C | T | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.680-1827G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674906 | ||||||
chr2:55674908
|
G | A | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.680-1829C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674908 | ||||||
chr2:55674913
|
T | A | 1 | a0002c0002t0002g0269 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.680-1834A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674913 | ||||||
chr2:55674929
|
A | C | 12 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0116others(9): Show | 12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.680-1850T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674929 | ||||||
chr2:55675094
|
C | G | 1 | a0002c0002t0023g0257 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.680-2015G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675094 | ||||||
chr2:55675223
|
T | C | 62 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0129others(59): Show | 62 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.680-2144A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675223 | ||||||
chr2:55675234
|
C | A | 1 | a0003c0003t0004g0092 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.680-2155G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675234 | ||||||
chr2:55675260
|
T | C | 296 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(293): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.680-2181A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675260 | ||||||
chr2:55675281
|
A | G | 288 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(285): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.680-2202T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675281 | ||||||
chr2:55675360
|
G | C | 4 | a0002c0002t0002g0017a0002c0002t0002g0021a0002c0002t0002g0022others(1): Show | 4 | HG02559.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.680-2281C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675360 | ||||||
chr2:55675379
|
G | A | 4 | a0001c0001t0003g0353a0001c0001t0003g0354a0001c0001t0017g0325others(1): Show | 4 | HG02074.hp1 NA18975.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.680-2300C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675379 | ||||||
chr2:55675453
|
G | T | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.680-2374C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675453 | ||||||
chr2:55675611
|
T | C | 1 | a0002c0002t0023g0257 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.680-2532A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675611 | ||||||
chr2:55675661
|
G | A | 296 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(293): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.680-2582C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675661 | ||||||
chr2:55675733
|
T | C | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-2654A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675733 | ||||||
chr2:55675881
|
A | C | 137 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(134): Show | 137 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.680-2802T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675881 | ||||||
chr2:55675921
|
A | G | 9 | a0001c0001t0003g0307a0001c0001t0003g0313a0001c0001t0003g0314others(6): Show | 9 | HG00544.hp1 HG02080.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.680-2842T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675921 | ||||||
chr2:55675932
|
C | T | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.680-2853G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675932 | ||||||
chr2:55676113
|
A | G | 8 | a0002c0002t0002g0217a0002c0002t0002g0226a0002c0002t0002g0227others(5): Show | 8 | HG00738.hp1 HG02630.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.680-3034T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676113 | ||||||
chr2:55676128
|
T | G | 45 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(42): Show | 45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.680-3049A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676128 | ||||||
chr2:55676132
|
C | T | 45 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(42): Show | 45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.680-3053G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676132 | ||||||
chr2:55676164
|
T | G | 295 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(292): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.680-3085A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676164 | ||||||
chr2:55676174
|
C | T | 1 | a0002c0002t0002g0244 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.680-3095G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676174 | ||||||
chr2:55676262
|
C | CA | 136 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0034others(133): Show | 144 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.680-3184dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676262 | ||||||
chr2:55676262
|
C | CAA | 66 | a0001c0001t0001g0059a0001c0001t0006g0114a0001c0001t0006g0115others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG01168.hp2 others(63): Show |
intron_variant | MODIFIER | c.680-3185_680-3184d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676262 | ||||||
chr2:55676262
|
C | CAAA | 9 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0170others(6): Show | 9 | HG01175.hp2 HG01346.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.680-3186_680-3184d others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676262 | ||||||
chr2:55676262
|
CA | C | 8 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0055others(5): Show | 8 | HG02080.hp1 HG02273.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.680-3184delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676262 | ||||||
chr2:55676262
|
CAAAAAAA others(4): Show |
C | 6 | a0001c0001t0003g0307a0001c0001t0003g0313a0001c0001t0003g0314others(3): Show | 6 | HG02080.hp2 NA18947.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.680-3194_680-3184d others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676262 | ||||||
chr2:55676381
|
A | G | 1 | a0001c0001t0011g0158 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.679+3301T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676381 | ||||||
chr2:55676451
|
A | G | 2 | a0003c0003t0004g0066a0003c0003t0004g0080 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.679+3231T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676451 | ||||||
chr2:55676485
|
G | T | 297 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.679+3197C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676485 | ||||||
chr2:55676526
|
C | T | 5 | a0002c0002t0002g0373a0002c0002t0002g0374a0002c0002t0002g0375others(2): Show | 5 | HG01074.hp1 HG01168.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.679+3156G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676526 | ||||||
chr2:55676563
|
T | TA | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.679+3118dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676563 | ||||||
chr2:55676576
|
G | A | 12 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0116others(9): Show | 12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.679+3106C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676576 | ||||||
chr2:55676612
|
G | A | 295 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(292): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.679+3070C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676612 | ||||||
chr2:55676642
|
A | G | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.679+3040T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676642 | ||||||
chr2:55676643
|
C | T | 1 | a0002c0002t0002g0225 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.679+3039G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676643 | ||||||
chr2:55676652
|
A | G | 2 | a0003c0003t0016g0070a0003c0003t0016g0071 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.679+3030T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676652 | ||||||
chr2:55676710
|
A | C | 1 | a0002c0002t0005g0251 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.679+2972T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676710 | ||||||
chr2:55676837
|
C | G | 296 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(293): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.679+2845G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676837 | ||||||
chr2:55676910
|
T | C | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.679+2772A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676910 | ||||||
chr2:55676926
|
A | G | 31 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(28): Show | 31 | HG00423.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.679+2756T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676926 | ||||||
chr2:55677035
|
C | A | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.679+2647G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677035 | ||||||
chr2:55677217
|
T | G | 1 | a0001c0001t0006g0118 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.679+2465A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677217 | ||||||
chr2:55677268
|
G | T | 1 | a0002c0002t0002g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.679+2414C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677268 | ||||||
chr2:55677310
|
T | C | 1 | a0001c0001t0003g0361 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.679+2372A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677310 | ||||||
chr2:55677336
|
A | G | 2 | a0003c0003t0004g0083a0003c0003t0018g0082 | 2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.679+2346T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677336 | ||||||
chr2:55677365
|
G | A | 1 | a0001c0001t0003g0339 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.679+2317C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677365 | ||||||
chr2:55677391
|
A | C | 295 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(292): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.679+2291T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677391 | ||||||
chr2:55677391
|
A | T | 1 | a0003c0003t0004g0110 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.679+2291T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677391 | ||||||
chr2:55677596
|
C | CA | 27 | a0001c0004t0004g0008a0001c0004t0004g0025a0002c0002t0002g0009others(24): Show | 27 | HG01106.hp1 HG01433.hp1 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.679+2085dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677596 | ||||||
chr2:55677596
|
C | CAA | 7 | a0001c0001t0001g0058a0001c0001t0013g0141a0001c0001t0014g0171others(4): Show | 7 | HG01109.hp2 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.679+2084_679+2085d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677596 | ||||||
chr2:55677596
|
C | CAAA | 96 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(93): Show | 96 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.679+2083_679+2085d others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677596 | ||||||
chr2:55677596
|
C | CAAAA | 39 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0122others(36): Show | 39 | HG00140.hp1 HG00621.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.679+2082_679+2085d others(6): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677596 | ||||||
chr2:55677596
|
CA | C | 74 | a0001c0001t0002g0346a0001c0001t0002g0356a0001c0001t0003g0004others(71): Show | 76 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.679+2085delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677596 | ||||||
chr2:55677596
|
CAAA | C | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.679+2083_679+2085d others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677596 | ||||||
chr2:55677627
|
A | G | 12 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0116others(9): Show | 12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.679+2055T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677627 | ||||||
chr2:55677679
|
A | AGG | 18 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(15): Show | 18 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.679+2001_679+2002d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677679 | ||||||
chr2:55677808
|
C | T | 1 | a0002c0002t0001g0052 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.679+1874G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677808 | ||||||
chr2:55677827
|
C | A | 4 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.679+1855G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677827 | ||||||
chr2:55677835
|
G | A | 1 | a0001c0001t0001g0365 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.679+1847C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677835 | ||||||
chr2:55677896
|
G | A | 1 | a0003c0003t0004g0080 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.679+1786C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677896 | ||||||
chr2:55677987
|
T | G | 117 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(114): Show | 125 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.679+1695A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677987 | ||||||
chr2:55678021
|
G | A | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.679+1661C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55678021 | ||||||
chr2:55678051
|
C | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(3): Show | 6 | HG01192.hp2 HG03490.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.679+1631G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55678051 | ||||||
chr2:55678094
|
C | A | 1 | a0003c0003t0016g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.679+1588G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55678094 | ||||||
chr2:55678174
|
A | G | 1 | a0001c0001t0013g0169 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.679+1508T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55678174 | ||||||
chr2:55678214
|
G | C | 1 | a0001c0001t0001g0190 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.679+1468C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55678214 | ||||||
chr2:55678240
|
C | G | 1 | a0002c0002t0002g0218 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.679+1442G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55678240 | ||||||
chr2:55678488
|
G | A | 4 | a0002c0002t0002g0258a0002c0002t0002g0266a0002c0002t0002g0267others(1): Show | 4 | HG01099.hp2 HG01106.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.679+1194C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55678488 | ||||||
chr2:55678610
|
G | T | 2 | a0002c0002t0002g0220a0002c0002t0002g0221 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.679+1072C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55678610 | ||||||
chr2:55679185
|
A | G | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.679+497T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55679185 | ||||||
chr2:55679321
|
A | G | 2 | a0002c0002t0002g0245a0002c0002t0002g0276 | 2 | HG01109.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.679+361T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55679321 | ||||||
chr2:55679405
|
A | T | 1 | a0002c0002t0002g0219 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.679+277T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55679405 | ||||||
chr2:55679417
|
T | C | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.679+265A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55679417 | ||||||
chr2:55679551
|
G | C | 3 | a0001c0001t0003g0335a0001c0001t0003g0361a0001c0001t0009g0336 | 3 | HG00621.hp2 HG02056.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.679+131C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55679551 | ||||||
chr2:55679633
|
G | C | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.679+49C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55679633 | ||||||
chr2:55680169
|
T | C | 8 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0170others(5): Show | 8 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-374A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680169 | ||||||
chr2:55680196
|
G | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0055 | 3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.566-401C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680196 | ||||||
chr2:55680217
|
C | T | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0187others(11): Show | 14 | HG00438.hp1 HG03710.hp2 HG03942.hp1 others(11): Show |
intron_variant | MODIFIER | c.566-422G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680217 | ||||||
chr2:55680222
|
C | T | 297 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.566-427G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680222 | ||||||
chr2:55680227
|
G | A | 1 | a0001c0001t0003g0330 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.566-432C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680227 | ||||||
chr2:55680292
|
C | G | 1 | a0002c0002t0023g0257 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.565+420G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680292 | ||||||
chr2:55680328
|
C | G | 297 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.565+384G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680328 | ||||||
chr2:55680347
|
C | T | 45 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(42): Show | 45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.565+365G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680347 | ||||||
chr2:55680425
|
TA | T | 290 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0033others(287): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.565+286delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680425 | ||||||
chr2:55680425
|
TAA | T | 10 | a0001c0001t0001g0198a0001c0001t0001g0207a0001c0001t0014g0176others(7): Show | 10 | HG00639.hp2 HG01069.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+285_565+286del others(2): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680425 | ||||||
chr2:55680427
|
A | T | 1 | a0001c0001t0014g0171 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.565+285T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680427 | ||||||
chr2:55680622
|
G | A | 17 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(14): Show | 17 | HG01192.hp2 HG01243.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.565+90C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680622 | ||||||
chr2:55681013
|
G | A | 1 | a0002c0002t0005g0255 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.454-95C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681013 | ||||||
chr2:55681152
|
A | G | 15 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(12): Show | 15 | HG00423.hp2 HG02027.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.454-234T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681152 | ||||||
chr2:55681182
|
G | C | 118 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(115): Show | 126 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.454-264C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681182 | ||||||
chr2:55681239
|
G | A | 1 | a0002c0002t0002g0247 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.454-321C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681239 | ||||||
chr2:55681293
|
A | G | 296 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(293): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.454-375T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681293 | ||||||
chr2:55681482
|
G | A | 1 | a0001c0001t0001g0309 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.454-564C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681482 | ||||||
chr2:55681494
|
T | G | 296 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(293): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.454-576A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681494 | ||||||
chr2:55681501
|
C | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0055 | 3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.454-583G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681501 | ||||||
chr2:55681543
|
T | C | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.454-625A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681543 | ||||||
chr2:55681718
|
G | A | 45 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(42): Show | 45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.454-800C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681718 | ||||||
chr2:55681798
|
C | T | 2 | a0003c0003t0004g0076a0003c0003t0004g0081 | 2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.454-880G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681798 | ||||||
chr2:55681828
|
G | A | 1 | a0001c0001t0003g0339 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.454-910C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681828 | ||||||
chr2:55681844
|
C | CA | 288 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(285): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.454-927dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681844 | ||||||
chr2:55681844
|
C | CAAA | 8 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0170others(5): Show | 8 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.454-929_454-927dup others(3): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681844 | ||||||
chr2:55681869
|
C | T | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.454-951G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681869 | ||||||
chr2:55681892
|
A | G | 2 | a0002c0002t0002g0275a0002c0002t0002g0282 | 2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.454-974T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681892 | ||||||
chr2:55681955
|
C | T | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.454-1037G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681955 | ||||||
chr2:55682016
|
G | A | 1 | a0002c0002t0002g0245 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.454-1098C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682016 | ||||||
chr2:55682053
|
T | G | 377 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(374): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.454-1135A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682053 | ||||||
chr2:55682122
|
G | A | 1 | a0002c0002t0002g0269 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.454-1204C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682122 | ||||||
chr2:55682186
|
G | A | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.454-1268C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682186 | ||||||
chr2:55682190
|
A | G | 298 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(295): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.454-1272T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682190 | ||||||
chr2:55682414
|
T | C | 76 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0129others(73): Show | 76 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.453+1371A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682414 | ||||||
chr2:55682418
|
G | A | 1 | a0010c0014t0010g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.453+1367C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682418 | ||||||
chr2:55682473
|
T | A | 1 | a0001c0001t0001g0157 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.453+1312A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682473 | ||||||
chr2:55682595
|
T | C | 6 | a0001c0001t0006g0115a0001c0001t0006g0116a0001c0001t0006g0120others(3): Show | 6 | HG01261.hp1 HG01496.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.453+1190A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682595 | ||||||
chr2:55682687
|
C | G | 2 | a0003c0003t0004g0066a0003c0003t0004g0080 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.453+1098G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682687 | ||||||
chr2:55682856
|
G | C | 297 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.453+929C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682856 | ||||||
chr2:55683094
|
T | C | 1 | a0001c0001t0006g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.453+691A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683094 | ||||||
chr2:55683179
|
G | A | 1 | a0002c0002t0002g0246 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.453+606C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683179 | ||||||
chr2:55683217
|
C | G | 1 | a0002c0002t0023g0257 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.453+568G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683217 | ||||||
chr2:55683231
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.453+554A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683231 | ||||||
chr2:55683352
|
C | T | 1 | a0001c0001t0006g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.453+433G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683352 | ||||||
chr2:55683383
|
G | A | 1 | a0001c0004t0007g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.453+402C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683383 | ||||||
chr2:55683389
|
C | T | 1 | a0001c0001t0003g0311 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.453+396G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683389 | ||||||
chr2:55683410
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.453+375G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683410 | ||||||
chr2:55683539
|
G | A | 8 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0170others(5): Show | 8 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.453+246C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683539 | ||||||
chr2:55683575
|
T | C | 45 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(42): Show | 45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.453+210A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683575 | ||||||
chr2:55683612
|
C | CA | 62 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(59): Show | 62 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.453+172dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683612 | ||||||
chr2:55683612
|
C | CAA | 6 | a0001c0001t0001g0056a0001c0001t0006g0117a0001c0001t0006g0121others(3): Show | 6 | HG01168.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.453+171_453+172dup others(2): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683612 | ||||||
chr2:55684216
|
A | G | 296 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(293): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.404-382T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684216 | ||||||
chr2:55684231
|
G | A | 14 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0187others(11): Show | 14 | HG00438.hp1 HG03710.hp2 HG03942.hp1 others(11): Show |
intron_variant | MODIFIER | c.404-397C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684231 | ||||||
chr2:55684305
|
A | C | 298 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(295): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.404-471T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684305 | ||||||
chr2:55684319
|
A | T | 18 | a0002c0002t0002g0258a0002c0002t0002g0259a0002c0002t0002g0261others(15): Show | 18 | HG00099.hp1 HG00735.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.404-485T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684319 | ||||||
chr2:55684324
|
G | A | 45 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(42): Show | 45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.404-490C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684324 | ||||||
chr2:55684388
|
C | T | 6 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(3): Show | 6 | HG01192.hp2 HG03490.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.404-554G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684388 | ||||||
chr2:55684519
|
T | C | 1 | a0001c0001t0006g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.403+424A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684519 | ||||||
chr2:55684554
|
T | G | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.403+389A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684554 | ||||||
chr2:55684559
|
C | T | 1 | a0001c0001t0003g0342 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.403+384G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684559 | ||||||
chr2:55684736
|
G | A | 1 | a0001c0001t0003g0298 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.403+207C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684736 | ||||||
chr2:55685056
|
A | C | 1 | a0002c0002t0002g0019 | 1 | HG02717.hp1 | splice_region_variant&intron_variant | LOW | c.298-8T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55685056 | ||||||
chr2:55685229
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298-181C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55685229 | ||||||
chr2:55685527
|
TC | T | 12 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0116others(9): Show | 12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-480delG | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55685527 | ||||||
chr2:55685619
|
T | C | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.298-571A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55685619 | ||||||
chr2:55685826
|
T | C | 118 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(115): Show | 126 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.297+544A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55685826 | ||||||
chr2:55685996
|
G | A | 99 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(96): Show | 99 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.297+374C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55685996 | ||||||
chr2:55686062
|
A | G | 1 | a0001c0001t0031g0372 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.297+308T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55686062 | ||||||
chr2:55686071
|
G | A | 1 | a0002c0002t0002g0270 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.297+299C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55686071 | ||||||
chr2:55686128
|
C | G | 1 | a0002c0002t0002g0222 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.297+242G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55686128 | ||||||
chr2:55686136
|
AT | A | 12 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0116others(9): Show | 12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.297+233delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55686136 | ||||||
chr2:55686333
|
A | T | 1 | a0003c0003t0004g0090 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.297+37T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55686333 | ||||||
chr2:55686509
|
C | A | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-65G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55686509 | ||||||
chr2:55686520
|
C | T | 4 | a0003c0003t0004g0102a0003c0003t0004g0103a0003c0003t0004g0104others(1): Show | 4 | NA18612.hp2 NA18984.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-76G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55686520 | ||||||
chr2:55686762
|
A | G | 297 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.223-318T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55686762 | ||||||
chr2:55686835
|
C | G | 299 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(296): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.223-391G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55686835 | ||||||
chr2:55686872
|
G | A | 1 | a0002c0002t0041g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.223-428C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55686872 | ||||||
chr2:55686874
|
A | C | 53 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0170others(50): Show | 53 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(50): Show |
intron_variant | MODIFIER | c.223-430T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55686874 | ||||||
chr2:55686890
|
G | A | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-446C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55686890 | ||||||
chr2:55686990
|
G | A | 1 | a0001c0004t0007g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.223-546C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55686990 | ||||||
chr2:55687030
|
C | T | 5 | a0001c0001t0001g0168a0001c0001t0001g0211a0001c0001t0001g0212others(2): Show | 5 | NA18963.hp1 NA18983.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-586G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687030 | ||||||
chr2:55687048
|
A | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0053 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.222+597T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687048 | ||||||
chr2:55687075
|
G | A | 1 | a0001c0004t0004g0008 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.222+570C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687075 | ||||||
chr2:55687110
|
A | C | 2 | a0001c0001t0001g0188a0001c0001t0026g0130 | 2 | HG03710.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.222+535T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687110 | ||||||
chr2:55687147
|
G | A | 1 | a0001c0001t0003g0291 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.222+498C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687147 | ||||||
chr2:55687168
|
C | T | 2 | a0002c0002t0002g0220a0002c0002t0002g0221 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.222+477G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687168 | ||||||
chr2:55687169
|
G | A | 45 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(42): Show | 45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.222+476C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687169 | ||||||
chr2:55687173
|
C | T | 1 | a0003c0003t0004g0089 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.222+472G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687173 | ||||||
chr2:55687213
|
C | CA | 142 | a0001c0001t0001g0028a0001c0001t0001g0056a0001c0001t0001g0057others(139): Show | 142 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.222+431dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687213 | ||||||
chr2:55687213
|
C | CAA | 142 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(139): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.222+430_222+431dup others(2): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687213 | ||||||
chr2:55687213
|
C | CAAA | 7 | a0001c0001t0001g0034a0001c0001t0028g0111a0002c0002t0001g0045others(4): Show | 7 | HG01192.hp2 HG01261.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+429_222+431dup others(3): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687213 | ||||||
chr2:55687221
|
A | AC | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+423_222+424ins others(1): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687221 | ||||||
chr2:55687438
|
C | CA | 120 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(117): Show | 128 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.222+206dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687438 | ||||||
chr2:55687486
|
T | C | 118 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(115): Show | 126 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.222+159A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687486 | ||||||
chr2:55687745
|
C | A | 1 | a0002c0002t0002g0283 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.162-40G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55687745 | ||||||
chr2:55687814
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.162-109G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55687814 | ||||||
chr2:55687827
|
C | T | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.162-122G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55687827 | ||||||
chr2:55687927
|
C | T | 1 | a0001c0001t0001g0370 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.162-222G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55687927 | ||||||
chr2:55687993
|
A | AT | 15 | a0001c0001t0001g0131a0001c0001t0001g0139a0001c0001t0001g0142others(12): Show | 15 | HG02155.hp1 HG02273.hp1 NA18940.hp2 others(12): Show |
intron_variant | MODIFIER | c.162-289dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55687993 | ||||||
chr2:55688020
|
T | A | 299 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(296): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.162-315A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688020 | ||||||
chr2:55688232
|
T | A | 296 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(293): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.162-527A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688232 | ||||||
chr2:55688304
|
T | C | 1 | a0006c0008t0001g0043 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.162-599A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688304 | ||||||
chr2:55688309
|
G | C | 1 | a0001c0001t0011g0158 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.162-604C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688309 | ||||||
chr2:55688337
|
G | C | 2 | a0003c0003t0004g0074a0003c0003t0004g0075 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.162-632C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688337 | ||||||
chr2:55688383
|
T | C | 1 | a0002c0002t0002g0248 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.162-678A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688383 | ||||||
chr2:55688446
|
A | T | 3 | a0001c0001t0006g0114a0001c0001t0006g0117a0001c0001t0028g0111 | 3 | HG04204.hp1 HG04228.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.162-741T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688446 | ||||||
chr2:55688508
|
C | T | 1 | a0001c0001t0003g0310 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.162-803G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688508 | ||||||
chr2:55688625
|
C | T | 1 | a0003c0003t0004g0096 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.162-920G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688625 | ||||||
chr2:55688691
|
G | C | 191 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(188): Show | 193 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.162-986C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688691 | ||||||
chr2:55688760
|
C | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | NA18969.hp1 NA18985.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.162-1055G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688760 | ||||||
chr2:55688760
|
C | CA | 6 | a0001c0001t0001g0122a0001c0001t0001g0170a0001c0001t0001g0173others(3): Show | 6 | HG01346.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.162-1056dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688760 | ||||||
chr2:55688763
|
C | A | 90 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0131others(87): Show | 90 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.162-1058G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688763 | ||||||
chr2:55688766
|
C | A | 189 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(186): Show | 191 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.162-1061G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688766 | ||||||
chr2:55688769
|
A | C | 104 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0007others(101): Show | 112 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.162-1064T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688769 | ||||||
chr2:55688873
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.162-1168T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688873 | ||||||
chr2:55688967
|
G | C | 1 | a0002c0002t0002g0249 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.162-1262C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688967 | ||||||
chr2:55688975
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0055 | 3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.162-1270G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688975 | ||||||
chr2:55689019
|
G | A | 12 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0116others(9): Show | 12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.162-1314C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55689019 | ||||||
chr2:55689168
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.162-1463A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55689168 | ||||||
chr2:55689212
|
A | G | 1 | a0001c0001t0037g0178 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.162-1507T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55689212 | ||||||
chr2:55689268
|
T | C | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.162-1563A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55689268 | ||||||
chr2:55689284
|
T | A | 2 | a0003c0003t0016g0070a0003c0003t0016g0071 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.162-1579A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55689284 | ||||||
chr2:55689371
|
C | T | 1 | a0002c0002t0038g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.162-1666G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55689371 | ||||||
chr2:55689524
|
C | T | 1 | a0003c0003t0020g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-1819G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55689524 | ||||||
chr2:55689723
|
AT | A | 7 | a0001c0001t0008g0194a0001c0001t0008g0195a0001c0001t0008g0196others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.162-2019delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55689723 | ||||||
chr2:55690034
|
C | G | 2 | a0001c0001t0019g0215a0001c0001t0019g0216 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.162-2329G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690034 | ||||||
chr2:55690121
|
C | T | 7 | a0001c0001t0008g0194a0001c0001t0008g0195a0001c0001t0008g0196others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.162-2416G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690121 | ||||||
chr2:55690348
|
CAGAGAA | C | 295 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(292): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.162-2649_162-2644d others(8): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690348 | ||||||
chr2:55690408
|
C | G | 8 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0170others(5): Show | 8 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.162-2703G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690408 | ||||||
chr2:55690469
|
A | G | 143 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(140): Show | 153 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.162-2764T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690469 | ||||||
chr2:55690479
|
T | C | 1 | a0002c0002t0041g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.162-2774A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690479 | ||||||
chr2:55690607
|
T | C | 1 | a0001c0001t0006g0114 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.162-2902A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690607 | ||||||
chr2:55690670
|
A | G | 296 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(293): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.162-2965T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690670 | ||||||
chr2:55690843
|
G | A | 377 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(374): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.161+2820C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690843 | ||||||
chr2:55690961
|
G | C | 6 | a0002c0002t0005g0250a0002c0002t0005g0251a0002c0002t0005g0252others(3): Show | 6 | NA18947.hp1 NA18973.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+2702C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690961 | ||||||
chr2:55690967
|
C | T | 295 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(292): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.161+2696G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690967 | ||||||
chr2:55691054
|
T | G | 107 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0125others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.161+2609A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691054 | ||||||
chr2:55691222
|
T | C | 42 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(39): Show | 44 | HG00423.hp2 HG01070.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.161+2441A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691222 | ||||||
chr2:55691247
|
A | G | 1 | a0002c0005t0001g0175 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.161+2416T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691247 | ||||||
chr2:55691264
|
T | C | 1 | a0002c0002t0002g0019 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.161+2399A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691264 | ||||||
chr2:55691445
|
G | T | 2 | a0003c0003t0004g0107a0003c0003t0004g0108 | 2 | NA18979.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.161+2218C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691445 | ||||||
chr2:55691549
|
G | A | 1 | a0002c0002t0002g0256 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.161+2114C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691549 | ||||||
chr2:55691718
|
T | C | 1 | a0001c0001t0031g0372 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.161+1945A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691718 | ||||||
chr2:55691722
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.161+1941G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691722 | ||||||
chr2:55691791
|
G | A | 1 | a0003c0003t0004g0098 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.161+1872C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691791 | ||||||
chr2:55691848
|
T | TATATATA others(4): Show |
1 | a0001c0001t0001g0056 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.161+1814_161+1815i others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691848 | ||||||
chr2:55691848
|
T | TTATATAT others(3): Show |
4 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | HG02055.hp1 HG02451.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+1805_161+1814d others(12): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691848 | ||||||
chr2:55691848
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.161+1803_161+1814d others(14): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691848 | ||||||
chr2:55691848
|
TTA | T | 10 | a0001c0001t0001g0126a0001c0001t0001g0340a0001c0001t0003g0337others(7): Show | 11 | HG01081.hp1 HG01099.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.161+1813_161+1814d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691848 | ||||||
chr2:55691848
|
TTATA | T | 10 | a0001c0001t0001g0125a0001c0001t0001g0131a0001c0001t0001g0132others(7): Show | 10 | HG00558.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.161+1811_161+1814d others(6): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691848 | ||||||
chr2:55691848
|
TTATATA | T | 5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG02698.hp2 HG03688.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+1809_161+1814d others(8): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691848 | ||||||
chr2:55691848
|
TTATATAT others(7): Show |
T | 16 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(13): Show | 16 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.161+1801_161+1814d others(16): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691848 | ||||||
chr2:55691848
|
TTATATAT others(9): Show |
T | 6 | a0001c0001t0003g0334a0001c0001t0003g0335a0001c0001t0003g0366others(3): Show | 6 | HG00423.hp1 HG00621.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.161+1799_161+1814d others(18): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691848 | ||||||
chr2:55691863
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0013g0169 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.161+1787_161+1799d others(15): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691863 | ||||||
chr2:55691864
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0003g0361 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.161+1782_161+1798d others(19): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691864 | ||||||
chr2:55691864
|
ATATATAT others(13): Show |
A | 1 | a0002c0002t0002g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.161+1779_161+1798d others(22): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691864 | ||||||
chr2:55691865
|
TATATATA others(4): Show |
T | 6 | a0001c0001t0001g0028a0001c0001t0001g0170a0001c0001t0001g0173others(3): Show | 6 | HG01346.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+1787_161+1797d others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691865 | ||||||
chr2:55691865
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0192 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.161+1785_161+1797d others(15): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691865 | ||||||
chr2:55691866
|
ATATATAT others(12): Show |
A | 1 | a0002c0002t0002g0218 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.161+1778_161+1796d others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691866 | ||||||
chr2:55691866
|
ATATATAT others(13): Show |
A | 46 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0007others(43): Show | 51 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.161+1777_161+1796d others(22): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691866 | ||||||
chr2:55691866
|
ATATATAT others(14): Show |
A | 14 | a0002c0002t0002g0258a0002c0002t0002g0259a0002c0002t0002g0261others(11): Show | 14 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.161+1776_161+1796d others(23): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691866 | ||||||
chr2:55691866
|
ATATATAT others(15): Show |
A | 1 | a0002c0002t0002g0273 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.161+1775_161+1796d others(24): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691866 | ||||||
chr2:55691867
|
TATATA | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0211a0002c0005t0002g0128 | 3 | HG02071.hp2 NA18963.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.161+1791_161+1795d others(7): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691867 | ||||||
chr2:55691867
|
TATATATA others(4): Show |
T | 1 | a0001c0001t0024g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.161+1785_161+1795d others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691867 | ||||||
chr2:55691868
|
A | G | 1 | a0002c0002t0002g0021 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161+1795T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691868 | ||||||
chr2:55691868
|
ATATATAT others(12): Show |
A | 2 | a0002c0002t0002g0271a0002c0002t0041g0272 | 2 | HG03453.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.161+1776_161+1794d others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691868 | ||||||
chr2:55691868
|
ATATATAT others(13): Show |
A | 25 | a0002c0002t0002g0014a0002c0002t0002g0015a0002c0002t0002g0016others(22): Show | 28 | HG00099.hp1 HG01074.hp1 HG01258.hp1 others(25): Show |
intron_variant | MODIFIER | c.161+1775_161+1794d others(22): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691868 | ||||||
chr2:55691868
|
ATATATAT others(14): Show |
A | 3 | a0002c0002t0002g0284a0002c0002t0002g0285a0002c0002t0002g0363 | 3 | HG01106.hp1 HG02735.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.161+1774_161+1794d others(23): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691868 | ||||||
chr2:55691869
|
TATATA | T | 26 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0142others(23): Show | 26 | HG00438.hp2 HG00621.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.161+1789_161+1793d others(7): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691869 | ||||||
chr2:55691870
|
ATATATAT others(11): Show |
A | 1 | a0002c0002t0002g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.161+1775_161+1792d others(20): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691870 | ||||||
chr2:55691870
|
ATATATAT others(12): Show |
A | 3 | a0002c0002t0002g0021a0002c0002t0002g0022a0002c0002t0002g0023 | 3 | HG02559.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.161+1774_161+1792d others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691870 | ||||||
chr2:55691871
|
TATA | T | 6 | a0001c0004t0004g0008a0001c0004t0007g0006a0001c0004t0007g0061others(3): Show | 7 | HG01433.hp2 HG03017.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.161+1789_161+1791d others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691871 | ||||||
chr2:55691871
|
TATATA | T | 3 | a0001c0001t0001g0177a0001c0001t0014g0176a0002c0005t0001g0175 | 3 | HG01346.hp2 HG02155.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.161+1787_161+1791d others(7): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691871 | ||||||
chr2:55691872
|
A | T | 5 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0006g0123others(2): Show | 5 | HG02698.hp2 NA18950.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+1791T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691872 | ||||||
chr2:55691872
|
ATATATAT others(12): Show |
A | 2 | a0002c0002t0021g0286a0002c0002t0021g0287 | 2 | HG01167.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.161+1772_161+1790d others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691872 | ||||||
chr2:55691873
|
TATATA | T | 3 | a0001c0001t0008g0194a0001c0001t0008g0195a0001c0001t0008g0196 | 3 | HG02258.hp1 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.161+1785_161+1789d others(7): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691873 | ||||||
chr2:55691874
|
A | AT | 3 | a0001c0001t0003g0289a0001c0001t0003g0290a0001c0001t0003g0291 | 3 | HG02273.hp2 NA18993.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.161+1788dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691874 | ||||||
chr2:55691874
|
A | T | 17 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0129others(14): Show | 18 | HG00558.hp2 HG01081.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+1789T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691874 | ||||||
chr2:55691876
|
A | AT | 6 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295others(3): Show | 6 | HG01928.hp2 HG01934.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+1786dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691876 | ||||||
chr2:55691876
|
A | T | 59 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0129others(56): Show | 61 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.161+1787T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691876 | ||||||
chr2:55691877
|
TA | T | 27 | a0001c0001t0001g0309a0001c0001t0003g0004a0001c0001t0003g0310others(24): Show | 29 | HG00558.hp1 HG02074.hp1 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.161+1785delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691877 | ||||||
chr2:55691878
|
A | ATATATAT others(4): Show |
2 | a0002c0002t0001g0047a0002c0002t0001g0048 | 2 | NA18966.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.161+1784_161+1785i others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(31): Show |
1 | a0001c0001t0028g0111 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(40): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0122 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(33): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0006g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(33): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0030g0046 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(22): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0044 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0006g0162 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(23): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(10): Show |
3 | a0001c0001t0001g0041a0004c0016t0001g0042a0006c0008t0001g0043 | 3 | HG02523.hp1 HG03490.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.161+1784_161+1785i others(19): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0037 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(20): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(22): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(8): Show |
1 | a0002c0002t0001g0369 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(17): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0026 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0006g0118 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(24): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0036 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(16): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG01496.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.161+1784_161+1785i others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0006g0191a0002c0002t0001g0045 | 2 | HG01261.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.161+1784_161+1785i others(12): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(4): Show |
3 | a0001c0001t0001g0038a0002c0002t0001g0039a0002c0002t0001g0040 | 3 | NA19064.hp2 NA19065.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.161+1784_161+1785i others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(5): Show |
3 | a0001c0001t0001g0033a0001c0001t0001g0034a0002c0002t0001g0035 | 3 | HG01192.hp2 HG03834.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.161+1784_161+1785i others(14): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(6): Show |
1 | a0002c0002t0001g0032 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(15): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(10): Show |
1 | a0001c0009t0029g0119 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(19): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0006g0116 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(22): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(4): Show |
2 | a0002c0002t0001g0030a0002c0002t0001g0031 | 2 | NA19002.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.161+1784_161+1785i others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0006g0115 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(20): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0006g0114 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATTT others(3): Show |
2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | NA18988.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.161+1784_161+1785i others(12): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATTT others(4): Show |
1 | a0001c0001t0026g0130 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | ATATATTT others(5): Show |
1 | a0002c0011t0001g0029 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(14): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
A | T | 103 | a0001c0001t0001g0028a0001c0001t0001g0125a0001c0001t0001g0126others(100): Show | 105 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.161+1785T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
AT | A | 17 | a0001c0001t0002g0356a0001c0001t0003g0353a0001c0001t0003g0354others(14): Show | 17 | HG01175.hp2 HG01255.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.161+1784delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
ATT | A | 9 | a0001c0001t0003g0358a0001c0001t0009g0359a0003c0003t0004g0073others(6): Show | 9 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.161+1783_161+1784d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691878
|
ATTT | A | 15 | a0003c0003t0004g0079a0003c0003t0004g0080a0003c0003t0004g0081others(12): Show | 15 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.161+1782_161+1784d others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | ||||||
chr2:55691879
|
T | TATATATA others(8): Show |
1 | a0005c0006t0004g0106 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161+1783_161+1784i others(17): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691879 | ||||||
chr2:55691880
|
T | A | 8 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(5): Show | 8 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.161+1783A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691880 | ||||||
chr2:55691881
|
T | A | 14 | a0001c0001t0003g0362a0003c0003t0004g0072a0003c0003t0004g0088others(11): Show | 14 | HG01175.hp2 HG01243.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.161+1782A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691881 | ||||||
chr2:55691882
|
T | A | 12 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(9): Show | 12 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.161+1781A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691882 | ||||||
chr2:55691882
|
T | C | 4 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | NA18963.hp1 NA18983.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.161+1781A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691882 | ||||||
chr2:55691883
|
T | A | 26 | a0003c0003t0004g0079a0003c0003t0004g0080a0003c0003t0004g0081others(23): Show | 26 | HG01175.hp2 HG01243.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.161+1780A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691883 | ||||||
chr2:55691884
|
T | A | 7 | a0003c0003t0004g0096a0003c0003t0004g0097a0003c0003t0004g0098others(4): Show | 7 | HG03225.hp2 HG03486.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.161+1779A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691884 | ||||||
chr2:55691885
|
T | A | 7 | a0003c0003t0004g0102a0003c0003t0004g0103a0003c0003t0004g0104others(4): Show | 7 | HG02451.hp1 NA18612.hp2 NA18906.hp2 others(4): Show |
intron_variant | MODIFIER | c.161+1778A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691885 | ||||||
chr2:55691886
|
T | A | 2 | a0003c0003t0004g0107a0003c0003t0004g0108 | 2 | NA18979.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.161+1777A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691886 | ||||||
chr2:55691887
|
T | A | 1 | a0003c0003t0032g0109 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.161+1776A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691887 | ||||||
chr2:55691889
|
T | A | 1 | a0003c0003t0032g0109 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.161+1774A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691889 | ||||||
chr2:55691910
|
A | G | 196 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(193): Show | 198 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.161+1753T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691910 | ||||||
chr2:55691988
|
C | T | 2 | a0002c0002t0010g0112a0002c0002t0010g0113 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.161+1675G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691988 | ||||||
chr2:55692066
|
G | A | 8 | a0001c0004t0007g0005a0001c0004t0007g0006a0001c0004t0007g0060others(5): Show | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.161+1597C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692066 | ||||||
chr2:55692104
|
C | T | 1 | a0001c0001t0028g0111 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.161+1559G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692104 | ||||||
chr2:55692185
|
G | A | 45 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(42): Show | 45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.161+1478C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692185 | ||||||
chr2:55692191
|
T | A | 1 | a0003c0003t0004g0110 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.161+1472A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692191 | ||||||
chr2:55692266
|
G | C | 42 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(39): Show | 44 | HG00423.hp2 HG01070.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.161+1397C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692266 | ||||||
chr2:55692356
|
C | T | 297 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.161+1307G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692356 | ||||||
chr2:55692501
|
C | G | 45 | a0003c0003t0004g0066a0003c0003t0004g0068a0003c0003t0004g0069others(42): Show | 45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.161+1162G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692501 | ||||||
chr2:55692523
|
T | A | 2 | a0001c0001t0003g0364a0002c0002t0002g0363 | 2 | HG01106.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.161+1140A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692523 | ||||||
chr2:55692531
|
G | T | 42 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(39): Show | 44 | HG00423.hp2 HG01070.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.161+1132C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692531 | ||||||
chr2:55692711
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.161+952G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692711 | ||||||
chr2:55693026
|
T | C | 1 | a0001c0001t0001g0365 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.161+637A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693026 | ||||||
chr2:55693125
|
T | G | 3 | a0001c0001t0003g0366a0001c0001t0003g0367a0001c0001t0003g0368 | 3 | HG00423.hp1 NA19003.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.161+538A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693125 | ||||||
chr2:55693170
|
C | T | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.161+493G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693170 | ||||||
chr2:55693243
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02683.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.161+420G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693243 | ||||||
chr2:55693286
|
C | T | 2 | a0001c0004t0004g0008a0001c0004t0004g0025 | 2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.161+377G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693286 | ||||||
chr2:55693374
|
G | A | 1 | a0002c0002t0001g0369 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.161+289C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693374 | ||||||
chr2:55693475
|
T | C | 2 | a0001c0001t0001g0370a0001c0001t0001g0371 | 2 | HG00438.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.161+188A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693475 | ||||||
chr2:55693486
|
G | A | 1 | a0001c0001t0031g0372 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.161+177C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693486 | ||||||
chr2:55693509
|
C | T | 1 | a0002c0002t0038g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.161+154G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693509 | ||||||
chr2:55693528
|
T | C | 5 | a0002c0002t0002g0373a0002c0002t0002g0374a0002c0002t0002g0375others(2): Show | 5 | HG01074.hp1 HG01168.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+135A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693528 | ||||||
chr2:55693614
|
C | T | 15 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(12): Show | 15 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.161+49G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693614 | ||||||
chr2:55693646
|
C | G | 1 | a0001c0004t0004g0008 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.161+17G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693646 |