geneid | 23175 |
---|---|
ensemblid | ENSG00000134324.12 |
hgncid | 13345 |
symbol | LPIN1 |
name | lipin 1 |
refseq_nuc | NM_001349206.2 |
refseq_prot | NP_001336135.1 |
ensembl_nuc | ENST00000674199.1 |
ensembl_prot | ENSP00000501331.1 |
mane_status | MANE Select |
chr | chr2 |
start | 11746632 |
end | 11827409 |
strand | + |
ver | v1.2 |
region | chr2:11746632-11827409 |
region5000 | chr2:11741632-11832409 |
regionname0 | LPIN1_chr2_11746632_11827409 |
regionname5000 | LPIN1_chr2_11741632_11832409 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 926 | 268 | 81 | 51 | 91 | 13 | 30 | 62 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0002 | 0/0 | 925 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0003 | 0/0 | 926 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0004 | 0/0 | 926 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2781 | 230 | 57 | 42 | 91 | 11 | 27 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
c0002 | 0/0 | 2781 | 13 | 12 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
c0003 | 0/0 | 2781 | 10 | 0 | 6 | 0 | 2 | 2 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
c0004 | 0/0 | 2781 | 6 | 4 | 2 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
c0005 | 0/0 | 2781 | 5 | 5 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
c0006 | 0/0 | 2781 | 3 | 0 | 2 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
c0007 | 0/0 | 2778 | 3 | 2 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
c0008 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
c0009 | 0/0 | 2778 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
c0010 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
c0011 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
c0012 | 0/0 | 2781 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
c0013 | 0/0 | 2781 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2668 | 61 | 4 | 8 | 33 | 4 | 11 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0002 | 0/0 | 2667 | 48 | 13 | 15 | 8 | 6 | 6 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0003 | 0/0 | 2668 | 33 | 16 | 4 | 13 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0004 | 0/0 | 2667 | 33 | 2 | 6 | 22 | 1 | 2 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0005 | 0/0 | 2667 | 12 | 12 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0006 | 0/0 | 2667 | 11 | 10 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0007 | 0/0 | 2667 | 9 | 5 | 3 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0008 | 0/0 | 2666 | 8 | 6 | 2 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0009 | 0/0 | 2667 | 7 | 0 | 4 | 0 | 0 | 3 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0010 | 0/0 | 2667 | 7 | 4 | 3 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0011 | 0/1 | 2666 | 7 | 0 | 1 | 0 | 1 | 4 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0012 | 0/0 | 2668 | 5 | 1 | 1 | 2 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0013 | 0/0 | 2669 | 4 | 0 | 1 | 3 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0014 | 0/0 | 2667 | 4 | 0 | 0 | 3 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0015 | 0/0 | 2668 | 3 | 3 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0016 | 0/0 | 2669 | 3 | 0 | 0 | 3 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0017 | 0/0 | 2667 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0018 | 0/0 | 2667 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0019 | 0/0 | 2669 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0020 | 0/0 | 2668 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0021 | 0/0 | 2669 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0022 | 0/0 | 2668 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0023 | 0/0 | 2669 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0024 | 0/0 | 2668 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0025 | 0/0 | 2667 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0026 | 0/0 | 2666 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0027 | 0/0 | 2668 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0028 | 0/0 | 2668 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0029 | 0/0 | 2668 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0030 | 0/0 | 2667 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0031 | 0/0 | 2666 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0032 | 0/0 | 2667 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0033 | 0/0 | 2666 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0034 | 0/0 | 2668 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0035 | 0/0 | 2667 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0036 | 0/0 | 2668 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0037 | 0/0 | 2667 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
t0038 | 0/0 | 2665 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0203 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2781 | 230 | 57 | 42 | 91 | 11 | 27 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0002 | 0/0 | 2781 | 13 | 12 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0003 | 0/0 | 2781 | 10 | 0 | 6 | 0 | 2 | 2 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0004 | 0/0 | 2781 | 6 | 4 | 2 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0005 | 0/0 | 2781 | 5 | 5 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0008 | 0/0 | 2781 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0011 | 0/0 | 2781 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0013 | 0/0 | 2781 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0002c0007 | 0/0 | 2778 | 3 | 2 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0002c0009 | 0/0 | 2778 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0002c0010 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0003c0006 | 0/0 | 2781 | 3 | 0 | 2 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0004c0012 | 0/0 | 2781 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5448 | 58 | 4 | 6 | 32 | 4 | 11 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0002 | 0/0 | 5447 | 41 | 10 | 14 | 8 | 4 | 5 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0003 | 0/0 | 5448 | 28 | 11 | 4 | 13 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0004 | 0/0 | 5447 | 31 | 2 | 4 | 22 | 1 | 2 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0005 | 0/0 | 5447 | 9 | 9 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0006 | 0/0 | 5447 | 8 | 7 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0007 | 0/0 | 5447 | 3 | 0 | 2 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0008 | 0/0 | 5446 | 7 | 5 | 2 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0009 | 0/0 | 5447 | 2 | 0 | 0 | 0 | 0 | 2 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0010 | 0/0 | 5447 | 3 | 1 | 2 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0011 | 0/1 | 5446 | 6 | 0 | 0 | 0 | 1 | 4 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0012 | 0/0 | 5448 | 5 | 1 | 1 | 2 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0013 | 0/0 | 5449 | 4 | 0 | 1 | 3 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0014 | 0/0 | 5447 | 3 | 0 | 0 | 3 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0016 | 0/0 | 5449 | 3 | 0 | 0 | 3 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0017 | 0/0 | 5447 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0018 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0019 | 0/0 | 5449 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0020 | 0/0 | 5448 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0021 | 0/0 | 5449 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0022 | 0/0 | 5448 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0023 | 0/0 | 5449 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0024 | 0/0 | 5448 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0025 | 0/0 | 5447 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0026 | 0/0 | 5446 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0027 | 0/0 | 5448 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0028 | 0/0 | 5448 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0029 | 0/0 | 5448 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0031 | 0/0 | 5446 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0033 | 0/0 | 5446 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0036 | 0/0 | 5448 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0037 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0001t0038 | 0/0 | 5445 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0002t0002 | 0/0 | 5447 | 2 | 1 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0002t0003 | 0/0 | 5448 | 5 | 5 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0002t0006 | 0/0 | 5447 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0002t0008 | 0/0 | 5446 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0002t0015 | 0/0 | 5448 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0002t0030 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0003t0001 | 0/0 | 5448 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0003t0002 | 0/0 | 5447 | 3 | 0 | 1 | 0 | 2 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0003t0009 | 0/0 | 5447 | 5 | 0 | 4 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0003t0014 | 0/0 | 5447 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0004t0006 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0004t0007 | 0/0 | 5447 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0004t0010 | 0/0 | 5447 | 4 | 3 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0005t0007 | 0/0 | 5447 | 5 | 5 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0008t0005 | 0/0 | 5447 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0011t0015 | 0/0 | 5448 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0001c0013t0001 | 0/0 | 5448 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0002c0007t0011 | 0/0 | 5443 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0002c0007t0034 | 0/0 | 5445 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0002c0007t0035 | 0/0 | 5444 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0002c0009t0002 | 0/0 | 5444 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0002c0010t0005 | 0/0 | 5444 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0003c0006t0004 | 0/0 | 5447 | 2 | 0 | 2 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0003c0006t0032 | 0/0 | 5447 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
a0004c0012t0001 | 0/0 | 5448 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | copy fasta | chr2 | 11741632 | 11832409 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0203 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0007g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0007g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0008g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0008g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0009g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0009g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0010g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0010g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0011g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0011g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0011g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0011g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0011g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0011g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0012g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0012g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0012g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0012g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0012g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0013g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0013g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0013g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0013g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0014g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0014g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0014g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0016g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0016g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0016g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0017g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0017g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0018g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0019g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0020g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0021g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0022g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0023g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0024g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0025g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0026g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0027g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0028g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0029g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0031g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0033g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0036g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0037g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0001t0038g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0002t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0002t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0002t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0002t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0002t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0002t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0002t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0002t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0002t0015g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0002t0015g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0002t0030g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0003t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0003t0009g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0003t0009g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0003t0009g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0003t0009g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0003t0009g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0003t0014g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0004t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0004t0007g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0004t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0004t0010g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0004t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0004t0010g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0005t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0005t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0005t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0005t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0005t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0008t0005g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0008t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0011t0015g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0001c0013t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0002c0007t0011g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0002c0007t0034g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0002c0007t0035g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0002c0009t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0002c0009t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0002c0010t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0003c0006t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0003c0006t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0003c0006t0032g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
a0004c0012t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | GBR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0101 | EUR | GBR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00280 | hp1 | a0001 | c0003 | t0002 | g0052 | EUR | FIN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0256 | EUR | FIN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | CHS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00558 | hp1 | a0001 | c0001 | t0014 | g0177 | EAS | CHS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | CHS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0219 | EAS | CHS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00639 | hp1 | a0001 | c0001 | t0031 | g0184 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00639 | hp2 | a0001 | c0001 | t0008 | g0038 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | CHS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00733 | hp1 | a0001 | c0003 | t0001 | g0048 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0227 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00735 | hp1 | a0001 | c0001 | t0007 | g0112 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00738 | hp1 | a0001 | c0003 | t0009 | g0137 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0218 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01070 | hp2 | a0001 | c0013 | t0001 | g0021 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01074 | hp2 | a0001 | c0003 | t0002 | g0087 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01081 | hp1 | a0001 | c0003 | t0009 | g0049 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01109 | hp1 | a0001 | c0001 | t0010 | g0020 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01109 | hp2 | a0001 | c0004 | t0007 | g0274 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01167 | hp2 | a0002 | c0007 | t0011 | g0025 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0181 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01175 | hp2 | a0001 | c0001 | t0006 | g0039 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01243 | hp1 | a0003 | c0006 | t0004 | g0174 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0189 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0190 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01257 | hp1 | a0001 | c0001 | t0038 | g0001 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01257 | hp2 | a0001 | c0003 | t0009 | g0050 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01258 | hp1 | a0001 | c0001 | t0007 | g0188 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01258 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01261 | hp1 | a0001 | c0001 | t0010 | g0078 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01346 | hp2 | a0001 | c0001 | t0012 | g0251 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01361 | hp1 | a0001 | c0001 | t0021 | g0102 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01433 | hp2 | a0001 | c0003 | t0009 | g0090 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01496 | hp1 | a0003 | c0006 | t0004 | g0105 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | IBS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01515 | hp2 | a0001 | c0003 | t0002 | g0088 | EUR | IBS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0200 | EUR | IBS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0171 | EUR | IBS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0254 | EUR | IBS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0170 | EUR | IBS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01884 | hp1 | a0001 | c0001 | t0012 | g0066 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0037 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0019 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01934 | hp1 | a0001 | c0004 | t0010 | g0076 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01934 | hp2 | a0001 | c0001 | t0023 | g0159 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01952 | hp1 | a0001 | c0001 | t0024 | g0195 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01981 | hp1 | a0001 | c0001 | t0013 | g0220 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02015 | hp2 | a0001 | c0001 | t0012 | g0113 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02055 | hp1 | a0001 | c0004 | t0006 | g0072 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02055 | hp2 | a0002 | c0007 | t0034 | g0023 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02074 | hp2 | a0001 | c0001 | t0020 | g0110 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02080 | hp1 | a0001 | c0001 | t0016 | g0098 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02155 | hp1 | a0001 | c0001 | t0016 | g0120 | EAS | CDX | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | CDX | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | CDX | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02257 | hp2 | a0001 | c0004 | t0010 | g0004 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02258 | hp2 | a0001 | c0005 | t0007 | g0157 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02280 | hp1 | a0002 | c0010 | t0005 | g0008 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0042 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02523 | hp1 | a0001 | c0001 | t0027 | g0142 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02523 | hp2 | a0004 | c0012 | t0001 | g0198 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02572 | hp2 | a0001 | c0002 | t0008 | g0081 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02615 | hp2 | a0001 | c0002 | t0006 | g0153 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02622 | hp1 | a0001 | c0001 | t0018 | g0032 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02622 | hp2 | a0001 | c0002 | t0015 | g0156 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02630 | hp1 | a0001 | c0002 | t0015 | g0152 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02723 | hp2 | a0001 | c0001 | t0006 | g0056 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02735 | hp1 | a0001 | c0003 | t0014 | g0089 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02735 | hp2 | a0001 | c0001 | t0011 | g0125 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02738 | hp1 | a0001 | c0001 | t0029 | g0136 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0204 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02809 | hp1 | a0001 | c0002 | t0003 | g0009 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02809 | hp2 | a0001 | c0004 | t0010 | g0074 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02896 | hp1 | a0001 | c0001 | t0017 | g0061 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02896 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02897 | hp1 | a0001 | c0001 | t0017 | g0062 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0079 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02922 | hp1 | a0001 | c0008 | t0005 | g0003 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0092 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02970 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02970 | hp2 | a0001 | c0005 | t0007 | g0017 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0163 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03017 | hp1 | a0001 | c0001 | t0011 | g0093 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03041 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0035 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | MSL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | MSL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03130 | hp2 | a0001 | c0001 | t0028 | g0080 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0075 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03139 | hp2 | a0001 | c0001 | t0022 | g0160 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03195 | hp1 | a0001 | c0008 | t0005 | g0002 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03209 | hp1 | a0001 | c0005 | t0007 | g0151 | AFR | MSL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03209 | hp2 | a0002 | c0009 | t0002 | g0047 | AFR | MSL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | MSL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03225 | hp2 | a0001 | c0002 | t0003 | g0015 | AFR | MSL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03239 | hp1 | a0001 | c0001 | t0009 | g0108 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03486 | hp1 | a0001 | c0001 | t0010 | g0071 | AFR | MSL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03486 | hp2 | a0001 | c0001 | t0037 | g0236 | AFR | MSL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03491 | hp1 | a0001 | c0001 | t0012 | g0161 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03516 | hp2 | a0001 | c0005 | t0007 | g0154 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0044 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0091 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | STU | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03688 | hp2 | a0001 | c0001 | t0011 | g0085 | SAS | STU | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0269 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03710 | hp2 | a0001 | c0001 | t0011 | g0217 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0016 | SAS | BEB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | BEB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | STU | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | STU | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG04228 | hp2 | a0001 | c0003 | t0009 | g0051 | SAS | STU | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18522 | hp1 | a0001 | c0005 | t0007 | g0018 | AFR | YRI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0045 | AFR | YRI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | CHB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | CHB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18906 | hp1 | a0002 | c0009 | t0002 | g0022 | AFR | YRI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18906 | hp2 | a0001 | c0002 | t0030 | g0007 | AFR | YRI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18950 | hp1 | a0001 | c0001 | t0019 | g0197 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18951 | hp1 | a0001 | c0001 | t0014 | g0275 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18960 | hp2 | a0001 | c0001 | t0014 | g0187 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18961 | hp1 | a0001 | c0001 | t0033 | g0268 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18975 | hp1 | a0001 | c0001 | t0012 | g0216 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18975 | hp2 | a0001 | c0001 | t0016 | g0139 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18991 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18991 | hp2 | a0001 | c0001 | t0013 | g0206 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18995 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19000 | hp1 | a0001 | c0001 | t0013 | g0214 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19000 | hp2 | a0001 | c0001 | t0013 | g0133 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19005 | hp2 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0082 | AFR | LWK | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19030 | hp2 | a0002 | c0007 | t0035 | g0024 | AFR | LWK | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0277 | AFR | LWK | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19081 | hp1 | a0001 | c0001 | t0036 | g0262 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19086 | hp1 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19086 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0070 | AFR | YRI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA19240 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | YRI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ASW | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA20129 | hp2 | a0001 | c0004 | t0010 | g0005 | AFR | ASW | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA20752 | hp1 | a0003 | c0006 | t0032 | g0111 | EUR | TSI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0245 | EUR | TSI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA20805 | hp1 | a0001 | c0001 | t0007 | g0172 | EUR | TSI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA20805 | hp2 | a0001 | c0001 | t0011 | g0084 | EUR | TSI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA20905 | hp1 | a0001 | c0001 | t0009 | g0229 | SAS | GIH | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA20905 | hp2 | a0001 | c0001 | t0025 | g0100 | SAS | GIH | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0036 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02486 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0043 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02559 | hp1 | a0001 | c0002 | t0006 | g0155 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG06807 | hp1 | a0001 | c0011 | t0015 | g0073 | AFR | USA | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | USA | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0243 | AFR | USA | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | USA | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA21309 | hp1 | a0001 | c0001 | t0026 | g0034 | AFR | LWK | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0095 | AFR | LWK | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0011 | g0086 | REF | REF | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0203 | REF | REF | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:11782200
|
GTCT | G | 1 | a0002 | 6 | HG01167.hp2 HG02055.hp2 HG02280.hp1 others(3): Show |
conservative_inframe_deletion | MODERATE | c.964_966delTCT | p.Ser322del | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/21 | 1013/5448 | 964/2781 | 322/926 | INFO_REALIGN_3_PRIME | chr2 | 11782200 | |
chr2:11802956
|
C | T | 1 | a0003 | 3 | HG01243.hp1 HG01496.hp1 NA20752.hp1 |
missense_variant | MODERATE | c.1936C>T | p.Pro646Ser | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/21 | 1985/5448 | 1936/2781 | 646/926 | chr2 | 11802956 | ||
chr2:11802990
|
A | G | 1 | a0004 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1970A>G | p.Asn657Ser | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/21 | 2019/5448 | 1970/2781 | 657/926 | chr2 | 11802990 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:11771503
|
C | T | 3 | a0001c0013a0002c0007a0002c0009 | 6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
synonymous_variant | LOW | c.420C>T | p.Ile140Ile | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/21 | 469/5448 | 420/2781 | 140/926 | chr2 | 11771503 | ||
chr2:11771635
|
C | T | 1 | a0001c0003 | 10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
synonymous_variant | LOW | c.552C>T | p.Ile184Ile | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/21 | 601/5448 | 552/2781 | 184/926 | chr2 | 11771635 | ||
chr2:11773680
|
G | A | 4 | a0001c0002a0001c0005a0001c0008others(1): Show | 21 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(18): Show |
synonymous_variant | LOW | c.657G>A | p.Leu219Leu | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/21 | 706/5448 | 657/2781 | 219/926 | chr2 | 11773680 | ||
chr2:11804452
|
C | T | 1 | a0002c0010 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.2043C>T | p.Asn681Asn | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/21 | 2092/5448 | 2043/2781 | 681/926 | chr2 | 11804452 | ||
chr2:11805136
|
G | A | 1 | a0001c0011 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.2229G>A | p.Lys743Lys | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/21 | 2278/5448 | 2229/2781 | 743/926 | chr2 | 11805136 | ||
chr2:11815196
|
G | C | 4 | a0001c0004a0001c0005a0002c0007others(1): Show | 15 | HG01109.hp2 HG01167.hp2 HG01934.hp1 others(12): Show |
synonymous_variant | LOW | c.2358G>C | p.Gly786Gly | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/21 | 2407/5448 | 2358/2781 | 786/926 | chr2 | 11815196 | ||
chr2:11820488
|
G | A | 1 | a0001c0008 | 2 | HG02922.hp1 HG03195.hp1 |
synonymous_variant | LOW | c.2595G>A | p.Gln865Gln | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/21 | 2644/5448 | 2595/2781 | 865/926 | chr2 | 11820488 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:11825117
|
C | T | 4 | a0001c0001t0008a0001c0001t0037a0001c0001t0038others(1): Show | 10 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*326C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 326 | chr2 | 11825117 | |||||
chr2:11825138
|
C | T | 1 | a0001c0001t0036 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*347C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 347 | chr2 | 11825138 | |||||
chr2:11825216
|
G | A | 3 | a0001c0001t0009a0001c0001t0018a0001c0003t0009 | 8 | HG00738.hp1 HG01081.hp1 HG01257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*425G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 425 | chr2 | 11825216 | |||||
chr2:11825414
|
A | C | 2 | a0002c0007t0034a0002c0007t0035 | 2 | HG02055.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*623A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 623 | chr2 | 11825414 | |||||
chr2:11825415
|
A | G | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(41): Show | 202 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*624A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 624 | chr2 | 11825415 | |||||
chr2:11825473
|
G | C | 1 | a0001c0001t0017 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*682G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 682 | chr2 | 11825473 | |||||
chr2:11825503
|
G | A | 1 | a0001c0001t0025 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*712G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 712 | chr2 | 11825503 | |||||
chr2:11825688
|
C | T | 4 | a0001c0001t0004a0001c0001t0033a0003c0006t0004others(1): Show | 35 | HG00609.hp2 HG00673.hp1 HG00733.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*897C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 897 | chr2 | 11825688 | |||||
chr2:11825872
|
AG | A | 5 | a0001c0001t0008a0001c0001t0026a0001c0001t0037others(2): Show | 11 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1082delG | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1082 | chr2 | 11825872 | |||||
chr2:11826063
|
G | A | 2 | a0001c0002t0015a0001c0011t0015 | 3 | HG02622.hp2 HG02630.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1272G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1272 | chr2 | 11826063 | |||||
chr2:11826191
|
T | C | 23 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(20): Show | 90 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1400T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1400 | chr2 | 11826191 | |||||
chr2:11826194
|
T | C | 1 | a0001c0001t0019 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1403T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1403 | chr2 | 11826194 | |||||
chr2:11826361
|
C | G | 6 | a0001c0001t0007a0001c0001t0031a0001c0004t0007others(3): Show | 12 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1570C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1570 | chr2 | 11826361 | |||||
chr2:11826411
|
T | C | 2 | a0001c0001t0020a0001c0001t0036 | 2 | HG02074.hp2 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1620T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1620 | chr2 | 11826411 | |||||
chr2:11826447
|
G | C | 1 | a0001c0001t0018 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1656G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1656 | chr2 | 11826447 | |||||
chr2:11826457
|
T | C | 1 | a0001c0001t0027 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1666T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1666 | chr2 | 11826457 | |||||
chr2:11826462
|
C | T | 2 | a0001c0001t0023a0001c0001t0024 | 2 | HG01934.hp2 HG01952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1671C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1671 | chr2 | 11826462 | |||||
chr2:11826490
|
G | A | 4 | a0001c0001t0006a0001c0001t0028a0001c0002t0006others(1): Show | 12 | HG01175.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1699G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1699 | chr2 | 11826490 | |||||
chr2:11826513
|
C | CA | 5 | a0001c0001t0013a0001c0001t0016a0001c0001t0019others(2): Show | 10 | HG01361.hp1 HG01934.hp2 HG01981.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1746dupA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1747 | INFO_REALIGN_3_PRIME | chr2 | 11826513 | ||||
chr2:11826513
|
CA | C | 30 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(27): Show | 147 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*1746delA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1746 | INFO_REALIGN_3_PRIME | chr2 | 11826513 | ||||
chr2:11826513
|
CAA | C | 5 | a0001c0001t0011a0001c0001t0031a0001c0001t0033others(2): Show | 10 | HG00639.hp1 HG01167.hp2 HG01257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1745_*1746delAA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1745 | INFO_REALIGN_3_PRIME | chr2 | 11826513 | ||||
chr2:11826584
|
A | T | 1 | a0001c0002t0030 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1793A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1793 | chr2 | 11826584 | |||||
chr2:11826877
|
C | G | 3 | a0001c0001t0009a0001c0001t0018a0001c0003t0009 | 8 | HG00738.hp1 HG01081.hp1 HG01257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2086C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 2086 | chr2 | 11826877 | |||||
chr2:11826913
|
A | G | 1 | a0001c0001t0022 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2122A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 2122 | chr2 | 11826913 | |||||
chr2:11826999
|
T | C | 1 | a0003c0006t0032 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2208T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 2208 | chr2 | 11826999 | |||||
chr2:11827065
|
C | G | 1 | a0001c0001t0021 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2274C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 2274 | chr2 | 11827065 | |||||
chr2:11827075
|
A | G | 1 | a0001c0001t0029 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2284A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 2284 | chr2 | 11827075 | |||||
chr2:11827282
|
G | A | 2 | a0001c0001t0010a0001c0004t0010 | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2491G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 2491 | chr2 | 11827282 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:11746723
|
C | T | 1 | a0001c0001t0005g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+52C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11746723 | ||||||
chr2:11746791
|
G | A | 19 | a0001c0001t0003g0011a0001c0001t0008g0006a0001c0001t0008g0019others(16): Show | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10+120G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11746791 | ||||||
chr2:11746792
|
G | A | 6 | a0001c0001t0001g0026a0001c0013t0001g0021a0002c0007t0011g0025others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+121G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11746792 | ||||||
chr2:11746826
|
G | C | 81 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0027others(78): Show | 81 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.-10+155G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11746826 | ||||||
chr2:11746907
|
C | T | 1 | a0001c0001t0002g0276 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-10+236C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11746907 | ||||||
chr2:11746925
|
C | T | 35 | a0001c0001t0001g0026a0001c0001t0002g0060a0001c0001t0002g0063others(32): Show | 35 | HG01070.hp2 HG01109.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.-10+254C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11746925 | ||||||
chr2:11747059
|
C | T | 1 | a0001c0001t0014g0275 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-10+388C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747059 | ||||||
chr2:11747109
|
C | T | 1 | a0001c0002t0008g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-10+438C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747109 | ||||||
chr2:11747111
|
C | T | 1 | a0001c0004t0007g0274 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-10+440C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747111 | ||||||
chr2:11747129
|
G | C | 5 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(2): Show | 5 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+458G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747129 | ||||||
chr2:11747151
|
C | G | 2 | a0001c0001t0001g0272a0001c0001t0001g0273 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-10+480C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747151 | ||||||
chr2:11747309
|
G | A | 162 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(159): Show | 162 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.-10+638G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747309 | ||||||
chr2:11747395
|
C | T | 2 | a0001c0001t0006g0079a0001c0001t0028g0080 | 2 | HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-10+724C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747395 | ||||||
chr2:11747426
|
C | T | 7 | a0001c0001t0001g0265a0001c0001t0001g0271a0001c0001t0003g0266others(4): Show | 7 | HG02071.hp1 HG03710.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+755C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747426 | ||||||
chr2:11747428
|
G | T | 17 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0067others(14): Show | 17 | HG01261.hp1 HG01261.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10+757G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747428 | ||||||
chr2:11747805
|
C | T | 10 | a0001c0002t0002g0016a0001c0002t0006g0153a0001c0002t0006g0155others(7): Show | 10 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+1134C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747805 | ||||||
chr2:11747921
|
A | G | 3 | a0001c0001t0004g0148a0001c0001t0004g0149a0001c0001t0004g0150 | 3 | NA19064.hp1 NA19074.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-10+1250A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747921 | ||||||
chr2:11747927
|
C | T | 1 | a0001c0001t0002g0264 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-10+1256C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747927 | ||||||
chr2:11748010
|
A | C | 5 | a0001c0003t0001g0048a0001c0003t0002g0052a0001c0003t0009g0049others(2): Show | 5 | HG00280.hp1 HG00733.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+1339A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748010 | ||||||
chr2:11748045
|
G | A | 7 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0003g0031others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+1374G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748045 | ||||||
chr2:11748192
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-10+1521G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748192 | ||||||
chr2:11748325
|
C | T | 3 | a0001c0001t0001g0263a0001c0001t0004g0261a0001c0001t0036g0262 | 3 | HG02071.hp2 NA18989.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-10+1654C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748325 | ||||||
chr2:11748340
|
G | A | 2 | a0001c0008t0005g0002a0001c0008t0005g0003 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-10+1669G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748340 | ||||||
chr2:11748348
|
C | T | 32 | a0001c0001t0001g0026a0001c0001t0003g0011a0001c0001t0008g0006others(29): Show | 32 | HG01070.hp2 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10+1677C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748348 | ||||||
chr2:11748372
|
G | T | 9 | a0001c0001t0002g0060a0001c0001t0002g0063a0001c0001t0002g0064others(6): Show | 9 | HG01884.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+1701G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748372 | ||||||
chr2:11748561
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-10+1890A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748561 | ||||||
chr2:11748631
|
G | C | 1 | a0001c0001t0023g0159 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-10+1960G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748631 | ||||||
chr2:11748693
|
C | T | 62 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(59): Show | 62 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-10+2022C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748693 | ||||||
chr2:11748715
|
T | G | 32 | a0001c0001t0003g0011a0001c0001t0003g0055a0001c0001t0003g0057others(29): Show | 32 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10+2044T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748715 | ||||||
chr2:11748874
|
A | G | 1 | a0001c0001t0011g0093 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-10+2203A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748874 | ||||||
chr2:11748895
|
A | G | 14 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0003g0069others(11): Show | 14 | HG01261.hp1 HG01496.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10+2224A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748895 | ||||||
chr2:11748922
|
G | T | 1 | a0001c0001t0001g0258 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-10+2251G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748922 | ||||||
chr2:11749007
|
A | G | 7 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0003g0031others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+2336A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749007 | ||||||
chr2:11749259
|
G | T | 163 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(160): Show | 163 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.-10+2588G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749259 | ||||||
chr2:11749286
|
A | G | 4 | a0001c0001t0005g0082a0001c0001t0005g0091a0001c0001t0005g0092others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+2615A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749286 | ||||||
chr2:11749296
|
G | A | 1 | a0001c0001t0022g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-10+2625G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749296 | ||||||
chr2:11749398
|
C | T | 1 | a0001c0001t0022g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-10+2727C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749398 | ||||||
chr2:11749403
|
G | A | 14 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0003g0069others(11): Show | 14 | HG01261.hp1 HG01496.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10+2732G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749403 | ||||||
chr2:11749526
|
G | T | 12 | a0001c0001t0003g0040a0001c0001t0003g0046a0001c0001t0005g0042others(9): Show | 12 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10+2855G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749526 | ||||||
chr2:11749539
|
C | G | 67 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-10+2868C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749539 | ||||||
chr2:11749783
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-10+3112A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749783 | ||||||
chr2:11749942
|
A | G | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+3271A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749942 | ||||||
chr2:11750012
|
T | C | 168 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.-10+3341T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750012 | ||||||
chr2:11750030
|
T | C | 1 | a0001c0001t0012g0161 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-10+3359T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750030 | ||||||
chr2:11750087
|
C | A | 1 | a0001c0001t0004g0094 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-10+3416C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750087 | ||||||
chr2:11750091
|
C | T | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+3420C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750091 | ||||||
chr2:11750148
|
C | G | 3 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158 | 3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-10+3477C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750148 | ||||||
chr2:11750181
|
C | T | 14 | a0001c0002t0002g0014a0001c0002t0002g0016a0001c0002t0003g0012others(11): Show | 14 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10+3510C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750181 | ||||||
chr2:11750302
|
C | G | 142 | a0001c0001t0001g0026a0001c0001t0001g0103a0001c0001t0001g0107others(139): Show | 142 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.-10+3631C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750302 | ||||||
chr2:11750472
|
G | A | 3 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158 | 3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-10+3801G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750472 | ||||||
chr2:11750520
|
G | A | 1 | a0001c0001t0005g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-10+3849G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750520 | ||||||
chr2:11750533
|
C | T | 5 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(2): Show | 5 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+3862C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750533 | ||||||
chr2:11750638
|
T | C | 84 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-10+3967T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750638 | ||||||
chr2:11750698
|
G | C | 1 | a0001c0001t0022g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-10+4027G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750698 | ||||||
chr2:11750774
|
G | A | 2 | a0001c0001t0002g0027a0001c0001t0002g0028 | 2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-10+4103G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750774 | ||||||
chr2:11750794
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-10+4123A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750794 | ||||||
chr2:11750806
|
T | TAGAC | 149 | a0001c0001t0001g0026a0001c0001t0001g0103a0001c0001t0001g0107others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.-10+4137_-10+4138i others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11750806 | |||||
chr2:11750906
|
A | G | 2 | a0001c0008t0005g0002a0001c0008t0005g0003 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-10+4235A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750906 | ||||||
chr2:11751198
|
C | G | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-10+4527C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11751198 | ||||||
chr2:11751290
|
T | TGG | 125 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-10+4620_-10+4621d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11751290 | |||||
chr2:11751330
|
T | C | 3 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158 | 3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-10+4659T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11751330 | ||||||
chr2:11751395
|
G | T | 1 | a0001c0001t0012g0251 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-10+4724G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11751395 | ||||||
chr2:11751462
|
C | T | 1 | a0001c0001t0005g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+4791C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11751462 | ||||||
chr2:11751824
|
C | G | 12 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0068others(9): Show | 12 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10+5153C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11751824 | ||||||
chr2:11751910
|
T | C | 5 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(2): Show | 5 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+5239T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11751910 | ||||||
chr2:11752008
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-10+5337A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752008 | ||||||
chr2:11752064
|
G | A | 118 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-10+5393G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752064 | ||||||
chr2:11752284
|
T | C | 1 | a0001c0001t0008g0019 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-10+5613T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752284 | ||||||
chr2:11752363
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-10+5692A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752363 | ||||||
chr2:11752396
|
G | C | 1 | a0001c0001t0022g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-10+5725G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752396 | ||||||
chr2:11752432
|
C | CTTTTTTT others(7): Show |
3 | a0001c0001t0002g0060a0001c0001t0017g0061a0001c0001t0017g0062 | 3 | HG02896.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-10+5761_-10+5762i others(16): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752432 | ||||||
chr2:11752432
|
C | CTTTTTTT others(8): Show |
5 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+5761_-10+5762i others(17): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752432 | ||||||
chr2:11752433
|
A | ATTTTTTT others(1): Show |
8 | a0001c0001t0003g0040a0001c0001t0005g0042a0001c0001t0006g0035others(5): Show | 8 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+5771_-10+5778d others(10): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | |||||
chr2:11752433
|
A | ATTTTTTT others(2): Show |
37 | a0001c0001t0001g0103a0001c0001t0001g0259a0001c0001t0001g0260others(34): Show | 37 | HG00099.hp2 HG01361.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.-10+5770_-10+5778d others(11): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | |||||
chr2:11752433
|
A | ATTTTTTT others(3): Show |
44 | a0001c0001t0001g0107a0001c0001t0001g0121a0001c0001t0001g0123others(41): Show | 44 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.-10+5769_-10+5778d others(12): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | |||||
chr2:11752433
|
A | ATTTTTTT others(4): Show |
13 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0146others(10): Show | 13 | HG00558.hp2 HG00738.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10+5768_-10+5778d others(13): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | |||||
chr2:11752433
|
A | ATTTTTTT others(5): Show |
8 | a0001c0001t0001g0026a0001c0001t0005g0075a0001c0001t0006g0079others(5): Show | 8 | HG02257.hp2 HG02809.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+5767_-10+5778d others(14): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | |||||
chr2:11752433
|
A | ATTTTTTT others(6): Show |
10 | a0001c0001t0002g0067a0001c0001t0003g0055a0001c0001t0003g0077others(7): Show | 10 | HG01261.hp1 HG01884.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+5766_-10+5778d others(15): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | |||||
chr2:11752433
|
A | ATTTTTTT others(7): Show |
6 | a0001c0001t0002g0053a0001c0001t0002g0158a0001c0001t0003g0057others(3): Show | 6 | HG01167.hp2 HG01261.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+5765_-10+5778d others(16): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | |||||
chr2:11752433
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0054 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-10+5764_-10+5778d others(17): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | |||||
chr2:11752433
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0008g0019a0001c0001t0010g0020 | 2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-10+5763_-10+5778d others(18): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | |||||
chr2:11752433
|
A | ATTTTTTT others(11): Show |
2 | a0001c0001t0002g0068a0001c0001t0003g0069 | 2 | HG01496.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-10+5778_-10+5779i others(20): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | |||||
chr2:11752433
|
A | ATTTTTTT others(14): Show |
1 | a0001c0001t0005g0070 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-10+5778_-10+5779i others(23): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | |||||
chr2:11752433
|
A | ATTTTTTT others(16): Show |
8 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0003g0031others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+5778_-10+5779i others(25): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | |||||
chr2:11752433
|
A | ATTTTTTT others(17): Show |
1 | a0001c0001t0003g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-10+5778_-10+5779i others(26): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | |||||
chr2:11752433
|
A | T | 9 | a0001c0001t0002g0060a0001c0001t0002g0063a0001c0001t0002g0064others(6): Show | 9 | HG02145.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+5762A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752433 | ||||||
chr2:11752433
|
AT | A | 10 | a0001c0001t0002g0162a0001c0001t0005g0082a0001c0001t0005g0091others(7): Show | 10 | HG01069.hp1 HG01109.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+5778delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | |||||
chr2:11752433
|
ATT | A | 8 | a0001c0003t0001g0048a0001c0003t0002g0052a0001c0003t0002g0087others(5): Show | 8 | HG00280.hp1 HG00733.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+5777_-10+5778d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | |||||
chr2:11752451
|
A | T | 1 | a0001c0001t0003g0046 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-10+5780A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752451 | ||||||
chr2:11752455
|
G | A | 21 | a0001c0001t0003g0011a0001c0002t0002g0014a0001c0002t0002g0016others(18): Show | 21 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.-10+5784G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752455 | ||||||
chr2:11752483
|
G | GT | 113 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-10+5813dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752483 | |||||
chr2:11752582
|
C | T | 1 | a0001c0001t0005g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+5911C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752582 | ||||||
chr2:11752588
|
C | T | 79 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.-10+5917C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752588 | ||||||
chr2:11752611
|
T | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0006g0163others(3): Show | 6 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+5940T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752611 | ||||||
chr2:11752635
|
T | G | 113 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-10+5964T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752635 | ||||||
chr2:11752652
|
C | T | 4 | a0001c0003t0002g0087a0001c0003t0002g0088a0001c0003t0009g0090others(1): Show | 4 | HG01074.hp2 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+5981C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752652 | ||||||
chr2:11752678
|
G | A | 3 | a0001c0001t0001g0167a0001c0001t0003g0166a0001c0001t0003g0168 | 3 | HG02132.hp2 HG02155.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.-10+6007G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752678 | ||||||
chr2:11752789
|
T | A | 3 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158 | 3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-10+6118T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752789 | ||||||
chr2:11752871
|
T | C | 132 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-10+6200T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752871 | ||||||
chr2:11752906
|
G | C | 1 | a0001c0001t0005g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+6235G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752906 | ||||||
chr2:11753036
|
T | C | 4 | a0001c0001t0001g0026a0001c0001t0008g0019a0001c0001t0010g0020others(1): Show | 4 | HG01109.hp1 HG01891.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+6365T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753036 | ||||||
chr2:11753087
|
T | C | 146 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-10+6416T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753087 | ||||||
chr2:11753113
|
G | A | 1 | a0001c0003t0009g0137 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-10+6442G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753113 | ||||||
chr2:11753206
|
G | GGGCTTTG others(2): Show |
129 | a0001c0001t0001g0026a0001c0001t0001g0103a0001c0001t0001g0107others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.-10+6539_-10+6547d others(11): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11753206 | |||||
chr2:11753274
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-10+6603A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753274 | ||||||
chr2:11753326
|
T | A | 10 | a0001c0002t0002g0016a0001c0002t0006g0153a0001c0002t0006g0155others(7): Show | 10 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+6655T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753326 | ||||||
chr2:11753379
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-10+6708C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753379 | ||||||
chr2:11753390
|
G | A | 4 | a0001c0003t0002g0087a0001c0003t0002g0088a0001c0003t0009g0090others(1): Show | 4 | HG01074.hp2 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+6719G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753390 | ||||||
chr2:11753491
|
T | A | 3 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0004t0007g0274 | 3 | HG01109.hp2 HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-10+6820T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753491 | ||||||
chr2:11753578
|
C | T | 1 | a0001c0001t0026g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-10+6907C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753578 | ||||||
chr2:11753692
|
C | G | 4 | a0001c0001t0001g0026a0001c0001t0008g0019a0001c0001t0010g0020others(1): Show | 4 | HG01109.hp1 HG01891.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+7021C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753692 | ||||||
chr2:11753895
|
C | A | 1 | a0001c0001t0005g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+7224C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753895 | ||||||
chr2:11753916
|
G | C | 1 | a0001c0001t0001g0265 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-10+7245G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753916 | ||||||
chr2:11753944
|
G | A | 4 | a0001c0001t0001g0026a0001c0001t0008g0019a0001c0001t0010g0020others(1): Show | 4 | HG01109.hp1 HG01891.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+7273G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753944 | ||||||
chr2:11754084
|
C | T | 2 | a0001c0001t0002g0162a0001c0001t0002g0247 | 2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-10+7413C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754084 | ||||||
chr2:11754223
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-10+7552G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754223 | ||||||
chr2:11754316
|
C | T | 1 | a0001c0001t0029g0136 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-10+7645C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754316 | ||||||
chr2:11754401
|
C | G | 3 | a0001c0001t0001g0246a0001c0001t0002g0244a0001c0001t0004g0245 | 3 | HG01081.hp2 HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-10+7730C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754401 | ||||||
chr2:11754458
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-10+7787G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754458 | ||||||
chr2:11754463
|
G | A | 1 | a0001c0001t0003g0138 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-10+7792G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754463 | ||||||
chr2:11754504
|
C | G | 1 | a0001c0001t0001g0257 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-10+7833C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754504 | ||||||
chr2:11754591
|
G | A | 1 | a0001c0001t0004g0261 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-10+7920G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754591 | ||||||
chr2:11754601
|
T | C | 6 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+7930T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754601 | ||||||
chr2:11754670
|
A | G | 1 | a0001c0001t0005g0042 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-10+7999A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754670 | ||||||
chr2:11754676
|
A | G | 7 | a0001c0001t0003g0011a0001c0002t0003g0009a0001c0002t0003g0010others(4): Show | 7 | HG02280.hp1 HG02809.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+8005A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754676 | ||||||
chr2:11754817
|
C | T | 62 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(59): Show | 62 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-10+8146C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754817 | ||||||
chr2:11754840
|
C | G | 1 | a0001c0001t0026g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-10+8169C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754840 | ||||||
chr2:11754976
|
A | AT | 7 | a0001c0001t0001g0242a0001c0001t0002g0135a0001c0001t0004g0106others(4): Show | 7 | HG02559.hp1 HG03098.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+8322dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11754976 | |||||
chr2:11754980
|
T | C | 3 | a0001c0001t0004g0148a0001c0001t0004g0149a0001c0001t0004g0150 | 3 | NA19064.hp1 NA19074.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-10+8309T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754980 | ||||||
chr2:11755028
|
C | A | 1 | a0001c0001t0036g0262 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-10+8357C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755028 | ||||||
chr2:11755045
|
A | G | 1 | a0001c0001t0005g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+8374A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755045 | ||||||
chr2:11755103
|
C | T | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+8432C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755103 | ||||||
chr2:11755115
|
G | A | 4 | a0001c0001t0001g0026a0001c0001t0008g0019a0001c0001t0010g0020others(1): Show | 4 | HG01109.hp1 HG01891.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+8444G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755115 | ||||||
chr2:11755157
|
C | T | 1 | a0001c0001t0012g0161 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-10+8486C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755157 | ||||||
chr2:11755177
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-10+8506C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755177 | ||||||
chr2:11755262
|
C | T | 7 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0011g0084others(4): Show | 7 | HG01109.hp2 HG02922.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+8591C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755262 | ||||||
chr2:11755354
|
GT | G | 3 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158 | 3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-10+8687delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11755354 | |||||
chr2:11755360
|
C | T | 1 | a0001c0001t0003g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-10+8689C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755360 | ||||||
chr2:11755374
|
G | A | 2 | a0001c0001t0002g0170a0001c0001t0002g0171 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-10+8703G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755374 | ||||||
chr2:11755479
|
G | A | 1 | a0001c0001t0007g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-10+8808G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755479 | ||||||
chr2:11755570
|
C | T | 1 | a0001c0001t0005g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+8899C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755570 | ||||||
chr2:11755723
|
C | CT | 20 | a0001c0001t0001g0146a0001c0001t0001g0241a0001c0001t0003g0011others(17): Show | 20 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10+9068dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11755723 | |||||
chr2:11755723
|
CT | C | 6 | a0001c0001t0001g0026a0001c0001t0001g0173a0001c0001t0002g0244others(3): Show | 6 | HG00733.hp1 HG01109.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+9068delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11755723 | |||||
chr2:11755828
|
T | C | 6 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+9157T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755828 | ||||||
chr2:11755869
|
G | A | 1 | a0001c0001t0002g0244 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-10+9198G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755869 | ||||||
chr2:11755903
|
A | G | 11 | a0001c0001t0001g0026a0001c0001t0002g0060a0001c0001t0002g0063others(8): Show | 11 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10+9232A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755903 | ||||||
chr2:11755922
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-10+9251C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755922 | ||||||
chr2:11755944
|
G | A | 4 | a0001c0001t0011g0084a0001c0001t0011g0085a0001c0001t0011g0086others(1): Show | 4 | HG03017.hp1 HG03688.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+9273G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755944 | ||||||
chr2:11756012
|
C | A | 6 | a0001c0003t0001g0048a0001c0003t0002g0052a0001c0003t0009g0049others(3): Show | 6 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+9341C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756012 | ||||||
chr2:11756012
|
C | T | 6 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+9341C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756012 | ||||||
chr2:11756038
|
A | G | 11 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0060others(8): Show | 11 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10+9367A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756038 | ||||||
chr2:11756099
|
C | T | 10 | a0001c0003t0001g0048a0001c0003t0002g0052a0001c0003t0002g0087others(7): Show | 10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+9428C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756099 | ||||||
chr2:11756113
|
G | A | 1 | a0001c0002t0003g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-9-9420G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756113 | ||||||
chr2:11756114
|
T | G | 13 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(10): Show | 13 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-9419T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756114 | ||||||
chr2:11756352
|
C | T | 1 | a0001c0001t0004g0106 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-9-9181C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756352 | ||||||
chr2:11756357
|
A | C | 13 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(10): Show | 13 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-9176A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756357 | ||||||
chr2:11756513
|
C | G | 1 | a0001c0001t0001g0239 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-9-9020C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756513 | ||||||
chr2:11756676
|
C | T | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-9-8857C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756676 | ||||||
chr2:11756712
|
C | T | 1 | a0001c0001t0004g0145 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-9-8821C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756712 | ||||||
chr2:11756849
|
G | A | 158 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(155): Show | 158 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-9-8684G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756849 | ||||||
chr2:11757034
|
G | A | 6 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-8499G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757034 | ||||||
chr2:11757099
|
C | T | 55 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(52): Show | 55 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.-9-8434C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757099 | ||||||
chr2:11757486
|
G | T | 23 | a0001c0001t0003g0055a0001c0001t0003g0057a0001c0001t0003g0058others(20): Show | 23 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.-9-8047G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757486 | ||||||
chr2:11757623
|
T | A | 1 | a0001c0001t0005g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-9-7910T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757623 | ||||||
chr2:11757786
|
C | G | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-7747C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757786 | ||||||
chr2:11757813
|
A | AT | 67 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(64): Show | 67 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.-9-7720_-9-7719ins others(1): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757813 | ||||||
chr2:11757813
|
A | T | 23 | a0001c0001t0005g0277a0001c0001t0012g0066a0001c0002t0002g0014others(20): Show | 23 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.-9-7720A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757813 | ||||||
chr2:11757932
|
TCCGCTTC others(2): Show |
T | 4 | a0001c0003t0002g0087a0001c0003t0002g0088a0001c0003t0009g0090others(1): Show | 4 | HG01074.hp2 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-7598_-9-7590del others(9): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11757932 | |||||
chr2:11757967
|
T | A | 2 | a0001c0001t0005g0277a0001c0001t0012g0066 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-9-7566T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757967 | ||||||
chr2:11757986
|
G | A | 13 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(10): Show | 13 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-7547G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757986 | ||||||
chr2:11758130
|
C | T | 1 | a0001c0001t0002g0238 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-9-7403C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758130 | ||||||
chr2:11758261
|
G | GT | 28 | a0001c0001t0001g0054a0001c0001t0002g0027a0001c0001t0002g0028others(25): Show | 28 | HG01109.hp1 HG01261.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.-9-7261dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11758261 | |||||
chr2:11758273
|
G | T | 6 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-7260G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758273 | ||||||
chr2:11758274
|
A | T | 1 | a0001c0001t0001g0237 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-9-7259A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758274 | ||||||
chr2:11758323
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-9-7210A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758323 | ||||||
chr2:11758355
|
G | T | 1 | a0001c0001t0003g0131 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-9-7178G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758355 | ||||||
chr2:11758565
|
A | G | 13 | a0001c0001t0002g0067a0001c0001t0003g0011a0001c0001t0003g0077others(10): Show | 13 | HG01261.hp1 HG01934.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-6968A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758565 | ||||||
chr2:11758613
|
T | G | 5 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(2): Show | 5 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-6920T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758613 | ||||||
chr2:11758756
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-9-6777C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758756 | ||||||
chr2:11758805
|
C | T | 90 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(87): Show | 90 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.-9-6728C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758805 | ||||||
chr2:11758962
|
T | C | 90 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(87): Show | 90 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.-9-6571T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758962 | ||||||
chr2:11759049
|
T | C | 90 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(87): Show | 90 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.-9-6484T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759049 | ||||||
chr2:11759118
|
A | T | 1 | a0001c0004t0010g0005 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-9-6415A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759118 | ||||||
chr2:11759123
|
G | T | 13 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(10): Show | 13 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-6410G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759123 | ||||||
chr2:11759123
|
GCTTTCTT others(6): Show |
G | 2 | a0001c0001t0011g0084a0001c0001t0011g0085 | 2 | HG03688.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-9-6397_-9-6385del others(13): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759123 | |||||
chr2:11759123
|
GCTTTCTT others(10): Show |
G | 1 | a0001c0001t0011g0093 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-9-6397_-9-6381del others(17): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759123 | |||||
chr2:11759127
|
T | G | 5 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0175others(2): Show | 5 | HG01243.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-6406T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759127 | ||||||
chr2:11759133
|
T | TTTC | 3 | a0001c0001t0002g0176a0001c0002t0003g0015a0001c0004t0010g0005 | 3 | HG01071.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-9-6398_-9-6397ins others(3): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | |||||
chr2:11759133
|
T | TTTTC | 48 | a0001c0001t0001g0185a0001c0001t0001g0192a0001c0001t0001g0193others(45): Show | 48 | HG00639.hp1 HG00673.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.-9-6344_-9-6341dup others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | |||||
chr2:11759133
|
T | TTTTCTTT others(1): Show |
19 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0242others(16): Show | 19 | HG01175.hp1 HG01346.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.-9-6348_-9-6341dup others(8): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | |||||
chr2:11759133
|
T | TTTTCTTT others(5): Show |
6 | a0001c0001t0001g0179a0001c0001t0003g0178a0001c0001t0014g0177others(3): Show | 6 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-6352_-9-6341dup others(12): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | |||||
chr2:11759133
|
TTTTC | T | 52 | a0001c0001t0001g0103a0001c0001t0001g0134a0001c0001t0001g0141others(49): Show | 52 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.-9-6344_-9-6341del others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | |||||
chr2:11759133
|
TTTTCTTT others(1): Show |
T | 38 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0127others(35): Show | 38 | HG00609.hp1 HG00733.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.-9-6348_-9-6341del others(8): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | |||||
chr2:11759133
|
TTTTCTTT others(5): Show |
T | 9 | a0001c0001t0001g0026a0001c0001t0001g0144a0001c0001t0001g0173others(6): Show | 9 | HG00733.hp1 HG01346.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-6352_-9-6341del others(12): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | |||||
chr2:11759133
|
TTTTCTTT others(9): Show |
T | 3 | a0001c0001t0002g0234a0001c0001t0003g0040a0001c0001t0004g0243 | 3 | HG01978.hp1 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-9-6356_-9-6341del others(16): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | |||||
chr2:11759133
|
TTTTCTTT others(13): Show |
T | 2 | a0001c0001t0002g0235a0001c0001t0037g0236 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-9-6360_-9-6341del others(20): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | |||||
chr2:11759133
|
TTTTCTTT others(17): Show |
T | 1 | a0001c0001t0026g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-9-6364_-9-6341del others(24): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | |||||
chr2:11759136
|
T | G | 1 | a0001c0001t0011g0086 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-9-6397T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759136 | ||||||
chr2:11759140
|
T | G | 2 | a0001c0001t0011g0084a0001c0001t0011g0085 | 2 | HG03688.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-9-6393T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759140 | ||||||
chr2:11759144
|
T | G | 1 | a0001c0001t0011g0093 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-9-6389T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759144 | ||||||
chr2:11759145
|
C | A | 2 | a0001c0001t0003g0011a0001c0001t0006g0079 | 2 | HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-9-6388C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759145 | ||||||
chr2:11759177
|
CTTTCTTT others(6): Show |
C | 3 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0009t0002g0022 | 3 | HG01070.hp2 HG01167.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-9-6340_-9-6328del others(13): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759177 | |||||
chr2:11759190
|
T | TTTCTTTC others(8): Show |
1 | a0001c0005t0007g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-9-6341_-9-6340ins others(15): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759190 | |||||
chr2:11759346
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-9-6187T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759346 | ||||||
chr2:11759351
|
C | T | 2 | a0001c0001t0005g0277a0001c0001t0012g0066 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-9-6182C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759351 | ||||||
chr2:11759437
|
G | A | 13 | a0001c0001t0002g0067a0001c0001t0003g0011a0001c0001t0003g0077others(10): Show | 13 | HG01261.hp1 HG01934.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-6096G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759437 | ||||||
chr2:11759529
|
C | T | 1 | a0001c0001t0003g0213 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-9-6004C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759529 | ||||||
chr2:11759569
|
T | C | 1 | a0001c0002t0030g0007 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-9-5964T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759569 | ||||||
chr2:11759586
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-9-5947A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759586 | ||||||
chr2:11759666
|
A | G | 12 | a0001c0001t0003g0040a0001c0001t0003g0046a0001c0001t0005g0042others(9): Show | 12 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9-5867A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759666 | ||||||
chr2:11759685
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-9-5848G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759685 | ||||||
chr2:11759709
|
C | CG | 36 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0164others(33): Show | 36 | HG00735.hp1 HG00735.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-9-5820dupG | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759709 | |||||
chr2:11759710
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-9-5823G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759710 | ||||||
chr2:11759758
|
T | C | 13 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(10): Show | 13 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-5775T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759758 | ||||||
chr2:11759759
|
G | A | 12 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(9): Show | 12 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-9-5774G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759759 | ||||||
chr2:11759769
|
G | GCCCCCCA others(40): Show |
1 | a0001c0001t0001g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-5717_-9-5671dup others(47): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759769 | |||||
chr2:11759787
|
G | A | 2 | a0001c0001t0002g0162a0001c0001t0002g0247 | 2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-9-5746G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759787 | ||||||
chr2:11759817
|
C | T | 1 | a0001c0001t0026g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-9-5716C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759817 | ||||||
chr2:11759843
|
G | A | 13 | a0001c0001t0002g0067a0001c0001t0003g0011a0001c0001t0003g0077others(10): Show | 13 | HG01261.hp1 HG01934.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-5690G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759843 | ||||||
chr2:11759850
|
C | T | 6 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-5683C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759850 | ||||||
chr2:11759870
|
C | T | 1 | a0001c0002t0030g0007 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-9-5663C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759870 | ||||||
chr2:11759895
|
C | T | 1 | a0001c0003t0002g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-9-5638C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759895 | ||||||
chr2:11759899
|
C | T | 1 | a0001c0003t0009g0137 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-9-5634C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759899 | ||||||
chr2:11759924
|
G | A | 1 | a0001c0001t0006g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-9-5609G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759924 | ||||||
chr2:11759946
|
G | T | 5 | a0001c0001t0003g0055a0001c0001t0003g0057a0001c0001t0003g0058others(2): Show | 5 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-5587G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759946 | ||||||
chr2:11759963
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-5570C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759963 | ||||||
chr2:11759964
|
G | A | 8 | a0001c0001t0005g0082a0001c0001t0005g0091a0001c0001t0005g0092others(5): Show | 8 | HG01109.hp2 HG02922.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-5569G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759964 | ||||||
chr2:11760086
|
G | A | 2 | a0001c0001t0006g0079a0001c0001t0028g0080 | 2 | HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-9-5447G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760086 | ||||||
chr2:11760102
|
T | G | 12 | a0001c0001t0003g0040a0001c0001t0003g0046a0001c0001t0005g0042others(9): Show | 12 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9-5431T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760102 | ||||||
chr2:11760156
|
C | T | 29 | a0001c0001t0003g0055a0001c0001t0003g0057a0001c0001t0003g0058others(26): Show | 29 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-9-5377C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760156 | ||||||
chr2:11760165
|
G | A | 6 | a0001c0002t0003g0009a0001c0002t0003g0010a0001c0002t0030g0007others(3): Show | 6 | HG02280.hp1 HG02809.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-5368G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760165 | ||||||
chr2:11760278
|
G | A | 2 | a0001c0001t0005g0277a0001c0001t0012g0066 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-9-5255G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760278 | ||||||
chr2:11760319
|
G | A | 2 | a0001c0001t0006g0035a0001c0001t0006g0037 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-9-5214G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760319 | ||||||
chr2:11760354
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-5179G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760354 | ||||||
chr2:11760383
|
C | T | 6 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-5150C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760383 | ||||||
chr2:11760438
|
A | G | 13 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(10): Show | 13 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-5095A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760438 | ||||||
chr2:11760633
|
G | C | 1 | a0001c0001t0005g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9-4900G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760633 | ||||||
chr2:11760800
|
G | A | 1 | a0001c0001t0031g0184 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-9-4733G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760800 | ||||||
chr2:11760838
|
G | A | 12 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(9): Show | 12 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-9-4695G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760838 | ||||||
chr2:11760858
|
G | C | 2 | a0001c0001t0008g0019a0001c0001t0010g0020 | 2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-9-4675G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760858 | ||||||
chr2:11760883
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-9-4650G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760883 | ||||||
chr2:11760934
|
C | T | 5 | a0001c0001t0002g0194a0001c0001t0004g0212a0001c0001t0004g0230others(2): Show | 5 | NA18747.hp2 NA18983.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-4599C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760934 | ||||||
chr2:11761168
|
TTTAGAG | T | 35 | a0001c0001t0003g0040a0001c0001t0003g0046a0001c0001t0005g0042others(32): Show | 35 | HG00639.hp2 HG01175.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.-9-4358_-9-4353del others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11761168 | |||||
chr2:11761235
|
A | C | 21 | a0001c0002t0002g0014a0001c0002t0002g0016a0001c0002t0003g0009others(18): Show | 21 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.-9-4298A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11761235 | ||||||
chr2:11761544
|
G | A | 1 | a0001c0001t0012g0113 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-9-3989G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11761544 | ||||||
chr2:11761564
|
CT | C | 3 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158 | 3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-9-3967delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11761564 | |||||
chr2:11761616
|
T | C | 1 | a0001c0001t0004g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9-3917T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11761616 | ||||||
chr2:11761682
|
G | C | 1 | a0001c0001t0003g0046 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-9-3851G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11761682 | ||||||
chr2:11761730
|
G | A | 63 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-9-3803G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11761730 | ||||||
chr2:11761936
|
G | A | 2 | a0001c0001t0002g0060a0001c0001t0002g0063 | 2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-9-3597G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11761936 | ||||||
chr2:11761942
|
A | G | 1 | a0001c0001t0026g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-9-3591A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11761942 | ||||||
chr2:11762086
|
C | T | 6 | a0001c0001t0003g0055a0001c0001t0003g0057a0001c0001t0003g0058others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-3447C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11762086 | ||||||
chr2:11762217
|
T | C | 2 | a0001c0001t0008g0019a0001c0001t0010g0020 | 2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-9-3316T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11762217 | ||||||
chr2:11762334
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-9-3199G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11762334 | ||||||
chr2:11762374
|
A | C | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-3159A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11762374 | ||||||
chr2:11762380
|
C | T | 10 | a0001c0001t0001g0265a0001c0001t0001g0271a0001c0001t0003g0266others(7): Show | 10 | HG01884.hp1 HG02071.hp1 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-3153C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11762380 | ||||||
chr2:11762655
|
A | G | 1 | a0001c0001t0026g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-9-2878A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11762655 | ||||||
chr2:11762885
|
G | T | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-2648G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11762885 | ||||||
chr2:11763035
|
C | T | 6 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-2498C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763035 | ||||||
chr2:11763043
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-9-2490C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763043 | ||||||
chr2:11763313
|
G | A | 22 | a0001c0001t0005g0070a0001c0002t0002g0014a0001c0002t0002g0016others(19): Show | 22 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.-9-2220G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763313 | ||||||
chr2:11763452
|
C | T | 1 | a0001c0001t0012g0113 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-9-2081C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763452 | ||||||
chr2:11763536
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0004g0199 | 2 | HG00673.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.-9-1997T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763536 | ||||||
chr2:11763555
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-9-1978G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763555 | ||||||
chr2:11763589
|
T | C | 10 | a0001c0003t0001g0048a0001c0003t0002g0052a0001c0003t0002g0087others(7): Show | 10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-1944T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763589 | ||||||
chr2:11763671
|
C | A | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-1862C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763671 | ||||||
chr2:11763688
|
C | T | 6 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-1845C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763688 | ||||||
chr2:11763702
|
C | T | 10 | a0001c0003t0001g0048a0001c0003t0002g0052a0001c0003t0002g0087others(7): Show | 10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-1831C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763702 | ||||||
chr2:11763714
|
C | T | 6 | a0001c0001t0003g0055a0001c0001t0003g0057a0001c0001t0003g0058others(3): Show | 6 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-1819C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763714 | ||||||
chr2:11763728
|
A | T | 152 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(149): Show | 152 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.-9-1805A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763728 | ||||||
chr2:11763729
|
G | C | 152 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(149): Show | 152 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.-9-1804G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763729 | ||||||
chr2:11763730
|
T | C | 1 | a0001c0001t0005g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9-1803T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763730 | ||||||
chr2:11763848
|
G | A | 1 | a0001c0001t0003g0266 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-9-1685G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763848 | ||||||
chr2:11763854
|
G | GTCC | 152 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(149): Show | 152 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.-9-1675_-9-1673dup others(3): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763854 | |||||
chr2:11763964
|
A | AGT | 21 | a0001c0001t0001g0026a0001c0001t0001g0107a0001c0001t0001g0144others(18): Show | 21 | HG00609.hp1 HG00735.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-9-1546_-9-1545dup others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763964 | |||||
chr2:11763964
|
A | AGTGT | 58 | a0001c0001t0001g0103a0001c0001t0001g0121a0001c0001t0001g0123others(55): Show | 58 | HG00099.hp2 HG00558.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.-9-1548_-9-1545dup others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763964 | |||||
chr2:11763964
|
A | AGTGTGT | 6 | a0001c0001t0001g0134a0001c0001t0002g0067a0001c0001t0002g0132others(3): Show | 6 | HG01261.hp1 HG01934.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-1550_-9-1545dup others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763964 | |||||
chr2:11763964
|
A | AGTGTGTG others(1): Show |
11 | a0001c0001t0002g0053a0001c0001t0002g0158a0001c0001t0003g0011others(8): Show | 11 | HG01261.hp2 HG01981.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-1552_-9-1545dup others(8): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763964 | |||||
chr2:11763964
|
A | AGTGTGTG others(3): Show |
17 | a0001c0001t0001g0054a0001c0001t0008g0019a0001c0001t0010g0020others(14): Show | 17 | HG01070.hp2 HG01109.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.-9-1554_-9-1545dup others(10): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763964 | |||||
chr2:11763964
|
A | AGTGTGTG others(5): Show |
14 | a0001c0002t0006g0153a0001c0002t0006g0155a0001c0002t0015g0152others(11): Show | 14 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9-1556_-9-1545dup others(12): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763964 | |||||
chr2:11763964
|
A | AGTGTGTG others(7): Show |
10 | a0001c0002t0002g0014a0001c0002t0002g0016a0001c0002t0003g0012others(7): Show | 10 | HG01433.hp2 HG02258.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9-1558_-9-1545dup others(14): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763964 | |||||
chr2:11763964
|
A | T | 7 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0005g0277others(4): Show | 7 | HG02922.hp2 HG03017.hp1 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-1569A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763964 | ||||||
chr2:11763987
|
G | A | 2 | a0001c0001t0001g0239a0001c0001t0002g0238 | 2 | HG04228.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.-9-1546G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763987 | ||||||
chr2:11763987
|
G | GTA | 8 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0068others(5): Show | 8 | HG01496.hp2 HG01516.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-1528_-9-1527dup others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763987 | |||||
chr2:11763987
|
GTA | G | 4 | a0001c0001t0002g0264a0001c0001t0003g0040a0001c0001t0008g0038others(1): Show | 4 | HG00639.hp2 HG02723.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-1528_-9-1527del others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763987 | |||||
chr2:11763989
|
A | G | 133 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(130): Show | 133 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-9-1544A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763989 | ||||||
chr2:11763991
|
A | G | 55 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0144others(52): Show | 55 | HG01070.hp2 HG01109.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.-9-1542A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763991 | ||||||
chr2:11763993
|
A | G | 33 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(30): Show | 33 | HG01070.hp2 HG01109.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.-9-1540A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763993 | ||||||
chr2:11763995
|
A | G | 28 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(25): Show | 28 | HG01070.hp2 HG01109.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-9-1538A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763995 | ||||||
chr2:11763997
|
A | G | 17 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158others(14): Show | 17 | HG01070.hp2 HG01109.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.-9-1536A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763997 | ||||||
chr2:11763999
|
A | G | 8 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0005g0277others(5): Show | 8 | HG01109.hp2 HG02922.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-1534A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763999 | ||||||
chr2:11764001
|
A | G | 8 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0005g0277others(5): Show | 8 | HG01109.hp2 HG02922.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-1532A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764001 | ||||||
chr2:11764016
|
G | A | 62 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(59): Show | 62 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-9-1517G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764016 | ||||||
chr2:11764034
|
G | C | 1 | a0001c0001t0012g0216 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-9-1499G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764034 | ||||||
chr2:11764054
|
A | ATG | 11 | a0001c0001t0001g0179a0001c0001t0001g0192a0001c0001t0001g0223others(8): Show | 11 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-1455_-9-1454dup others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764054 | |||||
chr2:11764054
|
ATG | A | 5 | a0001c0001t0005g0042a0001c0001t0006g0041a0001c0001t0008g0043others(2): Show | 5 | HG02451.hp2 HG02486.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-1455_-9-1454del others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764054 | |||||
chr2:11764054
|
ATGTG | A | 11 | a0001c0002t0008g0081a0001c0002t0030g0007a0001c0003t0002g0087others(8): Show | 11 | HG00738.hp1 HG01074.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9-1457_-9-1454del others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764054 | |||||
chr2:11764072
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-1461G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764072 | ||||||
chr2:11764074
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-1459G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764074 | ||||||
chr2:11764074
|
GTGTGTA | G | 18 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0011g0084others(15): Show | 18 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9-1457_-9-1452del others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764074 | |||||
chr2:11764074
|
GTGTGTAT others(3): Show |
G | 2 | a0001c0001t0005g0277a0001c0001t0012g0066 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-9-1457_-9-1448del others(10): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764074 | |||||
chr2:11764076
|
G | A | 13 | a0001c0001t0001g0026a0001c0001t0003g0040a0001c0001t0003g0046others(10): Show | 13 | HG01175.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-1457G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764076 | ||||||
chr2:11764076
|
G | GTATA | 6 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0234others(3): Show | 6 | HG01496.hp2 HG01978.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-1456_-9-1455ins others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764076 | |||||
chr2:11764078
|
G | A | 54 | a0001c0001t0001g0026a0001c0001t0002g0027a0001c0001t0002g0028others(51): Show | 54 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.-9-1455G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764078 | ||||||
chr2:11764078
|
G | GTA | 50 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0167others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-9-1430_-9-1429dup others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764078 | |||||
chr2:11764078
|
G | GTATA | 5 | a0001c0001t0001g0242a0001c0001t0002g0162a0001c0001t0002g0247others(2): Show | 5 | HG01069.hp1 HG01074.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-1432_-9-1429dup others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764078 | |||||
chr2:11764078
|
G | GTATATA | 3 | a0001c0001t0001g0228a0001c0001t0001g0265a0001c0001t0004g0269 | 3 | HG01361.hp2 HG03710.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-9-1434_-9-1429dup others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764078 | |||||
chr2:11764078
|
G | GTGTATAT others(1): Show |
5 | a0001c0001t0001g0250a0001c0001t0001g0271a0001c0001t0004g0211others(2): Show | 5 | HG02056.hp1 HG02071.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-1454_-9-1453ins others(8): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764078 | |||||
chr2:11764078
|
G | GTGTATAT others(3): Show |
2 | a0001c0001t0003g0266a0001c0001t0033g0268 | 2 | NA18747.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.-9-1454_-9-1453ins others(10): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764078 | |||||
chr2:11764078
|
GTA | G | 7 | a0001c0001t0007g0172a0001c0001t0026g0034a0001c0013t0001g0021others(4): Show | 7 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-1430_-9-1429del others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764078 | |||||
chr2:11764078
|
GTATA | G | 6 | a0001c0001t0001g0054a0001c0001t0001g0246a0001c0001t0002g0053others(3): Show | 6 | HG01081.hp2 HG01261.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-1432_-9-1429del others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764078 | |||||
chr2:11764078
|
GTATATAT others(1): Show |
G | 6 | a0001c0001t0002g0060a0001c0001t0002g0063a0001c0001t0002g0064others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-1436_-9-1429del others(8): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764078 | |||||
chr2:11764080
|
A | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0223a0001c0001t0025g0100others(1): Show | 4 | HG01243.hp1 HG02015.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-1453A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764080 | ||||||
chr2:11764086
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-9-1447A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764086 | ||||||
chr2:11764091
|
T | C | 2 | a0001c0002t0002g0014a0001c0002t0003g0015 | 2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-9-1442T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764091 | ||||||
chr2:11764093
|
T | C | 4 | a0001c0002t0002g0014a0001c0002t0003g0015a0001c0002t0030g0007others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-1440T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764093 | ||||||
chr2:11764095
|
T | C | 19 | a0001c0002t0002g0014a0001c0002t0002g0016a0001c0002t0003g0009others(16): Show | 19 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.-9-1438T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764095 | ||||||
chr2:11764097
|
T | C | 30 | a0001c0001t0001g0134a0001c0001t0002g0115a0001c0001t0002g0116others(27): Show | 30 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.-9-1436T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764097 | ||||||
chr2:11764097
|
T | TAC | 46 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0123others(43): Show | 46 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.-9-1435_-9-1434ins others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764097 | |||||
chr2:11764099
|
T | C | 89 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0123others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-9-1434T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764099 | ||||||
chr2:11764099
|
T | TACAC | 5 | a0001c0001t0001g0121a0001c0001t0001g0272a0001c0001t0001g0273others(2): Show | 5 | HG01243.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-1433_-9-1432ins others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764099 | |||||
chr2:11764101
|
T | C | 105 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(102): Show | 105 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.-9-1432T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764101 | ||||||
chr2:11764101
|
T | TAC | 6 | a0001c0001t0003g0057a0001c0001t0003g0058a0001c0001t0003g0059others(3): Show | 6 | HG02723.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-1431_-9-1430ins others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764101 | |||||
chr2:11764103
|
T | C | 124 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.-9-1430T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764103 | ||||||
chr2:11764103
|
T | TAC | 3 | a0001c0001t0003g0033a0001c0001t0008g0038a0001c0001t0008g0044 | 3 | HG00639.hp2 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-9-1414_-9-1413dup others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764103 | |||||
chr2:11764103
|
T | TACACACA others(1): Show |
7 | a0001c0001t0003g0011a0001c0001t0003g0077a0001c0001t0006g0079others(4): Show | 7 | HG02257.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-1420_-9-1413dup others(8): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764103 | |||||
chr2:11764103
|
T | TATAC | 3 | a0001c0001t0003g0031a0001c0001t0005g0030a0001c0001t0018g0032 | 3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-9-1429_-9-1428ins others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764103 | |||||
chr2:11764103
|
T | TATACACA others(3): Show |
3 | a0001c0001t0010g0078a0001c0004t0010g0076a0001c0011t0015g0073 | 3 | HG01261.hp1 HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-9-1429_-9-1428ins others(10): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764103 | |||||
chr2:11764103
|
T | TATATACA others(5): Show |
2 | a0001c0001t0002g0067a0001c0004t0010g0074 | 2 | HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-9-1429_-9-1428ins others(12): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764103 | |||||
chr2:11764105
|
C | T | 8 | a0001c0001t0001g0271a0001c0001t0003g0266a0001c0001t0004g0211others(5): Show | 8 | HG02071.hp1 HG03710.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-1428C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764105 | ||||||
chr2:11764328
|
G | A | 4 | a0001c0001t0001g0167a0001c0001t0003g0166a0001c0001t0003g0168others(1): Show | 4 | HG02132.hp2 HG02155.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-1205G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764328 | ||||||
chr2:11764360
|
T | C | 157 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-9-1173T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764360 | ||||||
chr2:11764436
|
T | G | 1 | a0001c0001t0002g0135 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-9-1097T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764436 | ||||||
chr2:11764535
|
C | T | 2 | a0001c0001t0002g0235a0001c0001t0037g0236 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-9-998C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764535 | ||||||
chr2:11764536
|
A | G | 1 | a0001c0001t0026g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-9-997A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764536 | ||||||
chr2:11764617
|
G | T | 6 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(3): Show | 6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-916G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764617 | ||||||
chr2:11764894
|
A | G | 14 | a0001c0002t0002g0014a0001c0002t0002g0016a0001c0002t0003g0012others(11): Show | 14 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9-639A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764894 | ||||||
chr2:11765191
|
T | C | 67 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-9-342T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11765191 | ||||||
chr2:11765264
|
G | C | 1 | a0001c0001t0005g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-9-269G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11765264 | ||||||
chr2:11765291
|
T | C | 1 | a0001c0003t0001g0048 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-9-242T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11765291 | ||||||
chr2:11765341
|
C | T | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-9-192C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11765341 | ||||||
chr2:11765372
|
C | T | 14 | a0001c0002t0002g0014a0001c0002t0002g0016a0001c0002t0003g0012others(11): Show | 14 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9-161C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11765372 | ||||||
chr2:11765413
|
A | G | 1 | a0001c0001t0003g0083 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-9-120A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11765413 | ||||||
chr2:11765510
|
GT | G | 152 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(149): Show | 152 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.-9-14delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11765510 | |||||
chr2:11765512
|
T | G | 2 | a0001c0001t0002g0027a0001c0001t0002g0028 | 2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-9-21T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11765512 | ||||||
chr2:11765750
|
C | T | 62 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(59): Show | 62 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.192+17C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11765750 | ||||||
chr2:11765819
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.192+86T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11765819 | ||||||
chr2:11765880
|
T | C | 5 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(2): Show | 5 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+147T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11765880 | ||||||
chr2:11765904
|
C | T | 14 | a0001c0001t0001g0026a0001c0001t0002g0060a0001c0001t0002g0063others(11): Show | 14 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.192+171C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11765904 | ||||||
chr2:11765923
|
G | A | 5 | a0001c0001t0001g0121a0001c0001t0001g0272a0001c0001t0001g0273others(2): Show | 5 | HG02738.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+190G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11765923 | ||||||
chr2:11765930
|
A | C | 13 | a0001c0001t0002g0067a0001c0001t0003g0011a0001c0001t0003g0077others(10): Show | 13 | HG01261.hp1 HG01934.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.192+197A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11765930 | ||||||
chr2:11765968
|
G | A | 1 | a0001c0002t0003g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.192+235G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11765968 | ||||||
chr2:11766111
|
C | T | 13 | a0001c0001t0002g0067a0001c0001t0003g0011a0001c0001t0003g0077others(10): Show | 13 | HG01261.hp1 HG01934.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.192+378C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766111 | ||||||
chr2:11766258
|
T | C | 6 | a0001c0001t0003g0055a0001c0001t0003g0057a0001c0001t0003g0058others(3): Show | 6 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.192+525T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766258 | ||||||
chr2:11766261
|
C | A | 10 | a0001c0003t0001g0048a0001c0003t0002g0052a0001c0003t0002g0087others(7): Show | 10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.192+528C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766261 | ||||||
chr2:11766262
|
G | A | 1 | a0001c0001t0003g0213 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.192+529G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766262 | ||||||
chr2:11766291
|
G | GC | 12 | a0001c0001t0003g0040a0001c0001t0003g0046a0001c0001t0005g0042others(9): Show | 12 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.192+560dupC | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr2 | 11766291 | |||||
chr2:11766370
|
A | G | 1 | a0001c0001t0005g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.192+637A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766370 | ||||||
chr2:11766378
|
G | A | 5 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(2): Show | 5 | HG00099.hp1 HG00280.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+645G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766378 | ||||||
chr2:11766549
|
G | T | 1 | a0001c0001t0002g0194 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.192+816G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766549 | ||||||
chr2:11766623
|
C | T | 1 | a0001c0001t0004g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.192+890C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766623 | ||||||
chr2:11766762
|
AACAAAC | A | 89 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(86): Show | 89 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.193-993_193-988del others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr2 | 11766762 | |||||
chr2:11766768
|
CACAA | C | 3 | a0001c0001t0001g0164a0001c0001t0006g0163a0001c0001t0022g0160 | 3 | HG02257.hp1 HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.193-969_193-966del others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr2 | 11766768 | |||||
chr2:11766768
|
CACAAACA others(5): Show |
C | 3 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0003g0138 | 3 | HG00558.hp2 NA19009.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.193-977_193-966del others(12): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr2 | 11766768 | |||||
chr2:11766903
|
G | A | 6 | a0001c0001t0002g0060a0001c0001t0002g0063a0001c0001t0002g0064others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-860G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766903 | ||||||
chr2:11766915
|
C | T | 1 | a0001c0001t0005g0092 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.193-848C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766915 | ||||||
chr2:11766988
|
A | AG | 18 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0005g0277others(15): Show | 18 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.193-770dupG | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr2 | 11766988 | |||||
chr2:11766995
|
C | G | 2 | a0001c0001t0008g0019a0001c0001t0010g0020 | 2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.193-768C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766995 | ||||||
chr2:11767077
|
C | G | 5 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(2): Show | 5 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-686C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11767077 | ||||||
chr2:11767109
|
A | G | 2 | a0001c0001t0007g0172a0001c0001t0007g0188 | 2 | HG01258.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.193-654A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11767109 | ||||||
chr2:11767124
|
G | A | 1 | a0001c0001t0005g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.193-639G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11767124 | ||||||
chr2:11767140
|
T | C | 1 | a0001c0001t0024g0195 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.193-623T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11767140 | ||||||
chr2:11767386
|
C | G | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.193-377C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11767386 | ||||||
chr2:11767666
|
C | G | 3 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0004t0007g0274 | 3 | HG01109.hp2 HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.193-97C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11767666 | ||||||
chr2:11767716
|
C | T | 19 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0005g0277others(16): Show | 19 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.193-47C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11767716 | ||||||
chr2:11767720
|
G | T | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.193-43G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11767720 | ||||||
chr2:11768012
|
T | C | 5 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158others(2): Show | 5 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.288+154T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768012 | ||||||
chr2:11768158
|
C | T | 1 | a0001c0001t0005g0092 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.288+300C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768158 | ||||||
chr2:11768184
|
T | A | 11 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158others(8): Show | 11 | HG01070.hp2 HG01109.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.288+326T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768184 | ||||||
chr2:11768663
|
A | G | 1 | a0001c0001t0002g0101 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.288+805A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768663 | ||||||
chr2:11768664
|
T | C | 1 | a0001c0001t0002g0101 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.288+806T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768664 | ||||||
chr2:11768795
|
G | A | 3 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158 | 3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.288+937G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768795 | ||||||
chr2:11768830
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.288+972G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768830 | ||||||
chr2:11768852
|
C | T | 148 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(145): Show | 148 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.288+994C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768852 | ||||||
chr2:11768922
|
C | T | 1 | a0001c0004t0006g0072 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.288+1064C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768922 | ||||||
chr2:11768967
|
C | A | 1 | a0001c0001t0003g0114 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.288+1109C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768967 | ||||||
chr2:11768976
|
C | A | 6 | a0001c0001t0003g0055a0001c0001t0003g0057a0001c0001t0003g0058others(3): Show | 6 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.288+1118C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768976 | ||||||
chr2:11769005
|
G | A | 35 | a0001c0001t0003g0040a0001c0001t0003g0046a0001c0001t0005g0042others(32): Show | 35 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.288+1147G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11769005 | ||||||
chr2:11769013
|
CA | C | 17 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0011g0084others(14): Show | 17 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+1157delA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr2 | 11769013 | |||||
chr2:11769016
|
C | T | 17 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0011g0084others(14): Show | 17 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+1158C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11769016 | ||||||
chr2:11769017
|
A | G | 17 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0011g0084others(14): Show | 17 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+1159A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11769017 | ||||||
chr2:11769267
|
G | A | 11 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158others(8): Show | 11 | HG01070.hp2 HG01109.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.288+1409G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11769267 | ||||||
chr2:11769400
|
G | T | 1 | a0001c0002t0008g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.288+1542G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11769400 | ||||||
chr2:11769545
|
A | G | 2 | a0001c0001t0008g0019a0001c0001t0010g0020 | 2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.288+1687A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11769545 | ||||||
chr2:11769591
|
AT | A | 9 | a0001c0001t0003g0055a0001c0001t0003g0057a0001c0001t0003g0058others(6): Show | 9 | HG01884.hp1 HG02615.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.288+1744delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr2 | 11769591 | |||||
chr2:11769603
|
A | T | 1 | a0001c0001t0002g0101 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.288+1745A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11769603 | ||||||
chr2:11770265
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.289-1107G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770265 | ||||||
chr2:11770314
|
A | T | 1 | a0001c0001t0009g0229 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.289-1058A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770314 | ||||||
chr2:11770370
|
C | G | 1 | a0001c0001t0005g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.289-1002C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770370 | ||||||
chr2:11770432
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.289-940C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770432 | ||||||
chr2:11770495
|
C | T | 13 | a0001c0001t0003g0040a0001c0001t0003g0046a0001c0001t0005g0042others(10): Show | 13 | HG00639.hp2 HG01175.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.289-877C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770495 | ||||||
chr2:11770592
|
C | T | 59 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(56): Show | 59 | HG01070.hp2 HG01109.hp1 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.289-780C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770592 | ||||||
chr2:11770625
|
A | G | 2 | a0001c0001t0006g0079a0001c0001t0028g0080 | 2 | HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.289-747A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770625 | ||||||
chr2:11770673
|
A | G | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.289-699A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770673 | ||||||
chr2:11770775
|
T | C | 14 | a0001c0001t0001g0026a0001c0001t0002g0060a0001c0001t0002g0063others(11): Show | 14 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.289-597T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770775 | ||||||
chr2:11770877
|
C | T | 90 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(87): Show | 90 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.289-495C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770877 | ||||||
chr2:11770929
|
TACA | T | 21 | a0001c0002t0002g0014a0001c0002t0002g0016a0001c0002t0003g0009others(18): Show | 21 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.289-442_289-440del others(3): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770929 | ||||||
chr2:11770948
|
GTCTT | G | 17 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0011g0084others(14): Show | 17 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.289-420_289-417del others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr2 | 11770948 | |||||
chr2:11771820
|
G | A | 7 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0011g0084others(4): Show | 7 | HG01109.hp2 HG02922.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.596+141G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11771820 | ||||||
chr2:11771831
|
G | T | 18 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0011g0084others(15): Show | 18 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.596+152G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11771831 | ||||||
chr2:11771855
|
C | G | 17 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0011g0084others(14): Show | 17 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.596+176C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11771855 | ||||||
chr2:11772010
|
C | T | 23 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158others(20): Show | 23 | HG00639.hp2 HG01070.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.596+331C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772010 | ||||||
chr2:11772072
|
G | A | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.596+393G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772072 | ||||||
chr2:11772119
|
C | G | 1 | a0001c0001t0026g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.596+440C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772119 | ||||||
chr2:11772196
|
C | T | 18 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0011g0084others(15): Show | 18 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.596+517C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772196 | ||||||
chr2:11772225
|
C | G | 6 | a0001c0001t0003g0055a0001c0001t0003g0057a0001c0001t0003g0058others(3): Show | 6 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+546C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772225 | ||||||
chr2:11772257
|
T | G | 1 | a0001c0001t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.596+578T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772257 | ||||||
chr2:11772265
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.596+586G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772265 | ||||||
chr2:11772281
|
G | T | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.596+602G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772281 | ||||||
chr2:11772367
|
A | G | 6 | a0001c0001t0002g0060a0001c0001t0002g0063a0001c0001t0002g0064others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+688A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772367 | ||||||
chr2:11772403
|
C | G | 3 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158 | 3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.596+724C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772403 | ||||||
chr2:11772509
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.596+830C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772509 | ||||||
chr2:11772670
|
G | A | 5 | a0001c0001t0003g0055a0001c0001t0003g0057a0001c0001t0003g0058others(2): Show | 5 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.597-950G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772670 | ||||||
chr2:11772779
|
C | T | 8 | a0001c0001t0001g0026a0001c0001t0002g0060a0001c0001t0002g0063others(5): Show | 8 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.597-841C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772779 | ||||||
chr2:11772932
|
CTCTA | C | 164 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(161): Show | 164 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(161): Show |
intron_variant | MODIFIER | c.597-683_597-680del others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr2 | 11772932 | |||||
chr2:11772965
|
G | A | 3 | a0001c0002t0003g0009a0001c0002t0003g0010a0002c0010t0005g0008 | 3 | HG02280.hp1 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.597-655G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772965 | ||||||
chr2:11773119
|
C | T | 120 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(117): Show | 120 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.597-501C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11773119 | ||||||
chr2:11773260
|
G | A | 47 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158others(44): Show | 47 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.597-360G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11773260 | ||||||
chr2:11773303
|
G | C | 2 | a0003c0006t0004g0105a0003c0006t0004g0174 | 2 | HG01243.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.597-317G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11773303 | ||||||
chr2:11773312
|
C | T | 62 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(59): Show | 62 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.597-308C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11773312 | ||||||
chr2:11773422
|
C | G | 2 | a0001c0002t0006g0153a0001c0002t0006g0155 | 2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.597-198C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11773422 | ||||||
chr2:11773602
|
T | A | 8 | a0001c0001t0001g0026a0001c0001t0002g0060a0001c0001t0002g0063others(5): Show | 8 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.597-18T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11773602 | ||||||
chr2:11773775
|
T | A | 1 | a0001c0001t0001g0237 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.722+30T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11773775 | ||||||
chr2:11773793
|
A | T | 1 | a0001c0001t0003g0213 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.722+48A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11773793 | ||||||
chr2:11774091
|
G | A | 1 | a0001c0001t0004g0124 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.722+346G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11774091 | ||||||
chr2:11774681
|
C | T | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.722+936C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11774681 | ||||||
chr2:11774815
|
C | T | 61 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(58): Show | 61 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.722+1070C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11774815 | ||||||
chr2:11774948
|
G | T | 3 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158 | 3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.723-1138G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11774948 | ||||||
chr2:11774965
|
T | TAAAA | 13 | a0001c0001t0001g0026a0001c0001t0002g0060a0001c0001t0002g0063others(10): Show | 13 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.723-1108_723-1105d others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 11774965 | |||||
chr2:11775095
|
A | T | 152 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(149): Show | 152 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.723-991A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775095 | ||||||
chr2:11775119
|
A | G | 1 | a0001c0001t0006g0079 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.723-967A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775119 | ||||||
chr2:11775158
|
A | C | 152 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(149): Show | 152 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.723-928A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775158 | ||||||
chr2:11775314
|
A | G | 1 | a0001c0001t0003g0099 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.723-772A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775314 | ||||||
chr2:11775334
|
A | G | 6 | a0001c0001t0002g0060a0001c0001t0002g0063a0001c0001t0002g0064others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.723-752A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775334 | ||||||
chr2:11775404
|
C | T | 1 | a0001c0001t0004g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.723-682C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775404 | ||||||
chr2:11775414
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.723-672G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775414 | ||||||
chr2:11775481
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.723-605G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775481 | ||||||
chr2:11775569
|
C | A | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.723-517C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775569 | ||||||
chr2:11775640
|
G | T | 1 | a0001c0001t0001g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.723-446G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775640 | ||||||
chr2:11775777
|
T | TTCTTTAT others(2307): Show |
1 | a0001c0001t0017g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.723-296_723-295ins others(2314): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 11775777 | |||||
chr2:11775777
|
T | TTCTTTAT others(2306): Show |
1 | a0001c0001t0017g0062 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.723-296_723-295ins others(2313): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 11775777 | |||||
chr2:11775777
|
T | TTCTTTAT others(2305): Show |
3 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065 | 3 | HG02559.hp2 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.723-296_723-295ins others(2312): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 11775777 | |||||
chr2:11775777
|
T | TTCTTTAT others(2304): Show |
1 | a0001c0001t0002g0060 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.723-296_723-295ins others(2311): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 11775777 | |||||
chr2:11775881
|
T | TTATATAT others(29): Show |
1 | a0001c0001t0012g0251 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.723-203_723-168dup others(36): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 11775881 | |||||
chr2:11775883
|
A | ATATATAA others(29): Show |
1 | a0001c0001t0005g0075 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.723-191_723-156dup others(36): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 11775883 | |||||
chr2:11775915
|
T | C | 12 | a0001c0001t0003g0040a0001c0001t0003g0046a0001c0001t0005g0042others(9): Show | 12 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.723-171T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775915 | ||||||
chr2:11775929
|
TTATA | T | 12 | a0001c0001t0003g0040a0001c0001t0003g0046a0001c0001t0005g0042others(9): Show | 12 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.723-152_723-149del others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 11775929 | |||||
chr2:11776229
|
A | G | 12 | a0001c0001t0003g0040a0001c0001t0003g0046a0001c0001t0005g0042others(9): Show | 12 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.830+36A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11776229 | ||||||
chr2:11776395
|
T | C | 1 | a0002c0010t0005g0008 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.830+202T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11776395 | ||||||
chr2:11776406
|
C | T | 14 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0127others(11): Show | 14 | HG00609.hp1 HG02056.hp2 NA18943.hp2 others(11): Show |
intron_variant | MODIFIER | c.830+213C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11776406 | ||||||
chr2:11776432
|
AT | A | 16 | a0001c0001t0001g0026a0001c0001t0002g0060a0001c0001t0002g0063others(13): Show | 16 | HG00558.hp1 HG01516.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.830+254delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr2 | 11776432 | |||||
chr2:11776622
|
A | G | 5 | a0001c0001t0003g0055a0001c0001t0003g0057a0001c0001t0003g0058others(2): Show | 5 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.830+429A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11776622 | ||||||
chr2:11776678
|
C | T | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.830+485C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11776678 | ||||||
chr2:11776893
|
G | T | 14 | a0001c0001t0002g0067a0001c0001t0003g0011a0001c0001t0003g0077others(11): Show | 14 | HG01261.hp1 HG01934.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.830+700G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11776893 | ||||||
chr2:11776979
|
A | G | 14 | a0001c0001t0002g0067a0001c0001t0003g0011a0001c0001t0003g0077others(11): Show | 14 | HG01261.hp1 HG01934.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.830+786A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11776979 | ||||||
chr2:11776990
|
T | A | 93 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0002g0053others(90): Show | 93 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.830+797T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11776990 | ||||||
chr2:11777139
|
C | A | 1 | a0001c0001t0004g0261 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.830+946C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777139 | ||||||
chr2:11777152
|
T | C | 63 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.830+959T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777152 | ||||||
chr2:11777240
|
T | G | 1 | a0003c0006t0004g0105 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.830+1047T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777240 | ||||||
chr2:11777386
|
G | A | 14 | a0001c0001t0001g0026a0001c0001t0002g0060a0001c0001t0002g0063others(11): Show | 14 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.830+1193G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777386 | ||||||
chr2:11777393
|
G | A | 121 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.830+1200G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777393 | ||||||
chr2:11777402
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.830+1209A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777402 | ||||||
chr2:11777431
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.830+1238C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777431 | ||||||
chr2:11777583
|
C | T | 1 | a0001c0001t0026g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.830+1390C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777583 | ||||||
chr2:11777651
|
C | T | 1 | a0001c0001t0012g0216 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.830+1458C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777651 | ||||||
chr2:11777719
|
C | T | 7 | a0001c0013t0001g0021a0002c0007t0011g0025a0002c0007t0034g0023others(4): Show | 7 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.830+1526C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777719 | ||||||
chr2:11777779
|
T | C | 89 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0121others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.830+1586T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777779 | ||||||
chr2:11777907
|
A | G | 20 | a0001c0001t0002g0067a0001c0001t0005g0082a0001c0001t0008g0006others(17): Show | 20 | HG01261.hp1 HG01934.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.831-1612A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777907 | ||||||
chr2:11778025
|
C | T | 1 | a0001c0001t0005g0075 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.831-1494C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11778025 | ||||||
chr2:11778138
|
G | GT | 147 | a0001c0001t0001g0054a0001c0001t0001g0103a0001c0001t0001g0107others(144): Show | 147 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.831-1381_831-1380i others(3): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11778138 | ||||||
chr2:11778139
|
G | T | 9 | a0001c0001t0001g0026a0001c0001t0003g0055a0001c0001t0003g0057others(6): Show | 9 | HG00639.hp2 HG02615.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.831-1380G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11778139 | ||||||
chr2:11778144
|
G | C | 147 | a0001c0001t0001g0054a0001c0001t0001g0103a0001c0001t0001g0107others(144): Show | 147 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.831-1375G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11778144 | ||||||
chr2:11778582
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0025g0100 | 2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.831-937G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11778582 | ||||||
chr2:11778638
|
C | T | 1 | a0001c0004t0010g0076 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.831-881C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11778638 | ||||||
chr2:11778871
|
G | A | 21 | a0001c0001t0002g0060a0001c0001t0002g0063a0001c0001t0002g0064others(18): Show | 21 | HG01175.hp2 HG01891.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.831-648G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11778871 | ||||||
chr2:11778962
|
T | C | 1 | a0001c0001t0004g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.831-557T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11778962 | ||||||
chr2:11779049
|
A | G | 88 | a0001c0001t0001g0054a0001c0001t0001g0103a0001c0001t0001g0121others(85): Show | 88 | HG00099.hp2 HG01070.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.831-470A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11779049 | ||||||
chr2:11779372
|
G | A | 44 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0127others(41): Show | 44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.831-147G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11779372 | ||||||
chr2:11779775
|
G | T | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.957+130G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11779775 | ||||||
chr2:11779881
|
CT | C | 16 | a0001c0001t0003g0040a0001c0001t0003g0046a0001c0001t0005g0042others(13): Show | 16 | HG01175.hp2 HG01891.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.957+250delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr2 | 11779881 | |||||
chr2:11779894
|
T | G | 6 | a0001c0001t0001g0228a0001c0001t0004g0189a0001c0001t0004g0204others(3): Show | 6 | HG00738.hp2 HG01255.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.957+249T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11779894 | ||||||
chr2:11779898
|
TGA | T | 10 | a0001c0003t0001g0048a0001c0003t0002g0052a0001c0003t0002g0087others(7): Show | 10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.957+256_957+257del others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr2 | 11779898 | |||||
chr2:11779924
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.957+279G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11779924 | ||||||
chr2:11780021
|
C | G | 62 | a0001c0001t0001g0103a0001c0001t0001g0121a0001c0001t0001g0272others(59): Show | 62 | HG00099.hp2 HG01175.hp2 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.957+376C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780021 | ||||||
chr2:11780073
|
G | C | 46 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0127others(43): Show | 46 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.957+428G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780073 | ||||||
chr2:11780081
|
G | A | 3 | a0001c0001t0003g0011a0001c0001t0003g0077a0001c0001t0005g0075 | 3 | HG02451.hp1 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.957+436G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780081 | ||||||
chr2:11780095
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.957+450G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780095 | ||||||
chr2:11780171
|
G | A | 2 | a0001c0002t0015g0152a0001c0002t0015g0156 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.957+526G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780171 | ||||||
chr2:11780415
|
G | C | 2 | a0001c0005t0007g0017a0001c0005t0007g0018 | 2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.957+770G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780415 | ||||||
chr2:11780619
|
G | A | 3 | a0001c0001t0003g0011a0001c0001t0003g0077a0001c0001t0005g0075 | 3 | HG02451.hp1 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.957+974G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780619 | ||||||
chr2:11780658
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0003g0140 | 2 | HG00609.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.957+1013G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780658 | ||||||
chr2:11780864
|
G | C | 1 | a0001c0001t0007g0188 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.957+1219G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780864 | ||||||
chr2:11781237
|
G | A | 1 | a0001c0001t0002g0244 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.958-964G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11781237 | ||||||
chr2:11781364
|
A | C | 2 | a0001c0001t0001g0121a0001c0001t0025g0100 | 2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.958-837A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11781364 | ||||||
chr2:11781379
|
A | G | 2 | a0001c0001t0002g0170a0001c0001t0002g0171 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.958-822A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11781379 | ||||||
chr2:11781571
|
T | C | 268 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.958-630T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11781571 | ||||||
chr2:11781770
|
G | T | 1 | a0001c0001t0001g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.958-431G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11781770 | ||||||
chr2:11781928
|
A | G | 67 | a0001c0001t0001g0103a0001c0001t0001g0121a0001c0001t0001g0272others(64): Show | 67 | HG00099.hp2 HG00738.hp2 HG01167.hp2 others(64): Show |
intron_variant | MODIFIER | c.958-273A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11781928 | ||||||
chr2:11782005
|
A | G | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.958-196A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11782005 | ||||||
chr2:11782622
|
A | C | 1 | a0001c0002t0008g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1264+115A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11782622 | ||||||
chr2:11782729
|
A | G | 63 | a0001c0001t0001g0054a0001c0001t0001g0107a0001c0001t0001g0123others(60): Show | 63 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.1264+222A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11782729 | ||||||
chr2:11782780
|
C | T | 29 | a0001c0001t0001g0103a0001c0001t0001g0121a0001c0001t0001g0272others(26): Show | 29 | HG00099.hp2 HG00738.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1264+273C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11782780 | ||||||
chr2:11782861
|
C | T | 44 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0127others(41): Show | 44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1264+354C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11782861 | ||||||
chr2:11783053
|
C | T | 61 | a0001c0001t0001g0103a0001c0001t0001g0121a0001c0001t0001g0272others(58): Show | 61 | HG00099.hp2 HG00738.hp2 HG01175.hp2 others(58): Show |
intron_variant | MODIFIER | c.1264+546C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783053 | ||||||
chr2:11783135
|
C | T | 1 | a0001c0001t0003g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1264+628C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783135 | ||||||
chr2:11783209
|
C | T | 6 | a0001c0003t0001g0048a0001c0003t0002g0052a0001c0003t0009g0049others(3): Show | 6 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1265-620C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783209 | ||||||
chr2:11783219
|
G | A | 3 | a0001c0001t0005g0277a0001c0001t0008g0038a0001c0001t0008g0044 | 3 | HG00639.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1265-610G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783219 | ||||||
chr2:11783282
|
A | G | 44 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0127others(41): Show | 44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1265-547A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783282 | ||||||
chr2:11783292
|
A | G | 168 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(165): Show | 168 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.1265-537A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783292 | ||||||
chr2:11783497
|
C | T | 19 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158others(16): Show | 19 | HG01109.hp1 HG01175.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1265-332C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783497 | ||||||
chr2:11783526
|
C | T | 5 | a0001c0001t0002g0180a0001c0001t0003g0178a0001c0001t0003g0190others(2): Show | 5 | HG00423.hp1 HG01255.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1265-303C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783526 | ||||||
chr2:11783549
|
A | G | 23 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158others(20): Show | 23 | HG01109.hp1 HG01175.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.1265-280A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783549 | ||||||
chr2:11783761
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1265-68A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783761 | ||||||
chr2:11784033
|
G | A | 1 | a0001c0001t0009g0108 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1358+111G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784033 | ||||||
chr2:11784167
|
G | A | 43 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0127others(40): Show | 43 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1358+245G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784167 | ||||||
chr2:11784289
|
GTGAGACT others(53): Show |
G | 48 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0127others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1358+369_1358+428d others(62): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr2 | 11784289 | |||||
chr2:11784303
|
C | CA | 22 | a0001c0001t0001g0026a0001c0001t0002g0027a0001c0001t0002g0028others(19): Show | 22 | HG01175.hp1 HG01496.hp2 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.1358+402dupA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr2 | 11784303 | |||||
chr2:11784303
|
C | CAA | 45 | a0001c0001t0001g0103a0001c0001t0001g0272a0001c0001t0001g0273others(42): Show | 45 | HG00738.hp2 HG01167.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.1358+401_1358+402d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr2 | 11784303 | |||||
chr2:11784303
|
C | CAAA | 11 | a0001c0001t0002g0101a0001c0001t0004g0204a0001c0001t0005g0082others(8): Show | 11 | HG00099.hp2 HG01109.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.1358+400_1358+402d others(5): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr2 | 11784303 | |||||
chr2:11784303
|
C | CAAAAA | 8 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0060others(5): Show | 8 | HG01109.hp1 HG01261.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358+398_1358+402d others(7): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr2 | 11784303 | |||||
chr2:11784303
|
C | CACAAAAA | 9 | a0001c0001t0003g0040a0001c0001t0003g0046a0001c0001t0005g0042others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1358+382_1358+383i others(9): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr2 | 11784303 | |||||
chr2:11784303
|
CA | C | 11 | a0001c0001t0002g0202a0001c0001t0003g0055a0001c0001t0003g0057others(8): Show | 11 | HG01070.hp1 HG01515.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.1358+402delA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr2 | 11784303 | |||||
chr2:11784352
|
C | T | 48 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0127others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1358+430C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784352 | ||||||
chr2:11784438
|
C | T | 1 | a0001c0001t0002g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1359-448C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784438 | ||||||
chr2:11784502
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1359-384T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784502 | ||||||
chr2:11784692
|
T | G | 14 | a0001c0001t0003g0040a0001c0001t0003g0046a0001c0001t0005g0042others(11): Show | 14 | HG01175.hp2 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1359-194T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784692 | ||||||
chr2:11784813
|
T | C | 1 | a0001c0001t0002g0147 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1359-73T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784813 | ||||||
chr2:11784824
|
T | C | 166 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(163): Show | 166 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.1359-62T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784824 | ||||||
chr2:11784835
|
C | G | 2 | a0001c0002t0002g0014a0001c0002t0003g0015 | 2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1359-51C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784835 | ||||||
chr2:11785209
|
A | G | 54 | a0001c0001t0001g0103a0001c0001t0001g0121a0001c0001t0001g0272others(51): Show | 54 | HG00099.hp2 HG00738.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.1549+133A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785209 | ||||||
chr2:11785372
|
T | C | 2 | a0001c0002t0015g0152a0001c0002t0015g0156 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1549+296T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785372 | ||||||
chr2:11785403
|
G | C | 1 | a0001c0001t0005g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1549+327G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785403 | ||||||
chr2:11785430
|
T | G | 6 | a0001c0001t0005g0082a0001c0001t0005g0091a0001c0001t0005g0092others(3): Show | 6 | HG02922.hp1 HG02922.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1549+354T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785430 | ||||||
chr2:11785656
|
C | T | 53 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0127others(50): Show | 53 | HG00558.hp2 HG00609.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1549+580C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785656 | ||||||
chr2:11785666
|
A | T | 6 | a0001c0001t0005g0082a0001c0001t0005g0091a0001c0001t0005g0092others(3): Show | 6 | HG02922.hp1 HG02922.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1549+590A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785666 | ||||||
chr2:11785765
|
T | G | 61 | a0001c0001t0001g0054a0001c0001t0001g0107a0001c0001t0001g0123others(58): Show | 61 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.1549+689T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785765 | ||||||
chr2:11785774
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1549+698G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785774 | ||||||
chr2:11785809
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1549+733C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785809 | ||||||
chr2:11785937
|
A | T | 1 | a0001c0001t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1549+861A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785937 | ||||||
chr2:11785938
|
C | T | 1 | a0001c0001t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1549+862C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785938 | ||||||
chr2:11786157
|
G | C | 6 | a0001c0001t0005g0082a0001c0001t0005g0091a0001c0001t0005g0092others(3): Show | 6 | HG02922.hp1 HG02922.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1550-917G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786157 | ||||||
chr2:11786245
|
T | G | 1 | a0004c0012t0001g0198 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1550-829T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786245 | ||||||
chr2:11786315
|
G | A | 1 | a0001c0001t0008g0044 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1550-759G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786315 | ||||||
chr2:11786479
|
A | G | 6 | a0001c0002t0008g0081a0002c0007t0011g0025a0002c0007t0034g0023others(3): Show | 6 | HG01167.hp2 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1550-595A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786479 | ||||||
chr2:11786568
|
C | T | 2 | a0001c0002t0015g0152a0001c0002t0015g0156 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1550-506C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786568 | ||||||
chr2:11786706
|
C | T | 1 | a0001c0002t0008g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1550-368C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786706 | ||||||
chr2:11786728
|
C | A | 1 | a0001c0001t0002g0143 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1550-346C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786728 | ||||||
chr2:11786844
|
C | T | 1 | a0001c0002t0002g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1550-230C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786844 | ||||||
chr2:11786957
|
A | G | 1 | a0001c0001t0003g0083 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1550-117A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786957 | ||||||
chr2:11787326
|
A | C | 1 | a0001c0001t0011g0217 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1643+159A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787326 | ||||||
chr2:11787376
|
A | G | 1 | a0001c0001t0003g0099 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1643+209A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787376 | ||||||
chr2:11787392
|
C | CT | 12 | a0001c0001t0001g0144a0001c0001t0001g0259a0001c0001t0001g0260others(9): Show | 12 | HG00673.hp1 HG00735.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.1643+230dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787392 | |||||
chr2:11787392
|
C | CTT | 33 | a0001c0001t0001g0054a0001c0001t0001g0107a0001c0001t0001g0123others(30): Show | 33 | HG00558.hp2 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1643+229_1643+230d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787392 | |||||
chr2:11787392
|
C | CTTT | 9 | a0001c0001t0002g0135a0001c0001t0002g0143a0001c0001t0003g0140others(6): Show | 9 | HG02055.hp2 HG02056.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1643+228_1643+230d others(5): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787392 | |||||
chr2:11787392
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0005g0082a0001c0001t0005g0091a0001c0001t0005g0092 | 3 | HG02922.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1643+230_1643+231i others(14): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787392 | |||||
chr2:11787392
|
C | CTTTTTTT others(13): Show |
1 | a0001c0008t0005g0002 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1643+230_1643+231i others(22): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787392 | |||||
chr2:11787392
|
C | CTTTTTTT others(14): Show |
1 | a0001c0002t0030g0007 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1643+230_1643+231i others(23): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787392 | |||||
chr2:11787392
|
C | CTTTTTTT others(18): Show |
1 | a0001c0008t0005g0003 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1643+230_1643+231i others(27): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787392 | |||||
chr2:11787396
|
TTC | T | 17 | a0001c0001t0002g0147a0001c0001t0002g0171a0001c0001t0008g0019others(14): Show | 17 | HG00738.hp1 HG01109.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.1643+231_1643+232d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787396 | |||||
chr2:11787397
|
TC | T | 63 | a0001c0001t0001g0103a0001c0001t0001g0121a0001c0001t0002g0028others(60): Show | 63 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.1643+231delC | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787397 | ||||||
chr2:11787398
|
C | T | 85 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0107others(82): Show | 85 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1643+231C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787398 | ||||||
chr2:11787566
|
C | T | 43 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0127others(40): Show | 43 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1643+399C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787566 | ||||||
chr2:11787615
|
G | A | 2 | a0001c0002t0015g0152a0001c0002t0015g0156 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1643+448G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787615 | ||||||
chr2:11787626
|
C | G | 2 | a0001c0002t0015g0152a0001c0002t0015g0156 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1643+459C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787626 | ||||||
chr2:11787781
|
G | A | 2 | a0001c0002t0015g0152a0001c0002t0015g0156 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1644-606G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787781 | ||||||
chr2:11787857
|
C | T | 2 | a0001c0001t0002g0027a0001c0001t0002g0028 | 2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1644-530C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787857 | ||||||
chr2:11787865
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1644-522T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787865 | ||||||
chr2:11787898
|
G | A | 2 | a0001c0001t0006g0079a0001c0001t0028g0080 | 2 | HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1644-489G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787898 | ||||||
chr2:11787940
|
C | CA | 39 | a0001c0001t0001g0026a0001c0001t0002g0027a0001c0001t0002g0028others(36): Show | 39 | HG00639.hp2 HG01175.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.1644-432dupA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787940 | |||||
chr2:11788123
|
C | T | 6 | a0001c0001t0002g0060a0001c0001t0002g0063a0001c0001t0002g0064others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1644-264C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11788123 | ||||||
chr2:11788172
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1644-215G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11788172 | ||||||
chr2:11788188
|
T | C | 5 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158others(2): Show | 5 | HG01261.hp2 HG01981.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1644-199T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11788188 | ||||||
chr2:11788287
|
G | A | 2 | a0001c0001t0008g0019a0001c0001t0010g0020 | 2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1644-100G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11788287 | ||||||
chr2:11788351
|
C | T | 3 | a0001c0001t0005g0277a0001c0001t0008g0038a0001c0001t0008g0044 | 3 | HG00639.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1644-36C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11788351 | ||||||
chr2:11788543
|
G | A | 5 | a0002c0007t0011g0025a0002c0007t0034g0023a0002c0007t0035g0024others(2): Show | 5 | HG01167.hp2 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1713+87G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11788543 | ||||||
chr2:11788682
|
G | A | 5 | a0001c0001t0002g0194a0001c0001t0004g0212a0001c0001t0004g0230others(2): Show | 5 | NA18747.hp2 NA18983.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.1713+226G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11788682 | ||||||
chr2:11788732
|
G | C | 1 | a0001c0001t0004g0204 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1713+276G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11788732 | ||||||
chr2:11788997
|
G | A | 1 | a0001c0001t0013g0133 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1713+541G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11788997 | ||||||
chr2:11789140
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1713+684A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789140 | ||||||
chr2:11789186
|
G | A | 1 | a0001c0002t0008g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1713+730G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789186 | ||||||
chr2:11789198
|
G | C | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1713+742G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789198 | ||||||
chr2:11789202
|
A | T | 108 | a0001c0001t0001g0026a0001c0001t0001g0103a0001c0001t0001g0121others(105): Show | 108 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(105): Show |
intron_variant | MODIFIER | c.1713+746A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789202 | ||||||
chr2:11789267
|
T | TTG | 5 | a0001c0001t0001g0271a0001c0001t0004g0219a0001c0001t0013g0220others(2): Show | 5 | HG00609.hp2 HG01934.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1713+830_1713+831d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr2 | 11789267 | |||||
chr2:11789273
|
G | A | 167 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(164): Show | 167 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.1713+817G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789273 | ||||||
chr2:11789333
|
G | A | 3 | a0001c0001t0003g0011a0001c0001t0003g0077a0001c0001t0005g0075 | 3 | HG02451.hp1 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1713+877G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789333 | ||||||
chr2:11789338
|
T | C | 44 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0127others(41): Show | 44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1713+882T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789338 | ||||||
chr2:11789357
|
G | A | 12 | a0001c0001t0001g0026a0001c0001t0002g0027a0001c0001t0002g0028others(9): Show | 12 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1713+901G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789357 | ||||||
chr2:11789386
|
C | T | 6 | a0001c0001t0002g0060a0001c0001t0002g0063a0001c0001t0002g0064others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1713+930C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789386 | ||||||
chr2:11789484
|
G | A | 1 | a0001c0001t0002g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1713+1028G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789484 | ||||||
chr2:11789486
|
A | G | 6 | a0001c0002t0008g0081a0002c0007t0011g0025a0002c0007t0034g0023others(3): Show | 6 | HG01167.hp2 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1713+1030A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789486 | ||||||
chr2:11789492
|
A | T | 1 | a0001c0001t0001g0107 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1713+1036A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789492 | ||||||
chr2:11789528
|
ACATGTGT others(5): Show |
A | 2 | a0001c0001t0002g0053a0001c0001t0002g0158 | 2 | HG01261.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1713+1081_1713+109 others(16): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr2 | 11789528 | |||||
chr2:11789571
|
T | C | 29 | a0001c0001t0001g0103a0001c0001t0001g0121a0001c0001t0001g0272others(26): Show | 29 | HG00099.hp2 HG00738.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1713+1115T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789571 | ||||||
chr2:11789575
|
C | T | 4 | a0001c0001t0002g0068a0001c0001t0003g0069a0001c0001t0026g0034others(1): Show | 4 | HG01496.hp2 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1713+1119C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789575 | ||||||
chr2:11789577
|
T | C | 4 | a0001c0001t0002g0068a0001c0001t0003g0069a0001c0001t0026g0034others(1): Show | 4 | HG01496.hp2 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1713+1121T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789577 | ||||||
chr2:11789610
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1713+1154C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789610 | ||||||
chr2:11789614
|
G | A | 145 | a0001c0001t0001g0026a0001c0001t0001g0103a0001c0001t0001g0107others(142): Show | 145 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.1713+1158G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789614 | ||||||
chr2:11790133
|
C | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0006g0163others(3): Show | 6 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1713+1677C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790133 | ||||||
chr2:11790153
|
A | G | 136 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(133): Show | 136 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(133): Show |
intron_variant | MODIFIER | c.1713+1697A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790153 | ||||||
chr2:11790207
|
G | A | 2 | a0001c0001t0008g0038a0001c0001t0008g0044 | 2 | HG00639.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1714-1707G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790207 | ||||||
chr2:11790274
|
G | A | 2 | a0001c0001t0007g0112a0001c0001t0009g0108 | 2 | HG00735.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1714-1640G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790274 | ||||||
chr2:11790370
|
C | T | 10 | a0001c0003t0001g0048a0001c0003t0002g0052a0001c0003t0002g0087others(7): Show | 10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1714-1544C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790370 | ||||||
chr2:11790377
|
A | G | 1 | a0001c0001t0012g0251 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1714-1537A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790377 | ||||||
chr2:11790396
|
G | A | 1 | a0001c0001t0011g0086 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1714-1518G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790396 | ||||||
chr2:11790406
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1714-1508C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790406 | ||||||
chr2:11790798
|
C | G | 1 | a0001c0001t0001g0237 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1714-1116C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790798 | ||||||
chr2:11790931
|
G | A | 2 | a0001c0002t0015g0152a0001c0002t0015g0156 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1714-983G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790931 | ||||||
chr2:11790986
|
A | T | 21 | a0001c0001t0003g0040a0001c0001t0003g0046a0001c0001t0005g0042others(18): Show | 21 | HG01167.hp2 HG01175.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1714-928A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790986 | ||||||
chr2:11791159
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1714-755T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11791159 | ||||||
chr2:11791227
|
C | T | 1 | a0001c0001t0010g0020 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1714-687C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11791227 | ||||||
chr2:11791255
|
G | A | 2 | a0001c0008t0005g0002a0001c0008t0005g0003 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1714-659G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11791255 | ||||||
chr2:11791306
|
A | C | 1 | a0001c0001t0004g0267 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1714-608A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11791306 | ||||||
chr2:11791372
|
A | G | 43 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0127others(40): Show | 43 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1714-542A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11791372 | ||||||
chr2:11791596
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0002g0027a0001c0001t0002g0028 | 3 | HG02145.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1714-318A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11791596 | ||||||
chr2:11791647
|
G | T | 4 | a0001c0003t0002g0087a0001c0003t0002g0088a0001c0003t0009g0090others(1): Show | 4 | HG01074.hp2 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714-267G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11791647 | ||||||
chr2:11791805
|
A | AT | 44 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0127others(41): Show | 44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1714-100dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr2 | 11791805 | |||||
chr2:11792047
|
G | T | 167 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(164): Show | 167 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.1806+41G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11792047 | ||||||
chr2:11792209
|
T | C | 167 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(164): Show | 167 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.1806+203T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11792209 | ||||||
chr2:11792388
|
C | T | 4 | a0001c0003t0002g0087a0001c0003t0002g0088a0001c0003t0009g0090others(1): Show | 4 | HG01074.hp2 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+382C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11792388 | ||||||
chr2:11792513
|
G | T | 1 | a0002c0009t0002g0047 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1806+507G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11792513 | ||||||
chr2:11792587
|
T | A | 3 | a0001c0001t0003g0011a0001c0001t0003g0077a0001c0001t0005g0075 | 3 | HG02451.hp1 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1806+581T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11792587 | ||||||
chr2:11792621
|
G | A | 1 | a0001c0001t0003g0138 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1806+615G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11792621 | ||||||
chr2:11792810
|
C | T | 1 | a0001c0013t0001g0021 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1806+804C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11792810 | ||||||
chr2:11793120
|
C | T | 2 | a0001c0001t0004g0261a0001c0001t0036g0262 | 2 | HG02071.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1806+1114C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11793120 | ||||||
chr2:11793174
|
A | G | 1 | a0001c0001t0026g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1806+1168A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11793174 | ||||||
chr2:11793260
|
A | G | 48 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0127others(45): Show | 48 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.1806+1254A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11793260 | ||||||
chr2:11793604
|
C | T | 12 | a0001c0001t0002g0060a0001c0001t0002g0063a0001c0001t0002g0064others(9): Show | 12 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.1806+1598C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11793604 | ||||||
chr2:11793909
|
AGG | A | 3 | a0001c0001t0005g0277a0001c0001t0008g0038a0001c0001t0008g0044 | 3 | HG00639.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1807-1496_1807-149 others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr2 | 11793909 | |||||
chr2:11794047
|
G | A | 2 | a0001c0008t0005g0002a0001c0008t0005g0003 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1807-1361G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794047 | ||||||
chr2:11794057
|
G | A | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1807-1351G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794057 | ||||||
chr2:11794073
|
C | G | 25 | a0001c0001t0001g0026a0001c0001t0002g0027a0001c0001t0002g0028others(22): Show | 25 | HG00639.hp2 HG01496.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1807-1335C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794073 | ||||||
chr2:11794122
|
C | A | 10 | a0001c0003t0001g0048a0001c0003t0002g0052a0001c0003t0002g0087others(7): Show | 10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1807-1286C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794122 | ||||||
chr2:11794539
|
T | C | 1 | a0001c0001t0002g0238 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1807-869T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794539 | ||||||
chr2:11794561
|
C | T | 11 | a0001c0001t0001g0182a0001c0001t0001g0223a0001c0001t0001g0250others(8): Show | 11 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1807-847C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794561 | ||||||
chr2:11794630
|
C | T | 2 | a0001c0001t0007g0172a0001c0001t0007g0188 | 2 | HG01258.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1807-778C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794630 | ||||||
chr2:11794641
|
CAGAG | C | 60 | a0001c0001t0001g0103a0001c0001t0001g0121a0001c0001t0001g0272others(57): Show | 60 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.1807-765_1807-762d others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr2 | 11794641 | |||||
chr2:11794718
|
C | A | 1 | a0001c0001t0002g0235 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1807-690C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794718 | ||||||
chr2:11794726
|
G | A | 2 | a0001c0002t0015g0152a0001c0002t0015g0156 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1807-682G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794726 | ||||||
chr2:11794888
|
C | G | 10 | a0001c0003t0001g0048a0001c0003t0002g0052a0001c0003t0002g0087others(7): Show | 10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1807-520C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794888 | ||||||
chr2:11795150
|
C | T | 1 | a0001c0001t0002g0147 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1807-258C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11795150 | ||||||
chr2:11795160
|
T | C | 1 | a0001c0002t0008g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1807-248T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11795160 | ||||||
chr2:11795528
|
C | T | 1 | a0001c0001t0005g0075 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1886+41C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11795528 | ||||||
chr2:11795546
|
G | C | 1 | a0001c0002t0008g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1886+59G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11795546 | ||||||
chr2:11795874
|
A | G | 1 | a0001c0001t0016g0139 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1886+387A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11795874 | ||||||
chr2:11795890
|
A | G | 6 | a0001c0001t0003g0011a0001c0001t0003g0077a0001c0001t0005g0075others(3): Show | 6 | HG02451.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1886+403A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11795890 | ||||||
chr2:11796014
|
C | T | 1 | a0001c0001t0011g0125 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1886+527C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796014 | ||||||
chr2:11796216
|
G | A | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1886+729G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796216 | ||||||
chr2:11796394
|
C | G | 6 | a0001c0001t0002g0060a0001c0001t0002g0063a0001c0001t0002g0064others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1886+907C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796394 | ||||||
chr2:11796465
|
C | G | 29 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0146others(26): Show | 29 | HG00558.hp2 HG00673.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.1886+978C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796465 | ||||||
chr2:11796514
|
T | C | 3 | a0001c0001t0005g0277a0001c0001t0008g0038a0001c0001t0008g0044 | 3 | HG00639.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1886+1027T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796514 | ||||||
chr2:11796556
|
G | A | 2 | a0001c0001t0002g0235a0001c0001t0037g0236 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1886+1069G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796556 | ||||||
chr2:11796672
|
A | G | 153 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(150): Show | 153 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(150): Show |
intron_variant | MODIFIER | c.1886+1185A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796672 | ||||||
chr2:11796770
|
C | T | 1 | a0001c0001t0016g0139 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1886+1283C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796770 | ||||||
chr2:11796791
|
C | T | 20 | a0001c0001t0003g0040a0001c0001t0003g0046a0001c0001t0005g0042others(17): Show | 20 | HG01167.hp2 HG01175.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1886+1304C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796791 | ||||||
chr2:11796906
|
T | G | 1 | a0001c0001t0005g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1886+1419T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796906 | ||||||
chr2:11796915
|
C | T | 1 | a0001c0001t0004g0245 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1886+1428C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796915 | ||||||
chr2:11797032
|
G | C | 90 | a0001c0001t0001g0054a0001c0001t0001g0103a0001c0001t0001g0121others(87): Show | 90 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(87): Show |
intron_variant | MODIFIER | c.1886+1545G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11797032 | ||||||
chr2:11797123
|
C | T | 16 | a0001c0001t0002g0060a0001c0001t0002g0063a0001c0001t0002g0064others(13): Show | 16 | HG00639.hp2 HG02559.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1886+1636C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11797123 | ||||||
chr2:11797211
|
G | C | 5 | a0001c0001t0002g0194a0001c0001t0004g0212a0001c0001t0004g0230others(2): Show | 5 | NA18747.hp2 NA18983.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.1886+1724G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11797211 | ||||||
chr2:11797222
|
C | A | 1 | a0001c0001t0006g0035 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1886+1735C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11797222 | ||||||
chr2:11797308
|
G | C | 1 | a0001c0002t0002g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1886+1821G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11797308 | ||||||
chr2:11797648
|
CA | C | 6 | a0001c0001t0002g0060a0001c0001t0002g0063a0001c0001t0002g0064others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1886+2163delA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 11797648 | |||||
chr2:11797687
|
A | G | 6 | a0001c0001t0002g0060a0001c0001t0002g0063a0001c0001t0002g0064others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1886+2200A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11797687 | ||||||
chr2:11797829
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1886+2342T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11797829 | ||||||
chr2:11798250
|
C | T | 1 | a0001c0002t0030g0007 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1886+2763C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798250 | ||||||
chr2:11798360
|
G | A | 5 | a0001c0001t0002g0180a0001c0001t0003g0178a0001c0001t0003g0190others(2): Show | 5 | HG00423.hp1 HG01255.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1886+2873G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798360 | ||||||
chr2:11798586
|
C | A | 2 | a0001c0002t0002g0014a0001c0002t0003g0015 | 2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1886+3099C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798586 | ||||||
chr2:11798615
|
T | G | 8 | a0001c0001t0001g0127a0001c0001t0004g0124a0001c0001t0004g0128others(5): Show | 8 | NA18960.hp1 NA18989.hp2 NA18995.hp2 others(5): Show |
intron_variant | MODIFIER | c.1886+3128T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798615 | ||||||
chr2:11798664
|
T | C | 1 | a0001c0001t0006g0163 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1886+3177T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798664 | ||||||
chr2:11798670
|
C | T | 2 | a0001c0001t0002g0235a0001c0001t0037g0236 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1886+3183C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798670 | ||||||
chr2:11798731
|
G | A | 2 | a0001c0002t0015g0152a0001c0002t0015g0156 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1886+3244G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798731 | ||||||
chr2:11798775
|
T | TA | 8 | a0001c0001t0001g0054a0001c0001t0002g0053a0001c0001t0002g0158others(5): Show | 8 | HG01167.hp2 HG01261.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1886+3302dupA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 11798775 | |||||
chr2:11798820
|
G | A | 98 | a0001c0001t0001g0026a0001c0001t0001g0103a0001c0001t0001g0121others(95): Show | 98 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(95): Show |
intron_variant | MODIFIER | c.1886+3333G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798820 | ||||||
chr2:11798848
|
C | G | 10 | a0001c0003t0001g0048a0001c0003t0002g0052a0001c0003t0002g0087others(7): Show | 10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1886+3361C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798848 | ||||||
chr2:11798892
|
G | A | 32 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0146others(29): Show | 32 | HG00558.hp2 HG00673.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1886+3405G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798892 | ||||||
chr2:11798993
|
T | C | 1 | a0001c0001t0004g0231 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1886+3506T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798993 | ||||||
chr2:11799030
|
T | G | 12 | a0001c0001t0001g0026a0001c0001t0002g0027a0001c0001t0002g0028others(9): Show | 12 | HG01496.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1886+3543T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799030 | ||||||
chr2:11799292
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1887-3615G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799292 | ||||||
chr2:11799391
|
T | C | 5 | a0002c0007t0011g0025a0002c0007t0034g0023a0002c0007t0035g0024others(2): Show | 5 | HG01167.hp2 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1887-3516T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799391 | ||||||
chr2:11799432
|
CCT | C | 76 | a0001c0001t0001g0026a0001c0001t0001g0103a0001c0001t0001g0121others(73): Show | 76 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.1887-3473_1887-347 others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 11799432 | |||||
chr2:11799482
|
C | T | 1 | a0001c0001t0016g0120 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1887-3425C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799482 | ||||||
chr2:11799483
|
G | A | 7 | a0001c0001t0003g0011a0001c0001t0003g0055a0001c0001t0003g0057others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1887-3424G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799483 | ||||||
chr2:11799504
|
G | C | 1 | a0001c0001t0005g0070 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1887-3403G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799504 | ||||||
chr2:11799505
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1887-3402C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799505 | ||||||
chr2:11799567
|
A | G | 1 | a0001c0002t0002g0016 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1887-3340A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799567 | ||||||
chr2:11799850
|
C | T | 50 | a0001c0001t0001g0103a0001c0001t0001g0121a0001c0001t0001g0272others(47): Show | 50 | HG00099.hp2 HG00738.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1887-3057C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799850 | ||||||
chr2:11800002
|
C | T | 1 | a0003c0006t0032g0111 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1887-2905C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800002 | ||||||
chr2:11800020
|
C | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0006g0163others(3): Show | 6 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1887-2887C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800020 | ||||||
chr2:11800045
|
G | A | 30 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0146others(27): Show | 30 | HG00558.hp2 HG00673.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1887-2862G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800045 | ||||||
chr2:11800191
|
C | T | 1 | a0001c0001t0007g0188 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1887-2716C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800191 | ||||||
chr2:11800309
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1887-2598C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800309 | ||||||
chr2:11800359
|
A | G | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1887-2548A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800359 | ||||||
chr2:11800414
|
T | G | 1 | a0003c0006t0004g0105 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1887-2493T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800414 | ||||||
chr2:11800468
|
C | T | 1 | a0001c0001t0005g0092 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1887-2439C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800468 | ||||||
chr2:11800469
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1887-2438G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800469 | ||||||
chr2:11800649
|
G | A | 3 | a0001c0001t0002g0053a0001c0001t0002g0117a0001c0001t0002g0158 | 3 | HG01261.hp2 HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1887-2258G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800649 | ||||||
chr2:11800661
|
T | G | 258 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1887-2246T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800661 | ||||||
chr2:11800693
|
G | A | 147 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0134others(144): Show | 147 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.1887-2214G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800693 | ||||||
chr2:11800720
|
G | A | 57 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0141others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1887-2187G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800720 | ||||||
chr2:11800893
|
C | T | 2 | a0001c0008t0005g0002a0001c0008t0005g0003 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1887-2014C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800893 | ||||||
chr2:11800959
|
T | A | 1 | a0001c0001t0001g0260 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1887-1948T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800959 | ||||||
chr2:11801007
|
T | G | 1 | a0001c0001t0003g0069 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1887-1900T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801007 | ||||||
chr2:11801020
|
T | A | 1 | a0002c0009t0002g0047 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1887-1887T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801020 | ||||||
chr2:11801022
|
A | G | 13 | a0001c0001t0003g0031a0001c0001t0003g0040a0001c0001t0003g0046others(10): Show | 13 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1887-1885A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801022 | ||||||
chr2:11801134
|
G | A | 1 | a0001c0001t0005g0075 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1887-1773G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801134 | ||||||
chr2:11801256
|
A | G | 6 | a0001c0001t0018g0032a0001c0008t0005g0002a0001c0008t0005g0003others(3): Show | 6 | HG01167.hp2 HG02055.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1887-1651A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801256 | ||||||
chr2:11801337
|
G | A | 1 | a0001c0001t0007g0188 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1887-1570G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801337 | ||||||
chr2:11801352
|
C | T | 1 | a0001c0001t0005g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1887-1555C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801352 | ||||||
chr2:11801424
|
A | G | 1 | a0001c0004t0010g0076 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1887-1483A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801424 | ||||||
chr2:11801520
|
G | A | 3 | a0001c0004t0007g0274a0001c0005t0007g0017a0001c0005t0007g0018 | 3 | HG01109.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1887-1387G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801520 | ||||||
chr2:11801535
|
T | C | 1 | a0001c0001t0025g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1887-1372T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801535 | ||||||
chr2:11801563
|
G | C | 1 | a0001c0001t0001g0141 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1887-1344G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801563 | ||||||
chr2:11801571
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1887-1336G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801571 | ||||||
chr2:11801681
|
G | A | 5 | a0001c0008t0005g0002a0001c0008t0005g0003a0002c0007t0011g0025others(2): Show | 5 | HG01167.hp2 HG02055.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1887-1226G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801681 | ||||||
chr2:11801863
|
A | G | 47 | a0001c0001t0001g0228a0001c0001t0002g0067a0001c0001t0002g0068others(44): Show | 47 | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1887-1044A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801863 | ||||||
chr2:11802121
|
AG | A | 3 | a0001c0005t0007g0151a0001c0005t0007g0154a0001c0005t0007g0157 | 3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1887-784delG | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 11802121 | |||||
chr2:11802123
|
G | T | 3 | a0001c0005t0007g0151a0001c0005t0007g0154a0001c0005t0007g0157 | 3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1887-784G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802123 | ||||||
chr2:11802124
|
C | A | 3 | a0001c0005t0007g0151a0001c0005t0007g0154a0001c0005t0007g0157 | 3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1887-783C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802124 | ||||||
chr2:11802125
|
A | G | 3 | a0001c0005t0007g0151a0001c0005t0007g0154a0001c0005t0007g0157 | 3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1887-782A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802125 | ||||||
chr2:11802127
|
T | G | 3 | a0001c0005t0007g0151a0001c0005t0007g0154a0001c0005t0007g0157 | 3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1887-780T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802127 | ||||||
chr2:11802128
|
T | G | 3 | a0001c0005t0007g0151a0001c0005t0007g0154a0001c0005t0007g0157 | 3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1887-779T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802128 | ||||||
chr2:11802240
|
A | G | 10 | a0001c0001t0002g0067a0001c0001t0006g0035a0001c0001t0006g0037others(7): Show | 10 | HG01261.hp1 HG01891.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1887-667A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802240 | ||||||
chr2:11802354
|
G | A | 3 | a0001c0001t0006g0056a0001c0002t0006g0153a0001c0002t0006g0155 | 3 | HG02559.hp1 HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1887-553G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802354 | ||||||
chr2:11802365
|
T | C | 5 | a0001c0001t0001g0228a0001c0001t0005g0070a0001c0001t0007g0112others(2): Show | 5 | HG00735.hp1 HG01258.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1887-542T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802365 | ||||||
chr2:11802593
|
T | A | 1 | a0001c0001t0003g0178 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1887-314T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802593 | ||||||
chr2:11803154
|
C | A | 3 | a0001c0005t0007g0151a0001c0005t0007g0154a0001c0005t0007g0157 | 3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2013+121C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11803154 | ||||||
chr2:11803181
|
T | C | 4 | a0001c0004t0010g0004a0001c0004t0010g0005a0001c0004t0010g0074others(1): Show | 4 | HG01934.hp1 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2013+148T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11803181 | ||||||
chr2:11803236
|
G | A | 1 | a0001c0001t0002g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2013+203G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11803236 | ||||||
chr2:11803249
|
G | C | 1 | a0001c0001t0004g0129 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2013+216G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11803249 | ||||||
chr2:11803387
|
T | C | 3 | a0001c0001t0001g0183a0001c0001t0001g0193a0001c0001t0001g0242 | 3 | NA18963.hp1 NA18978.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.2013+354T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11803387 | ||||||
chr2:11803607
|
T | C | 2 | a0001c0008t0005g0002a0001c0008t0005g0003 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2013+574T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11803607 | ||||||
chr2:11803657
|
A | G | 1 | a0001c0001t0003g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2013+624A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11803657 | ||||||
chr2:11803941
|
AT | A | 7 | a0001c0001t0002g0060a0001c0001t0002g0063a0001c0001t0002g0064others(4): Show | 7 | HG02559.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2014-480delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr2 | 11803941 | |||||
chr2:11804197
|
A | G | 1 | a0001c0011t0015g0073 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2014-226A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11804197 | ||||||
chr2:11804206
|
A | G | 3 | a0001c0005t0007g0151a0001c0005t0007g0154a0001c0005t0007g0157 | 3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2014-217A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11804206 | ||||||
chr2:11804610
|
T | C | 5 | a0001c0004t0006g0072a0001c0004t0010g0004a0001c0004t0010g0005others(2): Show | 5 | HG01934.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2162+39T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/20 | chr2 | 11804610 | ||||||
chr2:11804620
|
TG | T | 81 | a0001c0001t0001g0196a0001c0001t0002g0067a0001c0001t0002g0068others(78): Show | 81 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.2162+54delG | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 11804620 | |||||
chr2:11804655
|
C | G | 2 | a0001c0008t0005g0002a0001c0008t0005g0003 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2162+84C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/20 | chr2 | 11804655 | ||||||
chr2:11804782
|
G | A | 1 | a0001c0002t0002g0016 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2162+211G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/20 | chr2 | 11804782 | ||||||
chr2:11804830
|
C | A | 1 | a0001c0001t0007g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2163-240C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/20 | chr2 | 11804830 | ||||||
chr2:11804982
|
G | GT | 7 | a0001c0001t0001g0127a0001c0001t0001g0169a0001c0001t0002g0068others(4): Show | 7 | HG02735.hp2 HG03098.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.2163-72dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 11804982 | |||||
chr2:11804982
|
G | GTT | 5 | a0001c0001t0004g0148a0001c0001t0004g0150a0001c0004t0007g0274others(2): Show | 5 | HG01109.hp2 HG02970.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.2163-73_2163-72dup others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 11804982 | |||||
chr2:11804985
|
T | G | 2 | a0001c0002t0015g0152a0001c0002t0015g0156 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2163-85T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/20 | chr2 | 11804985 | ||||||
chr2:11805369
|
A | C | 1 | a0003c0006t0032g0111 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2249+213A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11805369 | ||||||
chr2:11805374
|
C | T | 3 | a0001c0001t0002g0067a0001c0001t0010g0071a0001c0001t0010g0078 | 3 | HG01261.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2249+218C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11805374 | ||||||
chr2:11805407
|
C | A | 53 | a0001c0001t0001g0196a0001c0001t0002g0180a0001c0001t0003g0031others(50): Show | 53 | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.2249+251C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11805407 | ||||||
chr2:11805603
|
T | C | 2 | a0001c0001t0010g0020a0001c0001t0026g0034 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2249+447T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11805603 | ||||||
chr2:11805713
|
G | C | 3 | a0001c0001t0006g0036a0001c0001t0006g0079a0001c0001t0028g0080 | 3 | HG02109.hp2 HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2249+557G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11805713 | ||||||
chr2:11806004
|
C | T | 19 | a0001c0001t0001g0134a0001c0001t0001g0146a0001c0001t0001g0182others(16): Show | 19 | HG00673.hp2 HG02015.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.2249+848C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806004 | ||||||
chr2:11806009
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2249+853A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806009 | ||||||
chr2:11806011
|
A | T | 3 | a0001c0001t0002g0067a0001c0001t0010g0071a0001c0001t0010g0078 | 3 | HG01261.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2249+855A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806011 | ||||||
chr2:11806644
|
T | G | 5 | a0001c0004t0006g0072a0001c0004t0010g0004a0001c0004t0010g0005others(2): Show | 5 | HG01934.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2249+1488T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806644 | ||||||
chr2:11806660
|
A | G | 5 | a0001c0001t0002g0067a0001c0001t0010g0020a0001c0001t0010g0071others(2): Show | 5 | HG01109.hp1 HG01261.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2249+1504A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806660 | ||||||
chr2:11806678
|
A | C | 1 | a0001c0001t0003g0011 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2249+1522A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806678 | ||||||
chr2:11806685
|
A | T | 1 | a0001c0001t0003g0011 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2249+1529A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806685 | ||||||
chr2:11806863
|
T | C | 3 | a0001c0004t0007g0274a0001c0005t0007g0017a0001c0005t0007g0018 | 3 | HG01109.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2249+1707T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806863 | ||||||
chr2:11806878
|
A | G | 1 | a0001c0001t0003g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2249+1722A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806878 | ||||||
chr2:11806908
|
A | G | 4 | a0001c0001t0003g0077a0001c0001t0008g0043a0001c0001t0008g0045others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2249+1752A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806908 | ||||||
chr2:11807012
|
T | C | 4 | a0001c0001t0003g0077a0001c0001t0008g0043a0001c0001t0008g0045others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2249+1856T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11807012 | ||||||
chr2:11807064
|
C | A | 2 | a0001c0001t0006g0079a0001c0001t0028g0080 | 2 | HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2249+1908C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11807064 | ||||||
chr2:11807077
|
T | C | 83 | a0001c0001t0001g0196a0001c0001t0002g0067a0001c0001t0002g0068others(80): Show | 83 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.2249+1921T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11807077 | ||||||
chr2:11807106
|
T | C | 1 | a0001c0001t0003g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2249+1950T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11807106 | ||||||
chr2:11807156
|
T | C | 2 | a0001c0002t0002g0014a0001c0002t0003g0015 | 2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2249+2000T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11807156 | ||||||
chr2:11807274
|
T | C | 57 | a0001c0001t0001g0196a0001c0001t0002g0180a0001c0001t0003g0011others(54): Show | 57 | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.2249+2118T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11807274 | ||||||
chr2:11807306
|
G | A | 3 | a0001c0001t0003g0083a0001c0001t0005g0075a0001c0002t0030g0007 | 3 | HG02280.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2249+2150G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11807306 | ||||||
chr2:11807512
|
A | AT | 16 | a0001c0001t0002g0162a0001c0001t0002g0247a0001c0001t0004g0104others(13): Show | 16 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.2249+2372dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11807512 | |||||
chr2:11807928
|
T | C | 1 | a0001c0001t0004g0109 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2249+2772T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11807928 | ||||||
chr2:11808059
|
C | T | 3 | a0001c0001t0002g0067a0001c0001t0010g0071a0001c0001t0010g0078 | 3 | HG01261.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2249+2903C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808059 | ||||||
chr2:11808120
|
A | C | 2 | a0001c0001t0017g0061a0001c0001t0017g0062 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2249+2964A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808120 | ||||||
chr2:11808245
|
A | G | 1 | a0001c0001t0012g0113 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2249+3089A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808245 | ||||||
chr2:11808256
|
C | G | 2 | a0001c0001t0003g0168a0001c0001t0016g0098 | 2 | HG02080.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.2249+3100C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808256 | ||||||
chr2:11808276
|
G | T | 1 | a0001c0001t0003g0138 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2249+3120G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808276 | ||||||
chr2:11808299
|
G | T | 1 | a0001c0001t0001g0248 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2249+3143G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808299 | ||||||
chr2:11808334
|
G | A | 1 | a0001c0001t0004g0219 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2249+3178G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808334 | ||||||
chr2:11808586
|
A | G | 2 | a0001c0008t0005g0002a0001c0008t0005g0003 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2249+3430A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808586 | ||||||
chr2:11808639
|
C | T | 14 | a0001c0001t0004g0227a0001c0001t0004g0245a0001c0001t0009g0108others(11): Show | 14 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.2249+3483C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808639 | ||||||
chr2:11808707
|
C | A | 1 | a0001c0011t0015g0073 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2249+3551C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808707 | ||||||
chr2:11808749
|
C | T | 1 | a0001c0001t0003g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2249+3593C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808749 | ||||||
chr2:11808870
|
C | CA | 13 | a0001c0001t0001g0054a0001c0001t0002g0067a0001c0001t0002g0135others(10): Show | 13 | HG01261.hp1 HG02040.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2249+3730dupA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11808870 | |||||
chr2:11808870
|
C | CAA | 6 | a0001c0001t0010g0020a0001c0004t0006g0072a0001c0004t0010g0004others(3): Show | 6 | HG01109.hp1 HG01934.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2249+3729_2249+373 others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11808870 | |||||
chr2:11808884
|
AAAG | A | 13 | a0001c0001t0004g0227a0001c0001t0004g0245a0001c0001t0009g0108others(10): Show | 13 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.2249+3730_2249+373 others(7): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11808884 | |||||
chr2:11809137
|
C | CAAAACTA others(1260): Show |
7 | a0001c0001t0005g0092a0001c0001t0008g0001a0001c0001t0008g0006others(4): Show | 7 | HG01257.hp1 HG01258.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.2249+3999_2249+400 others(1271): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11809137 | |||||
chr2:11809137
|
C | CAAAACTA others(1259): Show |
1 | a0001c0001t0005g0070 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2249+3999_2249+400 others(1270): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11809137 | |||||
chr2:11809137
|
C | CAAAACTA others(1259): Show |
1 | a0001c0011t0015g0073 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2249+3999_2249+400 others(1270): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11809137 | |||||
chr2:11809137
|
C | CAAAACTA others(1259): Show |
3 | a0001c0001t0002g0068a0001c0001t0008g0038a0001c0001t0008g0044 | 3 | HG00639.hp2 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2249+3999_2249+400 others(1270): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11809137 | |||||
chr2:11809312
|
A | T | 1 | a0001c0001t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2249+4156A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11809312 | ||||||
chr2:11809331
|
G | C | 25 | a0001c0001t0002g0067a0001c0001t0003g0011a0001c0001t0004g0227others(22): Show | 25 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.2249+4175G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11809331 | ||||||
chr2:11809422
|
C | CT | 8 | a0001c0002t0002g0014a0001c0002t0003g0015a0001c0004t0007g0274others(5): Show | 8 | HG01109.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2249+4276dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11809422 | |||||
chr2:11809519
|
C | A | 2 | a0001c0001t0008g0038a0001c0001t0008g0044 | 2 | HG00639.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2249+4363C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11809519 | ||||||
chr2:11809703
|
A | C | 5 | a0001c0004t0006g0072a0001c0004t0010g0004a0001c0004t0010g0005others(2): Show | 5 | HG01934.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2249+4547A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11809703 | ||||||
chr2:11809743
|
G | A | 1 | a0001c0003t0009g0049 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2249+4587G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11809743 | ||||||
chr2:11809909
|
A | T | 1 | a0001c0001t0003g0011 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2249+4753A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11809909 | ||||||
chr2:11810216
|
A | G | 275 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0103others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.2250-4872A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810216 | ||||||
chr2:11810369
|
A | G | 2 | a0001c0001t0002g0232a0001c0001t0002g0238 | 2 | NA18997.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2250-4719A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810369 | ||||||
chr2:11810385
|
GA | G | 14 | a0001c0001t0004g0227a0001c0001t0004g0245a0001c0001t0009g0108others(11): Show | 14 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.2250-4702delA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810385 | ||||||
chr2:11810387
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2250-4701G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810387 | ||||||
chr2:11810516
|
G | A | 2 | a0001c0001t0017g0061a0001c0001t0017g0062 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2250-4572G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810516 | ||||||
chr2:11810588
|
A | T | 1 | a0001c0001t0002g0101 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2250-4500A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810588 | ||||||
chr2:11810630
|
G | T | 21 | a0001c0001t0002g0068a0001c0001t0005g0070a0001c0001t0005g0092others(18): Show | 21 | HG00639.hp2 HG01109.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.2250-4458G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810630 | ||||||
chr2:11810717
|
C | G | 1 | a0001c0001t0002g0175 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2250-4371C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810717 | ||||||
chr2:11810872
|
C | T | 1 | a0001c0001t0004g0149 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2250-4216C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810872 | ||||||
chr2:11811227
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2250-3861A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811227 | ||||||
chr2:11811324
|
G | A | 14 | a0001c0001t0004g0227a0001c0001t0004g0245a0001c0001t0009g0108others(11): Show | 14 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.2250-3764G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811324 | ||||||
chr2:11811420
|
A | T | 1 | a0004c0012t0001g0198 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2250-3668A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811420 | ||||||
chr2:11811502
|
C | T | 3 | a0001c0001t0008g0043a0001c0001t0008g0045a0002c0009t0002g0047 | 3 | HG02486.hp2 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2250-3586C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811502 | ||||||
chr2:11811507
|
A | G | 1 | a0001c0001t0005g0070 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2250-3581A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811507 | ||||||
chr2:11811539
|
A | G | 1 | a0001c0001t0026g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2250-3549A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811539 | ||||||
chr2:11811593
|
C | A | 1 | a0001c0001t0003g0099 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2250-3495C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811593 | ||||||
chr2:11811841
|
T | C | 95 | a0001c0001t0001g0026a0001c0001t0001g0196a0001c0001t0001g0228others(92): Show | 95 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.2250-3247T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811841 | ||||||
chr2:11811899
|
C | T | 3 | a0001c0001t0004g0212a0001c0001t0004g0230a0001c0001t0004g0231 | 3 | NA18983.hp1 NA19005.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2250-3189C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811899 | ||||||
chr2:11811941
|
T | C | 5 | a0001c0001t0002g0068a0001c0001t0003g0213a0001c0001t0005g0070others(2): Show | 5 | HG00639.hp2 HG03098.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2250-3147T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811941 | ||||||
chr2:11811970
|
C | T | 4 | a0001c0004t0010g0004a0001c0004t0010g0005a0001c0004t0010g0074others(1): Show | 4 | HG01934.hp1 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2250-3118C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811970 | ||||||
chr2:11812253
|
G | GT | 11 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0046others(8): Show | 11 | HG01496.hp2 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2250-2830dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11812253 | |||||
chr2:11812255
|
T | A | 11 | a0001c0001t0001g0123a0001c0001t0001g0127a0001c0001t0004g0094others(8): Show | 11 | NA18943.hp1 NA18943.hp2 NA18960.hp1 others(8): Show |
intron_variant | MODIFIER | c.2250-2833T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812255 | ||||||
chr2:11812263
|
C | T | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2250-2825C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812263 | ||||||
chr2:11812444
|
G | T | 1 | a0001c0001t0001g0223 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2250-2644G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812444 | ||||||
chr2:11812496
|
A | T | 40 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0002g0180others(37): Show | 40 | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.2250-2592A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812496 | ||||||
chr2:11812610
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2250-2478G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812610 | ||||||
chr2:11812711
|
T | C | 3 | a0001c0002t0015g0152a0001c0002t0015g0156a0001c0011t0015g0073 | 3 | HG02622.hp2 HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2250-2377T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812711 | ||||||
chr2:11812787
|
C | T | 6 | a0001c0001t0002g0067a0001c0001t0003g0083a0001c0001t0005g0075others(3): Show | 6 | HG02280.hp2 HG02886.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2250-2301C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812787 | ||||||
chr2:11812807
|
C | T | 1 | a0001c0001t0009g0229 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2250-2281C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812807 | ||||||
chr2:11812939
|
G | C | 2 | a0001c0001t0001g0255a0001c0001t0002g0130 | 2 | HG01099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2250-2149G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812939 | ||||||
chr2:11812979
|
G | A | 2 | a0001c0003t0001g0048a0001c0003t0014g0089 | 2 | HG00733.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2250-2109G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812979 | ||||||
chr2:11813062
|
G | A | 1 | a0001c0001t0011g0086 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2250-2026G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813062 | ||||||
chr2:11813172
|
G | A | 2 | a0001c0001t0002g0101a0001c0003t0002g0088 | 2 | HG00099.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.2250-1916G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813172 | ||||||
chr2:11813195
|
A | G | 31 | a0001c0001t0002g0180a0001c0001t0003g0031a0001c0001t0003g0033others(28): Show | 31 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.2250-1893A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813195 | ||||||
chr2:11813281
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2250-1807G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813281 | ||||||
chr2:11813302
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2250-1786C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813302 | ||||||
chr2:11813416
|
C | T | 1 | a0001c0001t0002g0232 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2250-1672C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813416 | ||||||
chr2:11813461
|
C | T | 2 | a0001c0001t0005g0070a0001c0001t0005g0092 | 2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2250-1627C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813461 | ||||||
chr2:11813771
|
C | T | 3 | a0001c0005t0007g0151a0001c0005t0007g0154a0001c0005t0007g0157 | 3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2250-1317C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813771 | ||||||
chr2:11813774
|
C | T | 5 | a0001c0001t0018g0032a0001c0003t0009g0049a0001c0003t0009g0050others(2): Show | 5 | HG00738.hp1 HG01081.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2250-1314C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813774 | ||||||
chr2:11813873
|
C | T | 3 | a0002c0007t0011g0025a0002c0007t0034g0023a0002c0007t0035g0024 | 3 | HG01167.hp2 HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2250-1215C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813873 | ||||||
chr2:11814057
|
G | T | 30 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0040others(27): Show | 30 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2250-1031G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11814057 | ||||||
chr2:11814243
|
C | T | 2 | a0001c0001t0005g0070a0001c0001t0005g0092 | 2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2250-845C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11814243 | ||||||
chr2:11814244
|
G | A | 2 | a0001c0001t0005g0070a0001c0001t0005g0092 | 2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2250-844G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11814244 | ||||||
chr2:11814372
|
A | G | 77 | a0001c0001t0002g0067a0001c0001t0003g0011a0001c0001t0003g0031others(74): Show | 77 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.2250-716A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11814372 | ||||||
chr2:11814511
|
C | T | 1 | a0001c0001t0002g0147 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2250-577C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11814511 | ||||||
chr2:11814512
|
A | ATG | 35 | a0001c0001t0001g0123a0001c0001t0001g0164a0001c0001t0001g0173others(32): Show | 35 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2250-539_2250-538d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11814512 | |||||
chr2:11814512
|
A | ATGTG | 61 | a0001c0001t0001g0054a0001c0001t0001g0103a0001c0001t0001g0107others(58): Show | 61 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.2250-541_2250-538d others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11814512 | |||||
chr2:11814512
|
A | ATGTGTG | 6 | a0001c0001t0001g0141a0001c0001t0008g0038a0001c0001t0013g0133others(3): Show | 6 | HG00639.hp2 HG02523.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2250-543_2250-538d others(8): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11814512 | |||||
chr2:11814512
|
A | ATGTGTGT others(1): Show |
5 | a0001c0001t0002g0238a0001c0004t0006g0072a0001c0004t0007g0274others(2): Show | 5 | HG01109.hp2 HG02055.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2250-545_2250-538d others(10): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11814512 | |||||
chr2:11814512
|
A | G | 2 | a0001c0001t0002g0147a0001c0001t0027g0142 | 2 | HG02145.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.2250-576A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11814512 | ||||||
chr2:11814512
|
ATG | A | 34 | a0001c0001t0001g0127a0001c0001t0002g0053a0001c0001t0002g0097others(31): Show | 34 | HG00609.hp2 HG00673.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.2250-539_2250-538d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11814512 | |||||
chr2:11814512
|
ATGTG | A | 10 | a0001c0001t0001g0241a0001c0001t0001g0246a0001c0001t0002g0180others(7): Show | 10 | HG01081.hp2 HG01496.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.2250-541_2250-538d others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11814512 | |||||
chr2:11814512
|
ATGTGTG | A | 3 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078 | 3 | HG01109.hp1 HG01261.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2250-543_2250-538d others(8): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11814512 | |||||
chr2:11814567
|
TTGTTTTA others(16): Show |
T | 1 | a0002c0010t0005g0008 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2250-519_2250-497d others(25): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11814567 | |||||
chr2:11814732
|
G | A | 2 | a0001c0001t0008g0043a0001c0001t0008g0045 | 2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2250-356G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11814732 | ||||||
chr2:11814816
|
T | C | 23 | a0001c0001t0003g0011a0001c0001t0008g0001a0001c0001t0008g0006others(20): Show | 23 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.2250-272T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11814816 | ||||||
chr2:11815014
|
T | C | 11 | a0001c0001t0008g0001a0001c0001t0008g0006a0001c0001t0008g0019others(8): Show | 11 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2250-74T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11815014 | ||||||
chr2:11815334
|
G | A | 3 | a0001c0001t0002g0238a0001c0001t0013g0206a0001c0001t0013g0214 | 3 | NA18991.hp2 NA18997.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2402+94G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11815334 | ||||||
chr2:11815477
|
C | T | 7 | a0001c0001t0002g0053a0001c0001t0002g0158a0001c0001t0011g0084others(4): Show | 7 | HG01261.hp2 HG01981.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.2402+237C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11815477 | ||||||
chr2:11815576
|
C | T | 2 | a0001c0003t0001g0048a0001c0003t0014g0089 | 2 | HG00733.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2402+336C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11815576 | ||||||
chr2:11815741
|
A | G | 2 | a0001c0001t0005g0070a0001c0001t0005g0092 | 2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2402+501A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11815741 | ||||||
chr2:11815786
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2402+546C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11815786 | ||||||
chr2:11815906
|
G | A | 1 | a0001c0001t0002g0232 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2402+666G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11815906 | ||||||
chr2:11816120
|
T | G | 3 | a0001c0002t0015g0152a0001c0002t0015g0156a0001c0011t0015g0073 | 3 | HG02622.hp2 HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2402+880T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816120 | ||||||
chr2:11816205
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2402+965C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816205 | ||||||
chr2:11816251
|
C | T | 1 | a0001c0001t0020g0110 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2402+1011C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816251 | ||||||
chr2:11816261
|
G | T | 5 | a0001c0001t0002g0060a0001c0001t0002g0063a0001c0001t0002g0064others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2402+1021G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816261 | ||||||
chr2:11816392
|
T | C | 30 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0040others(27): Show | 30 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2402+1152T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816392 | ||||||
chr2:11816619
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2402+1379A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816619 | ||||||
chr2:11816629
|
C | T | 6 | a0001c0001t0002g0067a0001c0001t0003g0083a0001c0001t0005g0075others(3): Show | 6 | HG02280.hp2 HG02886.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2402+1389C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816629 | ||||||
chr2:11816741
|
C | CT | 8 | a0001c0001t0007g0112a0001c0001t0007g0172a0001c0001t0007g0188others(5): Show | 8 | HG00735.hp1 HG01258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2402+1519dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11816741 | |||||
chr2:11816741
|
CT | C | 47 | a0001c0001t0001g0246a0001c0001t0001g0253a0001c0001t0001g0273others(44): Show | 47 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.2402+1519delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11816741 | |||||
chr2:11816749
|
T | C | 30 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0040others(27): Show | 30 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2402+1509T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816749 | ||||||
chr2:11816829
|
T | C | 3 | a0001c0005t0007g0151a0001c0005t0007g0154a0001c0005t0007g0157 | 3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2402+1589T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816829 | ||||||
chr2:11816920
|
C | A | 6 | a0001c0001t0008g0043a0001c0001t0008g0045a0001c0002t0015g0152others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2402+1680C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816920 | ||||||
chr2:11816920
|
C | G | 8 | a0001c0001t0009g0108a0001c0001t0009g0229a0001c0001t0018g0032others(5): Show | 8 | HG00738.hp1 HG01081.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2402+1680C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816920 | ||||||
chr2:11816921
|
C | A | 31 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0040others(28): Show | 31 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.2402+1681C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816921 | ||||||
chr2:11817090
|
A | G | 1 | a0001c0001t0010g0020 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2402+1850A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817090 | ||||||
chr2:11817092
|
G | C | 2 | a0001c0001t0013g0206a0001c0001t0013g0214 | 2 | NA18991.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.2402+1852G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817092 | ||||||
chr2:11817144
|
A | G | 24 | a0001c0001t0001g0258a0001c0001t0002g0143a0001c0001t0002g0186others(21): Show | 24 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.2402+1904A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817144 | ||||||
chr2:11817187
|
C | T | 1 | a0002c0009t0002g0047 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2402+1947C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817187 | ||||||
chr2:11817586
|
A | AT | 13 | a0001c0001t0005g0042a0001c0001t0006g0035a0001c0001t0006g0036others(10): Show | 13 | HG01175.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2403-1888dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11817586 | |||||
chr2:11817628
|
T | C | 3 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078 | 3 | HG01109.hp1 HG01261.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2403-1856T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817628 | ||||||
chr2:11817643
|
G | T | 8 | a0001c0001t0009g0108a0001c0001t0009g0229a0001c0001t0018g0032others(5): Show | 8 | HG00738.hp1 HG01081.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2403-1841G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817643 | ||||||
chr2:11817655
|
C | T | 3 | a0001c0001t0003g0031a0001c0002t0003g0009a0001c0002t0003g0010 | 3 | HG02109.hp1 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2403-1829C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817655 | ||||||
chr2:11817696
|
A | G | 5 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(2): Show | 5 | HG01109.hp1 HG01261.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403-1788A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817696 | ||||||
chr2:11817704
|
T | C | 5 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(2): Show | 5 | HG01109.hp1 HG01261.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403-1780T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817704 | ||||||
chr2:11817730
|
C | T | 3 | a0001c0002t0015g0152a0001c0002t0015g0156a0001c0011t0015g0073 | 3 | HG02622.hp2 HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2403-1754C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817730 | ||||||
chr2:11817760
|
G | C | 124 | a0001c0001t0002g0101a0001c0001t0002g0115a0001c0001t0002g0116others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.2403-1724G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817760 | ||||||
chr2:11817797
|
A | G | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2403-1687A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817797 | ||||||
chr2:11817803
|
CTGTAG | C | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2403-1674_2403-167 others(9): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11817803 | |||||
chr2:11817919
|
A | G | 100 | a0001c0001t0003g0011a0001c0001t0003g0031a0001c0001t0003g0033others(97): Show | 100 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.2403-1565A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817919 | ||||||
chr2:11817926
|
T | C | 1 | a0001c0001t0005g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2403-1558T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817926 | ||||||
chr2:11817929
|
CTCAAAAA others(2): Show |
C | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2403-1554_2403-154 others(13): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817929 | ||||||
chr2:11817931
|
C | CA | 60 | a0001c0001t0001g0107a0001c0001t0001g0144a0001c0001t0001g0146others(57): Show | 60 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.2403-1524dupA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11817931 | |||||
chr2:11817931
|
C | CAA | 8 | a0001c0001t0005g0277a0001c0001t0006g0037a0001c0001t0008g0006others(5): Show | 8 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.2403-1525_2403-152 others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11817931 | |||||
chr2:11817931
|
CA | C | 29 | a0001c0001t0001g0253a0001c0001t0002g0028a0001c0001t0002g0060others(26): Show | 29 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.2403-1524delA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11817931 | |||||
chr2:11817931
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0005g0070a0001c0001t0005g0092 | 2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2403-1533_2403-152 others(14): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11817931 | |||||
chr2:11817931
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0005g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2403-1534_2403-152 others(15): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11817931 | |||||
chr2:11818021
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2403-1463C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818021 | ||||||
chr2:11818022
|
G | A | 3 | a0001c0001t0017g0061a0001c0001t0017g0062a0002c0009t0002g0047 | 3 | HG02896.hp1 HG02897.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2403-1462G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818022 | ||||||
chr2:11818067
|
G | A | 8 | a0001c0001t0009g0108a0001c0001t0009g0229a0001c0001t0018g0032others(5): Show | 8 | HG00738.hp1 HG01081.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2403-1417G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818067 | ||||||
chr2:11818128
|
C | T | 3 | a0001c0001t0004g0212a0001c0001t0004g0230a0001c0001t0004g0231 | 3 | NA18983.hp1 NA19005.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2403-1356C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818128 | ||||||
chr2:11818195
|
A | G | 12 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0037others(9): Show | 12 | HG01175.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2403-1289A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818195 | ||||||
chr2:11818197
|
C | G | 2 | a0001c0001t0017g0061a0001c0001t0017g0062 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2403-1287C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818197 | ||||||
chr2:11818213
|
C | A | 6 | a0001c0001t0005g0277a0001c0002t0015g0152a0001c0002t0015g0156others(3): Show | 6 | HG02622.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2403-1271C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818213 | ||||||
chr2:11818451
|
A | T | 8 | a0001c0001t0009g0108a0001c0001t0009g0229a0001c0001t0018g0032others(5): Show | 8 | HG00738.hp1 HG01081.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2403-1033A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818451 | ||||||
chr2:11818495
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2403-989C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818495 | ||||||
chr2:11818510
|
CT | C | 14 | a0001c0001t0003g0077a0001c0001t0007g0112a0001c0001t0007g0172others(11): Show | 14 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2403-963delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11818510 | |||||
chr2:11818514
|
T | A | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2403-970T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818514 | ||||||
chr2:11818640
|
T | C | 2 | a0002c0007t0034g0023a0002c0007t0035g0024 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2403-844T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818640 | ||||||
chr2:11818644
|
G | A | 80 | a0001c0001t0003g0011a0001c0001t0003g0031a0001c0001t0003g0033others(77): Show | 80 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.2403-840G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818644 | ||||||
chr2:11818659
|
A | G | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2403-825A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818659 | ||||||
chr2:11818674
|
A | G | 1 | a0001c0001t0004g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2403-810A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818674 | ||||||
chr2:11818807
|
C | T | 1 | a0001c0002t0002g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2403-677C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818807 | ||||||
chr2:11819043
|
T | TAC | 17 | a0001c0001t0001g0141a0001c0001t0002g0115a0001c0001t0002g0132others(14): Show | 17 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.2403-416_2403-415d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11819043 | |||||
chr2:11819043
|
TAC | T | 43 | a0001c0001t0002g0117a0001c0001t0003g0011a0001c0001t0003g0031others(40): Show | 43 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.2403-416_2403-415d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11819043 | |||||
chr2:11819043
|
TACAC | T | 27 | a0001c0001t0003g0077a0001c0001t0003g0099a0001c0001t0003g0114others(24): Show | 27 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.2403-418_2403-415d others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11819043 | |||||
chr2:11819045
|
C | A | 2 | a0001c0001t0004g0227a0001c0001t0004g0245 | 2 | HG00733.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2403-439C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819045 | ||||||
chr2:11819055
|
C | T | 1 | a0001c0004t0007g0274 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2403-429C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819055 | ||||||
chr2:11819138
|
A | G | 39 | a0001c0001t0003g0011a0001c0001t0003g0031a0001c0001t0003g0033others(36): Show | 39 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2403-346A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819138 | ||||||
chr2:11819178
|
C | T | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2403-306C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819178 | ||||||
chr2:11819184
|
G | A | 6 | a0001c0001t0005g0277a0001c0002t0015g0152a0001c0002t0015g0156others(3): Show | 6 | HG02622.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2403-300G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819184 | ||||||
chr2:11819256
|
C | T | 100 | a0001c0001t0003g0011a0001c0001t0003g0031a0001c0001t0003g0033others(97): Show | 100 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.2403-228C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819256 | ||||||
chr2:11819275
|
C | T | 2 | a0001c0001t0005g0042a0002c0010t0005g0008 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2403-209C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819275 | ||||||
chr2:11819286
|
T | C | 2 | a0002c0007t0034g0023a0002c0007t0035g0024 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2403-198T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819286 | ||||||
chr2:11819363
|
A | G | 2 | a0001c0001t0001g0241a0001c0001t0004g0106 | 2 | NA18940.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.2403-121A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819363 | ||||||
chr2:11819779
|
T | C | 100 | a0001c0001t0003g0011a0001c0001t0003g0031a0001c0001t0003g0033others(97): Show | 100 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.2517+181T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11819779 | ||||||
chr2:11819803
|
G | A | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2517+205G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11819803 | ||||||
chr2:11819824
|
A | G | 24 | a0001c0001t0005g0277a0001c0001t0008g0001a0001c0001t0008g0006others(21): Show | 24 | HG00639.hp2 HG01109.hp1 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.2517+226A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11819824 | ||||||
chr2:11819857
|
A | G | 26 | a0001c0001t0003g0077a0001c0001t0003g0083a0001c0001t0003g0099others(23): Show | 26 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.2517+259A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11819857 | ||||||
chr2:11819903
|
A | G | 6 | a0001c0001t0005g0277a0001c0002t0015g0152a0001c0002t0015g0156others(3): Show | 6 | HG02622.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2517+305A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11819903 | ||||||
chr2:11819958
|
C | T | 1 | a0001c0001t0029g0136 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2517+360C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11819958 | ||||||
chr2:11819999
|
G | A | 1 | a0001c0001t0026g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2517+401G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11819999 | ||||||
chr2:11820001
|
T | G | 2 | a0001c0001t0005g0070a0001c0001t0005g0092 | 2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2517+403T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11820001 | ||||||
chr2:11820025
|
G | A | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2518-386G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11820025 | ||||||
chr2:11820107
|
C | T | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2518-304C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11820107 | ||||||
chr2:11820285
|
A | G | 3 | a0001c0001t0005g0070a0001c0001t0005g0092a0001c0001t0005g0095 | 3 | HG02922.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2518-126A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11820285 | ||||||
chr2:11820388
|
T | C | 2 | a0001c0001t0003g0140a0001c0001t0003g0178 | 2 | HG00423.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.2518-23T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11820388 | ||||||
chr2:11820646
|
T | C | 1 | a0001c0001t0026g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2621+132T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11820646 | ||||||
chr2:11820658
|
C | G | 1 | a0001c0001t0001g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2621+144C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11820658 | ||||||
chr2:11820778
|
A | C | 1 | a0001c0001t0010g0071 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2621+264A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11820778 | ||||||
chr2:11820783
|
G | C | 1 | a0001c0001t0001g0226 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2621+269G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11820783 | ||||||
chr2:11820983
|
C | T | 3 | a0001c0001t0005g0070a0001c0001t0005g0092a0001c0001t0005g0095 | 3 | HG02922.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2621+469C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11820983 | ||||||
chr2:11821164
|
T | G | 6 | a0001c0001t0005g0277a0001c0002t0015g0152a0001c0002t0015g0156others(3): Show | 6 | HG02622.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2621+650T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821164 | ||||||
chr2:11821230
|
T | TG | 23 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0037others(20): Show | 23 | HG00639.hp2 HG01175.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2621+718dupG | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr2 | 11821230 | |||||
chr2:11821282
|
T | C | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2621+768T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821282 | ||||||
chr2:11821287
|
T | C | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2621+773T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821287 | ||||||
chr2:11821288
|
G | A | 1 | a0001c0001t0010g0078 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2621+774G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821288 | ||||||
chr2:11821314
|
C | T | 1 | a0001c0001t0003g0191 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2621+800C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821314 | ||||||
chr2:11821385
|
T | C | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2621+871T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821385 | ||||||
chr2:11821440
|
T | C | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2621+926T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821440 | ||||||
chr2:11821471
|
C | T | 2 | a0001c0001t0008g0038a0001c0001t0008g0044 | 2 | HG00639.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2621+957C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821471 | ||||||
chr2:11821495
|
C | T | 3 | a0001c0005t0007g0151a0001c0005t0007g0154a0001c0005t0007g0157 | 3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2621+981C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821495 | ||||||
chr2:11821564
|
G | T | 36 | a0001c0001t0003g0011a0001c0001t0003g0031a0001c0001t0003g0033others(33): Show | 36 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.2621+1050G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821564 | ||||||
chr2:11821565
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2621+1051G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821565 | ||||||
chr2:11821570
|
T | C | 1 | a0001c0001t0005g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2621+1056T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821570 | ||||||
chr2:11821593
|
G | C | 1 | a0001c0001t0001g0256 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2621+1079G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821593 | ||||||
chr2:11821648
|
G | C | 1 | a0001c0001t0037g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2621+1134G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821648 | ||||||
chr2:11821670
|
G | T | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2621+1156G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821670 | ||||||
chr2:11821728
|
C | T | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2621+1214C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821728 | ||||||
chr2:11821732
|
G | C | 1 | a0001c0001t0012g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2621+1218G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821732 | ||||||
chr2:11821915
|
G | A | 3 | a0001c0004t0007g0274a0001c0005t0007g0017a0001c0005t0007g0018 | 3 | HG01109.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2621+1401G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821915 | ||||||
chr2:11821951
|
C | G | 23 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0037others(20): Show | 23 | HG00639.hp2 HG01175.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2621+1437C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821951 | ||||||
chr2:11822277
|
C | CA | 20 | a0001c0001t0001g0103a0001c0001t0001g0185a0001c0001t0002g0067others(17): Show | 20 | HG01257.hp1 HG01258.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.2621+1787dupA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr2 | 11822277 | |||||
chr2:11822277
|
CA | C | 91 | a0001c0001t0001g0259a0001c0001t0001g0273a0001c0001t0002g0147others(88): Show | 91 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.2621+1787delA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr2 | 11822277 | |||||
chr2:11822277
|
CAA | C | 32 | a0001c0001t0003g0011a0001c0001t0003g0031a0001c0001t0003g0033others(29): Show | 32 | HG00423.hp1 HG01255.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.2621+1786_2621+178 others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr2 | 11822277 | |||||
chr2:11822382
|
G | A | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2621+1868G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822382 | ||||||
chr2:11822427
|
G | A | 2 | a0001c0001t0005g0042a0002c0010t0005g0008 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2621+1913G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822427 | ||||||
chr2:11822433
|
G | C | 4 | a0001c0001t0007g0112a0001c0001t0007g0172a0001c0001t0007g0188others(1): Show | 4 | HG00639.hp1 HG00735.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2621+1919G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822433 | ||||||
chr2:11822484
|
C | T | 1 | a0001c0001t0003g0168 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2621+1970C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822484 | ||||||
chr2:11822487
|
A | G | 87 | a0001c0001t0003g0011a0001c0001t0003g0031a0001c0001t0003g0033others(84): Show | 87 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.2621+1973A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822487 | ||||||
chr2:11822521
|
A | G | 2 | a0002c0007t0034g0023a0002c0007t0035g0024 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2621+2007A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822521 | ||||||
chr2:11822861
|
T | C | 3 | a0001c0005t0007g0151a0001c0005t0007g0154a0001c0005t0007g0157 | 3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2622-1771T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822861 | ||||||
chr2:11822895
|
G | A | 1 | a0002c0010t0005g0008 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2622-1737G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822895 | ||||||
chr2:11822960
|
T | C | 1 | a0001c0001t0002g0117 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2622-1672T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822960 | ||||||
chr2:11823142
|
C | T | 2 | a0001c0001t0005g0042a0002c0010t0005g0008 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2622-1490C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823142 | ||||||
chr2:11823145
|
A | C | 3 | a0001c0001t0012g0161a0001c0001t0029g0136a0001c0002t0002g0016 | 3 | HG02738.hp1 HG03491.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2622-1487A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823145 | ||||||
chr2:11823236
|
G | A | 39 | a0001c0001t0003g0011a0001c0001t0003g0031a0001c0001t0003g0033others(36): Show | 39 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2622-1396G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823236 | ||||||
chr2:11823251
|
G | A | 8 | a0001c0001t0009g0108a0001c0001t0009g0229a0001c0001t0018g0032others(5): Show | 8 | HG00738.hp1 HG01081.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2622-1381G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823251 | ||||||
chr2:11823294
|
G | GCC | 87 | a0001c0001t0003g0011a0001c0001t0003g0031a0001c0001t0003g0033others(84): Show | 87 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.2622-1337_2622-133 others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr2 | 11823294 | |||||
chr2:11823329
|
G | A | 6 | a0001c0001t0005g0277a0001c0002t0015g0152a0001c0002t0015g0156others(3): Show | 6 | HG02622.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2622-1303G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823329 | ||||||
chr2:11823509
|
TATTAAAT others(16): Show |
T | 31 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0037others(28): Show | 31 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.2622-1119_2622-109 others(27): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr2 | 11823509 | |||||
chr2:11823527
|
G | A | 6 | a0001c0001t0005g0277a0001c0002t0015g0152a0001c0002t0015g0156others(3): Show | 6 | HG02622.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2622-1105G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823527 | ||||||
chr2:11823821
|
G | A | 1 | a0001c0003t0009g0049 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2622-811G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823821 | ||||||
chr2:11823821
|
G | C | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | NA19074.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2622-811G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823821 | ||||||
chr2:11823883
|
A | C | 1 | a0001c0001t0004g0181 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2622-749A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823883 | ||||||
chr2:11824003
|
G | T | 7 | a0001c0001t0001g0026a0001c0001t0001g0164a0001c0001t0001g0165others(4): Show | 7 | HG00733.hp1 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2622-629G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11824003 | ||||||
chr2:11824277
|
A | T | 2 | a0002c0007t0034g0023a0002c0007t0035g0024 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2622-355A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11824277 | ||||||
chr2:11824335
|
G | C | 7 | a0001c0001t0010g0020a0001c0001t0010g0071a0001c0001t0010g0078others(4): Show | 7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2622-297G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11824335 | ||||||
chr2:11824410
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2622-222C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11824410 | ||||||
chr2:11824460
|
C | T | 12 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0037others(9): Show | 12 | HG01175.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2622-172C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11824460 | ||||||
chr2:11824461
|
A | G | 18 | a0001c0001t0005g0277a0001c0001t0006g0035a0001c0001t0006g0036others(15): Show | 18 | HG01175.hp2 HG01891.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.2622-171A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11824461 |