geneid | 27132 |
---|---|
ensemblid | ENSG00000178773.15 |
hgncid | 2320 |
symbol | CPNE7 |
name | copine 7 |
refseq_nuc | NM_153636.3 |
refseq_prot | NP_705900.1 |
ensembl_nuc | ENST00000319518.13 |
ensembl_prot | ENSP00000317374.8 |
mane_status | MANE Select |
chr | chr16 |
start | 89575758 |
end | 89597246 |
strand | + |
ver | v1.2 |
region | chr16:89575758-89597246 |
region5000 | chr16:89570758-89602246 |
regionname0 | CPNE7_chr16_89575758_89597246 |
regionname5000 | CPNE7_chr16_89570758_89602246 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 558 | 277 | 88 | 56 | 80 | 13 | 38 | 60 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0002 | 0/0 | 558 | 47 | 1 | 11 | 32 | 1 | 2 | 22 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0003 | 0/0 | 558 | 14 | 0 | 0 | 14 | 0 | 0 | 9 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0004 | 0/0 | 558 | 3 | 1 | 0 | 0 | 2 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0005 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0006 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0007 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0008 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0009 | 0/0 | 259 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0010 | 0/0 | 558 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0011 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1677 | 123 | 31 | 35 | 18 | 11 | 27 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0002 | 0/1 | 1677 | 104 | 29 | 8 | 55 | 2 | 9 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0003 | 0/0 | 1677 | 26 | 0 | 1 | 24 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0004 | 0/0 | 1677 | 18 | 1 | 9 | 6 | 1 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0005 | 0/0 | 1677 | 18 | 0 | 11 | 6 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0006 | 0/0 | 1677 | 14 | 0 | 0 | 14 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0007 | 0/0 | 1677 | 13 | 13 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0008 | 0/0 | 1677 | 6 | 5 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0009 | 0/0 | 1677 | 3 | 2 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0010 | 0/0 | 1677 | 2 | 0 | 1 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0011 | 0/0 | 1677 | 2 | 0 | 0 | 0 | 2 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0012 | 0/0 | 1677 | 2 | 1 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0013 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0014 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0015 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0016 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0017 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0018 | 0/0 | 1677 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0019 | 0/0 | 1658 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0020 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0021 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0022 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0023 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0024 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0025 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0026 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0027 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0028 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
c0029 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 766 | 145 | 48 | 37 | 19 | 13 | 27 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
t0002 | 0/1 | 766 | 76 | 13 | 25 | 28 | 3 | 6 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
t0003 | 0/0 | 748 | 61 | 0 | 1 | 59 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
t0004 | 0/0 | 766 | 28 | 4 | 3 | 18 | 0 | 3 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
t0005 | 0/0 | 766 | 14 | 12 | 2 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
t0006 | 0/0 | 757 | 13 | 13 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
t0007 | 0/0 | 748 | 3 | 0 | 0 | 3 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
t0008 | 0/0 | 766 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
t0009 | 0/0 | 766 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
t0010 | 0/0 | 748 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
t0011 | 0/0 | 766 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
t0012 | 0/0 | 766 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
t0013 | 0/0 | 766 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
t0014 | 0/0 | 766 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1677 | 123 | 31 | 35 | 18 | 11 | 27 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0002 | 0/1 | 1677 | 104 | 29 | 8 | 55 | 2 | 9 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0005 | 0/0 | 1677 | 18 | 0 | 11 | 6 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0007 | 0/0 | 1677 | 13 | 13 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0008 | 0/0 | 1677 | 6 | 5 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0009 | 0/0 | 1677 | 3 | 2 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0012 | 0/0 | 1677 | 2 | 1 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0013 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0015 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0023 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0024 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0025 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0027 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0028 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0029 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0002c0003 | 0/0 | 1677 | 26 | 0 | 1 | 24 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0002c0004 | 0/0 | 1677 | 18 | 1 | 9 | 6 | 1 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0002c0010 | 0/0 | 1677 | 2 | 0 | 1 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0002c0017 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0003c0006 | 0/0 | 1677 | 14 | 0 | 0 | 14 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0004c0011 | 0/0 | 1677 | 2 | 0 | 0 | 0 | 2 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0004c0020 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0005c0026 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0006c0014 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0007c0022 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0008c0021 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0009c0019 | 0/0 | 1658 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0010c0018 | 0/0 | 1677 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0011c0016 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2442 | 121 | 31 | 35 | 17 | 11 | 26 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0001t0008 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0001t0012 | 0/0 | 2442 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0002t0001 | 0/0 | 2442 | 6 | 5 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0002t0002 | 0/1 | 2442 | 30 | 8 | 2 | 13 | 2 | 4 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0002t0003 | 0/0 | 2424 | 24 | 0 | 0 | 24 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0002t0004 | 0/0 | 2442 | 26 | 4 | 3 | 16 | 0 | 3 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0002t0005 | 0/0 | 2442 | 12 | 10 | 2 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0002t0007 | 0/0 | 2424 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0002t0009 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0002t0010 | 0/0 | 2424 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0002t0011 | 0/0 | 2442 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0002t0013 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0005t0002 | 0/0 | 2442 | 18 | 0 | 11 | 6 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0007t0006 | 0/0 | 2433 | 13 | 13 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0008t0001 | 0/0 | 2442 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0008t0002 | 0/0 | 2442 | 3 | 2 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0008t0005 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0009t0001 | 0/0 | 2442 | 3 | 2 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0012t0002 | 0/0 | 2442 | 2 | 1 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0013t0002 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0015t0001 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0023t0001 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0024t0001 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0025t0001 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0027t0005 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0028t0001 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0001c0029t0001 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0002c0003t0002 | 0/0 | 2442 | 3 | 0 | 0 | 3 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0002c0003t0003 | 0/0 | 2424 | 21 | 0 | 1 | 19 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0002c0003t0004 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0002c0003t0007 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0002c0004t0002 | 0/0 | 2442 | 17 | 1 | 9 | 5 | 1 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0002c0004t0014 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0002c0010t0001 | 0/0 | 2442 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0002c0010t0008 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0002c0017t0003 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0003c0006t0003 | 0/0 | 2424 | 14 | 0 | 0 | 14 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0004c0011t0001 | 0/0 | 2442 | 2 | 0 | 0 | 0 | 2 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0004c0020t0001 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0005c0026t0001 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0006c0014t0001 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0007c0022t0004 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0008c0021t0001 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0009c0019t0002 | 0/0 | 2423 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0010c0018t0002 | 0/0 | 2442 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
a0011c0016t0003 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | copy fasta | chr16 | 89570758 | 89602246 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0008g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0001t0012g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0004g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0005g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0007g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0007g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0009g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0010g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0011g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0002t0013g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0005t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0005t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0005t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0005t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0005t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0005t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0005t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0005t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0005t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0005t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0005t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0005t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0005t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0005t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0005t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0005t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0007t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0007t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0007t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0007t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0007t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0007t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0007t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0007t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0007t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0007t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0007t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0007t0006g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0007t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0008t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0008t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0008t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0008t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0008t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0008t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0009t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0009t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0009t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0012t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0012t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0013t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0015t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0023t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0024t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0025t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0027t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0028t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0001c0029t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0003t0007g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0004t0002g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0004t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0004t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0004t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0004t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0004t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0004t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0004t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0004t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0004t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0004t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0004t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0004t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0004t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0004t0014g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0010t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0010t0008g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0002c0017t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0003c0006t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0003c0006t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0003c0006t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0003c0006t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0003c0006t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0003c0006t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0003c0006t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0003c0006t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0003c0006t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0003c0006t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0003c0006t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0003c0006t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0003c0006t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0003c0006t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0004c0011t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0004c0011t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0004c0020t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0005c0026t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0006c0014t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0007c0022t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0008c0021t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0009c0019t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0010c0018t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
a0011c0016t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | GBR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0341 | EUR | GBR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | GBR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0196 | EUR | FIN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0265 | EUR | FIN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | FIN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | FIN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00423 | hp2 | a0002 | c0003 | t0002 | g0119 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00438 | hp1 | a0001 | c0005 | t0002 | g0302 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00438 | hp2 | a0001 | c0002 | t0003 | g0236 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00544 | hp1 | a0001 | c0002 | t0004 | g0150 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00544 | hp2 | a0001 | c0002 | t0003 | g0290 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0316 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00597 | hp1 | a0002 | c0003 | t0002 | g0153 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00597 | hp2 | a0003 | c0006 | t0003 | g0146 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00609 | hp1 | a0001 | c0002 | t0004 | g0151 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00609 | hp2 | a0002 | c0017 | t0003 | g0136 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00621 | hp1 | a0003 | c0006 | t0003 | g0342 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00621 | hp2 | a0002 | c0003 | t0004 | g0306 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0287 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00642 | hp2 | a0002 | c0003 | t0003 | g0137 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00673 | hp1 | a0001 | c0001 | t0008 | g0055 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00673 | hp2 | a0002 | c0004 | t0002 | g0307 | EAS | CHS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01070 | hp2 | a0001 | c0005 | t0002 | g0003 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01071 | hp1 | a0001 | c0005 | t0002 | g0003 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01074 | hp1 | a0002 | c0004 | t0002 | g0308 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01081 | hp2 | a0001 | c0008 | t0002 | g0015 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0084 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01167 | hp2 | a0001 | c0012 | t0002 | g0296 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01168 | hp2 | a0002 | c0004 | t0002 | g0001 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01169 | hp1 | a0002 | c0004 | t0002 | g0001 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01192 | hp2 | a0001 | c0002 | t0005 | g0320 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01243 | hp2 | a0001 | c0002 | t0005 | g0186 | AMR | PUR | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01257 | hp2 | a0001 | c0005 | t0002 | g0002 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01258 | hp1 | a0002 | c0004 | t0002 | g0001 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01258 | hp2 | a0001 | c0005 | t0002 | g0002 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01261 | hp1 | a0001 | c0005 | t0002 | g0072 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01261 | hp2 | a0001 | c0002 | t0002 | g0278 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01346 | hp2 | a0002 | c0004 | t0002 | g0319 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01361 | hp2 | a0002 | c0004 | t0002 | g0311 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01496 | hp2 | a0001 | c0005 | t0002 | g0212 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | IBS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0046 | EUR | IBS | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01891 | hp1 | a0006 | c0014 | t0001 | g0008 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0024 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01928 | hp1 | a0002 | c0010 | t0001 | g0245 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01943 | hp1 | a0001 | c0002 | t0004 | g0133 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01943 | hp2 | a0002 | c0004 | t0002 | g0314 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01952 | hp1 | a0001 | c0002 | t0004 | g0131 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01975 | hp2 | a0002 | c0004 | t0002 | g0309 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01978 | hp1 | a0001 | c0005 | t0002 | g0247 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01993 | hp2 | a0001 | c0005 | t0002 | g0193 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02027 | hp1 | a0002 | c0003 | t0003 | g0171 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02027 | hp2 | a0001 | c0002 | t0004 | g0123 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02071 | hp1 | a0002 | c0003 | t0003 | g0116 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02080 | hp1 | a0001 | c0002 | t0004 | g0223 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02080 | hp2 | a0003 | c0006 | t0003 | g0230 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02083 | hp1 | a0001 | c0002 | t0004 | g0227 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02083 | hp2 | a0003 | c0006 | t0003 | g0232 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02129 | hp1 | a0002 | c0003 | t0003 | g0073 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02129 | hp2 | a0001 | c0002 | t0004 | g0225 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02132 | hp1 | a0001 | c0005 | t0002 | g0317 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02132 | hp2 | a0001 | c0002 | t0004 | g0226 | EAS | KHV | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0023 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02148 | hp2 | a0001 | c0005 | t0002 | g0240 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02155 | hp1 | a0001 | c0005 | t0002 | g0310 | EAS | CDX | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02155 | hp2 | a0002 | c0003 | t0007 | g0298 | EAS | CDX | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02165 | hp1 | a0001 | c0002 | t0004 | g0118 | EAS | CDX | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02165 | hp2 | a0002 | c0003 | t0003 | g0124 | EAS | CDX | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02257 | hp1 | a0001 | c0025 | t0001 | g0276 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02258 | hp1 | a0001 | c0002 | t0004 | g0327 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02273 | hp1 | a0001 | c0005 | t0002 | g0107 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02273 | hp2 | a0001 | c0002 | t0004 | g0132 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02280 | hp1 | a0001 | c0007 | t0006 | g0158 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02280 | hp2 | a0001 | c0009 | t0001 | g0013 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02293 | hp1 | a0010 | c0018 | t0002 | g0246 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02293 | hp2 | a0002 | c0004 | t0002 | g0001 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02300 | hp1 | a0001 | c0005 | t0002 | g0250 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02602 | hp1 | a0002 | c0004 | t0002 | g0279 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02615 | hp1 | a0001 | c0002 | t0005 | g0292 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02615 | hp2 | a0005 | c0026 | t0001 | g0017 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02622 | hp1 | a0001 | c0012 | t0002 | g0297 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02622 | hp2 | a0001 | c0029 | t0001 | g0270 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0331 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02723 | hp2 | a0001 | c0007 | t0006 | g0064 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02735 | hp2 | a0001 | c0002 | t0004 | g0134 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02738 | hp2 | a0001 | c0002 | t0011 | g0200 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02809 | hp1 | a0001 | c0002 | t0005 | g0291 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02809 | hp2 | a0004 | c0020 | t0001 | g0340 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02818 | hp1 | a0001 | c0002 | t0005 | g0163 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02818 | hp2 | a0001 | c0007 | t0006 | g0157 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02896 | hp2 | a0001 | c0002 | t0004 | g0326 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02922 | hp1 | a0001 | c0002 | t0005 | g0295 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02922 | hp2 | a0001 | c0008 | t0001 | g0009 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02970 | hp1 | a0001 | c0002 | t0005 | g0020 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02970 | hp2 | a0001 | c0002 | t0002 | g0337 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02976 | hp2 | a0001 | c0002 | t0005 | g0289 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03017 | hp1 | a0001 | c0009 | t0001 | g0061 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03041 | hp1 | a0001 | c0008 | t0001 | g0005 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03041 | hp2 | a0001 | c0013 | t0002 | g0006 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0321 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03098 | hp2 | a0001 | c0007 | t0006 | g0165 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03139 | hp1 | a0001 | c0002 | t0004 | g0271 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03139 | hp2 | a0001 | c0008 | t0002 | g0010 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03195 | hp1 | a0001 | c0007 | t0006 | g0166 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03195 | hp2 | a0001 | c0007 | t0006 | g0161 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03209 | hp1 | a0001 | c0007 | t0006 | g0282 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0264 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03225 | hp1 | a0001 | c0007 | t0006 | g0162 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03225 | hp2 | a0001 | c0007 | t0006 | g0071 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0104 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03453 | hp2 | a0001 | c0008 | t0005 | g0014 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0329 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0322 | AFR | ESN | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03579 | hp2 | a0001 | c0015 | t0001 | g0330 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03669 | hp2 | a0001 | c0001 | t0012 | g0142 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0209 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03927 | hp1 | a0002 | c0003 | t0003 | g0129 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03927 | hp2 | a0001 | c0005 | t0002 | g0303 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03942 | hp1 | a0001 | c0002 | t0004 | g0266 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0210 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG04228 | hp2 | a0001 | c0002 | t0010 | g0219 | SAS | STU | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18522 | hp1 | a0001 | c0007 | t0006 | g0159 | AFR | YRI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0338 | AFR | YRI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18612 | hp1 | a0003 | c0006 | t0003 | g0148 | EAS | CHB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0254 | EAS | CHB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18747 | hp1 | a0001 | c0002 | t0004 | g0228 | EAS | CHB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18747 | hp2 | a0009 | c0019 | t0002 | g0253 | EAS | CHB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18906 | hp1 | a0001 | c0007 | t0006 | g0293 | AFR | YRI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18906 | hp2 | a0001 | c0007 | t0006 | g0160 | AFR | YRI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18940 | hp1 | a0003 | c0006 | t0003 | g0145 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18940 | hp2 | a0001 | c0002 | t0004 | g0039 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18941 | hp1 | a0002 | c0003 | t0003 | g0138 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18941 | hp2 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18942 | hp2 | a0002 | c0003 | t0003 | g0114 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18943 | hp1 | a0002 | c0003 | t0003 | g0208 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18943 | hp2 | a0003 | c0006 | t0003 | g0149 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18944 | hp1 | a0001 | c0002 | t0003 | g0076 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18944 | hp2 | a0007 | c0022 | t0004 | g0288 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18945 | hp1 | a0002 | c0003 | t0003 | g0128 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18945 | hp2 | a0001 | c0002 | t0004 | g0038 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18946 | hp1 | a0003 | c0006 | t0003 | g0274 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18946 | hp2 | a0001 | c0002 | t0003 | g0048 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18947 | hp1 | a0001 | c0005 | t0002 | g0056 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18947 | hp2 | a0001 | c0002 | t0003 | g0233 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18950 | hp2 | a0002 | c0004 | t0002 | g0324 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18952 | hp1 | a0011 | c0016 | t0003 | g0112 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18952 | hp2 | a0001 | c0002 | t0007 | g0235 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18959 | hp1 | a0002 | c0003 | t0003 | g0207 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18959 | hp2 | a0002 | c0003 | t0003 | g0113 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18962 | hp1 | a0001 | c0002 | t0004 | g0155 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18964 | hp1 | a0001 | c0002 | t0003 | g0034 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18966 | hp1 | a0001 | c0002 | t0004 | g0237 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18970 | hp1 | a0001 | c0002 | t0003 | g0192 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18977 | hp1 | a0001 | c0002 | t0003 | g0018 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18977 | hp2 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18979 | hp2 | a0002 | c0004 | t0002 | g0016 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18980 | hp1 | a0002 | c0004 | t0014 | g0305 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18980 | hp2 | a0001 | c0002 | t0003 | g0044 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18982 | hp1 | a0001 | c0024 | t0001 | g0218 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18982 | hp2 | a0001 | c0002 | t0003 | g0177 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18983 | hp1 | a0002 | c0003 | t0003 | g0126 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18990 | hp1 | a0003 | c0006 | t0003 | g0231 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18994 | hp1 | a0001 | c0005 | t0002 | g0323 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18994 | hp2 | a0003 | c0006 | t0003 | g0144 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18995 | hp1 | a0002 | c0003 | t0003 | g0122 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18995 | hp2 | a0001 | c0002 | t0003 | g0211 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18998 | hp1 | a0001 | c0002 | t0003 | g0180 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA18998 | hp2 | a0002 | c0003 | t0003 | g0135 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19004 | hp2 | a0002 | c0003 | t0003 | g0125 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19005 | hp1 | a0002 | c0003 | t0003 | g0111 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19005 | hp2 | a0002 | c0004 | t0002 | g0332 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19009 | hp2 | a0002 | c0003 | t0003 | g0139 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19010 | hp1 | a0002 | c0003 | t0002 | g0312 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19011 | hp2 | a0003 | c0006 | t0003 | g0275 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19012 | hp1 | a0002 | c0003 | t0003 | g0130 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19030 | hp1 | a0001 | c0023 | t0001 | g0195 | AFR | LWK | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19030 | hp2 | a0001 | c0002 | t0013 | g0194 | AFR | LWK | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | LWK | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19054 | hp2 | a0002 | c0010 | t0008 | g0127 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19055 | hp1 | a0001 | c0002 | t0003 | g0047 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19057 | hp1 | a0008 | c0021 | t0001 | g0224 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19057 | hp2 | a0001 | c0002 | t0003 | g0272 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19064 | hp1 | a0001 | c0002 | t0004 | g0169 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19064 | hp2 | a0001 | c0002 | t0003 | g0143 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19065 | hp1 | a0001 | c0002 | t0003 | g0313 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19065 | hp2 | a0001 | c0002 | t0003 | g0260 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19066 | hp2 | a0003 | c0006 | t0003 | g0268 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19067 | hp1 | a0001 | c0002 | t0003 | g0181 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19067 | hp2 | a0001 | c0002 | t0003 | g0049 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19070 | hp1 | a0001 | c0002 | t0003 | g0053 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19070 | hp2 | a0001 | c0002 | t0003 | g0206 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19074 | hp2 | a0003 | c0006 | t0003 | g0147 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19080 | hp1 | a0002 | c0003 | t0003 | g0152 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19080 | hp2 | a0001 | c0002 | t0007 | g0234 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19082 | hp1 | a0001 | c0005 | t0002 | g0043 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19082 | hp2 | a0001 | c0002 | t0003 | g0229 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19084 | hp1 | a0002 | c0004 | t0002 | g0304 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19084 | hp2 | a0001 | c0002 | t0004 | g0117 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19085 | hp1 | a0001 | c0002 | t0004 | g0037 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19087 | hp1 | a0002 | c0003 | t0003 | g0170 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19087 | hp2 | a0003 | c0006 | t0003 | g0168 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19240 | hp1 | a0001 | c0027 | t0005 | g0156 | AFR | YRI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA19240 | hp2 | a0001 | c0028 | t0001 | g0164 | AFR | YRI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA20129 | hp1 | a0001 | c0002 | t0005 | g0197 | AFR | ASW | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA20129 | hp2 | a0001 | c0009 | t0001 | g0011 | AFR | ASW | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA20752 | hp1 | a0004 | c0011 | t0001 | g0077 | EUR | TSI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA20752 | hp2 | a0002 | c0004 | t0002 | g0301 | EUR | TSI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA20805 | hp1 | a0004 | c0011 | t0001 | g0092 | EUR | TSI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | TSI | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0204 | SAS | GIH | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA20905 | hp2 | a0001 | c0002 | t0004 | g0110 | SAS | GIH | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02109 | hp1 | a0001 | c0008 | t0002 | g0012 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02486 | hp1 | a0001 | c0002 | t0005 | g0074 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02559 | hp1 | a0001 | c0007 | t0006 | g0259 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG02559 | hp2 | a0001 | c0002 | t0005 | g0187 | AFR | ACB | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03471 | hp1 | a0001 | c0002 | t0004 | g0325 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | USA | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
HG06807 | hp2 | a0001 | c0002 | t0005 | g0019 | AFR | USA | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | USA | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA20300 | hp2 | a0002 | c0004 | t0002 | g0315 | AFR | USA | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA21309 | hp1 | a0001 | c0002 | t0009 | g0328 | AFR | LWK | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0042 | REF | REF | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0283 | REF | REF | CPNE7_chr16_89570758_89602246 | CPNE7 | chr16 | 89570758 | 89602246 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:89577593
|
T | C | 2 | a0002a0011 | 48 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(45): Show |
missense_variant | MODERATE | c.229T>C | p.Phe77Leu | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/15 | 369/2442 | 229/1677 | 77/558 | chr16 | 89577593 | ||
chr16:89577698
|
G | A | 1 | a0010 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.334G>A | p.Gly112Ser | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/15 | 474/2442 | 334/1677 | 112/558 | chr16 | 89577698 | ||
chr16:89585766
|
AGGCCTTT others(67): Show |
A | 1 | a0009 | 1 | NA18747.hp2 | frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.768_780+61delTGAGG others(69): Show |
p.Phe256fs | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/15 | 908/2442 | 768/1677 | 256/558 | INFO_REALIGN_3_PRIME | chr16 | 89585766 | |
chr16:89586712
|
C | T | 1 | a0005 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.823C>T | p.Arg275Cys | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/15 | 963/2442 | 823/1677 | 275/558 | chr16 | 89586712 | ||
chr16:89588712
|
G | A | 1 | a0004 | 3 | HG02809.hp2 NA20752.hp1 NA20805.hp1 |
missense_variant | MODERATE | c.965G>A | p.Arg322Gln | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/15 | 1105/2442 | 965/1677 | 322/558 | chr16 | 89588712 | ||
chr16:89591252
|
A | G | 1 | a0006 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.1294A>G | p.Lys432Glu | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/15 | 1434/2442 | 1294/1677 | 432/558 | chr16 | 89591252 | ||
chr16:89595425
|
G | A | 1 | a0007 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.1361G>A | p.Arg454Gln | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/15 | 1501/2442 | 1361/1677 | 454/558 | chr16 | 89595425 | ||
chr16:89595428
|
A | G | 1 | a0008 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.1364A>G | p.Glu455Gly | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/15 | 1504/2442 | 1364/1677 | 455/558 | chr16 | 89595428 | ||
chr16:89596617
|
C | T | 2 | a0003a0011 | 15 | HG00597.hp2 HG00621.hp1 HG02080.hp2 others(12): Show |
missense_variant | MODERATE | c.1673C>T | p.Pro558Leu | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 1813/2442 | 1673/1677 | 558/558 | chr16 | 89596617 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:89576050
|
G | A | 4 | a0001c0008a0001c0009a0001c0013others(1): Show | 11 | HG01081.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
synonymous_variant | LOW | c.153G>A | p.Gln51Gln | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/15 | 293/2442 | 153/1677 | 51/558 | chr16 | 89576050 | ||
chr16:89577589
|
G | A | 1 | a0001c0015 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.225G>A | p.Lys75Lys | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/15 | 365/2442 | 225/1677 | 75/558 | chr16 | 89577589 | ||
chr16:89584791
|
C | T | 1 | a0001c0029 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.525C>T | p.Ser175Ser | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/15 | 665/2442 | 525/1677 | 175/558 | chr16 | 89584791 | ||
chr16:89584800
|
C | T | 2 | a0001c0027a0001c0028 | 2 | NA19240.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.534C>T | p.Phe178Phe | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/15 | 674/2442 | 534/1677 | 178/558 | chr16 | 89584800 | ||
chr16:89591137
|
C | T | 1 | a0001c0025 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1179C>T | p.Gly393Gly | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/15 | 1319/2442 | 1179/1677 | 393/558 | chr16 | 89591137 | ||
chr16:89591173
|
C | A | 1 | a0008c0021 | 1 | NA19057.hp1 | synonymous_variant | LOW | c.1215C>A | p.Val405Val | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/15 | 1355/2442 | 1215/1677 | 405/558 | chr16 | 89591173 | ||
chr16:89595381
|
G | C | 1 | a0001c0007 | 13 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(10): Show |
synonymous_variant | LOW | c.1317G>C | p.Leu439Leu | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/15 | 1457/2442 | 1317/1677 | 439/558 | chr16 | 89595381 | ||
chr16:89595396
|
C | T | 2 | a0001c0012a0001c0013 | 3 | HG01167.hp2 HG02622.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.1332C>T | p.Asp444Asp | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/15 | 1472/2442 | 1332/1677 | 444/558 | chr16 | 89595396 | ||
chr16:89595399
|
C | T | 4 | a0001c0005a0001c0024a0002c0004others(1): Show | 38 | HG00438.hp1 HG00673.hp2 HG01070.hp2 others(35): Show |
synonymous_variant | LOW | c.1335C>T | p.Gly445Gly | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/15 | 1475/2442 | 1335/1677 | 445/558 | chr16 | 89595399 | ||
chr16:89595429
|
G | A | 1 | a0008c0021 | 1 | NA19057.hp1 | synonymous_variant | LOW | c.1365G>A | p.Glu455Glu | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/15 | 1505/2442 | 1365/1677 | 455/558 | chr16 | 89595429 | ||
chr16:89595519
|
C | T | 1 | a0002c0017 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.1455C>T | p.Gly485Gly | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/15 | 1595/2442 | 1455/1677 | 485/558 | chr16 | 89595519 | ||
chr16:89596495
|
G | A | 1 | a0001c0023 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1551G>A | p.Ala517Ala | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 1691/2442 | 1551/1677 | 517/558 | chr16 | 89596495 | ||
chr16:89596582
|
T | C | 19 | a0001c0002a0001c0005a0001c0007others(16): Show | 212 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(209): Show |
synonymous_variant | LOW | c.1638T>C | p.Gly546Gly | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 1778/2442 | 1638/1677 | 546/558 | chr16 | 89596582 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:89575795
|
G | A | 1 | a0001c0002t0009 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-103G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/15 | 103 | chr16 | 89575795 | |||||
chr16:89575872
|
C | G | 1 | a0002c0004t0014 | 1 | NA18980.hp1 | 5_prime_UTR_variant | MODIFIER | c.-26C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/15 | 26 | chr16 | 89575872 | |||||
chr16:89596664
|
G | A | 19 | a0001c0002t0002a0001c0002t0004a0001c0002t0005others(16): Show | 122 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*43G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 43 | chr16 | 89596664 | |||||
chr16:89596735
|
C | A | 1 | a0001c0001t0012 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 114 | chr16 | 89596735 | |||||
chr16:89596782
|
C | T | 4 | a0001c0002t0004a0001c0002t0011a0002c0003t0004others(1): Show | 29 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*161C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 161 | chr16 | 89596782 | |||||
chr16:89596924
|
A | G | 1 | a0001c0001t0012 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*303A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 303 | chr16 | 89596924 | |||||
chr16:89596959
|
G | A | 3 | a0001c0002t0005a0001c0008t0005a0001c0027t0005 | 14 | HG01192.hp2 HG01243.hp2 HG02486.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*338G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 338 | chr16 | 89596959 | |||||
chr16:89597005
|
C | T | 2 | a0001c0002t0007a0002c0003t0007 | 3 | HG02155.hp2 NA18952.hp2 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*384C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 384 | chr16 | 89597005 | |||||
chr16:89597066
|
C | T | 1 | a0001c0002t0011 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*445C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 445 | chr16 | 89597066 | |||||
chr16:89597157
|
A | G | 1 | a0001c0002t0013 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*536A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 536 | chr16 | 89597157 | |||||
chr16:89597158
|
TGGGGTCT others(2): Show |
T | 1 | a0001c0007t0006 | 13 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*556_*564delGGGGTC others(3): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 556 | INFO_REALIGN_3_PRIME | chr16 | 89597158 | ||||
chr16:89597158
|
TGGGGTCT others(11): Show |
T | 8 | a0001c0002t0003a0001c0002t0007a0001c0002t0010others(5): Show | 65 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*547_*564delGGGGTC others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 547 | INFO_REALIGN_3_PRIME | chr16 | 89597158 | ||||
chr16:89597189
|
G | T | 2 | a0001c0001t0008a0002c0010t0008 | 2 | HG00673.hp1 NA19054.hp2 |
3_prime_UTR_variant | MODIFIER | c.*568G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 15/15 | 568 | chr16 | 89597189 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:89576088
|
G | C | 11 | a0001c0001t0001g0007a0001c0008t0001g0005a0001c0008t0001g0009others(8): Show | 11 | HG01081.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.174+17G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576088 | ||||||
chr16:89576095
|
G | T | 1 | a0003c0006t0003g0342 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.174+24G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576095 | ||||||
chr16:89576299
|
G | A | 1 | a0002c0004t0002g0016 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.174+228G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576299 | ||||||
chr16:89576417
|
G | T | 1 | a0001c0001t0001g0341 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.174+346G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576417 | ||||||
chr16:89576606
|
C | A | 46 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(43): Show | 46 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.174+535C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576606 | ||||||
chr16:89576673
|
T | A | 1 | a0001c0001t0001g0062 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.174+602T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576673 | ||||||
chr16:89576702
|
C | T | 1 | a0001c0009t0001g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.174+631C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576702 | ||||||
chr16:89576720
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.174+649C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576720 | ||||||
chr16:89576752
|
A | G | 1 | a0001c0009t0001g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.174+681A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576752 | ||||||
chr16:89576839
|
C | T | 41 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(38): Show | 41 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.175-700C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576839 | ||||||
chr16:89576913
|
G | A | 4 | a0001c0002t0001g0025a0001c0002t0002g0022a0001c0002t0002g0023others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-626G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89576913 | ||||||
chr16:89577056
|
C | G | 48 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(45): Show | 48 | HG00323.hp2 HG00673.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.175-483C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577056 | ||||||
chr16:89577124
|
T | C | 51 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(48): Show | 51 | HG00323.hp2 HG00673.hp1 HG01261.hp1 others(48): Show |
intron_variant | MODIFIER | c.175-415T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577124 | ||||||
chr16:89577193
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.175-346C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577193 | ||||||
chr16:89577226
|
T | G | 1 | a0001c0002t0003g0076 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.175-313T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577226 | ||||||
chr16:89577268
|
G | A | 32 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.175-271G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577268 | ||||||
chr16:89577268
|
G | T | 1 | a0002c0004t0002g0332 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.175-271G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577268 | ||||||
chr16:89577292
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.175-247C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577292 | ||||||
chr16:89577338
|
G | A | 1 | a0001c0005t0002g0107 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.175-201G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577338 | ||||||
chr16:89577410
|
A | C | 1 | a0001c0001t0001g0075 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.175-129A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577410 | ||||||
chr16:89577452
|
C | T | 2 | a0001c0002t0005g0019a0001c0002t0005g0020 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.175-87C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577452 | ||||||
chr16:89577463
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028 | 3 | HG02602.hp2 HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.175-76G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 1/14 | chr16 | 89577463 | ||||||
chr16:89577770
|
C | A | 73 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0066others(70): Show | 73 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.357+49C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89577770 | ||||||
chr16:89577796
|
A | G | 1 | a0002c0003t0003g0171 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.357+75A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89577796 | ||||||
chr16:89577952
|
G | A | 3 | a0001c0001t0001g0172a0001c0002t0001g0025a0004c0011t0001g0077 | 3 | HG03540.hp1 HG03834.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.357+231G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89577952 | ||||||
chr16:89578052
|
C | A | 3 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0336 | 3 | HG02723.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.357+331C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578052 | ||||||
chr16:89578067
|
C | CT | 16 | a0001c0001t0001g0339a0001c0002t0001g0331a0001c0002t0002g0329others(13): Show | 16 | HG01081.hp2 HG01109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.357+361dupT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89578067 | |||||
chr16:89578067
|
CT | C | 202 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(199): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.357+361delT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89578067 | |||||
chr16:89578127
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.357+406T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578127 | ||||||
chr16:89578167
|
C | T | 4 | a0001c0002t0001g0322a0001c0002t0002g0321a0001c0002t0005g0074others(1): Show | 4 | HG01192.hp2 HG02486.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+446C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578167 | ||||||
chr16:89578288
|
A | C | 2 | a0001c0001t0001g0339a0004c0020t0001g0340 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.357+567A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578288 | ||||||
chr16:89578309
|
T | C | 3 | a0001c0001t0001g0339a0001c0002t0001g0025a0004c0020t0001g0340 | 3 | HG01109.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.357+588T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578309 | ||||||
chr16:89578314
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.357+593T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578314 | ||||||
chr16:89578363
|
C | T | 2 | a0001c0001t0001g0339a0004c0020t0001g0340 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.357+642C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578363 | ||||||
chr16:89578399
|
T | C | 7 | a0001c0001t0001g0175a0001c0008t0001g0005a0001c0008t0002g0012others(4): Show | 7 | HG02109.hp1 HG02451.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.357+678T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578399 | ||||||
chr16:89578408
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.357+687C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578408 | ||||||
chr16:89578418
|
C | T | 2 | a0001c0008t0001g0005a0001c0009t0001g0061 | 2 | HG03017.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.357+697C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578418 | ||||||
chr16:89578452
|
A | G | 14 | a0001c0001t0001g0339a0001c0002t0001g0025a0001c0002t0001g0331others(11): Show | 14 | HG01081.hp2 HG01109.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.357+731A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578452 | ||||||
chr16:89578525
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.357+804C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578525 | ||||||
chr16:89578657
|
G | A | 1 | a0001c0002t0004g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.357+936G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578657 | ||||||
chr16:89578675
|
G | A | 4 | a0002c0003t0003g0111a0002c0003t0003g0113a0002c0003t0003g0114others(1): Show | 4 | NA18942.hp2 NA18952.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+954G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578675 | ||||||
chr16:89578759
|
C | CA | 9 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0001g0339others(6): Show | 9 | HG01109.hp2 HG02071.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.357+1057dupA | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89578759 | |||||
chr16:89578759
|
CA | C | 8 | a0001c0001t0001g0030a0001c0001t0001g0179a0001c0002t0001g0025others(5): Show | 8 | HG02615.hp2 HG02738.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.357+1057delA | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89578759 | |||||
chr16:89578759
|
CAA | C | 201 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(198): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.357+1056_357+1057d others(4): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89578759 | |||||
chr16:89578759
|
CAAA | C | 29 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0059others(26): Show | 32 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.357+1055_357+1057d others(5): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89578759 | |||||
chr16:89578898
|
T | A | 3 | a0001c0002t0001g0025a0001c0002t0002g0022a0001c0008t0001g0005 | 3 | HG03041.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.357+1177T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578898 | ||||||
chr16:89578913
|
C | T | 18 | a0001c0002t0001g0167a0001c0002t0002g0321a0001c0002t0005g0074others(15): Show | 18 | HG01192.hp2 HG02280.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.357+1192C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578913 | ||||||
chr16:89578928
|
C | T | 1 | a0001c0002t0002g0278 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.357+1207C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578928 | ||||||
chr16:89578937
|
C | A | 2 | a0001c0001t0001g0339a0004c0020t0001g0340 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.357+1216C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578937 | ||||||
chr16:89578952
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0294 | 2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.357+1231G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578952 | ||||||
chr16:89578960
|
C | G | 2 | a0001c0002t0001g0331a0001c0015t0001g0330 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.357+1239C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578960 | ||||||
chr16:89578966
|
T | G | 1 | a0001c0008t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.357+1245T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578966 | ||||||
chr16:89578976
|
G | A | 2 | a0001c0002t0001g0025a0001c0002t0002g0022 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.357+1255G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89578976 | ||||||
chr16:89579029
|
G | T | 204 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(201): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.357+1308G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579029 | ||||||
chr16:89579067
|
G | A | 6 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0002t0005g0019others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.357+1346G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579067 | ||||||
chr16:89579162
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.357+1441C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579162 | ||||||
chr16:89579163
|
G | A | 1 | a0001c0008t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.357+1442G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579163 | ||||||
chr16:89579289
|
C | CA | 13 | a0001c0001t0001g0175a0001c0001t0001g0188a0001c0001t0001g0189others(10): Show | 13 | HG02109.hp1 HG02451.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.357+1583dupA | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89579289 | |||||
chr16:89579289
|
CA | C | 6 | a0001c0001t0001g0106a0001c0001t0001g0280a0001c0001t0001g0339others(3): Show | 6 | HG01109.hp2 HG01168.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.357+1583delA | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89579289 | |||||
chr16:89579339
|
G | A | 1 | a0001c0002t0005g0295 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.357+1618G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579339 | ||||||
chr16:89579438
|
C | T | 245 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(242): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.357+1717C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579438 | ||||||
chr16:89579475
|
G | A | 2 | a0001c0002t0001g0322a0006c0014t0001g0008 | 2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.357+1754G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579475 | ||||||
chr16:89579484
|
G | A | 3 | a0001c0001t0001g0063a0001c0007t0006g0064a0001c0007t0006g0282 | 3 | HG02723.hp2 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.357+1763G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579484 | ||||||
chr16:89579487
|
C | T | 63 | a0001c0001t0001g0078a0001c0001t0001g0115a0001c0001t0001g0120others(60): Show | 63 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.357+1766C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579487 | ||||||
chr16:89579549
|
G | C | 253 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(250): Show | 259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.357+1828G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579549 | ||||||
chr16:89579615
|
C | T | 216 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(213): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.357+1894C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579615 | ||||||
chr16:89579671
|
ATCACATG others(18): Show |
A | 8 | a0001c0001t0001g0175a0001c0002t0001g0331a0001c0008t0001g0005others(5): Show | 8 | HG02109.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.357+1967_357+1991d others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89579671 | |||||
chr16:89579676
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.357+1955A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579676 | ||||||
chr16:89579717
|
C | G | 1 | a0001c0002t0001g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.357+1996C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579717 | ||||||
chr16:89579722
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.357+2001C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579722 | ||||||
chr16:89579746
|
CACACAGA others(513): Show |
C | 1 | a0001c0001t0001g0081 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.357+2076_357+2595d others(2): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89579746 | |||||
chr16:89579781
|
CGTCACCC others(237): Show |
C | 1 | a0001c0002t0002g0104 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.357+2108_357+2351d others(2): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89579781 | |||||
chr16:89579797
|
G | A | 1 | a0001c0005t0002g0193 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.357+2076G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579797 | ||||||
chr16:89579797
|
GGAACATC others(467): Show |
G | 1 | a0001c0001t0001g0082 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.357+2090_357+2563d others(2): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89579797 | |||||
chr16:89579811
|
GTCACACG others(421): Show |
G | 214 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(211): Show | 217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.357+2108_357+2535d others(2): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89579811 | |||||
chr16:89579836
|
C | G | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2115C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579836 | ||||||
chr16:89579841
|
G | A | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2120G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579841 | ||||||
chr16:89579872
|
G | A | 2 | a0001c0002t0001g0322a0006c0014t0001g0008 | 2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.357+2151G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579872 | ||||||
chr16:89579878
|
T | C | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2157T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579878 | ||||||
chr16:89579887
|
G | A | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2166G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579887 | ||||||
chr16:89579901
|
A | G | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2180A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579901 | ||||||
chr16:89579907
|
C | T | 3 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0338 | 3 | HG01891.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.357+2186C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579907 | ||||||
chr16:89579918
|
G | A | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2197G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579918 | ||||||
chr16:89579928
|
G | C | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2207G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579928 | ||||||
chr16:89579933
|
A | G | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2212A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579933 | ||||||
chr16:89579964
|
G | A | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2243G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579964 | ||||||
chr16:89579971
|
G | A | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2250G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579971 | ||||||
chr16:89579988
|
A | G | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2267A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579988 | ||||||
chr16:89579992
|
C | G | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2271C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579992 | ||||||
chr16:89579993
|
A | C | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2272A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579993 | ||||||
chr16:89579995
|
G | A | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2274G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579995 | ||||||
chr16:89579996
|
G | T | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2275G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579996 | ||||||
chr16:89579997
|
A | C | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2276A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89579997 | ||||||
chr16:89580009
|
A | G | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2288A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580009 | ||||||
chr16:89580016
|
G | A | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2295G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580016 | ||||||
chr16:89580025
|
T | C | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2304T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580025 | ||||||
chr16:89580026
|
G | T | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2305G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580026 | ||||||
chr16:89580033
|
G | A | 8 | a0001c0001t0001g0175a0001c0002t0001g0331a0001c0008t0001g0005others(5): Show | 8 | HG02109.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.357+2312G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580033 | ||||||
chr16:89580034
|
C | A | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2313C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580034 | ||||||
chr16:89580036
|
G | C | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2315G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580036 | ||||||
chr16:89580040
|
C | T | 2 | a0001c0002t0005g0289a0001c0008t0001g0009 | 2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.357+2319C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580040 | ||||||
chr16:89580055
|
G | A | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2334G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580055 | ||||||
chr16:89580060
|
A | C | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2339A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580060 | ||||||
chr16:89580062
|
G | A | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2341G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580062 | ||||||
chr16:89580063
|
G | T | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2342G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580063 | ||||||
chr16:89580064
|
A | C | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2343A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580064 | ||||||
chr16:89580078
|
T | C | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2357T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580078 | ||||||
chr16:89580081
|
A | T | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2360A>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580081 | ||||||
chr16:89580082
|
G | C | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2361G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580082 | ||||||
chr16:89580086
|
C | T | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2365C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580086 | ||||||
chr16:89580087
|
G | A | 3 | a0001c0002t0002g0104a0001c0008t0001g0005a0002c0004t0002g0016 | 3 | HG03041.hp1 HG03239.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.357+2366G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580087 | ||||||
chr16:89580107
|
C | T | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2386C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580107 | ||||||
chr16:89580108
|
A | G | 10 | a0001c0001t0001g0175a0001c0002t0001g0331a0001c0002t0002g0104others(7): Show | 10 | HG02109.hp1 HG02451.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.357+2387A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580108 | ||||||
chr16:89580109
|
G | A | 25 | a0001c0001t0001g0318a0001c0002t0002g0316a0001c0002t0003g0313others(22): Show | 28 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.357+2388G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580109 | ||||||
chr16:89580122
|
C | T | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2401C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580122 | ||||||
chr16:89580124
|
C | T | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2403C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580124 | ||||||
chr16:89580128
|
G | C | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2407G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580128 | ||||||
chr16:89580132
|
C | T | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2411C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580132 | ||||||
chr16:89580133
|
A | G | 30 | a0001c0001t0001g0318a0001c0002t0001g0029a0001c0002t0001g0322others(27): Show | 33 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.357+2412A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580133 | ||||||
chr16:89580147
|
G | A | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2426G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580147 | ||||||
chr16:89580163
|
CGTCACCC others(153): Show |
C | 1 | a0001c0002t0002g0104 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.357+2443_357+2602d others(2): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580163 | ||||||
chr16:89580164
|
G | A | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2443G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580164 | ||||||
chr16:89580172
|
C | A | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2451C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580172 | ||||||
chr16:89580174
|
G | C | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2453G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580174 | ||||||
chr16:89580192
|
C | T | 1 | a0002c0004t0002g0319 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.357+2471C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580192 | ||||||
chr16:89580193
|
G | A | 1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+2472G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580193 | ||||||
chr16:89580193
|
G | GTCACACG others(39): Show |
3 | a0002c0003t0002g0153a0002c0003t0003g0152a0002c0003t0003g0171 | 3 | HG00597.hp1 HG02027.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.357+2489_357+2534d others(48): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580193 | |||||
chr16:89580235
|
C | A | 38 | a0001c0001t0001g0175a0001c0001t0001g0318a0001c0002t0001g0029others(35): Show | 41 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.357+2514C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580235 | ||||||
chr16:89580239
|
A | G | 41 | a0001c0001t0001g0175a0001c0001t0001g0318a0001c0001t0001g0339others(38): Show | 44 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.357+2518A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580239 | ||||||
chr16:89580245
|
C | T | 2 | a0001c0001t0001g0300a0001c0008t0002g0010 | 2 | HG00741.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.357+2524C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580245 | ||||||
chr16:89580271
|
A | G | 8 | a0001c0001t0001g0175a0001c0002t0001g0331a0001c0008t0001g0005others(5): Show | 8 | HG02109.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.357+2550A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580271 | ||||||
chr16:89580285
|
A | G | 8 | a0001c0001t0001g0175a0001c0002t0001g0331a0001c0008t0001g0005others(5): Show | 8 | HG02109.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.357+2564A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580285 | ||||||
chr16:89580302
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.357+2581G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580302 | ||||||
chr16:89580320
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.357+2599A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580320 | ||||||
chr16:89580324
|
C | A | 1 | a0001c0002t0002g0104 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.357+2603C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580324 | ||||||
chr16:89580331
|
G | GTCACACG others(591): Show |
1 | a0001c0008t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.357+2626_357+2627i others(600): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580331 | |||||
chr16:89580331
|
G | GTCACACG others(1445): Show |
1 | a0001c0015t0001g0330 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.357+2626_357+2627i others(1454): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580331 | |||||
chr16:89580331
|
G | GTCACACG others(591): Show |
5 | a0001c0001t0001g0175a0001c0008t0002g0012a0001c0008t0005g0014others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.357+2626_357+2627i others(600): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580331 | |||||
chr16:89580331
|
G | GTCACACG others(1445): Show |
1 | a0001c0002t0001g0331 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.357+2626_357+2627i others(1454): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580331 | |||||
chr16:89580338
|
G | A | 1 | a0001c0002t0005g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.357+2617G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580338 | ||||||
chr16:89580348
|
ATCACCCG others(153): Show |
A | 1 | a0001c0001t0001g0060 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.357+2682_357+2841d others(2): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580348 | |||||
chr16:89580355
|
G | A | 2 | a0001c0002t0001g0322a0006c0014t0001g0008 | 2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.357+2634G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580355 | ||||||
chr16:89580361
|
C | T | 1 | a0001c0002t0002g0104 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.357+2640C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580361 | ||||||
chr16:89580369
|
C | T | 2 | a0001c0002t0002g0329a0001c0002t0009g0328 | 2 | HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.357+2648C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580369 | ||||||
chr16:89580379
|
G | A | 1 | a0001c0027t0005g0156 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.357+2658G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580379 | ||||||
chr16:89580385
|
T | C | 2 | a0001c0001t0001g0339a0004c0020t0001g0340 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.357+2664T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580385 | ||||||
chr16:89580396
|
ATCACCCG others(38): Show |
A | 1 | a0001c0009t0001g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.357+2682_357+2726d others(47): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580396 | |||||
chr16:89580403
|
G | A | 215 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(212): Show | 218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.357+2682G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580403 | ||||||
chr16:89580420
|
ATCACCCA others(14): Show |
A | 1 | a0001c0002t0001g0322 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.357+2713_357+2733d others(23): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580420 | |||||
chr16:89580434
|
A | AGAACATC others(14): Show |
1 | a0007c0022t0004g0288 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.357+2742_357+2762d others(23): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580434 | |||||
chr16:89580434
|
A | G | 244 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(241): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.357+2713A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580434 | ||||||
chr16:89580473
|
C | G | 1 | a0001c0002t0004g0151 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.357+2752C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580473 | ||||||
chr16:89580485
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.357+2764C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580485 | ||||||
chr16:89580516
|
T | C | 2 | a0001c0001t0001g0339a0004c0020t0001g0340 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.357+2795T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580516 | ||||||
chr16:89580545
|
T | C | 2 | a0001c0002t0003g0031a0001c0002t0003g0034 | 2 | NA18941.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.357+2824T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580545 | ||||||
chr16:89580556
|
ATCACCCA others(14): Show |
A | 1 | a0001c0002t0013g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.357+2857_357+2877d others(23): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580556 | |||||
chr16:89580607
|
C | T | 219 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(216): Show | 222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.357+2886C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580607 | ||||||
chr16:89580623
|
CTCACCTG others(697): Show |
C | 2 | a0001c0001t0001g0339a0004c0020t0001g0340 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.357+2908_358-2365d others(2): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580623 | |||||
chr16:89580629
|
T | C | 257 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(254): Show | 263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.357+2908T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580629 | ||||||
chr16:89580659
|
A | G | 1 | a0001c0001t0008g0055 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.357+2938A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580659 | ||||||
chr16:89580713
|
C | T | 8 | a0001c0001t0001g0175a0001c0002t0001g0331a0001c0008t0001g0005others(5): Show | 8 | HG02109.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.358-2984C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580713 | ||||||
chr16:89580793
|
CACACGGA others(17): Show |
C | 1 | a0001c0002t0005g0295 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.358-2883_358-2860d others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580793 | |||||
chr16:89580832
|
G | A | 25 | a0001c0001t0001g0318a0001c0002t0002g0316a0001c0002t0003g0313others(22): Show | 28 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.358-2865G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580832 | ||||||
chr16:89580839
|
ATCACACG others(17): Show |
A | 1 | a0001c0001t0001g0103 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.358-2844_358-2821d others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580839 | |||||
chr16:89580889
|
C | T | 1 | a0001c0002t0001g0322 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.358-2808C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580889 | ||||||
chr16:89580893
|
C | T | 2 | a0001c0002t0004g0117a0001c0002t0004g0150 | 2 | HG00544.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.358-2804C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580893 | ||||||
chr16:89580917
|
T | TGGAACAT others(14): Show |
3 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0338 | 3 | HG01891.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.358-2771_358-2751d others(23): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89580917 | |||||
chr16:89580938
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.358-2759C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580938 | ||||||
chr16:89580963
|
T | C | 1 | a0001c0008t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.358-2734T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580963 | ||||||
chr16:89580978
|
A | G | 334 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(331): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.358-2719A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89580978 | ||||||
chr16:89581019
|
G | A | 1 | a0001c0009t0001g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.358-2678G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581019 | ||||||
chr16:89581033
|
G | A | 1 | a0001c0002t0009g0328 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.358-2664G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581033 | ||||||
chr16:89581131
|
A | G | 1 | a0001c0008t0002g0015 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.358-2566A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581131 | ||||||
chr16:89581180
|
C | T | 2 | a0001c0002t0001g0029a0005c0026t0001g0017 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.358-2517C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581180 | ||||||
chr16:89581196
|
G | A | 2 | a0001c0002t0001g0029a0005c0026t0001g0017 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.358-2501G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581196 | ||||||
chr16:89581219
|
T | TGGAACAT others(42): Show |
25 | a0001c0001t0001g0318a0001c0002t0002g0316a0001c0002t0003g0313others(22): Show | 28 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.358-2436_358-2435i others(51): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89581219 | |||||
chr16:89581261
|
C | T | 1 | a0001c0002t0001g0322 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.358-2436C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581261 | ||||||
chr16:89581268
|
C | T | 207 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(204): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.358-2429C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581268 | ||||||
chr16:89581273
|
C | T | 1 | a0001c0025t0001g0276 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.358-2424C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581273 | ||||||
chr16:89581297
|
C | T | 223 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(220): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.358-2400C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581297 | ||||||
chr16:89581351
|
G | A | 2 | a0001c0001t0001g0339a0004c0020t0001g0340 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.358-2346G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581351 | ||||||
chr16:89581364
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.358-2333C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581364 | ||||||
chr16:89581424
|
C | T | 2 | a0003c0006t0003g0274a0003c0006t0003g0275 | 2 | NA18946.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.358-2273C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581424 | ||||||
chr16:89581519
|
C | T | 2 | a0001c0001t0001g0339a0004c0020t0001g0340 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.358-2178C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581519 | ||||||
chr16:89581543
|
G | C | 259 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(256): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.358-2154G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581543 | ||||||
chr16:89581615
|
G | C | 1 | a0001c0002t0002g0196 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.358-2082G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581615 | ||||||
chr16:89581873
|
C | T | 57 | a0001c0001t0001g0078a0001c0001t0001g0115a0001c0001t0001g0120others(54): Show | 57 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.358-1824C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581873 | ||||||
chr16:89581883
|
G | A | 25 | a0001c0001t0001g0318a0001c0002t0002g0316a0001c0002t0003g0313others(22): Show | 28 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.358-1814G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581883 | ||||||
chr16:89581992
|
G | A | 1 | a0001c0002t0005g0197 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.358-1705G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89581992 | ||||||
chr16:89582023
|
C | T | 1 | a0001c0002t0001g0322 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.358-1674C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582023 | ||||||
chr16:89582078
|
C | G | 9 | a0001c0001t0001g0175a0001c0002t0001g0167a0001c0002t0001g0331others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.358-1619C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582078 | ||||||
chr16:89582095
|
T | C | 4 | a0001c0001t0001g0083a0001c0001t0001g0105a0001c0001t0001g0334others(1): Show | 4 | HG00733.hp1 HG01106.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-1602T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582095 | ||||||
chr16:89582172
|
C | T | 76 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.358-1525C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582172 | ||||||
chr16:89582245
|
A | C | 5 | a0001c0001t0001g0175a0001c0008t0002g0012a0001c0008t0005g0014others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.358-1452A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582245 | ||||||
chr16:89582396
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.358-1301G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582396 | ||||||
chr16:89582406
|
T | A | 5 | a0001c0002t0002g0321a0001c0002t0005g0074a0001c0002t0005g0291others(2): Show | 5 | HG01192.hp2 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.358-1291T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582406 | ||||||
chr16:89582412
|
C | T | 1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.358-1285C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582412 | ||||||
chr16:89582443
|
C | A | 1 | a0001c0001t0001g0335 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.358-1254C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582443 | ||||||
chr16:89582568
|
C | T | 39 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(36): Show | 39 | HG00323.hp2 HG00673.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.358-1129C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582568 | ||||||
chr16:89582571
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.358-1126G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582571 | ||||||
chr16:89582629
|
T | G | 1 | a0001c0001t0001g0060 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.358-1068T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582629 | ||||||
chr16:89582656
|
G | T | 2 | a0001c0002t0001g0322a0006c0014t0001g0008 | 2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.358-1041G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582656 | ||||||
chr16:89582761
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.358-936G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582761 | ||||||
chr16:89582774
|
C | G | 2 | a0001c0002t0001g0322a0006c0014t0001g0008 | 2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.358-923C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582774 | ||||||
chr16:89582814
|
G | A | 1 | a0001c0025t0001g0276 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.358-883G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582814 | ||||||
chr16:89582837
|
A | G | 216 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(213): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.358-860A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89582837 | ||||||
chr16:89583140
|
C | T | 1 | a0001c0025t0001g0276 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.358-557C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89583140 | ||||||
chr16:89583227
|
G | A | 224 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(221): Show | 227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.358-470G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89583227 | ||||||
chr16:89583267
|
G | A | 225 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(222): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.358-430G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89583267 | ||||||
chr16:89583276
|
G | C | 25 | a0001c0001t0001g0318a0001c0002t0002g0316a0001c0002t0003g0313others(22): Show | 28 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.358-421G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89583276 | ||||||
chr16:89583384
|
G | A | 1 | a0001c0002t0002g0199 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.358-313G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89583384 | ||||||
chr16:89583471
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.358-226G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89583471 | ||||||
chr16:89583591
|
G | A | 1 | a0001c0007t0006g0259 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.358-106G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89583591 | ||||||
chr16:89583609
|
T | C | 2 | a0001c0002t0001g0331a0001c0015t0001g0330 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.358-88T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | chr16 | 89583609 | ||||||
chr16:89583797
|
C | A | 2 | a0001c0008t0005g0014a0001c0009t0001g0011 | 2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.432+26C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 3/14 | chr16 | 89583797 | ||||||
chr16:89583861
|
G | A | 1 | a0001c0002t0011g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.432+90G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 3/14 | chr16 | 89583861 | ||||||
chr16:89583963
|
T | G | 266 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(263): Show | 272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.433-65T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 3/14 | chr16 | 89583963 | ||||||
chr16:89583974
|
G | A | 4 | a0001c0001t0001g0075a0001c0002t0002g0199a0001c0002t0002g0201others(1): Show | 4 | HG00423.hp1 NA19012.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-54G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 3/14 | chr16 | 89583974 | ||||||
chr16:89584010
|
C | T | 5 | a0001c0001t0001g0175a0001c0008t0002g0012a0001c0008t0005g0014others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-18C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 3/14 | chr16 | 89584010 | ||||||
chr16:89584123
|
C | T | 3 | a0001c0002t0004g0325a0001c0002t0004g0326a0001c0002t0004g0327 | 3 | HG02258.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.507+21C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584123 | ||||||
chr16:89584152
|
G | A | 2 | a0001c0002t0001g0322a0006c0014t0001g0008 | 2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.507+50G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584152 | ||||||
chr16:89584189
|
C | T | 7 | a0001c0001t0001g0175a0001c0001t0001g0184a0001c0001t0001g0185others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+87C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584189 | ||||||
chr16:89584218
|
G | A | 2 | a0001c0001t0001g0339a0004c0020t0001g0340 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.507+116G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584218 | ||||||
chr16:89584258
|
C | T | 1 | a0001c0002t0001g0331 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.507+156C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584258 | ||||||
chr16:89584273
|
C | T | 1 | a0004c0011t0001g0077 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.507+171C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584273 | ||||||
chr16:89584398
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.507+296G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584398 | ||||||
chr16:89584422
|
C | T | 27 | a0001c0001t0001g0318a0001c0002t0002g0316a0001c0002t0002g0329others(24): Show | 30 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.507+320C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584422 | ||||||
chr16:89584436
|
C | G | 1 | a0001c0002t0001g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.507+334C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584436 | ||||||
chr16:89584485
|
T | A | 1 | a0001c0009t0001g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.508-289T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584485 | ||||||
chr16:89584510
|
G | C | 1 | a0001c0001t0001g0335 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.508-264G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584510 | ||||||
chr16:89584593
|
A | G | 12 | a0001c0001t0001g0075a0001c0002t0002g0004a0001c0002t0002g0196others(9): Show | 13 | HG00280.hp1 HG00423.hp1 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.508-181A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584593 | ||||||
chr16:89584634
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.508-140G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584634 | ||||||
chr16:89584671
|
C | T | 1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.508-103C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584671 | ||||||
chr16:89584729
|
C | T | 2 | a0001c0001t0001g0252a0001c0002t0002g0337 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.508-45C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584729 | ||||||
chr16:89584762
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | NA18971.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.508-12G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | chr16 | 89584762 | ||||||
chr16:89584767
|
T | TC | 25 | a0001c0001t0001g0318a0001c0002t0002g0316a0001c0002t0003g0313others(22): Show | 28 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(25): Show |
splice_acceptor_variant&intron_variant | HIGH | c.508-3dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 89584767 | |||||
chr16:89584862
|
G | C | 1 | a0001c0002t0003g0260 | 1 | NA19065.hp2 | splice_region_variant&intron_variant | LOW | c.591+5G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/14 | chr16 | 89584862 | ||||||
chr16:89584913
|
C | T | 2 | a0001c0002t0001g0322a0006c0014t0001g0008 | 2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.591+56C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/14 | chr16 | 89584913 | ||||||
chr16:89585027
|
C | T | 1 | a0001c0008t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.591+170C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/14 | chr16 | 89585027 | ||||||
chr16:89585095
|
C | G | 1 | a0001c0002t0003g0143 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.591+238C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/14 | chr16 | 89585095 | ||||||
chr16:89585205
|
G | A | 1 | a0001c0002t0002g0204 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.592-259G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/14 | chr16 | 89585205 | ||||||
chr16:89585239
|
G | A | 2 | a0001c0002t0004g0271a0001c0029t0001g0270 | 2 | HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.592-225G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/14 | chr16 | 89585239 | ||||||
chr16:89585409
|
C | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0058 | 3 | HG03688.hp1 HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.592-55C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 5/14 | chr16 | 89585409 | ||||||
chr16:89585628
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.682-59C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 6/14 | chr16 | 89585628 | ||||||
chr16:89585629
|
G | A | 1 | a0002c0004t0002g0301 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.682-58G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 6/14 | chr16 | 89585629 | ||||||
chr16:89585802
|
A | AG | 86 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0036others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.780+22dupG | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89585802 | |||||
chr16:89585838
|
G | A | 13 | a0001c0001t0001g0109a0001c0002t0005g0163a0001c0007t0006g0064others(10): Show | 13 | HG02280.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.780+53G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89585838 | ||||||
chr16:89585871
|
T | TG | 19 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0093others(16): Show | 19 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.780+93dupG | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89585871 | |||||
chr16:89585907
|
TG | T | 36 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(33): Show | 38 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.780+128delG | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89585907 | |||||
chr16:89585966
|
G | C | 71 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(68): Show | 73 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.780+181G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89585966 | ||||||
chr16:89585971
|
T | C | 79 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(76): Show | 81 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.780+186T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89585971 | ||||||
chr16:89586046
|
AGGGAGGG others(20): Show |
A | 35 | a0001c0001t0001g0040a0001c0001t0001g0091a0001c0001t0001g0115others(32): Show | 35 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.780+278_780+304del others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89586046 | |||||
chr16:89586071
|
C | G | 1 | a0003c0006t0003g0168 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.780+286C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89586071 | ||||||
chr16:89586388
|
G | C | 29 | a0001c0001t0001g0040a0001c0001t0001g0175a0001c0002t0002g0316others(26): Show | 29 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.781-282G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89586388 | ||||||
chr16:89586406
|
GC | G | 69 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0154others(66): Show | 69 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.781-261delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89586406 | |||||
chr16:89586409
|
C | G | 69 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0154others(66): Show | 69 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.781-261C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89586409 | ||||||
chr16:89586544
|
G | GCCCTC | 6 | a0001c0002t0001g0322a0001c0002t0004g0325a0001c0002t0004g0326others(3): Show | 6 | HG02258.hp1 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-112_781-108dup others(5): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89586544 | |||||
chr16:89586557
|
C | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG01074.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.781-113C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89586557 | ||||||
chr16:89586597
|
G | T | 1 | a0001c0002t0013g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.781-73G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89586597 | ||||||
chr16:89586624
|
G | A | 134 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0030others(131): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.781-46G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 7/14 | chr16 | 89586624 | ||||||
chr16:89586765
|
T | C | 65 | a0001c0001t0001g0075a0001c0001t0001g0120a0001c0001t0001g0121others(62): Show | 66 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.867+9T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586765 | ||||||
chr16:89586767
|
G | C | 2 | a0001c0001t0001g0238a0001c0001t0001g0300 | 2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.867+11G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586767 | ||||||
chr16:89586768
|
C | T | 1 | a0001c0015t0001g0330 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.867+12C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586768 | ||||||
chr16:89586776
|
G | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0154 | 3 | NA18962.hp2 NA18990.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.867+20G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586776 | ||||||
chr16:89586797
|
G | C | 2 | a0001c0002t0002g0024a0001c0002t0002g0338 | 2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.867+41G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586797 | ||||||
chr16:89586896
|
C | G | 51 | a0001c0001t0001g0090a0001c0001t0001g0102a0001c0001t0001g0120others(48): Show | 51 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.867+140C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586896 | ||||||
chr16:89586898
|
A | G | 1 | a0001c0005t0002g0250 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.867+142A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586898 | ||||||
chr16:89586964
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.868-79G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586964 | ||||||
chr16:89586993
|
T | C | 5 | a0001c0002t0001g0322a0001c0002t0004g0271a0001c0008t0001g0005others(2): Show | 5 | HG01081.hp2 HG02615.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.868-50T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89586993 | ||||||
chr16:89587011
|
C | T | 4 | a0001c0001t0001g0273a0001c0002t0003g0053a0001c0002t0003g0272others(1): Show | 4 | HG01928.hp2 HG02809.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-32C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 8/14 | chr16 | 89587011 | ||||||
chr16:89587111
|
A | ATGGCCCC others(148): Show |
1 | a0001c0015t0001g0330 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.927+52_927+53insTC others(153): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587111 | |||||
chr16:89587112
|
T | C | 12 | a0001c0001t0001g0175a0001c0002t0001g0322a0001c0002t0004g0271others(9): Show | 12 | HG01081.hp2 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.927+10T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587112 | ||||||
chr16:89587116
|
C | CCCGCCCC others(3): Show |
108 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(105): Show | 110 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.927+22_927+31dupAT others(8): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587116 | |||||
chr16:89587124
|
A | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0172a0004c0020t0001g0340 | 3 | HG02809.hp2 HG03834.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.927+22A>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587124 | ||||||
chr16:89587125
|
T | C | 3 | a0001c0001t0001g0060a0001c0001t0001g0172a0004c0020t0001g0340 | 3 | HG02809.hp2 HG03834.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.927+23T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587125 | ||||||
chr16:89587125
|
T | G | 5 | a0001c0002t0002g0321a0001c0002t0005g0074a0001c0002t0005g0291others(2): Show | 5 | HG01192.hp2 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+23T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587125 | ||||||
chr16:89587126
|
G | C | 3 | a0001c0001t0001g0060a0001c0001t0001g0172a0004c0020t0001g0340 | 3 | HG02809.hp2 HG03834.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.927+24G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587126 | ||||||
chr16:89587126
|
G | GCCGCCCC others(34): Show |
1 | a0003c0006t0003g0145 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.927+31_927+32insAT others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587126 | |||||
chr16:89587126
|
G | GCCGCCCC others(126): Show |
3 | a0001c0002t0007g0234a0001c0002t0007g0235a0002c0003t0007g0298 | 3 | HG02155.hp2 NA18952.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.927+31_927+32insAT others(131): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587126 | |||||
chr16:89587126
|
G | GCCGCCCC others(279): Show |
1 | a0001c0002t0003g0018 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+31_927+32insAT others(284): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587126 | |||||
chr16:89587129
|
G | GCCCCATG others(4): Show |
1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.927+31_927+32insAT others(9): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587129 | |||||
chr16:89587134
|
C | A | 3 | a0001c0002t0002g0023a0001c0002t0013g0194a0001c0025t0001g0276 | 3 | HG02145.hp1 HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.927+32C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587134 | ||||||
chr16:89587135
|
TCAGTCCG others(14): Show |
T | 3 | a0001c0002t0002g0023a0001c0002t0013g0194a0001c0025t0001g0276 | 3 | HG02145.hp1 HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.927+35_927+55delAG others(19): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587135 | |||||
chr16:89587141
|
C | T | 4 | a0001c0001t0001g0060a0001c0002t0003g0018a0003c0006t0003g0145others(1): Show | 4 | HG02809.hp2 HG03834.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+39C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587141 | ||||||
chr16:89587154
|
C | A | 14 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0213others(11): Show | 14 | HG01109.hp2 HG01243.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.927+52C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587154 | ||||||
chr16:89587155
|
G | A | 1 | a0001c0002t0002g0255 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.927+53G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587155 | ||||||
chr16:89587155
|
G | C | 1 | a0001c0001t0001g0262 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.927+53G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587155 | ||||||
chr16:89587155
|
G | T | 269 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(266): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.927+53G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587155 | ||||||
chr16:89587156
|
C | T | 1 | a0001c0002t0002g0255 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.927+54C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587156 | ||||||
chr16:89587157
|
C | G | 4 | a0001c0002t0002g0023a0001c0002t0002g0255a0001c0002t0013g0194others(1): Show | 4 | HG02145.hp1 HG02257.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+55C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587157 | ||||||
chr16:89587159
|
C | T | 3 | a0001c0002t0007g0234a0001c0002t0007g0235a0002c0003t0007g0298 | 3 | HG02155.hp2 NA18952.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.927+57C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587159 | ||||||
chr16:89587160
|
G | GC | 7 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0001g0214others(4): Show | 7 | HG01192.hp2 HG02896.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+63dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587160 | |||||
chr16:89587172
|
C | T | 121 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(118): Show | 123 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.927+70C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587172 | ||||||
chr16:89587185
|
C | A | 117 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(114): Show | 119 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.927+83C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587185 | ||||||
chr16:89587186
|
T | G | 27 | a0001c0002t0003g0076a0001c0002t0003g0143a0001c0002t0003g0177others(24): Show | 27 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.927+84T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587186 | ||||||
chr16:89587186
|
T | TC | 6 | a0001c0001t0001g0103a0001c0001t0001g0109a0001c0002t0002g0210others(3): Show | 6 | HG02080.hp1 HG02738.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+88dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587186 | |||||
chr16:89587191
|
GC | G | 23 | a0001c0001t0001g0040a0001c0002t0002g0316a0001c0005t0002g0302others(20): Show | 26 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.927+94delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587191 | |||||
chr16:89587192
|
C | G | 3 | a0001c0002t0004g0325a0001c0002t0004g0326a0001c0002t0004g0327 | 3 | HG02258.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.927+90C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587192 | ||||||
chr16:89587203
|
T | A | 1 | a0001c0001t0001g0339 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.927+101T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587203 | ||||||
chr16:89587203
|
T | C | 120 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(117): Show | 122 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.927+101T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587203 | ||||||
chr16:89587216
|
A | C | 233 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.927+114A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587216 | ||||||
chr16:89587217
|
T | A | 1 | a0007c0022t0004g0288 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.927+115T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587217 | ||||||
chr16:89587217
|
T | C | 1 | a0003c0006t0003g0145 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.927+115T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587217 | ||||||
chr16:89587217
|
TC | T | 98 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0054others(95): Show | 100 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.927+119delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587217 | |||||
chr16:89587218
|
C | T | 1 | a0007c0022t0004g0288 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.927+116C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587218 | ||||||
chr16:89587219
|
C | G | 1 | a0007c0022t0004g0288 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.927+117C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587219 | ||||||
chr16:89587221
|
C | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0078a0001c0001t0001g0103others(5): Show | 8 | HG00544.hp2 HG01099.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+119C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587221 | ||||||
chr16:89587221
|
C | T | 10 | a0001c0001t0001g0175a0001c0002t0001g0322a0001c0002t0004g0271others(7): Show | 10 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.927+119C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587221 | ||||||
chr16:89587222
|
G | C | 8 | a0001c0001t0001g0027a0001c0001t0001g0078a0001c0001t0001g0103others(5): Show | 8 | HG00544.hp2 HG01099.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+120G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587222 | ||||||
chr16:89587222
|
GC | G | 41 | a0001c0001t0001g0060a0001c0001t0001g0120a0001c0001t0001g0121others(38): Show | 41 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.927+125delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587222 | |||||
chr16:89587234
|
C | T | 115 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(112): Show | 117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.927+132C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587234 | ||||||
chr16:89587235
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.927+133G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587235 | ||||||
chr16:89587246
|
C | CA | 98 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(95): Show | 100 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.927+144_927+145ins others(1): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587246 | ||||||
chr16:89587247
|
C | A | 9 | a0001c0001t0001g0079a0001c0001t0001g0178a0001c0002t0001g0331others(6): Show | 9 | HG01516.hp2 HG01891.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.927+145C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587247 | ||||||
chr16:89587247
|
C | CA | 10 | a0001c0001t0001g0175a0001c0002t0001g0322a0001c0002t0004g0271others(7): Show | 10 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.927+145_927+146ins others(1): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587247 | ||||||
chr16:89587248
|
T | C | 112 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(109): Show | 114 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.927+146T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587248 | ||||||
chr16:89587248
|
T | TC | 119 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0030others(116): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.927+149dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587248 | |||||
chr16:89587251
|
C | CT | 5 | a0001c0001t0001g0060a0002c0004t0002g0311a0003c0006t0003g0145others(2): Show | 5 | HG01361.hp2 HG02809.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+149_927+150ins others(1): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587251 | ||||||
chr16:89587252
|
G | C | 4 | a0001c0001t0001g0172a0001c0007t0006g0071a0001c0023t0001g0195others(1): Show | 4 | HG03225.hp2 HG03834.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+150G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587252 | ||||||
chr16:89587252
|
G | GC | 7 | a0001c0001t0001g0179a0001c0001t0001g0251a0001c0002t0005g0186others(4): Show | 7 | HG00621.hp1 HG01243.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+155dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587252 | |||||
chr16:89587253
|
C | G | 2 | a0001c0001t0001g0172a0001c0007t0006g0071 | 2 | HG03225.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.927+151C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587253 | ||||||
chr16:89587264
|
T | A | 5 | a0001c0001t0001g0175a0001c0008t0002g0012a0001c0008t0005g0014others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+162T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587264 | ||||||
chr16:89587264
|
T | C | 129 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(126): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.927+162T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587264 | ||||||
chr16:89587275
|
C | CCCCTCCA | 4 | a0001c0002t0001g0322a0001c0002t0004g0271a0001c0008t0001g0005others(1): Show | 4 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+174_927+175ins others(7): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587275 | |||||
chr16:89587277
|
A | C | 231 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(228): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.927+175A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587277 | ||||||
chr16:89587278
|
T | C | 14 | a0001c0001t0001g0175a0001c0002t0001g0322a0001c0002t0002g0023others(11): Show | 14 | HG02109.hp1 HG02145.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.927+176T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587278 | ||||||
chr16:89587278
|
T | G | 1 | a0004c0020t0001g0340 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.927+176T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587278 | ||||||
chr16:89587278
|
T | TCCCCGCC others(24): Show |
1 | a0002c0003t0003g0111 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.927+185_927+186ins others(31): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587278 | |||||
chr16:89587279
|
C | CGGGA | 4 | a0001c0002t0001g0322a0001c0002t0004g0271a0001c0008t0001g0005others(1): Show | 4 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+177_927+178ins others(4): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587279 | ||||||
chr16:89587279
|
C | CTCCACAC others(5): Show |
2 | a0001c0008t0005g0014a0001c0009t0001g0011 | 2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.927+177_927+178ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587279 | ||||||
chr16:89587280
|
C | T | 2 | a0001c0001t0001g0175a0001c0008t0002g0012 | 2 | HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.927+178C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587280 | ||||||
chr16:89587281
|
C | A | 1 | a0001c0008t0002g0015 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.927+179C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587281 | ||||||
chr16:89587282
|
C | T | 113 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(110): Show | 115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.927+180C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587282 | ||||||
chr16:89587283
|
G | A | 3 | a0001c0001t0001g0175a0001c0008t0002g0012a0001c0008t0002g0015 | 3 | HG01081.hp2 HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.927+181G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587283 | ||||||
chr16:89587283
|
G | C | 1 | a0001c0013t0002g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+181G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587283 | ||||||
chr16:89587283
|
GC | G | 82 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0035others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.927+186delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587283 | |||||
chr16:89587285
|
C | A | 3 | a0001c0001t0001g0175a0001c0008t0002g0012a0001c0013t0002g0006 | 3 | HG02109.hp1 HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.927+183C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587285 | ||||||
chr16:89587287
|
C | A | 1 | a0001c0013t0002g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+185C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587287 | ||||||
chr16:89587287
|
C | CCCG | 6 | a0001c0002t0001g0322a0001c0002t0004g0271a0001c0008t0001g0005others(3): Show | 6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+186_927+187ins others(3): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587287 | |||||
chr16:89587288
|
C | G | 2 | a0001c0001t0001g0175a0001c0008t0002g0012 | 2 | HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.927+186C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587288 | ||||||
chr16:89587289
|
T | C | 7 | a0001c0002t0001g0322a0001c0002t0004g0271a0001c0008t0001g0005others(4): Show | 7 | HG02615.hp2 HG03041.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+187T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587289 | ||||||
chr16:89587289
|
T | G | 3 | a0001c0001t0001g0175a0001c0008t0002g0012a0001c0008t0002g0015 | 3 | HG01081.hp2 HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.927+187T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587289 | ||||||
chr16:89587290
|
C | G | 3 | a0001c0001t0001g0175a0001c0008t0002g0012a0001c0013t0002g0006 | 3 | HG02109.hp1 HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.927+188C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587290 | ||||||
chr16:89587291
|
A | G | 1 | a0001c0013t0002g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+189A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587291 | ||||||
chr16:89587291
|
A | T | 1 | a0001c0025t0001g0276 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.927+189A>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587291 | ||||||
chr16:89587292
|
G | C | 6 | a0001c0002t0001g0322a0001c0002t0004g0271a0001c0008t0001g0005others(3): Show | 6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+190G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587292 | ||||||
chr16:89587293
|
T | A | 1 | a0001c0013t0002g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+191T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587293 | ||||||
chr16:89587293
|
T | C | 8 | a0001c0001t0001g0175a0001c0002t0001g0322a0001c0002t0004g0271others(5): Show | 8 | HG02109.hp1 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.927+191T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587293 | ||||||
chr16:89587295
|
T | C | 160 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0030others(157): Show | 164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.927+193T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587295 | ||||||
chr16:89587295
|
T | G | 6 | a0001c0002t0001g0322a0001c0002t0004g0271a0001c0008t0001g0005others(3): Show | 6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+193T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587295 | ||||||
chr16:89587296
|
G | C | 1 | a0001c0013t0002g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+194G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587296 | ||||||
chr16:89587297
|
T | A | 6 | a0001c0002t0001g0322a0001c0002t0004g0271a0001c0008t0001g0005others(3): Show | 6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+195T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587297 | ||||||
chr16:89587297
|
T | G | 1 | a0001c0013t0002g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+195T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587297 | ||||||
chr16:89587298
|
G | C | 3 | a0001c0001t0001g0175a0001c0008t0002g0012a0001c0013t0002g0006 | 3 | HG02109.hp1 HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.927+196G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587298 | ||||||
chr16:89587299
|
G | C | 4 | a0001c0001t0001g0175a0001c0008t0002g0012a0001c0008t0002g0015others(1): Show | 4 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+197G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587299 | ||||||
chr16:89587299
|
G | GAGGAA | 6 | a0001c0002t0001g0322a0001c0002t0004g0271a0001c0008t0001g0005others(3): Show | 6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+197_927+198ins others(5): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587299 | ||||||
chr16:89587302
|
C | A | 6 | a0001c0002t0001g0322a0001c0002t0004g0271a0001c0008t0001g0005others(3): Show | 6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+200C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587302 | ||||||
chr16:89587303
|
C | G | 6 | a0001c0002t0001g0322a0001c0002t0004g0271a0001c0008t0001g0005others(3): Show | 6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+201C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587303 | ||||||
chr16:89587304
|
G | GC | 5 | a0001c0001t0001g0028a0001c0001t0001g0079a0001c0001t0001g0101others(2): Show | 5 | HG00639.hp2 HG01516.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+205dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587304 | |||||
chr16:89587306
|
C | CA | 6 | a0001c0002t0001g0322a0001c0002t0004g0271a0001c0008t0001g0005others(3): Show | 6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+204_927+205ins others(1): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587306 | ||||||
chr16:89587307
|
C | G | 6 | a0001c0002t0001g0322a0001c0002t0004g0271a0001c0008t0001g0005others(3): Show | 6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+205C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587307 | ||||||
chr16:89587308
|
A | ACCCGGAG others(28): Show |
2 | a0001c0008t0002g0015a0001c0013t0002g0006 | 2 | HG01081.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.927+206_927+207ins others(35): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587308 | ||||||
chr16:89587308
|
A | C | 262 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0026others(259): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.927+206A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587308 | ||||||
chr16:89587309
|
T | A | 4 | a0001c0001t0001g0101a0001c0001t0001g0172a0001c0001t0001g0183others(1): Show | 4 | HG00639.hp2 HG03225.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+207T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587309 | ||||||
chr16:89587309
|
T | C | 6 | a0001c0001t0001g0175a0001c0008t0002g0012a0001c0008t0002g0015others(3): Show | 6 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+207T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587309 | ||||||
chr16:89587309
|
T | G | 108 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(105): Show | 110 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.927+207T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587309 | ||||||
chr16:89587310
|
C | A | 6 | a0001c0002t0001g0322a0001c0002t0004g0271a0001c0008t0001g0005others(3): Show | 6 | HG02615.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+208C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587310 | ||||||
chr16:89587311
|
C | CGGAGGAG others(31): Show |
2 | a0001c0001t0001g0175a0001c0008t0002g0012 | 2 | HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.927+209_927+210ins others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587311 | ||||||
chr16:89587311
|
C | T | 1 | a0004c0020t0001g0340 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.927+209C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587311 | ||||||
chr16:89587312
|
C | CTGGAGT | 4 | a0001c0002t0004g0271a0001c0008t0001g0005a0001c0008t0005g0014others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+210_927+211ins others(6): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587312 | ||||||
chr16:89587313
|
C | A | 2 | a0001c0002t0001g0322a0005c0026t0001g0017 | 2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.927+211C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587313 | ||||||
chr16:89587313
|
C | CACACCGG others(48): Show |
1 | a0004c0020t0001g0340 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.927+211_927+212ins others(55): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587313 | ||||||
chr16:89587313
|
C | T | 137 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0030others(134): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.927+211C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587313 | ||||||
chr16:89587314
|
G | C | 4 | a0001c0002t0004g0271a0001c0008t0001g0005a0001c0008t0005g0014others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+212G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587314 | ||||||
chr16:89587315
|
C | T | 3 | a0001c0002t0001g0322a0004c0020t0001g0340a0005c0026t0001g0017 | 3 | HG02615.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.927+213C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587315 | ||||||
chr16:89587317
|
C | G | 2 | a0001c0008t0002g0015a0001c0013t0002g0006 | 2 | HG01081.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.927+215C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587317 | ||||||
chr16:89587320
|
T | C | 11 | a0001c0001t0001g0175a0001c0002t0001g0322a0001c0007t0006g0158others(8): Show | 11 | HG01081.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+218T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587320 | ||||||
chr16:89587320
|
T | G | 4 | a0001c0002t0004g0271a0001c0008t0001g0005a0001c0008t0005g0014others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+218T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587320 | ||||||
chr16:89587322
|
A | C | 10 | a0001c0001t0001g0175a0001c0002t0001g0322a0001c0002t0004g0271others(7): Show | 10 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.927+220A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587322 | ||||||
chr16:89587322
|
A | T | 1 | a0001c0013t0002g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+220A>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587322 | ||||||
chr16:89587324
|
T | C | 11 | a0001c0001t0001g0175a0001c0002t0001g0322a0001c0002t0004g0271others(8): Show | 11 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+222T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587324 | ||||||
chr16:89587325
|
CCGT | C | 3 | a0001c0002t0001g0322a0004c0020t0001g0340a0005c0026t0001g0017 | 3 | HG02615.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.927+224_927+226del others(3): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587325 | ||||||
chr16:89587326
|
C | A | 4 | a0001c0001t0001g0101a0001c0001t0001g0172a0001c0001t0001g0183others(1): Show | 4 | HG00639.hp2 HG03225.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+224C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587326 | ||||||
chr16:89587326
|
C | T | 51 | a0001c0001t0001g0040a0001c0001t0001g0060a0001c0001t0001g0263others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.927+224C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587326 | ||||||
chr16:89587327
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+225G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587327 | ||||||
chr16:89587327
|
G | C | 7 | a0001c0001t0001g0175a0001c0008t0001g0005a0001c0008t0002g0012others(4): Show | 7 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+225G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587327 | ||||||
chr16:89587328
|
T | C | 5 | a0001c0001t0001g0175a0001c0008t0001g0005a0001c0008t0002g0012others(2): Show | 5 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+226T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587328 | ||||||
chr16:89587330
|
G | C | 10 | a0001c0001t0001g0175a0001c0002t0001g0322a0001c0008t0001g0005others(7): Show | 10 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.927+228G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587330 | ||||||
chr16:89587330
|
G | GCCCCCGC others(179): Show |
1 | a0001c0005t0002g0302 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.927+232_927+233ins others(186): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(168): Show |
6 | a0002c0003t0003g0113a0002c0003t0003g0114a0002c0003t0003g0135others(3): Show | 6 | HG00609.hp2 HG00642.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+236_927+237ins others(175): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(122): Show |
1 | a0001c0001t0001g0030 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(129): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(120): Show |
1 | a0001c0005t0002g0056 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(127): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(119): Show |
1 | a0001c0001t0001g0095 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(126): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(120): Show |
1 | a0001c0001t0001g0281 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(127): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(120): Show |
1 | a0001c0001t0001g0262 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(127): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(127): Show |
1 | a0001c0001t0001g0057 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(134): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(119): Show |
1 | a0004c0011t0001g0077 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(126): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(137): Show |
1 | a0001c0002t0002g0199 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(144): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(113): Show |
1 | a0001c0001t0001g0174 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(120): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(126): Show |
1 | a0001c0002t0003g0044 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(133): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(119): Show |
60 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0035others(57): Show | 60 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(126): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(120): Show |
3 | a0001c0001t0001g0088a0001c0001t0001g0341a0001c0002t0003g0034 | 3 | HG00140.hp1 HG00642.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.927+237_927+238ins others(127): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(125): Show |
8 | a0001c0001t0001g0058a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG00280.hp1 HG01243.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(132): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(126): Show |
2 | a0001c0002t0002g0201a0001c0002t0003g0033 | 2 | HG00423.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.927+237_927+238ins others(133): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(169): Show |
1 | a0002c0004t0002g0304 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(176): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(182): Show |
1 | a0002c0004t0002g0311 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(189): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(178): Show |
1 | a0002c0004t0002g0279 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(185): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(164): Show |
1 | a0002c0004t0014g0305 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(171): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(176): Show |
1 | a0002c0004t0002g0016 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(183): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(176): Show |
1 | a0002c0003t0004g0306 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(183): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(131): Show |
2 | a0002c0004t0002g0308a0002c0004t0002g0309 | 2 | HG01074.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.927+237_927+238ins others(138): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(164): Show |
1 | a0001c0001t0001g0040 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(171): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(176): Show |
3 | a0002c0004t0002g0001a0002c0004t0002g0314a0002c0004t0002g0315 | 6 | HG01168.hp2 HG01169.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(183): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(164): Show |
2 | a0002c0004t0002g0301a0002c0004t0002g0324 | 2 | NA18950.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.927+237_927+238ins others(171): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(170): Show |
1 | a0002c0004t0002g0332 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(177): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(163): Show |
1 | a0002c0004t0002g0307 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(170): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(172): Show |
1 | a0002c0004t0002g0319 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(179): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(175): Show |
1 | a0001c0005t0002g0310 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(182): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(174): Show |
1 | a0001c0005t0002g0317 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(181): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(114): Show |
1 | a0001c0002t0004g0327 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(121): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(113): Show |
2 | a0001c0002t0004g0325a0001c0002t0004g0326 | 2 | HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.927+237_927+238ins others(120): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(125): Show |
1 | a0001c0002t0002g0202 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(132): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(76): Show |
8 | a0001c0001t0001g0028a0001c0001t0001g0059a0001c0001t0001g0216others(5): Show | 8 | HG02602.hp2 HG03579.hp1 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+238_927+239ins others(83): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(94): Show |
1 | a0001c0001t0001g0215 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.927+238_927+239ins others(101): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(100): Show |
1 | a0001c0002t0002g0209 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.927+238_927+239ins others(107): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(82): Show |
2 | a0001c0001t0001g0079a0001c0009t0001g0061 | 2 | HG01516.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.927+238_927+239ins others(89): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(113): Show |
1 | a0001c0002t0001g0331 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.927+238_927+239ins others(120): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(88): Show |
4 | a0001c0001t0001g0101a0001c0001t0001g0172a0001c0001t0001g0183others(1): Show | 4 | HG00639.hp2 HG03225.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+238_927+239ins others(95): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(114): Show |
1 | a0001c0008t0002g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.927+243_927+244ins others(121): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(145): Show |
1 | a0001c0015t0001g0330 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.927+243_927+244ins others(152): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(125): Show |
1 | a0001c0002t0005g0074 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.927+243_927+244ins others(132): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(86): Show |
1 | a0001c0025t0001g0276 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(93): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(107): Show |
1 | a0001c0002t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(114): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(161): Show |
1 | a0001c0002t0005g0292 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(168): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(145): Show |
1 | a0001c0002t0005g0291 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(152): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(124): Show |
1 | a0001c0002t0005g0320 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(131): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(125): Show |
1 | a0001c0002t0002g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(132): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(219): Show |
1 | a0001c0002t0002g0256 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(226): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(218): Show |
1 | a0001c0002t0002g0299 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(225): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(218): Show |
6 | a0001c0002t0002g0004a0001c0002t0002g0042a0001c0002t0002g0254others(3): Show | 7 | NA18612.hp2 NA18747.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(225): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(397): Show |
4 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(1): Show | 4 | HG00323.hp2 HG02300.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(404): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(335): Show |
1 | a0001c0001t0001g0060 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(342): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(186): Show |
1 | a0001c0001t0001g0263 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(193): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(151): Show |
1 | a0001c0001t0001g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(158): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(156): Show |
1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(163): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(192): Show |
1 | a0001c0002t0002g0024 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(199): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(185): Show |
1 | a0001c0002t0005g0289 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(192): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(191): Show |
1 | a0001c0002t0002g0338 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(198): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(137): Show |
30 | a0001c0002t0003g0076a0001c0002t0003g0143a0001c0002t0003g0177others(27): Show | 30 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(144): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(138): Show |
2 | a0001c0002t0004g0123a0002c0003t0003g0152 | 2 | HG02027.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.927+237_927+238ins others(145): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(163): Show |
1 | a0001c0001t0001g0120 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(170): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(143): Show |
3 | a0001c0002t0004g0131a0001c0002t0004g0132a0001c0002t0004g0228 | 3 | HG01952.hp1 HG02273.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.927+237_927+238ins others(150): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(155): Show |
1 | a0001c0001t0001g0154 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(162): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(161): Show |
1 | a0001c0001t0001g0121 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(168): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(167): Show |
5 | a0001c0007t0006g0159a0001c0007t0006g0160a0001c0007t0006g0161others(2): Show | 5 | HG02559.hp1 HG03195.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(174): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(181): Show |
1 | a0001c0007t0006g0165 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(188): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(179): Show |
7 | a0001c0001t0001g0062a0001c0001t0001g0284a0001c0001t0001g0285others(4): Show | 7 | HG00639.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(186): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(185): Show |
2 | a0001c0002t0005g0163a0001c0007t0006g0166 | 2 | HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.927+237_927+238ins others(192): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(191): Show |
4 | a0001c0007t0006g0064a0001c0007t0006g0162a0001c0007t0006g0282others(1): Show | 4 | HG02723.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(198): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(203): Show |
1 | a0001c0007t0006g0158 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(210): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587330
|
G | GCCCCGCC others(185): Show |
1 | a0001c0001t0001g0335 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(192): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587330 | |||||
chr16:89587332
|
C | CCCGCCCC others(102): Show |
1 | a0001c0001t0001g0109 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(109): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587332 | |||||
chr16:89587332
|
C | CCCGCCCC others(71): Show |
1 | a0001c0002t0003g0236 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.927+238_927+239ins others(78): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587332 | |||||
chr16:89587332
|
C | CCCGCCCC others(71): Show |
4 | a0001c0001t0001g0179a0001c0002t0003g0018a0001c0005t0002g0072others(1): Show | 4 | HG00621.hp1 HG01261.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+238_927+239ins others(78): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587332 | |||||
chr16:89587332
|
C | CCCGCCCC others(70): Show |
72 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0063others(69): Show | 74 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.927+238_927+239ins others(77): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587332 | |||||
chr16:89587332
|
C | CCCGCCCC others(109): Show |
1 | a0006c0014t0001g0008 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.927+243_927+244ins others(116): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587332 | |||||
chr16:89587332
|
C | CCCGCCCC others(109): Show |
1 | a0001c0023t0001g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.927+243_927+244ins others(116): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587332 | |||||
chr16:89587332
|
C | CCCGCCCC others(101): Show |
5 | a0001c0002t0007g0234a0001c0002t0007g0235a0001c0002t0013g0194others(2): Show | 5 | HG02155.hp2 NA18940.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+237_927+238ins others(108): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587332 | |||||
chr16:89587334
|
C | CGCCCCAC others(107): Show |
1 | a0004c0011t0001g0092 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(114): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587334 | |||||
chr16:89587334
|
C | CGCCCCCG others(108): Show |
2 | a0001c0002t0002g0329a0001c0002t0009g0328 | 2 | HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.927+243_927+244ins others(115): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587334 | |||||
chr16:89587335
|
G | GCCCCACC others(121): Show |
1 | a0001c0001t0001g0094 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(128): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | |||||
chr16:89587335
|
G | GCCCCACC others(123): Show |
1 | a0001c0005t0002g0043 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(130): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | |||||
chr16:89587335
|
G | GCCCCACC others(120): Show |
2 | a0001c0001t0001g0096a0001c0002t0002g0032 | 2 | HG00741.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.927+237_927+238ins others(127): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | |||||
chr16:89587335
|
G | GCCCCACC others(177): Show |
1 | a0001c0005t0002g0323 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(184): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | |||||
chr16:89587335
|
G | GCCCCACC others(133): Show |
1 | a0001c0002t0002g0316 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(140): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | |||||
chr16:89587335
|
G | GCCCCCCT others(72): Show |
3 | a0001c0002t0003g0229a0001c0002t0011g0200a0001c0005t0002g0240 | 3 | HG02148.hp2 HG02738.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.927+238_927+239ins others(79): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | |||||
chr16:89587335
|
G | GCCCCCCT others(72): Show |
1 | a0001c0002t0004g0223 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.927+238_927+239ins others(79): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | |||||
chr16:89587335
|
G | GCCCCCCT others(71): Show |
5 | a0001c0001t0001g0068a0001c0001t0001g0078a0001c0002t0003g0180others(2): Show | 5 | HG01099.hp2 HG02080.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+238_927+239ins others(78): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | |||||
chr16:89587335
|
G | GCCCCCCT others(78): Show |
1 | a0001c0001t0001g0027 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.927+238_927+239ins others(85): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | |||||
chr16:89587335
|
G | GCCCCCCT others(108): Show |
1 | a0001c0002t0002g0278 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.927+238_927+239ins others(115): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | |||||
chr16:89587335
|
G | GCCCCTCC others(138): Show |
1 | a0002c0003t0003g0111 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.927+237_927+238ins others(145): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587335 | |||||
chr16:89587336
|
C | CCCCACCC others(184): Show |
1 | a0001c0005t0002g0303 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.927+237_927+238ins others(191): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587336 | |||||
chr16:89587340
|
C | A | 1 | a0001c0005t0002g0303 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.927+238C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587340 | ||||||
chr16:89587340
|
C | CCCCCACA others(71): Show |
1 | a0001c0001t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.927+238_927+239ins others(78): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587340 | ||||||
chr16:89587340
|
C | CCTCCACA others(72): Show |
1 | a0001c0005t0002g0212 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.927+238_927+239ins others(79): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587340 | ||||||
chr16:89587340
|
C | CCTCCACA others(71): Show |
3 | a0001c0001t0001g0238a0001c0029t0001g0270a0003c0006t0003g0146 | 3 | HG00597.hp2 HG01175.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.927+238_927+239ins others(78): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587340 | ||||||
chr16:89587340
|
C | CCTCCACA others(71): Show |
1 | a0001c0001t0001g0249 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.927+238_927+239ins others(78): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587340 | ||||||
chr16:89587341
|
G | C | 7 | a0001c0001t0001g0214a0001c0001t0001g0238a0001c0001t0001g0249others(4): Show | 7 | HG00558.hp2 HG00597.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+239G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587341 | ||||||
chr16:89587341
|
G | GC | 7 | a0001c0001t0001g0184a0001c0002t0005g0320a0001c0005t0002g0043others(4): Show | 7 | HG01192.hp2 HG02055.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+244dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587341 | |||||
chr16:89587344
|
C | G | 1 | a0001c0002t0002g0316 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.927+242C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587344 | ||||||
chr16:89587347
|
G | GC | 12 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0094others(9): Show | 12 | HG00597.hp2 HG01192.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.927+250dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587347 | |||||
chr16:89587408
|
G | A | 101 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.927+306G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587408 | ||||||
chr16:89587473
|
T | A | 3 | a0001c0002t0004g0037a0001c0002t0004g0038a0001c0002t0004g0039 | 3 | NA18940.hp2 NA18945.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.927+371T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587473 | ||||||
chr16:89587521
|
C | T | 7 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0002t0005g0019others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+419C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587521 | ||||||
chr16:89587535
|
C | T | 31 | a0001c0001t0001g0248a0001c0005t0002g0002a0001c0005t0002g0003others(28): Show | 36 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.927+433C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587535 | ||||||
chr16:89587591
|
TTGAG | T | 83 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0035others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.927+493_927+496del others(4): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587591 | |||||
chr16:89587600
|
C | G | 1 | a0001c0002t0004g0118 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.927+498C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587600 | ||||||
chr16:89587634
|
C | T | 2 | a0001c0002t0002g0321a0001c0002t0005g0320 | 2 | HG01192.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.927+532C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587634 | ||||||
chr16:89587665
|
CCGCAGAC others(19): Show |
C | 1 | a0001c0008t0002g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.927+568_927+593del others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587665 | |||||
chr16:89587670
|
G | C | 1 | a0002c0004t0002g0319 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+568G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587670 | ||||||
chr16:89587677
|
C | T | 1 | a0002c0004t0002g0319 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+575C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587677 | ||||||
chr16:89587685
|
A | C | 1 | a0002c0004t0002g0319 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+583A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587685 | ||||||
chr16:89587686
|
T | C | 1 | a0002c0004t0002g0319 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+584T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587686 | ||||||
chr16:89587688
|
G | T | 1 | a0002c0004t0002g0319 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+586G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587688 | ||||||
chr16:89587697
|
A | ACCCCGTG others(79): Show |
1 | a0001c0001t0001g0269 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.927+619_927+620ins others(86): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587697 | |||||
chr16:89587705
|
TCACCCCC others(4): Show |
T | 1 | a0002c0003t0003g0171 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.927+611_927+621del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587705 | |||||
chr16:89587707
|
A | ACCCACAG others(387): Show |
1 | a0001c0008t0002g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.927+608_927+609ins others(394): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587707 | |||||
chr16:89587707
|
A | ACCCCCCA others(234): Show |
1 | a0001c0001t0001g0088 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.927+610_927+611ins others(241): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587707 | |||||
chr16:89587707
|
ACCCCCAT others(94): Show |
A | 1 | a0001c0001t0001g0075 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.927+611_927+711del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587707 | |||||
chr16:89587711
|
C | A | 1 | a0002c0004t0002g0319 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+609C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587711 | ||||||
chr16:89587713
|
A | ATGTCACC others(30): Show |
1 | a0001c0001t0001g0243 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.927+612_927+613ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587713 | |||||
chr16:89587713
|
A | G | 5 | a0001c0001t0001g0088a0001c0001t0001g0205a0001c0002t0001g0322others(2): Show | 5 | HG00642.hp1 HG01243.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+611A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587713 | ||||||
chr16:89587713
|
ATAGCACC others(94): Show |
A | 1 | a0001c0001t0001g0058 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.927+613_927+713del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587713 | |||||
chr16:89587713
|
ATAGCACC others(403): Show |
A | 1 | a0001c0002t0002g0104 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.927+613_928-551del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587713 | |||||
chr16:89587715
|
A | G | 81 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(78): Show | 82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.927+613A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587715 | ||||||
chr16:89587716
|
G | GCACCCGC others(31): Show |
1 | a0002c0004t0002g0324 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.927+619_927+620ins others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587716 | |||||
chr16:89587716
|
G | GCACCCGC others(69): Show |
1 | a0001c0002t0001g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.927+619_927+620ins others(76): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587716 | |||||
chr16:89587716
|
G | GCACCCGC others(111): Show |
1 | a0001c0015t0001g0330 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.927+619_927+620ins others(118): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587716 | |||||
chr16:89587716
|
G | T | 81 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(78): Show | 82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.927+614G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587716 | ||||||
chr16:89587716
|
GCACCCCC others(30): Show |
G | 1 | a0001c0001t0001g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.927+620_927+656del others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587716 | |||||
chr16:89587716
|
GCACCCCC others(94): Show |
G | 1 | a0001c0012t0002g0297 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+620_927+720del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587716 | |||||
chr16:89587716
|
GCACCCCC others(403): Show |
G | 1 | a0001c0001t0001g0021 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.927+620_928-544del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587716 | |||||
chr16:89587718
|
A | ACCCCCGT others(20): Show |
1 | a0001c0002t0002g0210 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.927+621_927+647dup others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | |||||
chr16:89587718
|
A | ACCCCCGT others(2461): Show |
1 | a0001c0002t0001g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(2468): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | |||||
chr16:89587718
|
A | ACCCCCGT others(120): Show |
1 | a0001c0001t0001g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(127): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | |||||
chr16:89587718
|
A | ACCCCCGT others(520): Show |
1 | a0001c0001t0001g0294 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.927+656_927+657ins others(527): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | |||||
chr16:89587718
|
A | ACCCGCGT others(241): Show |
1 | a0001c0001t0001g0120 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.927+619_927+620ins others(248): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | |||||
chr16:89587718
|
A | ACCCGCGT others(19): Show |
1 | a0001c0013t0002g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+619_927+620ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | |||||
chr16:89587718
|
A | ACCCGCGT others(20): Show |
1 | a0003c0006t0003g0145 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.927+619_927+620ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | |||||
chr16:89587718
|
ACCCCCGT others(56): Show |
A | 4 | a0001c0002t0001g0287a0001c0002t0004g0228a0001c0002t0005g0019others(1): Show | 4 | HG00639.hp1 HG03041.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+648_927+710del others(63): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | |||||
chr16:89587718
|
ACCCCCGT others(366): Show |
A | 3 | a0001c0001t0001g0089a0001c0002t0002g0257a0001c0002t0005g0163 | 3 | HG01099.hp1 HG02818.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.927+673_928-528del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587718 | |||||
chr16:89587721
|
C | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0057others(2): Show | 5 | HG02602.hp2 HG03688.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+619C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587721 | ||||||
chr16:89587722
|
C | CCGTGTCA others(541): Show |
1 | a0001c0001t0001g0215 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.927+635_927+636ins others(548): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587722 | |||||
chr16:89587722
|
C | CCGTGTCA others(95): Show |
1 | a0001c0002t0005g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.927+647_927+648ins others(102): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587722 | |||||
chr16:89587722
|
C | CCGTGTCA others(1381): Show |
1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.927+656_927+657ins others(1388): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587722 | |||||
chr16:89587722
|
C | CCGTGTCA others(108): Show |
2 | a0001c0001t0001g0191a0008c0021t0001g0224 | 2 | NA18970.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.927+656_927+657ins others(115): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587722 | |||||
chr16:89587722
|
C | CCGTGTCA others(56): Show |
2 | a0001c0001t0001g0063a0001c0002t0004g0223 | 2 | HG02080.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.927+656_927+657ins others(63): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587722 | |||||
chr16:89587722
|
C | G | 121 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(118): Show | 122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.927+620C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587722 | ||||||
chr16:89587722
|
C | T | 3 | a0001c0007t0006g0157a0001c0007t0006g0166a0001c0007t0006g0282 | 3 | HG02818.hp2 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.927+620C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587722 | ||||||
chr16:89587722
|
CCGTGTCA others(313): Show |
C | 1 | a0001c0025t0001g0276 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.927+648_928-606del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587722 | |||||
chr16:89587722
|
CCGTGTCA others(403): Show |
C | 1 | a0001c0001t0001g0078 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.927+673_928-491del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587722 | |||||
chr16:89587725
|
T | C | 2 | a0001c0002t0002g0041a0001c0002t0002g0042 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.927+623T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587725 | ||||||
chr16:89587728
|
C | T | 3 | a0001c0002t0001g0331a0001c0007t0006g0293a0002c0003t0003g0152 | 3 | HG02717.hp2 NA18906.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.927+626C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587728 | ||||||
chr16:89587728
|
CACCCACA others(120): Show |
C | 4 | a0001c0001t0001g0090a0001c0002t0002g0337a0001c0002t0003g0049others(1): Show | 4 | HG01109.hp1 HG02970.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+648_927+774del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587728 | |||||
chr16:89587728
|
CACCCACA others(340): Show |
C | 1 | a0002c0010t0008g0127 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.927+657_928-570del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587728 | |||||
chr16:89587731
|
C | CCACAGAT others(741): Show |
1 | a0001c0002t0002g0316 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.927+647_927+648ins others(748): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587731 | |||||
chr16:89587734
|
C | T | 2 | a0001c0002t0002g0041a0001c0002t0002g0042 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.927+632C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587734 | ||||||
chr16:89587738
|
T | A | 27 | a0001c0001t0001g0115a0001c0001t0001g0121a0001c0001t0001g0140others(24): Show | 27 | HG00423.hp2 HG02080.hp2 HG02155.hp2 others(24): Show |
intron_variant | MODIFIER | c.927+636T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587738 | ||||||
chr16:89587738
|
TACACGGC others(30): Show |
T | 2 | a0001c0002t0003g0272a0002c0003t0003g0152 | 2 | NA19057.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.927+657_927+693del others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587738 | |||||
chr16:89587741
|
A | G | 2 | a0001c0002t0002g0041a0001c0002t0002g0042 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.927+639A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587741 | ||||||
chr16:89587741
|
ACGGCCCC others(55): Show |
A | 1 | a0001c0002t0003g0018 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+640_927+701del others(62): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587741 | ||||||
chr16:89587742
|
C | T | 1 | a0001c0002t0004g0327 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.927+640C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587742 | ||||||
chr16:89587743
|
G | A | 2 | a0001c0002t0002g0041a0001c0002t0002g0042 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.927+641G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587743 | ||||||
chr16:89587744
|
G | C | 2 | a0001c0002t0002g0041a0001c0002t0002g0042 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.927+642G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587744 | ||||||
chr16:89587744
|
G | GC | 106 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0050others(103): Show | 107 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.927+647dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCCG others(32): Show |
3 | a0002c0003t0003g0113a0002c0003t0003g0114a0011c0016t0003g0112 | 3 | NA18942.hp2 NA18952.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.927+647_927+648ins others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCCG others(123): Show |
1 | a0001c0002t0003g0143 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.927+647_927+648ins others(130): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCCG others(32): Show |
3 | a0001c0002t0003g0177a0003c0006t0003g0274a0003c0006t0003g0275 | 3 | NA18946.hp1 NA18982.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.927+647_927+648ins others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCCG others(69): Show |
1 | a0001c0001t0001g0045 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.927+647_927+648ins others(76): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCCG others(145): Show |
1 | a0002c0003t0003g0073 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.927+647_927+648ins others(152): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCCG others(58): Show |
1 | a0002c0003t0002g0119 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.927+647_927+648ins others(65): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCCG others(208): Show |
1 | a0001c0001t0001g0062 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.927+647_927+648ins others(215): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCGT others(20): Show |
1 | a0001c0001t0001g0285 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCGT others(46): Show |
1 | a0003c0006t0003g0268 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.927+656_927+657ins others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCGT others(573): Show |
1 | a0001c0024t0001g0218 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(580): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCGT others(200): Show |
1 | a0001c0002t0004g0123 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.927+656_927+657ins others(207): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCGT others(57): Show |
1 | a0001c0012t0002g0296 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.927+656_927+657ins others(64): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCGT others(372): Show |
1 | a0002c0004t0014g0305 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(379): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCGT others(20): Show |
1 | a0003c0006t0003g0148 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCGT others(325): Show |
1 | a0001c0001t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(332): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCGT others(31): Show |
1 | a0003c0006t0003g0231 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.927+672_927+673ins others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCGT others(169): Show |
1 | a0001c0001t0001g0263 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.927+672_927+673ins others(176): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587744
|
G | GCCCCCGT others(20): Show |
1 | a0001c0001t0001g0121 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.927+651_927+652ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587744 | |||||
chr16:89587745
|
C | A | 2 | a0001c0002t0002g0041a0001c0002t0002g0042 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.927+643C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587745 | ||||||
chr16:89587745
|
C | T | 3 | a0002c0004t0002g0279a0002c0004t0002g0309a0002c0004t0002g0311 | 3 | HG01361.hp2 HG01975.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.927+643C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587745 | ||||||
chr16:89587745
|
CCCCCGTG others(29): Show |
C | 2 | a0001c0002t0004g0133a0001c0007t0006g0157 | 2 | HG01943.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.927+648_927+683del others(36): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587745 | |||||
chr16:89587745
|
CCCCCGTG others(365): Show |
C | 2 | a0001c0001t0001g0108a0001c0008t0005g0014 | 2 | HG03453.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.927+648_928-554del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587745 | |||||
chr16:89587745
|
CCCCCGTG others(402): Show |
C | 1 | a0005c0026t0001g0017 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.927+648_928-517del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587745 | |||||
chr16:89587748
|
CCGTGTCA others(4): Show |
C | 7 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0086others(4): Show | 7 | HG00597.hp2 HG01516.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+657_927+667del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587748 | |||||
chr16:89587748
|
CCGTGTCA others(169): Show |
C | 1 | a0002c0003t0003g0116 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.927+657_928-741del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587748 | |||||
chr16:89587749
|
CGTGTCAC others(67): Show |
C | 1 | a0001c0007t0006g0293 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.927+648_927+721del others(74): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587749 | ||||||
chr16:89587754
|
C | T | 9 | a0001c0001t0001g0121a0001c0001t0001g0182a0001c0001t0001g0217others(6): Show | 9 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+652C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587754 | ||||||
chr16:89587754
|
CACCCGCG others(249): Show |
C | 1 | a0001c0001t0001g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.927+657_928-661del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587754 | |||||
chr16:89587755
|
A | ACCCACAG others(8): Show |
3 | a0002c0003t0003g0129a0002c0003t0004g0306a0003c0006t0003g0147 | 3 | HG00621.hp2 HG03927.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.927+656_927+657ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587755 | |||||
chr16:89587755
|
A | ACCCACAG others(9): Show |
1 | a0001c0001t0001g0335 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587755 | |||||
chr16:89587755
|
A | ACCCACAG others(10): Show |
1 | a0001c0002t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(17): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587755 | |||||
chr16:89587755
|
A | ACCCACAG others(34): Show |
1 | a0001c0007t0006g0064 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.927+656_927+657ins others(41): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587755 | |||||
chr16:89587755
|
A | ACCCACAG others(73): Show |
1 | a0001c0001t0008g0055 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(80): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587755 | |||||
chr16:89587755
|
A | ACCCACAG others(82): Show |
1 | a0001c0001t0001g0216 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.927+656_927+657ins others(89): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587755 | |||||
chr16:89587755
|
ACCCGCGT others(19): Show |
A | 5 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0105others(2): Show | 5 | HG01074.hp1 HG01074.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+657_927+682del others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587755 | |||||
chr16:89587755
|
ACCCGCGT others(83): Show |
A | 1 | a0004c0011t0001g0092 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.927+657_927+746del others(90): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587755 | |||||
chr16:89587759
|
G | A | 1 | a0001c0008t0002g0015 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.927+657G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587759 | ||||||
chr16:89587759
|
G | C | 20 | a0001c0001t0001g0036a0001c0001t0001g0081a0001c0001t0001g0101others(17): Show | 20 | HG00558.hp2 HG00621.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.927+657G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587759 | ||||||
chr16:89587759
|
G | GCGTGTCA others(287): Show |
1 | a0002c0003t0003g0128 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.927+672_927+673ins others(294): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587759 | |||||
chr16:89587759
|
G | GCGTGTCA others(95): Show |
1 | a0001c0002t0003g0206 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.927+672_927+673ins others(102): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587759 | |||||
chr16:89587759
|
G | GCGTGTCA others(383): Show |
1 | a0001c0001t0001g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.927+672_927+673ins others(390): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587759 | |||||
chr16:89587759
|
G | GCGTGTCA others(104): Show |
1 | a0001c0001t0001g0030 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.927+672_927+673ins others(111): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587759 | |||||
chr16:89587759
|
GCGTGTCA others(19): Show |
G | 8 | a0001c0001t0001g0026a0001c0001t0001g0035a0001c0001t0001g0096others(5): Show | 8 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+673_927+698del others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587759 | |||||
chr16:89587759
|
GCGTGTCA others(329): Show |
G | 2 | a0001c0002t0005g0289a0001c0028t0001g0164 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.927+673_928-565del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587759 | |||||
chr16:89587761
|
G | A | 2 | a0001c0002t0002g0041a0001c0002t0002g0042 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.927+659G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587761 | ||||||
chr16:89587763
|
G | A | 2 | a0001c0002t0002g0041a0001c0002t0002g0042 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.927+661G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587763 | ||||||
chr16:89587764
|
T | G | 2 | a0001c0002t0002g0041a0001c0002t0002g0042 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.927+662T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587764 | ||||||
chr16:89587765
|
C | CACCCACA others(20): Show |
1 | a0001c0001t0001g0154 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.927+672_927+673ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587765 | |||||
chr16:89587765
|
C | T | 6 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0002t0002g0023others(3): Show | 6 | HG01516.hp1 HG01517.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+663C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587765 | ||||||
chr16:89587765
|
CACCCACA others(83): Show |
C | 6 | a0001c0001t0001g0115a0001c0002t0003g0031a0001c0002t0003g0047others(3): Show | 6 | HG02155.hp2 HG03195.hp2 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+673_927+762del others(90): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587765 | |||||
chr16:89587765
|
CACCCACA others(185): Show |
C | 1 | a0001c0002t0004g0132 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.927+673_928-709del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587765 | |||||
chr16:89587765
|
CACCCACA others(238): Show |
C | 7 | a0001c0001t0001g0252a0001c0007t0006g0071a0001c0007t0006g0158others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+673_928-656del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587765 | |||||
chr16:89587765
|
CACCCACA others(303): Show |
C | 3 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0256 | 4 | NA18950.hp1 NA19000.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+673_928-591del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587765 | |||||
chr16:89587767
|
C | CCCACAGA others(19): Show |
1 | a0001c0008t0002g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.927+672_927+673ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587767 | |||||
chr16:89587767
|
C | G | 2 | a0001c0002t0001g0322a0002c0003t0003g0129 | 2 | HG03516.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.927+665C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587767 | ||||||
chr16:89587770
|
A | G | 2 | a0001c0002t0002g0041a0001c0002t0002g0042 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.927+668A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587770 | ||||||
chr16:89587775
|
A | AACACGGC others(195): Show |
1 | a0001c0002t0004g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.927+684_927+685ins others(202): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587775 | |||||
chr16:89587775
|
A | AACACGGC others(321): Show |
1 | a0002c0003t0003g0135 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.927+688_927+689ins others(328): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587775 | |||||
chr16:89587775
|
A | AACACGGC others(120): Show |
1 | a0001c0001t0001g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.927+688_927+689ins others(127): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587775 | |||||
chr16:89587775
|
A | T | 219 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0028others(216): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.927+673A>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587775 | ||||||
chr16:89587775
|
AACACGGC others(19): Show |
A | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.927+685_927+710del others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587775 | |||||
chr16:89587775
|
AACACGGC others(83): Show |
A | 1 | a0001c0001t0001g0261 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.927+685_927+774del others(90): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587775 | |||||
chr16:89587775
|
AACACGGC others(303): Show |
A | 1 | a0001c0001t0001g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.927+711_928-553del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587775 | |||||
chr16:89587779
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.927+677C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587779 | ||||||
chr16:89587781
|
G | GC | 24 | a0001c0001t0001g0036a0001c0001t0001g0065a0001c0001t0001g0091others(21): Show | 24 | HG00544.hp1 HG00621.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.927+684dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | |||||
chr16:89587781
|
G | GCCCCCCG others(5): Show |
4 | a0001c0001t0001g0088a0001c0001t0001g0097a0001c0024t0001g0218others(1): Show | 4 | HG00642.hp1 HG01071.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+684_927+685ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | |||||
chr16:89587781
|
G | GCCCCCCG others(903): Show |
1 | a0001c0002t0001g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.927+684_927+685ins others(910): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | |||||
chr16:89587781
|
G | GCCCCCCG others(392): Show |
1 | a0001c0002t0004g0155 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(399): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | |||||
chr16:89587781
|
G | GCCCCCCG others(32): Show |
1 | a0002c0003t0003g0111 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | |||||
chr16:89587781
|
G | GCCCCCGT others(4): Show |
1 | a0001c0001t0001g0277 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.927+683_927+693dup others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | |||||
chr16:89587781
|
G | GCCCCCGT others(318): Show |
1 | a0003c0006t0003g0145 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.927+710_927+711ins others(325): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | |||||
chr16:89587781
|
G | GCCCCCGT others(209): Show |
1 | a0002c0004t0002g0307 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.927+710_927+711ins others(216): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | |||||
chr16:89587781
|
G | GCCCCCGT others(106): Show |
1 | a0001c0001t0001g0334 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(113): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | |||||
chr16:89587781
|
G | GCCCCCGT others(964): Show |
1 | a0001c0001t0001g0188 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(971): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | |||||
chr16:89587781
|
G | GCCCCCGT others(575): Show |
1 | a0001c0002t0002g0210 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(582): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | |||||
chr16:89587781
|
GCCCCCGT others(20): Show |
G | 5 | a0001c0001t0001g0106a0001c0002t0002g0084a0001c0002t0003g0229others(2): Show | 5 | HG01106.hp2 HG01346.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+694_927+720del others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | |||||
chr16:89587781
|
GCCCCCGT others(84): Show |
G | 4 | a0001c0001t0001g0141a0001c0001t0001g0280a0001c0002t0004g0039others(1): Show | 4 | HG01168.hp1 NA18940.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+694_927+784del others(91): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | |||||
chr16:89587781
|
GCCCCCGT others(239): Show |
G | 1 | a0001c0001t0001g0265 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.927+694_928-634del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587781 | |||||
chr16:89587782
|
CCCCCGTG others(120): Show |
C | 2 | a0001c0001t0001g0087a0001c0002t0002g0022 | 2 | HG01978.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.927+685_928-762del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587782 | |||||
chr16:89587782
|
CCCCCGTG others(328): Show |
C | 2 | a0001c0001t0001g0060a0001c0002t0004g0271 | 2 | HG03139.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.927+685_928-554del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587782 | |||||
chr16:89587782
|
CCCCCGTG others(365): Show |
C | 1 | a0001c0007t0006g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.927+685_928-517del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587782 | |||||
chr16:89587782
|
CCCCCGTG others(402): Show |
C | 1 | a0001c0002t0009g0328 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.927+685_928-480del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587782 | |||||
chr16:89587785
|
C | CCCCGTGT others(17): Show |
1 | a0001c0002t0011g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.927+684_927+685ins others(24): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCCGTGTC others(95): Show |
1 | a0001c0001t0001g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(102): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCCGTGTC others(58): Show |
1 | a0001c0001t0001g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.927+684_927+685ins others(65): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCCGTGTC others(231): Show |
1 | a0001c0001t0001g0176 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(238): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCCGTGTC others(5): Show |
20 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0095others(17): Show | 20 | HG00544.hp2 HG00558.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.927+684_927+685ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCCGTGTC others(301): Show |
1 | a0001c0002t0004g0237 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(308): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCCGTGTC others(208): Show |
1 | a0001c0001t0001g0054 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(215): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCCGTGTC others(43): Show |
2 | a0003c0006t0003g0168a0003c0006t0003g0230 | 2 | HG02080.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.927+684_927+685ins others(50): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCCGTGTC others(194): Show |
1 | a0001c0002t0004g0227 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(201): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCCGTGTC others(42): Show |
1 | a0001c0001t0001g0007 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.927+684_927+685ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCCGTGTC others(301): Show |
1 | a0001c0001t0001g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.927+684_927+685ins others(308): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCCGTGTC others(68): Show |
1 | a0006c0014t0001g0008 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.927+684_927+685ins others(75): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCCGTGTT others(5): Show |
4 | a0001c0001t0008g0055a0001c0002t0004g0223a0002c0003t0003g0125others(1): Show | 4 | HG00673.hp1 HG02080.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+684_927+685ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCCGTGTT others(42): Show |
1 | a0002c0003t0003g0139 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.927+684_927+685ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTCA others(820): Show |
1 | a0001c0001t0001g0189 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.927+698_927+699ins others(827): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTCA others(41): Show |
1 | a0001c0001t0001g0198 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.927+693_927+694ins others(48): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTCA others(116): Show |
1 | a0002c0004t0002g0301 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.927+693_927+694ins others(123): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTCA others(4): Show |
20 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0082others(17): Show | 20 | HG00323.hp2 HG01257.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.927+693_927+694ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTCA others(67): Show |
1 | a0001c0002t0005g0197 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(74): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTCA others(42): Show |
1 | a0001c0001t0001g0336 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTCA others(79): Show |
3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0059 | 3 | HG02602.hp2 HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.927+693_927+694ins others(86): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTCA others(105): Show |
1 | a0001c0001t0001g0215 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.927+693_927+694ins others(112): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTCA others(267): Show |
1 | a0004c0011t0001g0077 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(274): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTCA others(78): Show |
1 | a0001c0001t0001g0241 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(85): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTCA others(78): Show |
1 | a0001c0001t0001g0269 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(85): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTCA others(169): Show |
1 | a0001c0002t0002g0278 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.927+693_927+694ins others(176): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTCA others(31): Show |
1 | a0001c0002t0004g0151 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.927+690_927+691ins others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTTA others(637): Show |
1 | a0001c0001t0001g0238 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.927+688_927+689ins others(644): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTTA others(31): Show |
1 | a0002c0017t0003g0136 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.927+688_927+689ins others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTTA others(285): Show |
1 | a0001c0002t0002g0338 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.927+688_927+689ins others(292): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | CCGTGTTA others(155): Show |
1 | a0001c0002t0003g0233 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.927+688_927+689ins others(162): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
C | G | 2 | a0001c0002t0001g0287a0001c0002t0004g0228 | 2 | HG00639.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.927+683C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587785 | ||||||
chr16:89587785
|
CCGTGTCA others(95): Show |
C | 1 | a0001c0001t0001g0318 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.927+711_928-761del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587785
|
CCGTGTCA others(250): Show |
C | 1 | a0001c0002t0004g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.927+716_928-601del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587785 | |||||
chr16:89587786
|
C | CGTGTCAC others(251): Show |
1 | a0002c0003t0003g0122 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.927+693_927+694ins others(258): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587786 | |||||
chr16:89587786
|
CGTGTCAC others(30): Show |
C | 1 | a0001c0002t0003g0034 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.927+685_927+721del others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587786 | ||||||
chr16:89587786
|
CGTGTCAC others(249): Show |
C | 1 | a0001c0002t0002g0299 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.927+685_928-633del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587786 | ||||||
chr16:89587788
|
T | C | 2 | a0001c0002t0002g0041a0001c0002t0002g0042 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.927+686T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587788 | ||||||
chr16:89587791
|
C | T | 39 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0068others(36): Show | 39 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.927+689C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587791 | ||||||
chr16:89587792
|
ACCCACAG others(46): Show |
A | 15 | a0001c0001t0001g0050a0001c0001t0001g0093a0001c0001t0001g0094others(12): Show | 15 | HG00140.hp1 HG00639.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.927+694_927+746del others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587792 | |||||
chr16:89587792
|
ACCCACAG others(292): Show |
A | 8 | a0001c0001t0001g0036a0001c0001t0001g0081a0001c0001t0001g0091others(5): Show | 8 | HG01070.hp1 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+694_928-581del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587792 | |||||
chr16:89587793
|
C | CCCACAGA others(294): Show |
1 | a0002c0004t0002g0311 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.927+710_927+711ins others(301): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587793 | |||||
chr16:89587793
|
C | CCCGCGTG others(31): Show |
1 | a0001c0008t0002g0015 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.927+693_927+694ins others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587793 | |||||
chr16:89587793
|
C | CCCGCGTG others(30): Show |
1 | a0002c0004t0002g0324 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.927+693_927+694ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587793 | |||||
chr16:89587793
|
C | G | 13 | a0001c0001t0001g0069a0001c0001t0001g0183a0001c0001t0001g0281others(10): Show | 13 | HG00423.hp1 HG01361.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.927+691C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587793 | ||||||
chr16:89587797
|
C | T | 2 | a0001c0002t0002g0041a0001c0002t0002g0042 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.927+695C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587797 | ||||||
chr16:89587801
|
T | A | 8 | a0001c0001t0001g0103a0001c0001t0001g0215a0001c0001t0001g0220others(5): Show | 8 | HG02615.hp1 HG03239.hp2 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.927+699T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587801 | ||||||
chr16:89587804
|
A | G | 2 | a0001c0002t0002g0041a0001c0002t0002g0042 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.927+702A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587804 | ||||||
chr16:89587805
|
C | T | 9 | a0001c0001t0001g0109a0001c0001t0001g0184a0001c0008t0002g0010others(6): Show | 9 | HG00597.hp2 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.927+703C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587805 | ||||||
chr16:89587807
|
G | A | 2 | a0001c0002t0002g0041a0001c0002t0002g0042 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.927+705G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587807 | ||||||
chr16:89587807
|
GC | G | 81 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0051others(78): Show | 86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.927+711delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587807 | |||||
chr16:89587807
|
GCCCCCCG others(58): Show |
G | 1 | a0004c0020t0001g0340 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.927+711_927+775del others(65): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587807 | |||||
chr16:89587807
|
GCCCCCCG others(186): Show |
G | 1 | a0001c0002t0002g0329 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.927+711_928-670del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587807 | |||||
chr16:89587808
|
C | CCCCCCGT others(452): Show |
1 | a0002c0004t0002g0332 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.927+720_927+721ins others(459): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | |||||
chr16:89587808
|
C | CCCCCGTG others(18): Show |
1 | a0001c0002t0010g0219 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.927+710_927+711ins others(25): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | |||||
chr16:89587808
|
C | CCCCCGTG others(108): Show |
1 | a0001c0001t0001g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.927+710_927+711ins others(115): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | |||||
chr16:89587808
|
C | CCCCCGTG others(40): Show |
1 | a0001c0002t0002g0196 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.927+710_927+711ins others(47): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | |||||
chr16:89587808
|
C | CCCCCGTG others(29): Show |
1 | a0001c0001t0001g0273 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.927+710_927+711ins others(36): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | |||||
chr16:89587808
|
C | CCCCCGTG others(617): Show |
1 | a0001c0002t0004g0169 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.927+710_927+711ins others(624): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | |||||
chr16:89587808
|
C | CCCCCGTG others(179): Show |
1 | a0001c0001t0001g0062 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.927+710_927+711ins others(186): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | |||||
chr16:89587808
|
C | CCCCCGTG others(18): Show |
1 | a0001c0002t0004g0151 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.927+710_927+711ins others(25): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | |||||
chr16:89587808
|
C | CCCCCGTG others(757): Show |
1 | a0002c0004t0002g0279 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.927+710_927+711ins others(764): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | |||||
chr16:89587808
|
C | CCCCCGTG others(56): Show |
1 | a0002c0003t0003g0137 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.927+710_927+711ins others(63): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | |||||
chr16:89587808
|
CCCCCCGT others(302): Show |
C | 1 | a0001c0002t0005g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.927+753_928-512del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587808 | |||||
chr16:89587809
|
C | A | 2 | a0001c0002t0002g0041a0001c0002t0002g0042 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.927+707C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587809 | ||||||
chr16:89587811
|
CCCGTGTC others(5): Show |
C | 5 | a0001c0001t0001g0040a0001c0001t0001g0220a0001c0001t0001g0239others(2): Show | 5 | HG01361.hp1 HG02071.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+711_927+722del others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587811 | |||||
chr16:89587811
|
CCCGTGTC others(69): Show |
C | 2 | a0001c0002t0003g0192a0001c0005t0002g0310 | 2 | HG02155.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.927+711_927+786del others(76): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587811 | |||||
chr16:89587811
|
CCCGTGTC others(106): Show |
C | 1 | a0002c0004t0002g0309 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.927+711_928-750del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587811 | |||||
chr16:89587812
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.927+710C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587812 | ||||||
chr16:89587812
|
CCGTGTCA others(223): Show |
C | 1 | a0001c0002t0005g0320 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.927+721_928-623del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587812 | |||||
chr16:89587812
|
CCGTGTCA others(387): Show |
C | 1 | a0001c0002t0007g0234 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.927+721_928-459del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587812 | |||||
chr16:89587817
|
T | TCACCCCC others(4): Show |
1 | a0001c0002t0002g0042 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.927+720_927+721ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587817 | |||||
chr16:89587818
|
C | T | 24 | a0001c0001t0001g0068a0001c0001t0001g0120a0001c0001t0001g0154others(21): Show | 24 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.927+716C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587818 | ||||||
chr16:89587818
|
CACCCGCG others(30): Show |
C | 1 | a0001c0002t0003g0211 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.927+721_927+757del others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587818 | |||||
chr16:89587819
|
A | ACCCACAG others(8): Show |
2 | a0001c0001t0001g0173a0001c0002t0003g0076 | 2 | NA18944.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.927+720_927+721ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587819 | |||||
chr16:89587819
|
A | ACCCACAG others(9): Show |
1 | a0001c0001t0001g0217 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.927+720_927+721ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587819 | |||||
chr16:89587819
|
A | ACCCACAG others(34): Show |
2 | a0001c0001t0001g0065a0001c0007t0006g0064 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.927+720_927+721ins others(41): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587819 | |||||
chr16:89587819
|
A | ACCCACAG others(60): Show |
1 | a0001c0001t0001g0109 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.927+720_927+721ins others(67): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587819 | |||||
chr16:89587819
|
A | AGCCACAG others(9): Show |
1 | a0001c0005t0002g0107 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.927+717_927+718ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587819 | ||||||
chr16:89587819
|
A | AGCCACAG others(274): Show |
1 | a0002c0004t0002g0016 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.927+717_927+718ins others(281): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587819 | ||||||
chr16:89587819
|
A | AGCCACAG others(706): Show |
1 | a0001c0005t0002g0056 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.927+717_927+718ins others(713): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587819 | ||||||
chr16:89587819
|
A | AGCCACAG others(197): Show |
1 | a0001c0005t0002g0043 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.927+717_927+718ins others(204): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587819 | ||||||
chr16:89587819
|
A | AGCCACAG others(34): Show |
1 | a0002c0003t0004g0306 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.927+717_927+718ins others(41): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587819 | ||||||
chr16:89587823
|
G | C | 14 | a0001c0001t0001g0065a0001c0001t0001g0082a0001c0001t0001g0109others(11): Show | 14 | HG00558.hp1 HG00621.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.927+721G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587823 | ||||||
chr16:89587823
|
G | GCGTGTCA others(251): Show |
1 | a0001c0001t0001g0103 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.927+736_927+737ins others(258): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587823 | |||||
chr16:89587823
|
G | GCGTGTCA others(270): Show |
1 | a0002c0004t0002g0319 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+736_927+737ins others(277): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587823 | |||||
chr16:89587823
|
GCGTGTCA others(265): Show |
G | 1 | a0001c0002t0002g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.927+753_928-549del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587823 | |||||
chr16:89587829
|
C | CACCCACA others(20): Show |
2 | a0003c0006t0003g0274a0003c0006t0003g0275 | 2 | NA18946.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.927+748_927+749ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587829 | |||||
chr16:89587829
|
C | T | 1 | a0001c0002t0004g0225 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.927+727C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587829 | ||||||
chr16:89587829
|
CACCCACA others(19): Show |
C | 5 | a0001c0001t0001g0102a0001c0001t0001g0121a0001c0002t0002g0046others(2): Show | 5 | HG00099.hp2 HG01517.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+749_927+774del others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587829 | |||||
chr16:89587831
|
C | G | 2 | a0001c0001t0001g0281a0001c0002t0013g0194 | 2 | HG01361.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.927+729C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587831 | ||||||
chr16:89587834
|
A | C | 1 | a0001c0002t0003g0076 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.927+732A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587834 | ||||||
chr16:89587835
|
C | T | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+733C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587835 | ||||||
chr16:89587837
|
G | T | 1 | a0001c0002t0003g0076 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.927+735G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587837 | ||||||
chr16:89587839
|
T | A | 26 | a0001c0001t0001g0054a0001c0001t0001g0063a0001c0001t0001g0080others(23): Show | 26 | HG00323.hp1 HG00733.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.927+737T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587839 | ||||||
chr16:89587839
|
T | TACACGGC others(131): Show |
1 | a0002c0003t0003g0130 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.927+752_927+753ins others(138): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587839 | |||||
chr16:89587840
|
A | G | 1 | a0001c0002t0003g0076 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.927+738A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587840 | ||||||
chr16:89587843
|
C | T | 4 | a0001c0001t0001g0066a0001c0001t0001g0243a0001c0008t0001g0009others(1): Show | 4 | HG01123.hp1 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+741C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587843 | ||||||
chr16:89587845
|
G | GC | 37 | a0001c0001t0001g0040a0001c0001t0001g0079a0001c0001t0001g0098others(34): Show | 37 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.927+748dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587845 | |||||
chr16:89587845
|
G | GCCCCCCG others(5): Show |
1 | a0001c0001t0001g0097 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.927+748_927+749ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587845 | |||||
chr16:89587845
|
G | GCCCCCCG others(785): Show |
1 | a0002c0003t0003g0124 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.927+748_927+749ins others(792): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587845 | |||||
chr16:89587845
|
G | GCCCCCCG others(32): Show |
1 | a0002c0003t0003g0126 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.927+748_927+749ins others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587845 | |||||
chr16:89587845
|
G | GCCCCCGT others(4): Show |
3 | a0001c0001t0001g0277a0001c0001t0001g0334a0001c0002t0005g0292 | 3 | HG00733.hp1 HG02615.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.927+752_927+753ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587845 | |||||
chr16:89587845
|
G | GCCCCCGT others(481): Show |
1 | a0001c0002t0003g0290 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.927+752_927+753ins others(488): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587845 | |||||
chr16:89587845
|
GCCCCCGT others(20): Show |
G | 7 | a0001c0001t0001g0035a0001c0001t0001g0096a0001c0001t0001g0140others(4): Show | 7 | HG00597.hp2 HG00741.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+753_927+779del others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587845 | |||||
chr16:89587845
|
GCCCCCGT others(148): Show |
G | 1 | a0001c0002t0004g0117 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.928-760_928-606del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587845 | |||||
chr16:89587846
|
CCCCCGTG others(264): Show |
C | 2 | a0001c0002t0003g0313a0001c0007t0006g0157 | 2 | HG02818.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.927+749_928-554del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587846 | |||||
chr16:89587849
|
C | CCCCGTGT others(6): Show |
2 | a0001c0001t0001g0088a0001c0002t0013g0194 | 2 | HG00642.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.927+748_927+749ins others(13): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | |||||
chr16:89587849
|
C | CCCGTGTC others(5): Show |
12 | a0001c0001t0001g0066a0001c0001t0001g0175a0001c0001t0001g0176others(9): Show | 12 | HG00099.hp1 HG00558.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.927+748_927+749ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | |||||
chr16:89587849
|
C | CCCGTGTC others(119): Show |
1 | a0001c0002t0003g0181 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.927+748_927+749ins others(126): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | |||||
chr16:89587849
|
C | CCCGTGTC others(569): Show |
1 | a0001c0001t0001g0249 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.927+748_927+749ins others(576): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | |||||
chr16:89587849
|
C | CCCGTGTC others(42): Show |
2 | a0001c0001t0001g0184a0001c0001t0001g0216 | 2 | HG02055.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.927+748_927+749ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | |||||
chr16:89587849
|
C | CCCGTGTC others(270): Show |
1 | a0001c0001t0001g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.927+748_927+749ins others(277): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | |||||
chr16:89587849
|
C | CCCGTGTT others(5): Show |
6 | a0001c0001t0001g0154a0001c0002t0004g0225a0002c0003t0003g0125others(3): Show | 6 | HG02129.hp2 NA18945.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+748_927+749ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | |||||
chr16:89587849
|
C | CCCGTGTT others(230): Show |
1 | a0001c0001t0001g0243 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.927+748_927+749ins others(237): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | |||||
chr16:89587849
|
C | CCGTGTCA others(57): Show |
1 | a0002c0004t0002g0311 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.927+752_927+753ins others(64): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | |||||
chr16:89587849
|
C | CCGTGTCA others(4): Show |
21 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0068others(18): Show | 21 | HG01081.hp2 HG01175.hp1 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.927+752_927+753ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | |||||
chr16:89587849
|
C | CCGTGTCA others(67): Show |
1 | a0001c0013t0002g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.927+752_927+753ins others(74): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | |||||
chr16:89587849
|
C | CCGTGTCA others(367): Show |
1 | a0003c0006t0003g0147 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.927+752_927+753ins others(374): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587849 | |||||
chr16:89587849
|
C | G | 17 | a0001c0001t0001g0050a0001c0001t0001g0093a0001c0001t0001g0094others(14): Show | 17 | HG00140.hp1 HG00639.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.927+747C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587849 | ||||||
chr16:89587850
|
CGTGTTAC others(30): Show |
C | 1 | a0001c0005t0002g0317 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.927+749_927+785del others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587850 | ||||||
chr16:89587851
|
G | A | 2 | a0001c0001t0001g0251a0001c0002t0002g0210 | 2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.927+749G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587851 | ||||||
chr16:89587855
|
T | C | 198 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0030others(195): Show | 203 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.927+753T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587855 | ||||||
chr16:89587855
|
T | TACCCGCG others(4): Show |
1 | a0001c0002t0001g0322 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.927+757_927+758ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587855 | |||||
chr16:89587856
|
ACCCACAG others(228): Show |
A | 1 | a0001c0002t0004g0327 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.927+758_928-581del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587856 | |||||
chr16:89587857
|
C | CCCGCGTG others(56): Show |
1 | a0001c0002t0005g0187 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.927+757_927+758ins others(63): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587857 | |||||
chr16:89587857
|
C | G | 20 | a0001c0001t0001g0059a0001c0001t0001g0069a0001c0001t0001g0075others(17): Show | 20 | HG00621.hp2 HG00673.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.927+755C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587857 | ||||||
chr16:89587865
|
T | A | 11 | a0001c0001t0001g0066a0001c0001t0001g0080a0001c0001t0001g0088others(8): Show | 11 | HG00099.hp1 HG00558.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+763T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587865 | ||||||
chr16:89587869
|
C | T | 9 | a0001c0001t0001g0183a0001c0001t0001g0185a0001c0001t0001g0273others(6): Show | 9 | HG01928.hp2 HG03195.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+767C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587869 | ||||||
chr16:89587871
|
GC | G | 69 | a0001c0001t0001g0026a0001c0001t0001g0050a0001c0001t0001g0051others(66): Show | 70 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.927+775delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587871 | |||||
chr16:89587871
|
GCCCCCCG others(187): Show |
G | 1 | a0001c0002t0002g0202 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.927+775_928-605del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587871 | |||||
chr16:89587872
|
C | CCCCCCGT others(82): Show |
1 | a0001c0001t0001g0258 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.928-755_928-754ins others(89): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587872 | |||||
chr16:89587872
|
C | CCCCCGTG others(3): Show |
1 | a0001c0002t0002g0254 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.927+774_927+775ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587872 | |||||
chr16:89587872
|
C | CCCCCGTG others(18): Show |
1 | a0001c0002t0002g0338 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.927+774_927+775ins others(25): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587872 | |||||
chr16:89587872
|
C | CCCCCGTG others(66): Show |
1 | a0001c0005t0002g0303 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.927+774_927+775ins others(73): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587872 | |||||
chr16:89587872
|
C | CCCCCGTG others(29): Show |
1 | a0001c0001t0001g0269 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.927+774_927+775ins others(36): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587872 | |||||
chr16:89587872
|
C | CCCCCGTG others(56): Show |
1 | a0001c0002t0004g0134 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.927+774_927+775ins others(63): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587872 | |||||
chr16:89587872
|
CCCCCCGT others(94): Show |
C | 1 | a0001c0002t0004g0133 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.927+785_928-688del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587872 | |||||
chr16:89587875
|
CCCGTGTC others(5): Show |
C | 10 | a0001c0001t0001g0098a0001c0001t0001g0242a0001c0002t0001g0322others(7): Show | 10 | HG01123.hp2 HG01891.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.927+775_927+786del others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587875 | |||||
chr16:89587875
|
CCCGTGTC others(42): Show |
C | 1 | a0002c0004t0002g0308 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.927+775_928-750del others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587875 | |||||
chr16:89587876
|
C | T | 2 | a0001c0002t0003g0033a0001c0002t0003g0044 | 2 | NA18977.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.927+774C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587876 | ||||||
chr16:89587876
|
CCGTGTCA others(4): Show |
C | 4 | a0001c0001t0001g0040a0001c0001t0001g0154a0002c0003t0003g0207others(1): Show | 4 | NA18942.hp1 NA18959.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+785_928-778del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587876 | |||||
chr16:89587877
|
CGTGTCAC others(3): Show |
C | 1 | a0001c0002t0003g0236 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.927+776_927+785del others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587877 | ||||||
chr16:89587878
|
G | A | 2 | a0001c0002t0002g0254a0001c0002t0004g0226 | 2 | HG02132.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.927+776G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587878 | ||||||
chr16:89587882
|
C | T | 9 | a0001c0001t0001g0182a0001c0001t0001g0339a0001c0001t0008g0055others(6): Show | 9 | HG00673.hp1 HG01109.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+780C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587882 | ||||||
chr16:89587883
|
A | ACCCACAG others(8): Show |
1 | a0002c0003t0003g0208 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.927+784_927+785ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587883 | |||||
chr16:89587883
|
A | ACCCACAG others(9): Show |
2 | a0001c0001t0001g0120a0002c0004t0002g0304 | 2 | NA18990.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.927+784_927+785ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587883 | |||||
chr16:89587883
|
A | ACCCACAG others(36): Show |
1 | a0001c0001t0001g0188 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.927+784_927+785ins others(43): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587883 | |||||
chr16:89587883
|
A | ACCCACAG others(141): Show |
1 | a0002c0004t0002g0016 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.927+784_927+785ins others(148): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587883 | |||||
chr16:89587883
|
A | ACCCACAG others(115): Show |
1 | a0001c0005t0002g0212 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.927+784_927+785ins others(122): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587883 | |||||
chr16:89587883
|
A | ACCCACAG others(61): Show |
1 | a0001c0001t0001g0190 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.927+784_927+785ins others(68): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587883 | |||||
chr16:89587883
|
A | ACCCACAG others(45): Show |
1 | a0001c0007t0006g0064 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.927+784_927+785ins others(52): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587883 | |||||
chr16:89587883
|
A | ACCCACAG others(62): Show |
1 | a0002c0004t0002g0279 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.927+784_927+785ins others(69): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587883 | |||||
chr16:89587883
|
A | AGCCACAG others(8): Show |
2 | a0001c0001t0001g0068a0002c0003t0004g0306 | 2 | HG00621.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.927+781_927+782ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587883 | ||||||
chr16:89587883
|
A | AGCCACAG others(9): Show |
1 | a0001c0005t0002g0107 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.927+781_927+782ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587883 | ||||||
chr16:89587883
|
A | AGCCACAG others(146): Show |
1 | a0001c0005t0002g0302 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.927+781_927+782ins others(153): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587883 | ||||||
chr16:89587883
|
A | AGCCACAG others(88): Show |
10 | a0001c0001t0001g0248a0001c0005t0002g0003a0001c0005t0002g0072others(7): Show | 14 | HG01070.hp2 HG01071.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.927+781_927+782ins others(95): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587883 | ||||||
chr16:89587887
|
G | A | 1 | a0001c0002t0002g0337 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.927+785G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587887 | ||||||
chr16:89587887
|
G | C | 29 | a0001c0001t0001g0068a0001c0001t0001g0079a0001c0001t0001g0083others(26): Show | 33 | HG00438.hp1 HG00621.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.927+785G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587887 | ||||||
chr16:89587887
|
G | GCGTGTCA others(308): Show |
1 | a0001c0001t0001g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.928-773_928-772ins others(315): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587887 | |||||
chr16:89587887
|
G | GCGTGTCA others(19): Show |
3 | a0001c0002t0002g0196a0001c0002t0004g0150a0001c0007t0006g0165 | 3 | HG00280.hp1 HG00544.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.928-777_928-752dup others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587887 | |||||
chr16:89587887
|
G | GCGTGTCA others(72): Show |
1 | a0002c0004t0002g0319 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.928-752_928-751ins others(79): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587887 | |||||
chr16:89587887
|
G | GCGTGTCA others(407): Show |
1 | a0001c0001t0001g0241 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.928-769_928-768ins others(414): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587887 | |||||
chr16:89587887
|
GCGTGTCA others(83): Show |
G | 2 | a0001c0002t0004g0037a0001c0002t0004g0325 | 2 | HG03471.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.928-760_928-671del others(90): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587887 | |||||
chr16:89587887
|
GCGTGTCA others(201): Show |
G | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.928-723_928-516del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587887 | |||||
chr16:89587893
|
C | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0154a0001c0002t0004g0110others(1): Show | 4 | HG02080.hp1 NA18962.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-782C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587893 | ||||||
chr16:89587895
|
C | G | 4 | a0001c0001t0001g0068a0001c0005t0002g0310a0001c0005t0002g0323others(1): Show | 4 | HG02145.hp2 HG02155.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-780C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587895 | ||||||
chr16:89587903
|
T | A | 9 | a0001c0001t0001g0095a0001c0001t0001g0103a0001c0001t0001g0217others(6): Show | 9 | HG00558.hp1 HG00733.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.928-772T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587903 | ||||||
chr16:89587907
|
C | T | 9 | a0001c0001t0001g0054a0001c0001t0001g0069a0001c0001t0001g0198others(6): Show | 9 | HG00140.hp2 HG00741.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.928-768C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587907 | ||||||
chr16:89587909
|
G | GC | 79 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0054others(76): Show | 79 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.928-761dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | |||||
chr16:89587909
|
G | GCCCCCCG others(21): Show |
2 | a0001c0002t0001g0167a0003c0006t0003g0232 | 2 | HG02083.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.928-761_928-760ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | |||||
chr16:89587909
|
G | GCCCCCCG others(21): Show |
2 | a0001c0001t0001g0284a0001c0001t0001g0335 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.928-761_928-760ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | |||||
chr16:89587909
|
G | GCCCCCCG others(236): Show |
1 | a0002c0003t0003g0114 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.928-761_928-760ins others(243): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | |||||
chr16:89587909
|
G | GCCCCCGT others(20): Show |
2 | a0001c0002t0003g0180a0001c0002t0004g0123 | 2 | HG02027.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.928-752_928-751ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | |||||
chr16:89587909
|
G | GCCCCCGT others(177): Show |
2 | a0001c0001t0001g0191a0008c0021t0001g0224 | 2 | NA18970.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.928-752_928-751ins others(184): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | |||||
chr16:89587909
|
G | GCCCCCGT others(196): Show |
1 | a0003c0006t0003g0148 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.928-752_928-751ins others(203): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | |||||
chr16:89587909
|
G | GCCCCCGT others(46): Show |
1 | a0001c0002t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.928-752_928-751ins others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | |||||
chr16:89587909
|
G | GCCCCCGT others(20): Show |
1 | a0001c0002t0011g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.928-755_928-754ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | |||||
chr16:89587909
|
G | GCCCCCGT others(20): Show |
1 | a0001c0001t0001g0103 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.928-757_928-756ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | |||||
chr16:89587909
|
G | GCCCCCGT others(427): Show |
1 | a0001c0001t0001g0285 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.928-757_928-756ins others(434): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | |||||
chr16:89587909
|
GCCCCCGT others(4): Show |
G | 1 | a0002c0003t0003g0126 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.928-762_928-752del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587909 | |||||
chr16:89587910
|
CCCCCGTG others(274): Show |
C | 1 | a0001c0001t0001g0079 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.928-760_928-480del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587910 | |||||
chr16:89587913
|
C | CCCGTGTC others(166): Show |
1 | a0001c0001t0001g0217 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.928-761_928-760ins others(173): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587913 | |||||
chr16:89587913
|
CCGTGTCA others(4): Show |
C | 9 | a0001c0001t0001g0057a0001c0001t0001g0120a0001c0002t0003g0076others(6): Show | 9 | HG00597.hp2 HG02486.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-751_928-741del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587913 | |||||
chr16:89587913
|
CCGTGTCA others(122): Show |
C | 3 | a0001c0002t0002g0199a0001c0002t0002g0201a0002c0003t0002g0312 | 3 | HG00423.hp1 NA19010.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.928-751_928-623del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587913 | |||||
chr16:89587913
|
CCGTGTCA others(212): Show |
C | 1 | a0001c0002t0002g0209 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.928-751_928-533del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587913 | |||||
chr16:89587913
|
CCGTGTCA others(286): Show |
C | 1 | a0001c0001t0001g0080 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.928-751_928-459del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587913 | |||||
chr16:89587914
|
CGTGTCAC others(3): Show |
C | 8 | a0001c0001t0001g0154a0001c0001t0001g0182a0001c0001t0001g0244others(5): Show | 8 | HG00323.hp1 HG02155.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-760_928-751del others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587914 | ||||||
chr16:89587915
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.928-760G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587915 | ||||||
chr16:89587919
|
C | T | 13 | a0001c0001t0001g0103a0001c0001t0001g0198a0001c0001t0001g0277others(10): Show | 13 | HG00140.hp2 HG00642.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.928-756C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587919 | ||||||
chr16:89587919
|
CACCCGCG others(84): Show |
C | 3 | a0001c0001t0001g0172a0001c0002t0004g0118a0009c0019t0002g0253 | 3 | HG02165.hp1 HG03834.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.928-751_928-661del others(91): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587919 | |||||
chr16:89587919
|
CACCCGCG others(149): Show |
C | 1 | a0001c0001t0001g0075 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.928-751_928-596del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587919 | |||||
chr16:89587920
|
A | ACCCACAG others(35): Show |
1 | a0001c0001t0001g0040 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.928-752_928-751ins others(42): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587920 | |||||
chr16:89587920
|
A | ACCCACAG others(8): Show |
5 | a0001c0001t0001g0277a0001c0002t0003g0236a0002c0003t0003g0138others(2): Show | 5 | HG00438.hp2 HG00621.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.928-752_928-751ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587920 | |||||
chr16:89587920
|
A | ACCCACAG others(9): Show |
6 | a0001c0001t0001g0214a0001c0002t0003g0206a0001c0002t0004g0155others(3): Show | 7 | HG01257.hp2 HG01258.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-752_928-751ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587920 | |||||
chr16:89587920
|
A | ACCCACAG others(46): Show |
2 | a0003c0006t0003g0274a0003c0006t0003g0275 | 2 | NA18946.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.928-752_928-751ins others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587920 | |||||
chr16:89587920
|
A | AGCCACAG others(9): Show |
1 | a0002c0004t0002g0016 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.928-755_928-754ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587920 | ||||||
chr16:89587920
|
A | AGCCACAG others(47): Show |
1 | a0001c0002t0005g0187 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.928-755_928-754ins others(54): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587920 | ||||||
chr16:89587924
|
G | C | 28 | a0001c0001t0001g0040a0001c0001t0001g0062a0001c0001t0001g0083others(25): Show | 29 | HG00438.hp2 HG00621.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.928-751G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587924 | ||||||
chr16:89587924
|
GCGTGTCA others(164): Show |
G | 4 | a0001c0001t0001g0052a0001c0001t0001g0058a0001c0001t0001g0093others(1): Show | 4 | HG00323.hp2 HG01106.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-723_928-553del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587924 | |||||
chr16:89587926
|
G | A | 1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-749G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587926 | ||||||
chr16:89587930
|
C | T | 3 | a0001c0001t0001g0182a0001c0002t0004g0150a0001c0002t0004g0266 | 3 | HG00544.hp1 HG02257.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.928-745C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587930 | ||||||
chr16:89587930
|
CACCCACA others(20): Show |
C | 4 | a0001c0001t0001g0115a0001c0001t0001g0141a0001c0002t0003g0018others(1): Show | 4 | NA18966.hp2 NA18970.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-723_928-697del others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587930 | |||||
chr16:89587930
|
CACCCACA others(73): Show |
C | 6 | a0001c0001t0001g0140a0001c0002t0002g0084a0001c0002t0003g0031others(3): Show | 6 | HG01106.hp2 NA18941.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-718_928-639del others(80): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587930 | |||||
chr16:89587930
|
CACCCACA others(138): Show |
C | 1 | a0001c0001t0001g0267 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.928-723_928-579del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587930 | |||||
chr16:89587932
|
C | CCCACAGA others(19): Show |
1 | a0002c0004t0002g0324 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.928-724_928-723ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587932 | |||||
chr16:89587932
|
C | G | 5 | a0001c0005t0002g0002a0001c0008t0001g0005a0002c0003t0004g0306others(2): Show | 6 | HG00621.hp2 HG01074.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-743C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587932 | ||||||
chr16:89587933
|
C | T | 1 | a0001c0002t0002g0316 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.928-742C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587933 | ||||||
chr16:89587935
|
A | G | 1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-740A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587935 | ||||||
chr16:89587940
|
T | A | 32 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0066others(29): Show | 36 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.928-735T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587940 | ||||||
chr16:89587944
|
C | T | 2 | a0001c0001t0001g0109a0001c0002t0001g0167 | 2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.928-731C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587944 | ||||||
chr16:89587946
|
GC | G | 72 | a0001c0001t0001g0028a0001c0001t0001g0051a0001c0001t0001g0057others(69): Show | 72 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.928-723delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587946 | |||||
chr16:89587946
|
GCCCCCCG others(47): Show |
G | 1 | a0001c0001t0001g0341 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.928-723_928-670del others(54): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587946 | |||||
chr16:89587946
|
GCCCCCCG others(74): Show |
G | 8 | a0001c0001t0001g0050a0001c0001t0001g0101a0001c0002t0002g0041others(5): Show | 8 | HG00639.hp2 HG01928.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-723_928-643del others(81): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587946 | |||||
chr16:89587947
|
C | A | 1 | a0001c0002t0004g0151 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.928-728C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587947 | ||||||
chr16:89587947
|
C | CCCCCCCG others(20): Show |
1 | a0001c0005t0002g0072 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.928-723_928-722ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | |||||
chr16:89587947
|
C | CCCCCCGT others(4): Show |
1 | a0001c0008t0002g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.928-719_928-718ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | |||||
chr16:89587947
|
C | CCCCCCGT others(19): Show |
8 | a0001c0001t0001g0248a0001c0005t0002g0003a0001c0005t0002g0193others(5): Show | 9 | HG01070.hp2 HG01071.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-719_928-718ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | |||||
chr16:89587947
|
C | CCCCCCGT others(104): Show |
1 | a0001c0002t0003g0177 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.928-719_928-718ins others(111): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | |||||
chr16:89587947
|
C | CCCCCGTG others(3): Show |
1 | a0001c0001t0001g0030 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.928-724_928-723ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | |||||
chr16:89587947
|
C | CCCCCGTG others(29): Show |
1 | a0001c0002t0005g0197 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.928-724_928-723ins others(36): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | |||||
chr16:89587947
|
C | CCCCCGTG others(409): Show |
1 | a0001c0001t0001g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-724_928-723ins others(416): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | |||||
chr16:89587947
|
C | CCCCCGTG others(251): Show |
1 | a0001c0002t0004g0169 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.928-724_928-723ins others(258): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | |||||
chr16:89587947
|
C | CCCCCGTG others(98): Show |
1 | a0002c0004t0002g0307 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.928-724_928-723ins others(105): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | |||||
chr16:89587947
|
C | CCCCTCGT others(4): Show |
1 | a0001c0001t0001g0045 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.928-725_928-724ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | |||||
chr16:89587947
|
C | CCTCCCGT others(4): Show |
1 | a0001c0008t0002g0015 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.928-727_928-726ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | |||||
chr16:89587947
|
CCCCCCGT others(163): Show |
C | 4 | a0001c0001t0001g0082a0001c0001t0001g0090a0001c0007t0006g0161others(1): Show | 4 | HG01109.hp1 HG03195.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-718_928-549del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | |||||
chr16:89587947
|
CCCCCCGT others(200): Show |
C | 2 | a0001c0001t0001g0102a0001c0001t0001g0106 | 2 | HG00099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.928-718_928-512del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587947 | |||||
chr16:89587950
|
CCCGTGTT others(175): Show |
C | 1 | a0004c0020t0001g0340 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.928-723_928-542del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587950 | |||||
chr16:89587951
|
C | CCATGTCA others(4): Show |
2 | a0001c0001t0001g0191a0008c0021t0001g0224 | 2 | NA18970.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.928-723_928-722ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | |||||
chr16:89587951
|
C | CCCGTGTC others(43): Show |
1 | a0003c0006t0003g0144 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.928-723_928-722ins others(50): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | |||||
chr16:89587951
|
C | CCGTGTCA others(31): Show |
2 | a0001c0002t0003g0233a0001c0002t0004g0134 | 2 | HG02735.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.928-719_928-718ins others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | |||||
chr16:89587951
|
C | CCGTGTCA others(95): Show |
1 | a0001c0002t0004g0123 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.928-719_928-718ins others(102): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | |||||
chr16:89587951
|
C | CCGTGTCA others(43): Show |
1 | a0001c0001t0001g0088 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.928-719_928-718ins others(50): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | |||||
chr16:89587951
|
C | CCGTGTCA others(4): Show |
17 | a0001c0001t0001g0175a0001c0001t0001g0241a0001c0001t0001g0333others(14): Show | 17 | HG01952.hp2 HG02027.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.928-719_928-718ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | |||||
chr16:89587951
|
C | CCGTGTCA others(639): Show |
1 | a0002c0004t0002g0301 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.928-719_928-718ins others(646): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | |||||
chr16:89587951
|
C | CCGTGTCA others(42): Show |
1 | a0001c0001t0001g0189 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.928-719_928-718ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | |||||
chr16:89587951
|
C | CCGTGTCA others(42): Show |
3 | a0002c0003t0002g0119a0003c0006t0003g0231a0003c0006t0003g0342 | 3 | HG00423.hp2 HG00621.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.928-719_928-718ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | |||||
chr16:89587951
|
C | CCGTGTCA others(199): Show |
1 | a0003c0006t0003g0147 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.928-719_928-718ins others(206): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | |||||
chr16:89587951
|
C | CCGTGTCA others(41): Show |
2 | a0002c0003t0003g0111a0011c0016t0003g0112 | 2 | NA18952.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.928-719_928-718ins others(48): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | |||||
chr16:89587951
|
C | CCGTGTTA others(4): Show |
1 | a0001c0001t0001g0249 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.928-714_928-713ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | |||||
chr16:89587951
|
C | CGTGTCAC others(30): Show |
2 | a0001c0002t0002g0210a0001c0007t0006g0064 | 2 | HG02723.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.928-724_928-723ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | ||||||
chr16:89587951
|
C | CGTGTCAC others(158): Show |
1 | a0001c0002t0004g0227 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.928-724_928-723ins others(165): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | ||||||
chr16:89587951
|
C | CGTGTCAC others(30): Show |
1 | a0001c0002t0004g0225 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.928-724_928-723ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | ||||||
chr16:89587951
|
C | CGTGTCAC others(193): Show |
1 | a0001c0002t0002g0316 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.928-724_928-723ins others(200): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | ||||||
chr16:89587951
|
C | CGTGTCAC others(3): Show |
29 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0054others(26): Show | 29 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.928-724_928-723ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | ||||||
chr16:89587951
|
C | CGTGTCAC others(67): Show |
1 | a0001c0001t0001g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.928-724_928-723ins others(74): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | ||||||
chr16:89587951
|
C | CGTGTCAC others(79): Show |
1 | a0003c0006t0003g0149 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.928-724_928-723ins others(86): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | ||||||
chr16:89587951
|
C | CGTGTCAG others(313): Show |
1 | a0002c0004t0002g0304 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.928-724_928-723ins others(320): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | ||||||
chr16:89587951
|
C | CGTGTCAG others(68): Show |
1 | a0001c0001t0001g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.928-724_928-723ins others(75): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | ||||||
chr16:89587951
|
C | CGTGTTAC others(320): Show |
1 | a0001c0001t0001g0027 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.928-724_928-723ins others(327): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | ||||||
chr16:89587951
|
C | CGTGTTAC others(3): Show |
1 | a0002c0003t0003g0073 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.928-724_928-723ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | ||||||
chr16:89587951
|
C | G | 2 | a0001c0001t0001g0045a0001c0008t0002g0015 | 2 | HG01081.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.928-724C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | ||||||
chr16:89587951
|
C | T | 3 | a0001c0001t0001g0095a0001c0002t0003g0049a0001c0002t0010g0219 | 3 | HG00733.hp2 HG04228.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.928-724C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587951 | ||||||
chr16:89587951
|
CCGTGTTA others(174): Show |
C | 1 | a0001c0002t0002g0337 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.928-718_928-538del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587951 | |||||
chr16:89587953
|
G | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0251 | 2 | HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.928-722G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587953 | ||||||
chr16:89587954
|
T | C | 1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-721T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587954 | ||||||
chr16:89587957
|
T | C | 200 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0027others(197): Show | 205 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.928-718T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587957 | ||||||
chr16:89587957
|
T | TACCCACA others(371): Show |
1 | a0001c0001t0008g0055 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.928-697_928-696ins others(378): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587957 | |||||
chr16:89587957
|
T | TACCCACA others(460): Show |
1 | a0003c0006t0003g0275 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.928-666_928-665ins others(467): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587957 | |||||
chr16:89587957
|
T | TACCCCGC others(5): Show |
1 | a0001c0001t0001g0300 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.928-714_928-713ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587957 | |||||
chr16:89587957
|
T | TACCCGCG others(4): Show |
1 | a0001c0001t0001g0339 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.928-714_928-713ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587957 | |||||
chr16:89587957
|
T | TACCCGCG others(261): Show |
1 | a0002c0003t0003g0135 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.928-714_928-713ins others(268): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587957 | |||||
chr16:89587958
|
ACCCACAG others(8): Show |
A | 11 | a0001c0001t0001g0026a0001c0001t0001g0097a0001c0001t0001g0221others(8): Show | 11 | HG00597.hp2 HG01071.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.928-713_928-699del others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587958 | |||||
chr16:89587958
|
ACCCACAG others(35): Show |
A | 15 | a0001c0001t0001g0035a0001c0001t0001g0083a0001c0001t0001g0085others(12): Show | 15 | HG00733.hp2 HG01081.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.928-713_928-672del others(42): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587958 | |||||
chr16:89587958
|
ACCCACAG others(126): Show |
A | 8 | a0001c0001t0001g0051a0001c0001t0001g0094a0001c0001t0001g0220others(5): Show | 8 | HG01175.hp2 HG01192.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-713_928-581del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587958 | |||||
chr16:89587959
|
C | G | 9 | a0001c0001t0001g0068a0001c0001t0001g0269a0001c0001t0001g0281others(6): Show | 9 | HG00621.hp2 HG00673.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.928-716C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587959 | ||||||
chr16:89587963
|
C | T | 1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-712C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587963 | ||||||
chr16:89587967
|
T | A | 10 | a0001c0001t0001g0040a0001c0001t0001g0277a0001c0001t0012g0142others(7): Show | 10 | HG00423.hp2 HG00544.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.928-708T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587967 | ||||||
chr16:89587970
|
A | G | 1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-705A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587970 | ||||||
chr16:89587971
|
C | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0109a0001c0008t0001g0005others(1): Show | 4 | HG02896.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-704C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587971 | ||||||
chr16:89587972
|
G | A | 1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-703G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587972 | ||||||
chr16:89587973
|
G | C | 1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-702G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587973 | ||||||
chr16:89587973
|
G | GC | 25 | a0001c0001t0001g0045a0001c0001t0001g0103a0001c0001t0001g0185others(22): Show | 25 | HG00558.hp2 HG01074.hp1 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.928-697dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587973 | |||||
chr16:89587973
|
G | GCCCCCCG others(5): Show |
2 | a0001c0008t0002g0012a0002c0004t0002g0279 | 2 | HG02109.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.928-697_928-696ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587973 | |||||
chr16:89587973
|
G | GCCCCCCG others(74): Show |
1 | a0002c0004t0002g0016 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(81): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587973 | |||||
chr16:89587973
|
G | GCCCCCCG others(26): Show |
1 | a0001c0001t0001g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(33): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587973 | |||||
chr16:89587973
|
G | GCCCCCGT others(4): Show |
3 | a0001c0001t0001g0062a0001c0001t0001g0099a0001c0001t0001g0333 | 3 | HG01257.hp1 HG01952.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.928-698_928-688dup others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587973 | |||||
chr16:89587973
|
GCCCCCGT others(47): Show |
G | 3 | a0001c0001t0001g0141a0001c0001t0001g0318a0001c0007t0006g0293 | 3 | NA18906.hp1 NA19054.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.928-687_928-634del others(54): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587973 | |||||
chr16:89587974
|
C | A | 1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-701C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587974 | ||||||
chr16:89587974
|
CCCCCGTG others(210): Show |
C | 1 | a0001c0002t0004g0228 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.928-696_928-480del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587974 | |||||
chr16:89587975
|
C | A | 1 | a0002c0003t0003g0125 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.928-700C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587975 | ||||||
chr16:89587977
|
C | CCATGTCA others(41): Show |
1 | a0001c0001t0001g0030 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.928-697_928-696ins others(48): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCCGTGTC others(5): Show |
17 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0068others(14): Show | 17 | HG00323.hp1 HG00597.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.928-697_928-696ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCCGTGTC others(371): Show |
1 | a0001c0001t0001g0176 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.928-697_928-696ins others(378): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCCGTGTC others(256): Show |
1 | a0001c0001t0001g0215 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(263): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCCGTGTC others(433): Show |
1 | a0002c0004t0014g0305 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.928-697_928-696ins others(440): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCCGTGTC others(198): Show |
1 | a0002c0004t0002g0311 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(205): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCCGTGTC others(386): Show |
1 | a0002c0003t0003g0137 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(393): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCCGTGTC others(207): Show |
1 | a0001c0002t0003g0143 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(214): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCCGTGTT others(5): Show |
6 | a0001c0001t0001g0213a0001c0002t0003g0177a0002c0003t0003g0122others(3): Show | 6 | HG00609.hp2 HG02083.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-697_928-696ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCCGTGTT others(208): Show |
1 | a0003c0006t0003g0268 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(215): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCCGTGTT others(42): Show |
1 | a0002c0003t0003g0128 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.928-697_928-696ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCCGTGTT others(145): Show |
1 | a0002c0003t0003g0114 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(152): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCGTGTCA others(4): Show |
1 | a0001c0008t0002g0015 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.928-696_928-686dup others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCGTGTCA others(881): Show |
1 | a0001c0001t0001g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.928-671_928-670ins others(888): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCGTGTCA others(31): Show |
1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.928-679_928-678ins others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCGTGTCA others(4): Show |
20 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0269others(17): Show | 20 | HG00438.hp2 HG00741.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.928-688_928-687ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCGTGTCA others(105): Show |
1 | a0001c0001t0001g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.928-688_928-687ins others(112): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCGTGTCA others(681): Show |
1 | a0003c0006t0003g0168 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.928-688_928-687ins others(688): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCGTGTCA others(80): Show |
1 | a0001c0002t0003g0180 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.928-688_928-687ins others(87): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCGTGTCA others(1153): Show |
1 | a0002c0003t0003g0124 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.928-688_928-687ins others(1160): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCGTGTCA others(79): Show |
1 | a0001c0002t0001g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.928-688_928-687ins others(86): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | CCTGTGTC others(5): Show |
1 | a0001c0002t0001g0322 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.928-697_928-696ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587977
|
C | G | 12 | a0001c0001t0001g0026a0001c0001t0001g0097a0001c0001t0001g0221others(9): Show | 12 | HG00597.hp2 HG01071.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.928-698C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587977 | ||||||
chr16:89587977
|
CCGTGTCA others(185): Show |
C | 1 | a0001c0002t0002g0024 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.928-670_928-479del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587977 | |||||
chr16:89587979
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.928-696G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587979 | ||||||
chr16:89587979
|
G | T | 1 | a0001c0002t0001g0322 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.928-696G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587979 | ||||||
chr16:89587983
|
C | CACCCGCG others(191): Show |
1 | a0001c0001t0001g0249 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.928-688_928-687ins others(198): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587983 | |||||
chr16:89587983
|
C | T | 3 | a0001c0001t0001g0277a0001c0002t0002g0023a0001c0007t0006g0165 | 3 | HG02145.hp1 HG03098.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.928-692C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587983 | ||||||
chr16:89587983
|
CACCCACA others(20): Show |
C | 2 | a0001c0002t0007g0235a0002c0003t0007g0298 | 2 | HG02155.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.928-665_928-639del others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587983 | |||||
chr16:89587983
|
CACCCACA others(85): Show |
C | 1 | a0001c0001t0001g0280 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.928-670_928-579del others(92): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587983 | |||||
chr16:89587984
|
ACCCACAG others(9): Show |
A | 11 | a0001c0001t0001g0098a0001c0001t0001g0115a0001c0001t0001g0178others(8): Show | 11 | HG00639.hp1 HG01123.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.928-687_928-672del others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587984 | |||||
chr16:89587984
|
ACCCACAG others(100): Show |
A | 2 | a0001c0001t0001g0087a0001c0001t0001g0096 | 2 | HG00741.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.928-687_928-581del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587984 | |||||
chr16:89587985
|
C | CCCACAGA others(19): Show |
1 | a0001c0005t0002g0002 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.928-671_928-670ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587985 | |||||
chr16:89587985
|
C | G | 11 | a0001c0001t0001g0054a0001c0001t0001g0069a0001c0001t0001g0198others(8): Show | 11 | HG00140.hp2 HG00438.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.928-690C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587985 | ||||||
chr16:89587988
|
A | C | 1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-687A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587988 | ||||||
chr16:89587991
|
G | T | 1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-684G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587991 | ||||||
chr16:89587993
|
T | A | 11 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0099others(8): Show | 11 | HG01123.hp1 HG01257.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-682T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587993 | ||||||
chr16:89587997
|
C | T | 9 | a0001c0001t0001g0068a0001c0001t0001g0182a0001c0001t0001g0214others(6): Show | 9 | HG01928.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-678C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587997 | ||||||
chr16:89587999
|
G | C | 2 | a0001c0002t0002g0022a0001c0002t0004g0151 | 2 | HG00609.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.928-676G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89587999 | ||||||
chr16:89587999
|
GC | G | 62 | a0001c0001t0001g0026a0001c0001t0001g0062a0001c0001t0001g0065others(59): Show | 66 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.928-670delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587999 | |||||
chr16:89587999
|
GCCCCCCG others(21): Show |
G | 1 | a0001c0002t0003g0192 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.928-670_928-643del others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89587999 | |||||
chr16:89588000
|
C | A | 1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-675C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588000 | ||||||
chr16:89588000
|
C | CCCCCCGT others(4): Show |
1 | a0001c0001t0001g0334 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.928-666_928-665ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588000 | |||||
chr16:89588000
|
C | CCCCCCGT others(206): Show |
1 | a0001c0001t0001g0238 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.928-666_928-665ins others(213): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588000 | |||||
chr16:89588000
|
C | CCCCCCGT others(832): Show |
1 | a0003c0006t0003g0274 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.928-666_928-665ins others(839): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588000 | |||||
chr16:89588000
|
C | CCCCCCGT others(30): Show |
2 | a0001c0002t0003g0076a0001c0002t0003g0181 | 2 | NA18944.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.928-666_928-665ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588000 | |||||
chr16:89588000
|
C | CCCCCGTG others(3): Show |
4 | a0001c0001t0001g0030a0001c0001t0001g0099a0001c0001t0001g0241others(1): Show | 4 | HG01257.hp1 HG01952.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-671_928-670ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588000 | |||||
chr16:89588000
|
C | CCCCCGTG others(507): Show |
1 | a0001c0001t0001g0109 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.928-671_928-670ins others(514): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588000 | |||||
chr16:89588000
|
C | CCCCCGTG others(67): Show |
1 | a0001c0001t0001g0054 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.928-671_928-670ins others(74): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588000 | |||||
chr16:89588000
|
C | CCCCCGTG others(18): Show |
1 | a0002c0003t0004g0306 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.928-671_928-670ins others(25): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588000 | |||||
chr16:89588003
|
CCCGTGTT others(32): Show |
C | 1 | a0001c0001t0001g0174 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.928-670_928-632del others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588003 | |||||
chr16:89588004
|
C | CCCGTGTC others(107): Show |
1 | a0003c0006t0003g0144 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.928-670_928-669ins others(114): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588004 | |||||
chr16:89588004
|
C | CCGTGTCA others(4): Show |
23 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0057others(20): Show | 23 | HG00741.hp2 HG01071.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.928-666_928-665ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588004 | |||||
chr16:89588004
|
C | CCGTGTCA others(171): Show |
1 | a0002c0004t0002g0324 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.928-666_928-665ins others(178): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588004 | |||||
chr16:89588004
|
C | CCGTGTCA others(79): Show |
1 | a0001c0001t0001g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.928-666_928-665ins others(86): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588004 | |||||
chr16:89588004
|
C | CCGTGTCA others(190): Show |
1 | a0003c0006t0003g0149 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.928-666_928-665ins others(197): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588004 | |||||
chr16:89588004
|
C | CGTGTCAC others(14): Show |
1 | a0001c0002t0002g0196 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.928-671_928-670ins others(21): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | ||||||
chr16:89588004
|
C | CGTGTCAC others(3): Show |
23 | a0001c0001t0001g0027a0001c0001t0001g0059a0001c0001t0001g0067others(20): Show | 23 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.928-671_928-670ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | ||||||
chr16:89588004
|
C | CGTGTCAC others(230): Show |
1 | a0001c0001t0001g0294 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.928-671_928-670ins others(237): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | ||||||
chr16:89588004
|
C | CGTGTCAC others(167): Show |
1 | a0001c0001t0001g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.928-671_928-670ins others(174): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | ||||||
chr16:89588004
|
C | CGTGTCAC others(214): Show |
1 | a0001c0001t0001g0028 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.928-671_928-670ins others(221): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | ||||||
chr16:89588004
|
C | CGTGTCAC others(79): Show |
1 | a0001c0002t0004g0151 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.928-671_928-670ins others(86): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | ||||||
chr16:89588004
|
C | CGTGTCAC others(131): Show |
1 | a0001c0024t0001g0218 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.928-671_928-670ins others(138): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | ||||||
chr16:89588004
|
C | CGTGTCAC others(67): Show |
1 | a0001c0002t0001g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.928-671_928-670ins others(74): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | ||||||
chr16:89588004
|
C | G | 24 | a0001c0001t0001g0035a0001c0001t0001g0085a0001c0001t0001g0086others(21): Show | 24 | HG00639.hp1 HG00733.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.928-671C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588004 | ||||||
chr16:89588005
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.928-670C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588005 | ||||||
chr16:89588006
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.928-669G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588006 | ||||||
chr16:89588010
|
T | C | 189 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0027others(186): Show | 194 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.928-665T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588010 | ||||||
chr16:89588010
|
T | TACCCGCG others(4): Show |
4 | a0001c0001t0001g0045a0001c0002t0004g0223a0002c0003t0003g0139others(1): Show | 4 | HG02080.hp1 NA19009.hp2 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-661_928-660ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588010 | |||||
chr16:89588011
|
ACCCACAG others(9): Show |
A | 1 | a0001c0002t0002g0254 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.928-660_928-645del others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588011 | |||||
chr16:89588012
|
C | CCCGCGTG others(30): Show |
1 | a0001c0001t0001g0339 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.928-661_928-660ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588012 | |||||
chr16:89588012
|
C | G | 18 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0103others(15): Show | 19 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.928-663C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588012 | ||||||
chr16:89588020
|
T | A | 10 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0095others(7): Show | 10 | HG00558.hp1 HG00733.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.928-655T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588020 | ||||||
chr16:89588024
|
C | T | 7 | a0001c0001t0001g0069a0001c0002t0001g0029a0001c0002t0002g0329others(4): Show | 7 | HG00673.hp2 HG01884.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-651C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588024 | ||||||
chr16:89588025
|
G | A | 1 | a0009c0019t0002g0253 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.928-650G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588025 | ||||||
chr16:89588026
|
GC | G | 89 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0059others(86): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.928-643delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588026 | |||||
chr16:89588026
|
GCCCCCCG others(5): Show |
G | 2 | a0002c0003t0003g0125a0002c0003t0003g0170 | 2 | NA19004.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.928-645_928-634del others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588026 | |||||
chr16:89588027
|
C | CCCCCGTG others(109): Show |
2 | a0001c0005t0002g0043a0001c0005t0002g0056 | 2 | NA18947.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.928-644_928-643ins others(116): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588027 | |||||
chr16:89588030
|
CCCGTGTC others(5): Show |
C | 5 | a0001c0001t0001g0184a0001c0002t0001g0322a0001c0005t0002g0107others(2): Show | 5 | HG02027.hp1 HG02055.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-643_928-632del others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588030 | |||||
chr16:89588031
|
C | T | 6 | a0001c0001t0001g0269a0001c0002t0003g0031a0001c0002t0003g0033others(3): Show | 6 | HG03669.hp1 NA18941.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-644C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588031 | ||||||
chr16:89588031
|
CCGTGTCA others(4): Show |
C | 3 | a0001c0005t0002g0310a0001c0005t0002g0317a0001c0005t0002g0323 | 3 | HG02132.hp1 HG02155.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.928-633_928-623del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588031 | |||||
chr16:89588033
|
G | A | 2 | a0001c0002t0002g0254a0001c0002t0004g0227 | 2 | HG02083.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.928-642G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588033 | ||||||
chr16:89588037
|
C | CACCCGCG others(68): Show |
1 | a0002c0003t0003g0122 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.928-606_928-605ins others(75): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588037 | |||||
chr16:89588037
|
C | T | 12 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0154others(9): Show | 12 | HG01361.hp1 HG01517.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.928-638C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588037 | ||||||
chr16:89588038
|
A | ACCCACAG others(8): Show |
2 | a0001c0001t0001g0248a0002c0003t0003g0208 | 2 | HG01975.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.928-634_928-633ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588038 | |||||
chr16:89588038
|
A | ACCCACAG others(9): Show |
3 | a0001c0001t0001g0068a0001c0005t0002g0302a0002c0004t0002g0016 | 3 | HG00438.hp1 HG02145.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.928-634_928-633ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588038 | |||||
chr16:89588038
|
A | ACCCACAG others(352): Show |
1 | a0001c0001t0001g0190 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.928-634_928-633ins others(359): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588038 | |||||
chr16:89588038
|
A | ACCCACAG others(34): Show |
8 | a0001c0005t0002g0003a0001c0005t0002g0072a0001c0005t0002g0193others(5): Show | 9 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.928-634_928-633ins others(41): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588038 | |||||
chr16:89588038
|
A | ACCCACAG others(34): Show |
1 | a0001c0008t0002g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.928-634_928-633ins others(41): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588038 | |||||
chr16:89588038
|
A | AGCCACAG others(34): Show |
2 | a0002c0004t0002g0001a0002c0004t0002g0314 | 5 | HG01168.hp2 HG01169.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-637_928-636ins others(41): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588038 | ||||||
chr16:89588038
|
ACCCGCGT others(46): Show |
A | 1 | a0001c0001t0001g0026 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.928-633_928-581del others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588038 | |||||
chr16:89588042
|
G | A | 1 | a0011c0016t0003g0112 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.928-633G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588042 | ||||||
chr16:89588042
|
G | C | 20 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0098others(17): Show | 24 | HG00438.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.928-633G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588042 | ||||||
chr16:89588042
|
G | GCGTGTCA others(19): Show |
1 | a0001c0002t0004g0155 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.928-631_928-606dup others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588042 | |||||
chr16:89588042
|
GCGTGTCA others(46): Show |
G | 1 | a0001c0001t0001g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.928-605_928-553del others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588042 | |||||
chr16:89588043
|
C | T | 1 | a0001c0002t0002g0084 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.928-632C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588043 | ||||||
chr16:89588048
|
CACCCACA others(20): Show |
C | 6 | a0001c0001t0001g0244a0001c0002t0002g0299a0001c0002t0003g0272others(3): Show | 6 | HG00323.hp1 HG00597.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-605_928-579del others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588048 | |||||
chr16:89588050
|
C | G | 9 | a0001c0005t0002g0003a0001c0005t0002g0072a0001c0005t0002g0107others(6): Show | 10 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.928-625C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588050 | ||||||
chr16:89588058
|
T | A | 22 | a0001c0001t0001g0027a0001c0001t0001g0083a0001c0001t0001g0095others(19): Show | 23 | HG00733.hp2 HG01106.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.928-617T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588058 | ||||||
chr16:89588058
|
T | TACACGGC others(82): Show |
1 | a0001c0001t0012g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(89): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588058 | |||||
chr16:89588062
|
C | T | 8 | a0001c0001t0001g0103a0001c0001t0001g0243a0001c0001t0001g0300others(5): Show | 8 | HG00741.hp2 HG01123.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-613C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588062 | ||||||
chr16:89588064
|
GC | G | 79 | a0001c0001t0001g0050a0001c0001t0001g0062a0001c0001t0001g0098others(76): Show | 82 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.928-605delC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588064 | |||||
chr16:89588065
|
C | CCCCCCAT others(30): Show |
2 | a0001c0001t0001g0191a0008c0021t0001g0224 | 2 | NA18970.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.928-605_928-604ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | |||||
chr16:89588065
|
C | CCCCCCGT others(4): Show |
2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.928-601_928-600ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | |||||
chr16:89588065
|
C | CCCCCCGT others(131): Show |
1 | a0001c0002t0011g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.928-601_928-600ins others(138): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | |||||
chr16:89588065
|
C | CCCCCCGT others(30): Show |
1 | a0002c0003t0003g0126 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.928-601_928-600ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | |||||
chr16:89588065
|
C | CCCCCCGT others(82): Show |
1 | a0001c0001t0001g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-601_928-600ins others(89): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | |||||
chr16:89588065
|
C | CCCCCGTG others(3): Show |
1 | a0001c0008t0002g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.928-606_928-605ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | |||||
chr16:89588065
|
C | CCCCCGTG others(83): Show |
1 | a0001c0002t0004g0225 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(90): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | |||||
chr16:89588065
|
C | CCCCCGTG others(120): Show |
1 | a0001c0002t0004g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(127): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | |||||
chr16:89588065
|
CCCCCCGT others(19): Show |
C | 1 | a0001c0002t0001g0331 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.928-600_928-575del others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | |||||
chr16:89588065
|
CCCCCCGT others(45): Show |
C | 6 | a0001c0001t0001g0140a0001c0002t0004g0132a0001c0007t0006g0071others(3): Show | 6 | HG02071.hp1 HG02273.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-600_928-549del others(52): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588065 | |||||
chr16:89588068
|
CCCGTGTT others(57): Show |
C | 6 | a0001c0001t0001g0252a0001c0001t0001g0261a0001c0002t0001g0287others(3): Show | 6 | HG00639.hp1 HG01081.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-605_928-542del others(64): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588068 | |||||
chr16:89588068
|
CCCGTGTT others(131): Show |
C | 2 | a0001c0002t0002g0022a0001c0002t0003g0018 | 2 | HG03579.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.928-605_928-468del | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588068 | |||||
chr16:89588069
|
C | CCCGTGTC others(5): Show |
1 | a0001c0001t0001g0238 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.928-605_928-604ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | |||||
chr16:89588069
|
C | CCGTGTCA others(229): Show |
1 | a0001c0002t0003g0177 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.928-601_928-600ins others(236): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | |||||
chr16:89588069
|
C | CCGTGTCA others(130): Show |
1 | a0001c0001t0001g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.928-601_928-600ins others(137): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | |||||
chr16:89588069
|
C | CCGTGTCA others(4): Show |
14 | a0001c0001t0001g0040a0001c0001t0001g0059a0001c0001t0001g0097others(11): Show | 14 | HG00099.hp1 HG00438.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.928-601_928-600ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | |||||
chr16:89588069
|
C | CCGTGTCA others(91): Show |
1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.928-601_928-600ins others(98): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | |||||
chr16:89588069
|
C | CCGTGTCA others(196): Show |
1 | a0001c0001t0001g0103 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.928-601_928-600ins others(203): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | |||||
chr16:89588069
|
C | CCGTGTCA others(197): Show |
1 | a0011c0016t0003g0112 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.928-601_928-600ins others(204): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | |||||
chr16:89588069
|
C | CCGTGTCA others(263): Show |
1 | a0002c0003t0003g0135 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.928-601_928-600ins others(270): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | |||||
chr16:89588069
|
C | CCGTGTCA others(155): Show |
1 | a0001c0001t0001g0045 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.928-601_928-600ins others(162): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | |||||
chr16:89588069
|
C | CCGTGTTA others(4): Show |
1 | a0001c0001t0001g0249 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.928-596_928-595ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588069 | |||||
chr16:89588069
|
C | CGTGTCAC others(3): Show |
1 | a0001c0008t0002g0015 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | ||||||
chr16:89588069
|
C | CGTGTCAC others(67): Show |
1 | a0002c0004t0002g0332 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(74): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | ||||||
chr16:89588069
|
C | CGTGTCAC others(30): Show |
1 | a0002c0003t0003g0073 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.928-606_928-605ins others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | ||||||
chr16:89588069
|
C | CGTGTCAC others(158): Show |
1 | a0002c0003t0002g0119 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(165): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | ||||||
chr16:89588069
|
C | CGTGTCAC others(29): Show |
2 | a0001c0001t0001g0054a0001c0002t0004g0134 | 2 | HG02735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.928-606_928-605ins others(36): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | ||||||
chr16:89588069
|
C | CGTGTCAC others(232): Show |
1 | a0001c0001t0001g0334 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.928-606_928-605ins others(239): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | ||||||
chr16:89588069
|
C | CGTGTCAC others(697): Show |
1 | a0001c0005t0002g0303 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(704): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | ||||||
chr16:89588069
|
C | CGTGTCAC others(41): Show |
1 | a0001c0001t0001g0099 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.928-606_928-605ins others(48): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | ||||||
chr16:89588069
|
C | CGTGTCAC others(4): Show |
1 | a0001c0001t0001g0030 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.928-606_928-605ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | ||||||
chr16:89588069
|
C | CGTGTCAC others(3): Show |
26 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0057others(23): Show | 26 | HG00140.hp2 HG01167.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.928-606_928-605ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | ||||||
chr16:89588069
|
C | CGTGTCAC others(41): Show |
1 | a0001c0001t0001g0088 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.928-606_928-605ins others(48): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | ||||||
chr16:89588069
|
C | CGTGTCAC others(192): Show |
1 | a0001c0001t0001g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(199): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | ||||||
chr16:89588069
|
C | CGTGTTAC others(92): Show |
1 | a0001c0001t0001g0028 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(99): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | ||||||
chr16:89588069
|
C | CGTGTTAC others(3): Show |
1 | a0001c0001t0001g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.928-606_928-605ins others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | ||||||
chr16:89588069
|
C | T | 1 | a0001c0002t0003g0044 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.928-606C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588069 | ||||||
chr16:89588075
|
T | C | 208 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0030others(205): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.928-600T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588075 | ||||||
chr16:89588075
|
T | TACCCGCG others(4): Show |
4 | a0001c0001t0001g0120a0001c0001t0001g0154a0001c0002t0002g0278others(1): Show | 4 | HG01261.hp2 HG01346.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-596_928-595ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588075 | |||||
chr16:89588075
|
T | TACCCGCG others(79): Show |
1 | a0001c0001t0001g0243 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.928-596_928-595ins others(86): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588075 | |||||
chr16:89588075
|
T | TACCCGCG others(2867): Show |
1 | a0001c0002t0003g0143 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.928-596_928-595ins others(2874): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588075 | |||||
chr16:89588075
|
T | TACCCGCG others(42): Show |
1 | a0001c0002t0003g0181 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.928-596_928-595ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588075 | |||||
chr16:89588075
|
T | TACCCGCG others(1087): Show |
1 | a0001c0001t0001g0300 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.928-596_928-595ins others(1094): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588075 | |||||
chr16:89588075
|
TACCCACA others(45): Show |
T | 2 | a0001c0002t0004g0038a0002c0010t0001g0245 | 2 | HG01928.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.928-595_928-544del others(52): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588075 | |||||
chr16:89588076
|
ACCCACAG others(8): Show |
A | 38 | a0001c0001t0001g0035a0001c0001t0001g0050a0001c0001t0001g0083others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.928-595_928-581del others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588076 | |||||
chr16:89588077
|
C | G | 7 | a0001c0001t0001g0248a0001c0001t0001g0258a0001c0001t0001g0269others(4): Show | 10 | HG01168.hp2 HG01169.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.928-598C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588077 | ||||||
chr16:89588085
|
T | A | 8 | a0001c0001t0001g0062a0001c0001t0001g0103a0001c0001t0001g0182others(5): Show | 8 | HG00423.hp2 HG02257.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-590T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588085 | ||||||
chr16:89588089
|
C | T | 5 | a0001c0001t0001g0173a0001c0002t0004g0326a0001c0008t0002g0010others(2): Show | 5 | HG00673.hp2 HG02896.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.928-586C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588089 | ||||||
chr16:89588091
|
G | GC | 38 | a0001c0001t0001g0040a0001c0001t0001g0069a0001c0001t0001g0099others(35): Show | 41 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.928-579dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588091 | |||||
chr16:89588091
|
G | GCCCCCCG others(5): Show |
2 | a0001c0002t0003g0180a0001c0008t0002g0012 | 2 | HG02109.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.928-579_928-578ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588091 | |||||
chr16:89588091
|
G | GCCCCCCG others(84): Show |
1 | a0002c0003t0003g0138 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.928-579_928-578ins others(91): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588091 | |||||
chr16:89588091
|
G | GCCCCCCG others(682): Show |
1 | a0002c0003t0003g0124 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.928-579_928-578ins others(689): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588091 | |||||
chr16:89588091
|
G | GCCCCCGT others(4): Show |
2 | a0001c0001t0001g0333a0006c0014t0001g0008 | 2 | HG01891.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.928-580_928-570dup others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588091 | |||||
chr16:89588091
|
G | GCCCCCGT others(461): Show |
1 | a0001c0002t0003g0206 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.928-570_928-569ins others(468): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588091 | |||||
chr16:89588091
|
G | GCCCCCGT others(625): Show |
1 | a0001c0013t0002g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.928-570_928-569ins others(632): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588091 | |||||
chr16:89588092
|
CCCCCGTG others(18): Show |
C | 4 | a0001c0002t0004g0110a0001c0002t0004g0131a0001c0002t0004g0266others(1): Show | 4 | HG01952.hp1 HG03942.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-578_928-554del others(25): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588092 | |||||
chr16:89588092
|
CCCCCGTG others(55): Show |
C | 5 | a0001c0002t0003g0031a0001c0002t0003g0034a0001c0007t0006g0166others(2): Show | 5 | HG03195.hp1 HG03209.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-578_928-517del others(62): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588092 | |||||
chr16:89588095
|
C | CCCGTGTC others(5): Show |
10 | a0001c0001t0001g0088a0001c0001t0001g0173a0001c0002t0002g0278others(7): Show | 10 | HG00642.hp1 HG00673.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.928-579_928-578ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | |||||
chr16:89588095
|
C | CCCGTGTC others(70): Show |
1 | a0002c0003t0003g0113 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.928-579_928-578ins others(77): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | |||||
chr16:89588095
|
C | CCCGTGTC others(42): Show |
1 | a0001c0001t0001g0045 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.928-579_928-578ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | |||||
chr16:89588095
|
C | CCCGTGTT others(32): Show |
1 | a0002c0003t0003g0137 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.928-579_928-578ins others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | |||||
chr16:89588095
|
C | CCCGTGTT others(571): Show |
1 | a0001c0002t0003g0233 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.928-579_928-578ins others(578): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | |||||
chr16:89588095
|
C | CCCGTGTT others(5): Show |
5 | a0001c0002t0004g0151a0002c0003t0003g0125a0002c0003t0003g0128others(2): Show | 5 | HG00609.hp1 HG03927.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-579_928-578ins others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | |||||
chr16:89588095
|
C | CCGTGTCA others(30): Show |
1 | a0001c0001t0001g0062 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.928-463_928-427dup others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | |||||
chr16:89588095
|
C | CCGTGTCA others(15): Show |
1 | a0001c0002t0002g0196 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.928-570_928-569ins others(22): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | |||||
chr16:89588095
|
C | CCGTGTCA others(189): Show |
1 | a0001c0001t0001g0030 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.928-570_928-569ins others(196): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | |||||
chr16:89588095
|
C | CCGTGTCA others(4): Show |
30 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0057others(27): Show | 30 | HG00140.hp2 HG01346.hp2 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.928-570_928-569ins others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | |||||
chr16:89588095
|
C | CCGTGTCA others(42): Show |
1 | a0001c0001t0001g0109 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.928-570_928-569ins others(49): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | |||||
chr16:89588095
|
C | CCGTGTCA others(118): Show |
1 | a0003c0006t0003g0149 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.928-570_928-569ins others(125): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | |||||
chr16:89588095
|
C | CCGTGTCA others(107): Show |
1 | a0003c0006t0003g0268 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.928-570_928-569ins others(114): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | |||||
chr16:89588095
|
C | CCGTGTCA others(41): Show |
2 | a0001c0002t0002g0316a0001c0002t0005g0291 | 2 | HG00558.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.928-570_928-569ins others(48): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | |||||
chr16:89588095
|
C | G | 58 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0050others(55): Show | 58 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.928-580C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588095 | ||||||
chr16:89588095
|
CCGTGTCA others(67): Show |
C | 1 | a0001c0002t0002g0329 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.928-500_928-427del others(74): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588095 | |||||
chr16:89588096
|
CGTGTCAC others(66): Show |
C | 3 | a0001c0002t0004g0117a0001c0002t0004g0133a0001c0002t0007g0235 | 3 | HG01943.hp1 NA18952.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.928-578_928-506del others(73): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588096 | ||||||
chr16:89588097
|
G | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0221 | 2 | HG02109.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.928-578G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588097 | ||||||
chr16:89588101
|
C | CACCCGCG others(442): Show |
1 | a0001c0001t0001g0249 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.928-570_928-569ins others(449): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588101 | |||||
chr16:89588101
|
C | T | 13 | a0001c0001t0001g0099a0001c0001t0001g0213a0001c0002t0003g0076others(10): Show | 13 | HG00609.hp2 HG01257.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.928-574C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588101 | ||||||
chr16:89588103
|
C | G | 6 | a0001c0001t0001g0203a0001c0001t0001g0214a0001c0001t0001g0280others(3): Show | 6 | HG01168.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-572C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588103 | ||||||
chr16:89588111
|
T | A | 6 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0001g0109others(3): Show | 6 | HG00741.hp1 HG01106.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-564T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588111 | ||||||
chr16:89588115
|
C | T | 4 | a0001c0002t0003g0272a0001c0002t0004g0327a0001c0005t0002g0303others(1): Show | 4 | HG02258.hp1 HG03927.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-560C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588115 | ||||||
chr16:89588117
|
G | C | 1 | a0001c0002t0002g0255 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.928-558G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588117 | ||||||
chr16:89588117
|
G | GC | 81 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0045others(78): Show | 81 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.928-553dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | |||||
chr16:89588117
|
G | GCCCCCCG others(21): Show |
1 | a0002c0004t0002g0279 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.928-553_928-552ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | |||||
chr16:89588117
|
G | GCCCCCCG others(58): Show |
1 | a0001c0001t0001g0336 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.928-553_928-552ins others(65): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | |||||
chr16:89588117
|
G | GCCCCCCG others(32): Show |
1 | a0001c0012t0002g0296 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.928-553_928-552ins others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | |||||
chr16:89588117
|
G | GCCCCCCG others(21): Show |
2 | a0001c0007t0006g0064a0002c0003t0003g0135 | 2 | HG02723.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.928-553_928-552ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | |||||
chr16:89588117
|
G | GCCCCCGT others(174): Show |
1 | a0001c0001t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.928-544_928-543ins others(181): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | |||||
chr16:89588117
|
G | GCCCCCGT others(57): Show |
2 | a0001c0005t0002g0043a0001c0005t0002g0056 | 2 | NA18947.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.928-528_928-527ins others(64): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | |||||
chr16:89588117
|
G | GCCCCCGT others(31): Show |
3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0335 | 3 | HG02258.hp2 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.928-553_928-516dup others(38): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | |||||
chr16:89588117
|
G | GCCCCCGT others(68): Show |
1 | a0001c0001t0001g0284 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.928-553_928-479dup others(75): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | |||||
chr16:89588117
|
G | GCCCCCGT others(20): Show |
1 | a0002c0004t0002g0311 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.928-547_928-546ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | |||||
chr16:89588117
|
G | GCCCCCGT others(403): Show |
1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.928-547_928-546ins others(410): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588117 | |||||
chr16:89588121
|
C | CT | 5 | a0001c0001t0001g0179a0001c0002t0003g0049a0001c0002t0003g0053others(2): Show | 5 | HG01346.hp2 HG02027.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.928-554_928-553ins others(1): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588121 | ||||||
chr16:89588121
|
CCGTGTCA others(4): Show |
C | 10 | a0001c0001t0001g0098a0001c0001t0001g0239a0001c0001t0001g0242others(7): Show | 10 | HG00544.hp1 HG01123.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.928-543_928-533del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588121 | |||||
chr16:89588122
|
CGTGTCAC others(3): Show |
C | 12 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0174others(9): Show | 12 | HG00438.hp2 HG00597.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.928-552_928-543del others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588122 | ||||||
chr16:89588123
|
G | GTGTCACC others(130): Show |
1 | a0001c0002t0002g0196 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.928-523_928-522ins others(137): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588123 | |||||
chr16:89588127
|
C | CACCCGCG others(57): Show |
1 | a0001c0001t0001g0277 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.928-528_928-527ins others(64): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588127 | |||||
chr16:89588127
|
C | T | 5 | a0001c0001t0001g0205a0001c0002t0005g0186a0002c0003t0003g0128others(2): Show | 5 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-548C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588127 | ||||||
chr16:89588128
|
A | ACCCACAG others(8): Show |
7 | a0001c0001t0001g0068a0001c0001t0001g0248a0001c0002t0005g0019others(4): Show | 7 | HG00438.hp1 HG01975.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-544_928-543ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588128 | |||||
chr16:89588128
|
A | ACCCACAG others(9): Show |
7 | a0001c0001t0001g0185a0001c0001t0001g0213a0001c0002t0003g0076others(4): Show | 7 | HG02129.hp2 HG02132.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-544_928-543ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588128 | |||||
chr16:89588128
|
A | ACCCACAG others(35): Show |
1 | a0001c0001t0001g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.928-544_928-543ins others(42): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588128 | |||||
chr16:89588128
|
A | ACCCACAG others(36): Show |
1 | a0001c0001t0001g0154 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.928-544_928-543ins others(43): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588128 | |||||
chr16:89588128
|
A | ACCCACAG others(88): Show |
1 | a0001c0002t0004g0227 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.928-544_928-543ins others(95): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588128 | |||||
chr16:89588128
|
A | ACCCACAG others(46): Show |
1 | a0001c0001t0001g0217 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.928-544_928-543ins others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588128 | |||||
chr16:89588128
|
A | ACCCACAG others(98): Show |
2 | a0002c0004t0002g0001a0002c0004t0002g0314 | 5 | HG01168.hp2 HG01169.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-544_928-543ins others(105): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588128 | |||||
chr16:89588128
|
A | ACCCACAG others(255): Show |
1 | a0001c0005t0002g0002 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.928-544_928-543ins others(262): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588128 | |||||
chr16:89588128
|
A | AGCCACAG others(9): Show |
2 | a0001c0005t0002g0107a0003c0006t0003g0274 | 2 | HG02273.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.928-547_928-546ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588128 | ||||||
chr16:89588128
|
A | AGCCACAG others(73): Show |
1 | a0001c0005t0002g0247 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.928-547_928-546ins others(80): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588128 | ||||||
chr16:89588128
|
A | AGCCACAG others(72): Show |
7 | a0001c0005t0002g0003a0001c0005t0002g0072a0001c0005t0002g0193others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-547_928-546ins others(79): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588128 | ||||||
chr16:89588132
|
G | A | 1 | a0001c0008t0002g0015 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.928-543G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588132 | ||||||
chr16:89588132
|
G | C | 34 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0154others(31): Show | 39 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.928-543G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588132 | ||||||
chr16:89588132
|
G | GCGTGTCA others(19): Show |
2 | a0001c0002t0001g0029a0001c0015t0001g0330 | 2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.928-532_928-507dup others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588132 | |||||
chr16:89588132
|
G | GCGTGTCA others(20): Show |
3 | a0001c0001t0008g0055a0001c0002t0002g0204a0001c0002t0004g0134 | 3 | HG00673.hp1 HG02735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.928-542_928-516dup others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588132 | |||||
chr16:89588132
|
G | GCGTGTCA others(391): Show |
1 | a0001c0001t0001g0188 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.928-516_928-515ins others(398): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588132 | |||||
chr16:89588132
|
G | GCGTGTCA others(93): Show |
1 | a0001c0001t0001g0028 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.928-532_928-433dup others(100): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588132 | |||||
chr16:89588138
|
C | CACCCACA others(46): Show |
1 | a0002c0003t0003g0126 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.928-528_928-527ins others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588138 | |||||
chr16:89588138
|
C | T | 8 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0154others(5): Show | 8 | HG01928.hp1 HG02165.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-537C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588138 | ||||||
chr16:89588140
|
C | CCCACAGA others(19): Show |
1 | a0001c0002t0004g0325 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.928-524_928-523ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588140 | |||||
chr16:89588140
|
C | G | 4 | a0001c0001t0001g0098a0001c0001t0001g0239a0001c0001t0001g0242others(1): Show | 4 | HG01123.hp2 HG02071.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-535C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588140 | ||||||
chr16:89588148
|
T | A | 25 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0096others(22): Show | 30 | HG00323.hp1 HG00621.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.928-527T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588148 | ||||||
chr16:89588152
|
C | T | 1 | a0001c0025t0001g0276 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.928-523C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588152 | ||||||
chr16:89588153
|
G | A | 9 | a0001c0001t0001g0075a0001c0002t0002g0196a0001c0002t0002g0199others(6): Show | 9 | HG00280.hp1 HG00423.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-522G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588153 | ||||||
chr16:89588154
|
G | GC | 106 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(103): Show | 111 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.928-516dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | |||||
chr16:89588154
|
G | GCCCCCCG others(21): Show |
1 | a0002c0004t0002g0304 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.928-516_928-515ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | |||||
chr16:89588154
|
G | GCCCCCCG others(59): Show |
1 | a0003c0006t0003g0232 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.928-516_928-515ins others(66): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | |||||
chr16:89588154
|
G | GCCCCCCG others(2922): Show |
1 | a0001c0002t0003g0143 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.928-516_928-515ins others(2929): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | |||||
chr16:89588154
|
G | GCCCCCCG others(21): Show |
1 | a0001c0007t0006g0064 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.928-516_928-515ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | |||||
chr16:89588154
|
G | GCCCCCGT others(20): Show |
2 | a0002c0003t0004g0306a0002c0004t0002g0307 | 2 | HG00621.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.928-507_928-506ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | |||||
chr16:89588154
|
G | GCCCCCGT others(20): Show |
3 | a0001c0001t0001g0103a0002c0004t0014g0305a0003c0006t0003g0144 | 3 | HG03831.hp2 NA18980.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.928-507_928-506ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | |||||
chr16:89588154
|
G | GCCCCCGT others(47): Show |
1 | a0001c0002t0004g0123 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.928-507_928-506ins others(54): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | |||||
chr16:89588154
|
G | GCCCCCGT others(20): Show |
1 | a0001c0001t0001g0273 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.928-507_928-506ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | |||||
chr16:89588154
|
G | GCCCGCGT others(84): Show |
1 | a0002c0003t0003g0139 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.928-518_928-517ins others(91): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | |||||
chr16:89588154
|
G | GCCCGCGT others(202): Show |
2 | a0002c0003t0003g0113a0002c0003t0003g0114 | 2 | NA18942.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.928-518_928-517ins others(209): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588154 | |||||
chr16:89588158
|
C | G | 1 | a0002c0003t0003g0129 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.928-517C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588158 | ||||||
chr16:89588158
|
CCGTGTCA others(4): Show |
C | 14 | a0001c0001t0001g0050a0001c0001t0001g0095a0001c0001t0001g0205others(11): Show | 14 | HG00597.hp1 HG00733.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.928-506_928-496del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588158 | |||||
chr16:89588158
|
CCGTGTCA others(41): Show |
C | 2 | a0001c0002t0003g0192a0001c0009t0001g0013 | 2 | HG02280.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.928-506_928-459del others(48): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588158 | |||||
chr16:89588159
|
CGTGTCAC others(3): Show |
C | 2 | a0001c0002t0004g0038a0002c0003t0007g0298 | 2 | HG02155.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.928-515_928-506del others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588159 | ||||||
chr16:89588160
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.928-515G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588160 | ||||||
chr16:89588164
|
C | CACCCACA others(58): Show |
1 | a0001c0001t0001g0243 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.928-507_928-506ins others(65): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588164 | |||||
chr16:89588164
|
C | T | 2 | a0001c0002t0004g0037a0001c0002t0005g0292 | 2 | HG02615.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.928-511C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588164 | ||||||
chr16:89588165
|
A | ACCCACAG others(74): Show |
1 | a0002c0003t0003g0129 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.928-507_928-506ins others(81): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | |||||
chr16:89588165
|
A | ACCCACAG others(8): Show |
6 | a0001c0001t0001g0221a0001c0002t0003g0290a0001c0002t0004g0225others(3): Show | 6 | HG00544.hp2 HG01346.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-507_928-506ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | |||||
chr16:89588165
|
A | ACCCACAG others(9): Show |
4 | a0002c0003t0003g0130a0002c0003t0003g0208a0003c0006t0003g0145others(1): Show | 4 | NA18940.hp1 NA18943.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-507_928-506ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | |||||
chr16:89588165
|
A | ACCCACAG others(748): Show |
1 | a0002c0003t0003g0128 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.928-507_928-506ins others(755): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | |||||
chr16:89588165
|
A | ACCCACAG others(1789): Show |
1 | a0001c0002t0004g0237 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.928-507_928-506ins others(1796): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | |||||
chr16:89588165
|
A | ACCCACAG others(110): Show |
1 | a0001c0002t0011g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.928-507_928-506ins others(117): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | |||||
chr16:89588165
|
A | ACCCACAG others(99): Show |
1 | a0001c0001t0001g0339 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.928-507_928-506ins others(106): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | |||||
chr16:89588165
|
A | ACCCACAG others(61): Show |
1 | a0002c0017t0003g0136 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.928-507_928-506ins others(68): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | |||||
chr16:89588165
|
A | ACCCACAG others(306): Show |
1 | a0003c0006t0003g0275 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.928-507_928-506ins others(313): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | |||||
chr16:89588165
|
A | ACCCACAG others(36): Show |
1 | a0001c0002t0004g0155 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.928-507_928-506ins others(43): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588165 | |||||
chr16:89588165
|
A | AGCCACAG others(9): Show |
1 | a0001c0001t0001g0248 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.928-510_928-509ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588165 | ||||||
chr16:89588165
|
A | AGCCACAG others(138): Show |
1 | a0001c0002t0005g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.928-510_928-509ins others(145): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588165 | ||||||
chr16:89588169
|
G | C | 25 | a0001c0001t0001g0083a0001c0001t0001g0105a0001c0001t0001g0221others(22): Show | 25 | HG00544.hp2 HG00609.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.928-506G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588169 | ||||||
chr16:89588169
|
G | GCGTGTCA others(137): Show |
1 | a0003c0006t0003g0232 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.928-470_928-469ins others(144): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588169 | |||||
chr16:89588170
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.928-505C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588170 | ||||||
chr16:89588171
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0221 | 2 | HG00099.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.928-504G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588171 | ||||||
chr16:89588175
|
C | T | 11 | a0001c0001t0001g0045a0001c0001t0001g0243a0001c0002t0004g0038others(8): Show | 11 | HG00597.hp1 HG01123.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-500C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588175 | ||||||
chr16:89588177
|
C | CCCACAGA others(19): Show |
1 | a0001c0001t0001g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.928-473_928-472ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588177 | |||||
chr16:89588177
|
C | G | 1 | a0001c0002t0004g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.928-498C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588177 | ||||||
chr16:89588185
|
T | A | 11 | a0001c0001t0001g0030a0001c0001t0001g0067a0001c0001t0001g0068others(8): Show | 11 | HG01257.hp1 HG01361.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-490T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588185 | ||||||
chr16:89588189
|
C | T | 4 | a0001c0001t0001g0205a0001c0002t0002g0329a0001c0008t0002g0010others(1): Show | 4 | HG01243.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-486C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588189 | ||||||
chr16:89588190
|
G | A | 1 | a0001c0002t0002g0254 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.928-485G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588190 | ||||||
chr16:89588191
|
G | C | 1 | a0001c0001t0001g0057 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.928-484G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588191 | ||||||
chr16:89588191
|
G | GC | 107 | a0001c0001t0001g0035a0001c0001t0001g0045a0001c0001t0001g0066others(104): Show | 112 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.928-479dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCCG others(85): Show |
1 | a0001c0001t0001g0263 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.928-479_928-478ins others(92): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCCG others(21): Show |
1 | a0001c0002t0004g0123 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.928-479_928-478ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCCG others(70): Show |
2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.928-479_928-478ins others(77): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCCG others(146): Show |
1 | a0001c0001t0001g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.928-479_928-478ins others(153): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCCG others(250): Show |
1 | a0001c0002t0004g0151 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.928-479_928-478ins others(257): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCCG others(58): Show |
1 | a0001c0008t0002g0010 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.928-479_928-478ins others(65): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCCG others(21): Show |
2 | a0001c0002t0004g0037a0002c0003t0003g0111 | 2 | NA19005.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.928-479_928-478ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCCG others(1119): Show |
1 | a0002c0003t0003g0122 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.928-479_928-478ins others(1126): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCCG others(84): Show |
1 | a0001c0002t0003g0177 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.928-479_928-478ins others(91): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCGT others(20): Show |
3 | a0001c0002t0002g0210a0001c0008t0002g0012a0002c0003t0002g0119 | 3 | HG00423.hp2 HG02109.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.928-470_928-469ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCGT others(871): Show |
1 | a0001c0002t0003g0206 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.928-470_928-469ins others(878): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCGT others(201): Show |
1 | a0003c0006t0003g0274 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(208): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCGT others(74): Show |
1 | a0001c0002t0003g0076 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(81): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCGT others(100): Show |
1 | a0001c0001t0001g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.928-470_928-469ins others(107): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCGT others(57): Show |
1 | a0001c0002t0005g0197 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(64): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCGT others(916): Show |
1 | a0001c0001t0001g0269 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(923): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCGT others(95): Show |
1 | a0001c0001t0001g0027 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(102): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588191
|
G | GCCCCCGT others(281): Show |
1 | a0001c0001t0001g0059 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.928-427_928-426ins others(288): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588191 | |||||
chr16:89588195
|
C | CCGTGTCA others(142): Show |
1 | a0001c0001t0008g0055 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.928-427_928-426ins others(149): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588195 | |||||
chr16:89588195
|
CCGTGTCA others(4): Show |
C | 78 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0058others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.928-469_928-459del others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588195 | |||||
chr16:89588196
|
CGTGTCAC others(3): Show |
C | 17 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0093others(14): Show | 17 | HG01106.hp1 HG01243.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.928-478_928-469del others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588196 | ||||||
chr16:89588201
|
C | T | 3 | a0001c0001t0001g0057a0001c0001t0001g0103a0002c0003t0003g0073 | 3 | HG02129.hp1 HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.928-474C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588201 | ||||||
chr16:89588202
|
A | ACCCACAG others(8): Show |
3 | a0001c0001t0001g0277a0001c0002t0001g0029a0002c0004t0002g0332 | 3 | HG02572.hp2 HG03239.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.928-470_928-469ins others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | |||||
chr16:89588202
|
A | ACCCACAG others(137): Show |
1 | a0003c0006t0003g0144 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.928-470_928-469ins others(144): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | |||||
chr16:89588202
|
A | ACCCACAG others(46): Show |
2 | a0001c0001t0001g0103a0001c0002t0004g0227 | 2 | HG02083.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.928-470_928-469ins others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | |||||
chr16:89588202
|
A | ACCCACAG others(47): Show |
1 | a0001c0001t0001g0057 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(54): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | |||||
chr16:89588202
|
A | ACCCACAG others(147): Show |
1 | a0001c0001t0001g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-470_928-469ins others(154): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | |||||
chr16:89588202
|
A | ACCCACAG others(190): Show |
1 | a0011c0016t0003g0112 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(197): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | |||||
chr16:89588202
|
A | ACCCACAG others(136): Show |
1 | a0001c0001t0001g0189 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.928-470_928-469ins others(143): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | |||||
chr16:89588202
|
A | ACCCACAG others(124): Show |
1 | a0001c0002t0004g0223 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(131): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | |||||
chr16:89588202
|
A | ACCCACAG others(71): Show |
2 | a0001c0001t0001g0007a0003c0006t0003g0342 | 2 | HG00621.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.928-470_928-469ins others(78): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | |||||
chr16:89588202
|
A | ACCCACAG others(485): Show |
1 | a0001c0001t0001g0241 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(492): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | |||||
chr16:89588202
|
A | ACCCACAG others(45): Show |
1 | a0001c0001t0001g0217 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(52): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | |||||
chr16:89588202
|
A | ACCCACAG others(774): Show |
1 | a0001c0024t0001g0218 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(781): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | |||||
chr16:89588202
|
A | ACCCCCCG others(59): Show |
1 | a0001c0001t0001g0088 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.928-470_928-469ins others(66): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588202 | |||||
chr16:89588202
|
A | AGCCACAG others(9): Show |
1 | a0001c0005t0002g0107 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.928-473_928-472ins others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588202 | ||||||
chr16:89588202
|
A | AGCCACAG others(88): Show |
1 | a0002c0004t0002g0315 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.928-473_928-472ins others(95): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588202 | ||||||
chr16:89588202
|
A | AGCCACAG others(46): Show |
2 | a0001c0001t0001g0065a0001c0001t0001g0109 | 2 | HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.928-473_928-472ins others(53): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588202 | ||||||
chr16:89588202
|
A | AGCCACAG others(1344): Show |
1 | a0001c0002t0001g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.928-473_928-472ins others(1351): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588202 | ||||||
chr16:89588202
|
A | AGCCACAG others(2535): Show |
1 | a0001c0008t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.928-473_928-472ins others(2542): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588202 | ||||||
chr16:89588202
|
A | AGCCACAG others(327): Show |
1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.928-473_928-472ins others(334): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588202 | ||||||
chr16:89588202
|
A | AGCCGCGT others(57): Show |
1 | a0001c0001t0001g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.928-473_928-472ins others(64): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588202 | ||||||
chr16:89588206
|
G | C | 27 | a0001c0001t0001g0007a0001c0001t0001g0057a0001c0001t0001g0065others(24): Show | 27 | HG00558.hp1 HG00621.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.928-469G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588206 | ||||||
chr16:89588206
|
G | GCGTGTCA others(310): Show |
1 | a0001c0002t0013g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.928-454_928-453ins others(317): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(209): Show |
1 | a0001c0001t0001g0334 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.928-454_928-453ins others(216): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(94): Show |
1 | a0001c0001t0001g0249 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.928-454_928-453ins others(101): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(122): Show |
1 | a0001c0001t0001g0248 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.928-454_928-453ins others(129): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(82): Show |
1 | a0002c0003t0003g0138 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.928-449_928-448ins others(89): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(19): Show |
27 | a0001c0001t0001g0051a0001c0001t0001g0095a0001c0001t0001g0184others(24): Show | 27 | HG00544.hp2 HG00558.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.928-458_928-433dup others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(20): Show |
24 | a0001c0002t0002g0042a0001c0002t0005g0020a0001c0005t0002g0002others(21): Show | 29 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.928-468_928-442dup others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(21): Show |
1 | a0001c0005t0002g0303 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(237): Show |
1 | a0001c0001t0001g0190 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.928-442_928-441ins others(244): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(1467): Show |
1 | a0001c0002t0004g0134 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(1474): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(2084): Show |
1 | a0001c0002t0003g0181 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.928-442_928-441ins others(2091): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(386): Show |
1 | a0001c0002t0002g0278 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(393): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(799): Show |
1 | a0003c0006t0003g0231 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.928-442_928-441ins others(806): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(234): Show |
1 | a0003c0006t0003g0168 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(241): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(196): Show |
1 | a0003c0006t0003g0149 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(203): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(232): Show |
1 | a0001c0001t0001g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.928-442_928-441ins others(239): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(604): Show |
1 | a0008c0021t0001g0224 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.928-442_928-441ins others(611): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(174): Show |
1 | a0002c0003t0003g0073 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.928-442_928-441ins others(181): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(109): Show |
1 | a0001c0001t0001g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(116): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(2604): Show |
1 | a0001c0001t0001g0300 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(2611): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(45): Show |
2 | a0001c0002t0002g0210a0001c0002t0002g0338 | 2 | HG04204.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.928-433_928-432ins others(52): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(227): Show |
1 | a0003c0006t0003g0148 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.928-433_928-432ins others(234): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(71): Show |
1 | a0001c0001t0001g0185 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.928-433_928-432ins others(78): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(135): Show |
1 | a0001c0001t0001g0336 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.928-433_928-432ins others(142): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(173): Show |
1 | a0001c0001t0001g0191 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.928-433_928-432ins others(180): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(390): Show |
1 | a0001c0001t0001g0215 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.928-433_928-432ins others(397): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(364): Show |
1 | a0002c0004t0002g0324 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.928-433_928-432ins others(371): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(56): Show |
1 | a0001c0001t0001g0198 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.928-427_928-426ins others(63): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(966): Show |
1 | a0001c0001t0001g0216 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.928-427_928-426ins others(973): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(269): Show |
1 | a0004c0011t0001g0077 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.928-427_928-426ins others(276): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(296): Show |
1 | a0001c0001t0001g0054 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.928-450_928-449ins others(303): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(169): Show |
1 | a0001c0001t0001g0333 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-450_928-449ins others(176): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GCGTGTCA others(94): Show |
1 | a0001c0002t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.928-451_928-450ins others(101): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588206 | |||||
chr16:89588206
|
G | GTGTGTCA others(195): Show |
1 | a0001c0001t0001g0097 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.928-469_928-468ins others(202): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588206 | ||||||
chr16:89588208
|
G | A | 1 | a0001c0009t0001g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.928-467G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588208 | ||||||
chr16:89588212
|
C | CACCCACA others(19): Show |
1 | a0002c0003t0003g0128 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.928-438_928-437ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588212 | |||||
chr16:89588212
|
C | T | 4 | a0001c0001t0001g0057a0001c0007t0006g0162a0002c0003t0002g0153others(1): Show | 4 | HG00597.hp1 HG02071.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-463C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588212 | ||||||
chr16:89588214
|
C | CCCACAGA others(19): Show |
1 | a0001c0001t0001g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.928-436_928-435ins others(26): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588214 | |||||
chr16:89588214
|
C | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0109 | 2 | HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.928-461C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588214 | ||||||
chr16:89588228
|
G | GC | 8 | a0001c0002t0002g0321a0001c0002t0005g0074a0001c0002t0005g0320others(5): Show | 8 | HG01192.hp2 HG02486.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-442dupC | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588228 | |||||
chr16:89588228
|
G | GCCCCCCG others(21): Show |
1 | a0002c0004t0002g0016 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.928-442_928-441ins others(28): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588228 | |||||
chr16:89588228
|
G | GCCCCCCG others(32): Show |
1 | a0001c0002t0005g0292 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.928-442_928-441ins others(39): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588228 | |||||
chr16:89588228
|
G | GCCCCCCG others(132): Show |
1 | a0001c0002t0005g0291 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.928-442_928-441ins others(139): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588228 | |||||
chr16:89588228
|
G | GCCCCCGT others(20): Show |
1 | a0001c0002t0005g0197 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.928-433_928-432ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588228 | |||||
chr16:89588236
|
G | A | 2 | a0001c0005t0002g0302a0001c0005t0002g0323 | 2 | HG00438.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.928-439G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588236 | ||||||
chr16:89588239
|
A | ACCCACAG others(20): Show |
1 | a0001c0001t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.928-433_928-432ins others(27): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 89588239 | |||||
chr16:89588245
|
G | A | 1 | a0001c0002t0003g0272 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.928-430G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588245 | ||||||
chr16:89588258
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.928-417A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588258 | ||||||
chr16:89588262
|
G | A | 1 | a0001c0001t0001g0333 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-413G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588262 | ||||||
chr16:89588270
|
G | A | 1 | a0002c0003t0003g0135 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.928-405G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588270 | ||||||
chr16:89588352
|
C | T | 3 | a0001c0002t0005g0163a0001c0027t0005g0156a0001c0028t0001g0164 | 3 | HG02818.hp1 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.928-323C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588352 | ||||||
chr16:89588392
|
C | T | 53 | a0001c0001t0001g0007a0001c0001t0001g0054a0001c0001t0001g0063others(50): Show | 53 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.928-283C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588392 | ||||||
chr16:89588393
|
G | A | 4 | a0001c0002t0004g0223a0001c0002t0004g0225a0001c0002t0004g0226others(1): Show | 4 | HG02080.hp1 HG02083.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-282G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588393 | ||||||
chr16:89588413
|
G | A | 1 | a0001c0002t0002g0278 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.928-262G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588413 | ||||||
chr16:89588421
|
C | T | 109 | a0001c0001t0001g0035a0001c0001t0001g0079a0001c0001t0001g0108others(106): Show | 110 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.928-254C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588421 | ||||||
chr16:89588503
|
C | T | 1 | a0001c0013t0002g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.928-172C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588503 | ||||||
chr16:89588599
|
G | A | 4 | a0001c0001t0001g0243a0001c0001t0001g0249a0001c0001t0001g0333others(1): Show | 4 | HG01123.hp1 HG01496.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-76G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588599 | ||||||
chr16:89588629
|
G | A | 3 | a0001c0002t0005g0163a0001c0027t0005g0156a0001c0028t0001g0164 | 3 | HG02818.hp1 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.928-46G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 9/14 | chr16 | 89588629 | ||||||
chr16:89588813
|
G | A | 99 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0079others(96): Show | 99 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
splice_region_variant&intron_variant | LOW | c.1061+5G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89588813 | ||||||
chr16:89588816
|
C | T | 1 | a0004c0020t0001g0340 | 1 | HG02809.hp2 | splice_region_variant&intron_variant | LOW | c.1061+8C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89588816 | ||||||
chr16:89588865
|
G | A | 3 | a0001c0012t0002g0296a0001c0012t0002g0297a0001c0013t0002g0006 | 3 | HG01167.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1061+57G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89588865 | ||||||
chr16:89588940
|
C | T | 4 | a0001c0002t0001g0287a0001c0002t0001g0331a0001c0015t0001g0330others(1): Show | 4 | HG00639.hp1 HG02717.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1061+132C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89588940 | ||||||
chr16:89588953
|
C | T | 1 | a0001c0002t0002g0316 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1061+145C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89588953 | ||||||
chr16:89588966
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1061+158G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89588966 | ||||||
chr16:89589013
|
C | T | 103 | a0001c0001t0001g0079a0001c0001t0001g0108a0001c0001t0001g0120others(100): Show | 103 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1061+205C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589013 | ||||||
chr16:89589014
|
G | A | 1 | a0001c0001t0012g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1061+206G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589014 | ||||||
chr16:89589153
|
G | A | 40 | a0001c0001t0001g0175a0001c0001t0001g0248a0001c0005t0002g0002others(37): Show | 45 | HG00438.hp1 HG00673.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.1061+345G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589153 | ||||||
chr16:89589175
|
C | T | 1 | a0001c0002t0003g0290 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1061+367C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589175 | ||||||
chr16:89589206
|
C | T | 1 | a0002c0004t0002g0315 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1061+398C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589206 | ||||||
chr16:89589207
|
A | G | 231 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0036others(228): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1061+399A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589207 | ||||||
chr16:89589218
|
G | A | 3 | a0001c0001t0001g0238a0001c0001t0001g0281a0001c0001t0001g0300 | 3 | HG00741.hp2 HG01175.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1061+410G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589218 | ||||||
chr16:89589219
|
G | A | 195 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0058others(192): Show | 201 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.1061+411G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589219 | ||||||
chr16:89589287
|
G | A | 1 | a0004c0020t0001g0340 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1061+479G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589287 | ||||||
chr16:89589303
|
ACT | A | 3 | a0001c0002t0001g0025a0001c0002t0001g0167a0001c0008t0001g0009 | 3 | HG02922.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1061+498_1061+499d others(4): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 89589303 | |||||
chr16:89589328
|
C | T | 1 | a0006c0014t0001g0008 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1061+520C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589328 | ||||||
chr16:89589358
|
C | T | 6 | a0001c0002t0002g0264a0001c0002t0002g0329a0001c0002t0002g0337others(3): Show | 6 | HG01891.hp1 HG02970.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1062-539C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589358 | ||||||
chr16:89589468
|
C | T | 1 | a0001c0002t0001g0331 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1062-429C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589468 | ||||||
chr16:89589469
|
C | T | 2 | a0001c0001t0001g0079a0001c0009t0001g0061 | 2 | HG01516.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1062-428C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589469 | ||||||
chr16:89589553
|
C | A | 5 | a0001c0002t0002g0264a0001c0002t0002g0329a0001c0002t0002g0337others(2): Show | 5 | HG02970.hp2 HG03139.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1062-344C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589553 | ||||||
chr16:89589611
|
C | T | 29 | a0001c0002t0003g0031a0001c0002t0003g0033a0001c0002t0003g0034others(26): Show | 29 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1062-286C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589611 | ||||||
chr16:89589661
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1062-236C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589661 | ||||||
chr16:89589702
|
G | A | 5 | a0001c0002t0002g0264a0001c0002t0002g0329a0001c0002t0002g0337others(2): Show | 5 | HG02970.hp2 HG03139.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1062-195G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589702 | ||||||
chr16:89589754
|
C | T | 14 | a0001c0001t0001g0248a0001c0005t0002g0002a0001c0005t0002g0003others(11): Show | 19 | HG01070.hp2 HG01071.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1062-143C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589754 | ||||||
chr16:89589755
|
A | G | 203 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(200): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1062-142A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589755 | ||||||
chr16:89589814
|
G | A | 1 | a0001c0008t0002g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1062-83G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589814 | ||||||
chr16:89589843
|
T | C | 201 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(198): Show | 207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1062-54T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 10/14 | chr16 | 89589843 | ||||||
chr16:89590016
|
C | A | 102 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0075others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1116+65C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590016 | ||||||
chr16:89590016
|
C | T | 1 | a0006c0014t0001g0008 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1116+65C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590016 | ||||||
chr16:89590089
|
G | A | 1 | a0001c0002t0004g0169 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1116+138G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590089 | ||||||
chr16:89590137
|
T | G | 20 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0045others(17): Show | 20 | HG00323.hp2 HG00673.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1116+186T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590137 | ||||||
chr16:89590169
|
C | T | 30 | a0001c0002t0003g0031a0001c0002t0003g0033a0001c0002t0003g0034others(27): Show | 30 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1116+218C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590169 | ||||||
chr16:89590223
|
A | G | 199 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(196): Show | 205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1116+272A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590223 | ||||||
chr16:89590301
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1116+350G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590301 | ||||||
chr16:89590396
|
A | G | 5 | a0001c0002t0002g0264a0001c0002t0002g0329a0001c0002t0002g0337others(2): Show | 5 | HG02970.hp2 HG03139.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1116+445A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590396 | ||||||
chr16:89590454
|
G | A | 1 | a0001c0025t0001g0276 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1116+503G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590454 | ||||||
chr16:89590589
|
G | T | 1 | a0001c0002t0003g0233 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1117-418G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590589 | ||||||
chr16:89590645
|
C | T | 2 | a0001c0002t0002g0024a0001c0002t0002g0338 | 2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1117-362C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590645 | ||||||
chr16:89590750
|
C | CGGGGGAG others(32): Show |
4 | a0001c0002t0004g0132a0001c0002t0004g0133a0001c0002t0004g0151others(1): Show | 4 | HG00609.hp1 HG01943.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1117-202_1117-164d others(41): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 89590750 | |||||
chr16:89590750
|
C | T | 1 | a0001c0002t0001g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1117-257C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590750 | ||||||
chr16:89590750
|
CGGGGGAG others(32): Show |
C | 51 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0054others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1117-202_1117-164d others(41): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 89590750 | |||||
chr16:89590776
|
GGGGGCCG others(31): Show |
G | 1 | a0001c0001t0001g0027 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1117-226_1117-189d others(40): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 89590776 | |||||
chr16:89590789
|
G | A | 1 | a0001c0002t0002g0209 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1117-218G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590789 | ||||||
chr16:89590789
|
GGGGGGAG others(31): Show |
G | 1 | a0001c0001t0001g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1117-212_1117-175d others(40): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 89590789 | |||||
chr16:89590839
|
C | G | 1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1117-168C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590839 | ||||||
chr16:89590862
|
C | T | 24 | a0001c0001t0001g0269a0001c0002t0002g0046a0001c0002t0002g0084others(21): Show | 24 | HG01106.hp2 HG01192.hp2 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.1117-145C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590862 | ||||||
chr16:89590975
|
G | A | 1 | a0003c0006t0003g0232 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1117-32G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 11/14 | chr16 | 89590975 | ||||||
chr16:89591102
|
C | T | 31 | a0001c0002t0003g0018a0001c0002t0003g0076a0001c0002t0003g0180others(28): Show | 31 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1169-25C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 12/14 | chr16 | 89591102 | ||||||
chr16:89591311
|
T | A | 73 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0108others(70): Show | 73 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1302+51T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591311 | ||||||
chr16:89591321
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1302+61C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591321 | ||||||
chr16:89591420
|
G | A | 2 | a0001c0002t0002g0084a0001c0002t0002g0104 | 2 | HG01106.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1302+160G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591420 | ||||||
chr16:89591445
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1302+185C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591445 | ||||||
chr16:89591506
|
T | A | 1 | a0001c0002t0002g0196 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1302+246T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591506 | ||||||
chr16:89591534
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1302+274C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591534 | ||||||
chr16:89591536
|
C | T | 3 | a0001c0002t0005g0163a0001c0027t0005g0156a0001c0028t0001g0164 | 3 | HG02818.hp1 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1302+276C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591536 | ||||||
chr16:89591541
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1302+281A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591541 | ||||||
chr16:89591547
|
A | G | 2 | a0001c0002t0002g0041a0001c0002t0002g0042 | 2 | NA18983.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1302+287A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591547 | ||||||
chr16:89591628
|
T | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0294 | 3 | HG02630.hp2 HG02886.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1302+368T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591628 | ||||||
chr16:89591634
|
C | G | 8 | a0001c0002t0001g0287a0001c0002t0001g0331a0001c0002t0004g0271others(5): Show | 8 | HG00639.hp1 HG01081.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1302+374C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591634 | ||||||
chr16:89591704
|
C | G | 1 | a0001c0025t0001g0276 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1302+444C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591704 | ||||||
chr16:89591723
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1302+463A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591723 | ||||||
chr16:89591739
|
A | C | 4 | a0001c0001t0001g0174a0001c0001t0001g0183a0001c0001t0001g0184others(1): Show | 4 | HG02055.hp1 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+479A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591739 | ||||||
chr16:89591741
|
C | A | 8 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(5): Show | 8 | HG01109.hp2 HG02451.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.1302+481C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591741 | ||||||
chr16:89591767
|
C | T | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0069others(1): Show | 4 | HG01884.hp1 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+507C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591767 | ||||||
chr16:89591786
|
G | C | 10 | a0001c0001t0001g0284a0001c0002t0001g0287a0001c0002t0001g0331others(7): Show | 10 | HG00639.hp1 HG01081.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1302+526G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591786 | ||||||
chr16:89591793
|
G | A | 2 | a0001c0002t0002g0022a0004c0020t0001g0340 | 2 | HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1302+533G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591793 | ||||||
chr16:89591801
|
C | A | 21 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0070others(18): Show | 21 | HG00639.hp1 HG01081.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1302+541C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591801 | ||||||
chr16:89591801
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0244 | 2 | HG00323.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1302+541C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591801 | ||||||
chr16:89591804
|
C | A | 21 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0070others(18): Show | 21 | HG00639.hp1 HG01081.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1302+544C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591804 | ||||||
chr16:89591814
|
C | G | 8 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0070others(5): Show | 8 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+554C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591814 | ||||||
chr16:89591826
|
A | G | 86 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0027others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.1302+566A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591826 | ||||||
chr16:89591829
|
G | T | 76 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(73): Show |
intron_variant | MODIFIER | c.1302+569G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591829 | ||||||
chr16:89591838
|
C | T | 171 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0030others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1302+578C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591838 | ||||||
chr16:89591845
|
C | T | 98 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0045others(95): Show | 98 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1302+585C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591845 | ||||||
chr16:89591846
|
G | A | 4 | a0001c0001t0001g0284a0001c0002t0001g0287a0001c0002t0001g0331others(1): Show | 4 | HG00639.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+586G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591846 | ||||||
chr16:89591846
|
G | T | 131 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0036others(128): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1302+586G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591846 | ||||||
chr16:89591858
|
T | G | 1 | a0001c0002t0001g0322 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1302+598T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591858 | ||||||
chr16:89591859
|
T | C | 1 | a0001c0002t0001g0322 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1302+599T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591859 | ||||||
chr16:89591861
|
T | C | 1 | a0001c0002t0001g0322 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1302+601T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591861 | ||||||
chr16:89591900
|
C | T | 3 | a0001c0002t0001g0025a0001c0002t0001g0167a0001c0008t0001g0009 | 3 | HG02922.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1302+640C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591900 | ||||||
chr16:89591916
|
G | A | 8 | a0001c0001t0001g0108a0001c0001t0001g0188a0001c0001t0001g0189others(5): Show | 8 | HG01109.hp2 HG02451.hp2 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+656G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591916 | ||||||
chr16:89591935
|
A | G | 1 | a0001c0002t0001g0029 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1302+675A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591935 | ||||||
chr16:89591935
|
ATGATCCA others(308): Show |
A | 1 | a0001c0009t0001g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1302+718_1302+1032 others(3): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89591935 | |||||
chr16:89591995
|
G | A | 206 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0069others(203): Show | 212 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.1302+735G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89591995 | ||||||
chr16:89592001
|
C | G | 57 | a0001c0001t0001g0248a0001c0002t0002g0004a0001c0002t0002g0032others(54): Show | 63 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1302+741C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592001 | ||||||
chr16:89592010
|
G | T | 4 | a0001c0002t0004g0271a0001c0002t0004g0325a0001c0002t0004g0326others(1): Show | 4 | HG02258.hp1 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+750G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592010 | ||||||
chr16:89592013
|
G | GT | 71 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0040others(68): Show | 71 | HG00323.hp2 HG00673.hp1 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.1302+765dupT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89592013 | |||||
chr16:89592016
|
T | G | 4 | a0001c0002t0004g0271a0001c0002t0004g0325a0001c0002t0004g0326others(1): Show | 4 | HG02258.hp1 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+756T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592016 | ||||||
chr16:89592031
|
G | A | 3 | a0001c0002t0005g0163a0001c0027t0005g0156a0001c0028t0001g0164 | 3 | HG02818.hp1 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1302+771G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592031 | ||||||
chr16:89592039
|
G | A | 43 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0269others(40): Show | 43 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1302+779G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592039 | ||||||
chr16:89592051
|
A | C | 5 | a0001c0001t0001g0115a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01928.hp2 NA18966.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+791A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592051 | ||||||
chr16:89592053
|
G | A | 5 | a0001c0001t0001g0115a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01928.hp2 NA18966.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+793G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592053 | ||||||
chr16:89592063
|
T | C | 269 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0035others(266): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1302+803T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592063 | ||||||
chr16:89592069
|
C | T | 214 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0108others(211): Show | 220 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.1302+809C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592069 | ||||||
chr16:89592091
|
C | T | 4 | a0001c0002t0004g0271a0001c0002t0004g0325a0001c0002t0004g0326others(1): Show | 4 | HG02258.hp1 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+831C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592091 | ||||||
chr16:89592095
|
C | A | 201 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0069others(198): Show | 207 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.1302+835C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592095 | ||||||
chr16:89592108
|
G | A | 45 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0269others(42): Show | 45 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1302+848G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592108 | ||||||
chr16:89592109
|
C | T | 44 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0269others(41): Show | 44 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1302+849C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592109 | ||||||
chr16:89592110
|
G | A | 44 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0269others(41): Show | 44 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1302+850G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592110 | ||||||
chr16:89592113
|
A | T | 43 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0269others(40): Show | 43 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1302+853A>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592113 | ||||||
chr16:89592175
|
A | AT | 103 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0057others(100): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1302+927dupT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89592175 | |||||
chr16:89592175
|
A | ATTTTTTT others(311): Show |
1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1302+927_1302+928i others(320): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89592175 | |||||
chr16:89592215
|
C | T | 1 | a0001c0025t0001g0276 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1302+955C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592215 | ||||||
chr16:89592223
|
C | T | 4 | a0001c0002t0001g0025a0001c0002t0001g0167a0001c0008t0001g0009others(1): Show | 4 | HG01891.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+963C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592223 | ||||||
chr16:89592249
|
C | T | 2 | a0001c0001t0001g0175a0001c0002t0005g0295 | 2 | HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1302+989C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592249 | ||||||
chr16:89592280
|
CTGGGATT others(796): Show |
C | 1 | a0001c0002t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1302+1046_1302+184 others(4): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89592280 | |||||
chr16:89592306
|
G | A | 57 | a0001c0001t0001g0248a0001c0002t0002g0004a0001c0002t0002g0032others(54): Show | 63 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1302+1046G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592306 | ||||||
chr16:89592366
|
C | T | 40 | a0001c0001t0001g0269a0001c0002t0001g0287a0001c0002t0001g0331others(37): Show | 40 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1302+1106C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592366 | ||||||
chr16:89592395
|
G | C | 4 | a0001c0002t0004g0271a0001c0002t0004g0325a0001c0002t0004g0326others(1): Show | 4 | HG02258.hp1 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+1135G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592395 | ||||||
chr16:89592448
|
A | AT | 59 | a0001c0001t0001g0052a0001c0001t0001g0248a0001c0002t0001g0029others(56): Show | 65 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1302+1205dupT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89592448 | |||||
chr16:89592448
|
AT | A | 14 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0102others(11): Show | 14 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(11): Show |
intron_variant | MODIFIER | c.1302+1205delT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89592448 | |||||
chr16:89592471
|
A | G | 29 | a0001c0001t0001g0078a0001c0001t0001g0099a0001c0001t0001g0176others(26): Show | 29 | HG00099.hp1 HG01099.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.1302+1211A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592471 | ||||||
chr16:89592505
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0203 | 2 | HG04199.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1302+1245C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592505 | ||||||
chr16:89592658
|
G | C | 1 | a0001c0002t0001g0331 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1302+1398G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592658 | ||||||
chr16:89592732
|
G | A | 1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1302+1472G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592732 | ||||||
chr16:89592743
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1302+1483A>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592743 | ||||||
chr16:89592805
|
C | A | 1 | a0004c0011t0001g0092 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1302+1545C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592805 | ||||||
chr16:89592810
|
C | CT | 103 | a0001c0001t0001g0078a0001c0001t0001g0108a0001c0001t0001g0176others(100): Show | 109 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1302+1569dupT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89592810 | |||||
chr16:89592810
|
C | CTT | 36 | a0001c0001t0001g0269a0001c0002t0002g0022a0001c0002t0002g0046others(33): Show | 36 | HG00609.hp1 HG00621.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.1302+1568_1302+156 others(6): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89592810 | |||||
chr16:89592814
|
T | TC | 58 | a0001c0002t0003g0018a0001c0002t0003g0031a0001c0002t0003g0033others(55): Show | 58 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1302+1554_1302+155 others(5): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592814 | ||||||
chr16:89592815
|
T | C | 5 | a0001c0002t0003g0044a0001c0002t0003g0047a0001c0002t0003g0053others(2): Show | 5 | HG02083.hp2 NA18980.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1302+1555T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592815 | ||||||
chr16:89592848
|
T | C | 4 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0186others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+1588T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592848 | ||||||
chr16:89592914
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1302+1654G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592914 | ||||||
chr16:89592950
|
G | C | 1 | a0001c0008t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1302+1690G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592950 | ||||||
chr16:89592961
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1302+1701C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592961 | ||||||
chr16:89592975
|
G | C | 1 | a0001c0002t0001g0322 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1302+1715G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592975 | ||||||
chr16:89592998
|
G | C | 65 | a0001c0002t0003g0018a0001c0002t0003g0031a0001c0002t0003g0033others(62): Show | 65 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1302+1738G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89592998 | ||||||
chr16:89593042
|
C | A | 37 | a0001c0001t0001g0269a0001c0002t0002g0024a0001c0002t0002g0046others(34): Show | 37 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1302+1782C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593042 | ||||||
chr16:89593071
|
C | T | 4 | a0001c0002t0004g0271a0001c0002t0004g0325a0001c0002t0004g0326others(1): Show | 4 | HG02258.hp1 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+1811C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593071 | ||||||
chr16:89593103
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1302+1843C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593103 | ||||||
chr16:89593130
|
T | A | 211 | a0001c0001t0001g0078a0001c0001t0001g0099a0001c0001t0001g0176others(208): Show | 217 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.1302+1870T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593130 | ||||||
chr16:89593214
|
C | G | 64 | a0001c0002t0003g0018a0001c0002t0003g0031a0001c0002t0003g0033others(61): Show | 64 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1302+1954C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593214 | ||||||
chr16:89593240
|
T | A | 3 | a0001c0002t0002g0329a0001c0002t0009g0328a0001c0008t0002g0010 | 3 | HG03139.hp2 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1302+1980T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593240 | ||||||
chr16:89593292
|
C | G | 1 | a0001c0002t0013g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1302+2032C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593292 | ||||||
chr16:89593292
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1302+2032C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593292 | ||||||
chr16:89593294
|
C | T | 14 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0074others(11): Show | 14 | HG01192.hp2 HG01243.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1302+2034C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593294 | ||||||
chr16:89593310
|
G | A | 2 | a0001c0002t0001g0322a0001c0002t0002g0022 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1302+2050G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593310 | ||||||
chr16:89593358
|
A | AT | 86 | a0001c0001t0001g0078a0001c0001t0001g0099a0001c0001t0001g0176others(83): Show | 86 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1303-1996dupT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89593358 | |||||
chr16:89593365
|
T | C | 3 | a0001c0001t0001g0238a0001c0001t0001g0281a0001c0001t0001g0300 | 3 | HG00741.hp2 HG01175.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1303-2002T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593365 | ||||||
chr16:89593404
|
G | C | 1 | a0001c0024t0001g0218 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1303-1963G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593404 | ||||||
chr16:89593462
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1303-1905C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593462 | ||||||
chr16:89593519
|
A | AT | 63 | a0001c0002t0003g0018a0001c0002t0003g0031a0001c0002t0003g0033others(60): Show | 63 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1303-1842dupT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89593519 | |||||
chr16:89593553
|
T | C | 3 | a0001c0002t0001g0322a0001c0002t0002g0022a0001c0008t0002g0010 | 3 | HG03139.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1303-1814T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593553 | ||||||
chr16:89593554
|
G | A | 1 | a0001c0002t0001g0322 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1303-1813G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593554 | ||||||
chr16:89593642
|
G | A | 1 | a0001c0002t0001g0322 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1303-1725G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593642 | ||||||
chr16:89593661
|
C | G | 1 | a0001c0002t0002g0046 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1303-1706C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593661 | ||||||
chr16:89593809
|
T | A | 1 | a0006c0014t0001g0008 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1303-1558T>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593809 | ||||||
chr16:89593826
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1303-1541T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593826 | ||||||
chr16:89593895
|
C | T | 1 | a0001c0002t0002g0104 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1303-1472C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593895 | ||||||
chr16:89593907
|
G | T | 40 | a0001c0001t0001g0269a0001c0002t0002g0023a0001c0002t0002g0024others(37): Show | 40 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1303-1460G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593907 | ||||||
chr16:89593935
|
G | A | 19 | a0001c0001t0001g0054a0001c0001t0001g0063a0001c0001t0001g0067others(16): Show | 19 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1303-1432G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89593935 | ||||||
chr16:89594101
|
A | G | 86 | a0001c0001t0001g0078a0001c0001t0001g0099a0001c0001t0001g0176others(83): Show | 86 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1303-1266A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594101 | ||||||
chr16:89594103
|
C | G | 115 | a0001c0001t0001g0269a0001c0002t0001g0287a0001c0002t0001g0331others(112): Show | 121 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1303-1264C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594103 | ||||||
chr16:89594140
|
G | A | 5 | a0001c0002t0005g0074a0001c0002t0005g0197a0001c0002t0005g0292others(2): Show | 5 | HG01192.hp2 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303-1227G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594140 | ||||||
chr16:89594192
|
C | T | 7 | a0001c0002t0001g0025a0001c0002t0001g0029a0001c0002t0001g0167others(4): Show | 7 | HG00639.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1303-1175C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594192 | ||||||
chr16:89594227
|
G | C | 2 | a0001c0001t0008g0055a0002c0010t0008g0127 | 2 | HG00673.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1303-1140G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594227 | ||||||
chr16:89594270
|
G | A | 1 | a0002c0003t0003g0122 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1303-1097G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594270 | ||||||
chr16:89594367
|
G | C | 1 | a0001c0002t0002g0046 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1303-1000G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594367 | ||||||
chr16:89594376
|
G | A | 4 | a0001c0002t0001g0025a0001c0002t0001g0029a0001c0002t0001g0167others(1): Show | 4 | HG02572.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303-991G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594376 | ||||||
chr16:89594378
|
G | A | 1 | a0001c0002t0005g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1303-989G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594378 | ||||||
chr16:89594442
|
C | A | 14 | a0001c0007t0006g0064a0001c0007t0006g0071a0001c0007t0006g0157others(11): Show | 14 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1303-925C>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594442 | ||||||
chr16:89594473
|
C | T | 1 | a0001c0002t0002g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1303-894C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594473 | ||||||
chr16:89594560
|
G | A | 5 | a0003c0006t0003g0231a0003c0006t0003g0268a0003c0006t0003g0274others(2): Show | 5 | NA18946.hp1 NA18952.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303-807G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594560 | ||||||
chr16:89594624
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1303-743T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594624 | ||||||
chr16:89594642
|
C | CT | 32 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0054others(29): Show | 32 | HG00099.hp2 HG00558.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1303-696dupT | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | |||||
chr16:89594642
|
C | CTT | 46 | a0001c0002t0003g0018a0001c0002t0003g0031a0001c0002t0003g0034others(43): Show | 46 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1303-697_1303-696d others(4): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | |||||
chr16:89594642
|
C | CTTT | 14 | a0001c0002t0003g0033a0001c0002t0003g0180a0001c0002t0003g0181others(11): Show | 14 | HG00597.hp2 HG02129.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.1303-698_1303-696d others(5): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | |||||
chr16:89594642
|
CTTTTTTT | C | 10 | a0001c0002t0001g0029a0001c0002t0002g0023a0001c0002t0004g0266others(7): Show | 10 | HG00438.hp1 HG01361.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1303-702_1303-696d others(9): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | |||||
chr16:89594642
|
CTTTTTTT others(1): Show |
C | 93 | a0001c0001t0001g0269a0001c0002t0001g0287a0001c0002t0001g0322others(90): Show | 99 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1303-703_1303-696d others(10): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | |||||
chr16:89594642
|
CTTTTTTT others(2): Show |
C | 19 | a0001c0001t0001g0063a0001c0002t0004g0223a0001c0002t0004g0326others(16): Show | 19 | HG01192.hp2 HG01243.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.1303-704_1303-696d others(11): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | |||||
chr16:89594642
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0024t0001g0218 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1303-705_1303-696d others(12): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | |||||
chr16:89594642
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0002t0001g0025a0001c0002t0001g0167a0001c0008t0001g0009 | 3 | HG02922.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1303-708_1303-696d others(15): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | |||||
chr16:89594642
|
CTTTTTTT others(7): Show |
C | 16 | a0001c0002t0013g0194a0001c0007t0006g0064a0001c0007t0006g0071others(13): Show | 16 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.1303-709_1303-696d others(16): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89594642 | |||||
chr16:89594668
|
T | G | 8 | a0001c0001t0001g0269a0001c0002t0002g0046a0001c0002t0002g0084others(5): Show | 8 | HG01106.hp2 HG01261.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.1303-699T>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594668 | ||||||
chr16:89594691
|
C | T | 14 | a0001c0007t0006g0064a0001c0007t0006g0071a0001c0007t0006g0157others(11): Show | 14 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1303-676C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594691 | ||||||
chr16:89594715
|
G | A | 64 | a0001c0002t0003g0018a0001c0002t0003g0031a0001c0002t0003g0033others(61): Show | 64 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1303-652G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594715 | ||||||
chr16:89594726
|
A | T | 3 | a0001c0002t0001g0287a0001c0002t0001g0331a0001c0015t0001g0330 | 3 | HG00639.hp1 HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1303-641A>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594726 | ||||||
chr16:89594769
|
A | G | 1 | a0001c0008t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1303-598A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594769 | ||||||
chr16:89594830
|
T | C | 65 | a0001c0002t0003g0018a0001c0002t0003g0031a0001c0002t0003g0033others(62): Show | 65 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1303-537T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594830 | ||||||
chr16:89594899
|
G | A | 1 | a0003c0006t0003g0144 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1303-468G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89594899 | ||||||
chr16:89595098
|
A | G | 206 | a0001c0001t0001g0269a0001c0002t0001g0025a0001c0002t0001g0029others(203): Show | 212 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.1303-269A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89595098 | ||||||
chr16:89595129
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0176 | 2 | HG00099.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.1303-238G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89595129 | ||||||
chr16:89595267
|
C | T | 26 | a0001c0002t0004g0037a0001c0002t0004g0038a0001c0002t0004g0039others(23): Show | 26 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.1303-100C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89595267 | ||||||
chr16:89595362
|
C | T | 30 | a0001c0002t0004g0037a0001c0002t0004g0038a0001c0002t0004g0039others(27): Show | 30 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(27): Show |
splice_region_variant&intron_variant | LOW | c.1303-5C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 13/14 | chr16 | 89595362 | ||||||
chr16:89595635
|
G | A | 1 | a0001c0002t0001g0322 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1539+32G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595635 | ||||||
chr16:89595655
|
T | C | 34 | a0001c0002t0003g0018a0001c0002t0003g0076a0001c0002t0003g0180others(31): Show | 34 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.1539+52T>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595655 | ||||||
chr16:89595741
|
C | T | 1 | a0001c0008t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1539+138C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595741 | ||||||
chr16:89595824
|
A | T | 3 | a0001c0002t0001g0287a0001c0002t0001g0331a0001c0015t0001g0330 | 3 | HG00639.hp1 HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1539+221A>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595824 | ||||||
chr16:89595879
|
G | A | 2 | a0001c0001t0001g0120a0001c0002t0002g0204 | 2 | NA18990.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1539+276G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595879 | ||||||
chr16:89595911
|
C | T | 29 | a0001c0002t0004g0037a0001c0002t0004g0038a0001c0002t0004g0039others(26): Show | 29 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1539+308C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595911 | ||||||
chr16:89595942
|
G | A | 1 | a0001c0002t0002g0024 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1539+339G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595942 | ||||||
chr16:89595953
|
A | G | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1539+350A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595953 | ||||||
chr16:89595955
|
C | G | 1 | a0001c0002t0004g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1539+352C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595955 | ||||||
chr16:89595976
|
G | A | 3 | a0001c0002t0001g0287a0001c0002t0001g0331a0001c0015t0001g0330 | 3 | HG00639.hp1 HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1539+373G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595976 | ||||||
chr16:89595979
|
GAGACGCA others(28): Show |
G | 4 | a0001c0001t0001g0174a0001c0001t0001g0183a0001c0001t0001g0184others(1): Show | 4 | HG02055.hp1 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1539+381_1539+415d others(37): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 89595979 | |||||
chr16:89595980
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1539+377A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89595980 | ||||||
chr16:89596014
|
A | G | 203 | a0001c0002t0001g0025a0001c0002t0001g0029a0001c0002t0001g0167others(200): Show | 209 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.1539+411A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596014 | ||||||
chr16:89596045
|
G | T | 1 | a0005c0026t0001g0017 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1540-439G>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596045 | ||||||
chr16:89596052
|
G | C | 1 | a0005c0026t0001g0017 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1540-432G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596052 | ||||||
chr16:89596063
|
A | G | 6 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(3): Show | 6 | HG02602.hp2 HG02738.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540-421A>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596063 | ||||||
chr16:89596082
|
C | G | 6 | a0001c0001t0001g0243a0001c0001t0001g0248a0001c0001t0001g0249others(3): Show | 6 | HG01123.hp1 HG01496.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-402C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596082 | ||||||
chr16:89596113
|
C | T | 13 | a0001c0007t0006g0064a0001c0007t0006g0071a0001c0007t0006g0157others(10): Show | 13 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1540-371C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596113 | ||||||
chr16:89596122
|
G | A | 1 | a0002c0004t0002g0016 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1540-362G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596122 | ||||||
chr16:89596208
|
G | A | 1 | a0001c0023t0001g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1540-276G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596208 | ||||||
chr16:89596238
|
AG | A | 13 | a0001c0007t0006g0064a0001c0007t0006g0071a0001c0007t0006g0157others(10): Show | 13 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1540-244delG | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 89596238 | |||||
chr16:89596419
|
G | A | 1 | a0001c0001t0012g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1540-65G>A | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596419 | ||||||
chr16:89596429
|
C | T | 55 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0041others(52): Show | 61 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1540-55C>T | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596429 | ||||||
chr16:89596467
|
G | C | 83 | a0001c0002t0001g0025a0001c0002t0001g0167a0001c0002t0003g0018others(80): Show | 83 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1540-17G>C | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596467 | ||||||
chr16:89596472
|
C | G | 1 | a0001c0002t0013g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1540-12C>G | CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 14/14 | chr16 | 89596472 |