geneid | 8492 |
---|---|
ensemblid | ENSG00000164099.3 |
hgncid | 9477 |
symbol | PRSS12 |
name | serine protease 12 |
refseq_nuc | NM_003619.4 |
refseq_prot | NP_003610.2 |
ensembl_nuc | ENST00000296498.3 |
ensembl_prot | ENSP00000296498.3 |
mane_status | MANE Select |
chr | chr4 |
start | 118280038 |
end | 118353003 |
strand | - |
ver | v1.2 |
region | chr4:118280038-118353003 |
region5000 | chr4:118275038-118358003 |
regionname0 | PRSS12_chr4_118280038_118353003 |
regionname5000 | PRSS12_chr4_118275038_118358003 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 875 | 162 | 46 | 10 | 93 | 0 | 11 | 75 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002 | 0/0 | 875 | 143 | 20 | 40 | 61 | 7 | 15 | 48 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0003 | 0/0 | 875 | 41 | 7 | 4 | 16 | 2 | 12 | 13 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0004 | 0/0 | 875 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0005 | 0/0 | 875 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0006 | 0/0 | 875 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0007 | 0/0 | 875 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0008 | 0/0 | 875 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0009 | 0/0 | 875 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0010 | 0/0 | 875 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0011 | 0/0 | 875 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0012 | 0/0 | 875 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2628 | 89 | 29 | 6 | 47 | 0 | 5 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0002 | 0/0 | 2628 | 83 | 17 | 21 | 37 | 4 | 4 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0003 | 0/0 | 2628 | 57 | 3 | 19 | 21 | 3 | 11 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0004 | 0/0 | 2628 | 56 | 12 | 3 | 35 | 0 | 6 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0005 | 0/0 | 2628 | 41 | 7 | 4 | 16 | 2 | 12 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0006 | 0/0 | 2628 | 8 | 0 | 1 | 7 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0007 | 0/0 | 2628 | 4 | 1 | 3 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0008 | 0/0 | 2628 | 4 | 0 | 0 | 4 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0009 | 0/0 | 2628 | 4 | 4 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0010 | 0/0 | 2628 | 3 | 2 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0011 | 0/0 | 2628 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0012 | 0/0 | 2628 | 2 | 0 | 2 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0013 | 0/0 | 2628 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0014 | 0/0 | 2628 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0015 | 0/0 | 2628 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0016 | 0/0 | 2628 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0017 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0018 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0019 | 0/0 | 2628 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0020 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0021 | 0/0 | 2628 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
c0022 | 0/0 | 2628 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2182 | 232 | 62 | 31 | 122 | 5 | 10 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0002 | 0/0 | 2180 | 60 | 2 | 19 | 23 | 3 | 13 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0003 | 0/0 | 2182 | 38 | 2 | 6 | 17 | 2 | 11 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0004 | 0/0 | 2182 | 4 | 4 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0005 | 0/0 | 2180 | 3 | 3 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0006 | 0/0 | 2182 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0007 | 0/0 | 2182 | 3 | 0 | 1 | 0 | 0 | 2 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0008 | 0/0 | 2180 | 3 | 0 | 2 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0009 | 0/0 | 2182 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0010 | 0/0 | 2182 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0011 | 0/0 | 2182 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0012 | 0/0 | 2182 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0013 | 0/0 | 2182 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0014 | 0/0 | 2182 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0015 | 0/0 | 2182 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0016 | 0/0 | 2182 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0017 | 0/0 | 2182 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0018 | 0/0 | 2182 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0019 | 0/0 | 2182 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0020 | 0/0 | 2182 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0021 | 0/0 | 2182 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0022 | 0/0 | 2182 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0023 | 0/0 | 2182 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
t0024 | 0/0 | 2182 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0002 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0003 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0005 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0009 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0199 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2628 | 89 | 29 | 6 | 47 | 0 | 5 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0004 | 0/0 | 2628 | 56 | 12 | 3 | 35 | 0 | 6 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0006 | 0/0 | 2628 | 8 | 0 | 1 | 7 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0008 | 0/0 | 2628 | 4 | 0 | 0 | 4 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0009 | 0/0 | 2628 | 4 | 4 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0021 | 0/0 | 2628 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002c0002 | 0/0 | 2628 | 83 | 17 | 21 | 37 | 4 | 4 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002c0003 | 0/0 | 2628 | 57 | 3 | 19 | 21 | 3 | 11 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002c0017 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002c0018 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002c0020 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0003c0005 | 0/0 | 2628 | 41 | 7 | 4 | 16 | 2 | 12 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0004c0007 | 0/0 | 2628 | 4 | 1 | 3 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0005c0010 | 0/0 | 2628 | 3 | 2 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0006c0011 | 0/0 | 2628 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0007c0012 | 0/0 | 2628 | 2 | 0 | 2 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0008c0015 | 0/0 | 2628 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0008c0016 | 0/0 | 2628 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0009c0013 | 0/0 | 2628 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0010c0022 | 0/0 | 2628 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0011c0019 | 0/0 | 2628 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0012c0014 | 0/0 | 2628 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4809 | 74 | 25 | 4 | 41 | 0 | 2 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0001t0002 | 0/0 | 4807 | 2 | 0 | 0 | 1 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0001t0005 | 0/0 | 4807 | 3 | 3 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0001t0006 | 0/0 | 4809 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0001t0008 | 0/0 | 4807 | 3 | 0 | 2 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0001t0013 | 0/0 | 4809 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0001t0015 | 0/0 | 4809 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0001t0017 | 0/0 | 4809 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0001t0023 | 0/0 | 4809 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0004t0001 | 0/0 | 4809 | 51 | 11 | 2 | 34 | 0 | 4 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0004t0007 | 0/0 | 4809 | 2 | 0 | 0 | 0 | 0 | 2 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0004t0012 | 0/0 | 4809 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0004t0014 | 0/0 | 4809 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0004t0020 | 0/0 | 4809 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0006t0001 | 0/0 | 4809 | 8 | 0 | 1 | 7 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0008t0001 | 0/0 | 4809 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0008t0019 | 0/0 | 4809 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0009t0001 | 0/0 | 4809 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0009t0009 | 0/0 | 4809 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0001c0021t0021 | 0/0 | 4809 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002c0002t0001 | 0/0 | 4809 | 79 | 16 | 20 | 36 | 4 | 3 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002c0002t0007 | 0/0 | 4809 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002c0002t0016 | 0/0 | 4809 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002c0002t0018 | 0/0 | 4809 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002c0002t0022 | 0/0 | 4809 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002c0003t0001 | 0/0 | 4809 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002c0003t0002 | 0/0 | 4807 | 55 | 2 | 19 | 20 | 3 | 11 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002c0003t0003 | 0/0 | 4809 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002c0017t0002 | 0/0 | 4807 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002c0018t0002 | 0/0 | 4807 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0002c0020t0001 | 0/0 | 4809 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0003c0005t0003 | 0/0 | 4809 | 35 | 2 | 4 | 16 | 2 | 11 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0003c0005t0004 | 0/0 | 4809 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0003c0005t0010 | 0/0 | 4809 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0003c0005t0011 | 0/0 | 4809 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0003c0005t0024 | 0/0 | 4809 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0004c0007t0001 | 0/0 | 4809 | 4 | 1 | 3 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0005c0010t0001 | 0/0 | 4809 | 3 | 2 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0006c0011t0001 | 0/0 | 4809 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0007c0012t0003 | 0/0 | 4809 | 2 | 0 | 2 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0008c0015t0002 | 0/0 | 4807 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0008c0016t0001 | 0/0 | 4809 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0009c0013t0004 | 0/0 | 4809 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0010c0022t0001 | 0/0 | 4809 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0011c0019t0001 | 0/0 | 4809 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
a0012c0014t0001 | 0/0 | 4809 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | copy fasta | chr4 | 118275038 | 118358003 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0199 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0008g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0008g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0008g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0013g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0015g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0017g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0023g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0007g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0007g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0012g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0014g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0020g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0006t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0006t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0006t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0006t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0006t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0006t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0006t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0006t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0008t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0008t0019g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0009t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0009t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0009t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0009t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0021t0021g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0002 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0007g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0016g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0018g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0022g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0003 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0005 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0009 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0017t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0018t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0020t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0010g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0010g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0011g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0024g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0004c0007t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0004c0007t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0004c0007t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0004c0007t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0005c0010t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0006c0011t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0006c0011t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0007c0012t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0007c0012t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0008c0015t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0008c0016t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0009c0013t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0009c0013t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0010c0022t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0011c0019t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0012c0014t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0005 | t0003 | g0229 | EUR | GBR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0070 | EUR | GBR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0078 | EUR | FIN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00323 | hp2 | a0002 | c0003 | t0002 | g0009 | EUR | FIN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00408 | hp1 | a0002 | c0003 | t0002 | g0137 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00408 | hp2 | a0002 | c0003 | t0002 | g0129 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00438 | hp1 | a0001 | c0006 | t0001 | g0285 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00438 | hp2 | a0002 | c0017 | t0002 | g0110 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00544 | hp2 | a0001 | c0004 | t0001 | g0274 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00597 | hp2 | a0003 | c0005 | t0003 | g0220 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00609 | hp1 | a0001 | c0006 | t0001 | g0284 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00621 | hp2 | a0001 | c0004 | t0001 | g0279 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00639 | hp1 | a0005 | c0010 | t0001 | g0014 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00639 | hp2 | a0002 | c0003 | t0002 | g0141 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00642 | hp2 | a0002 | c0003 | t0002 | g0135 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00673 | hp1 | a0001 | c0004 | t0001 | g0245 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00673 | hp2 | a0002 | c0003 | t0002 | g0003 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00733 | hp2 | a0002 | c0003 | t0002 | g0016 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00735 | hp1 | a0001 | c0001 | t0008 | g0295 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00738 | hp1 | a0001 | c0004 | t0001 | g0210 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00738 | hp2 | a0002 | c0003 | t0002 | g0142 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00741 | hp1 | a0002 | c0003 | t0002 | g0016 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00741 | hp2 | a0004 | c0007 | t0001 | g0107 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01071 | hp1 | a0002 | c0003 | t0002 | g0117 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01074 | hp1 | a0002 | c0003 | t0002 | g0144 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01074 | hp2 | a0001 | c0004 | t0012 | g0205 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0049 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01109 | hp2 | a0001 | c0006 | t0001 | g0278 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01167 | hp1 | a0007 | c0012 | t0003 | g0239 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0076 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01169 | hp1 | a0007 | c0012 | t0003 | g0237 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0081 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01175 | hp1 | a0002 | c0003 | t0002 | g0115 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0051 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01192 | hp1 | a0004 | c0007 | t0001 | g0106 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01192 | hp2 | a0002 | c0003 | t0002 | g0138 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01243 | hp1 | a0002 | c0003 | t0002 | g0132 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01255 | hp1 | a0003 | c0005 | t0003 | g0213 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01255 | hp2 | a0001 | c0004 | t0001 | g0255 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01256 | hp1 | a0003 | c0005 | t0003 | g0034 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01261 | hp1 | a0002 | c0003 | t0002 | g0134 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01261 | hp2 | a0002 | c0003 | t0002 | g0133 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01346 | hp1 | a0002 | c0003 | t0002 | g0023 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0055 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01361 | hp2 | a0002 | c0003 | t0002 | g0005 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01433 | hp2 | a0001 | c0001 | t0008 | g0294 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01496 | hp1 | a0004 | c0007 | t0001 | g0104 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0102 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01517 | hp1 | a0011 | c0019 | t0001 | g0088 | EUR | IBS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01517 | hp2 | a0003 | c0005 | t0003 | g0228 | EUR | IBS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01884 | hp1 | a0002 | c0003 | t0002 | g0139 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01891 | hp2 | a0003 | c0005 | t0003 | g0232 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0087 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01928 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0090 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01934 | hp2 | a0002 | c0003 | t0002 | g0024 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01975 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01978 | hp2 | a0003 | c0005 | t0003 | g0238 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02027 | hp1 | a0002 | c0003 | t0002 | g0123 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02040 | hp2 | a0002 | c0003 | t0002 | g0011 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02055 | hp1 | a0005 | c0010 | t0001 | g0014 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0056 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02074 | hp2 | a0001 | c0004 | t0001 | g0039 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02080 | hp2 | a0001 | c0004 | t0014 | g0273 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0053 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02148 | hp1 | a0002 | c0002 | t0007 | g0145 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02148 | hp2 | a0002 | c0003 | t0002 | g0112 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02155 | hp1 | a0002 | c0002 | t0016 | g0146 | EAS | CDX | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02155 | hp2 | a0001 | c0004 | t0001 | g0036 | EAS | CDX | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02165 | hp1 | a0001 | c0004 | t0001 | g0036 | EAS | CDX | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02258 | hp1 | a0010 | c0022 | t0001 | g0197 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02258 | hp2 | a0001 | c0004 | t0020 | g0293 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02273 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02280 | hp2 | a0001 | c0004 | t0001 | g0193 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02451 | hp2 | a0001 | c0004 | t0001 | g0246 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02572 | hp1 | a0004 | c0007 | t0001 | g0108 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02572 | hp2 | a0002 | c0003 | t0001 | g0059 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02602 | hp1 | a0002 | c0003 | t0002 | g0127 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02602 | hp2 | a0003 | c0005 | t0011 | g0040 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02630 | hp1 | a0001 | c0004 | t0001 | g0275 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0058 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02647 | hp1 | a0003 | c0005 | t0010 | g0236 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0143 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02698 | hp1 | a0002 | c0003 | t0002 | g0118 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0079 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0105 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02738 | hp2 | a0003 | c0005 | t0003 | g0223 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0198 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02895 | hp2 | a0003 | c0005 | t0010 | g0235 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02896 | hp2 | a0001 | c0004 | t0001 | g0258 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02922 | hp1 | a0003 | c0005 | t0004 | g0211 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02922 | hp2 | a0001 | c0004 | t0001 | g0179 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0050 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02970 | hp2 | a0006 | c0011 | t0001 | g0148 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02976 | hp2 | a0006 | c0011 | t0001 | g0190 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03017 | hp1 | a0003 | c0005 | t0003 | g0224 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03017 | hp2 | a0002 | c0003 | t0002 | g0009 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03041 | hp1 | a0001 | c0009 | t0009 | g0043 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03041 | hp2 | a0012 | c0014 | t0001 | g0044 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03098 | hp1 | a0001 | c0004 | t0001 | g0180 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0101 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03139 | hp1 | a0001 | c0009 | t0001 | g0289 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0062 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03195 | hp2 | a0001 | c0009 | t0001 | g0204 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0069 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03209 | hp2 | a0001 | c0001 | t0017 | g0182 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03239 | hp1 | a0003 | c0005 | t0003 | g0225 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03486 | hp1 | a0003 | c0005 | t0024 | g0300 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03486 | hp2 | a0001 | c0009 | t0009 | g0042 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03491 | hp1 | a0002 | c0003 | t0002 | g0005 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03491 | hp2 | a0001 | c0004 | t0001 | g0271 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03492 | hp1 | a0008 | c0016 | t0001 | g0045 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03492 | hp2 | a0002 | c0003 | t0002 | g0005 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0061 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03579 | hp2 | a0001 | c0004 | t0001 | g0257 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03654 | hp2 | a0002 | c0003 | t0002 | g0003 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03669 | hp1 | a0001 | c0004 | t0007 | g0268 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03669 | hp2 | a0003 | c0005 | t0003 | g0035 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03688 | hp1 | a0003 | c0005 | t0003 | g0233 | SAS | STU | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03688 | hp2 | a0001 | c0004 | t0001 | g0266 | SAS | STU | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03704 | hp1 | a0001 | c0004 | t0001 | g0192 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03704 | hp2 | a0003 | c0005 | t0003 | g0226 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03710 | hp1 | a0003 | c0005 | t0003 | g0247 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03710 | hp2 | a0002 | c0003 | t0002 | g0023 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0089 | SAS | BEB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03831 | hp2 | a0002 | c0003 | t0002 | g0009 | SAS | BEB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03834 | hp1 | a0001 | c0001 | t0008 | g0296 | SAS | BEB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03834 | hp2 | a0003 | c0005 | t0003 | g0234 | SAS | BEB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03942 | hp1 | a0002 | c0002 | t0022 | g0298 | SAS | BEB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03942 | hp2 | a0003 | c0005 | t0003 | g0248 | SAS | BEB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0113 | SAS | STU | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG04115 | hp2 | a0008 | c0015 | t0002 | g0046 | SAS | STU | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG04184 | hp1 | a0001 | c0001 | t0013 | g0188 | SAS | BEB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG04184 | hp2 | a0002 | c0003 | t0002 | g0119 | SAS | BEB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG04204 | hp1 | a0002 | c0003 | t0002 | g0005 | SAS | STU | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG04204 | hp2 | a0001 | c0004 | t0007 | g0249 | SAS | STU | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG04228 | hp1 | a0001 | c0004 | t0001 | g0272 | SAS | STU | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG04228 | hp2 | a0003 | c0005 | t0003 | g0230 | SAS | STU | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | YRI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18612 | hp1 | a0003 | c0005 | t0003 | g0227 | EAS | CHB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18747 | hp2 | a0003 | c0005 | t0003 | g0219 | EAS | CHB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18906 | hp1 | a0001 | c0021 | t0021 | g0297 | AFR | YRI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18939 | hp1 | a0001 | c0004 | t0001 | g0254 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18943 | hp1 | a0001 | c0004 | t0001 | g0264 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18943 | hp2 | a0001 | c0006 | t0001 | g0287 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18945 | hp1 | a0003 | c0005 | t0003 | g0240 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18946 | hp2 | a0001 | c0004 | t0001 | g0282 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18947 | hp1 | a0001 | c0004 | t0001 | g0037 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18948 | hp1 | a0003 | c0005 | t0003 | g0263 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18948 | hp2 | a0001 | c0004 | t0001 | g0243 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18952 | hp1 | a0001 | c0004 | t0001 | g0281 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18952 | hp2 | a0003 | c0005 | t0003 | g0218 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18953 | hp1 | a0001 | c0004 | t0001 | g0038 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18954 | hp1 | a0001 | c0001 | t0006 | g0177 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18954 | hp2 | a0003 | c0005 | t0003 | g0215 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18957 | hp2 | a0001 | c0004 | t0001 | g0253 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18959 | hp1 | a0001 | c0004 | t0001 | g0265 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18960 | hp1 | a0001 | c0001 | t0006 | g0174 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18960 | hp2 | a0001 | c0006 | t0001 | g0288 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18961 | hp1 | a0002 | c0003 | t0002 | g0130 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18961 | hp2 | a0001 | c0004 | t0001 | g0039 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18962 | hp1 | a0001 | c0004 | t0001 | g0267 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18962 | hp2 | a0002 | c0003 | t0002 | g0122 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18963 | hp1 | a0001 | c0004 | t0001 | g0250 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18963 | hp2 | a0002 | c0003 | t0002 | g0011 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18964 | hp2 | a0001 | c0004 | t0001 | g0252 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18965 | hp1 | a0001 | c0006 | t0001 | g0286 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18965 | hp2 | a0001 | c0004 | t0001 | g0260 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18966 | hp2 | a0003 | c0005 | t0003 | g0222 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18968 | hp2 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18969 | hp1 | a0001 | c0004 | t0001 | g0038 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18969 | hp2 | a0003 | c0005 | t0003 | g0004 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18972 | hp1 | a0003 | c0005 | t0003 | g0004 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18972 | hp2 | a0001 | c0004 | t0001 | g0259 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18973 | hp1 | a0003 | c0005 | t0003 | g0221 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18974 | hp1 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18974 | hp2 | a0003 | c0005 | t0003 | g0217 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18975 | hp1 | a0003 | c0005 | t0003 | g0216 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18975 | hp2 | a0001 | c0004 | t0001 | g0269 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18978 | hp1 | a0002 | c0018 | t0002 | g0128 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18978 | hp2 | a0001 | c0004 | t0001 | g0261 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18979 | hp2 | a0001 | c0004 | t0001 | g0251 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18980 | hp1 | a0002 | c0003 | t0002 | g0010 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18982 | hp1 | a0002 | c0003 | t0002 | g0120 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18982 | hp2 | a0001 | c0004 | t0001 | g0037 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18983 | hp1 | a0001 | c0006 | t0001 | g0283 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18983 | hp2 | a0001 | c0004 | t0001 | g0244 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18987 | hp2 | a0001 | c0001 | t0006 | g0176 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18994 | hp2 | a0001 | c0006 | t0001 | g0277 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18999 | hp2 | a0002 | c0003 | t0002 | g0111 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19000 | hp1 | a0002 | c0003 | t0002 | g0126 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19001 | hp1 | a0002 | c0003 | t0002 | g0010 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19002 | hp1 | a0002 | c0003 | t0002 | g0121 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19002 | hp2 | a0001 | c0004 | t0001 | g0262 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19004 | hp2 | a0002 | c0003 | t0002 | g0124 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19007 | hp1 | a0001 | c0008 | t0019 | g0241 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19007 | hp2 | a0002 | c0003 | t0002 | g0136 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19009 | hp1 | a0001 | c0001 | t0023 | g0299 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19012 | hp2 | a0002 | c0003 | t0002 | g0011 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19030 | hp2 | a0001 | c0004 | t0001 | g0256 | AFR | LWK | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19054 | hp1 | a0002 | c0003 | t0002 | g0024 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19057 | hp2 | a0003 | c0005 | t0003 | g0004 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19062 | hp1 | a0001 | c0004 | t0001 | g0280 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19072 | hp1 | a0001 | c0008 | t0001 | g0012 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19072 | hp2 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19074 | hp1 | a0003 | c0005 | t0003 | g0004 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19075 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19076 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19078 | hp1 | a0002 | c0003 | t0002 | g0125 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19078 | hp2 | a0001 | c0004 | t0001 | g0270 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19079 | hp2 | a0002 | c0003 | t0002 | g0010 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19081 | hp1 | a0001 | c0004 | t0001 | g0242 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19082 | hp1 | a0003 | c0005 | t0003 | g0004 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19082 | hp2 | a0001 | c0008 | t0001 | g0012 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19084 | hp2 | a0001 | c0001 | t0015 | g0168 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19085 | hp1 | a0001 | c0008 | t0001 | g0012 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19085 | hp2 | a0002 | c0020 | t0001 | g0100 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19089 | hp2 | a0002 | c0003 | t0003 | g0131 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19240 | hp1 | a0003 | c0005 | t0004 | g0212 | AFR | YRI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19240 | hp2 | a0005 | c0010 | t0001 | g0014 | AFR | YRI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20129 | hp1 | a0009 | c0013 | t0004 | g0291 | AFR | ASW | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ASW | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0103 | EUR | TSI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20752 | hp2 | a0002 | c0003 | t0002 | g0109 | EUR | TSI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0022 | EUR | TSI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20805 | hp2 | a0002 | c0003 | t0002 | g0114 | EUR | TSI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20905 | hp1 | a0003 | c0005 | t0003 | g0035 | SAS | GIH | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20905 | hp2 | a0002 | c0003 | t0002 | g0116 | SAS | GIH | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0022 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01123 | hp2 | a0003 | c0005 | t0003 | g0231 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02109 | hp1 | a0002 | c0003 | t0002 | g0140 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02109 | hp2 | a0009 | c0013 | t0004 | g0292 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02486 | hp1 | a0002 | c0002 | t0018 | g0080 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0041 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0052 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03471 | hp1 | a0001 | c0004 | t0001 | g0195 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03471 | hp2 | a0001 | c0004 | t0001 | g0162 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20300 | hp1 | a0003 | c0005 | t0003 | g0034 | AFR | USA | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | USA | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0063 | AFR | LWK | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0152 | REF | REF | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0199 | REF | REF | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:118282066
|
C | T | 1 | a0004 | 4 | HG00741.hp2 HG01192.hp1 HG01496.hp1 others(1): Show |
missense_variant | MODERATE | c.2498G>A | p.Arg833Gln | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 2781/4809 | 2498/2628 | 833/875 | chr4 | 118282066 | ||
chr4:118282171
|
T | C | 1 | a0011 | 1 | HG01517.hp1 | missense_variant | MODERATE | c.2393A>G | p.Tyr798Cys | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 2676/4809 | 2393/2628 | 798/875 | chr4 | 118282171 | ||
chr4:118295806
|
G | A | 1 | a0007 | 2 | HG01167.hp1 HG01169.hp1 |
missense_variant | MODERATE | c.1888C>T | p.Arg630Trp | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 10/13 | 2171/4809 | 1888/2628 | 630/875 | chr4 | 118295806 | ||
chr4:118298754
|
C | A | 4 | a0003a0006a0007others(1): Show | 47 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(44): Show |
missense_variant | MODERATE | c.1816G>T | p.Ala606Ser | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/13 | 2099/4809 | 1816/2628 | 606/875 | chr4 | 118298754 | ||
chr4:118316204
|
C | T | 1 | a0006 | 2 | HG02970.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.1270G>A | p.Val424Ile | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/13 | 1553/4809 | 1270/2628 | 424/875 | chr4 | 118316204 | ||
chr4:118338254
|
C | T | 1 | a0010 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.563G>A | p.Ser188Asn | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/13 | 846/4809 | 563/2628 | 188/875 | chr4 | 118338254 | ||
chr4:118352281
|
G | A | 1 | a0005 | 3 | HG00639.hp1 HG02055.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.440C>T | p.Pro147Leu | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 723/4809 | 440/2628 | 147/875 | chr4 | 118352281 | ||
chr4:118352405
|
C | G | 1 | a0008 | 2 | HG03492.hp1 HG04115.hp2 |
missense_variant | MODERATE | c.316G>C | p.Gly106Arg | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 599/4809 | 316/2628 | 106/875 | chr4 | 118352405 | ||
chr4:118352557
|
C | G | 4 | a0002a0004a0008others(1): Show | 150 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
missense_variant | MODERATE | c.164G>C | p.Arg55Thr | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 447/4809 | 164/2628 | 55/875 | chr4 | 118352557 | ||
chr4:118352657
|
C | G | 1 | a0012 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.64G>C | p.Asp22His | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 347/4809 | 64/2628 | 22/875 | chr4 | 118352657 | ||
chr4:118352693
|
G | C | 1 | a0009 | 2 | HG02109.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.28C>G | p.Leu10Val | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 311/4809 | 28/2628 | 10/875 | chr4 | 118352693 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:118281996
|
A | T | 1 | a0001c0008 | 4 | NA19007.hp1 NA19072.hp1 NA19082.hp2 others(1): Show |
synonymous_variant | LOW | c.2568T>A | p.Pro856Pro | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 2851/4809 | 2568/2628 | 856/875 | chr4 | 118281996 | ||
chr4:118282029
|
G | A | 1 | a0002c0017 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.2535C>T | p.Ser845Ser | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 2818/4809 | 2535/2628 | 845/875 | chr4 | 118282029 | ||
chr4:118298797
|
G | A | 1 | a0001c0009 | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.1773C>T | p.His591His | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/13 | 2056/4809 | 1773/2628 | 591/875 | chr4 | 118298797 | ||
chr4:118313334
|
G | A | 1 | a0002c0018 | 1 | NA18978.hp1 | synonymous_variant | LOW | c.1356C>T | p.Asp452Asp | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/13 | 1639/4809 | 1356/2628 | 452/875 | chr4 | 118313334 | ||
chr4:118316193
|
T | C | 12 | a0001c0004a0001c0009a0001c0021others(9): Show | 198 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(195): Show |
synonymous_variant | LOW | c.1281A>G | p.Gln427Gln | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/13 | 1564/4809 | 1281/2628 | 427/875 | chr4 | 118316193 | ||
chr4:118316202
|
A | C | 1 | a0001c0006 | 8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
synonymous_variant | LOW | c.1272T>G | p.Val424Val | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/13 | 1555/4809 | 1272/2628 | 424/875 | chr4 | 118316202 | ||
chr4:118318384
|
G | A | 1 | a0002c0020 | 1 | NA19085.hp2 | synonymous_variant | LOW | c.1144C>T | p.Leu382Leu | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/13 | 1427/4809 | 1144/2628 | 382/875 | chr4 | 118318384 | ||
chr4:118352412
|
C | G | 1 | a0001c0021 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.309G>C | p.Thr103Thr | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 592/4809 | 309/2628 | 103/875 | chr4 | 118352412 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:118280071
|
A | G | 1 | a0002c0002t0016 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1865T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1865 | chr4 | 118280071 | |||||
chr4:118280091
|
A | G | 1 | a0003c0005t0011 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1845T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1845 | chr4 | 118280091 | |||||
chr4:118280171
|
G | A | 1 | a0001c0001t0017 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1765C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1765 | chr4 | 118280171 | |||||
chr4:118280243
|
T | G | 1 | a0002c0002t0018 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1693A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1693 | chr4 | 118280243 | |||||
chr4:118280296
|
T | C | 1 | a0001c0008t0019 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1640A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1640 | chr4 | 118280296 | |||||
chr4:118280341
|
T | C | 1 | a0001c0004t0012 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1595A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1595 | chr4 | 118280341 | |||||
chr4:118280374
|
A | G | 1 | a0001c0001t0006 | 3 | NA18954.hp1 NA18960.hp1 NA18987.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1562T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1562 | chr4 | 118280374 | |||||
chr4:118280376
|
GTT | G | 7 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(4): Show | 66 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1558_*1559delAA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1558 | chr4 | 118280376 | |||||
chr4:118280389
|
A | T | 1 | a0001c0001t0015 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1547T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1547 | chr4 | 118280389 | |||||
chr4:118280432
|
C | T | 4 | a0002c0003t0003a0003c0005t0003a0003c0005t0011others(1): Show | 39 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1504G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1504 | chr4 | 118280432 | |||||
chr4:118280679
|
A | G | 1 | a0001c0021t0021 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1257T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1257 | chr4 | 118280679 | |||||
chr4:118280731
|
A | G | 1 | a0001c0004t0014 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1205T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1205 | chr4 | 118280731 | |||||
chr4:118280795
|
A | G | 1 | a0001c0001t0013 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1141T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1141 | chr4 | 118280795 | |||||
chr4:118280803
|
C | A | 1 | a0001c0021t0021 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1133G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1133 | chr4 | 118280803 | |||||
chr4:118281024
|
C | T | 1 | a0003c0005t0010 | 2 | HG02647.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*912G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 912 | chr4 | 118281024 | |||||
chr4:118281129
|
C | T | 2 | a0001c0004t0012a0001c0004t0020 | 2 | HG01074.hp2 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*807G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 807 | chr4 | 118281129 | |||||
chr4:118281264
|
G | A | 3 | a0003c0005t0004a0003c0005t0024a0009c0013t0004 | 5 | HG02109.hp2 HG02922.hp1 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*672C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 672 | chr4 | 118281264 | |||||
chr4:118281292
|
T | C | 1 | a0001c0021t0021 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*644A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 644 | chr4 | 118281292 | |||||
chr4:118281517
|
T | C | 1 | a0001c0021t0021 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*419A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 419 | chr4 | 118281517 | |||||
chr4:118281728
|
G | A | 2 | a0001c0004t0007a0002c0002t0007 | 3 | HG02148.hp1 HG03669.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*208C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 208 | chr4 | 118281728 | |||||
chr4:118352777
|
A | G | 2 | a0001c0001t0005a0001c0009t0009 | 5 | HG02486.hp2 HG02886.hp2 HG03041.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-57T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 57 | chr4 | 118352777 | |||||
chr4:118352793
|
G | C | 2 | a0001c0001t0008a0001c0004t0020 | 4 | HG00735.hp1 HG01433.hp2 HG02258.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-73C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 73 | chr4 | 118352793 | |||||
chr4:118352878
|
C | T | 1 | a0003c0005t0011 | 1 | HG02602.hp2 | 5_prime_UTR_variant | MODIFIER | c.-158G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 158 | chr4 | 118352878 | |||||
chr4:118352885
|
T | G | 1 | a0001c0021t0021 | 1 | NA18906.hp1 | 5_prime_UTR_variant | MODIFIER | c.-165A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 165 | chr4 | 118352885 | |||||
chr4:118352887
|
G | A | 1 | a0002c0002t0022 | 1 | HG03942.hp1 | 5_prime_UTR_variant | MODIFIER | c.-167C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 167 | chr4 | 118352887 | |||||
chr4:118352987
|
G | A | 1 | a0001c0001t0023 | 1 | NA19009.hp1 | 5_prime_UTR_variant | MODIFIER | c.-267C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 267 | chr4 | 118352987 | |||||
chr4:118353002
|
G | A | 1 | a0003c0005t0024 | 1 | HG03486.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-282C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | chr4 | 118353002 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:118282288
|
C | T | 1 | a0003c0005t0003g0226 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2321-45G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 12/12 | chr4 | 118282288 | ||||||
chr4:118282324
|
T | C | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2321-81A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 12/12 | chr4 | 118282324 | ||||||
chr4:118282553
|
A | C | 157 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(154): Show | 183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.2320+278T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 12/12 | chr4 | 118282553 | ||||||
chr4:118282678
|
A | G | 8 | a0001c0006t0001g0277a0001c0006t0001g0278a0001c0006t0001g0283others(5): Show | 8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2320+153T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 12/12 | chr4 | 118282678 | ||||||
chr4:118282693
|
A | C | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2320+138T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 12/12 | chr4 | 118282693 | ||||||
chr4:118283203
|
C | G | 1 | a0002c0002t0001g0097 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2040-92G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283203 | ||||||
chr4:118283311
|
T | C | 173 | a0001c0001t0001g0149a0001c0004t0001g0013a0001c0004t0001g0036others(170): Show | 199 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.2040-200A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283311 | ||||||
chr4:118283390
|
C | G | 1 | a0001c0004t0020g0293 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2040-279G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283390 | ||||||
chr4:118283517
|
A | G | 1 | a0002c0002t0001g0018 | 2 | NA18984.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2040-406T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283517 | ||||||
chr4:118283535
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2040-424C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283535 | ||||||
chr4:118283565
|
A | C | 182 | a0001c0001t0001g0149a0001c0004t0001g0013a0001c0004t0001g0036others(179): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2040-454T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283565 | ||||||
chr4:118283696
|
G | A | 47 | a0001c0001t0002g0214a0001c0001t0002g0290a0001c0001t0008g0294others(44): Show | 63 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.2040-585C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283696 | ||||||
chr4:118283862
|
G | A | 8 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(5): Show | 8 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2040-751C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283862 | ||||||
chr4:118283888
|
C | T | 8 | a0001c0006t0001g0277a0001c0006t0001g0278a0001c0006t0001g0283others(5): Show | 8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2040-777G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283888 | ||||||
chr4:118283934
|
A | C | 1 | a0002c0003t0002g0111 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2040-823T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283934 | ||||||
chr4:118283943
|
AATTG | A | 9 | a0001c0001t0001g0149a0001c0006t0001g0277a0001c0006t0001g0278others(6): Show | 9 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2040-836_2040-833d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283943 | ||||||
chr4:118283979
|
T | C | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2040-868A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283979 | ||||||
chr4:118284048
|
C | T | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2040-937G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284048 | ||||||
chr4:118284281
|
C | T | 1 | a0001c0004t0001g0251 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2040-1170G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284281 | ||||||
chr4:118284439
|
A | G | 2 | a0006c0011t0001g0148a0006c0011t0001g0190 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2040-1328T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284439 | ||||||
chr4:118284460
|
CCT | C | 3 | a0001c0004t0001g0255a0001c0004t0001g0257a0001c0004t0001g0258 | 3 | HG01255.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2040-1351_2040-135 others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284460 | ||||||
chr4:118284514
|
T | A | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2040-1403A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284514 | ||||||
chr4:118284566
|
A | C | 1 | a0001c0004t0001g0275 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2040-1455T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284566 | ||||||
chr4:118284608
|
T | C | 9 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(6): Show | 9 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2040-1497A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284608 | ||||||
chr4:118284696
|
A | T | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2040-1585T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284696 | ||||||
chr4:118284723
|
A | G | 115 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(112): Show | 135 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.2040-1612T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284723 | ||||||
chr4:118284962
|
C | G | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2040-1851G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284962 | ||||||
chr4:118285062
|
G | A | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2040-1951C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118285062 | ||||||
chr4:118285083
|
C | T | 1 | a0002c0002t0001g0096 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2040-1972G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118285083 | ||||||
chr4:118285386
|
T | G | 2 | a0006c0011t0001g0148a0006c0011t0001g0190 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2040-2275A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118285386 | ||||||
chr4:118285663
|
GA | G | 6 | a0002c0002t0001g0022a0003c0005t0004g0211a0003c0005t0004g0212others(3): Show | 7 | HG01123.hp1 HG02109.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2040-2553delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118285663 | ||||||
chr4:118285952
|
A | C | 17 | a0001c0004t0001g0038a0001c0004t0001g0279a0001c0004t0001g0280others(14): Show | 19 | HG00621.hp2 HG02080.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.2040-2841T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118285952 | ||||||
chr4:118285993
|
A | G | 1 | a0001c0001t0017g0182 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2040-2882T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118285993 | ||||||
chr4:118286145
|
A | G | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2040-3034T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118286145 | ||||||
chr4:118286375
|
G | A | 8 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(5): Show | 8 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2040-3264C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118286375 | ||||||
chr4:118286397
|
C | G | 1 | a0001c0001t0001g0209 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2040-3286G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118286397 | ||||||
chr4:118286489
|
C | T | 1 | a0003c0005t0003g0227 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2040-3378G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118286489 | ||||||
chr4:118286706
|
T | C | 1 | a0012c0014t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2040-3595A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118286706 | ||||||
chr4:118286868
|
C | G | 1 | a0001c0004t0001g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2040-3757G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118286868 | ||||||
chr4:118286891
|
T | G | 1 | a0003c0005t0024g0300 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2040-3780A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118286891 | ||||||
chr4:118286917
|
T | G | 2 | a0003c0005t0010g0235a0003c0005t0010g0236 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2040-3806A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118286917 | ||||||
chr4:118287053
|
A | T | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2040-3942T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118287053 | ||||||
chr4:118287141
|
A | G | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2040-4030T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118287141 | ||||||
chr4:118287147
|
C | T | 173 | a0001c0001t0001g0149a0001c0004t0001g0013a0001c0004t0001g0036others(170): Show | 199 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.2040-4036G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118287147 | ||||||
chr4:118287207
|
C | T | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2040-4096G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118287207 | ||||||
chr4:118287274
|
C | T | 2 | a0001c0004t0001g0243a0002c0002t0001g0068 | 2 | NA18948.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2040-4163G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118287274 | ||||||
chr4:118287286
|
C | A | 1 | a0001c0001t0001g0032 | 2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2040-4175G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118287286 | ||||||
chr4:118288108
|
C | T | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2040-4997G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288108 | ||||||
chr4:118288170
|
T | C | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2040-5059A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288170 | ||||||
chr4:118288183
|
G | T | 8 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(5): Show | 8 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2040-5072C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288183 | ||||||
chr4:118288229
|
T | C | 1 | a0011c0019t0001g0088 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2040-5118A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288229 | ||||||
chr4:118288287
|
CACAAATA others(9): Show |
C | 1 | a0002c0002t0001g0048 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2040-5192_2040-517 others(20): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288287 | ||||||
chr4:118288336
|
T | C | 1 | a0002c0002t0001g0022 | 2 | HG01123.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2040-5225A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288336 | ||||||
chr4:118288350
|
G | A | 2 | a0003c0005t0010g0235a0003c0005t0010g0236 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2040-5239C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288350 | ||||||
chr4:118288393
|
G | A | 1 | a0001c0004t0001g0275 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2040-5282C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288393 | ||||||
chr4:118288772
|
C | T | 7 | a0001c0006t0001g0277a0001c0006t0001g0283a0001c0006t0001g0284others(4): Show | 7 | HG00438.hp1 HG00609.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.2040-5661G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288772 | ||||||
chr4:118288881
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2040-5770T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288881 | ||||||
chr4:118288978
|
G | A | 2 | a0002c0003t0002g0132a0002c0003t0002g0133 | 2 | HG01243.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2040-5867C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288978 | ||||||
chr4:118289271
|
C | T | 9 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(6): Show | 9 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2039+5668G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118289271 | ||||||
chr4:118290001
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2039+4938G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290001 | ||||||
chr4:118290006
|
A | G | 2 | a0006c0011t0001g0148a0006c0011t0001g0190 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2039+4933T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290006 | ||||||
chr4:118290045
|
C | T | 3 | a0002c0003t0002g0111a0002c0003t0002g0112a0002c0003t0002g0129 | 3 | HG00408.hp2 HG02148.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.2039+4894G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290045 | ||||||
chr4:118290115
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2039+4824G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290115 | ||||||
chr4:118290119
|
G | T | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2039+4820C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290119 | ||||||
chr4:118290134
|
T | C | 3 | a0003c0005t0003g0231a0003c0005t0003g0232a0003c0005t0003g0233 | 3 | HG01123.hp2 HG01891.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2039+4805A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290134 | ||||||
chr4:118290217
|
A | G | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2039+4722T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290217 | ||||||
chr4:118290218
|
T | C | 2 | a0003c0005t0010g0235a0003c0005t0010g0236 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2039+4721A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290218 | ||||||
chr4:118290823
|
T | C | 231 | a0001c0001t0001g0149a0001c0001t0002g0214a0001c0001t0002g0290others(228): Show | 274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.2039+4116A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290823 | ||||||
chr4:118290830
|
A | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0025others(43): Show | 63 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.2039+4109T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290830 | ||||||
chr4:118290948
|
T | C | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2039+3991A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290948 | ||||||
chr4:118291076
|
CT | C | 5 | a0003c0005t0004g0211a0003c0005t0004g0212a0003c0005t0024g0300others(2): Show | 5 | HG02109.hp2 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2039+3862delA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118291076 | ||||||
chr4:118291197
|
A | C | 6 | a0002c0002t0001g0017a0002c0002t0001g0050a0002c0002t0001g0060others(3): Show | 7 | HG01243.hp2 HG02451.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2039+3742T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118291197 | ||||||
chr4:118291288
|
T | C | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2039+3651A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118291288 | ||||||
chr4:118291295
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2039+3644A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118291295 | ||||||
chr4:118291714
|
C | A | 1 | a0001c0004t0001g0266 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2039+3225G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118291714 | ||||||
chr4:118291756
|
G | A | 1 | a0002c0002t0001g0086 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2039+3183C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118291756 | ||||||
chr4:118291796
|
A | G | 2 | a0003c0005t0004g0211a0003c0005t0004g0212 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2039+3143T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118291796 | ||||||
chr4:118292188
|
A | G | 8 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(5): Show | 8 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2039+2751T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292188 | ||||||
chr4:118292275
|
T | C | 1 | a0002c0002t0001g0093 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2039+2664A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292275 | ||||||
chr4:118292374
|
G | C | 2 | a0003c0005t0003g0221a0003c0005t0003g0222 | 2 | NA18966.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2039+2565C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292374 | ||||||
chr4:118292380
|
G | T | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2039+2559C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292380 | ||||||
chr4:118292544
|
G | A | 1 | a0003c0005t0003g0223 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2039+2395C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292544 | ||||||
chr4:118292610
|
C | T | 1 | a0002c0003t0002g0125 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2039+2329G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292610 | ||||||
chr4:118292613
|
A | C | 1 | a0002c0002t0001g0048 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2039+2326T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292613 | ||||||
chr4:118292630
|
T | C | 6 | a0002c0003t0002g0023a0002c0003t0002g0109a0002c0003t0002g0114others(3): Show | 7 | HG01071.hp1 HG01175.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.2039+2309A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292630 | ||||||
chr4:118292737
|
T | C | 1 | a0001c0004t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2039+2202A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292737 | ||||||
chr4:118292874
|
G | A | 1 | a0002c0002t0001g0085 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2039+2065C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292874 | ||||||
chr4:118292875
|
C | T | 1 | a0002c0002t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2039+2064G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292875 | ||||||
chr4:118292968
|
T | C | 1 | a0002c0002t0016g0146 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2039+1971A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292968 | ||||||
chr4:118293018
|
A | AAAT | 3 | a0002c0002t0001g0097a0003c0005t0010g0235a0003c0005t0010g0236 | 3 | HG00609.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2039+1918_2039+192 others(7): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118293018 | ||||||
chr4:118293167
|
T | G | 1 | a0002c0002t0001g0020 | 2 | NA19001.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2039+1772A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118293167 | ||||||
chr4:118293776
|
CT | C | 92 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(89): Show | 111 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.2039+1162delA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118293776 | ||||||
chr4:118293957
|
T | C | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2039+982A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118293957 | ||||||
chr4:118293999
|
A | G | 1 | a0002c0003t0002g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2039+940T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118293999 | ||||||
chr4:118294093
|
G | T | 1 | a0001c0006t0001g0287 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2039+846C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294093 | ||||||
chr4:118294157
|
AT | A | 10 | a0003c0005t0003g0004a0003c0005t0003g0215a0003c0005t0003g0216others(7): Show | 14 | HG00597.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2039+781delA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294157 | ||||||
chr4:118294175
|
T | A | 1 | a0003c0005t0003g0234 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2039+764A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294175 | ||||||
chr4:118294267
|
T | C | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2039+672A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294267 | ||||||
chr4:118294392
|
C | T | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2039+547G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294392 | ||||||
chr4:118294412
|
A | G | 164 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(161): Show | 190 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.2039+527T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294412 | ||||||
chr4:118294495
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2039+444A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294495 | ||||||
chr4:118294613
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2039+326G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294613 | ||||||
chr4:118294614
|
G | A | 1 | a0001c0004t0012g0205 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2039+325C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294614 | ||||||
chr4:118294672
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2039+267T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294672 | ||||||
chr4:118294747
|
C | G | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2039+192G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294747 | ||||||
chr4:118294770
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0172 | 2 | HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2039+169T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294770 | ||||||
chr4:118294871
|
G | A | 1 | a0002c0002t0001g0084 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2039+68C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294871 | ||||||
chr4:118294899
|
T | C | 124 | a0001c0001t0001g0149a0001c0004t0001g0013a0001c0004t0001g0036others(121): Show | 144 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.2039+40A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294899 | ||||||
chr4:118295625
|
A | G | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1916+153T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 10/12 | chr4 | 118295625 | ||||||
chr4:118295759
|
C | A | 2 | a0002c0003t0002g0121a0002c0003t0002g0126 | 2 | NA19000.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1916+19G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 10/12 | chr4 | 118295759 | ||||||
chr4:118295900
|
CAG | C | 9 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(6): Show | 9 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1838-46_1838-45del others(2): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118295900 | ||||||
chr4:118295959
|
C | G | 297 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0025others(294): Show | 360 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(357): Show |
intron_variant | MODIFIER | c.1838-103G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118295959 | ||||||
chr4:118296063
|
C | T | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1838-207G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296063 | ||||||
chr4:118296100
|
G | A | 9 | a0001c0001t0001g0149a0001c0006t0001g0277a0001c0006t0001g0278others(6): Show | 9 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1838-244C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296100 | ||||||
chr4:118296419
|
C | T | 9 | a0001c0001t0001g0149a0001c0006t0001g0277a0001c0006t0001g0278others(6): Show | 9 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1838-563G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296419 | ||||||
chr4:118296530
|
T | G | 2 | a0006c0011t0001g0148a0006c0011t0001g0190 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1838-674A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296530 | ||||||
chr4:118296564
|
T | G | 1 | a0001c0006t0001g0285 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1838-708A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296564 | ||||||
chr4:118296686
|
T | C | 8 | a0001c0006t0001g0277a0001c0006t0001g0278a0001c0006t0001g0283others(5): Show | 8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1838-830A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296686 | ||||||
chr4:118296819
|
A | G | 10 | a0003c0005t0003g0004a0003c0005t0003g0215a0003c0005t0003g0216others(7): Show | 14 | HG00597.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.1838-963T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296819 | ||||||
chr4:118296881
|
T | C | 2 | a0001c0004t0001g0193a0001c0004t0001g0195 | 2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1838-1025A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296881 | ||||||
chr4:118296892
|
A | G | 2 | a0003c0005t0010g0235a0003c0005t0010g0236 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1838-1036T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296892 | ||||||
chr4:118297003
|
G | A | 1 | a0002c0002t0001g0085 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1838-1147C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297003 | ||||||
chr4:118297128
|
T | C | 1 | a0001c0006t0001g0283 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1838-1272A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297128 | ||||||
chr4:118297137
|
C | T | 4 | a0002c0003t0002g0114a0002c0003t0002g0115a0002c0003t0002g0117others(1): Show | 4 | HG01071.hp1 HG01175.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1838-1281G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297137 | ||||||
chr4:118297151
|
C | T | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1838-1295G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297151 | ||||||
chr4:118297513
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1837+1220A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297513 | ||||||
chr4:118297525
|
T | C | 1 | a0003c0005t0003g0217 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1837+1208A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297525 | ||||||
chr4:118297635
|
T | C | 2 | a0003c0005t0010g0235a0003c0005t0010g0236 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1837+1098A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297635 | ||||||
chr4:118297701
|
G | C | 1 | a0002c0002t0001g0051 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1837+1032C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297701 | ||||||
chr4:118297818
|
T | C | 1 | a0002c0002t0007g0145 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1837+915A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297818 | ||||||
chr4:118297909
|
G | T | 26 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(23): Show | 30 | HG00544.hp2 HG00673.hp1 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.1837+824C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297909 | ||||||
chr4:118297999
|
G | A | 6 | a0002c0002t0001g0017a0002c0002t0001g0050a0002c0002t0001g0060others(3): Show | 7 | HG01243.hp2 HG02451.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837+734C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297999 | ||||||
chr4:118298013
|
C | T | 50 | a0001c0001t0002g0214a0001c0001t0002g0290a0001c0001t0005g0015others(47): Show | 67 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.1837+720G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298013 | ||||||
chr4:118298024
|
G | A | 1 | a0001c0004t0001g0036 | 2 | HG02155.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1837+709C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298024 | ||||||
chr4:118298032
|
G | A | 48 | a0001c0001t0002g0214a0001c0001t0002g0290a0001c0001t0008g0294others(45): Show | 64 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1837+701C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298032 | ||||||
chr4:118298086
|
C | G | 32 | a0003c0005t0003g0004a0003c0005t0003g0034a0003c0005t0003g0035others(29): Show | 38 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.1837+647G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298086 | ||||||
chr4:118298140
|
C | CA | 22 | a0001c0001t0001g0170a0001c0001t0006g0176a0001c0001t0008g0295others(19): Show | 22 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1837+592dupT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298140 | ||||||
chr4:118298225
|
C | T | 1 | a0001c0001t0001g0152 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1837+508G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298225 | ||||||
chr4:118298345
|
T | G | 8 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(5): Show | 8 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1837+388A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298345 | ||||||
chr4:118298428
|
G | A | 1 | a0002c0003t0002g0119 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1837+305C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298428 | ||||||
chr4:118298529
|
T | C | 231 | a0001c0001t0001g0149a0001c0001t0002g0214a0001c0001t0002g0290others(228): Show | 274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1837+204A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298529 | ||||||
chr4:118298957
|
T | C | 1 | a0003c0005t0003g0218 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1632-19A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118298957 | ||||||
chr4:118298964
|
G | T | 1 | a0002c0003t0002g0138 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1632-26C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118298964 | ||||||
chr4:118299199
|
C | T | 1 | a0001c0004t0001g0253 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1632-261G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299199 | ||||||
chr4:118299403
|
G | A | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1632-465C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299403 | ||||||
chr4:118299408
|
C | T | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1632-470G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299408 | ||||||
chr4:118299452
|
G | A | 1 | a0002c0002t0001g0096 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1632-514C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299452 | ||||||
chr4:118299466
|
A | G | 2 | a0001c0004t0001g0039a0002c0002t0001g0064 | 3 | HG02074.hp2 NA18961.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1632-528T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299466 | ||||||
chr4:118299542
|
T | G | 1 | a0001c0001t0001g0183 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1632-604A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299542 | ||||||
chr4:118299548
|
C | T | 1 | a0002c0003t0002g0133 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1632-610G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299548 | ||||||
chr4:118299689
|
T | C | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1632-751A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299689 | ||||||
chr4:118299704
|
AAATAAAA others(1): Show |
A | 3 | a0002c0002t0001g0094a0002c0002t0001g0095a0002c0002t0001g0096 | 3 | NA18966.hp1 NA18987.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1632-774_1632-767d others(10): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299704 | ||||||
chr4:118299708
|
AAAAT | A | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | HG02145.hp2 HG02895.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1632-774_1632-771d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299708 | ||||||
chr4:118299712
|
T | TA | 4 | a0001c0009t0001g0289a0001c0009t0009g0042a0001c0009t0009g0043others(1): Show | 4 | HG01071.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1632-775dupT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299712 | ||||||
chr4:118299712
|
T | TAAAATAA others(4): Show |
1 | a0001c0009t0001g0204 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1632-775_1632-774i others(13): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299712 | ||||||
chr4:118299712
|
T | TAAATAAA others(3): Show |
29 | a0001c0001t0002g0290a0002c0003t0002g0003a0002c0003t0002g0005others(26): Show | 43 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1632-784_1632-775d others(12): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299712 | ||||||
chr4:118299712
|
T | TAAATAAA others(8): Show |
10 | a0001c0001t0002g0214a0001c0001t0008g0294a0001c0001t0008g0295others(7): Show | 12 | HG00735.hp1 HG00738.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1632-789_1632-775d others(17): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299712 | ||||||
chr4:118299712
|
T | TAATA | 3 | a0001c0004t0007g0249a0001c0004t0007g0268a0002c0002t0007g0145 | 3 | HG02148.hp1 HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1632-775_1632-774i others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299712 | ||||||
chr4:118299712
|
T | TAATAAAA others(7): Show |
1 | a0001c0004t0001g0257 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1632-775_1632-774i others(16): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299712 | ||||||
chr4:118299712
|
TAAATAAA others(3): Show |
T | 9 | a0001c0001t0001g0149a0001c0006t0001g0277a0001c0006t0001g0278others(6): Show | 9 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1632-784_1632-775d others(12): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299712 | ||||||
chr4:118299727
|
AAAATAAA others(31): Show |
A | 1 | a0002c0002t0001g0093 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1632-827_1632-790d others(40): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299727 | ||||||
chr4:118299732
|
AAAATAAA others(26): Show |
A | 8 | a0001c0004t0001g0210a0002c0002t0001g0051a0002c0002t0001g0052others(5): Show | 8 | HG00738.hp1 HG01175.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1632-827_1632-795d others(35): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299732 | ||||||
chr4:118299737
|
A | AAAAT | 4 | a0001c0001t0001g0028a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 5 | HG02559.hp1 HG03041.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1632-803_1632-800d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299737 | ||||||
chr4:118299737
|
A | AAAATAAA others(12): Show |
2 | a0002c0003t0002g0123a0002c0003t0002g0132 | 2 | HG01243.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1632-800_1632-799i others(21): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299737 | ||||||
chr4:118299737
|
AAAATAAA others(21): Show |
A | 1 | a0002c0002t0001g0058 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1632-827_1632-800d others(30): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299737 | ||||||
chr4:118299741
|
TAAAATAA others(22): Show |
T | 3 | a0002c0002t0001g0094a0002c0002t0001g0095a0002c0002t0001g0096 | 3 | NA18966.hp1 NA18987.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1632-832_1632-804d others(31): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299741 | ||||||
chr4:118299741
|
TAAAATAA others(27): Show |
T | 2 | a0002c0002t0001g0086a0002c0002t0001g0089 | 2 | HG03831.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1632-837_1632-804d others(36): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299741 | ||||||
chr4:118299742
|
AAAAT | A | 7 | a0001c0004t0001g0242a0001c0004t0001g0252a0001c0004t0001g0270others(4): Show | 11 | HG01346.hp2 HG01928.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1632-808_1632-805d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299742 | ||||||
chr4:118299742
|
AAAATAAA others(6): Show |
A | 1 | a0002c0002t0001g0143 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1632-817_1632-805d others(15): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299742 | ||||||
chr4:118299742
|
AAAATAAA others(16): Show |
A | 68 | a0001c0004t0001g0036a0001c0004t0001g0037a0001c0004t0001g0038others(65): Show | 78 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1632-827_1632-805d others(25): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299742 | ||||||
chr4:118299746
|
T | TA | 16 | a0001c0004t0001g0180a0001c0004t0001g0198a0001c0004t0001g0255others(13): Show | 16 | HG00639.hp2 HG01255.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1632-809dupT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299746 | ||||||
chr4:118299746
|
T | TAAAATAA others(4): Show |
3 | a0001c0004t0001g0246a0001c0004t0001g0256a0003c0005t0024g0300 | 3 | HG02451.hp2 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1632-809_1632-808i others(13): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299746 | ||||||
chr4:118299746
|
TAAATAAA others(22): Show |
T | 11 | a0001c0004t0001g0269a0002c0002t0001g0007a0002c0002t0001g0021others(8): Show | 14 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1632-837_1632-809d others(31): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299746 | ||||||
chr4:118299746
|
TAAATAAA others(32): Show |
T | 1 | a0002c0002t0001g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1632-847_1632-809d others(41): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299746 | ||||||
chr4:118299747
|
AAATAAAA others(11): Show |
A | 10 | a0001c0004t0001g0013a0001c0004t0001g0259a0001c0004t0001g0260others(7): Show | 13 | HG01123.hp1 HG01517.hp1 HG03491.hp2 others(10): Show |
intron_variant | MODIFIER | c.1632-827_1632-810d others(20): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299747 | ||||||
chr4:118299750
|
T | A | 2 | a0001c0001t0005g0015a0001c0001t0005g0041 | 3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1632-812A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299750 | ||||||
chr4:118299751
|
A | T | 2 | a0001c0001t0005g0015a0001c0001t0005g0041 | 3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1632-813T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299751 | ||||||
chr4:118299751
|
AAAAT | A | 31 | a0001c0001t0001g0276a0003c0005t0003g0004a0003c0005t0003g0034others(28): Show | 37 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.1632-817_1632-814d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299751 | ||||||
chr4:118299755
|
T | TA | 5 | a0001c0001t0008g0294a0001c0001t0008g0295a0001c0001t0008g0296others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1632-818dupT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299755 | ||||||
chr4:118299755
|
T | TAAAATAA others(17): Show |
1 | a0002c0003t0002g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1632-818_1632-817i others(26): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299755 | ||||||
chr4:118299755
|
T | TAAATA | 41 | a0001c0001t0001g0165a0001c0001t0001g0175a0001c0001t0001g0181others(38): Show | 55 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.1632-822_1632-818d others(7): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299755 | ||||||
chr4:118299755
|
T | TAAATAAA others(3): Show |
2 | a0001c0001t0001g0191a0001c0001t0006g0177 | 2 | HG02257.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1632-818_1632-817i others(12): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299755 | ||||||
chr4:118299759
|
T | A | 9 | a0001c0001t0005g0015a0001c0001t0005g0041a0001c0004t0012g0205others(6): Show | 10 | HG01074.hp2 HG02148.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1632-821A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299759 | ||||||
chr4:118299760
|
A | AAAATT | 13 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030others(10): Show | 18 | HG02165.hp2 NA18939.hp2 NA18945.hp2 others(15): Show |
intron_variant | MODIFIER | c.1632-827_1632-823d others(7): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299760 | ||||||
chr4:118299760
|
A | T | 10 | a0001c0001t0001g0276a0001c0001t0005g0015a0001c0001t0005g0041others(7): Show | 11 | HG01074.hp2 HG02148.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1632-822T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299760 | ||||||
chr4:118299763
|
AT | A | 4 | a0001c0009t0001g0289a0001c0009t0009g0042a0001c0009t0009g0043others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1632-826delA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299763 | ||||||
chr4:118299764
|
T | A | 7 | a0001c0004t0012g0205a0001c0004t0020g0293a0002c0002t0007g0145others(4): Show | 7 | HG01074.hp2 HG02148.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1632-826A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299764 | ||||||
chr4:118299764
|
TTAAATAA others(22): Show |
T | 5 | a0001c0004t0001g0242a0002c0002t0001g0002a0002c0002t0001g0065others(2): Show | 9 | HG01346.hp2 HG01928.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1632-855_1632-827d others(31): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299764 | ||||||
chr4:118299765
|
T | A | 120 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0165others(117): Show | 147 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1632-827A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299765 | ||||||
chr4:118299765
|
T | TAAATA | 20 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0025others(17): Show | 31 | HG01256.hp2 HG01258.hp1 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.1632-832_1632-828d others(7): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299765 | ||||||
chr4:118299765
|
T | TAAATAAA others(3): Show |
3 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0208 | 3 | HG00558.hp1 HG01433.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1632-837_1632-828d others(12): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299765 | ||||||
chr4:118299765
|
T | TAAATAAA others(8): Show |
1 | a0002c0003t0001g0059 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1632-842_1632-828d others(17): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299765 | ||||||
chr4:118299765
|
TAAATAAA others(3): Show |
T | 1 | a0001c0001t0001g0154 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1632-837_1632-828d others(12): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299765 | ||||||
chr4:118299769
|
TA | T | 35 | a0003c0005t0003g0004a0003c0005t0003g0034a0003c0005t0003g0035others(32): Show | 41 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1632-832delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299769 | ||||||
chr4:118299770
|
A | AAAAT | 7 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(4): Show | 7 | HG01255.hp2 HG02451.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1632-836_1632-833d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299770 | ||||||
chr4:118299774
|
TA | T | 83 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(80): Show | 96 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1632-837delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299774 | ||||||
chr4:118299774
|
TAAAATA | T | 4 | a0001c0004t0001g0180a0001c0004t0001g0198a0001c0004t0001g0252others(1): Show | 4 | HG02886.hp1 HG03098.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1632-842_1632-837d others(8): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299774 | ||||||
chr4:118299780
|
A | T | 1 | a0001c0001t0001g0154 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1632-842T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299780 | ||||||
chr4:118299784
|
TA | T | 8 | a0002c0002t0001g0051a0002c0002t0001g0052a0002c0002t0001g0053others(5): Show | 8 | HG01175.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1632-847delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299784 | ||||||
chr4:118299793
|
A | T | 7 | a0001c0004t0001g0210a0002c0002t0001g0093a0002c0002t0001g0094others(4): Show | 7 | HG00738.hp1 NA18941.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.1632-855T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299793 | ||||||
chr4:118299794
|
T | A | 12 | a0001c0004t0001g0210a0001c0004t0001g0242a0002c0002t0001g0002others(9): Show | 16 | HG00738.hp1 HG01346.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.1632-856A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299794 | ||||||
chr4:118299794
|
TAAATAAA others(12): Show |
T | 1 | a0003c0005t0010g0235 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1632-875_1632-857d others(21): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299794 | ||||||
chr4:118299798
|
T | A | 15 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(12): Show | 15 | HG01074.hp2 HG01255.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1632-860A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299798 | ||||||
chr4:118299799
|
A | T | 13 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(10): Show | 13 | HG01255.hp2 HG02451.hp2 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.1632-861T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299799 | ||||||
chr4:118299799
|
AAAATAAA others(2): Show |
A | 4 | a0001c0004t0001g0180a0001c0004t0001g0198a0001c0004t0001g0252others(1): Show | 4 | HG02886.hp1 HG03098.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1632-870_1632-862d others(11): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299799 | ||||||
chr4:118299807
|
A | T | 6 | a0002c0002t0001g0094a0002c0002t0001g0095a0002c0002t0001g0096others(3): Show | 6 | HG02027.hp1 NA18966.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1632-869T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299807 | ||||||
chr4:118299808
|
T | A | 6 | a0002c0002t0001g0094a0002c0002t0001g0095a0002c0002t0001g0096others(3): Show | 6 | HG02027.hp1 NA18966.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1632-870A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299808 | ||||||
chr4:118299808
|
T | TAAATA | 47 | a0001c0001t0001g0025a0001c0001t0001g0147a0001c0001t0001g0167others(44): Show | 64 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1632-875_1632-871d others(7): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299808 | ||||||
chr4:118299808
|
T | TAAATAAA others(3): Show |
4 | a0001c0001t0001g0160a0001c0001t0005g0015a0001c0001t0005g0041others(1): Show | 5 | HG01261.hp2 HG02486.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1632-880_1632-871d others(12): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299808 | ||||||
chr4:118299808
|
T | TAAATAAA others(8): Show |
1 | a0001c0001t0001g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1632-885_1632-871d others(17): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299808 | ||||||
chr4:118299808
|
TAAATA | T | 43 | a0001c0001t0001g0149a0001c0004t0001g0193a0001c0004t0001g0195others(40): Show | 49 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.1632-875_1632-871d others(7): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299808 | ||||||
chr4:118299808
|
TAAATAAA others(3): Show |
T | 8 | a0001c0006t0001g0277a0001c0006t0001g0278a0001c0006t0001g0283others(5): Show | 8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1632-880_1632-871d others(12): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299808 | ||||||
chr4:118299812
|
T | A | 17 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(14): Show | 17 | HG01074.hp2 HG01255.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1632-874A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299812 | ||||||
chr4:118299813
|
A | T | 17 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(14): Show | 17 | HG01074.hp2 HG01255.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1632-875T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299813 | ||||||
chr4:118299998
|
A | T | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1632-1060T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299998 | ||||||
chr4:118300017
|
C | CT | 5 | a0001c0001t0001g0181a0001c0001t0001g0189a0001c0001t0001g0191others(2): Show | 7 | HG00639.hp1 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1632-1080dupA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300017 | ||||||
chr4:118300158
|
A | G | 1 | a0001c0006t0001g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1632-1220T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300158 | ||||||
chr4:118300253
|
T | C | 1 | a0001c0006t0001g0286 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1632-1315A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300253 | ||||||
chr4:118300350
|
G | A | 115 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(112): Show | 135 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.1632-1412C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300350 | ||||||
chr4:118300412
|
T | C | 16 | a0001c0004t0001g0038a0001c0004t0001g0279a0001c0004t0001g0280others(13): Show | 18 | HG00621.hp2 HG02080.hp1 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.1632-1474A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300412 | ||||||
chr4:118300763
|
GAATATAC others(3): Show |
G | 1 | a0002c0003t0003g0131 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1632-1835_1632-182 others(14): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300763 | ||||||
chr4:118300785
|
T | G | 181 | a0001c0001t0001g0149a0001c0004t0001g0013a0001c0004t0001g0036others(178): Show | 207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1632-1847A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300785 | ||||||
chr4:118300824
|
A | G | 91 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(88): Show | 110 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1632-1886T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300824 | ||||||
chr4:118300919
|
C | T | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1632-1981G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300919 | ||||||
chr4:118301038
|
A | C | 34 | a0003c0005t0003g0004a0003c0005t0003g0034a0003c0005t0003g0035others(31): Show | 40 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1632-2100T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301038 | ||||||
chr4:118301066
|
CA | C | 34 | a0003c0005t0003g0004a0003c0005t0003g0034a0003c0005t0003g0035others(31): Show | 40 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1632-2129delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301066 | ||||||
chr4:118301100
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0178a0001c0001t0001g0203 | 8 | NA18940.hp1 NA18941.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.1632-2162G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301100 | ||||||
chr4:118301505
|
C | T | 1 | a0002c0003t0002g0138 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1632-2567G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301505 | ||||||
chr4:118301533
|
GA | G | 8 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(5): Show | 8 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1632-2596delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301533 | ||||||
chr4:118301609
|
C | T | 2 | a0003c0005t0010g0235a0003c0005t0010g0236 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1632-2671G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301609 | ||||||
chr4:118301685
|
A | C | 1 | a0001c0001t0001g0029 | 2 | NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1632-2747T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301685 | ||||||
chr4:118301815
|
T | A | 1 | a0002c0003t0003g0131 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1632-2877A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301815 | ||||||
chr4:118301890
|
T | C | 2 | a0001c0004t0001g0162a0001c0004t0001g0179 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1632-2952A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301890 | ||||||
chr4:118302039
|
A | T | 1 | a0002c0003t0003g0131 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1632-3101T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302039 | ||||||
chr4:118302064
|
G | A | 1 | a0002c0003t0002g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1632-3126C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302064 | ||||||
chr4:118302154
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1632-3216G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302154 | ||||||
chr4:118302197
|
A | G | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1632-3259T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302197 | ||||||
chr4:118302491
|
A | C | 50 | a0001c0001t0002g0214a0001c0001t0002g0290a0001c0001t0005g0015others(47): Show | 67 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.1632-3553T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302491 | ||||||
chr4:118302491
|
A | G | 1 | a0005c0010t0001g0014 | 3 | HG00639.hp1 HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1632-3553T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302491 | ||||||
chr4:118302590
|
C | T | 1 | a0002c0002t0022g0298 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1632-3652G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302590 | ||||||
chr4:118302661
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1632-3723C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302661 | ||||||
chr4:118302674
|
G | A | 8 | a0001c0006t0001g0277a0001c0006t0001g0278a0001c0006t0001g0283others(5): Show | 8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1632-3736C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302674 | ||||||
chr4:118302707
|
G | A | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1632-3769C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302707 | ||||||
chr4:118302765
|
T | C | 8 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(5): Show | 8 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1632-3827A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302765 | ||||||
chr4:118302790
|
T | C | 1 | a0002c0002t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1632-3852A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302790 | ||||||
chr4:118302806
|
TTG | T | 165 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(162): Show | 191 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1632-3870_1632-386 others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302806 | ||||||
chr4:118302926
|
T | C | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1632-3988A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302926 | ||||||
chr4:118302981
|
A | G | 8 | a0001c0006t0001g0277a0001c0006t0001g0278a0001c0006t0001g0283others(5): Show | 8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1632-4043T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302981 | ||||||
chr4:118303012
|
A | C | 1 | a0002c0003t0002g0122 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1632-4074T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118303012 | ||||||
chr4:118303194
|
C | T | 1 | a0003c0005t0003g0240 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1632-4256G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118303194 | ||||||
chr4:118303343
|
C | T | 181 | a0001c0001t0001g0149a0001c0004t0001g0013a0001c0004t0001g0036others(178): Show | 207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1632-4405G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118303343 | ||||||
chr4:118303478
|
A | G | 5 | a0001c0004t0001g0013a0001c0004t0001g0259a0001c0004t0001g0260others(2): Show | 7 | NA18965.hp2 NA18968.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.1632-4540T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118303478 | ||||||
chr4:118303500
|
C | T | 1 | a0002c0003t0002g0137 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1632-4562G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118303500 | ||||||
chr4:118303656
|
T | C | 3 | a0002c0002t0001g0008a0002c0002t0001g0047a0002c0002t0001g0048 | 5 | NA18940.hp2 NA18970.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1632-4718A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118303656 | ||||||
chr4:118303696
|
C | G | 6 | a0002c0002t0001g0022a0002c0002t0001g0049a0002c0002t0001g0079others(3): Show | 7 | HG01109.hp1 HG01123.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1631+4740G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118303696 | ||||||
chr4:118303982
|
CT | C | 8 | a0001c0006t0001g0277a0001c0006t0001g0278a0001c0006t0001g0283others(5): Show | 8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1631+4453delA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118303982 | ||||||
chr4:118304090
|
C | G | 2 | a0003c0005t0010g0235a0003c0005t0010g0236 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1631+4346G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304090 | ||||||
chr4:118304128
|
G | A | 1 | a0001c0004t0001g0271 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1631+4308C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304128 | ||||||
chr4:118304138
|
G | T | 1 | a0002c0003t0003g0131 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1631+4298C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304138 | ||||||
chr4:118304294
|
A | G | 230 | a0001c0001t0001g0149a0001c0001t0002g0214a0001c0001t0002g0290others(227): Show | 273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.1631+4142T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304294 | ||||||
chr4:118304403
|
A | G | 172 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(169): Show | 198 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1631+4033T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304403 | ||||||
chr4:118304410
|
T | C | 1 | a0003c0005t0003g0232 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1631+4026A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304410 | ||||||
chr4:118304572
|
T | A | 1 | a0012c0014t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1631+3864A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304572 | ||||||
chr4:118304574
|
CA | C | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1631+3861delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304574 | ||||||
chr4:118304785
|
C | T | 48 | a0001c0001t0002g0214a0001c0001t0002g0290a0001c0001t0008g0294others(45): Show | 64 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1631+3651G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304785 | ||||||
chr4:118304899
|
A | C | 9 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(6): Show | 9 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1631+3537T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304899 | ||||||
chr4:118305049
|
T | C | 2 | a0003c0005t0004g0211a0003c0005t0004g0212 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1631+3387A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305049 | ||||||
chr4:118305101
|
TTA | T | 17 | a0001c0001t0001g0149a0001c0004t0001g0162a0001c0004t0001g0179others(14): Show | 17 | HG01074.hp2 HG01255.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1631+3333_1631+333 others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305101 | ||||||
chr4:118305118
|
T | C | 2 | a0001c0001t0005g0015a0001c0004t0001g0270 | 3 | HG02886.hp2 HG03516.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1631+3318A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305118 | ||||||
chr4:118305120
|
T | C | 172 | a0001c0001t0002g0214a0001c0001t0002g0290a0001c0001t0005g0015others(169): Show | 213 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.1631+3316A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305120 | ||||||
chr4:118305120
|
T | TAC | 3 | a0002c0002t0001g0081a0003c0005t0003g0227a0003c0005t0003g0263 | 3 | HG01169.hp2 NA18612.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1631+3314_1631+331 others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305120 | ||||||
chr4:118305136
|
C | CAT | 18 | a0003c0005t0003g0034a0003c0005t0003g0213a0003c0005t0003g0216others(15): Show | 19 | HG01123.hp2 HG01255.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.1631+3298_1631+329 others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305136 | ||||||
chr4:118305136
|
C | T | 9 | a0001c0001t0001g0171a0003c0005t0003g0004a0003c0005t0003g0215others(6): Show | 13 | HG00597.hp2 HG01433.hp1 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.1631+3300G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305136 | ||||||
chr4:118305138
|
T | C | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1631+3298A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305138 | ||||||
chr4:118305165
|
T | C | 2 | a0001c0004t0001g0162a0001c0004t0001g0179 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1631+3271A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305165 | ||||||
chr4:118305321
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1631+3115C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305321 | ||||||
chr4:118305505
|
T | C | 1 | a0001c0006t0001g0287 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1631+2931A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305505 | ||||||
chr4:118305520
|
T | C | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1631+2916A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305520 | ||||||
chr4:118305738
|
C | T | 12 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(9): Show | 12 | HG01255.hp2 HG02109.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.1631+2698G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305738 | ||||||
chr4:118305739
|
G | A | 1 | a0002c0002t0001g0064 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1631+2697C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305739 | ||||||
chr4:118306104
|
T | C | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1631+2332A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306104 | ||||||
chr4:118306157
|
A | G | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1631+2279T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306157 | ||||||
chr4:118306161
|
T | C | 1 | a0002c0002t0001g0078 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1631+2275A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306161 | ||||||
chr4:118306258
|
T | C | 1 | a0009c0013t0004g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1631+2178A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306258 | ||||||
chr4:118306318
|
T | C | 1 | a0002c0003t0002g0130 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1631+2118A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306318 | ||||||
chr4:118306336
|
C | A | 1 | a0001c0001t0001g0147 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1631+2100G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306336 | ||||||
chr4:118306377
|
A | G | 9 | a0001c0001t0001g0149a0001c0006t0001g0277a0001c0006t0001g0278others(6): Show | 9 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1631+2059T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306377 | ||||||
chr4:118306441
|
C | T | 3 | a0002c0002t0001g0057a0002c0002t0001g0058a0002c0002t0001g0063 | 3 | HG02630.hp2 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1631+1995G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306441 | ||||||
chr4:118306517
|
C | T | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1631+1919G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306517 | ||||||
chr4:118306534
|
G | A | 3 | a0003c0005t0024g0300a0009c0013t0004g0291a0009c0013t0004g0292 | 3 | HG02109.hp2 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1631+1902C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306534 | ||||||
chr4:118306798
|
G | A | 231 | a0001c0001t0001g0149a0001c0001t0002g0214a0001c0001t0002g0290others(228): Show | 274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1631+1638C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306798 | ||||||
chr4:118307074
|
T | C | 1 | a0002c0002t0001g0087 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1631+1362A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118307074 | ||||||
chr4:118307198
|
T | C | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1631+1238A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118307198 | ||||||
chr4:118307205
|
T | C | 6 | a0002c0002t0001g0022a0002c0002t0001g0049a0002c0002t0001g0079others(3): Show | 7 | HG01109.hp1 HG01123.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1631+1231A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118307205 | ||||||
chr4:118307728
|
C | T | 32 | a0003c0005t0003g0004a0003c0005t0003g0034a0003c0005t0003g0035others(29): Show | 38 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.1631+708G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118307728 | ||||||
chr4:118308315
|
C | T | 3 | a0002c0002t0001g0057a0002c0002t0001g0058a0002c0002t0001g0063 | 3 | HG02630.hp2 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1631+121G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118308315 | ||||||
chr4:118308338
|
G | C | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1631+98C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118308338 | ||||||
chr4:118308412
|
C | G | 1 | a0004c0007t0001g0106 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1631+24G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118308412 | ||||||
chr4:118308584
|
C | T | 1 | a0003c0005t0024g0300 | 1 | HG03486.hp1 | splice_region_variant&intron_variant | LOW | c.1490-7G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118308584 | ||||||
chr4:118308597
|
T | C | 8 | a0001c0006t0001g0277a0001c0006t0001g0278a0001c0006t0001g0283others(5): Show | 8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1490-20A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118308597 | ||||||
chr4:118308822
|
G | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0185 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1490-245C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118308822 | ||||||
chr4:118308856
|
T | C | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1490-279A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118308856 | ||||||
chr4:118308896
|
A | G | 1 | a0001c0006t0001g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1490-319T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118308896 | ||||||
chr4:118308910
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1490-333A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118308910 | ||||||
chr4:118309023
|
A | G | 13 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(10): Show | 13 | HG01255.hp2 HG02109.hp2 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.1490-446T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118309023 | ||||||
chr4:118309184
|
T | C | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1490-607A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118309184 | ||||||
chr4:118309374
|
G | C | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1490-797C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118309374 | ||||||
chr4:118309385
|
A | G | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1490-808T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118309385 | ||||||
chr4:118309474
|
ATC | A | 230 | a0001c0001t0001g0149a0001c0001t0002g0214a0001c0001t0002g0290others(227): Show | 273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.1490-899_1490-898d others(4): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118309474 | ||||||
chr4:118309888
|
T | C | 1 | a0003c0005t0004g0211 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1490-1311A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118309888 | ||||||
chr4:118310181
|
A | C | 1 | a0002c0003t0002g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1490-1604T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310181 | ||||||
chr4:118310467
|
C | G | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1490-1890G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310467 | ||||||
chr4:118310468
|
T | C | 2 | a0006c0011t0001g0148a0006c0011t0001g0190 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1490-1891A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310468 | ||||||
chr4:118310506
|
A | G | 2 | a0002c0002t0001g0094a0002c0002t0001g0095 | 2 | NA18987.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1490-1929T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310506 | ||||||
chr4:118310516
|
T | C | 116 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(113): Show | 136 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.1490-1939A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310516 | ||||||
chr4:118310581
|
T | C | 48 | a0001c0001t0002g0214a0001c0001t0002g0290a0001c0001t0008g0294others(45): Show | 64 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1490-2004A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310581 | ||||||
chr4:118310744
|
C | T | 2 | a0002c0002t0001g0075a0002c0002t0001g0082 | 2 | NA18959.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1490-2167G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310744 | ||||||
chr4:118310879
|
C | T | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1490-2302G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310879 | ||||||
chr4:118310905
|
G | C | 1 | a0003c0005t0004g0212 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1489+2296C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310905 | ||||||
chr4:118310910
|
G | C | 1 | a0008c0015t0002g0046 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1489+2291C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310910 | ||||||
chr4:118311062
|
T | TAATTAAT others(11): Show |
1 | a0001c0006t0001g0288 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1489+2121_1489+213 others(22): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311062 | ||||||
chr4:118311075
|
A | T | 6 | a0002c0002t0001g0017a0002c0002t0001g0050a0002c0002t0001g0060others(3): Show | 7 | HG01243.hp2 HG02451.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1489+2126T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311075 | ||||||
chr4:118311189
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1489+2012G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311189 | ||||||
chr4:118311198
|
C | T | 2 | a0006c0011t0001g0148a0006c0011t0001g0190 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1489+2003G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311198 | ||||||
chr4:118311237
|
A | T | 2 | a0003c0005t0010g0235a0003c0005t0010g0236 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1489+1964T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311237 | ||||||
chr4:118311282
|
T | C | 1 | a0002c0003t0002g0137 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1489+1919A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311282 | ||||||
chr4:118311470
|
G | A | 8 | a0001c0006t0001g0277a0001c0006t0001g0278a0001c0006t0001g0283others(5): Show | 8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1489+1731C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311470 | ||||||
chr4:118311785
|
G | A | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1489+1416C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311785 | ||||||
chr4:118311863
|
T | C | 1 | a0002c0003t0002g0130 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1489+1338A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311863 | ||||||
chr4:118312046
|
G | T | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1489+1155C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118312046 | ||||||
chr4:118312070
|
G | T | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1489+1131C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118312070 | ||||||
chr4:118312312
|
T | C | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1489+889A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118312312 | ||||||
chr4:118312470
|
CATAT | C | 13 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(10): Show | 13 | HG01255.hp2 HG02109.hp2 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.1489+727_1489+730d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118312470 | ||||||
chr4:118312614
|
A | T | 3 | a0002c0002t0001g0094a0002c0002t0001g0095a0002c0002t0001g0096 | 3 | NA18966.hp1 NA18987.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1489+587T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118312614 | ||||||
chr4:118312709
|
T | A | 2 | a0003c0005t0010g0235a0003c0005t0010g0236 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1489+492A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118312709 | ||||||
chr4:118312791
|
T | C | 2 | a0002c0003t0002g0132a0002c0003t0002g0133 | 2 | HG01243.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1489+410A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118312791 | ||||||
chr4:118313102
|
A | G | 14 | a0001c0004t0001g0246a0001c0004t0001g0255a0001c0004t0001g0256others(11): Show | 14 | HG01255.hp2 HG02109.hp2 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.1489+99T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118313102 | ||||||
chr4:118313538
|
C | T | 2 | a0006c0011t0001g0148a0006c0011t0001g0190 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1293-141G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118313538 | ||||||
chr4:118313714
|
A | T | 115 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(112): Show | 135 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.1293-317T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118313714 | ||||||
chr4:118313875
|
T | A | 9 | a0001c0001t0001g0149a0001c0006t0001g0277a0001c0006t0001g0278others(6): Show | 9 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1293-478A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118313875 | ||||||
chr4:118313898
|
C | A | 1 | a0001c0004t0001g0198 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1293-501G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118313898 | ||||||
chr4:118314010
|
C | A | 5 | a0003c0005t0004g0211a0003c0005t0004g0212a0003c0005t0024g0300others(2): Show | 5 | HG02109.hp2 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1293-613G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314010 | ||||||
chr4:118314166
|
C | T | 1 | a0001c0001t0001g0028 | 2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1293-769G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314166 | ||||||
chr4:118314309
|
CT | C | 115 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(112): Show | 135 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.1293-913delA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314309 | ||||||
chr4:118314429
|
C | G | 235 | a0001c0001t0001g0149a0001c0001t0001g0181a0001c0001t0001g0189others(232): Show | 280 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.1293-1032G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314429 | ||||||
chr4:118314688
|
C | T | 2 | a0003c0005t0010g0235a0003c0005t0010g0236 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1293-1291G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314688 | ||||||
chr4:118314690
|
C | T | 115 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(112): Show | 135 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.1293-1293G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314690 | ||||||
chr4:118314714
|
C | T | 1 | a0003c0005t0003g0225 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1293-1317G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314714 | ||||||
chr4:118314814
|
TA | T | 7 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(4): Show | 7 | HG01169.hp2 HG02486.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1292+1367delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314814 | ||||||
chr4:118314983
|
C | A | 1 | a0002c0002t0001g0068 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1292+1199G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314983 | ||||||
chr4:118315098
|
G | A | 181 | a0001c0001t0001g0149a0001c0004t0001g0013a0001c0004t0001g0036others(178): Show | 207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1292+1084C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118315098 | ||||||
chr4:118315182
|
T | C | 32 | a0003c0005t0003g0004a0003c0005t0003g0034a0003c0005t0003g0035others(29): Show | 38 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.1292+1000A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118315182 | ||||||
chr4:118315187
|
T | A | 231 | a0001c0001t0001g0149a0001c0001t0002g0214a0001c0001t0002g0290others(228): Show | 274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1292+995A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118315187 | ||||||
chr4:118315315
|
T | C | 2 | a0001c0001t0005g0015a0001c0001t0005g0041 | 3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1292+867A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118315315 | ||||||
chr4:118315428
|
T | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0178a0001c0001t0001g0203 | 8 | NA18940.hp1 NA18941.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.1292+754A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118315428 | ||||||
chr4:118315655
|
A | T | 1 | a0002c0002t0001g0097 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1292+527T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118315655 | ||||||
chr4:118316159
|
C | T | 2 | a0003c0005t0010g0235a0003c0005t0010g0236 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1292+23G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118316159 | ||||||
chr4:118316533
|
T | C | 2 | a0003c0005t0010g0235a0003c0005t0010g0236 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1151-210A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316533 | ||||||
chr4:118316593
|
AG | A | 34 | a0003c0005t0003g0004a0003c0005t0003g0034a0003c0005t0003g0035others(31): Show | 40 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1151-271delC | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316593 | ||||||
chr4:118316649
|
C | T | 2 | a0006c0011t0001g0148a0006c0011t0001g0190 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1151-326G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316649 | ||||||
chr4:118316727
|
C | T | 3 | a0002c0002t0001g0057a0002c0002t0001g0058a0002c0002t0001g0063 | 3 | HG02630.hp2 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1151-404G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316727 | ||||||
chr4:118316776
|
C | T | 2 | a0002c0003t0002g0010a0002c0003t0002g0136 | 4 | NA18980.hp1 NA19001.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1151-453G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316776 | ||||||
chr4:118316777
|
G | A | 1 | a0001c0001t0013g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1151-454C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316777 | ||||||
chr4:118316808
|
C | T | 8 | a0001c0006t0001g0277a0001c0006t0001g0278a0001c0006t0001g0283others(5): Show | 8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1151-485G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316808 | ||||||
chr4:118316817
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1151-494C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316817 | ||||||
chr4:118316825
|
G | GAAAA | 25 | a0003c0005t0003g0004a0003c0005t0003g0034a0003c0005t0003g0035others(22): Show | 31 | HG00597.hp2 HG01123.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.1151-506_1151-503d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316825 | ||||||
chr4:118316825
|
G | GAAAAA | 7 | a0003c0005t0003g0218a0003c0005t0003g0222a0003c0005t0003g0223others(4): Show | 7 | HG00099.hp1 HG02738.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1151-507_1151-503d others(7): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316825 | ||||||
chr4:118316837
|
A | AAAAAAAA others(7): Show |
1 | a0002c0002t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1151-515_1151-514i others(16): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAAAAA others(9): Show |
1 | a0002c0002t0001g0061 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1151-515_1151-514i others(18): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAAAAA others(6): Show |
1 | a0004c0007t0001g0106 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1151-515_1151-514i others(15): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAAAAA others(5): Show |
6 | a0001c0004t0001g0253a0001c0004t0001g0254a0001c0004t0001g0262others(3): Show | 6 | HG03139.hp2 NA18939.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(14): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAAAAA others(7): Show |
6 | a0001c0004t0001g0192a0002c0002t0001g0017a0002c0002t0001g0050others(3): Show | 7 | HG01243.hp2 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(16): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAAAAA others(13): Show |
1 | a0001c0004t0001g0198 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1151-515_1151-514i others(22): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAAAAT others(4): Show |
3 | a0001c0004t0001g0271a0002c0003t0002g0129a0002c0003t0002g0130 | 3 | HG00408.hp2 HG03491.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1151-515_1151-514i others(13): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAAAAT others(6): Show |
5 | a0001c0004t0001g0260a0001c0004t0001g0261a0002c0002t0001g0087others(2): Show | 5 | HG01928.hp1 HG02080.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(15): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAAAAT others(8): Show |
1 | a0001c0004t0001g0264 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1151-515_1151-514i others(17): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAAAAT others(10): Show |
1 | a0001c0004t0001g0193 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1151-515_1151-514i others(19): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAAAAT others(20): Show |
1 | a0001c0004t0001g0179 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1151-515_1151-514i others(29): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAAATA others(3): Show |
2 | a0001c0004t0001g0242a0011c0019t0001g0088 | 2 | HG01517.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1151-515_1151-514i others(12): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAAATA others(5): Show |
61 | a0001c0001t0005g0041a0001c0004t0001g0013a0001c0004t0001g0036others(58): Show | 76 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(14): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAAATA others(7): Show |
18 | a0001c0004t0001g0180a0001c0004t0001g0250a0001c0004t0001g0259others(15): Show | 19 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(16): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAAATA others(9): Show |
5 | a0001c0004t0001g0195a0001c0004t0001g0210a0002c0002t0001g0099others(2): Show | 5 | HG00738.hp1 HG02922.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(18): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAAATA others(13): Show |
1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1151-515_1151-514i others(22): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAATAT others(4): Show |
21 | a0002c0003t0002g0003a0002c0003t0002g0005a0002c0003t0002g0010others(18): Show | 33 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(13): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAATAT others(6): Show |
5 | a0001c0004t0001g0266a0002c0002t0001g0048a0002c0003t0002g0120others(2): Show | 5 | HG03688.hp2 NA18982.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(15): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAATAT others(10): Show |
3 | a0001c0001t0008g0294a0001c0001t0008g0295a0001c0001t0008g0296 | 3 | HG00735.hp1 HG01433.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1151-515_1151-514i others(19): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAAATAT others(12): Show |
1 | a0001c0001t0002g0214 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1151-515_1151-514i others(21): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAATATA others(5): Show |
10 | a0001c0001t0005g0015a0001c0004t0001g0280a0001c0009t0001g0204others(7): Show | 13 | HG02155.hp1 HG02647.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(14): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAATATA others(7): Show |
3 | a0001c0009t0009g0043a0002c0002t0001g0007a0002c0002t0001g0055 | 5 | HG00733.hp1 HG01071.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(16): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAAATATA others(9): Show |
2 | a0002c0002t0001g0070a0002c0003t0002g0142 | 2 | HG00099.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.1151-515_1151-514i others(18): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAATATAT others(4): Show |
8 | a0001c0001t0002g0290a0002c0003t0002g0009a0002c0003t0002g0023others(5): Show | 11 | HG00323.hp2 HG01071.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(13): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAATATAT others(6): Show |
1 | a0002c0003t0002g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1151-515_1151-514i others(15): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAATATAT others(8): Show |
1 | a0002c0003t0002g0116 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1151-515_1151-514i others(17): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AAATATAT others(10): Show |
1 | a0002c0003t0002g0144 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1151-515_1151-514i others(19): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AATATATA others(5): Show |
1 | a0001c0009t0001g0289 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1151-526_1151-515d others(14): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | AT | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0184others(1): Show | 4 | HG02145.hp2 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(3): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316837
|
A | T | 12 | a0001c0001t0001g0155a0001c0001t0001g0167a0001c0001t0001g0169others(9): Show | 12 | HG01109.hp2 HG01975.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1151-514T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | ||||||
chr4:118316839
|
T | A | 32 | a0001c0001t0001g0206a0001c0004t0001g0162a0003c0005t0003g0004others(29): Show | 38 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.1151-516A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316839 | ||||||
chr4:118316841
|
T | A | 1 | a0001c0004t0001g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1151-518A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316841 | ||||||
chr4:118316856
|
A | C | 1 | a0002c0003t0002g0138 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1151-533T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316856 | ||||||
chr4:118317063
|
GA | G | 116 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(113): Show | 136 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.1151-741delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118317063 | ||||||
chr4:118317092
|
A | T | 1 | a0001c0004t0001g0279 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1151-769T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118317092 | ||||||
chr4:118317685
|
T | A | 1 | a0003c0005t0003g0240 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1150+693A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118317685 | ||||||
chr4:118317809
|
T | C | 3 | a0001c0004t0001g0180a0001c0004t0001g0198a0001c0004t0001g0210 | 3 | HG00738.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1150+569A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118317809 | ||||||
chr4:118317852
|
C | T | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1150+526G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118317852 | ||||||
chr4:118318035
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0196 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1150+343G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118318035 | ||||||
chr4:118318071
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1150+307G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118318071 | ||||||
chr4:118318112
|
T | C | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1150+266A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118318112 | ||||||
chr4:118318209
|
A | T | 1 | a0001c0009t0009g0043 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1150+169T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118318209 | ||||||
chr4:118318234
|
T | C | 1 | a0002c0002t0001g0089 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1150+144A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118318234 | ||||||
chr4:118318250
|
T | C | 32 | a0003c0005t0003g0004a0003c0005t0003g0034a0003c0005t0003g0035others(29): Show | 38 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.1150+128A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118318250 | ||||||
chr4:118318324
|
G | A | 1 | a0001c0004t0001g0265 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1150+54C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118318324 | ||||||
chr4:118318633
|
A | G | 114 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(111): Show | 134 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.972-77T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118318633 | ||||||
chr4:118318719
|
T | C | 1 | a0001c0004t0001g0198 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.972-163A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118318719 | ||||||
chr4:118318745
|
C | A | 228 | a0001c0001t0001g0149a0001c0001t0002g0214a0001c0001t0002g0290others(225): Show | 271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.972-189G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118318745 | ||||||
chr4:118318748
|
T | C | 2 | a0006c0011t0001g0148a0006c0011t0001g0190 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.972-192A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118318748 | ||||||
chr4:118318794
|
T | A | 1 | a0002c0002t0001g0090 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.972-238A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118318794 | ||||||
chr4:118318834
|
T | C | 2 | a0001c0001t0001g0184a0001c0001t0001g0186 | 2 | HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.972-278A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118318834 | ||||||
chr4:118318845
|
A | G | 170 | a0001c0001t0001g0167a0001c0004t0001g0013a0001c0004t0001g0036others(167): Show | 196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.972-289T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118318845 | ||||||
chr4:118319050
|
A | G | 1 | a0002c0003t0002g0142 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.972-494T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118319050 | ||||||
chr4:118319327
|
A | C | 34 | a0003c0005t0003g0004a0003c0005t0003g0034a0003c0005t0003g0035others(31): Show | 40 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.972-771T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118319327 | ||||||
chr4:118319368
|
A | G | 42 | a0001c0001t0001g0276a0001c0004t0001g0013a0001c0004t0001g0036others(39): Show | 46 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.972-812T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118319368 | ||||||
chr4:118319463
|
T | C | 89 | a0001c0004t0001g0038a0001c0004t0001g0039a0001c0004t0001g0162others(86): Show | 105 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.972-907A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118319463 | ||||||
chr4:118319465
|
A | G | 2 | a0001c0004t0007g0249a0001c0004t0007g0268 | 2 | HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.972-909T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118319465 | ||||||
chr4:118319612
|
C | T | 6 | a0002c0002t0001g0017a0002c0002t0001g0050a0002c0002t0001g0060others(3): Show | 7 | HG01243.hp2 HG02451.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.972-1056G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118319612 | ||||||
chr4:118319666
|
C | T | 2 | a0001c0001t0005g0015a0001c0001t0005g0041 | 3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.972-1110G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118319666 | ||||||
chr4:118320341
|
C | T | 2 | a0006c0011t0001g0148a0006c0011t0001g0190 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.972-1785G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118320341 | ||||||
chr4:118320503
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.972-1947C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118320503 | ||||||
chr4:118320615
|
T | G | 1 | a0003c0005t0024g0300 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.972-2059A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118320615 | ||||||
chr4:118320780
|
T | G | 1 | a0001c0004t0007g0268 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.972-2224A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118320780 | ||||||
chr4:118320794
|
G | T | 33 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(30): Show | 37 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.972-2238C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118320794 | ||||||
chr4:118320947
|
C | A | 33 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(30): Show | 37 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.972-2391G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118320947 | ||||||
chr4:118321056
|
A | G | 1 | a0002c0002t0001g0070 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.972-2500T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118321056 | ||||||
chr4:118321119
|
G | A | 88 | a0001c0004t0001g0038a0001c0004t0001g0039a0001c0004t0001g0162others(85): Show | 104 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.972-2563C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118321119 | ||||||
chr4:118321679
|
C | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0025others(294): Show | 360 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(357): Show |
intron_variant | MODIFIER | c.972-3123G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118321679 | ||||||
chr4:118321812
|
T | G | 33 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(30): Show | 37 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.972-3256A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118321812 | ||||||
chr4:118321880
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.972-3324A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118321880 | ||||||
chr4:118321889
|
G | A | 168 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(165): Show | 194 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.972-3333C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118321889 | ||||||
chr4:118322164
|
G | GTAGT | 34 | a0003c0005t0003g0004a0003c0005t0003g0034a0003c0005t0003g0035others(31): Show | 40 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.972-3612_972-3609d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322164 | ||||||
chr4:118322214
|
A | G | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.972-3658T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322214 | ||||||
chr4:118322271
|
T | A | 1 | a0001c0001t0008g0296 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.972-3715A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322271 | ||||||
chr4:118322398
|
A | C | 38 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(35): Show | 42 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.972-3842T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322398 | ||||||
chr4:118322423
|
G | A | 6 | a0002c0002t0001g0051a0002c0002t0001g0052a0002c0002t0001g0053others(3): Show | 6 | HG01175.hp2 HG01361.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.972-3867C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322423 | ||||||
chr4:118322428
|
C | A | 1 | a0003c0005t0003g0223 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.972-3872G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322428 | ||||||
chr4:118322448
|
C | T | 38 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(35): Show | 42 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.972-3892G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322448 | ||||||
chr4:118322454
|
G | A | 1 | a0001c0004t0001g0210 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.972-3898C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322454 | ||||||
chr4:118322482
|
G | A | 2 | a0006c0011t0001g0148a0006c0011t0001g0190 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.972-3926C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322482 | ||||||
chr4:118322549
|
TA | T | 176 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0154others(173): Show | 202 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.972-3994delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322549 | ||||||
chr4:118322724
|
A | C | 1 | a0002c0003t0002g0142 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.972-4168T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322724 | ||||||
chr4:118322756
|
C | T | 1 | a0003c0005t0003g0224 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.972-4200G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322756 | ||||||
chr4:118322775
|
G | A | 88 | a0001c0004t0001g0038a0001c0004t0001g0039a0001c0004t0001g0162others(85): Show | 104 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.972-4219C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322775 | ||||||
chr4:118322852
|
A | C | 231 | a0001c0001t0001g0149a0001c0001t0001g0276a0001c0001t0002g0214others(228): Show | 274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.972-4296T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322852 | ||||||
chr4:118322853
|
G | A | 88 | a0001c0004t0001g0038a0001c0004t0001g0039a0001c0004t0001g0162others(85): Show | 104 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.972-4297C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322853 | ||||||
chr4:118322893
|
T | G | 10 | a0001c0001t0001g0149a0001c0006t0001g0277a0001c0006t0001g0278others(7): Show | 10 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.972-4337A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322893 | ||||||
chr4:118323170
|
A | T | 1 | a0003c0005t0003g0215 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.972-4614T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118323170 | ||||||
chr4:118323414
|
G | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0025others(296): Show | 363 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(360): Show |
intron_variant | MODIFIER | c.972-4858C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118323414 | ||||||
chr4:118323448
|
A | G | 1 | a0002c0003t0002g0114 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.972-4892T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118323448 | ||||||
chr4:118323481
|
C | T | 2 | a0003c0005t0003g0230a0003c0005t0011g0040 | 2 | HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.972-4925G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118323481 | ||||||
chr4:118323639
|
A | C | 1 | a0001c0001t0001g0163 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.972-5083T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118323639 | ||||||
chr4:118323790
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.972-5234A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118323790 | ||||||
chr4:118323916
|
T | A | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-5360A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118323916 | ||||||
chr4:118324091
|
G | A | 4 | a0002c0002t0001g0022a0002c0002t0001g0090a0002c0002t0001g0102others(1): Show | 5 | HG01123.hp1 HG01496.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.972-5535C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324091 | ||||||
chr4:118324233
|
T | C | 66 | a0001c0004t0001g0038a0001c0004t0001g0039a0001c0004t0001g0279others(63): Show | 81 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.972-5677A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324233 | ||||||
chr4:118324279
|
G | A | 1 | a0002c0002t0001g0052 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.972-5723C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324279 | ||||||
chr4:118324410
|
T | G | 34 | a0003c0005t0003g0004a0003c0005t0003g0034a0003c0005t0003g0035others(31): Show | 40 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.972-5854A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324410 | ||||||
chr4:118324580
|
G | A | 8 | a0001c0006t0001g0277a0001c0006t0001g0278a0001c0006t0001g0283others(5): Show | 8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.972-6024C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324580 | ||||||
chr4:118324696
|
G | T | 32 | a0003c0005t0003g0004a0003c0005t0003g0034a0003c0005t0003g0035others(29): Show | 38 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.972-6140C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324696 | ||||||
chr4:118324766
|
G | A | 33 | a0001c0001t0001g0149a0003c0005t0003g0004a0003c0005t0003g0034others(30): Show | 39 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.972-6210C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324766 | ||||||
chr4:118324805
|
C | T | 33 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(30): Show | 37 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.972-6249G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324805 | ||||||
chr4:118324955
|
C | T | 4 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-6399G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324955 | ||||||
chr4:118324983
|
G | A | 72 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(69): Show | 82 | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.972-6427C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324983 | ||||||
chr4:118325041
|
G | A | 3 | a0003c0005t0024g0300a0009c0013t0004g0291a0009c0013t0004g0292 | 3 | HG02109.hp2 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.972-6485C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325041 | ||||||
chr4:118325042
|
T | A | 8 | a0001c0006t0001g0277a0001c0006t0001g0278a0001c0006t0001g0283others(5): Show | 8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.972-6486A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325042 | ||||||
chr4:118325081
|
A | G | 1 | a0002c0002t0001g0102 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.972-6525T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325081 | ||||||
chr4:118325199
|
G | A | 34 | a0003c0005t0003g0004a0003c0005t0003g0034a0003c0005t0003g0035others(31): Show | 40 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.971+6517C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325199 | ||||||
chr4:118325238
|
C | A | 5 | a0001c0004t0001g0013a0001c0004t0001g0259a0001c0004t0001g0260others(2): Show | 7 | NA18965.hp2 NA18968.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.971+6478G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325238 | ||||||
chr4:118325241
|
G | A | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.971+6475C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325241 | ||||||
chr4:118325243
|
T | A | 90 | a0001c0004t0001g0038a0001c0004t0001g0039a0001c0004t0001g0162others(87): Show | 106 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.971+6473A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325243 | ||||||
chr4:118325323
|
T | TA | 7 | a0001c0006t0001g0278a0002c0002t0001g0067a0002c0002t0001g0091others(4): Show | 7 | HG01109.hp2 HG02080.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.971+6392dupT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325323 | ||||||
chr4:118325323
|
TA | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0181a0001c0004t0001g0242others(5): Show | 9 | HG01169.hp1 HG02109.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.971+6392delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325323 | ||||||
chr4:118325386
|
A | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0025others(201): Show | 246 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.971+6330T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325386 | ||||||
chr4:118325439
|
G | A | 32 | a0003c0005t0003g0004a0003c0005t0003g0034a0003c0005t0003g0035others(29): Show | 38 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.971+6277C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325439 | ||||||
chr4:118325599
|
C | T | 2 | a0001c0004t0012g0205a0001c0004t0020g0293 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.971+6117G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325599 | ||||||
chr4:118325740
|
C | A | 6 | a0002c0002t0001g0017a0002c0002t0001g0050a0002c0002t0001g0060others(3): Show | 7 | HG01243.hp2 HG02451.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.971+5976G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325740 | ||||||
chr4:118325831
|
T | G | 10 | a0001c0004t0001g0039a0001c0006t0001g0277a0001c0006t0001g0278others(7): Show | 11 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+5885A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325831 | ||||||
chr4:118325858
|
T | G | 1 | a0003c0005t0003g0220 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.971+5858A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325858 | ||||||
chr4:118325930
|
T | C | 3 | a0001c0021t0021g0297a0003c0005t0010g0235a0003c0005t0010g0236 | 3 | HG02647.hp1 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.971+5786A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325930 | ||||||
chr4:118326158
|
T | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0025others(74): Show | 97 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.971+5558A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326158 | ||||||
chr4:118326168
|
A | G | 5 | a0001c0009t0001g0204a0001c0009t0001g0289a0001c0009t0009g0042others(2): Show | 5 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.971+5548T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326168 | ||||||
chr4:118326282
|
G | A | 2 | a0003c0005t0010g0235a0003c0005t0010g0236 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.971+5434C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326282 | ||||||
chr4:118326320
|
T | C | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0276others(2): Show | 5 | HG02895.hp1 HG02922.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.971+5396A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326320 | ||||||
chr4:118326341
|
T | C | 1 | a0001c0004t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.971+5375A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326341 | ||||||
chr4:118326514
|
T | G | 3 | a0002c0002t0001g0057a0002c0002t0001g0058a0002c0002t0001g0063 | 3 | HG02630.hp2 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.971+5202A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326514 | ||||||
chr4:118326590
|
G | A | 30 | a0001c0001t0002g0214a0003c0005t0003g0004a0003c0005t0003g0034others(27): Show | 36 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.971+5126C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326590 | ||||||
chr4:118326599
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.971+5117G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326599 | ||||||
chr4:118326705
|
A | G | 2 | a0003c0005t0010g0235a0003c0005t0010g0236 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.971+5011T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326705 | ||||||
chr4:118326755
|
C | A | 1 | a0002c0002t0001g0143 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.971+4961G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326755 | ||||||
chr4:118326831
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0163a0001c0001t0001g0164others(2): Show | 8 | HG00597.hp1 HG02027.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.971+4885G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326831 | ||||||
chr4:118326916
|
T | C | 1 | a0002c0002t0001g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.971+4800A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326916 | ||||||
chr4:118327055
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.971+4661G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327055 | ||||||
chr4:118327068
|
A | G | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.971+4648T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327068 | ||||||
chr4:118327102
|
G | A | 31 | a0001c0001t0002g0214a0003c0005t0003g0004a0003c0005t0003g0034others(28): Show | 37 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.971+4614C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327102 | ||||||
chr4:118327162
|
T | A | 5 | a0001c0001t0001g0153a0001c0009t0001g0204a0001c0009t0009g0042others(2): Show | 5 | HG02922.hp1 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.971+4554A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327162 | ||||||
chr4:118327200
|
G | A | 4 | a0001c0004t0001g0037a0001c0004t0001g0264a0001c0004t0001g0274others(1): Show | 5 | HG00544.hp2 HG02080.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.971+4516C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327200 | ||||||
chr4:118327349
|
A | T | 1 | a0003c0005t0003g0223 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.971+4367T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327349 | ||||||
chr4:118327432
|
G | A | 1 | a0001c0004t0012g0205 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.971+4284C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327432 | ||||||
chr4:118327447
|
T | C | 1 | a0001c0004t0001g0265 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.971+4269A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327447 | ||||||
chr4:118327468
|
G | C | 121 | a0001c0001t0001g0276a0001c0001t0002g0290a0002c0002t0001g0002others(118): Show | 151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.971+4248C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327468 | ||||||
chr4:118327556
|
C | A | 1 | a0002c0003t0003g0131 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.971+4160G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327556 | ||||||
chr4:118327702
|
T | A | 1 | a0004c0007t0001g0107 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.971+4014A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327702 | ||||||
chr4:118328107
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0025others(257): Show | 318 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.971+3609T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328107 | ||||||
chr4:118328197
|
T | C | 1 | a0004c0007t0001g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.971+3519A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328197 | ||||||
chr4:118328370
|
T | C | 1 | a0003c0005t0010g0236 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.971+3346A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328370 | ||||||
chr4:118328472
|
C | T | 2 | a0002c0002t0001g0074a0002c0002t0001g0099 | 2 | NA18991.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.971+3244G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328472 | ||||||
chr4:118328589
|
CAAA | C | 6 | a0002c0003t0002g0005a0002c0003t0002g0132a0002c0003t0002g0133others(3): Show | 9 | HG00642.hp2 HG00738.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.971+3124_971+3126d others(5): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328589 | ||||||
chr4:118328592
|
A | C | 214 | a0001c0001t0001g0276a0001c0001t0002g0214a0001c0001t0002g0290others(211): Show | 253 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.971+3124T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328592 | ||||||
chr4:118328648
|
G | C | 38 | a0001c0001t0001g0276a0001c0004t0001g0013a0001c0004t0001g0036others(35): Show | 42 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.971+3068C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328648 | ||||||
chr4:118328656
|
C | T | 38 | a0001c0001t0001g0276a0001c0004t0001g0013a0001c0004t0001g0036others(35): Show | 42 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.971+3060G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328656 | ||||||
chr4:118328680
|
G | A | 5 | a0001c0001t0008g0294a0001c0001t0008g0295a0001c0001t0008g0296others(2): Show | 5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.971+3036C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328680 | ||||||
chr4:118328841
|
T | C | 3 | a0002c0003t0002g0005a0002c0003t0002g0134a0002c0003t0002g0135 | 6 | HG00642.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.971+2875A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328841 | ||||||
chr4:118328860
|
C | A | 38 | a0001c0001t0001g0276a0001c0004t0001g0013a0001c0004t0001g0036others(35): Show | 42 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.971+2856G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328860 | ||||||
chr4:118328948
|
C | G | 1 | a0002c0003t0002g0112 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.971+2768G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328948 | ||||||
chr4:118328982
|
C | T | 213 | a0001c0001t0001g0276a0001c0001t0002g0214a0001c0001t0002g0290others(210): Show | 255 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.971+2734G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328982 | ||||||
chr4:118328984
|
G | A | 38 | a0001c0001t0001g0276a0001c0004t0001g0013a0001c0004t0001g0036others(35): Show | 42 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.971+2732C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328984 | ||||||
chr4:118328996
|
G | A | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.971+2720C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328996 | ||||||
chr4:118329082
|
G | C | 1 | a0001c0001t0001g0150 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.971+2634C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329082 | ||||||
chr4:118329103
|
A | T | 218 | a0001c0001t0001g0276a0001c0001t0002g0214a0001c0001t0002g0290others(215): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.971+2613T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329103 | ||||||
chr4:118329686
|
G | C | 5 | a0001c0001t0008g0294a0001c0001t0008g0295a0001c0001t0008g0296others(2): Show | 5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.971+2030C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329686 | ||||||
chr4:118329722
|
G | T | 5 | a0001c0001t0008g0294a0001c0001t0008g0295a0001c0001t0008g0296others(2): Show | 5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.971+1994C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329722 | ||||||
chr4:118329787
|
G | A | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.971+1929C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329787 | ||||||
chr4:118329804
|
T | C | 3 | a0002c0002t0001g0094a0002c0002t0001g0095a0002c0002t0001g0096 | 3 | NA18966.hp1 NA18987.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.971+1912A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329804 | ||||||
chr4:118329930
|
C | T | 1 | a0001c0004t0001g0245 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.971+1786G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329930 | ||||||
chr4:118329943
|
C | A | 2 | a0001c0001t0005g0015a0001c0001t0005g0041 | 3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.971+1773G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329943 | ||||||
chr4:118329956
|
C | G | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.971+1760G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329956 | ||||||
chr4:118329999
|
C | T | 1 | a0002c0003t0002g0111 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.971+1717G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329999 | ||||||
chr4:118330002
|
A | G | 120 | a0001c0001t0002g0290a0002c0002t0001g0002a0002c0002t0001g0007others(117): Show | 150 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.971+1714T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330002 | ||||||
chr4:118330018
|
A | G | 215 | a0001c0001t0001g0276a0001c0001t0002g0214a0001c0001t0002g0290others(212): Show | 259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.971+1698T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330018 | ||||||
chr4:118330043
|
T | C | 1 | a0001c0009t0001g0289 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.971+1673A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330043 | ||||||
chr4:118330055
|
C | T | 1 | a0002c0002t0001g0051 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.971+1661G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330055 | ||||||
chr4:118330138
|
T | C | 1 | a0002c0002t0001g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.971+1578A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330138 | ||||||
chr4:118330251
|
T | C | 1 | a0001c0004t0001g0266 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.971+1465A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330251 | ||||||
chr4:118330393
|
A | C | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.971+1323T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330393 | ||||||
chr4:118330460
|
G | T | 1 | a0002c0002t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.971+1256C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330460 | ||||||
chr4:118330636
|
G | A | 1 | a0001c0004t0001g0242 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.971+1080C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330636 | ||||||
chr4:118330651
|
T | C | 2 | a0001c0001t0005g0015a0001c0001t0005g0041 | 3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.971+1065A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330651 | ||||||
chr4:118330723
|
T | G | 1 | a0001c0006t0001g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.971+993A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330723 | ||||||
chr4:118330726
|
A | G | 1 | a0006c0011t0001g0148 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.971+990T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330726 | ||||||
chr4:118330780
|
G | C | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.971+936C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330780 | ||||||
chr4:118330895
|
G | T | 1 | a0002c0002t0001g0097 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.971+821C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330895 | ||||||
chr4:118330941
|
AT | A | 127 | a0001c0001t0002g0290a0002c0002t0001g0002a0002c0002t0001g0007others(124): Show | 157 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.971+774delA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330941 | ||||||
chr4:118330943
|
G | A | 127 | a0001c0001t0002g0290a0002c0002t0001g0002a0002c0002t0001g0007others(124): Show | 157 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.971+773C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330943 | ||||||
chr4:118330952
|
A | G | 3 | a0002c0002t0001g0057a0002c0002t0001g0058a0002c0002t0001g0063 | 3 | HG02630.hp2 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.971+764T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330952 | ||||||
chr4:118330978
|
C | T | 2 | a0002c0002t0001g0072a0002c0002t0001g0073 | 2 | HG00621.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.971+738G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330978 | ||||||
chr4:118331041
|
T | A | 222 | a0001c0001t0001g0276a0001c0001t0002g0214a0001c0001t0002g0290others(219): Show | 266 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.971+675A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118331041 | ||||||
chr4:118331099
|
C | T | 2 | a0001c0001t0001g0276a0001c0004t0001g0275 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.971+617G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118331099 | ||||||
chr4:118331168
|
C | T | 225 | a0001c0001t0001g0276a0001c0001t0002g0214a0001c0001t0002g0290others(222): Show | 270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.971+548G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118331168 | ||||||
chr4:118331213
|
G | A | 16 | a0001c0004t0001g0038a0001c0004t0001g0039a0001c0004t0001g0279others(13): Show | 18 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.971+503C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118331213 | ||||||
chr4:118331344
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.971+372A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118331344 | ||||||
chr4:118331352
|
C | T | 1 | a0002c0002t0001g0071 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.971+364G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118331352 | ||||||
chr4:118331424
|
T | A | 1 | a0001c0004t0001g0243 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.971+292A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118331424 | ||||||
chr4:118332002
|
C | T | 1 | a0001c0004t0001g0275 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.821-136G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332002 | ||||||
chr4:118332003
|
G | GTA | 31 | a0001c0001t0002g0214a0003c0005t0003g0004a0003c0005t0003g0034others(28): Show | 37 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.821-139_821-138dup others(2): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332003 | ||||||
chr4:118332012
|
T | C | 1 | a0002c0002t0001g0097 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.821-146A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332012 | ||||||
chr4:118332025
|
G | A | 1 | a0003c0005t0003g0228 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.821-159C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332025 | ||||||
chr4:118332114
|
C | T | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.821-248G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332114 | ||||||
chr4:118332272
|
A | G | 5 | a0001c0001t0008g0294a0001c0001t0008g0295a0001c0001t0008g0296others(2): Show | 5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.821-406T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332272 | ||||||
chr4:118332293
|
T | C | 1 | a0003c0005t0024g0300 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.821-427A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332293 | ||||||
chr4:118332698
|
G | A | 1 | a0001c0004t0012g0205 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.821-832C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332698 | ||||||
chr4:118332776
|
A | G | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.821-910T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332776 | ||||||
chr4:118332954
|
C | T | 1 | a0001c0001t0023g0299 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.821-1088G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332954 | ||||||
chr4:118333227
|
T | TA | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.821-1362dupT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118333227 | ||||||
chr4:118333398
|
G | A | 218 | a0001c0001t0001g0276a0001c0001t0002g0214a0001c0001t0002g0290others(215): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.821-1532C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118333398 | ||||||
chr4:118333849
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.820+1624G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118333849 | ||||||
chr4:118333863
|
C | A | 1 | a0003c0005t0024g0300 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.820+1610G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118333863 | ||||||
chr4:118334124
|
C | T | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.820+1349G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118334124 | ||||||
chr4:118334479
|
C | T | 1 | a0001c0004t0001g0270 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.820+994G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118334479 | ||||||
chr4:118334671
|
T | C | 183 | a0001c0001t0001g0276a0001c0001t0002g0290a0001c0004t0001g0013others(180): Show | 221 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.820+802A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118334671 | ||||||
chr4:118334680
|
C | T | 1 | a0002c0002t0001g0070 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.820+793G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118334680 | ||||||
chr4:118335063
|
T | C | 6 | a0002c0002t0001g0017a0002c0002t0001g0050a0002c0002t0001g0060others(3): Show | 7 | HG01243.hp2 HG02451.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.820+410A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118335063 | ||||||
chr4:118335122
|
T | G | 1 | a0002c0002t0001g0098 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.820+351A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118335122 | ||||||
chr4:118335141
|
T | G | 218 | a0001c0001t0001g0276a0001c0001t0002g0214a0001c0001t0002g0290others(215): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.820+332A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118335141 | ||||||
chr4:118335462
|
C | CT | 31 | a0001c0001t0002g0214a0003c0005t0003g0004a0003c0005t0003g0034others(28): Show | 37 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.820+10dupA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118335462 | ||||||
chr4:118335736
|
G | A | 2 | a0003c0005t0003g0230a0003c0005t0011g0040 | 2 | HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.642-85C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118335736 | ||||||
chr4:118335819
|
A | C | 5 | a0003c0005t0004g0211a0003c0005t0004g0212a0003c0005t0024g0300others(2): Show | 5 | HG02109.hp2 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.642-168T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118335819 | ||||||
chr4:118335834
|
C | T | 1 | a0001c0004t0007g0268 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.642-183G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118335834 | ||||||
chr4:118335861
|
T | C | 2 | a0001c0001t0005g0015a0001c0001t0005g0041 | 3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.642-210A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118335861 | ||||||
chr4:118335913
|
T | G | 5 | a0001c0001t0001g0026a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 6 | HG01256.hp2 HG01258.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.642-262A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118335913 | ||||||
chr4:118336303
|
G | A | 5 | a0001c0001t0008g0294a0001c0001t0008g0295a0001c0001t0008g0296others(2): Show | 5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-652C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336303 | ||||||
chr4:118336388
|
G | A | 1 | a0003c0005t0010g0236 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.642-737C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336388 | ||||||
chr4:118336399
|
TA | T | 222 | a0001c0001t0001g0276a0001c0001t0002g0214a0001c0001t0002g0290others(219): Show | 265 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.642-749delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336399 | ||||||
chr4:118336557
|
A | C | 1 | a0002c0002t0001g0069 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.642-906T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336557 | ||||||
chr4:118336564
|
T | C | 31 | a0001c0001t0002g0214a0003c0005t0003g0004a0003c0005t0003g0034others(28): Show | 37 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.642-913A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336564 | ||||||
chr4:118336584
|
T | G | 1 | a0001c0001t0001g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.642-933A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336584 | ||||||
chr4:118336615
|
A | G | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.642-964T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336615 | ||||||
chr4:118336706
|
A | G | 1 | a0001c0004t0001g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.642-1055T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336706 | ||||||
chr4:118336724
|
T | C | 2 | a0001c0001t0001g0189a0006c0011t0001g0190 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.642-1073A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336724 | ||||||
chr4:118336906
|
C | A | 1 | a0003c0005t0003g0233 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.642-1255G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336906 | ||||||
chr4:118336946
|
C | G | 1 | a0002c0002t0001g0053 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.641+1230G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336946 | ||||||
chr4:118337323
|
A | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.641+853T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337323 | ||||||
chr4:118337330
|
A | C | 14 | a0001c0004t0001g0038a0001c0004t0001g0039a0001c0004t0001g0279others(11): Show | 16 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.641+846T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337330 | ||||||
chr4:118337336
|
T | C | 5 | a0001c0001t0008g0294a0001c0001t0008g0295a0001c0001t0008g0296others(2): Show | 5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+840A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337336 | ||||||
chr4:118337382
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.641+794T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337382 | ||||||
chr4:118337392
|
C | G | 1 | a0002c0002t0001g0068 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.641+784G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337392 | ||||||
chr4:118337447
|
T | C | 8 | a0001c0001t0001g0033a0001c0001t0001g0196a0001c0001t0001g0201others(5): Show | 9 | HG01975.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.641+729A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337447 | ||||||
chr4:118337560
|
A | T | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.641+616T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337560 | ||||||
chr4:118337563
|
GCAGGA | G | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.641+608_641+612del others(5): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337563 | ||||||
chr4:118337645
|
C | T | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.641+531G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337645 | ||||||
chr4:118337993
|
T | C | 2 | a0009c0013t0004g0291a0009c0013t0004g0292 | 2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.641+183A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337993 | ||||||
chr4:118338044
|
C | G | 5 | a0001c0001t0008g0294a0001c0001t0008g0295a0001c0001t0008g0296others(2): Show | 5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+132G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118338044 | ||||||
chr4:118338075
|
C | T | 10 | a0003c0005t0003g0004a0003c0005t0003g0215a0003c0005t0003g0216others(7): Show | 14 | HG00597.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.641+101G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118338075 | ||||||
chr4:118338127
|
TATTC | T | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.641+45_641+48delGA others(2): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118338127 | ||||||
chr4:118339090
|
C | T | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.503-776G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118339090 | ||||||
chr4:118339147
|
C | T | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.503-833G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118339147 | ||||||
chr4:118339654
|
C | T | 1 | a0002c0002t0016g0146 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.503-1340G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118339654 | ||||||
chr4:118339746
|
G | C | 1 | a0001c0004t0001g0267 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.503-1432C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118339746 | ||||||
chr4:118339780
|
T | C | 1 | a0002c0002t0001g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.503-1466A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118339780 | ||||||
chr4:118339964
|
C | T | 1 | a0001c0006t0001g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.503-1650G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118339964 | ||||||
chr4:118340158
|
A | G | 2 | a0001c0001t0005g0015a0001c0001t0005g0041 | 3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.503-1844T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340158 | ||||||
chr4:118340544
|
G | C | 2 | a0003c0005t0010g0235a0003c0005t0010g0236 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.503-2230C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340544 | ||||||
chr4:118340572
|
C | T | 3 | a0002c0002t0022g0298a0003c0005t0010g0235a0003c0005t0010g0236 | 3 | HG02647.hp1 HG02895.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.503-2258G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340572 | ||||||
chr4:118340662
|
T | C | 1 | a0002c0002t0001g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-2348A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340662 | ||||||
chr4:118340663
|
C | T | 1 | a0002c0002t0001g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-2349G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340663 | ||||||
chr4:118340667
|
G | A | 1 | a0002c0002t0001g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-2353C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340667 | ||||||
chr4:118340756
|
C | T | 1 | a0002c0002t0001g0067 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.503-2442G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340756 | ||||||
chr4:118340784
|
A | G | 221 | a0001c0001t0001g0276a0001c0001t0002g0214a0001c0001t0002g0290others(218): Show | 263 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.503-2470T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340784 | ||||||
chr4:118340789
|
C | G | 1 | a0002c0002t0001g0066 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.503-2475G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340789 | ||||||
chr4:118340831
|
A | G | 1 | a0001c0004t0001g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.503-2517T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340831 | ||||||
chr4:118340833
|
G | A | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.503-2519C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340833 | ||||||
chr4:118340839
|
A | T | 1 | a0002c0002t0001g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-2525T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340839 | ||||||
chr4:118340868
|
A | T | 1 | a0002c0002t0001g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-2554T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340868 | ||||||
chr4:118340953
|
C | T | 1 | a0002c0002t0001g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-2639G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340953 | ||||||
chr4:118340954
|
T | C | 1 | a0002c0002t0001g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-2640A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340954 | ||||||
chr4:118340955
|
G | T | 1 | a0002c0002t0001g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-2641C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340955 | ||||||
chr4:118341211
|
T | C | 40 | a0001c0001t0001g0276a0001c0004t0001g0013a0001c0004t0001g0036others(37): Show | 46 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.503-2897A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341211 | ||||||
chr4:118341257
|
G | A | 1 | a0001c0004t0007g0268 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.503-2943C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341257 | ||||||
chr4:118341424
|
T | G | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.503-3110A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341424 | ||||||
chr4:118341449
|
G | A | 8 | a0003c0005t0003g0035a0003c0005t0003g0229a0003c0005t0003g0230others(5): Show | 9 | HG00099.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.503-3135C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341449 | ||||||
chr4:118341528
|
C | T | 1 | a0001c0006t0001g0277 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.503-3214G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341528 | ||||||
chr4:118341624
|
G | T | 1 | a0002c0002t0001g0065 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.503-3310C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341624 | ||||||
chr4:118341642
|
A | T | 1 | a0002c0002t0001g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-3328T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341642 | ||||||
chr4:118341801
|
C | A | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.503-3487G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341801 | ||||||
chr4:118341924
|
A | T | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.503-3610T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341924 | ||||||
chr4:118342149
|
A | G | 5 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(2): Show | 5 | HG01361.hp1 HG02055.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.503-3835T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118342149 | ||||||
chr4:118342250
|
T | C | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.503-3936A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118342250 | ||||||
chr4:118342434
|
G | A | 1 | a0001c0009t0001g0289 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.503-4120C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118342434 | ||||||
chr4:118342531
|
G | A | 1 | a0001c0004t0001g0269 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.503-4217C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118342531 | ||||||
chr4:118342557
|
A | G | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | NA18945.hp2 NA18956.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.503-4243T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118342557 | ||||||
chr4:118342734
|
T | A | 1 | a0002c0002t0001g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-4420A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118342734 | ||||||
chr4:118342850
|
T | TTTTCCTT others(8): Show |
1 | a0002c0020t0001g0100 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.503-4551_503-4537d others(17): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118342850 | ||||||
chr4:118343006
|
T | C | 127 | a0001c0001t0002g0290a0002c0002t0001g0002a0002c0002t0001g0007others(124): Show | 157 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.503-4692A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343006 | ||||||
chr4:118343007
|
A | T | 5 | a0001c0001t0008g0294a0001c0001t0008g0295a0001c0001t0008g0296others(2): Show | 5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-4693T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343007 | ||||||
chr4:118343048
|
T | C | 30 | a0001c0001t0002g0214a0003c0005t0003g0004a0003c0005t0003g0034others(27): Show | 36 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.503-4734A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343048 | ||||||
chr4:118343159
|
C | A | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.503-4845G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343159 | ||||||
chr4:118343192
|
C | A | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.503-4878G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343192 | ||||||
chr4:118343258
|
G | C | 1 | a0002c0003t0002g0136 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.503-4944C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343258 | ||||||
chr4:118343276
|
T | G | 1 | a0002c0003t0002g0137 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.503-4962A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343276 | ||||||
chr4:118343592
|
A | G | 1 | a0002c0017t0002g0110 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.503-5278T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343592 | ||||||
chr4:118343697
|
G | A | 1 | a0001c0004t0001g0270 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.503-5383C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343697 | ||||||
chr4:118344038
|
T | C | 1 | a0001c0009t0009g0043 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.503-5724A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118344038 | ||||||
chr4:118344301
|
A | T | 1 | a0001c0004t0001g0244 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.503-5987T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118344301 | ||||||
chr4:118344423
|
TAA | T | 30 | a0001c0001t0002g0214a0003c0005t0003g0004a0003c0005t0003g0034others(27): Show | 36 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.503-6111_503-6110d others(4): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118344423 | ||||||
chr4:118344459
|
T | C | 224 | a0001c0001t0001g0276a0001c0001t0002g0214a0001c0001t0002g0290others(221): Show | 269 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.503-6145A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118344459 | ||||||
chr4:118344460
|
G | A | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.503-6146C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118344460 | ||||||
chr4:118344476
|
A | G | 2 | a0003c0005t0010g0235a0003c0005t0010g0236 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.503-6162T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118344476 | ||||||
chr4:118344495
|
T | C | 1 | a0006c0011t0001g0190 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.503-6181A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118344495 | ||||||
chr4:118344933
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0152a0001c0001t0001g0153 | 4 | HG01256.hp2 HG01258.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.503-6619G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118344933 | ||||||
chr4:118345054
|
G | C | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.503-6740C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345054 | ||||||
chr4:118345168
|
C | G | 8 | a0003c0005t0003g0004a0003c0005t0003g0215a0003c0005t0003g0216others(5): Show | 12 | HG00597.hp2 NA18747.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.503-6854G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345168 | ||||||
chr4:118345463
|
T | C | 3 | a0003c0005t0003g0231a0003c0005t0003g0232a0003c0005t0003g0233 | 3 | HG01123.hp2 HG01891.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.502+6756A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345463 | ||||||
chr4:118345477
|
T | C | 1 | a0003c0005t0003g0234 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.502+6742A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345477 | ||||||
chr4:118345536
|
A | G | 1 | a0002c0002t0001g0052 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.502+6683T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345536 | ||||||
chr4:118345611
|
C | T | 1 | a0002c0002t0001g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.502+6608G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345611 | ||||||
chr4:118345699
|
A | C | 1 | a0002c0002t0001g0051 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.502+6520T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345699 | ||||||
chr4:118345782
|
T | G | 1 | a0001c0004t0001g0271 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.502+6437A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345782 | ||||||
chr4:118345809
|
T | C | 60 | a0001c0001t0002g0290a0002c0002t0001g0002a0002c0002t0001g0007others(57): Show | 73 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.502+6410A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345809 | ||||||
chr4:118345832
|
C | T | 2 | a0001c0004t0001g0242a0001c0004t0001g0243 | 2 | NA18948.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.502+6387G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345832 | ||||||
chr4:118345835
|
A | G | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.502+6384T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345835 | ||||||
chr4:118345906
|
C | A | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.502+6313G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345906 | ||||||
chr4:118345990
|
T | C | 2 | a0002c0002t0007g0145a0002c0003t0002g0144 | 2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.502+6229A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345990 | ||||||
chr4:118346275
|
G | A | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.502+5944C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346275 | ||||||
chr4:118346315
|
A | C | 1 | a0002c0002t0001g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.502+5904T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346315 | ||||||
chr4:118346384
|
TCA | T | 30 | a0001c0001t0002g0214a0003c0005t0003g0004a0003c0005t0003g0034others(27): Show | 36 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.502+5833_502+5834d others(4): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346384 | ||||||
chr4:118346389
|
G | A | 2 | a0001c0001t0001g0276a0001c0004t0001g0275 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.502+5830C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346389 | ||||||
chr4:118346405
|
T | C | 5 | a0002c0002t0001g0101a0002c0003t0002g0138a0002c0003t0002g0139others(2): Show | 5 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.502+5814A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346405 | ||||||
chr4:118346458
|
T | TTA | 6 | a0001c0001t0001g0191a0001c0001t0008g0294a0001c0001t0008g0295others(3): Show | 6 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+5759_502+5760d others(4): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346458 | ||||||
chr4:118346458
|
T | TTATA | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.502+5757_502+5760d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346458 | ||||||
chr4:118346458
|
TTA | T | 212 | a0001c0001t0001g0276a0001c0001t0002g0214a0001c0001t0002g0290others(209): Show | 254 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.502+5759_502+5760d others(4): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346458 | ||||||
chr4:118346565
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.502+5654A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346565 | ||||||
chr4:118346651
|
CCAGGAGG others(4): Show |
C | 2 | a0001c0001t0005g0015a0001c0001t0005g0041 | 3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.502+5557_502+5567d others(13): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346651 | ||||||
chr4:118346695
|
C | A | 44 | a0002c0002t0001g0113a0002c0002t0007g0145a0002c0003t0002g0003others(41): Show | 60 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.502+5524G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346695 | ||||||
chr4:118346721
|
C | T | 1 | a0002c0002t0001g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.502+5498G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346721 | ||||||
chr4:118346783
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.502+5436G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346783 | ||||||
chr4:118346947
|
G | A | 3 | a0003c0005t0003g0238a0007c0012t0003g0237a0007c0012t0003g0239 | 3 | HG01167.hp1 HG01169.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.502+5272C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346947 | ||||||
chr4:118347077
|
TA | T | 6 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0196others(3): Show | 6 | HG02280.hp1 HG03704.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+5141delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347077 | ||||||
chr4:118347157
|
G | A | 1 | a0002c0003t0002g0142 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.502+5062C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347157 | ||||||
chr4:118347263
|
C | A | 221 | a0001c0001t0001g0276a0001c0001t0002g0214a0001c0001t0002g0290others(218): Show | 263 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.502+4956G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347263 | ||||||
chr4:118347495
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.502+4724A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347495 | ||||||
chr4:118347551
|
G | C | 1 | a0003c0005t0003g0240 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.502+4668C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347551 | ||||||
chr4:118347558
|
A | G | 1 | a0003c0005t0004g0211 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.502+4661T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347558 | ||||||
chr4:118347725
|
G | A | 4 | a0001c0001t0001g0194a0001c0004t0001g0192a0001c0004t0001g0193others(1): Show | 4 | HG02280.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+4494C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347725 | ||||||
chr4:118347750
|
A | G | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.502+4469T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347750 | ||||||
chr4:118347970
|
C | T | 1 | a0003c0005t0003g0213 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.502+4249G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347970 | ||||||
chr4:118348060
|
T | A | 1 | a0001c0001t0001g0202 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.502+4159A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348060 | ||||||
chr4:118348144
|
G | A | 1 | a0001c0004t0001g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.502+4075C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348144 | ||||||
chr4:118348269
|
T | G | 224 | a0001c0001t0001g0206a0001c0001t0001g0276a0001c0001t0002g0214others(221): Show | 267 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.502+3950A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348269 | ||||||
chr4:118348344
|
C | T | 36 | a0001c0001t0001g0276a0001c0004t0001g0013a0001c0004t0001g0036others(33): Show | 40 | HG00673.hp1 HG01255.hp2 HG02155.hp2 others(37): Show |
intron_variant | MODIFIER | c.502+3875G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348344 | ||||||
chr4:118348355
|
A | C | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.502+3864T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348355 | ||||||
chr4:118348444
|
C | T | 5 | a0003c0005t0004g0211a0003c0005t0004g0212a0003c0005t0024g0300others(2): Show | 5 | HG02109.hp2 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.502+3775G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348444 | ||||||
chr4:118348651
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.502+3568T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348651 | ||||||
chr4:118348654
|
C | CT | 220 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0276others(217): Show | 261 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.502+3564dupA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348654 | ||||||
chr4:118348697
|
A | G | 224 | a0001c0001t0001g0206a0001c0001t0001g0276a0001c0001t0002g0214others(221): Show | 267 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.502+3522T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348697 | ||||||
chr4:118348720
|
C | T | 17 | a0001c0004t0001g0038a0001c0004t0001g0039a0001c0004t0001g0274others(14): Show | 19 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.502+3499G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348720 | ||||||
chr4:118348800
|
T | C | 226 | a0001c0001t0001g0206a0001c0001t0001g0276a0001c0001t0002g0214others(223): Show | 271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.502+3419A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348800 | ||||||
chr4:118348927
|
C | T | 3 | a0001c0009t0001g0204a0001c0009t0009g0042a0001c0009t0009g0043 | 3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.502+3292G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348927 | ||||||
chr4:118349074
|
TC | T | 34 | a0001c0004t0001g0013a0001c0004t0001g0036a0001c0004t0001g0037others(31): Show | 38 | HG00673.hp1 HG01255.hp2 HG02155.hp2 others(35): Show |
intron_variant | MODIFIER | c.502+3144delG | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118349074 | ||||||
chr4:118349346
|
G | C | 1 | a0006c0011t0001g0148 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.502+2873C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118349346 | ||||||
chr4:118349395
|
A | C | 222 | a0001c0001t0001g0206a0001c0001t0001g0276a0001c0001t0002g0214others(219): Show | 264 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.502+2824T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118349395 | ||||||
chr4:118349403
|
CA | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0025others(71): Show | 94 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.502+2815delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118349403 | ||||||
chr4:118349615
|
C | A | 1 | a0001c0001t0001g0203 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.502+2604G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118349615 | ||||||
chr4:118349639
|
T | C | 223 | a0001c0001t0001g0206a0001c0001t0001g0276a0001c0001t0002g0214others(220): Show | 265 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.502+2580A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118349639 | ||||||
chr4:118349873
|
G | A | 5 | a0002c0002t0001g0105a0004c0007t0001g0104a0004c0007t0001g0106others(2): Show | 5 | HG00741.hp2 HG01192.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.502+2346C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118349873 | ||||||
chr4:118350395
|
C | G | 1 | a0001c0021t0021g0297 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.502+1824G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118350395 | ||||||
chr4:118350556
|
G | A | 15 | a0001c0004t0001g0038a0001c0004t0001g0039a0001c0004t0001g0279others(12): Show | 17 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.502+1663C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118350556 | ||||||
chr4:118350641
|
A | T | 5 | a0001c0001t0005g0015a0001c0001t0005g0041a0001c0009t0009g0042others(2): Show | 6 | HG02486.hp2 HG02886.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+1578T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118350641 | ||||||
chr4:118350736
|
T | TGAAA | 222 | a0001c0001t0001g0276a0001c0001t0002g0214a0001c0001t0002g0290others(219): Show | 265 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.502+1482_502+1483i others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118350736 | ||||||
chr4:118350752
|
G | A | 1 | a0012c0014t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.502+1467C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118350752 | ||||||
chr4:118351009
|
T | G | 15 | a0001c0004t0001g0038a0001c0004t0001g0039a0001c0004t0001g0279others(12): Show | 17 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.502+1210A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351009 | ||||||
chr4:118351048
|
T | C | 44 | a0002c0002t0001g0113a0002c0002t0007g0145a0002c0003t0002g0003others(41): Show | 60 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.502+1171A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351048 | ||||||
chr4:118351134
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.502+1085A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351134 | ||||||
chr4:118351347
|
C | CA | 57 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0276others(54): Show | 65 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.502+871dupT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351347 | ||||||
chr4:118351617
|
T | C | 1 | a0002c0002t0001g0143 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.502+602A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351617 | ||||||
chr4:118351658
|
T | A | 215 | a0001c0001t0001g0276a0001c0001t0002g0214a0001c0001t0002g0290others(212): Show | 259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.502+561A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351658 | ||||||
chr4:118351667
|
G | A | 2 | a0002c0002t0007g0145a0002c0003t0002g0144 | 2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.502+552C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351667 | ||||||
chr4:118351803
|
T | C | 121 | a0001c0001t0002g0290a0002c0002t0001g0002a0002c0002t0001g0007others(118): Show | 151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.502+416A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351803 | ||||||
chr4:118351923
|
GCA | G | 5 | a0001c0001t0005g0015a0001c0001t0005g0041a0001c0009t0009g0042others(2): Show | 6 | HG02486.hp2 HG02886.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+294_502+295del others(2): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351923 | ||||||
chr4:118352040
|
T | C | 1 | a0002c0002t0016g0146 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.502+179A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118352040 | ||||||
chr4:118352057
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0147 | 3 | NA18970.hp2 NA18989.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.502+162G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118352057 | ||||||
chr4:118352178
|
A | G | 1 | a0002c0003t0002g0016 | 2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.502+41T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118352178 |