geneid | 25849 |
---|---|
ensemblid | ENSG00000169116.11 |
hgncid | 24536 |
symbol | PARM1 |
name | prostate androgen-regulated mucin-like protein 1 |
refseq_nuc | NM_015393.4 |
refseq_prot | NP_056208.2 |
ensembl_nuc | ENST00000307428.7 |
ensembl_prot | ENSP00000370224.3 |
mane_status | MANE Select |
chr | chr4 |
start | 74933116 |
end | 75050113 |
strand | + |
ver | v1.2 |
region | chr4:74933116-75050113 |
region5000 | chr4:74928116-75055113 |
regionname0 | PARM1_chr4_74933116_75050113 |
regionname5000 | PARM1_chr4_74928116_75055113 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 310 | 136 | 44 | 29 | 52 | 3 | 6 | 31 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002 | 0/0 | 310 | 52 | 23 | 12 | 7 | 1 | 9 | 5 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0003 | 0/0 | 310 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0004 | 0/0 | 310 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0005 | 0/0 | 310 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0006 | 0/0 | 310 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 933 | 111 | 31 | 24 | 47 | 2 | 5 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
c0002 | 0/0 | 933 | 47 | 20 | 10 | 7 | 1 | 9 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
c0003 | 0/0 | 933 | 24 | 13 | 5 | 4 | 1 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
c0004 | 0/0 | 933 | 5 | 3 | 2 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
c0005 | 0/0 | 933 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
c0006 | 0/0 | 933 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
c0007 | 0/0 | 933 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
c0008 | 0/0 | 933 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
c0009 | 0/0 | 933 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 4079 | 61 | 17 | 15 | 16 | 1 | 10 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0002 | 0/0 | 4079 | 54 | 6 | 11 | 33 | 2 | 2 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0003 | 0/0 | 4083 | 10 | 9 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0004 | 0/0 | 4080 | 8 | 5 | 3 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0005 | 0/0 | 4080 | 7 | 6 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0006 | 0/0 | 4080 | 5 | 0 | 5 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0007 | 0/0 | 4079 | 4 | 2 | 2 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0008 | 0/0 | 4079 | 4 | 0 | 0 | 3 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0009 | 0/0 | 4082 | 4 | 0 | 0 | 4 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0010 | 0/0 | 4083 | 4 | 3 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0011 | 0/0 | 4079 | 3 | 3 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0012 | 0/0 | 4077 | 3 | 2 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0013 | 0/0 | 4077 | 2 | 0 | 1 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0014 | 0/0 | 4078 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0015 | 0/0 | 4079 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0016 | 0/0 | 4079 | 2 | 0 | 0 | 2 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0017 | 0/0 | 4084 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0018 | 0/0 | 4079 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0019 | 0/0 | 4084 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0020 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0021 | 0/0 | 4079 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0022 | 0/0 | 4079 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0023 | 0/0 | 4079 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0024 | 0/0 | 4079 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0025 | 0/0 | 4081 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0026 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0027 | 0/0 | 4082 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0028 | 0/0 | 4078 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0029 | 0/0 | 4084 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0030 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0031 | 0/0 | 4079 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
t0032 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0020 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 933 | 111 | 31 | 24 | 47 | 2 | 5 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0003 | 0/0 | 933 | 24 | 13 | 5 | 4 | 1 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0006 | 0/0 | 933 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002c0002 | 0/0 | 933 | 47 | 20 | 10 | 7 | 1 | 9 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002c0004 | 0/0 | 933 | 5 | 3 | 2 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0003c0009 | 0/0 | 933 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0004c0005 | 0/0 | 933 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0005c0008 | 0/0 | 933 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0006c0007 | 0/0 | 933 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5011 | 29 | 11 | 7 | 8 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0001t0002 | 0/0 | 5011 | 52 | 5 | 11 | 32 | 2 | 2 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0001t0003 | 0/0 | 5015 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0001t0004 | 0/0 | 5012 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0001t0005 | 0/0 | 5012 | 7 | 6 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0001t0006 | 0/0 | 5012 | 5 | 0 | 5 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0001t0007 | 0/0 | 5011 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0001t0008 | 0/0 | 5011 | 4 | 0 | 0 | 3 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0001t0016 | 0/0 | 5011 | 2 | 0 | 0 | 2 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0001t0017 | 0/0 | 5016 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0001t0019 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0001t0020 | 0/0 | 5012 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0001t0021 | 0/0 | 5011 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0001t0022 | 0/0 | 5011 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0001t0023 | 0/0 | 5011 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0001t0026 | 0/0 | 5012 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0001t0030 | 0/0 | 5012 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0003t0001 | 0/0 | 5011 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0003t0002 | 0/0 | 5011 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0003t0003 | 0/0 | 5015 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0003t0004 | 0/0 | 5012 | 5 | 3 | 2 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0003t0009 | 0/0 | 5014 | 4 | 0 | 0 | 4 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0003t0010 | 0/0 | 5015 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0003t0011 | 0/0 | 5011 | 3 | 3 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0003t0012 | 0/0 | 5009 | 3 | 2 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0003t0013 | 0/0 | 5009 | 2 | 0 | 1 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0003t0014 | 0/0 | 5010 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0003t0028 | 0/0 | 5010 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0001c0006t0002 | 0/0 | 5011 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002c0002t0001 | 0/0 | 5011 | 28 | 4 | 8 | 7 | 1 | 8 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002c0002t0003 | 0/0 | 5015 | 7 | 7 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002c0002t0004 | 0/0 | 5012 | 2 | 1 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002c0002t0007 | 0/0 | 5011 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002c0002t0010 | 0/0 | 5015 | 3 | 3 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002c0002t0015 | 0/0 | 5011 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002c0002t0024 | 0/0 | 5011 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002c0002t0025 | 0/0 | 5013 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002c0002t0029 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002c0002t0031 | 0/0 | 5011 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002c0004t0001 | 0/0 | 5011 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002c0004t0007 | 0/0 | 5011 | 2 | 0 | 2 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002c0004t0018 | 0/0 | 5011 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0002c0004t0027 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0003c0009t0003 | 0/0 | 5015 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0004c0005t0001 | 0/0 | 5011 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0005c0008t0001 | 0/0 | 5011 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
a0006c0007t0032 | 0/0 | 5012 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | copy fasta | chr4 | 74928116 | 75055113 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0020 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0005g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0006g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0006g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0006g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0008g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0008g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0008g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0016g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0016g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0017g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0017g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0019g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0020g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0021g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0022g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0023g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0026g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0001t0030g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0004g0001 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0009g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0009g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0009g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0010g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0011g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0011g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0012g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0012g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0012g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0013g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0013g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0014g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0014g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0003t0028g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0001c0006t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0010g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0010g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0015g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0015g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0024g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0025g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0029g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0002t0031g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0004t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0004t0007g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0004t0007g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0004t0018g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0002c0004t0027g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0003c0009t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0004c0005t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0005c0008t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
a0006c0007t0032g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0001 | c0001 | t0002 | g0107 | EUR | FIN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0150 | EUR | FIN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG00438 | hp2 | a0001 | c0003 | t0009 | g0163 | EAS | CHS | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | CHS | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG00741 | hp2 | a0001 | c0003 | t0028 | g0067 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01070 | hp2 | a0001 | c0003 | t0004 | g0001 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01071 | hp2 | a0001 | c0003 | t0004 | g0001 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01167 | hp2 | a0002 | c0004 | t0007 | g0178 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01169 | hp1 | a0002 | c0004 | t0007 | g0177 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01255 | hp1 | a0001 | c0003 | t0012 | g0049 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01255 | hp2 | a0001 | c0001 | t0006 | g0126 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0151 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0138 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01361 | hp1 | a0001 | c0003 | t0013 | g0175 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01361 | hp2 | a0001 | c0001 | t0006 | g0146 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0089 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01884 | hp2 | a0001 | c0003 | t0002 | g0156 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01891 | hp1 | a0001 | c0001 | t0017 | g0051 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01891 | hp2 | a0002 | c0002 | t0004 | g0034 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01943 | hp1 | a0002 | c0002 | t0004 | g0162 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01943 | hp2 | a0002 | c0002 | t0024 | g0140 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01978 | hp1 | a0001 | c0001 | t0006 | g0039 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02129 | hp1 | a0001 | c0001 | t0008 | g0122 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02135 | hp2 | a0001 | c0001 | t0023 | g0084 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02145 | hp2 | a0001 | c0003 | t0004 | g0001 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02148 | hp2 | a0001 | c0001 | t0006 | g0166 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | CDX | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | CDX | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CDX | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | CDX | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02257 | hp1 | a0002 | c0002 | t0007 | g0179 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02258 | hp2 | a0002 | c0002 | t0003 | g0074 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02300 | hp2 | a0001 | c0001 | t0006 | g0036 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02615 | hp1 | a0002 | c0002 | t0003 | g0025 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02622 | hp2 | a0002 | c0002 | t0010 | g0004 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02717 | hp2 | a0002 | c0002 | t0010 | g0030 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02818 | hp2 | a0002 | c0002 | t0029 | g0023 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02895 | hp1 | a0001 | c0003 | t0012 | g0037 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02895 | hp2 | a0002 | c0002 | t0003 | g0003 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02896 | hp1 | a0002 | c0002 | t0003 | g0003 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02896 | hp2 | a0001 | c0001 | t0030 | g0072 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02922 | hp2 | a0001 | c0003 | t0004 | g0001 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02965 | hp1 | a0002 | c0004 | t0001 | g0155 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02965 | hp2 | a0002 | c0002 | t0003 | g0027 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02970 | hp1 | a0001 | c0001 | t0020 | g0172 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02970 | hp2 | a0001 | c0003 | t0011 | g0017 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0153 | SAS | PJL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03041 | hp1 | a0002 | c0002 | t0025 | g0181 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03130 | hp2 | a0001 | c0003 | t0014 | g0171 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0132 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03195 | hp2 | a0001 | c0003 | t0003 | g0013 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | MSL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03209 | hp2 | a0002 | c0004 | t0027 | g0029 | AFR | MSL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03225 | hp1 | a0006 | c0007 | t0032 | g0028 | AFR | MSL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | MSL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03453 | hp2 | a0001 | c0003 | t0011 | g0092 | AFR | MSL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03491 | hp1 | a0002 | c0002 | t0031 | g0043 | SAS | PJL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03540 | hp2 | a0002 | c0002 | t0015 | g0016 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0031 | SAS | STU | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03688 | hp2 | a0001 | c0001 | t0021 | g0044 | SAS | STU | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0142 | SAS | PJL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0160 | SAS | BEB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0161 | SAS | BEB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03942 | hp1 | a0001 | c0003 | t0010 | g0050 | SAS | BEB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0152 | SAS | BEB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0149 | SAS | BEB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG04184 | hp2 | a0001 | c0001 | t0008 | g0134 | SAS | BEB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG04204 | hp1 | a0004 | c0005 | t0001 | g0056 | SAS | STU | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0139 | SAS | STU | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0170 | AFR | YRI | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18522 | hp2 | a0002 | c0004 | t0018 | g0052 | AFR | YRI | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | CHB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18612 | hp2 | a0005 | c0008 | t0001 | g0082 | EAS | CHB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18906 | hp1 | a0002 | c0002 | t0010 | g0004 | AFR | YRI | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18941 | hp1 | a0001 | c0006 | t0002 | g0105 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18941 | hp2 | a0001 | c0003 | t0009 | g0055 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18960 | hp1 | a0001 | c0001 | t0008 | g0054 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18963 | hp1 | a0001 | c0001 | t0008 | g0077 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18963 | hp2 | a0001 | c0001 | t0022 | g0104 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18986 | hp2 | a0001 | c0001 | t0016 | g0117 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18990 | hp1 | a0001 | c0003 | t0009 | g0006 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19030 | hp2 | a0001 | c0003 | t0011 | g0018 | AFR | LWK | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0068 | AFR | LWK | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19043 | hp2 | a0002 | c0002 | t0003 | g0024 | AFR | LWK | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19088 | hp1 | a0001 | c0003 | t0009 | g0006 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19088 | hp2 | a0001 | c0001 | t0016 | g0053 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0158 | AFR | YRI | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | ASW | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA20129 | hp2 | a0001 | c0001 | t0017 | g0093 | AFR | ASW | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0065 | EUR | TSI | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
NA20752 | hp2 | a0001 | c0003 | t0013 | g0176 | EUR | TSI | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01123 | hp1 | a0003 | c0009 | t0003 | g0167 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0165 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02109 | hp1 | a0001 | c0003 | t0014 | g0174 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02109 | hp2 | a0001 | c0003 | t0004 | g0035 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02486 | hp2 | a0001 | c0003 | t0012 | g0045 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02559 | hp1 | a0002 | c0002 | t0015 | g0015 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0094 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03471 | hp1 | a0001 | c0001 | t0026 | g0021 | AFR | MSL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG03471 | hp2 | a0001 | c0001 | t0019 | g0173 | AFR | MSL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG06807 | hp1 | a0002 | c0002 | t0003 | g0033 | AFR | USA | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | USA | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0113 | REF | REF | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0020 | REF | REF | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:75012527
|
C | G | 1 | a0003 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.146C>G | p.Thr49Ser | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/4 | 358/5011 | 146/933 | 49/310 | chr4 | 75012527 | ||
chr4:75012704
|
G | C | 1 | a0004 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.323G>C | p.Gly108Ala | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/4 | 535/5011 | 323/933 | 108/310 | chr4 | 75012704 | ||
chr4:75012739
|
A | G | 1 | a0005 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.358A>G | p.Thr120Ala | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/4 | 570/5011 | 358/933 | 120/310 | chr4 | 75012739 | ||
chr4:75012761
|
C | T | 4 | a0002a0003a0005others(1): Show | 55 | HG01123.hp1 HG01123.hp2 HG01167.hp1 others(52): Show |
missense_variant | MODERATE | c.380C>T | p.Ser127Leu | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/4 | 592/5011 | 380/933 | 127/310 | chr4 | 75012761 | ||
chr4:75046222
|
A | G | 1 | a0006 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.908A>G | p.Asn303Ser | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1120/5011 | 908/933 | 303/310 | chr4 | 75046222 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:75012762
|
G | A | 1 | a0001c0006 | 1 | NA18941.hp1 | synonymous_variant | LOW | c.381G>A | p.Ser127Ser | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/4 | 593/5011 | 381/933 | 127/310 | chr4 | 75012762 | ||
chr4:75012969
|
G | A | 3 | a0002c0002a0003c0009a0005c0008 | 49 | HG01123.hp1 HG01123.hp2 HG01167.hp1 others(46): Show |
synonymous_variant | LOW | c.588G>A | p.Pro196Pro | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/4 | 800/5011 | 588/933 | 196/310 | chr4 | 75012969 | ||
chr4:75013026
|
A | G | 6 | a0001c0003a0002c0002a0002c0004others(3): Show | 79 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(76): Show |
synonymous_variant | LOW | c.645A>G | p.Val215Val | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/4 | 857/5011 | 645/933 | 215/310 | chr4 | 75013026 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:74933239
|
G | A | 1 | a0002c0004t0018 | 1 | NA18522.hp2 | 5_prime_UTR_variant | MODIFIER | c.-89G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/4 | 89 | chr4 | 74933239 | |||||
chr4:74933308
|
G | C | 7 | a0001c0001t0007a0001c0001t0019a0001c0001t0020others(4): Show | 10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-20G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/4 | 20 | chr4 | 74933308 | |||||
chr4:75046338
|
C | T | 1 | a0006c0007t0032 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 91 | chr4 | 75046338 | |||||
chr4:75046521
|
C | G | 1 | a0002c0002t0031 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*274C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 274 | chr4 | 75046521 | |||||
chr4:75046554
|
C | T | 20 | a0001c0001t0003a0001c0001t0005a0001c0001t0017others(17): Show | 42 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*307C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 307 | chr4 | 75046554 | |||||
chr4:75046696
|
C | T | 20 | a0001c0001t0003a0001c0001t0005a0001c0001t0017others(17): Show | 42 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*449C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 449 | chr4 | 75046696 | |||||
chr4:75046787
|
A | G | 21 | a0001c0001t0003a0001c0001t0005a0001c0001t0017others(18): Show | 43 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*540A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 540 | chr4 | 75046787 | |||||
chr4:75047078
|
G | A | 2 | a0001c0001t0017a0001c0001t0019 | 3 | HG01891.hp1 HG03471.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*831G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 831 | chr4 | 75047078 | |||||
chr4:75047191
|
G | A | 1 | a0001c0001t0021 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*944G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 944 | chr4 | 75047191 | |||||
chr4:75047203
|
C | T | 19 | a0001c0001t0003a0001c0001t0005a0001c0001t0017others(16): Show | 41 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*956C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 956 | chr4 | 75047203 | |||||
chr4:75047386
|
C | T | 1 | a0002c0002t0024 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1139C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1139 | chr4 | 75047386 | |||||
chr4:75047531
|
A | C | 20 | a0001c0001t0003a0001c0001t0005a0001c0001t0017others(17): Show | 42 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1284A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1284 | chr4 | 75047531 | |||||
chr4:75047602
|
A | G | 30 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(27): Show | 111 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1355A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1355 | chr4 | 75047602 | |||||
chr4:75047642
|
A | T | 20 | a0001c0001t0003a0001c0001t0005a0001c0001t0017others(17): Show | 42 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1395A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1395 | chr4 | 75047642 | |||||
chr4:75047822
|
G | A | 17 | a0001c0001t0003a0001c0001t0017a0001c0001t0019others(14): Show | 33 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1575G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1575 | chr4 | 75047822 | |||||
chr4:75047896
|
C | A | 3 | a0001c0001t0005a0001c0001t0020a0001c0001t0026 | 9 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1649C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1649 | chr4 | 75047896 | |||||
chr4:75047924
|
A | G | 17 | a0001c0001t0003a0001c0001t0017a0001c0001t0019others(14): Show | 33 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1677A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1677 | chr4 | 75047924 | |||||
chr4:75047983
|
C | T | 1 | a0001c0001t0016 | 2 | NA18986.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1736C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1736 | chr4 | 75047983 | |||||
chr4:75048090
|
C | T | 1 | a0001c0001t0023 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1843C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1843 | chr4 | 75048090 | |||||
chr4:75048250
|
C | T | 2 | a0001c0001t0017a0001c0001t0019 | 3 | HG01891.hp1 HG03471.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2003C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2003 | chr4 | 75048250 | |||||
chr4:75048392
|
C | G | 1 | a0001c0001t0030 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2145C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2145 | chr4 | 75048392 | |||||
chr4:75048393
|
A | G | 16 | a0001c0001t0003a0001c0001t0017a0001c0001t0019others(13): Show | 32 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2146A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2146 | chr4 | 75048393 | |||||
chr4:75048412
|
G | A | 1 | a0002c0002t0015 | 2 | HG02559.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2165G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2165 | chr4 | 75048412 | |||||
chr4:75048485
|
G | A | 1 | a0001c0003t0011 | 3 | HG02970.hp2 HG03453.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2238G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2238 | chr4 | 75048485 | |||||
chr4:75048620
|
C | T | 17 | a0001c0001t0003a0001c0001t0017a0001c0001t0019others(14): Show | 33 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2373C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2373 | chr4 | 75048620 | |||||
chr4:75048637
|
C | G | 17 | a0001c0001t0003a0001c0001t0017a0001c0001t0019others(14): Show | 33 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2390C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2390 | chr4 | 75048637 | |||||
chr4:75048802
|
C | T | 17 | a0001c0001t0003a0001c0001t0017a0001c0001t0019others(14): Show | 33 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2555C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2555 | chr4 | 75048802 | |||||
chr4:75048821
|
C | T | 1 | a0002c0002t0029 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2574C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2574 | chr4 | 75048821 | |||||
chr4:75048838
|
G | A | 1 | a0001c0001t0022 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2591G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2591 | chr4 | 75048838 | |||||
chr4:75048906
|
G | A | 17 | a0001c0001t0003a0001c0001t0017a0001c0001t0019others(14): Show | 33 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2659G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2659 | chr4 | 75048906 | |||||
chr4:75049143
|
G | A | 9 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(6): Show | 68 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2896G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2896 | chr4 | 75049143 | |||||
chr4:75049348
|
AATACTT | A | 4 | a0001c0003t0012a0001c0003t0013a0001c0003t0014others(1): Show | 8 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3105_*3110delCTTA others(2): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3105 | INFO_REALIGN_3_PRIME | chr4 | 75049348 | ||||
chr4:75049452
|
G | C | 1 | a0001c0001t0008 | 4 | HG02129.hp1 HG04184.hp2 NA18960.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3205G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3205 | chr4 | 75049452 | |||||
chr4:75049761
|
A | G | 1 | a0001c0001t0026 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3514A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3514 | chr4 | 75049761 | |||||
chr4:75049766
|
G | A | 1 | a0001c0001t0023 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3519G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3519 | chr4 | 75049766 | |||||
chr4:75049857
|
C | CT | 5 | a0001c0001t0005a0001c0001t0020a0001c0001t0026others(2): Show | 11 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3618dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3619 | INFO_REALIGN_3_PRIME | chr4 | 75049857 | ||||
chr4:75049857
|
C | CTT | 2 | a0001c0003t0009a0002c0002t0025 | 5 | HG00438.hp2 HG03041.hp1 NA18941.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3617_*3618dupTT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3619 | INFO_REALIGN_3_PRIME | chr4 | 75049857 | ||||
chr4:75049857
|
C | CTTT | 3 | a0001c0003t0010a0002c0002t0010a0002c0004t0027 | 5 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3616_*3618dupTTT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3619 | INFO_REALIGN_3_PRIME | chr4 | 75049857 | ||||
chr4:75049857
|
C | CTTTT | 6 | a0001c0001t0003a0001c0003t0003a0001c0003t0012others(3): Show | 15 | HG01123.hp1 HG01255.hp1 HG01361.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3615_*3618dupTTTT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3619 | INFO_REALIGN_3_PRIME | chr4 | 75049857 | ||||
chr4:75049857
|
C | CTTTTT | 5 | a0001c0001t0017a0001c0001t0019a0001c0003t0014others(2): Show | 7 | HG00741.hp2 HG01891.hp1 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3614_*3618dupTTTT others(1): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3619 | INFO_REALIGN_3_PRIME | chr4 | 75049857 | ||||
chr4:75049866
|
C | CT | 4 | a0001c0001t0004a0001c0001t0006a0001c0003t0004others(1): Show | 13 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3633dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3634 | INFO_REALIGN_3_PRIME | chr4 | 75049866 | ||||
chr4:75049866
|
C | T | 21 | a0001c0001t0003a0001c0001t0005a0001c0001t0017others(18): Show | 43 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3619C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3619 | chr4 | 75049866 | |||||
chr4:75049897
|
A | G | 1 | a0001c0001t0030 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3650A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3650 | chr4 | 75049897 | |||||
chr4:75049965
|
A | AT | 3 | a0001c0003t0009a0001c0003t0010a0002c0002t0010 | 8 | HG00438.hp2 HG02622.hp2 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3723dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3724 | INFO_REALIGN_3_PRIME | chr4 | 75049965 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:74933410
|
T | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0004g0009others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+40T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74933410 | ||||||
chr4:74933436
|
G | C | 1 | a0001c0003t0003g0013 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.43+66G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74933436 | ||||||
chr4:74933774
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.43+404C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74933774 | ||||||
chr4:74933836
|
G | T | 1 | a0002c0002t0025g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.43+466G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74933836 | ||||||
chr4:74933892
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43+522A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74933892 | ||||||
chr4:74934075
|
GGCTTCGT others(4): Show |
G | 1 | a0002c0002t0001g0014 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.43+708_43+718delTT others(9): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74934075 | |||||
chr4:74934352
|
T | C | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.43+982T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74934352 | ||||||
chr4:74934362
|
C | T | 10 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+992C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74934362 | ||||||
chr4:74934373
|
G | A | 2 | a0001c0003t0011g0017a0001c0003t0011g0018 | 2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.43+1003G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74934373 | ||||||
chr4:74934546
|
G | C | 12 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+1176G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74934546 | ||||||
chr4:74934836
|
G | A | 2 | a0001c0001t0005g0002a0001c0001t0005g0019 | 3 | HG02622.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.43+1466G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74934836 | ||||||
chr4:74934996
|
C | CT | 151 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0040others(148): Show | 159 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.43+1640dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74934996 | |||||
chr4:74934996
|
C | CTT | 8 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0002g0164others(5): Show | 8 | HG00438.hp2 HG00741.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.43+1639_43+1640dup others(2): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74934996 | |||||
chr4:74934996
|
CTT | C | 10 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+1639_43+1640del others(2): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74934996 | |||||
chr4:74935084
|
G | A | 3 | a0002c0002t0010g0004a0002c0002t0010g0030a0002c0004t0027g0029 | 4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.43+1714G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74935084 | ||||||
chr4:74935149
|
A | T | 2 | a0001c0003t0011g0017a0001c0003t0011g0018 | 2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.43+1779A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74935149 | ||||||
chr4:74935228
|
T | C | 10 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+1858T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74935228 | ||||||
chr4:74936373
|
C | T | 1 | a0002c0002t0004g0162 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.43+3003C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936373 | ||||||
chr4:74936379
|
C | T | 1 | a0001c0003t0003g0013 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.43+3009C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936379 | ||||||
chr4:74936445
|
T | TG | 11 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+3075_43+3076ins others(1): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936445 | ||||||
chr4:74936445
|
T | TTG | 148 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0040others(145): Show | 155 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.43+3076_43+3077ins others(2): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74936445 | |||||
chr4:74936449
|
G | T | 159 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0040others(156): Show | 167 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.43+3079G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936449 | ||||||
chr4:74936453
|
G | T | 155 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0040others(152): Show | 163 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.43+3083G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936453 | ||||||
chr4:74936453
|
GTTT | G | 11 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+3088_43+3090del others(3): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74936453 | |||||
chr4:74936456
|
T | G | 128 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0040others(125): Show | 134 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.43+3086T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936456 | ||||||
chr4:74936456
|
T | TG | 4 | a0001c0001t0001g0157a0001c0003t0001g0158a0001c0003t0002g0156others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+3086_43+3087ins others(1): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936456 | ||||||
chr4:74936457
|
T | G | 1 | a0001c0001t0002g0159 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.43+3087T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936457 | ||||||
chr4:74936461
|
G | T | 1 | a0001c0001t0002g0159 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.43+3091G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936461 | ||||||
chr4:74936515
|
G | A | 11 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+3145G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936515 | ||||||
chr4:74936528
|
A | T | 1 | a0001c0003t0001g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.43+3158A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936528 | ||||||
chr4:74936602
|
C | T | 10 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+3232C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936602 | ||||||
chr4:74936609
|
A | G | 1 | a0001c0001t0002g0135 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.43+3239A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936609 | ||||||
chr4:74936611
|
A | G | 1 | a0001c0001t0002g0135 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.43+3241A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936611 | ||||||
chr4:74936616
|
T | G | 1 | a0001c0001t0002g0135 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.43+3246T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936616 | ||||||
chr4:74936631
|
A | T | 2 | a0002c0002t0010g0004a0002c0002t0010g0030 | 3 | HG02622.hp2 HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.43+3261A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936631 | ||||||
chr4:74936757
|
G | A | 11 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+3387G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936757 | ||||||
chr4:74937018
|
A | G | 2 | a0001c0001t0002g0133a0001c0001t0008g0134 | 2 | HG04184.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.43+3648A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74937018 | ||||||
chr4:74937652
|
A | G | 1 | a0002c0002t0001g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.43+4282A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74937652 | ||||||
chr4:74937702
|
A | G | 1 | a0001c0001t0002g0154 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.43+4332A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74937702 | ||||||
chr4:74937902
|
T | C | 170 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0040others(167): Show | 178 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.43+4532T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74937902 | ||||||
chr4:74938086
|
G | A | 10 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+4716G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938086 | ||||||
chr4:74938259
|
G | A | 1 | a0002c0002t0001g0031 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.43+4889G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938259 | ||||||
chr4:74938267
|
A | G | 11 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+4897A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938267 | ||||||
chr4:74938328
|
G | A | 3 | a0002c0002t0010g0004a0002c0002t0010g0030a0002c0004t0027g0029 | 4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.43+4958G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938328 | ||||||
chr4:74938382
|
A | G | 4 | a0002c0002t0010g0004a0002c0002t0010g0030a0002c0002t0025g0181others(1): Show | 5 | HG02622.hp2 HG02717.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+5012A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938382 | ||||||
chr4:74938414
|
A | G | 10 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+5044A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938414 | ||||||
chr4:74938456
|
T | A | 4 | a0001c0001t0001g0157a0001c0003t0001g0158a0001c0003t0002g0156others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+5086T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938456 | ||||||
chr4:74938617
|
G | T | 6 | a0001c0003t0013g0175a0001c0003t0013g0176a0001c0003t0014g0174others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+5247G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938617 | ||||||
chr4:74938698
|
T | G | 4 | a0002c0002t0010g0004a0002c0002t0010g0030a0002c0002t0025g0181others(1): Show | 5 | HG02622.hp2 HG02717.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+5328T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938698 | ||||||
chr4:74938845
|
C | T | 10 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+5475C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938845 | ||||||
chr4:74938849
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.43+5479A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938849 | ||||||
chr4:74939047
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.43+5677G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74939047 | ||||||
chr4:74939048
|
A | T | 61 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(58): Show | 62 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.43+5678A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74939048 | ||||||
chr4:74939302
|
G | T | 1 | a0002c0002t0025g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.43+5932G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74939302 | ||||||
chr4:74939416
|
A | T | 1 | a0001c0001t0001g0168 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.43+6046A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74939416 | ||||||
chr4:74939572
|
CTT | C | 61 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(58): Show | 62 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.43+6205_43+6206del others(2): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74939572 | |||||
chr4:74939766
|
C | G | 2 | a0002c0002t0001g0152a0002c0002t0001g0153 | 2 | HG03017.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.43+6396C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74939766 | ||||||
chr4:74939803
|
T | C | 6 | a0002c0002t0003g0033a0002c0002t0004g0034a0002c0002t0010g0004others(3): Show | 7 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+6433T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74939803 | ||||||
chr4:74940019
|
G | C | 10 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+6649G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74940019 | ||||||
chr4:74940044
|
G | GT | 4 | a0001c0001t0001g0157a0001c0003t0001g0158a0001c0003t0002g0156others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+6682dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74940044 | |||||
chr4:74940588
|
A | T | 1 | a0001c0001t0001g0130 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.43+7218A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74940588 | ||||||
chr4:74940718
|
C | T | 1 | a0001c0001t0002g0129 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.43+7348C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74940718 | ||||||
chr4:74940869
|
G | A | 5 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0003t0003g0013others(2): Show | 9 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.43+7499G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74940869 | ||||||
chr4:74940884
|
A | G | 1 | a0001c0001t0005g0012 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.43+7514A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74940884 | ||||||
chr4:74940911
|
G | C | 1 | a0001c0001t0002g0032 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.43+7541G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74940911 | ||||||
chr4:74940944
|
A | T | 150 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0040others(147): Show | 157 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.43+7574A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74940944 | ||||||
chr4:74941050
|
T | C | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.43+7680T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74941050 | ||||||
chr4:74941372
|
A | G | 170 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0040others(167): Show | 178 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.43+8002A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74941372 | ||||||
chr4:74941473
|
C | G | 1 | a0002c0002t0025g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.43+8103C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74941473 | ||||||
chr4:74941519
|
C | T | 10 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+8149C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74941519 | ||||||
chr4:74941986
|
T | C | 151 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0040others(148): Show | 158 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.43+8616T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74941986 | ||||||
chr4:74941994
|
G | T | 3 | a0001c0001t0002g0150a0002c0002t0001g0151a0002c0002t0001g0161 | 3 | HG00323.hp2 HG01256.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.43+8624G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74941994 | ||||||
chr4:74942012
|
A | G | 171 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0040others(168): Show | 179 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.43+8642A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74942012 | ||||||
chr4:74942073
|
T | A | 62 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(59): Show | 63 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.43+8703T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74942073 | ||||||
chr4:74942501
|
G | A | 1 | a0001c0003t0012g0037 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.43+9131G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74942501 | ||||||
chr4:74942516
|
C | T | 10 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+9146C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74942516 | ||||||
chr4:74942554
|
T | G | 171 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0040others(168): Show | 179 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.43+9184T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74942554 | ||||||
chr4:74942836
|
G | A | 4 | a0001c0001t0001g0157a0001c0003t0001g0158a0001c0003t0002g0156others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+9466G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74942836 | ||||||
chr4:74942894
|
A | G | 1 | a0002c0002t0001g0008 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.43+9524A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74942894 | ||||||
chr4:74943155
|
T | C | 1 | a0001c0001t0005g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.43+9785T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74943155 | ||||||
chr4:74943345
|
A | T | 1 | a0001c0001t0001g0127 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.43+9975A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74943345 | ||||||
chr4:74943497
|
T | TA | 5 | a0002c0002t0003g0033a0002c0002t0004g0034a0002c0002t0010g0004others(2): Show | 6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+10140dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74943497 | |||||
chr4:74943799
|
G | A | 5 | a0002c0002t0003g0033a0002c0002t0004g0034a0002c0002t0010g0004others(2): Show | 6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+10429G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74943799 | ||||||
chr4:74943860
|
A | G | 5 | a0002c0002t0003g0033a0002c0002t0004g0034a0002c0002t0010g0004others(2): Show | 6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+10490A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74943860 | ||||||
chr4:74943868
|
G | A | 1 | a0002c0002t0001g0137 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+10498G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74943868 | ||||||
chr4:74944203
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.43+10833G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74944203 | ||||||
chr4:74944243
|
C | T | 8 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(5): Show | 8 | HG01255.hp2 HG01952.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.43+10873C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74944243 | ||||||
chr4:74944443
|
G | A | 1 | a0001c0001t0023g0084 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.43+11073G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74944443 | ||||||
chr4:74944611
|
C | T | 2 | a0001c0001t0002g0076a0001c0001t0008g0077 | 2 | NA18963.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.43+11241C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74944611 | ||||||
chr4:74944680
|
G | C | 9 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(6): Show | 9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+11310G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74944680 | ||||||
chr4:74944850
|
G | T | 1 | a0002c0002t0001g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.43+11480G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74944850 | ||||||
chr4:74945189
|
C | T | 1 | a0002c0002t0001g0075 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.43+11819C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945189 | ||||||
chr4:74945276
|
A | G | 27 | a0001c0001t0001g0157a0001c0001t0002g0022a0001c0001t0005g0002others(24): Show | 30 | HG01109.hp2 HG01167.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.43+11906A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945276 | ||||||
chr4:74945328
|
T | C | 9 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(6): Show | 9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+11958T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945328 | ||||||
chr4:74945396
|
G | T | 1 | a0002c0002t0001g0151 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.43+12026G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945396 | ||||||
chr4:74945430
|
C | T | 9 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(6): Show | 9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+12060C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945430 | ||||||
chr4:74945447
|
C | T | 8 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0003t0003g0013others(5): Show | 12 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+12077C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945447 | ||||||
chr4:74945492
|
C | A | 1 | a0001c0001t0006g0039 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.43+12122C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945492 | ||||||
chr4:74945573
|
G | A | 4 | a0001c0001t0001g0157a0001c0003t0001g0158a0001c0003t0002g0156others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+12203G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945573 | ||||||
chr4:74945670
|
G | A | 1 | a0001c0001t0002g0085 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.43+12300G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945670 | ||||||
chr4:74945712
|
A | T | 1 | a0002c0002t0001g0073 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.43+12342A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945712 | ||||||
chr4:74946499
|
T | G | 1 | a0001c0001t0002g0086 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.43+13129T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74946499 | ||||||
chr4:74947029
|
A | G | 1 | a0001c0001t0030g0072 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.43+13659A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74947029 | ||||||
chr4:74947398
|
A | G | 1 | a0002c0002t0001g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.43+14028A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74947398 | ||||||
chr4:74947494
|
T | A | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+14124T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74947494 | ||||||
chr4:74947512
|
G | T | 3 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071 | 3 | HG02074.hp1 HG02155.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.43+14142G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74947512 | ||||||
chr4:74947768
|
G | T | 27 | a0001c0001t0001g0157a0001c0001t0002g0022a0001c0001t0005g0002others(24): Show | 30 | HG01109.hp2 HG01167.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.43+14398G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74947768 | ||||||
chr4:74947836
|
T | C | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+14466T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74947836 | ||||||
chr4:74947871
|
C | T | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+14501C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74947871 | ||||||
chr4:74948135
|
A | G | 2 | a0002c0002t0004g0162a0002c0002t0007g0179 | 2 | HG01943.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.43+14765A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74948135 | ||||||
chr4:74948437
|
A | G | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+15067A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74948437 | ||||||
chr4:74948634
|
CAA | C | 4 | a0001c0001t0001g0157a0001c0003t0001g0158a0001c0003t0002g0156others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+15268_43+15269d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74948634 | |||||
chr4:74948788
|
C | T | 5 | a0002c0002t0003g0033a0002c0002t0004g0034a0002c0002t0010g0004others(2): Show | 6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+15418C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74948788 | ||||||
chr4:74948935
|
T | A | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+15565T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74948935 | ||||||
chr4:74948937
|
G | A | 1 | a0002c0002t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.43+15567G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74948937 | ||||||
chr4:74948951
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.43+15581G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74948951 | ||||||
chr4:74948990
|
C | G | 8 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0003t0003g0013others(5): Show | 12 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+15620C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74948990 | ||||||
chr4:74949060
|
G | T | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+15690G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949060 | ||||||
chr4:74949067
|
C | A | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+15697C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949067 | ||||||
chr4:74949238
|
C | T | 2 | a0001c0003t0012g0037a0002c0002t0001g0038 | 2 | HG01167.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.43+15868C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949238 | ||||||
chr4:74949239
|
G | A | 6 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+15869G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949239 | ||||||
chr4:74949461
|
C | T | 1 | a0002c0002t0003g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.43+16091C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949461 | ||||||
chr4:74949470
|
G | A | 2 | a0002c0002t0004g0162a0002c0002t0007g0179 | 2 | HG01943.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.43+16100G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949470 | ||||||
chr4:74949682
|
A | G | 27 | a0001c0001t0001g0157a0001c0001t0002g0022a0001c0001t0005g0002others(24): Show | 30 | HG01109.hp2 HG01167.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.43+16312A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949682 | ||||||
chr4:74949774
|
T | C | 9 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(6): Show | 9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+16404T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949774 | ||||||
chr4:74949821
|
G | A | 1 | a0001c0001t0002g0085 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.43+16451G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949821 | ||||||
chr4:74949835
|
C | CT | 7 | a0001c0001t0001g0157a0001c0001t0002g0125a0001c0003t0001g0158others(4): Show | 7 | HG01884.hp2 HG02027.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.43+16481dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74949835 | |||||
chr4:74949835
|
C | CTT | 4 | a0002c0002t0003g0033a0002c0002t0004g0034a0002c0002t0010g0004others(1): Show | 5 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+16480_43+16481d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74949835 | |||||
chr4:74949835
|
CT | C | 8 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(5): Show | 10 | HG01109.hp2 HG02622.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.43+16481delT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74949835 | |||||
chr4:74950612
|
T | C | 1 | a0001c0003t0001g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.43+17242T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74950612 | ||||||
chr4:74950842
|
A | AT | 9 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0003t0003g0013others(6): Show | 13 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.43+17486dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74950842 | |||||
chr4:74950921
|
C | G | 1 | a0001c0001t0002g0150 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.43+17551C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74950921 | ||||||
chr4:74951053
|
T | C | 14 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(11): Show | 17 | HG01109.hp2 HG01891.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.43+17683T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951053 | ||||||
chr4:74951268
|
G | A | 1 | a0001c0001t0017g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.43+17898G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951268 | ||||||
chr4:74951361
|
T | G | 5 | a0002c0002t0003g0033a0002c0002t0004g0034a0002c0002t0010g0004others(2): Show | 6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+17991T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951361 | ||||||
chr4:74951547
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.43+18177G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951547 | ||||||
chr4:74951586
|
C | T | 2 | a0001c0001t0002g0123a0001c0001t0002g0124 | 2 | HG02027.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.43+18216C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951586 | ||||||
chr4:74951611
|
C | T | 8 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0003t0003g0013others(5): Show | 12 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+18241C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951611 | ||||||
chr4:74951683
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.43+18313G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951683 | ||||||
chr4:74951868
|
C | T | 7 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0003t0003g0013others(4): Show | 11 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+18498C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951868 | ||||||
chr4:74951885
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.43+18515C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951885 | ||||||
chr4:74951977
|
G | A | 1 | a0001c0001t0017g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.43+18607G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951977 | ||||||
chr4:74951978
|
G | T | 1 | a0001c0001t0017g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.43+18608G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951978 | ||||||
chr4:74952594
|
A | T | 1 | a0001c0001t0019g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43+19224A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74952594 | ||||||
chr4:74952647
|
T | C | 4 | a0001c0001t0001g0157a0001c0003t0001g0158a0001c0003t0002g0156others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+19277T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74952647 | ||||||
chr4:74952676
|
A | G | 1 | a0002c0002t0015g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.43+19306A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74952676 | ||||||
chr4:74952728
|
C | T | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+19358C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74952728 | ||||||
chr4:74952978
|
A | G | 13 | a0001c0001t0001g0157a0001c0001t0002g0022a0001c0001t0005g0002others(10): Show | 15 | HG01109.hp2 HG01884.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.43+19608A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74952978 | ||||||
chr4:74953046
|
T | C | 1 | a0002c0002t0001g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.43+19676T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74953046 | ||||||
chr4:74953189
|
A | G | 178 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0040others(175): Show | 188 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.43+19819A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74953189 | ||||||
chr4:74953372
|
G | A | 9 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(6): Show | 9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+20002G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74953372 | ||||||
chr4:74953840
|
G | A | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+20470G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74953840 | ||||||
chr4:74953871
|
A | G | 1 | a0001c0001t0002g0007 | 2 | NA19004.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.43+20501A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74953871 | ||||||
chr4:74954157
|
G | T | 1 | a0001c0001t0008g0077 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.43+20787G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74954157 | ||||||
chr4:74954586
|
G | T | 9 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(6): Show | 9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+21216G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74954586 | ||||||
chr4:74954608
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+21238A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74954608 | ||||||
chr4:74954617
|
G | A | 2 | a0001c0001t0007g0170a0001c0003t0014g0171 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.43+21247G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74954617 | ||||||
chr4:74954621
|
A | G | 1 | a0001c0001t0006g0166 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.43+21251A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74954621 | ||||||
chr4:74954690
|
G | A | 4 | a0001c0001t0001g0157a0001c0003t0001g0158a0001c0003t0002g0156others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+21320G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74954690 | ||||||
chr4:74954887
|
A | G | 1 | a0001c0001t0008g0122 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.43+21517A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74954887 | ||||||
chr4:74954917
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.43+21547G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74954917 | ||||||
chr4:74955232
|
G | GA | 9 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0003t0003g0013others(6): Show | 13 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.43+21874dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74955232 | |||||
chr4:74955232
|
GA | G | 11 | a0001c0001t0002g0022a0001c0001t0002g0083a0001c0001t0005g0002others(8): Show | 13 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.43+21874delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74955232 | |||||
chr4:74955829
|
T | C | 9 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(6): Show | 9 | HG00438.hp2 HG01255.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.43+22459T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74955829 | ||||||
chr4:74956373
|
T | C | 1 | a0001c0001t0017g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.43+23003T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74956373 | ||||||
chr4:74956672
|
A | G | 2 | a0002c0002t0001g0065a0002c0002t0001g0066 | 2 | HG01433.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.43+23302A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74956672 | ||||||
chr4:74956709
|
TC | T | 4 | a0001c0001t0001g0157a0001c0003t0001g0158a0001c0003t0002g0156others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+23342delC | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74956709 | |||||
chr4:74956965
|
T | C | 9 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(6): Show | 9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+23595T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74956965 | ||||||
chr4:74957493
|
G | T | 1 | a0001c0001t0002g0150 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.43+24123G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74957493 | ||||||
chr4:74958052
|
G | T | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.43+24682G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74958052 | ||||||
chr4:74958424
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.43+25054C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74958424 | ||||||
chr4:74958482
|
T | G | 5 | a0002c0002t0003g0033a0002c0002t0004g0034a0002c0002t0010g0004others(2): Show | 6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+25112T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74958482 | ||||||
chr4:74958574
|
C | T | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+25204C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74958574 | ||||||
chr4:74958629
|
G | A | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0002c0002t0031g0043 | 3 | HG03491.hp1 NA19010.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.43+25259G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74958629 | ||||||
chr4:74958815
|
C | A | 4 | a0001c0001t0001g0157a0001c0003t0001g0158a0001c0003t0002g0156others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+25445C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74958815 | ||||||
chr4:74958867
|
G | C | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+25497G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74958867 | ||||||
chr4:74958988
|
G | A | 1 | a0002c0002t0001g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.43+25618G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74958988 | ||||||
chr4:74959448
|
T | C | 1 | a0002c0002t0001g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.43+26078T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74959448 | ||||||
chr4:74959651
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+26281A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74959651 | ||||||
chr4:74959696
|
T | G | 1 | a0002c0002t0024g0140 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.43+26326T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74959696 | ||||||
chr4:74959801
|
G | A | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+26431G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74959801 | ||||||
chr4:74959926
|
C | T | 1 | a0002c0002t0025g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.43+26556C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74959926 | ||||||
chr4:74960065
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | NA19010.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.43+26695G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74960065 | ||||||
chr4:74960222
|
T | C | 1 | a0002c0002t0003g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.43+26852T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74960222 | ||||||
chr4:74960287
|
T | C | 1 | a0001c0001t0002g0096 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.43+26917T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74960287 | ||||||
chr4:74960748
|
C | A | 1 | a0001c0001t0001g0127 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.43+27378C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74960748 | ||||||
chr4:74960852
|
CA | C | 18 | a0001c0001t0001g0157a0001c0001t0007g0170a0001c0001t0019g0173others(15): Show | 19 | HG01167.hp1 HG01361.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.43+27495delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74960852 | |||||
chr4:74960852
|
CAA | C | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+27494_43+27495d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74960852 | |||||
chr4:74961004
|
C | CA | 8 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(5): Show | 9 | HG01109.hp2 HG02622.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.43+27648dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74961004 | |||||
chr4:74961350
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43+27980C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74961350 | ||||||
chr4:74961465
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.43+28095A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74961465 | ||||||
chr4:74961608
|
A | G | 9 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(6): Show | 9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+28238A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74961608 | ||||||
chr4:74961784
|
G | A | 27 | a0001c0001t0001g0157a0001c0001t0002g0022a0001c0001t0005g0002others(24): Show | 30 | HG01109.hp2 HG01167.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.43+28414G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74961784 | ||||||
chr4:74961856
|
T | A | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+28486T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74961856 | ||||||
chr4:74961881
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.43+28511A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74961881 | ||||||
chr4:74962023
|
C | T | 1 | a0001c0001t0002g0129 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.43+28653C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74962023 | ||||||
chr4:74962136
|
G | T | 1 | a0002c0002t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.43+28766G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74962136 | ||||||
chr4:74962346
|
C | CA | 4 | a0001c0001t0001g0157a0001c0003t0001g0158a0001c0003t0002g0156others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+28984dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74962346 | |||||
chr4:74962573
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.43+29203A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74962573 | ||||||
chr4:74962612
|
G | A | 1 | a0001c0001t0005g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.43+29242G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74962612 | ||||||
chr4:74962618
|
C | T | 7 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(4): Show | 7 | HG01361.hp1 HG02109.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.43+29248C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74962618 | ||||||
chr4:74962639
|
G | A | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+29269G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74962639 | ||||||
chr4:74962993
|
A | G | 1 | a0001c0001t0002g0119 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.43+29623A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74962993 | ||||||
chr4:74963062
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.43+29692T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963062 | ||||||
chr4:74963148
|
G | T | 1 | a0001c0001t0002g0085 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.43+29778G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963148 | ||||||
chr4:74963166
|
C | G | 1 | a0002c0002t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.43+29796C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963166 | ||||||
chr4:74963201
|
A | T | 9 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(6): Show | 9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+29831A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963201 | ||||||
chr4:74963261
|
G | C | 36 | a0001c0001t0001g0157a0001c0001t0002g0005a0001c0001t0002g0022others(33): Show | 43 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.43+29891G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963261 | ||||||
chr4:74963281
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+29911A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963281 | ||||||
chr4:74963332
|
C | T | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.43+29962C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963332 | ||||||
chr4:74963333
|
G | A | 9 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(6): Show | 9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+29963G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963333 | ||||||
chr4:74963544
|
A | G | 5 | a0002c0002t0003g0033a0002c0002t0004g0034a0002c0002t0010g0004others(2): Show | 6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+30174A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963544 | ||||||
chr4:74963659
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+30289A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963659 | ||||||
chr4:74963661
|
A | G | 6 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0063others(3): Show | 6 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+30291A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963661 | ||||||
chr4:74963744
|
G | A | 10 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(7): Show | 12 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+30374G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963744 | ||||||
chr4:74963803
|
A | T | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+30433A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963803 | ||||||
chr4:74963815
|
T | C | 1 | a0001c0003t0012g0045 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.43+30445T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963815 | ||||||
chr4:74963836
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+30466A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963836 | ||||||
chr4:74964029
|
C | A | 1 | a0001c0001t0002g0131 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.43+30659C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964029 | ||||||
chr4:74964172
|
T | A | 9 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(6): Show | 9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+30802T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964172 | ||||||
chr4:74964198
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+30828A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964198 | ||||||
chr4:74964367
|
C | T | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+30997C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964367 | ||||||
chr4:74964383
|
C | T | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+31013C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964383 | ||||||
chr4:74964392
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.43+31022A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964392 | ||||||
chr4:74964407
|
C | T | 1 | a0006c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.43+31037C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964407 | ||||||
chr4:74964458
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+31088A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964458 | ||||||
chr4:74964503
|
G | A | 1 | a0001c0003t0009g0163 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.43+31133G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964503 | ||||||
chr4:74964553
|
G | GCA | 9 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(6): Show | 9 | HG01884.hp1 HG02258.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+31208_43+31209d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964553 | |||||
chr4:74964553
|
G | GCACACA | 3 | a0001c0001t0019g0173a0001c0001t0020g0172a0001c0003t0003g0013 | 3 | HG02970.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.43+31204_43+31209d others(8): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964553 | |||||
chr4:74964553
|
G | GCACACAC others(1): Show |
3 | a0002c0002t0003g0033a0002c0002t0004g0034a0002c0004t0027g0029 | 3 | HG01891.hp2 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.43+31202_43+31209d others(10): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964553 | |||||
chr4:74964553
|
G | GCACACAC others(3): Show |
16 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0007g0170others(13): Show | 21 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.43+31200_43+31209d others(12): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964553 | |||||
chr4:74964553
|
G | GCACACAC others(9): Show |
1 | a0001c0001t0001g0157 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.43+31194_43+31209d others(18): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964553 | |||||
chr4:74964553
|
G | GCACACAC others(11): Show |
2 | a0001c0003t0001g0158a0001c0003t0002g0156 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.43+31192_43+31209d others(20): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964553 | |||||
chr4:74964553
|
G | GCACACAC others(13): Show |
1 | a0002c0002t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.43+31190_43+31209d others(22): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964553 | |||||
chr4:74964553
|
G | GCACACAC others(17): Show |
1 | a0002c0002t0025g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.43+31186_43+31209d others(26): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964553 | |||||
chr4:74964577
|
A | ACACACAC others(9): Show |
5 | a0001c0001t0002g0022a0002c0002t0003g0003a0002c0002t0003g0024others(2): Show | 6 | HG02615.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+31209_43+31210i others(18): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964577 | |||||
chr4:74964577
|
A | ACACACAC others(7): Show |
4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+31209_43+31210i others(16): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964577 | |||||
chr4:74965115
|
C | T | 2 | a0001c0001t0002g0062a0001c0001t0002g0063 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.43+31745C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965115 | ||||||
chr4:74965300
|
T | C | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+31930T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965300 | ||||||
chr4:74965388
|
C | T | 1 | a0002c0002t0031g0043 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.43+32018C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965388 | ||||||
chr4:74965406
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43+32036G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965406 | ||||||
chr4:74965408
|
G | A | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32038G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965408 | ||||||
chr4:74965457
|
T | G | 1 | a0002c0002t0001g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.43+32087T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965457 | ||||||
chr4:74965560
|
G | A | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32190G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965560 | ||||||
chr4:74965646
|
TC | T | 2 | a0002c0002t0010g0004a0002c0002t0010g0030 | 3 | HG02622.hp2 HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.43+32277delC | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965646 | ||||||
chr4:74965686
|
G | A | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32316G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965686 | ||||||
chr4:74965825
|
G | T | 1 | a0001c0001t0002g0086 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.43+32455G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965825 | ||||||
chr4:74965874
|
G | A | 1 | a0006c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.43+32504G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965874 | ||||||
chr4:74965882
|
T | C | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32512T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965882 | ||||||
chr4:74966042
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32672A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966042 | ||||||
chr4:74966054
|
C | T | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32684C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966054 | ||||||
chr4:74966179
|
C | T | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32809C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966179 | ||||||
chr4:74966180
|
G | A | 7 | a0001c0001t0021g0044a0001c0003t0028g0067a0002c0002t0003g0033others(4): Show | 8 | HG00741.hp2 HG01891.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+32810G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966180 | ||||||
chr4:74966281
|
T | C | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32911T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966281 | ||||||
chr4:74966322
|
A | T | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32952A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966322 | ||||||
chr4:74966524
|
A | G | 1 | a0001c0001t0002g0154 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.43+33154A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966524 | ||||||
chr4:74966525
|
G | A | 5 | a0002c0002t0003g0033a0002c0002t0004g0034a0002c0002t0010g0004others(2): Show | 6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+33155G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966525 | ||||||
chr4:74966635
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+33265A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966635 | ||||||
chr4:74966693
|
C | T | 1 | a0002c0002t0001g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.43+33323C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966693 | ||||||
chr4:74966854
|
G | A | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+33484G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966854 | ||||||
chr4:74967331
|
G | A | 1 | a0002c0002t0001g0046 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.43+33961G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74967331 | ||||||
chr4:74967369
|
C | A | 6 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0063others(3): Show | 6 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+33999C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74967369 | ||||||
chr4:74967604
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.43+34234T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74967604 | ||||||
chr4:74967643
|
C | T | 9 | a0001c0001t0007g0170a0001c0001t0019g0173a0001c0001t0020g0172others(6): Show | 9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+34273C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74967643 | ||||||
chr4:74967673
|
C | A | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+34303C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74967673 | ||||||
chr4:74967924
|
T | C | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+34554T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74967924 | ||||||
chr4:74968032
|
C | G | 1 | a0001c0001t0002g0032 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.43+34662C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74968032 | ||||||
chr4:74968236
|
A | C | 16 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060others(13): Show | 16 | HG00438.hp2 HG01255.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.43+34866A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74968236 | ||||||
chr4:74968300
|
T | C | 1 | a0002c0002t0003g0025 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43+34930T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74968300 | ||||||
chr4:74968639
|
G | C | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.43+35269G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74968639 | ||||||
chr4:74969158
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0098 | 2 | HG03130.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.43+35788G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74969158 | ||||||
chr4:74969170
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.43+35800G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74969170 | ||||||
chr4:74969481
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.43+36111C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74969481 | ||||||
chr4:74969507
|
G | A | 6 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0130others(3): Show | 6 | HG00597.hp2 HG01169.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+36137G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74969507 | ||||||
chr4:74969691
|
G | A | 4 | a0001c0001t0001g0157a0001c0003t0001g0158a0001c0003t0002g0156others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+36321G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74969691 | ||||||
chr4:74969815
|
G | A | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+36445G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74969815 | ||||||
chr4:74969952
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43+36582A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74969952 | ||||||
chr4:74970008
|
C | T | 1 | a0001c0001t0016g0117 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.43+36638C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970008 | ||||||
chr4:74970013
|
C | T | 5 | a0001c0001t0002g0022a0002c0002t0003g0003a0002c0002t0003g0024others(2): Show | 6 | HG02615.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+36643C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970013 | ||||||
chr4:74970062
|
G | A | 1 | a0002c0002t0001g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.43+36692G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970062 | ||||||
chr4:74970073
|
C | T | 1 | a0004c0005t0001g0056 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.43+36703C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970073 | ||||||
chr4:74970096
|
G | A | 1 | a0001c0003t0009g0163 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.43+36726G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970096 | ||||||
chr4:74970115
|
T | C | 1 | a0002c0002t0001g0008 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.43+36745T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970115 | ||||||
chr4:74970249
|
T | A | 5 | a0002c0002t0003g0033a0002c0002t0004g0034a0002c0002t0010g0004others(2): Show | 6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+36879T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970249 | ||||||
chr4:74970371
|
C | T | 9 | a0001c0001t0002g0022a0001c0001t0005g0002a0001c0001t0005g0019others(6): Show | 11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+37001C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970371 | ||||||
chr4:74970700
|
A | C | 3 | a0001c0001t0002g0147a0001c0001t0006g0146a0002c0002t0024g0140 | 3 | HG01361.hp2 HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.43+37330A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970700 | ||||||
chr4:74971062
|
A | G | 23 | a0001c0001t0001g0098a0001c0001t0002g0032a0001c0001t0002g0069others(20): Show | 23 | HG00323.hp2 HG00597.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.43+37692A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971062 | ||||||
chr4:74971074
|
C | A | 2 | a0001c0001t0001g0048a0002c0002t0001g0094 | 2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.43+37704C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971074 | ||||||
chr4:74971130
|
C | T | 2 | a0001c0003t0001g0158a0001c0003t0002g0156 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.43+37760C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971130 | ||||||
chr4:74971251
|
G | C | 3 | a0001c0001t0003g0136a0001c0001t0005g0089a0002c0004t0001g0155 | 3 | HG01884.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.43+37881G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971251 | ||||||
chr4:74971349
|
T | C | 5 | a0002c0002t0003g0027a0002c0002t0003g0033a0002c0002t0004g0034others(2): Show | 6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+37979T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971349 | ||||||
chr4:74971424
|
G | A | 1 | a0002c0002t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.43+38054G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971424 | ||||||
chr4:74971496
|
T | C | 1 | a0001c0001t0002g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.43+38126T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971496 | ||||||
chr4:74971617
|
T | C | 3 | a0001c0003t0003g0013a0001c0003t0011g0017a0001c0003t0011g0018 | 3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.43+38247T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971617 | ||||||
chr4:74971640
|
T | A | 6 | a0001c0001t0002g0022a0002c0002t0003g0027a0002c0002t0003g0033others(3): Show | 7 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+38270T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971640 | ||||||
chr4:74971788
|
C | A | 65 | a0001c0001t0001g0121a0001c0001t0001g0168a0001c0001t0002g0007others(62): Show | 69 | HG00438.hp2 HG00597.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.43+38418C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971788 | ||||||
chr4:74971978
|
G | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.43+38608G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971978 | ||||||
chr4:74972059
|
A | G | 2 | a0001c0003t0001g0158a0001c0003t0002g0156 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.43+38689A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972059 | ||||||
chr4:74972210
|
A | G | 1 | a0002c0002t0001g0066 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43+38840A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972210 | ||||||
chr4:74972396
|
C | T | 2 | a0002c0002t0010g0004a0002c0002t0010g0030 | 3 | HG02622.hp2 HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.43+39026C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972396 | ||||||
chr4:74972557
|
C | T | 3 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026 | 4 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.43+39187C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972557 | ||||||
chr4:74972571
|
T | C | 3 | a0002c0002t0001g0065a0002c0004t0007g0177a0002c0004t0007g0178 | 3 | HG01167.hp2 HG01169.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.43+39201T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972571 | ||||||
chr4:74972706
|
CG | C | 65 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(62): Show | 68 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.43+39337delG | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972706 | ||||||
chr4:74972732
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.43+39362A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972732 | ||||||
chr4:74972887
|
C | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.43+39517C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972887 | ||||||
chr4:74972920
|
G | A | 1 | a0002c0002t0001g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.44-39505G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972920 | ||||||
chr4:74973013
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-39412A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973013 | ||||||
chr4:74973141
|
G | T | 1 | a0002c0002t0001g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.44-39284G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973141 | ||||||
chr4:74973233
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-39192A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973233 | ||||||
chr4:74973302
|
A | G | 3 | a0001c0003t0003g0013a0001c0003t0011g0017a0001c0003t0011g0018 | 3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.44-39123A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973302 | ||||||
chr4:74973850
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-38575A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973850 | ||||||
chr4:74973854
|
A | ATGTGTG | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-38559_44-38554d others(8): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74973854 | |||||
chr4:74973884
|
G | A | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.44-38541G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973884 | ||||||
chr4:74973897
|
G | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-38528G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973897 | ||||||
chr4:74973903
|
GAA | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-38520_44-38519d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74973903 | |||||
chr4:74973911
|
G | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-38514G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973911 | ||||||
chr4:74973923
|
G | A | 97 | a0001c0001t0001g0040a0001c0001t0001g0048a0001c0001t0001g0121others(94): Show | 106 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.44-38502G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973923 | ||||||
chr4:74974103
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.44-38322T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974103 | ||||||
chr4:74974223
|
A | C | 1 | a0002c0002t0001g0038 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.44-38202A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974223 | ||||||
chr4:74974513
|
T | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-37912T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974513 | ||||||
chr4:74974637
|
C | G | 2 | a0001c0003t0001g0158a0001c0003t0002g0156 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-37788C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974637 | ||||||
chr4:74974641
|
C | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-37784C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974641 | ||||||
chr4:74974728
|
G | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-37697G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974728 | ||||||
chr4:74974763
|
A | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-37662A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974763 | ||||||
chr4:74974838
|
A | G | 3 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0026g0021 | 4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-37587A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974838 | ||||||
chr4:74974958
|
G | A | 4 | a0001c0003t0013g0175a0001c0003t0013g0176a0001c0003t0014g0174others(1): Show | 4 | HG00741.hp2 HG01361.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-37467G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974958 | ||||||
chr4:74974989
|
A | T | 1 | a0001c0001t0016g0117 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.44-37436A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974989 | ||||||
chr4:74975106
|
C | A | 1 | a0002c0002t0001g0014 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.44-37319C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74975106 | ||||||
chr4:74975160
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-37265A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74975160 | ||||||
chr4:74975193
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-37232A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74975193 | ||||||
chr4:74975285
|
C | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-37140C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74975285 | ||||||
chr4:74975331
|
G | T | 55 | a0001c0001t0001g0121a0001c0001t0001g0168a0001c0001t0002g0007others(52): Show | 57 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.44-37094G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74975331 | ||||||
chr4:74975604
|
G | A | 2 | a0002c0004t0001g0155a0002c0004t0018g0052 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.44-36821G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74975604 | ||||||
chr4:74975878
|
A | G | 94 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(91): Show | 103 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.44-36547A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74975878 | ||||||
chr4:74976031
|
G | C | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-36394G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74976031 | ||||||
chr4:74976193
|
C | T | 1 | a0001c0001t0002g0129 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.44-36232C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74976193 | ||||||
chr4:74976210
|
C | T | 1 | a0002c0002t0003g0003 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.44-36215C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74976210 | ||||||
chr4:74976292
|
G | A | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-36133G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74976292 | ||||||
chr4:74976432
|
A | G | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-35993A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74976432 | ||||||
chr4:74976463
|
G | A | 2 | a0001c0003t0001g0158a0001c0003t0002g0156 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-35962G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74976463 | ||||||
chr4:74976856
|
T | G | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-35569T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74976856 | ||||||
chr4:74976894
|
C | A | 3 | a0001c0003t0003g0013a0001c0003t0011g0017a0001c0003t0011g0018 | 3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.44-35531C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74976894 | ||||||
chr4:74977408
|
GA | G | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-35010delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74977408 | |||||
chr4:74977473
|
G | A | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-34952G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74977473 | ||||||
chr4:74977505
|
G | C | 4 | a0001c0001t0002g0007a0001c0001t0002g0078a0001c0001t0002g0079others(1): Show | 5 | HG02015.hp1 HG02040.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-34920G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74977505 | ||||||
chr4:74977761
|
CAA | C | 2 | a0001c0003t0004g0001a0001c0003t0004g0035 | 5 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-34662_44-34661d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74977761 | |||||
chr4:74977781
|
C | G | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-34644C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74977781 | ||||||
chr4:74978081
|
G | C | 1 | a0001c0003t0012g0045 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.44-34344G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978081 | ||||||
chr4:74978172
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.44-34253C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978172 | ||||||
chr4:74978376
|
T | C | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-34049T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978376 | ||||||
chr4:74978381
|
G | A | 3 | a0001c0003t0003g0013a0001c0003t0011g0017a0001c0003t0011g0018 | 3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.44-34044G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978381 | ||||||
chr4:74978555
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.44-33870G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978555 | ||||||
chr4:74978809
|
T | G | 8 | a0001c0001t0007g0170a0001c0003t0012g0045a0001c0003t0012g0049others(5): Show | 8 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-33616T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978809 | ||||||
chr4:74978846
|
C | T | 1 | a0002c0002t0001g0031 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.44-33579C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978846 | ||||||
chr4:74978853
|
A | G | 3 | a0001c0003t0003g0013a0001c0003t0011g0017a0001c0003t0011g0018 | 3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.44-33572A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978853 | ||||||
chr4:74978948
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.44-33477G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978948 | ||||||
chr4:74979117
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-33308C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979117 | ||||||
chr4:74979134
|
GCA | G | 3 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0026g0021 | 4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-33278_44-33277d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74979134 | |||||
chr4:74979149
|
A | C | 8 | a0001c0003t0003g0013a0001c0003t0011g0017a0001c0003t0011g0018others(5): Show | 8 | HG02129.hp2 HG02965.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-33276A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979149 | ||||||
chr4:74979196
|
T | TA | 4 | a0002c0002t0003g0003a0002c0002t0003g0024a0002c0002t0003g0025others(1): Show | 5 | HG02615.hp1 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-33221dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74979196 | |||||
chr4:74979203
|
A | T | 51 | a0001c0001t0001g0121a0001c0001t0001g0168a0001c0001t0002g0007others(48): Show | 53 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.44-33222A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979203 | ||||||
chr4:74979482
|
C | T | 70 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(67): Show | 74 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.44-32943C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979482 | ||||||
chr4:74979514
|
C | A | 3 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0026g0021 | 4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-32911C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979514 | ||||||
chr4:74979624
|
A | G | 3 | a0001c0001t0017g0051a0001c0001t0017g0093a0001c0001t0019g0173 | 3 | HG01891.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.44-32801A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979624 | ||||||
chr4:74979732
|
A | G | 1 | a0002c0002t0001g0038 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.44-32693A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979732 | ||||||
chr4:74979806
|
T | C | 3 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0026g0021 | 4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-32619T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979806 | ||||||
chr4:74979830
|
G | A | 1 | a0002c0002t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.44-32595G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979830 | ||||||
chr4:74979840
|
C | T | 8 | a0001c0001t0007g0170a0001c0003t0012g0045a0001c0003t0012g0049others(5): Show | 8 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-32585C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979840 | ||||||
chr4:74979934
|
C | T | 8 | a0001c0001t0007g0170a0001c0003t0012g0045a0001c0003t0012g0049others(5): Show | 8 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-32491C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979934 | ||||||
chr4:74980002
|
A | G | 2 | a0002c0004t0001g0155a0002c0004t0018g0052 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.44-32423A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980002 | ||||||
chr4:74980083
|
T | C | 1 | a0001c0001t0002g0154 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.44-32342T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980083 | ||||||
chr4:74980127
|
C | T | 2 | a0002c0002t0001g0152a0002c0002t0001g0153 | 2 | HG03017.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.44-32298C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980127 | ||||||
chr4:74980229
|
C | T | 1 | a0001c0001t0001g0113 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.44-32196C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980229 | ||||||
chr4:74980239
|
T | C | 3 | a0001c0003t0003g0013a0001c0003t0011g0017a0001c0003t0011g0018 | 3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.44-32186T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980239 | ||||||
chr4:74980287
|
T | C | 69 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(66): Show | 73 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.44-32138T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980287 | ||||||
chr4:74980323
|
C | T | 2 | a0001c0003t0001g0158a0001c0003t0002g0156 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-32102C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980323 | ||||||
chr4:74980820
|
A | G | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-31605A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980820 | ||||||
chr4:74980996
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.44-31429A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980996 | ||||||
chr4:74981101
|
C | A | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-31324C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74981101 | ||||||
chr4:74981420
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.44-31005G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74981420 | ||||||
chr4:74981647
|
C | T | 2 | a0002c0002t0001g0068a0002c0002t0001g0132 | 2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.44-30778C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74981647 | ||||||
chr4:74981706
|
C | T | 8 | a0001c0001t0007g0170a0001c0003t0012g0045a0001c0003t0012g0049others(5): Show | 8 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-30719C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74981706 | ||||||
chr4:74981845
|
T | C | 94 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(91): Show | 103 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.44-30580T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74981845 | ||||||
chr4:74981879
|
C | CA | 10 | a0001c0001t0002g0005a0001c0001t0002g0061a0001c0001t0003g0136others(7): Show | 14 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.44-30527dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74981879 | |||||
chr4:74981996
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.44-30429T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74981996 | ||||||
chr4:74982203
|
C | A | 1 | a0001c0003t0028g0067 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.44-30222C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74982203 | ||||||
chr4:74982263
|
G | A | 2 | a0001c0001t0002g0086a0002c0002t0001g0057 | 2 | NA18960.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.44-30162G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74982263 | ||||||
chr4:74982417
|
A | C | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-30008A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74982417 | ||||||
chr4:74982459
|
A | ATAAAAT | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-29956_44-29951d others(8): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74982459 | |||||
chr4:74982566
|
C | T | 2 | a0001c0003t0001g0158a0001c0003t0002g0156 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-29859C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74982566 | ||||||
chr4:74982667
|
T | G | 6 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(3): Show | 7 | HG01109.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-29758T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74982667 | ||||||
chr4:74982678
|
G | A | 1 | a0002c0002t0001g0142 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.44-29747G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74982678 | ||||||
chr4:74982878
|
G | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-29547G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74982878 | ||||||
chr4:74983092
|
G | A | 1 | a0001c0001t0002g0005 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.44-29333G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983092 | ||||||
chr4:74983170
|
C | A | 1 | a0002c0002t0001g0066 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.44-29255C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983170 | ||||||
chr4:74983390
|
T | C | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-29035T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983390 | ||||||
chr4:74983647
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.44-28778T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983647 | ||||||
chr4:74983774
|
C | T | 2 | a0001c0001t0002g0086a0002c0002t0001g0057 | 2 | NA18960.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.44-28651C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983774 | ||||||
chr4:74983800
|
A | G | 1 | a0001c0003t0013g0176 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.44-28625A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983800 | ||||||
chr4:74983829
|
C | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-28596C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983829 | ||||||
chr4:74983896
|
G | A | 24 | a0001c0001t0001g0113a0001c0001t0002g0133a0001c0001t0002g0147others(21): Show | 25 | HG01167.hp1 HG01175.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.44-28529G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983896 | ||||||
chr4:74983934
|
C | A | 1 | a0001c0001t0005g0012 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.44-28491C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983934 | ||||||
chr4:74984013
|
A | G | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-28412A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984013 | ||||||
chr4:74984290
|
A | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-28135A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984290 | ||||||
chr4:74984445
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-27980C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984445 | ||||||
chr4:74984470
|
C | T | 2 | a0002c0002t0001g0068a0002c0002t0001g0132 | 2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.44-27955C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984470 | ||||||
chr4:74984471
|
G | A | 3 | a0001c0003t0003g0013a0001c0003t0011g0017a0001c0003t0011g0018 | 3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.44-27954G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984471 | ||||||
chr4:74984507
|
G | A | 10 | a0001c0001t0007g0170a0001c0003t0012g0045a0001c0003t0012g0049others(7): Show | 10 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.44-27918G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984507 | ||||||
chr4:74984766
|
C | G | 2 | a0001c0001t0001g0106a0001c0001t0002g0112 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.44-27659C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984766 | ||||||
chr4:74984827
|
TG | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-27597delG | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984827 | ||||||
chr4:74984892
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-27533C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984892 | ||||||
chr4:74984933
|
T | C | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-27492T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984933 | ||||||
chr4:74984935
|
A | G | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-27490A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984935 | ||||||
chr4:74985325
|
T | A | 10 | a0001c0001t0001g0040a0001c0001t0030g0072a0002c0002t0001g0068others(7): Show | 11 | HG01891.hp2 HG02258.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-27100T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74985325 | ||||||
chr4:74985334
|
A | G | 1 | a0001c0001t0002g0145 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.44-27091A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74985334 | ||||||
chr4:74985545
|
C | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0180a0002c0002t0001g0094 | 3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-26880C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74985545 | ||||||
chr4:74985598
|
A | G | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-26827A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74985598 | ||||||
chr4:74985641
|
T | A | 2 | a0001c0001t0002g0076a0001c0001t0022g0104 | 2 | NA18963.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.44-26784T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74985641 | ||||||
chr4:74985735
|
TGA | T | 2 | a0002c0004t0001g0155a0002c0004t0018g0052 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.44-26685_44-26684d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74985735 | |||||
chr4:74985785
|
T | C | 1 | a0001c0003t0009g0163 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.44-26640T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74985785 | ||||||
chr4:74985791
|
T | C | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-26634T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74985791 | ||||||
chr4:74985875
|
T | C | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-26550T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74985875 | ||||||
chr4:74986147
|
G | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-26278G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986147 | ||||||
chr4:74986152
|
T | C | 8 | a0001c0001t0007g0170a0001c0003t0012g0045a0001c0003t0012g0049others(5): Show | 8 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-26273T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986152 | ||||||
chr4:74986172
|
T | C | 2 | a0001c0003t0001g0158a0001c0003t0002g0156 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-26253T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986172 | ||||||
chr4:74986425
|
A | G | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-26000A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986425 | ||||||
chr4:74986548
|
T | C | 51 | a0001c0001t0001g0121a0001c0001t0001g0168a0001c0001t0002g0007others(48): Show | 53 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.44-25877T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986548 | ||||||
chr4:74986778
|
T | G | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-25647T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986778 | ||||||
chr4:74986808
|
G | C | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-25617G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986808 | ||||||
chr4:74986909
|
A | G | 94 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(91): Show | 103 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.44-25516A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986909 | ||||||
chr4:74986921
|
AGTCAG | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-25498_44-25494d others(7): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74986921 | |||||
chr4:74986950
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-25475C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986950 | ||||||
chr4:74987039
|
A | G | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-25386A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74987039 | ||||||
chr4:74987184
|
G | A | 1 | a0002c0002t0001g0014 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.44-25241G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74987184 | ||||||
chr4:74987624
|
C | T | 8 | a0001c0001t0007g0170a0001c0003t0012g0045a0001c0003t0012g0049others(5): Show | 8 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-24801C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74987624 | ||||||
chr4:74987777
|
A | T | 1 | a0001c0001t0001g0130 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.44-24648A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74987777 | ||||||
chr4:74987889
|
C | T | 1 | a0001c0001t0030g0072 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.44-24536C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74987889 | ||||||
chr4:74987984
|
T | C | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-24441T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74987984 | ||||||
chr4:74988359
|
G | A | 17 | a0001c0001t0001g0113a0001c0001t0002g0133a0001c0001t0002g0147others(14): Show | 18 | HG01167.hp1 HG01175.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.44-24066G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74988359 | ||||||
chr4:74988376
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-24049C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74988376 | ||||||
chr4:74988404
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0002g0112 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.44-24021C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74988404 | ||||||
chr4:74988405
|
G | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-24020G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74988405 | ||||||
chr4:74988487
|
G | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-23938G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74988487 | ||||||
chr4:74988516
|
G | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-23909G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74988516 | ||||||
chr4:74989070
|
G | C | 181 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0040others(178): Show | 191 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.44-23355G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74989070 | ||||||
chr4:74989302
|
A | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-23123A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74989302 | ||||||
chr4:74989308
|
C | G | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-23117C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74989308 | ||||||
chr4:74989341
|
T | C | 24 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0005g0002others(21): Show | 29 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.44-23084T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74989341 | ||||||
chr4:74989498
|
T | C | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-22927T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74989498 | ||||||
chr4:74989508
|
C | T | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-22917C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74989508 | ||||||
chr4:74989790
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-22635C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74989790 | ||||||
chr4:74990075
|
G | A | 2 | a0001c0003t0004g0001a0001c0003t0004g0035 | 5 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-22350G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74990075 | ||||||
chr4:74990252
|
C | G | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-22173C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74990252 | ||||||
chr4:74990404
|
G | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-22021G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74990404 | ||||||
chr4:74991051
|
A | T | 3 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026 | 4 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-21374A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74991051 | ||||||
chr4:74991514
|
CAG | C | 14 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(11): Show | 15 | HG00741.hp2 HG01109.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.44-20898_44-20897d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74991514 | |||||
chr4:74991574
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.44-20851T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74991574 | ||||||
chr4:74991581
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-20844C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74991581 | ||||||
chr4:74991746
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.44-20679G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74991746 | ||||||
chr4:74991792
|
C | T | 1 | a0001c0001t0002g0060 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.44-20633C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74991792 | ||||||
chr4:74992108
|
T | C | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-20317T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992108 | ||||||
chr4:74992115
|
T | G | 93 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(90): Show | 102 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.44-20310T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992115 | ||||||
chr4:74992133
|
C | T | 2 | a0001c0001t0002g0076a0001c0001t0022g0104 | 2 | NA18963.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.44-20292C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992133 | ||||||
chr4:74992150
|
G | A | 1 | a0001c0001t0002g0085 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.44-20275G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992150 | ||||||
chr4:74992247
|
T | C | 1 | a0001c0001t0004g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.44-20178T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992247 | ||||||
chr4:74992295
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-20130C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992295 | ||||||
chr4:74992296
|
G | A | 3 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0026g0021 | 4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-20129G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992296 | ||||||
chr4:74992374
|
T | A | 6 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(3): Show | 7 | HG01109.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-20051T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992374 | ||||||
chr4:74992438
|
C | A | 2 | a0002c0004t0001g0155a0002c0004t0018g0052 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.44-19987C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992438 | ||||||
chr4:74992438
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-19987C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992438 | ||||||
chr4:74992861
|
C | T | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-19564C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992861 | ||||||
chr4:74992893
|
G | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-19532G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992893 | ||||||
chr4:74993172
|
C | G | 1 | a0002c0002t0001g0014 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.44-19253C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74993172 | ||||||
chr4:74993249
|
G | C | 1 | a0001c0001t0002g0135 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.44-19176G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74993249 | ||||||
chr4:74993329
|
T | C | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-19096T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74993329 | ||||||
chr4:74993378
|
G | A | 2 | a0001c0003t0001g0158a0001c0003t0002g0156 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-19047G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74993378 | ||||||
chr4:74993413
|
G | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-19012G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74993413 | ||||||
chr4:74994209
|
C | T | 2 | a0001c0003t0001g0158a0001c0003t0002g0156 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-18216C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74994209 | ||||||
chr4:74994328
|
T | G | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-18097T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74994328 | ||||||
chr4:74994632
|
A | C | 1 | a0002c0002t0001g0038 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.44-17793A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74994632 | ||||||
chr4:74994699
|
A | G | 2 | a0001c0003t0004g0001a0001c0003t0004g0035 | 5 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-17726A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74994699 | ||||||
chr4:74994739
|
G | C | 2 | a0001c0001t0001g0040a0001c0001t0030g0072 | 2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.44-17686G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74994739 | ||||||
chr4:74994799
|
T | TATAA | 39 | a0001c0001t0001g0101a0001c0001t0001g0113a0001c0001t0001g0130others(36): Show | 41 | HG00438.hp1 HG01167.hp1 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.44-17591_44-17588d others(6): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74994799 | |||||
chr4:74994799
|
T | TATAAATA others(1): Show |
4 | a0001c0003t0013g0176a0001c0003t0014g0174a0002c0002t0001g0137others(1): Show | 4 | HG02109.hp1 HG02129.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-17595_44-17588d others(10): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74994799 | |||||
chr4:74994799
|
T | TATAAATA others(5): Show |
3 | a0001c0001t0007g0170a0001c0003t0012g0045a0001c0003t0014g0171 | 3 | HG02486.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.44-17599_44-17588d others(14): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74994799 | |||||
chr4:74994799
|
T | TATAAATA others(9): Show |
1 | a0001c0003t0028g0067 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.44-17603_44-17588d others(18): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74994799 | |||||
chr4:74994799
|
TATAA | T | 65 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(62): Show | 68 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.44-17591_44-17588d others(6): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74994799 | |||||
chr4:74995110
|
A | G | 2 | a0002c0004t0001g0155a0002c0004t0018g0052 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.44-17315A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74995110 | ||||||
chr4:74995766
|
T | C | 66 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(63): Show | 70 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.44-16659T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74995766 | ||||||
chr4:74995813
|
C | T | 8 | a0001c0001t0007g0170a0001c0003t0012g0045a0001c0003t0012g0049others(5): Show | 8 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-16612C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74995813 | ||||||
chr4:74995821
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-16604C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74995821 | ||||||
chr4:74995958
|
C | G | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-16467C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74995958 | ||||||
chr4:74996281
|
A | T | 2 | a0002c0002t0001g0068a0002c0002t0001g0132 | 2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.44-16144A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74996281 | ||||||
chr4:74996294
|
T | G | 1 | a0001c0001t0002g0087 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.44-16131T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74996294 | ||||||
chr4:74996330
|
A | C | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-16095A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74996330 | ||||||
chr4:74996404
|
G | A | 2 | a0002c0004t0001g0155a0002c0004t0018g0052 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.44-16021G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74996404 | ||||||
chr4:74996607
|
A | G | 6 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(3): Show | 7 | HG01109.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-15818A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74996607 | ||||||
chr4:74996834
|
G | C | 3 | a0001c0003t0009g0006a0001c0003t0009g0163a0001c0006t0002g0105 | 4 | HG00438.hp2 NA18941.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-15591G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74996834 | ||||||
chr4:74997083
|
C | T | 5 | a0002c0002t0003g0003a0002c0002t0003g0024a0002c0002t0003g0025others(2): Show | 6 | HG01123.hp1 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-15342C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997083 | ||||||
chr4:74997122
|
C | T | 2 | a0001c0003t0001g0158a0001c0003t0002g0156 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-15303C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997122 | ||||||
chr4:74997160
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | NA19010.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.44-15265C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997160 | ||||||
chr4:74997296
|
A | G | 50 | a0001c0001t0001g0121a0001c0001t0001g0168a0001c0001t0002g0007others(47): Show | 52 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.44-15129A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997296 | ||||||
chr4:74997359
|
G | A | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-15066G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997359 | ||||||
chr4:74997462
|
G | T | 3 | a0001c0001t0005g0012a0001c0001t0005g0128a0001c0001t0020g0172 | 3 | HG02818.hp1 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.44-14963G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997462 | ||||||
chr4:74997583
|
G | A | 1 | a0001c0001t0023g0084 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.44-14842G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997583 | ||||||
chr4:74997703
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-14722C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997703 | ||||||
chr4:74997828
|
A | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-14597A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997828 | ||||||
chr4:74997941
|
T | C | 25 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0005g0002others(22): Show | 30 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.44-14484T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997941 | ||||||
chr4:74997972
|
A | G | 1 | a0001c0001t0006g0166 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.44-14453A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997972 | ||||||
chr4:74998044
|
A | G | 2 | a0001c0003t0004g0001a0001c0003t0004g0035 | 5 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-14381A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998044 | ||||||
chr4:74998049
|
T | G | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-14376T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998049 | ||||||
chr4:74998151
|
T | A | 2 | a0001c0003t0004g0001a0001c0003t0004g0035 | 5 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-14274T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998151 | ||||||
chr4:74998215
|
T | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-14210T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998215 | ||||||
chr4:74998372
|
G | GT | 68 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(65): Show | 72 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.44-14052dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74998372 | |||||
chr4:74998425
|
A | T | 49 | a0001c0001t0001g0121a0001c0001t0001g0168a0001c0001t0002g0007others(46): Show | 51 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.44-14000A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998425 | ||||||
chr4:74998496
|
T | C | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-13929T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998496 | ||||||
chr4:74998573
|
T | G | 1 | a0001c0003t0010g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.44-13852T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998573 | ||||||
chr4:74998612
|
A | G | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-13813A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998612 | ||||||
chr4:74998632
|
T | A | 65 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(62): Show | 69 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.44-13793T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998632 | ||||||
chr4:74998757
|
C | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-13668C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998757 | ||||||
chr4:74998830
|
A | C | 3 | a0001c0003t0001g0158a0001c0003t0002g0156a0002c0002t0001g0014 | 3 | HG01884.hp2 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.44-13595A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998830 | ||||||
chr4:74998986
|
C | G | 49 | a0001c0001t0001g0121a0001c0001t0001g0168a0001c0001t0002g0007others(46): Show | 51 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.44-13439C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998986 | ||||||
chr4:74999194
|
G | A | 49 | a0001c0001t0001g0121a0001c0001t0001g0168a0001c0001t0002g0007others(46): Show | 51 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.44-13231G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74999194 | ||||||
chr4:74999207
|
T | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-13218T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74999207 | ||||||
chr4:74999220
|
G | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-13205G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74999220 | ||||||
chr4:75000048
|
A | G | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-12377A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000048 | ||||||
chr4:75000136
|
T | G | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-12289T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000136 | ||||||
chr4:75000297
|
A | G | 1 | a0001c0001t0002g0125 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.44-12128A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000297 | ||||||
chr4:75000312
|
T | C | 65 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(62): Show | 69 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.44-12113T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000312 | ||||||
chr4:75000365
|
G | A | 2 | a0001c0003t0004g0001a0001c0003t0004g0035 | 5 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-12060G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000365 | ||||||
chr4:75000430
|
C | G | 1 | a0001c0001t0002g0119 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.44-11995C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000430 | ||||||
chr4:75000668
|
C | G | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-11757C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000668 | ||||||
chr4:75000693
|
A | G | 8 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0026g0021others(5): Show | 12 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.44-11732A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000693 | ||||||
chr4:75000711
|
C | A | 1 | a0002c0002t0001g0161 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.44-11714C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000711 | ||||||
chr4:75000846
|
G | A | 2 | a0001c0001t0002g0159a0002c0002t0001g0073 | 2 | NA19005.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.44-11579G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000846 | ||||||
chr4:75000924
|
G | A | 6 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(3): Show | 7 | HG01109.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-11501G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000924 | ||||||
chr4:75000989
|
C | T | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-11436C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000989 | ||||||
chr4:75001088
|
G | T | 3 | a0001c0003t0003g0013a0001c0003t0011g0017a0001c0003t0011g0018 | 3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.44-11337G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75001088 | ||||||
chr4:75001108
|
G | A | 2 | a0001c0003t0001g0158a0001c0003t0002g0156 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-11317G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75001108 | ||||||
chr4:75001504
|
C | T | 3 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0026g0021 | 4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-10921C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75001504 | ||||||
chr4:75001698
|
G | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-10727G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75001698 | ||||||
chr4:75001948
|
G | A | 3 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0026g0021 | 4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-10477G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75001948 | ||||||
chr4:75001950
|
A | C | 7 | a0001c0001t0002g0164a0001c0001t0006g0036a0001c0001t0006g0039others(4): Show | 7 | HG01070.hp1 HG01123.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-10475A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75001950 | ||||||
chr4:75002006
|
A | T | 2 | a0001c0003t0004g0001a0001c0003t0004g0035 | 5 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-10419A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002006 | ||||||
chr4:75002087
|
G | T | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-10338G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002087 | ||||||
chr4:75002381
|
C | T | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-10044C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002381 | ||||||
chr4:75002415
|
C | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-10010C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002415 | ||||||
chr4:75002415
|
C | T | 40 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(37): Show | 40 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.44-10010C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002415 | ||||||
chr4:75002469
|
T | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-9956T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002469 | ||||||
chr4:75002538
|
G | A | 3 | a0001c0003t0003g0013a0001c0003t0011g0017a0001c0003t0011g0018 | 3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.44-9887G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002538 | ||||||
chr4:75002680
|
G | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-9745G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002680 | ||||||
chr4:75002694
|
G | A | 2 | a0001c0003t0001g0158a0001c0003t0002g0156 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-9731G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002694 | ||||||
chr4:75002728
|
G | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-9697G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002728 | ||||||
chr4:75002729
|
G | A | 49 | a0001c0001t0001g0121a0001c0001t0001g0168a0001c0001t0002g0007others(46): Show | 51 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.44-9696G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002729 | ||||||
chr4:75002988
|
A | G | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-9437A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002988 | ||||||
chr4:75002989
|
T | C | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-9436T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002989 | ||||||
chr4:75003072
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-9353C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75003072 | ||||||
chr4:75003162
|
G | T | 1 | a0002c0002t0001g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.44-9263G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75003162 | ||||||
chr4:75003232
|
C | G | 1 | a0001c0003t0011g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.44-9193C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75003232 | ||||||
chr4:75003280
|
G | GT | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-9144dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 75003280 | |||||
chr4:75003308
|
T | C | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-9117T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75003308 | ||||||
chr4:75003321
|
GA | G | 11 | a0001c0001t0002g0005a0001c0001t0002g0078a0001c0001t0002g0141others(8): Show | 13 | HG01891.hp2 HG02040.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.44-9090delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 75003321 | |||||
chr4:75003418
|
G | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-9007G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75003418 | ||||||
chr4:75003486
|
T | C | 2 | a0001c0001t0001g0048a0002c0002t0001g0094 | 2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-8939T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75003486 | ||||||
chr4:75003514
|
C | T | 8 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0026g0021others(5): Show | 12 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.44-8911C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75003514 | ||||||
chr4:75003516
|
C | T | 8 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0026g0021others(5): Show | 12 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.44-8909C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75003516 | ||||||
chr4:75003879
|
T | TTC | 3 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026 | 4 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-8528_44-8527dup others(2): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 75003879 | |||||
chr4:75004020
|
G | A | 1 | a0006c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.44-8405G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75004020 | ||||||
chr4:75004148
|
C | T | 92 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(89): Show | 101 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.44-8277C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75004148 | ||||||
chr4:75004227
|
T | G | 5 | a0002c0002t0003g0003a0002c0002t0003g0024a0002c0002t0003g0025others(2): Show | 6 | HG01123.hp1 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-8198T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75004227 | ||||||
chr4:75004440
|
G | T | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-7985G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75004440 | ||||||
chr4:75004936
|
G | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-7489G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75004936 | ||||||
chr4:75005210
|
C | T | 65 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(62): Show | 69 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.44-7215C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75005210 | ||||||
chr4:75005218
|
A | G | 92 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(89): Show | 101 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.44-7207A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75005218 | ||||||
chr4:75005297
|
G | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-7128G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75005297 | ||||||
chr4:75005581
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-6844C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75005581 | ||||||
chr4:75006206
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.44-6219A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75006206 | ||||||
chr4:75006476
|
CT | C | 5 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(2): Show | 6 | HG01109.hp2 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-5942delT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 75006476 | |||||
chr4:75006605
|
A | G | 6 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(3): Show | 7 | HG01109.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-5820A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75006605 | ||||||
chr4:75006713
|
G | A | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-5712G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75006713 | ||||||
chr4:75006944
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | NA19010.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.44-5481A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75006944 | ||||||
chr4:75006965
|
G | T | 1 | a0001c0003t0012g0037 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.44-5460G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75006965 | ||||||
chr4:75007025
|
C | G | 2 | a0001c0003t0001g0158a0001c0003t0002g0156 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-5400C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75007025 | ||||||
chr4:75007061
|
G | A | 3 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0026g0021 | 4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-5364G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75007061 | ||||||
chr4:75007129
|
C | G | 3 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0026g0021 | 4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-5296C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75007129 | ||||||
chr4:75007216
|
C | G | 1 | a0002c0002t0001g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.44-5209C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75007216 | ||||||
chr4:75007324
|
C | G | 24 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0005g0002others(21): Show | 29 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.44-5101C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75007324 | ||||||
chr4:75007493
|
G | GT | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-4931dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 75007493 | |||||
chr4:75007739
|
G | A | 49 | a0001c0001t0001g0121a0001c0001t0001g0168a0001c0001t0002g0007others(46): Show | 51 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.44-4686G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75007739 | ||||||
chr4:75007845
|
A | C | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-4580A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75007845 | ||||||
chr4:75007974
|
C | T | 1 | a0002c0002t0031g0043 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.44-4451C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75007974 | ||||||
chr4:75008063
|
C | G | 92 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(89): Show | 101 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.44-4362C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75008063 | ||||||
chr4:75008593
|
C | A | 1 | a0001c0001t0002g0079 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.44-3832C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75008593 | ||||||
chr4:75008669
|
T | C | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-3756T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75008669 | ||||||
chr4:75008828
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-3597C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75008828 | ||||||
chr4:75008887
|
A | G | 1 | a0002c0002t0001g0165 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.44-3538A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75008887 | ||||||
chr4:75008923
|
AT | A | 90 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0168others(87): Show | 99 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.44-3489delT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 75008923 | |||||
chr4:75009294
|
G | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-3131G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75009294 | ||||||
chr4:75009379
|
G | A | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-3046G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75009379 | ||||||
chr4:75009564
|
G | A | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-2861G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75009564 | ||||||
chr4:75009570
|
GATCTTTA others(7): Show |
G | 1 | a0001c0001t0001g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.44-2849_44-2836del others(14): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 75009570 | |||||
chr4:75009627
|
G | A | 1 | a0002c0002t0001g0143 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.44-2798G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75009627 | ||||||
chr4:75009652
|
C | T | 1 | a0006c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.44-2773C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75009652 | ||||||
chr4:75009667
|
G | A | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-2758G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75009667 | ||||||
chr4:75009748
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-2677C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75009748 | ||||||
chr4:75010516
|
C | T | 1 | a0002c0002t0003g0024 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.44-1909C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75010516 | ||||||
chr4:75010536
|
A | T | 1 | a0001c0001t0002g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.44-1889A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75010536 | ||||||
chr4:75010543
|
A | T | 1 | a0001c0001t0001g0127 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.44-1882A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75010543 | ||||||
chr4:75010544
|
T | A | 19 | a0001c0001t0002g0007a0001c0001t0002g0058a0001c0001t0002g0059others(16): Show | 20 | HG00597.hp2 HG01952.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.44-1881T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75010544 | ||||||
chr4:75010545
|
T | A | 1 | a0001c0001t0002g0141 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.44-1880T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75010545 | ||||||
chr4:75010589
|
G | A | 1 | a0006c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.44-1836G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75010589 | ||||||
chr4:75010590
|
G | C | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-1835G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75010590 | ||||||
chr4:75010608
|
CT | C | 4 | a0001c0003t0013g0175a0001c0003t0013g0176a0001c0003t0014g0174others(1): Show | 4 | HG00741.hp2 HG01361.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-1814delT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 75010608 | |||||
chr4:75010642
|
C | T | 4 | a0001c0003t0003g0013a0001c0003t0011g0017a0001c0003t0011g0018others(1): Show | 4 | HG01255.hp1 HG02970.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-1783C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75010642 | ||||||
chr4:75011062
|
T | G | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-1363T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75011062 | ||||||
chr4:75011119
|
A | T | 4 | a0001c0001t0005g0002a0001c0001t0005g0019a0001c0001t0005g0026others(1): Show | 5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-1306A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75011119 | ||||||
chr4:75011205
|
G | A | 1 | a0006c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.44-1220G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75011205 | ||||||
chr4:75011212
|
A | T | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-1213A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75011212 | ||||||
chr4:75011509
|
T | C | 12 | a0001c0001t0007g0170a0001c0003t0001g0158a0001c0003t0002g0156others(9): Show | 13 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-916T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75011509 | ||||||
chr4:75011584
|
T | A | 2 | a0001c0003t0004g0001a0001c0003t0004g0035 | 5 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-841T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75011584 | ||||||
chr4:75011859
|
G | C | 117 | a0001c0001t0001g0041a0001c0001t0001g0088a0001c0001t0001g0168others(114): Show | 127 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.44-566G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75011859 | ||||||
chr4:75012001
|
A | G | 1 | a0002c0002t0001g0073 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.44-424A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75012001 | ||||||
chr4:75012039
|
G | C | 6 | a0001c0003t0001g0158a0001c0003t0002g0156a0001c0003t0003g0013others(3): Show | 6 | HG01884.hp2 HG02970.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-386G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75012039 | ||||||
chr4:75012060
|
T | C | 1 | a0002c0002t0003g0003 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.44-365T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75012060 | ||||||
chr4:75012225
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.44-200G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75012225 | ||||||
chr4:75012273
|
A | G | 2 | a0001c0001t0001g0088a0002c0002t0001g0132 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.44-152A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75012273 | ||||||
chr4:75013163
|
C | G | 70 | a0001c0003t0003g0013a0001c0003t0004g0001a0001c0003t0004g0035others(67): Show | 77 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.769+13C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013163 | ||||||
chr4:75013353
|
T | G | 2 | a0002c0002t0010g0004a0002c0002t0010g0030 | 3 | HG02622.hp2 HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.769+203T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013353 | ||||||
chr4:75013422
|
G | A | 1 | a0002c0002t0003g0024 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.769+272G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013422 | ||||||
chr4:75013446
|
A | G | 2 | a0002c0004t0027g0029a0006c0007t0032g0028 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.769+296A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013446 | ||||||
chr4:75013577
|
G | C | 1 | a0002c0002t0001g0142 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.769+427G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013577 | ||||||
chr4:75013579
|
A | C | 1 | a0002c0002t0001g0142 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.769+429A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013579 | ||||||
chr4:75013581
|
T | A | 1 | a0002c0002t0001g0142 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.769+431T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013581 | ||||||
chr4:75013775
|
C | T | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.769+625C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013775 | ||||||
chr4:75013779
|
A | G | 70 | a0001c0003t0003g0013a0001c0003t0004g0001a0001c0003t0004g0035others(67): Show | 77 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.769+629A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013779 | ||||||
chr4:75013813
|
A | T | 1 | a0006c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.769+663A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013813 | ||||||
chr4:75013948
|
G | A | 7 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0005g0012others(4): Show | 8 | HG01884.hp1 HG02615.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+798G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013948 | ||||||
chr4:75013951
|
T | G | 72 | a0001c0003t0001g0158a0001c0003t0002g0156a0001c0003t0003g0013others(69): Show | 79 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.769+801T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013951 | ||||||
chr4:75013959
|
C | T | 1 | a0002c0002t0003g0025 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.769+809C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013959 | ||||||
chr4:75014027
|
G | A | 7 | a0001c0001t0002g0005a0001c0001t0003g0136a0001c0001t0005g0012others(4): Show | 8 | HG01884.hp1 HG02615.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+877G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75014027 | ||||||
chr4:75014050
|
C | G | 1 | a0002c0002t0001g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.769+900C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75014050 | ||||||
chr4:75014250
|
G | T | 1 | a0001c0001t0002g0081 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.769+1100G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75014250 | ||||||
chr4:75014520
|
C | T | 2 | a0001c0003t0012g0045a0001c0003t0012g0049 | 2 | HG01255.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.769+1370C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75014520 | ||||||
chr4:75014639
|
A | C | 22 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(19): Show | 24 | HG01123.hp1 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.769+1489A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75014639 | ||||||
chr4:75014750
|
A | T | 6 | a0001c0001t0002g0164a0001c0001t0006g0036a0001c0001t0006g0039others(3): Show | 6 | HG01070.hp1 HG01255.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+1600A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75014750 | ||||||
chr4:75014953
|
C | T | 1 | a0002c0002t0001g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.769+1803C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75014953 | ||||||
chr4:75015008
|
T | C | 34 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(31): Show | 39 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.769+1858T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75015008 | ||||||
chr4:75015412
|
G | C | 9 | a0001c0003t0009g0006a0001c0003t0009g0055a0001c0003t0009g0163others(6): Show | 11 | HG00438.hp2 HG02622.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.769+2262G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75015412 | ||||||
chr4:75015502
|
C | A | 1 | a0006c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.769+2352C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75015502 | ||||||
chr4:75015525
|
A | G | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.769+2375A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75015525 | ||||||
chr4:75015579
|
A | G | 1 | a0002c0002t0001g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.769+2429A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75015579 | ||||||
chr4:75015618
|
C | G | 13 | a0001c0001t0017g0051a0001c0001t0017g0093a0001c0001t0019g0173others(10): Show | 14 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.769+2468C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75015618 | ||||||
chr4:75015775
|
T | C | 1 | a0006c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.769+2625T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75015775 | ||||||
chr4:75015865
|
C | G | 12 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(9): Show | 16 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+2715C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75015865 | ||||||
chr4:75016173
|
A | G | 25 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(22): Show | 30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+3023A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75016173 | ||||||
chr4:75016512
|
G | T | 1 | a0001c0003t0001g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.769+3362G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75016512 | ||||||
chr4:75016924
|
C | T | 18 | a0001c0001t0030g0072a0001c0003t0009g0006a0001c0003t0009g0055others(15): Show | 20 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.769+3774C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75016924 | ||||||
chr4:75016988
|
T | C | 25 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(22): Show | 30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+3838T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75016988 | ||||||
chr4:75017326
|
G | A | 12 | a0001c0001t0017g0051a0001c0001t0017g0093a0001c0001t0019g0173others(9): Show | 13 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.769+4176G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75017326 | ||||||
chr4:75017470
|
A | G | 1 | a0001c0003t0001g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.769+4320A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75017470 | ||||||
chr4:75017473
|
G | T | 20 | a0001c0001t0003g0136a0001c0001t0030g0072a0001c0003t0009g0006others(17): Show | 22 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.769+4323G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75017473 | ||||||
chr4:75017627
|
T | A | 12 | a0001c0001t0017g0051a0001c0001t0017g0093a0001c0001t0019g0173others(9): Show | 13 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.769+4477T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75017627 | ||||||
chr4:75017737
|
G | A | 12 | a0001c0001t0017g0051a0001c0001t0017g0093a0001c0001t0019g0173others(9): Show | 13 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.769+4587G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75017737 | ||||||
chr4:75017908
|
C | T | 24 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(21): Show | 29 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.769+4758C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75017908 | ||||||
chr4:75018027
|
G | A | 24 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(21): Show | 29 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.769+4877G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75018027 | ||||||
chr4:75018082
|
T | G | 1 | a0001c0001t0006g0126 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.769+4932T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75018082 | ||||||
chr4:75018240
|
C | T | 1 | a0002c0002t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.769+5090C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75018240 | ||||||
chr4:75018298
|
A | C | 25 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(22): Show | 30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+5148A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75018298 | ||||||
chr4:75018888
|
T | C | 1 | a0001c0003t0001g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.769+5738T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75018888 | ||||||
chr4:75018920
|
G | A | 24 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(21): Show | 29 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.769+5770G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75018920 | ||||||
chr4:75018968
|
T | A | 1 | a0002c0002t0001g0014 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.769+5818T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75018968 | ||||||
chr4:75019243
|
T | C | 12 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(9): Show | 16 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+6093T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019243 | ||||||
chr4:75019496
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.769+6346C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019496 | ||||||
chr4:75019830
|
C | T | 1 | a0002c0002t0001g0153 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.769+6680C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019830 | ||||||
chr4:75019859
|
C | T | 1 | a0001c0001t0002g0060 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.769+6709C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019859 | ||||||
chr4:75019860
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.769+6710G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019860 | ||||||
chr4:75019864
|
G | A | 1 | a0006c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.769+6714G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019864 | ||||||
chr4:75019875
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.769+6725C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019875 | ||||||
chr4:75019989
|
G | A | 7 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(4): Show | 8 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+6839G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019989 | ||||||
chr4:75019995
|
A | G | 25 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(22): Show | 30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+6845A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019995 | ||||||
chr4:75020004
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.769+6854C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020004 | ||||||
chr4:75020009
|
C | CA | 39 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0090others(36): Show | 39 | HG00438.hp2 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.769+6887dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75020009 | |||||
chr4:75020009
|
CA | C | 6 | a0001c0001t0001g0091a0001c0001t0001g0182a0001c0001t0002g0063others(3): Show | 6 | HG01256.hp2 HG03041.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+6887delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75020009 | |||||
chr4:75020009
|
CAAAAAAA others(11): Show |
C | 25 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(22): Show | 30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+6870_769+6887d others(20): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75020009 | |||||
chr4:75020120
|
G | T | 27 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0168others(24): Show | 27 | HG01167.hp1 HG01175.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.769+6970G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020120 | ||||||
chr4:75020156
|
G | T | 27 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0168others(24): Show | 27 | HG01167.hp1 HG01175.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.769+7006G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020156 | ||||||
chr4:75020237
|
T | C | 5 | a0001c0001t0002g0085a0001c0001t0002g0107a0001c0001t0002g0119others(2): Show | 5 | HG00323.hp1 NA18986.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.769+7087T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020237 | ||||||
chr4:75020273
|
A | G | 2 | a0002c0004t0001g0155a0002c0004t0018g0052 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.769+7123A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020273 | ||||||
chr4:75020463
|
C | G | 1 | a0001c0006t0002g0105 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.769+7313C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020463 | ||||||
chr4:75020492
|
TC | T | 22 | a0001c0001t0001g0182a0001c0001t0003g0136a0001c0001t0030g0072others(19): Show | 24 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.769+7352delC | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75020492 | |||||
chr4:75020492
|
TCC | T | 25 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(22): Show | 30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+7351_769+7352d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75020492 | |||||
chr4:75020500
|
C | A | 2 | a0001c0001t0002g0005a0001c0001t0002g0112 | 3 | HG02615.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.769+7350C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020500 | ||||||
chr4:75020502
|
C | G | 25 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(22): Show | 30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+7352C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020502 | ||||||
chr4:75020606
|
C | G | 1 | a0006c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.769+7456C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020606 | ||||||
chr4:75020689
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.769+7539C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020689 | ||||||
chr4:75020749
|
C | T | 11 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(8): Show | 15 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+7599C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020749 | ||||||
chr4:75020901
|
CT | C | 25 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(22): Show | 30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+7752delT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020901 | ||||||
chr4:75021050
|
G | T | 12 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(9): Show | 16 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+7900G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021050 | ||||||
chr4:75021129
|
C | G | 1 | a0001c0001t0002g0131 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.769+7979C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021129 | ||||||
chr4:75021267
|
G | A | 13 | a0001c0001t0017g0051a0001c0001t0017g0093a0001c0001t0019g0173others(10): Show | 14 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.769+8117G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021267 | ||||||
chr4:75021390
|
A | G | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.769+8240A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021390 | ||||||
chr4:75021419
|
A | T | 3 | a0001c0003t0011g0017a0001c0003t0011g0018a0001c0003t0011g0092 | 3 | HG02970.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.769+8269A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021419 | ||||||
chr4:75021455
|
TC | T | 3 | a0001c0003t0011g0017a0001c0003t0011g0018a0001c0003t0011g0092 | 3 | HG02970.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.769+8307delC | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75021455 | |||||
chr4:75021586
|
G | GT | 12 | a0001c0001t0017g0051a0001c0001t0017g0093a0001c0001t0019g0173others(9): Show | 13 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.769+8445dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75021586 | |||||
chr4:75021586
|
G | GTT | 13 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(10): Show | 17 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.769+8444_769+8445d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75021586 | |||||
chr4:75021586
|
G | T | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.769+8436G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021586 | ||||||
chr4:75021586
|
GT | G | 7 | a0001c0001t0001g0047a0001c0001t0002g0007a0001c0001t0002g0058others(4): Show | 8 | HG01952.hp2 HG02040.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.769+8445delT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75021586 | |||||
chr4:75021602
|
A | T | 8 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(5): Show | 9 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.769+8452A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021602 | ||||||
chr4:75021689
|
T | C | 26 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(23): Show | 31 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.769+8539T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021689 | ||||||
chr4:75021819
|
G | A | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.769+8669G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021819 | ||||||
chr4:75021831
|
T | A | 20 | a0001c0001t0003g0136a0001c0001t0030g0072a0001c0003t0009g0006others(17): Show | 22 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.769+8681T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021831 | ||||||
chr4:75021831
|
T | TAC | 26 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(23): Show | 31 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.769+8682_769+8683d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75021831 | |||||
chr4:75021882
|
T | C | 83 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0168others(80): Show | 91 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.769+8732T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021882 | ||||||
chr4:75022130
|
T | A | 13 | a0001c0001t0017g0051a0001c0001t0017g0093a0001c0001t0019g0173others(10): Show | 14 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.769+8980T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022130 | ||||||
chr4:75022146
|
T | G | 1 | a0002c0002t0003g0025 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.769+8996T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022146 | ||||||
chr4:75022311
|
G | A | 46 | a0001c0001t0003g0136a0001c0001t0005g0002a0001c0001t0005g0012others(43): Show | 53 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.769+9161G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022311 | ||||||
chr4:75022420
|
G | A | 25 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(22): Show | 30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+9270G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022420 | ||||||
chr4:75022447
|
A | G | 13 | a0001c0001t0017g0051a0001c0001t0017g0093a0001c0001t0019g0173others(10): Show | 14 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.769+9297A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022447 | ||||||
chr4:75022448
|
T | C | 1 | a0001c0003t0001g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.769+9298T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022448 | ||||||
chr4:75022471
|
T | C | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.769+9321T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022471 | ||||||
chr4:75022474
|
A | C | 35 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0168others(32): Show | 36 | HG01123.hp2 HG01167.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.769+9324A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022474 | ||||||
chr4:75022649
|
A | T | 1 | a0001c0001t0002g0150 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.769+9499A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022649 | ||||||
chr4:75022816
|
C | A | 1 | a0001c0003t0013g0175 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.769+9666C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022816 | ||||||
chr4:75022954
|
T | C | 2 | a0001c0001t0003g0136a0002c0002t0003g0024 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.769+9804T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022954 | ||||||
chr4:75023220
|
C | A | 12 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(9): Show | 16 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+10070C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75023220 | ||||||
chr4:75023282
|
T | G | 1 | a0001c0003t0014g0171 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.769+10132T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75023282 | ||||||
chr4:75023326
|
T | C | 2 | a0001c0001t0003g0136a0002c0002t0003g0024 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.769+10176T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75023326 | ||||||
chr4:75023484
|
T | C | 13 | a0001c0001t0017g0051a0001c0001t0017g0093a0001c0001t0019g0173others(10): Show | 14 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.769+10334T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75023484 | ||||||
chr4:75023658
|
T | C | 32 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0168others(29): Show | 33 | HG01123.hp2 HG01167.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.770-10225T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75023658 | ||||||
chr4:75023980
|
G | T | 12 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(9): Show | 16 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.770-9903G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75023980 | ||||||
chr4:75024113
|
A | G | 13 | a0001c0001t0017g0051a0001c0001t0017g0093a0001c0001t0019g0173others(10): Show | 14 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.770-9770A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75024113 | ||||||
chr4:75024171
|
C | A | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.770-9712C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75024171 | ||||||
chr4:75024255
|
C | CA | 54 | a0001c0001t0001g0042a0001c0001t0002g0005a0001c0001t0002g0060others(51): Show | 57 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.770-9613dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75024255 | |||||
chr4:75024255
|
C | CAA | 8 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(5): Show | 9 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.770-9614_770-9613d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75024255 | |||||
chr4:75024255
|
C | CAAAA | 12 | a0001c0001t0017g0051a0001c0001t0017g0093a0001c0001t0019g0173others(9): Show | 13 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.770-9616_770-9613d others(6): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75024255 | |||||
chr4:75024386
|
T | C | 18 | a0001c0001t0030g0072a0001c0003t0009g0006a0001c0003t0009g0055others(15): Show | 20 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.770-9497T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75024386 | ||||||
chr4:75024481
|
G | C | 13 | a0001c0001t0017g0051a0001c0001t0017g0093a0001c0001t0019g0173others(10): Show | 14 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.770-9402G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75024481 | ||||||
chr4:75024724
|
T | C | 13 | a0001c0001t0017g0051a0001c0001t0017g0093a0001c0001t0019g0173others(10): Show | 14 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.770-9159T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75024724 | ||||||
chr4:75024767
|
C | T | 4 | a0001c0001t0005g0012a0001c0001t0005g0089a0001c0001t0005g0128others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-9116C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75024767 | ||||||
chr4:75024949
|
T | C | 45 | a0001c0001t0003g0136a0001c0001t0005g0002a0001c0001t0005g0012others(42): Show | 52 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.770-8934T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75024949 | ||||||
chr4:75024974
|
C | T | 35 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0168others(32): Show | 36 | HG01123.hp2 HG01167.hp1 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.770-8909C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75024974 | ||||||
chr4:75025033
|
C | T | 1 | a0002c0002t0001g0144 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.770-8850C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75025033 | ||||||
chr4:75025177
|
A | G | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.770-8706A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75025177 | ||||||
chr4:75025218
|
A | C | 1 | a0002c0002t0003g0025 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.770-8665A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75025218 | ||||||
chr4:75025261
|
A | T | 1 | a0001c0001t0006g0126 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.770-8622A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75025261 | ||||||
chr4:75025495
|
G | A | 18 | a0001c0001t0030g0072a0001c0003t0009g0006a0001c0003t0009g0055others(15): Show | 20 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.770-8388G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75025495 | ||||||
chr4:75025649
|
G | A | 10 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(7): Show | 14 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.770-8234G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75025649 | ||||||
chr4:75025701
|
C | T | 2 | a0001c0001t0003g0136a0002c0002t0003g0024 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.770-8182C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75025701 | ||||||
chr4:75025715
|
T | TTATTATC others(13): Show |
1 | a0002c0002t0003g0025 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.770-8167_770-8148d others(22): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75025715 | |||||
chr4:75025917
|
A | C | 3 | a0001c0003t0004g0001a0001c0003t0004g0035a0002c0002t0004g0034 | 6 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.770-7966A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75025917 | ||||||
chr4:75026258
|
A | AAAT | 9 | a0001c0003t0002g0156a0001c0003t0003g0013a0002c0002t0003g0003others(6): Show | 10 | HG01123.hp1 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.770-7619_770-7617d others(5): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75026258 | |||||
chr4:75026417
|
G | A | 1 | a0002c0002t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.770-7466G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75026417 | ||||||
chr4:75026509
|
G | A | 20 | a0001c0001t0003g0136a0001c0001t0030g0072a0001c0003t0009g0006others(17): Show | 22 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.770-7374G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75026509 | ||||||
chr4:75026809
|
T | A | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.770-7074T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75026809 | ||||||
chr4:75027041
|
A | C | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.770-6842A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75027041 | ||||||
chr4:75027289
|
A | C | 82 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0168others(79): Show | 90 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.770-6594A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75027289 | ||||||
chr4:75027374
|
G | A | 2 | a0001c0001t0017g0051a0001c0001t0019g0173 | 2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.770-6509G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75027374 | ||||||
chr4:75027483
|
C | G | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0130 | 3 | HG01169.hp2 HG01175.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.770-6400C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75027483 | ||||||
chr4:75027902
|
G | A | 32 | a0001c0001t0003g0136a0001c0001t0017g0051a0001c0001t0017g0093others(29): Show | 35 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.770-5981G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75027902 | ||||||
chr4:75027936
|
C | A | 1 | a0001c0001t0002g0115 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.770-5947C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75027936 | ||||||
chr4:75028203
|
A | G | 1 | a0006c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.770-5680A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75028203 | ||||||
chr4:75028332
|
C | T | 2 | a0002c0004t0001g0155a0002c0004t0018g0052 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.770-5551C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75028332 | ||||||
chr4:75028436
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.770-5447G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75028436 | ||||||
chr4:75028653
|
G | A | 1 | a0001c0003t0010g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.770-5230G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75028653 | ||||||
chr4:75028685
|
G | A | 13 | a0001c0001t0030g0072a0001c0003t0009g0006a0001c0003t0009g0055others(10): Show | 14 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.770-5198G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75028685 | ||||||
chr4:75028841
|
A | C | 3 | a0001c0003t0011g0017a0001c0003t0011g0018a0001c0003t0011g0092 | 3 | HG02970.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.770-5042A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75028841 | ||||||
chr4:75029040
|
A | G | 2 | a0001c0001t0002g0087a0001c0001t0002g0145 | 2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.770-4843A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75029040 | ||||||
chr4:75029099
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.770-4784G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75029099 | ||||||
chr4:75029262
|
C | T | 2 | a0002c0002t0015g0015a0002c0002t0015g0016 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.770-4621C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75029262 | ||||||
chr4:75029406
|
AC | A | 4 | a0001c0001t0005g0012a0001c0001t0005g0089a0001c0001t0005g0128others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-4474delC | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75029406 | |||||
chr4:75029704
|
G | C | 15 | a0001c0001t0003g0136a0001c0001t0017g0051a0001c0001t0017g0093others(12): Show | 16 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.770-4179G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75029704 | ||||||
chr4:75029840
|
A | C | 3 | a0002c0002t0001g0132a0002c0002t0015g0015a0002c0002t0015g0016 | 3 | HG02559.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.770-4043A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75029840 | ||||||
chr4:75029876
|
TA | T | 8 | a0001c0001t0001g0169a0001c0001t0002g0083a0001c0003t0004g0001others(5): Show | 11 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.770-3993delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75029876 | |||||
chr4:75029996
|
C | T | 14 | a0001c0001t0003g0136a0001c0001t0017g0051a0001c0001t0017g0093others(11): Show | 15 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.770-3887C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75029996 | ||||||
chr4:75030089
|
T | C | 1 | a0002c0002t0001g0161 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.770-3794T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75030089 | ||||||
chr4:75030160
|
G | A | 18 | a0001c0001t0030g0072a0001c0003t0009g0006a0001c0003t0009g0055others(15): Show | 20 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.770-3723G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75030160 | ||||||
chr4:75030476
|
A | T | 1 | a0001c0001t0002g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.770-3407A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75030476 | ||||||
chr4:75030838
|
GC | G | 4 | a0001c0003t0009g0006a0001c0003t0009g0055a0001c0003t0009g0163others(1): Show | 5 | HG00438.hp2 HG03942.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.770-3039delC | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75030838 | |||||
chr4:75031495
|
T | C | 1 | a0001c0001t0002g0060 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.770-2388T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75031495 | ||||||
chr4:75031527
|
T | TA | 14 | a0001c0001t0001g0130a0001c0001t0002g0097a0001c0001t0002g0109others(11): Show | 15 | HG00323.hp2 HG01109.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.770-2343dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75031527 | |||||
chr4:75031973
|
G | T | 6 | a0001c0001t0002g0164a0001c0001t0006g0036a0001c0001t0006g0039others(3): Show | 6 | HG01070.hp1 HG01255.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.770-1910G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75031973 | ||||||
chr4:75032013
|
A | G | 1 | a0006c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.770-1870A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75032013 | ||||||
chr4:75032048
|
G | T | 1 | a0001c0001t0002g0083 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.770-1835G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75032048 | ||||||
chr4:75032253
|
T | C | 1 | a0001c0003t0028g0067 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.770-1630T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75032253 | ||||||
chr4:75032315
|
T | C | 45 | a0001c0001t0003g0136a0001c0001t0005g0002a0001c0001t0005g0012others(42): Show | 52 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.770-1568T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75032315 | ||||||
chr4:75032607
|
T | C | 1 | a0001c0001t0002g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.770-1276T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75032607 | ||||||
chr4:75032662
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.770-1221C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75032662 | ||||||
chr4:75032725
|
T | G | 1 | a0002c0002t0001g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.770-1158T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75032725 | ||||||
chr4:75033001
|
C | G | 18 | a0001c0001t0030g0072a0001c0003t0009g0006a0001c0003t0009g0055others(15): Show | 20 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.770-882C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75033001 | ||||||
chr4:75033038
|
G | A | 1 | a0001c0003t0011g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.770-845G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75033038 | ||||||
chr4:75033318
|
C | G | 45 | a0001c0001t0003g0136a0001c0001t0005g0002a0001c0001t0005g0012others(42): Show | 52 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.770-565C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75033318 | ||||||
chr4:75033403
|
C | A | 24 | a0001c0001t0003g0136a0001c0001t0005g0002a0001c0001t0005g0012others(21): Show | 26 | HG01109.hp2 HG01123.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.770-480C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75033403 | ||||||
chr4:75033722
|
T | G | 10 | a0001c0001t0002g0007a0001c0001t0002g0058a0001c0001t0002g0078others(7): Show | 11 | HG01952.hp2 HG02015.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.770-161T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75033722 | ||||||
chr4:75033737
|
A | C | 1 | a0001c0001t0001g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.770-146A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75033737 | ||||||
chr4:75033874
|
C | T | 1 | a0001c0003t0003g0013 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.770-9C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75033874 | ||||||
chr4:75033996
|
C | A | 1 | a0002c0002t0001g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.848+35C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75033996 | ||||||
chr4:75034022
|
G | A | 4 | a0001c0003t0004g0001a0001c0003t0004g0035a0002c0002t0001g0008others(1): Show | 8 | HG01070.hp2 HG01071.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.848+61G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75034022 | ||||||
chr4:75034031
|
C | T | 3 | a0001c0003t0004g0001a0001c0003t0004g0035a0002c0002t0004g0034 | 6 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.848+70C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75034031 | ||||||
chr4:75034208
|
T | C | 1 | a0001c0001t0002g0119 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.848+247T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75034208 | ||||||
chr4:75034295
|
C | G | 18 | a0001c0001t0030g0072a0001c0003t0009g0006a0001c0003t0009g0055others(15): Show | 20 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.848+334C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75034295 | ||||||
chr4:75034320
|
G | T | 2 | a0002c0004t0001g0155a0002c0004t0018g0052 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.848+359G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75034320 | ||||||
chr4:75034638
|
A | T | 1 | a0001c0001t0005g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.848+677A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75034638 | ||||||
chr4:75034973
|
T | C | 1 | a0001c0001t0003g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.848+1012T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75034973 | ||||||
chr4:75035032
|
C | T | 2 | a0001c0001t0002g0097a0001c0001t0002g0109 | 2 | HG02015.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.848+1071C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75035032 | ||||||
chr4:75035088
|
C | T | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.848+1127C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75035088 | ||||||
chr4:75035325
|
G | T | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.848+1364G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75035325 | ||||||
chr4:75035366
|
C | T | 44 | a0001c0001t0003g0136a0001c0001t0005g0002a0001c0001t0005g0012others(41): Show | 51 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.848+1405C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75035366 | ||||||
chr4:75036594
|
G | A | 1 | a0002c0002t0004g0162 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.848+2633G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75036594 | ||||||
chr4:75036679
|
G | A | 1 | a0001c0001t0021g0044 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.848+2718G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75036679 | ||||||
chr4:75037432
|
A | G | 44 | a0001c0001t0003g0136a0001c0001t0005g0002a0001c0001t0005g0012others(41): Show | 51 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.848+3471A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75037432 | ||||||
chr4:75037754
|
C | T | 1 | a0001c0001t0002g0119 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.848+3793C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75037754 | ||||||
chr4:75037922
|
G | T | 1 | a0001c0001t0030g0072 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.848+3961G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75037922 | ||||||
chr4:75037948
|
G | A | 1 | a0002c0002t0003g0024 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.848+3987G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75037948 | ||||||
chr4:75038587
|
T | C | 4 | a0001c0003t0013g0175a0001c0003t0013g0176a0001c0003t0014g0174others(1): Show | 4 | HG00741.hp2 HG01361.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+4626T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75038587 | ||||||
chr4:75038626
|
G | A | 1 | a0001c0001t0002g0005 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.848+4665G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75038626 | ||||||
chr4:75039008
|
C | CTA | 3 | a0001c0001t0017g0051a0001c0001t0017g0093a0001c0001t0019g0173 | 3 | HG01891.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.848+5049_848+5050d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 75039008 | |||||
chr4:75039048
|
A | G | 3 | a0001c0003t0004g0001a0001c0003t0004g0035a0002c0002t0004g0034 | 6 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.848+5087A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039048 | ||||||
chr4:75039270
|
G | A | 8 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(5): Show | 9 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.848+5309G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039270 | ||||||
chr4:75039302
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0182 | 3 | HG03130.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.848+5341C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039302 | ||||||
chr4:75039460
|
G | A | 10 | a0001c0001t0003g0136a0001c0003t0003g0013a0002c0002t0003g0003others(7): Show | 11 | HG01123.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.848+5499G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039460 | ||||||
chr4:75039488
|
C | T | 3 | a0002c0002t0001g0073a0002c0002t0001g0075a0005c0008t0001g0082 | 3 | NA18612.hp2 NA18986.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.848+5527C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039488 | ||||||
chr4:75039510
|
C | T | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.848+5549C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039510 | ||||||
chr4:75039511
|
G | A | 18 | a0001c0001t0030g0072a0001c0003t0009g0006a0001c0003t0009g0055others(15): Show | 20 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.848+5550G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039511 | ||||||
chr4:75039550
|
A | G | 38 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0168others(35): Show | 39 | HG01123.hp2 HG01167.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.848+5589A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039550 | ||||||
chr4:75039690
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.848+5729C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039690 | ||||||
chr4:75039740
|
C | G | 1 | a0001c0001t0002g0078 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.848+5779C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039740 | ||||||
chr4:75039923
|
A | G | 2 | a0002c0004t0001g0155a0002c0004t0018g0052 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.848+5962A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039923 | ||||||
chr4:75040035
|
T | C | 107 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0022others(104): Show | 113 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.848+6074T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040035 | ||||||
chr4:75040167
|
A | G | 8 | a0001c0001t0005g0002a0001c0001t0005g0012a0001c0001t0005g0019others(5): Show | 9 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.849-5996A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040167 | ||||||
chr4:75040240
|
A | G | 1 | a0001c0001t0030g0072 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.849-5923A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040240 | ||||||
chr4:75040241
|
C | T | 32 | a0001c0001t0003g0136a0001c0001t0017g0051a0001c0001t0017g0093others(29): Show | 35 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.849-5922C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040241 | ||||||
chr4:75040244
|
C | T | 2 | a0001c0003t0014g0174a0001c0003t0028g0067 | 2 | HG00741.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.849-5919C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040244 | ||||||
chr4:75040291
|
A | C | 15 | a0001c0001t0002g0060a0001c0001t0002g0069a0001c0001t0002g0070others(12): Show | 15 | HG00438.hp1 HG00597.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.849-5872A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040291 | ||||||
chr4:75040313
|
T | G | 152 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0168others(149): Show | 162 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.849-5850T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040313 | ||||||
chr4:75040877
|
G | A | 2 | a0001c0003t0013g0175a0006c0007t0032g0028 | 2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.849-5286G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040877 | ||||||
chr4:75040898
|
G | C | 107 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0022others(104): Show | 113 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.849-5265G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040898 | ||||||
chr4:75040908
|
C | G | 1 | a0002c0002t0001g0038 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.849-5255C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040908 | ||||||
chr4:75040961
|
GA | G | 66 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0022others(63): Show | 68 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.849-5200delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 75040961 | |||||
chr4:75041777
|
T | C | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.849-4386T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75041777 | ||||||
chr4:75041890
|
A | G | 18 | a0001c0001t0030g0072a0001c0003t0009g0006a0001c0003t0009g0055others(15): Show | 20 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.849-4273A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75041890 | ||||||
chr4:75041990
|
G | T | 107 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0022others(104): Show | 113 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.849-4173G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75041990 | ||||||
chr4:75042221
|
A | G | 1 | a0001c0001t0002g0150 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.849-3942A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75042221 | ||||||
chr4:75042664
|
A | G | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.849-3499A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75042664 | ||||||
chr4:75042947
|
G | GA | 15 | a0001c0001t0003g0136a0001c0001t0017g0051a0001c0001t0017g0093others(12): Show | 16 | HG01123.hp1 HG01891.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.849-3203dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 75042947 | |||||
chr4:75044000
|
G | C | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.849-2163G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044000 | ||||||
chr4:75044046
|
C | CA | 21 | a0001c0001t0001g0127a0001c0001t0002g0059a0001c0001t0030g0072others(18): Show | 23 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.849-2103dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 75044046 | |||||
chr4:75044046
|
C | CAA | 74 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0022others(71): Show | 77 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.849-2104_849-2103d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 75044046 | |||||
chr4:75044046
|
CA | C | 8 | a0001c0001t0001g0098a0001c0001t0005g0002a0001c0001t0005g0012others(5): Show | 9 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.849-2103delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 75044046 | |||||
chr4:75044061
|
T | A | 1 | a0001c0001t0001g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.849-2102T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044061 | ||||||
chr4:75044062
|
T | A | 1 | a0001c0001t0001g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.849-2101T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044062 | ||||||
chr4:75044392
|
C | T | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.849-1771C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044392 | ||||||
chr4:75044465
|
C | T | 1 | a0002c0002t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.849-1698C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044465 | ||||||
chr4:75044566
|
C | T | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.849-1597C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044566 | ||||||
chr4:75044620
|
G | A | 1 | a0006c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.849-1543G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044620 | ||||||
chr4:75044663
|
G | A | 3 | a0001c0001t0017g0051a0001c0001t0017g0093a0001c0001t0019g0173 | 3 | HG01891.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.849-1500G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044663 | ||||||
chr4:75044768
|
TA | T | 107 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0022others(104): Show | 113 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.849-1393delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 75044768 | |||||
chr4:75044821
|
G | A | 1 | a0002c0002t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.849-1342G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044821 | ||||||
chr4:75045103
|
G | A | 6 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0005g0012others(3): Show | 6 | HG01884.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.849-1060G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75045103 | ||||||
chr4:75045282
|
A | G | 68 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0022others(65): Show | 70 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.849-881A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75045282 | ||||||
chr4:75045754
|
G | A | 14 | a0001c0001t0003g0136a0001c0001t0017g0051a0001c0001t0017g0093others(11): Show | 15 | HG01123.hp1 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.849-409G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75045754 | ||||||
chr4:75045862
|
A | C | 39 | a0001c0001t0003g0136a0001c0001t0005g0002a0001c0001t0005g0012others(36): Show | 43 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.849-301A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75045862 | ||||||
chr4:75046050
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.849-113A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75046050 | ||||||
chr4:75046079
|
C | G | 38 | a0001c0001t0003g0136a0001c0001t0005g0002a0001c0001t0005g0012others(35): Show | 42 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.849-84C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75046079 | ||||||
chr4:75046142
|
C | A | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.849-21C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75046142 |