geneid | 4670 |
---|---|
ensemblid | ENSG00000099783.13 |
hgncid | 5046 |
symbol | HNRNPM |
name | heterogeneous nuclear ribonucleoprotein M |
refseq_nuc | NM_005968.5 |
refseq_prot | NP_005959.2 |
ensembl_nuc | ENST00000325495.9 |
ensembl_prot | ENSP00000325376.2 |
mane_status | MANE Select |
chr | chr19 |
start | 8444975 |
end | 8489114 |
strand | + |
ver | v1.2 |
region | chr19:8444975-8489114 |
region5000 | chr19:8439975-8494114 |
regionname0 | HNRNPM_chr19_8444975_8489114 |
regionname5000 | HNRNPM_chr19_8439975_8494114 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 730 | 355 | 90 | 66 | 132 | 18 | 47 | 106 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0002 | 0/0 | 730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0003 | 0/0 | 730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0004 | 0/0 | 726 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0005 | 0/0 | 730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0006 | 0/0 | 523 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2193 | 282 | 42 | 59 | 121 | 15 | 44 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
c0002 | 1/0 | 2193 | 38 | 33 | 2 | 1 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
c0003 | 0/0 | 2193 | 15 | 0 | 5 | 6 | 3 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
c0004 | 0/0 | 2193 | 5 | 5 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
c0005 | 0/0 | 2193 | 3 | 3 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
c0006 | 0/0 | 2193 | 3 | 0 | 0 | 3 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
c0007 | 0/0 | 2193 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
c0008 | 0/0 | 2193 | 2 | 1 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
c0009 | 0/0 | 2193 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
c0010 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
c0011 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
c0012 | 0/0 | 2193 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
c0013 | 0/0 | 2181 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
c0014 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
c0015 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
c0016 | 0/0 | 2183 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
c0017 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 285 | 360 | 92 | 66 | 134 | 18 | 48 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0003 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0021 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0289 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2193 | 282 | 42 | 59 | 121 | 15 | 44 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0002 | 1/0 | 2193 | 38 | 33 | 2 | 1 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0003 | 0/0 | 2193 | 15 | 0 | 5 | 6 | 3 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0004 | 0/0 | 2193 | 5 | 5 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0005 | 0/0 | 2193 | 3 | 3 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0006 | 0/0 | 2193 | 3 | 0 | 0 | 3 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0007 | 0/0 | 2193 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0008 | 0/0 | 2193 | 2 | 1 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0009 | 0/0 | 2193 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0012 | 0/0 | 2193 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0014 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0015 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0002c0017 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0003c0010 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0004c0013 | 0/0 | 2181 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0005c0011 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0006c0016 | 0/0 | 2183 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2477 | 282 | 42 | 59 | 121 | 15 | 44 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0002t0001 | 1/0 | 2477 | 38 | 33 | 2 | 1 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0003t0001 | 0/0 | 2477 | 15 | 0 | 5 | 6 | 3 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0004t0001 | 0/0 | 2477 | 5 | 5 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0005t0001 | 0/0 | 2477 | 3 | 3 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0006t0001 | 0/0 | 2477 | 3 | 0 | 0 | 3 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0007t0001 | 0/0 | 2477 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0008t0001 | 0/0 | 2477 | 2 | 1 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0009t0001 | 0/0 | 2477 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0012t0001 | 0/0 | 2477 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0014t0001 | 0/0 | 2477 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0001c0015t0001 | 0/0 | 2477 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0002c0017t0001 | 0/0 | 2477 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0003c0010t0001 | 0/0 | 2477 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0004c0013t0001 | 0/0 | 2465 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0005c0011t0001 | 0/0 | 2477 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
a0006c0016t0001 | 0/0 | 2467 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | copy fasta | chr19 | 8439975 | 8494114 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0001t0001g0289 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0021 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0004t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0004t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0004t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0004t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0004t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0005t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0005t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0005t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0006t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0006t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0006t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0007t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0007t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0008t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0008t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0009t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0009t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0012t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0014t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0001c0015t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0002c0017t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0003c0010t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0004c0013t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0005c0011t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
a0006c0016t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0140 | EUR | GBR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0286 | EUR | FIN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | FIN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00544 | hp1 | a0001 | c0003 | t0001 | g0263 | EAS | CHS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00673 | hp1 | a0001 | c0003 | t0001 | g0258 | EAS | CHS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01081 | hp1 | a0001 | c0003 | t0001 | g0161 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0322 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01243 | hp1 | a0001 | c0003 | t0001 | g0159 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01255 | hp1 | a0001 | c0003 | t0001 | g0141 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01433 | hp1 | a0001 | c0003 | t0001 | g0124 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01516 | hp2 | a0001 | c0003 | t0001 | g0157 | EUR | IBS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0321 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0160 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0303 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0315 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02145 | hp2 | a0001 | c0009 | t0001 | g0026 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0327 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02280 | hp1 | a0001 | c0009 | t0001 | g0025 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0304 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0305 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02622 | hp1 | a0001 | c0004 | t0001 | g0294 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0311 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02647 | hp1 | a0001 | c0004 | t0001 | g0290 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02683 | hp2 | a0004 | c0013 | t0001 | g0062 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02717 | hp1 | a0001 | c0007 | t0001 | g0275 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0312 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0313 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0329 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0306 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0310 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0300 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02970 | hp1 | a0001 | c0004 | t0001 | g0291 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0309 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02976 | hp2 | a0001 | c0014 | t0001 | g0024 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0325 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0301 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03098 | hp1 | a0003 | c0010 | t0001 | g0079 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0293 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03130 | hp2 | a0001 | c0005 | t0001 | g0267 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0297 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0328 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0299 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03486 | hp2 | a0001 | c0015 | t0001 | g0319 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03490 | hp2 | a0001 | c0003 | t0001 | g0144 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0323 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03516 | hp2 | a0005 | c0011 | t0001 | g0307 | AFR | ESN | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0316 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03579 | hp2 | a0001 | c0004 | t0001 | g0308 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0314 | SAS | PJL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03834 | hp1 | a0001 | c0012 | t0001 | g0023 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | STU | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0292 | AFR | YRI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0320 | AFR | YRI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | YRI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0296 | AFR | YRI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18950 | hp2 | a0001 | c0008 | t0001 | g0150 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18961 | hp1 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18963 | hp1 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18973 | hp1 | a0002 | c0017 | t0001 | g0099 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18985 | hp2 | a0001 | c0006 | t0001 | g0069 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19000 | hp2 | a0001 | c0006 | t0001 | g0067 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19030 | hp2 | a0001 | c0005 | t0001 | g0268 | AFR | LWK | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | LWK | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0302 | AFR | LWK | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19060 | hp2 | a0001 | c0006 | t0001 | g0068 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19065 | hp2 | a0001 | c0003 | t0001 | g0257 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19084 | hp1 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19089 | hp1 | a0006 | c0016 | t0001 | g0071 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0298 | AFR | YRI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0326 | AFR | ASW | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ASW | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA20752 | hp1 | a0001 | c0003 | t0001 | g0158 | EUR | TSI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | GIH | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | GIH | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0330 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02109 | hp2 | a0001 | c0008 | t0001 | g0171 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02486 | hp1 | a0001 | c0004 | t0001 | g0295 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02559 | hp1 | a0001 | c0005 | t0001 | g0269 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0317 | AFR | ACB | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03471 | hp1 | a0001 | c0007 | t0001 | g0273 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0324 | AFR | MSL | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | USA | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | USA | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0318 | AFR | LWK | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0289 | REF | REF | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0021 | REF | REF | HNRNPM_chr19_8439975_8494114 | HNRNPM | chr19 | 8439975 | 8494114 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:8445105
|
C | T | 1 | a0002 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.107C>T | p.Pro36Leu | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/16 | 131/2477 | 107/2193 | 36/730 | chr19 | 8445105 | ||
chr19:8473704
|
G | A | 1 | a0003 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1038G>A | p.Met346Ile | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 11/16 | 1062/2477 | 1038/2193 | 346/730 | chr19 | 8473704 | ||
chr19:8483168
|
TAATGCAC others(3): Show |
T | 1 | a0006 | 1 | NA19089.hp1 | frameshift_variant | HIGH | c.1133_1142delATGCAC others(4): Show |
p.Asn378fs | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/16 | 1157/2477 | 1133/2193 | 378/730 | INFO_REALIGN_3_PRIME | chr19 | 8483168 | |
chr19:8485893
|
G | A | 1 | a0005 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.1465G>A | p.Gly489Ser | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1489/2477 | 1465/2193 | 489/730 | chr19 | 8485893 | ||
chr19:8486200
|
GCATGGGC others(5): Show |
G | 1 | a0004 | 1 | HG02683.hp2 | disruptive_inframe_deletion | MODERATE | c.1782_1793delTGCCAT others(6): Show |
p.Ala595_Pro598del | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1806/2477 | 1782/2193 | 594/730 | INFO_REALIGN_3_PRIME | chr19 | 8486200 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:8474177
|
G | A | 1 | a0001c0007 | 2 | HG02717.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.1053G>A | p.Gly351Gly | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/16 | 1077/2477 | 1053/2193 | 351/730 | chr19 | 8474177 | ||
chr19:8485688
|
C | T | 1 | a0001c0015 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1260C>T | p.Gly420Gly | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1284/2477 | 1260/2193 | 420/730 | chr19 | 8485688 | ||
chr19:8485805
|
G | A | 1 | a0001c0008 | 2 | HG02109.hp2 NA18950.hp2 |
synonymous_variant | LOW | c.1377G>A | p.Pro459Pro | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1401/2477 | 1377/2193 | 459/730 | chr19 | 8485805 | ||
chr19:8486066
|
C | T | 1 | a0001c0014 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.1638C>T | p.Pro546Pro | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1662/2477 | 1638/2193 | 546/730 | chr19 | 8486066 | ||
chr19:8486087
|
C | T | 1 | a0001c0009 | 2 | HG02145.hp2 HG02280.hp1 |
synonymous_variant | LOW | c.1659C>T | p.Thr553Thr | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1683/2477 | 1659/2193 | 553/730 | chr19 | 8486087 | ||
chr19:8486144
|
C | T | 1 | a0001c0006 | 3 | NA18985.hp2 NA19000.hp2 NA19060.hp2 |
synonymous_variant | LOW | c.1716C>T | p.Gly572Gly | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1740/2477 | 1716/2193 | 572/730 | chr19 | 8486144 | ||
chr19:8486210
|
T | C | 12 | a0001c0001a0001c0003a0001c0005others(9): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
synonymous_variant | LOW | c.1782T>C | p.Pro594Pro | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1806/2477 | 1782/2193 | 594/730 | chr19 | 8486210 | ||
chr19:8486228
|
G | T | 1 | a0001c0003 | 15 | HG00140.hp2 HG00544.hp1 HG00673.hp1 others(12): Show |
synonymous_variant | LOW | c.1800G>T | p.Leu600Leu | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1824/2477 | 1800/2193 | 600/730 | chr19 | 8486228 | ||
chr19:8486231
|
C | T | 1 | a0001c0005 | 3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.1803C>T | p.Gly601Gly | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/16 | 1827/2477 | 1803/2193 | 601/730 | chr19 | 8486231 | ||
chr19:8488746
|
C | T | 14 | a0001c0001a0001c0003a0001c0004others(11): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
synonymous_variant | LOW | c.2085C>T | p.Gly695Gly | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 16/16 | 2109/2477 | 2085/2193 | 695/730 | chr19 | 8488746 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:8445260
|
T | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.113+149T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445260 | ||||||
chr19:8445332
|
T | TC | 4 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(1): Show | 4 | HG00323.hp1 HG03688.hp1 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.113+222dupC | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8445332 | |||||
chr19:8445339
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG01952.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.113+228C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445339 | ||||||
chr19:8445347
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0282a0001c0001t0001g0283 | 4 | HG01981.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+236C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445347 | ||||||
chr19:8445492
|
C | G | 1 | a0001c0001t0001g0281 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.113+381C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445492 | ||||||
chr19:8445515
|
C | T | 2 | a0001c0002t0001g0329a0001c0002t0001g0330 | 2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.113+404C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445515 | ||||||
chr19:8445529
|
G | T | 20 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(17): Show | 20 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.113+418G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445529 | ||||||
chr19:8445542
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(305): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.113+431A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445542 | ||||||
chr19:8445593
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.113+482C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445593 | ||||||
chr19:8445642
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.113+531C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445642 | ||||||
chr19:8445657
|
C | T | 13 | a0001c0001t0001g0019a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG00323.hp1 HG01109.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.113+546C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445657 | ||||||
chr19:8445740
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.113+629C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8445740 | ||||||
chr19:8446042
|
CACTT | C | 5 | a0001c0001t0001g0006a0001c0009t0001g0025a0001c0009t0001g0026others(2): Show | 6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.113+933_113+936del others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8446042 | |||||
chr19:8446134
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.113+1023T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446134 | ||||||
chr19:8446250
|
T | C | 1 | a0001c0004t0001g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.113+1139T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446250 | ||||||
chr19:8446280
|
A | G | 2 | a0001c0002t0001g0327a0001c0002t0001g0328 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.113+1169A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446280 | ||||||
chr19:8446288
|
G | C | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.113+1177G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446288 | ||||||
chr19:8446320
|
C | T | 4 | a0001c0001t0001g0266a0001c0005t0001g0267a0001c0005t0001g0268others(1): Show | 4 | HG02559.hp1 HG02738.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+1209C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446320 | ||||||
chr19:8446403
|
A | C | 1 | a0001c0001t0001g0265 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.113+1292A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446403 | ||||||
chr19:8446441
|
C | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.113+1330C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446441 | ||||||
chr19:8446460
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.113+1349G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446460 | ||||||
chr19:8446528
|
G | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.113+1417G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446528 | ||||||
chr19:8446872
|
A | G | 1 | a0001c0004t0001g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.113+1761A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8446872 | ||||||
chr19:8447005
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.113+1894T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447005 | ||||||
chr19:8447234
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.113+2123A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447234 | ||||||
chr19:8447243
|
A | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.113+2132A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447243 | ||||||
chr19:8447260
|
C | CT | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(58): Show | 71 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.113+2165dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8447260 | |||||
chr19:8447260
|
C | CTT | 28 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(25): Show | 28 | HG00544.hp2 HG02145.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.113+2164_113+2165d others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8447260 | |||||
chr19:8447260
|
C | CTTT | 190 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 208 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.113+2163_113+2165d others(5): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8447260 | |||||
chr19:8447260
|
C | CTTTT | 8 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(5): Show | 8 | HG00544.hp1 HG01891.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.113+2162_113+2165d others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8447260 | |||||
chr19:8447417
|
A | G | 1 | a0001c0002t0001g0326 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.113+2306A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447417 | ||||||
chr19:8447444
|
A | T | 20 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(17): Show | 20 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.113+2333A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447444 | ||||||
chr19:8447503
|
G | T | 1 | a0001c0002t0001g0325 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.113+2392G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447503 | ||||||
chr19:8447518
|
A | G | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG01109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.113+2407A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447518 | ||||||
chr19:8447647
|
G | A | 3 | a0001c0005t0001g0267a0001c0005t0001g0268a0001c0005t0001g0269 | 3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.113+2536G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447647 | ||||||
chr19:8447955
|
G | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 7 | HG02071.hp1 HG02135.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.113+2844G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8447955 | ||||||
chr19:8448025
|
T | TCAAA | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.113+2930_113+2933d others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8448025 | |||||
chr19:8448026
|
C | T | 1 | a0001c0001t0001g0289 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.113+2915C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448026 | ||||||
chr19:8448056
|
T | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(84): Show | 94 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.113+2945T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448056 | ||||||
chr19:8448412
|
T | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(305): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.113+3301T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448412 | ||||||
chr19:8448452
|
A | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(88): Show | 99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.113+3341A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448452 | ||||||
chr19:8448473
|
A | AT | 9 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(6): Show | 9 | HG02080.hp1 HG02129.hp1 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.113+3377dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8448473 | |||||
chr19:8448473
|
AT | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(73): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.113+3377delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8448473 | |||||
chr19:8448509
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(305): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.113+3398T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448509 | ||||||
chr19:8448546
|
C | T | 5 | a0001c0003t0001g0157a0001c0003t0001g0158a0001c0003t0001g0159others(2): Show | 5 | HG01081.hp1 HG01243.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+3435C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448546 | ||||||
chr19:8448576
|
C | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.113+3465C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448576 | ||||||
chr19:8448607
|
A | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.113+3496A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448607 | ||||||
chr19:8448622
|
C | T | 10 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(7): Show | 10 | HG02257.hp2 HG02280.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.113+3511C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448622 | ||||||
chr19:8448651
|
T | A | 14 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(11): Show | 15 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.113+3540T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448651 | ||||||
chr19:8448656
|
T | C | 1 | a0001c0012t0001g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.113+3545T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448656 | ||||||
chr19:8448784
|
C | T | 1 | a0005c0011t0001g0307 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.113+3673C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448784 | ||||||
chr19:8448918
|
G | A | 20 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(17): Show | 20 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.113+3807G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448918 | ||||||
chr19:8448918
|
G | C | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.113+3807G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448918 | ||||||
chr19:8448942
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.113+3831C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8448942 | ||||||
chr19:8449010
|
A | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(88): Show | 99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.113+3899A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8449010 | ||||||
chr19:8449294
|
G | A | 7 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(4): Show | 8 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.113+4183G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8449294 | ||||||
chr19:8449313
|
T | A | 4 | a0001c0002t0001g0292a0001c0002t0001g0293a0001c0002t0001g0329others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.113+4202T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8449313 | ||||||
chr19:8449509
|
T | C | 1 | a0002c0017t0001g0099 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.113+4398T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8449509 | ||||||
chr19:8449526
|
GCTAAGAG others(300): Show |
G | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.113+4431_113+4737d others(2): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8449526 | |||||
chr19:8449537
|
C | CT | 19 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(16): Show | 19 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.113+4442dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8449537 | |||||
chr19:8449911
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.113+4800C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8449911 | ||||||
chr19:8449923
|
C | A | 1 | a0001c0014t0001g0024 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.113+4812C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8449923 | ||||||
chr19:8450105
|
T | A | 1 | a0001c0001t0001g0032 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.113+4994T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450105 | ||||||
chr19:8450182
|
TTA | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.113+5076_113+5077d others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8450182 | |||||
chr19:8450276
|
T | C | 2 | a0001c0009t0001g0025a0001c0009t0001g0026 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.114-5129T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450276 | ||||||
chr19:8450400
|
A | G | 4 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(1): Show | 4 | HG00323.hp1 HG03688.hp1 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-5005A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450400 | ||||||
chr19:8450459
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.114-4946T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450459 | ||||||
chr19:8450491
|
A | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(88): Show | 99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.114-4914A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450491 | ||||||
chr19:8450593
|
T | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.114-4812T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450593 | ||||||
chr19:8450689
|
G | A | 1 | a0001c0012t0001g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.114-4716G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450689 | ||||||
chr19:8450711
|
A | AATT | 18 | a0001c0001t0001g0019a0001c0001t0001g0088a0001c0001t0001g0089others(15): Show | 19 | HG00323.hp1 HG01109.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.114-4678_114-4676d others(5): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8450711 | |||||
chr19:8450727
|
A | AT | 12 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0070others(9): Show | 12 | HG00438.hp1 HG03195.hp1 HG03490.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-4664dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8450727 | |||||
chr19:8450727
|
A | ATT | 24 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0028others(21): Show | 25 | HG00741.hp1 HG01169.hp1 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.114-4665_114-4664d others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8450727 | |||||
chr19:8450727
|
A | T | 2 | a0001c0001t0001g0255a0001c0002t0001g0306 | 2 | HG02922.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.114-4678A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450727 | ||||||
chr19:8450728
|
T | TTA | 75 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(72): Show | 84 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.114-4676_114-4675i others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8450728 | |||||
chr19:8450729
|
T | TA | 54 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(51): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.114-4676_114-4675i others(3): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450729 | ||||||
chr19:8450729
|
T | TATTA | 4 | a0001c0001t0001g0006a0001c0009t0001g0025a0001c0009t0001g0026others(1): Show | 5 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-4676_114-4675i others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450729 | ||||||
chr19:8450729
|
T | TATTATTA | 85 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(82): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.114-4676_114-4675i others(9): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450729 | ||||||
chr19:8450729
|
T | TATTATTA others(3): Show |
3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG00639.hp2 NA19081.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.114-4676_114-4675i others(12): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450729 | ||||||
chr19:8450730
|
T | A | 27 | a0001c0001t0001g0033a0001c0001t0001g0088a0001c0001t0001g0089others(24): Show | 27 | HG01109.hp2 HG01516.hp1 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.114-4675T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450730 | ||||||
chr19:8450731
|
T | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | NA18977.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.114-4674T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450731 | ||||||
chr19:8450732
|
T | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(99): Show | 111 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.114-4673T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450732 | ||||||
chr19:8450733
|
T | A | 3 | a0001c0004t0001g0291a0001c0004t0001g0294a0001c0004t0001g0295 | 3 | HG02486.hp1 HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.114-4672T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450733 | ||||||
chr19:8450735
|
T | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(91): Show | 102 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.114-4670T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450735 | ||||||
chr19:8450744
|
G | T | 5 | a0001c0004t0001g0290a0001c0004t0001g0291a0001c0004t0001g0294others(2): Show | 5 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-4661G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450744 | ||||||
chr19:8450778
|
G | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0289 | 2 | HG00323.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.114-4627G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450778 | ||||||
chr19:8450792
|
T | G | 111 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(108): Show | 122 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.114-4613T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450792 | ||||||
chr19:8450855
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.114-4550G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450855 | ||||||
chr19:8450891
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.114-4514G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450891 | ||||||
chr19:8450928
|
C | T | 1 | a0001c0003t0001g0161 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.114-4477C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450928 | ||||||
chr19:8450932
|
G | T | 1 | a0001c0001t0001g0231 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.114-4473G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8450932 | ||||||
chr19:8451095
|
C | T | 2 | a0001c0001t0001g0080a0003c0010t0001g0079 | 2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.114-4310C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451095 | ||||||
chr19:8451126
|
C | T | 2 | a0001c0009t0001g0025a0001c0009t0001g0026 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.114-4279C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451126 | ||||||
chr19:8451142
|
G | A | 1 | a0001c0004t0001g0294 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.114-4263G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451142 | ||||||
chr19:8451182
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.114-4223C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451182 | ||||||
chr19:8451299
|
C | T | 2 | a0001c0001t0001g0080a0003c0010t0001g0079 | 2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.114-4106C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451299 | ||||||
chr19:8451394
|
A | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(88): Show | 99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.114-4011A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451394 | ||||||
chr19:8451413
|
C | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.114-3992C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451413 | ||||||
chr19:8451463
|
T | TA | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.114-3935dupA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8451463 | |||||
chr19:8451527
|
CTCCCCT | C | 116 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(113): Show | 127 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.114-3861_114-3856d others(8): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8451527 | |||||
chr19:8451571
|
C | A | 1 | a0001c0001t0001g0280 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.114-3834C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451571 | ||||||
chr19:8451789
|
C | T | 3 | a0001c0005t0001g0267a0001c0005t0001g0268a0001c0005t0001g0269 | 3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.114-3616C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451789 | ||||||
chr19:8451793
|
A | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(88): Show | 99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.114-3612A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451793 | ||||||
chr19:8451850
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.114-3555G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451850 | ||||||
chr19:8451890
|
A | G | 1 | a0001c0002t0001g0305 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.114-3515A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8451890 | ||||||
chr19:8452130
|
A | G | 20 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(17): Show | 20 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.114-3275A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452130 | ||||||
chr19:8452165
|
A | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.114-3240A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452165 | ||||||
chr19:8452274
|
C | T | 103 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(100): Show | 113 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.114-3131C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452274 | ||||||
chr19:8452327
|
C | T | 1 | a0006c0016t0001g0071 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.114-3078C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452327 | ||||||
chr19:8452328
|
A | C | 1 | a0006c0016t0001g0071 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.114-3077A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452328 | ||||||
chr19:8452429
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.114-2976G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452429 | ||||||
chr19:8452502
|
C | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(50): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.114-2903C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452502 | ||||||
chr19:8452802
|
G | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.114-2603G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452802 | ||||||
chr19:8452891
|
A | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.114-2514A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452891 | ||||||
chr19:8452921
|
A | G | 111 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(108): Show | 122 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.114-2484A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8452921 | ||||||
chr19:8453376
|
A | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG01070.hp1 HG01978.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.114-2029A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8453376 | ||||||
chr19:8453500
|
C | T | 6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.114-1905C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8453500 | ||||||
chr19:8453512
|
A | G | 3 | a0001c0005t0001g0267a0001c0005t0001g0268a0001c0005t0001g0269 | 3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.114-1893A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8453512 | ||||||
chr19:8453531
|
G | A | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(164): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.114-1874G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8453531 | ||||||
chr19:8453588
|
G | GT | 23 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0061others(20): Show | 24 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.114-1809dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8453588 | |||||
chr19:8453660
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | NA18948.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.114-1745C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8453660 | ||||||
chr19:8453738
|
T | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.114-1667T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8453738 | ||||||
chr19:8453774
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.114-1631C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8453774 | ||||||
chr19:8453994
|
C | T | 1 | a0001c0002t0001g0304 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.114-1411C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8453994 | ||||||
chr19:8454016
|
C | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.114-1389C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454016 | ||||||
chr19:8454080
|
AT | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.114-1320delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8454080 | |||||
chr19:8454082
|
T | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.114-1323T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454082 | ||||||
chr19:8454102
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.114-1303A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454102 | ||||||
chr19:8454135
|
T | G | 1 | a0001c0001t0001g0183 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.114-1270T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454135 | ||||||
chr19:8454164
|
A | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-1241A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454164 | ||||||
chr19:8454339
|
A | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(88): Show | 99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.114-1066A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454339 | ||||||
chr19:8454433
|
AT | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 7 | HG01099.hp2 HG01123.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.114-971delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454433 | ||||||
chr19:8454492
|
G | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0084 | 2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.114-913G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454492 | ||||||
chr19:8454557
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.114-848C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454557 | ||||||
chr19:8454673
|
G | GC | 94 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(91): Show | 103 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.114-721dupC | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8454673 | |||||
chr19:8454673
|
G | GCC | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(45): Show | 57 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.114-722_114-721dup others(2): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8454673 | |||||
chr19:8454683
|
C | CT | 4 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0007t0001g0273others(1): Show | 5 | HG02717.hp1 HG02809.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-722_114-721ins others(1): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454683 | ||||||
chr19:8454684
|
C | CT | 6 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(3): Show | 6 | HG00323.hp1 HG02922.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.114-710dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8454684 | |||||
chr19:8454684
|
C | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0277others(3): Show | 7 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.114-721C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454684 | ||||||
chr19:8454684
|
CT | C | 9 | a0001c0001t0001g0089a0001c0001t0001g0101a0001c0001t0001g0105others(6): Show | 9 | HG01074.hp1 HG02615.hp1 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.114-710delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8454684 | |||||
chr19:8454684
|
CTT | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.114-711_114-710del others(2): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 8454684 | |||||
chr19:8454685
|
T | C | 8 | a0001c0001t0001g0085a0001c0001t0001g0184a0001c0001t0001g0185others(5): Show | 8 | HG00735.hp2 HG01106.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-720T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454685 | ||||||
chr19:8454686
|
T | C | 10 | a0001c0001t0001g0089a0001c0001t0001g0101a0001c0001t0001g0105others(7): Show | 10 | HG01074.hp1 HG02615.hp1 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-719T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454686 | ||||||
chr19:8454687
|
T | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0084 | 2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.114-718T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454687 | ||||||
chr19:8454743
|
A | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.114-662A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454743 | ||||||
chr19:8454843
|
G | C | 1 | a0001c0014t0001g0024 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.114-562G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8454843 | ||||||
chr19:8455004
|
C | T | 5 | a0001c0004t0001g0290a0001c0004t0001g0291a0001c0004t0001g0294others(2): Show | 5 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-401C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455004 | ||||||
chr19:8455021
|
C | G | 1 | a0001c0002t0001g0325 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.114-384C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455021 | ||||||
chr19:8455082
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.114-323C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455082 | ||||||
chr19:8455106
|
C | G | 1 | a0005c0011t0001g0307 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.114-299C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455106 | ||||||
chr19:8455153
|
T | A | 105 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(102): Show | 115 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.114-252T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455153 | ||||||
chr19:8455156
|
T | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(50): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.114-249T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455156 | ||||||
chr19:8455165
|
T | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.114-240T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455165 | ||||||
chr19:8455217
|
A | G | 1 | a0001c0008t0001g0150 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.114-188A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455217 | ||||||
chr19:8455298
|
A | C | 1 | a0001c0002t0001g0306 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.114-107A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455298 | ||||||
chr19:8455361
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.114-44G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 1/15 | chr19 | 8455361 | ||||||
chr19:8455661
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.283+87A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8455661 | ||||||
chr19:8455725
|
G | GT | 7 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0085others(4): Show | 8 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+163dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8455725 | |||||
chr19:8455745
|
G | GT | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(95): Show | 107 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.283+181dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8455745 | |||||
chr19:8455746
|
TTTTTTTT others(3): Show |
T | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG01109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.283+177_283+186del others(10): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8455746 | |||||
chr19:8455750
|
T | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | NA18977.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.283+176T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8455750 | ||||||
chr19:8455751
|
T | G | 9 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(6): Show | 10 | HG00323.hp1 HG02055.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+177T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8455751 | ||||||
chr19:8455944
|
C | CT | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.283+386dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8455944 | |||||
chr19:8455944
|
C | CTT | 21 | a0001c0001t0001g0019a0001c0001t0001g0070a0001c0001t0001g0111others(18): Show | 22 | HG01109.hp2 HG01169.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.283+385_283+386dup others(2): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8455944 | |||||
chr19:8455944
|
C | CTTT | 63 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(60): Show | 71 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.283+384_283+386dup others(3): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8455944 | |||||
chr19:8456203
|
A | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+629A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8456203 | ||||||
chr19:8456296
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.283+722C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8456296 | ||||||
chr19:8456316
|
C | A | 1 | a0001c0001t0001g0114 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.283+742C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8456316 | ||||||
chr19:8456338
|
G | A | 1 | a0001c0012t0001g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.283+764G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8456338 | ||||||
chr19:8456474
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+900C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8456474 | ||||||
chr19:8456651
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | NA18977.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.283+1077C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8456651 | ||||||
chr19:8456932
|
A | G | 1 | a0001c0002t0001g0305 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.283+1358A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8456932 | ||||||
chr19:8457214
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.283+1640G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8457214 | ||||||
chr19:8457705
|
A | G | 1 | a0001c0002t0001g0311 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.283+2131A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8457705 | ||||||
chr19:8457994
|
G | T | 1 | a0001c0012t0001g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.283+2420G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8457994 | ||||||
chr19:8458119
|
T | G | 1 | a0001c0001t0001g0265 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.283+2545T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458119 | ||||||
chr19:8458122
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.283+2548T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458122 | ||||||
chr19:8458132
|
T | C | 1 | a0001c0002t0001g0304 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.283+2558T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458132 | ||||||
chr19:8458137
|
C | CG | 16 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(13): Show | 16 | HG01168.hp2 HG01934.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.283+2569dupG | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8458137 | |||||
chr19:8458138
|
G | C | 6 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(3): Show | 6 | HG02559.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+2564G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458138 | ||||||
chr19:8458242
|
T | C | 4 | a0001c0001t0001g0115a0001c0001t0001g0162a0001c0001t0001g0260others(1): Show | 4 | HG03017.hp2 HG04184.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+2668T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458242 | ||||||
chr19:8458266
|
A | C | 2 | a0001c0002t0001g0314a0001c0002t0001g0315 | 2 | HG02135.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.283+2692A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458266 | ||||||
chr19:8458324
|
C | A | 1 | a0001c0001t0001g0090 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+2750C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458324 | ||||||
chr19:8458325
|
C | G | 1 | a0001c0001t0001g0254 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.283+2751C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458325 | ||||||
chr19:8458529
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.283+2955C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458529 | ||||||
chr19:8458728
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.283+3154C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458728 | ||||||
chr19:8458749
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.283+3175A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458749 | ||||||
chr19:8458963
|
G | A | 4 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(1): Show | 4 | HG00323.hp1 HG03688.hp1 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+3389G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8458963 | ||||||
chr19:8459085
|
C | A | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.284-3444C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459085 | ||||||
chr19:8459085
|
C | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-3444C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459085 | ||||||
chr19:8459118
|
G | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-3411G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459118 | ||||||
chr19:8459265
|
T | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-3264T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459265 | ||||||
chr19:8459270
|
A | G | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | NA18957.hp1 NA18975.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-3259A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459270 | ||||||
chr19:8459308
|
C | T | 1 | a0001c0002t0001g0318 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.284-3221C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459308 | ||||||
chr19:8459368
|
C | CGTG | 3 | a0001c0002t0001g0022a0001c0002t0001g0297a0001c0002t0001g0298 | 4 | HG02809.hp2 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-3159_284-3157d others(5): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8459368 | |||||
chr19:8459384
|
T | C | 1 | a0004c0013t0001g0062 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.284-3145T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459384 | ||||||
chr19:8459571
|
A | G | 1 | a0001c0006t0001g0069 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.284-2958A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459571 | ||||||
chr19:8459690
|
A | G | 1 | a0001c0002t0001g0305 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.284-2839A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459690 | ||||||
chr19:8459717
|
G | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-2812G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459717 | ||||||
chr19:8459754
|
G | A | 4 | a0001c0006t0001g0067a0001c0006t0001g0068a0001c0006t0001g0069others(1): Show | 4 | NA18985.hp2 NA19000.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-2775G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459754 | ||||||
chr19:8459801
|
T | G | 8 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0170others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-2728T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459801 | ||||||
chr19:8459842
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.284-2687T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459842 | ||||||
chr19:8459877
|
A | G | 1 | a0001c0001t0001g0006 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.284-2652A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459877 | ||||||
chr19:8459970
|
A | C | 1 | a0001c0014t0001g0024 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.284-2559A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8459970 | ||||||
chr19:8460088
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.284-2441T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460088 | ||||||
chr19:8460420
|
T | C | 4 | a0001c0003t0001g0018a0001c0003t0001g0257a0001c0003t0001g0258others(1): Show | 5 | HG00544.hp1 HG00673.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-2109T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460420 | ||||||
chr19:8460550
|
C | T | 3 | a0001c0004t0001g0291a0001c0004t0001g0294a0001c0004t0001g0295 | 3 | HG02486.hp1 HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.284-1979C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460550 | ||||||
chr19:8460711
|
C | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(305): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.284-1818C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460711 | ||||||
chr19:8460756
|
G | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0054others(2): Show | 6 | HG00733.hp1 HG00741.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-1773G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460756 | ||||||
chr19:8460844
|
CTA | C | 4 | a0001c0002t0001g0312a0001c0002t0001g0313a0001c0002t0001g0314others(1): Show | 4 | HG02135.hp2 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-1683_284-1682d others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8460844 | |||||
chr19:8460864
|
AGTG | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG01074.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.284-1663_284-1661d others(5): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8460864 | |||||
chr19:8460953
|
G | A | 5 | a0001c0001t0001g0006a0001c0009t0001g0025a0001c0009t0001g0026others(2): Show | 6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-1576G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460953 | ||||||
chr19:8460967
|
T | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0084 | 2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.284-1562T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460967 | ||||||
chr19:8460987
|
G | A | 1 | a0001c0002t0001g0306 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.284-1542G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460987 | ||||||
chr19:8460994
|
A | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-1535A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8460994 | ||||||
chr19:8461103
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-1426G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461103 | ||||||
chr19:8461113
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.284-1416C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461113 | ||||||
chr19:8461178
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.284-1351C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461178 | ||||||
chr19:8461245
|
G | A | 3 | a0001c0005t0001g0267a0001c0005t0001g0268a0001c0005t0001g0269 | 3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.284-1284G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461245 | ||||||
chr19:8461253
|
G | C | 10 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(7): Show | 10 | HG02257.hp2 HG02280.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.284-1276G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461253 | ||||||
chr19:8461561
|
C | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.284-968C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461561 | ||||||
chr19:8461575
|
T | C | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.284-954T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461575 | ||||||
chr19:8461752
|
AAGCGGC | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(50): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.284-775_284-770del others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 8461752 | |||||
chr19:8461830
|
C | G | 4 | a0001c0002t0001g0292a0001c0002t0001g0293a0001c0002t0001g0329others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-699C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461830 | ||||||
chr19:8461938
|
A | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0054others(2): Show | 6 | HG00733.hp1 HG00741.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-591A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8461938 | ||||||
chr19:8462020
|
G | A | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.284-509G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 2/15 | chr19 | 8462020 | ||||||
chr19:8463036
|
T | C | 1 | a0001c0012t0001g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.336+455T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 3/15 | chr19 | 8463036 | ||||||
chr19:8463171
|
G | A | 1 | a0001c0002t0001g0322 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.337-326G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 3/15 | chr19 | 8463171 | ||||||
chr19:8463393
|
A | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.337-104A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 3/15 | chr19 | 8463393 | ||||||
chr19:8463420
|
T | A | 1 | a0001c0001t0001g0192 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.337-77T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 3/15 | chr19 | 8463420 | ||||||
chr19:8463426
|
A | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.337-71A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 3/15 | chr19 | 8463426 | ||||||
chr19:8463755
|
A | T | 1 | a0001c0001t0001g0280 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.438+69A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8463755 | ||||||
chr19:8463950
|
C | G | 1 | a0001c0009t0001g0026 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.438+264C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8463950 | ||||||
chr19:8464054
|
G | T | 2 | a0001c0002t0001g0302a0001c0002t0001g0303 | 2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.438+368G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464054 | ||||||
chr19:8464090
|
C | G | 1 | a0001c0001t0001g0286 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.438+404C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464090 | ||||||
chr19:8464219
|
C | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.438+533C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464219 | ||||||
chr19:8464228
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0116 | 2 | HG02615.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.438+542G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464228 | ||||||
chr19:8464248
|
TA | T | 313 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(310): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.438+569delA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr19 | 8464248 | |||||
chr19:8464316
|
C | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.438+630C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464316 | ||||||
chr19:8464349
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0100 | 2 | NA18951.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.438+663C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464349 | ||||||
chr19:8464362
|
C | T | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | NA19004.hp2 NA19086.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.438+676C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464362 | ||||||
chr19:8464524
|
C | T | 1 | a0001c0002t0001g0328 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.439-800C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464524 | ||||||
chr19:8464563
|
C | T | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(56): Show | 67 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.439-761C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464563 | ||||||
chr19:8464574
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.439-750G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464574 | ||||||
chr19:8464618
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.439-706G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464618 | ||||||
chr19:8464686
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.439-638A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464686 | ||||||
chr19:8464822
|
G | C | 1 | a0001c0004t0001g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.439-502G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464822 | ||||||
chr19:8464880
|
G | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 7 | HG01099.hp2 HG01123.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.439-444G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464880 | ||||||
chr19:8464912
|
T | C | 3 | a0001c0004t0001g0291a0001c0004t0001g0294a0001c0004t0001g0295 | 3 | HG02486.hp1 HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.439-412T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464912 | ||||||
chr19:8464959
|
C | T | 7 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(4): Show | 8 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.439-365C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8464959 | ||||||
chr19:8465003
|
A | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.439-321A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8465003 | ||||||
chr19:8465072
|
C | T | 3 | a0001c0005t0001g0267a0001c0005t0001g0268a0001c0005t0001g0269 | 3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.439-252C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8465072 | ||||||
chr19:8465165
|
C | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(50): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.439-159C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8465165 | ||||||
chr19:8465189
|
T | C | 16 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(13): Show | 16 | HG01168.hp2 HG01934.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.439-135T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8465189 | ||||||
chr19:8465207
|
G | C | 1 | a0001c0001t0001g0231 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.439-117G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8465207 | ||||||
chr19:8465246
|
A | C | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.439-78A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 5/15 | chr19 | 8465246 | ||||||
chr19:8465701
|
C | G | 1 | a0001c0001t0001g0053 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.630+186C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 6/15 | chr19 | 8465701 | ||||||
chr19:8465701
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.630+186C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 6/15 | chr19 | 8465701 | ||||||
chr19:8465747
|
G | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(305): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.630+232G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 6/15 | chr19 | 8465747 | ||||||
chr19:8465813
|
T | C | 20 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(17): Show | 20 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.630+298T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 6/15 | chr19 | 8465813 | ||||||
chr19:8465817
|
C | T | 5 | a0001c0002t0001g0320a0001c0002t0001g0321a0001c0002t0001g0324others(2): Show | 5 | HG01934.hp1 HG02258.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.630+302C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 6/15 | chr19 | 8465817 | ||||||
chr19:8465945
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG00735.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.631-290C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 6/15 | chr19 | 8465945 | ||||||
chr19:8465999
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.631-236A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 6/15 | chr19 | 8465999 | ||||||
chr19:8466472
|
G | GACTGTGT others(6): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0050a0001c0001t0001g0056 | 4 | HG01071.hp2 HG01256.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+86_784+98dupCT others(11): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466472 | |||||
chr19:8466594
|
A | G | 1 | a0001c0002t0001g0314 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.784+206A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | chr19 | 8466594 | ||||||
chr19:8466828
|
C | CA | 6 | a0001c0001t0001g0006a0001c0001t0001g0280a0001c0002t0001g0304others(3): Show | 7 | HG01891.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.784+464dupA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | |||||
chr19:8466828
|
C | CAA | 49 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(46): Show | 56 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.784+463_784+464dup others(2): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | |||||
chr19:8466828
|
C | CAAA | 56 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(53): Show | 59 | HG00423.hp1 HG01070.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.784+462_784+464dup others(3): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | |||||
chr19:8466828
|
C | CAAAA | 12 | a0001c0001t0001g0076a0001c0001t0001g0142a0001c0001t0001g0143others(9): Show | 12 | HG01070.hp1 HG01175.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.784+461_784+464dup others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | |||||
chr19:8466828
|
C | CAAAAA | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(48): Show | 59 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.784+460_784+464dup others(5): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | |||||
chr19:8466828
|
C | CAAAAAA | 25 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0112others(22): Show | 25 | HG00438.hp2 HG01081.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.784+459_784+464dup others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | |||||
chr19:8466828
|
C | CAAAAAAA | 7 | a0001c0001t0001g0105a0001c0001t0001g0116a0001c0001t0001g0117others(4): Show | 7 | HG01106.hp1 HG01192.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.784+458_784+464dup others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | |||||
chr19:8466828
|
CA | C | 18 | a0001c0001t0001g0042a0001c0001t0001g0053a0001c0001t0001g0057others(15): Show | 18 | HG00280.hp1 HG01192.hp1 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.784+464delA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | |||||
chr19:8466828
|
CAA | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(49): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.784+463_784+464del others(2): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | |||||
chr19:8466828
|
CAAA | C | 10 | a0001c0001t0001g0032a0001c0001t0001g0039a0001c0001t0001g0040others(7): Show | 10 | HG00323.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.784+462_784+464del others(3): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8466828 | |||||
chr19:8466890
|
A | T | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.784+502A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | chr19 | 8466890 | ||||||
chr19:8466917
|
T | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(50): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.784+529T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | chr19 | 8466917 | ||||||
chr19:8466983
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.785-552G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | chr19 | 8466983 | ||||||
chr19:8467076
|
GA | G | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(107): Show | 121 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.785-457delA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8467076 | |||||
chr19:8467088
|
TCTC | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.785-444_785-442del others(3): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr19 | 8467088 | |||||
chr19:8467335
|
G | A | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(107): Show | 121 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.785-200G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | chr19 | 8467335 | ||||||
chr19:8467356
|
G | A | 3 | a0001c0005t0001g0267a0001c0005t0001g0268a0001c0005t0001g0269 | 3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.785-179G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | chr19 | 8467356 | ||||||
chr19:8467390
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.785-145G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 7/15 | chr19 | 8467390 | ||||||
chr19:8467603
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.834+19T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8467603 | ||||||
chr19:8467634
|
A | G | 5 | a0001c0004t0001g0290a0001c0004t0001g0291a0001c0004t0001g0294others(2): Show | 5 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+50A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8467634 | ||||||
chr19:8467817
|
C | T | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(107): Show | 121 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.834+233C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8467817 | ||||||
chr19:8467823
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(70): Show | 80 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.834+239G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8467823 | ||||||
chr19:8467830
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.834+246G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8467830 | ||||||
chr19:8467885
|
G | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.834+301G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8467885 | ||||||
chr19:8467982
|
G | A | 3 | a0001c0005t0001g0267a0001c0005t0001g0268a0001c0005t0001g0269 | 3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.834+398G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8467982 | ||||||
chr19:8468021
|
T | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.834+437T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8468021 | ||||||
chr19:8468029
|
G | GA | 8 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0274others(5): Show | 9 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.834+454dupA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr19 | 8468029 | |||||
chr19:8468214
|
A | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.835-560A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8468214 | ||||||
chr19:8468320
|
C | A | 4 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(1): Show | 4 | HG00323.hp1 HG03688.hp1 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.835-454C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8468320 | ||||||
chr19:8468482
|
C | G | 1 | a0001c0001t0001g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.835-292C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8468482 | ||||||
chr19:8468484
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.835-290C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8468484 | ||||||
chr19:8468620
|
T | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.835-154T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8468620 | ||||||
chr19:8468621
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.835-153G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8468621 | ||||||
chr19:8468625
|
C | T | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(107): Show | 121 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.835-149C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 8/15 | chr19 | 8468625 | ||||||
chr19:8468881
|
C | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.895+47C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8468881 | ||||||
chr19:8468932
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.895+98G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8468932 | ||||||
chr19:8469041
|
A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.895+207A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469041 | ||||||
chr19:8469098
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.895+264G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469098 | ||||||
chr19:8469221
|
G | A | 1 | a0001c0002t0001g0299 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.895+387G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469221 | ||||||
chr19:8469567
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.895+733G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469567 | ||||||
chr19:8469632
|
A | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.895+798A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469632 | ||||||
chr19:8469677
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.895+843G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469677 | ||||||
chr19:8469742
|
G | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(50): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.895+908G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469742 | ||||||
chr19:8469794
|
G | A | 45 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(42): Show | 49 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.895+960G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469794 | ||||||
chr19:8469813
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.895+979C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469813 | ||||||
chr19:8469970
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.895+1136A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8469970 | ||||||
chr19:8470168
|
A | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.896-1158A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470168 | ||||||
chr19:8470204
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0084 | 2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.896-1122C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470204 | ||||||
chr19:8470230
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.896-1096A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470230 | ||||||
chr19:8470461
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.896-865G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470461 | ||||||
chr19:8470495
|
T | G | 19 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(16): Show | 19 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.896-831T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470495 | ||||||
chr19:8470497
|
T | TG | 7 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(4): Show | 8 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.896-829_896-828ins others(1): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470497 | ||||||
chr19:8470498
|
T | G | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(278): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.896-828T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470498 | ||||||
chr19:8470514
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.896-812G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470514 | ||||||
chr19:8470731
|
G | C | 1 | a0001c0001t0001g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.896-595G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470731 | ||||||
chr19:8470959
|
C | T | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG01070.hp1 HG01978.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.896-367C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8470959 | ||||||
chr19:8471100
|
T | G | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.896-226T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8471100 | ||||||
chr19:8471154
|
C | T | 1 | a0001c0002t0001g0325 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.896-172C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8471154 | ||||||
chr19:8471259
|
CTT | C | 3 | a0001c0001t0001g0006a0001c0012t0001g0023a0001c0014t0001g0024 | 4 | HG02257.hp1 HG02976.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.896-64_896-63delTT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr19 | 8471259 | |||||
chr19:8471306
|
T | G | 5 | a0001c0001t0001g0007a0001c0002t0001g0312a0001c0002t0001g0313others(2): Show | 6 | HG01099.hp2 HG01261.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.896-20T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 9/15 | chr19 | 8471306 | ||||||
chr19:8471489
|
A | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.997+62A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8471489 | ||||||
chr19:8471536
|
C | A | 5 | a0001c0001t0001g0006a0001c0009t0001g0025a0001c0009t0001g0026others(2): Show | 6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.997+109C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8471536 | ||||||
chr19:8471616
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.997+189T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8471616 | ||||||
chr19:8471648
|
G | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.997+221G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8471648 | ||||||
chr19:8471704
|
G | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0182a0001c0001t0001g0185others(4): Show | 8 | HG00423.hp1 HG01943.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.997+277G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8471704 | ||||||
chr19:8471870
|
T | C | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(164): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.997+443T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8471870 | ||||||
chr19:8472028
|
G | A | 1 | a0001c0004t0001g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.997+601G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472028 | ||||||
chr19:8472039
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.997+612C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472039 | ||||||
chr19:8472087
|
C | G | 1 | a0001c0005t0001g0269 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.997+660C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472087 | ||||||
chr19:8472090
|
G | A | 5 | a0001c0001t0001g0006a0001c0009t0001g0025a0001c0009t0001g0026others(2): Show | 6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.997+663G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472090 | ||||||
chr19:8472172
|
G | GA | 14 | a0001c0001t0001g0030a0001c0001t0001g0051a0001c0001t0001g0082others(11): Show | 14 | HG01109.hp2 HG01891.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.997+765dupA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr19 | 8472172 | |||||
chr19:8472172
|
GA | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(96): Show | 107 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.997+765delA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr19 | 8472172 | |||||
chr19:8472173
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0045 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.997+746A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472173 | ||||||
chr19:8472205
|
CTTTGATG others(3): Show |
C | 2 | a0001c0001t0001g0043a0001c0001t0001g0052 | 2 | HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.997+779_997+788del others(10): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472205 | ||||||
chr19:8472212
|
G | A | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.997+785G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472212 | ||||||
chr19:8472212
|
G | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.997+785G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472212 | ||||||
chr19:8472229
|
G | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0052 | 2 | HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.997+802G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472229 | ||||||
chr19:8472481
|
A | G | 20 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(17): Show | 20 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.997+1054A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472481 | ||||||
chr19:8472599
|
A | G | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG01109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.998-1065A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472599 | ||||||
chr19:8472782
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.998-882A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8472782 | ||||||
chr19:8473005
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.998-659G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473005 | ||||||
chr19:8473239
|
T | C | 23 | a0001c0001t0001g0014a0001c0001t0001g0184a0001c0001t0001g0189others(20): Show | 24 | HG02071.hp2 HG02074.hp2 HG02129.hp2 others(21): Show |
intron_variant | MODIFIER | c.998-425T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473239 | ||||||
chr19:8473243
|
A | C | 1 | a0001c0002t0001g0298 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.998-421A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473243 | ||||||
chr19:8473302
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.998-362C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473302 | ||||||
chr19:8473385
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.998-279C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473385 | ||||||
chr19:8473459
|
T | A | 1 | a0001c0001t0001g0164 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.998-205T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473459 | ||||||
chr19:8473459
|
TA | T | 12 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 13 | HG00733.hp2 HG01081.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.998-191delA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr19 | 8473459 | |||||
chr19:8473465
|
A | T | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.998-199A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473465 | ||||||
chr19:8473592
|
A | T | 1 | a0001c0001t0001g0138 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.998-72A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473592 | ||||||
chr19:8473614
|
A | G | 12 | a0001c0001t0001g0019a0001c0001t0001g0177a0001c0001t0001g0274others(9): Show | 13 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.998-50A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 10/15 | chr19 | 8473614 | ||||||
chr19:8473766
|
T | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0170a0001c0001t0001g0190others(4): Show | 8 | HG03209.hp2 NA18947.hp2 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.1042+58T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 11/15 | chr19 | 8473766 | ||||||
chr19:8473783
|
G | C | 4 | a0001c0003t0001g0018a0001c0003t0001g0257a0001c0003t0001g0258others(1): Show | 5 | HG00544.hp1 HG00673.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042+75G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 11/15 | chr19 | 8473783 | ||||||
chr19:8474002
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0126 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1043-165T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 11/15 | chr19 | 8474002 | ||||||
chr19:8474052
|
T | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0127 | 2 | HG01934.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1043-115T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 11/15 | chr19 | 8474052 | ||||||
chr19:8474111
|
C | G | 1 | a0001c0001t0001g0138 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1043-56C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 11/15 | chr19 | 8474111 | ||||||
chr19:8474529
|
A | C | 1 | a0001c0014t0001g0024 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1120+285A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474529 | ||||||
chr19:8474567
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1120+323C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474567 | ||||||
chr19:8474593
|
C | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0084 | 2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1120+349C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474593 | ||||||
chr19:8474609
|
A | G | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1120+365A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474609 | ||||||
chr19:8474661
|
T | C | 16 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(13): Show | 16 | HG01168.hp2 HG01934.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1120+417T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474661 | ||||||
chr19:8474714
|
C | CT | 8 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1120+488dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8474714 | |||||
chr19:8474714
|
CT | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1120+488delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8474714 | |||||
chr19:8474714
|
CTT | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0039a0001c0001t0001g0152others(5): Show | 9 | HG01070.hp1 HG01169.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1120+487_1120+488d others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8474714 | |||||
chr19:8474778
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1120+534G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474778 | ||||||
chr19:8474800
|
C | T | 2 | a0001c0009t0001g0025a0001c0009t0001g0026 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1120+556C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474800 | ||||||
chr19:8474828
|
C | T | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(172): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1120+584C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474828 | ||||||
chr19:8474911
|
C | A | 1 | a0001c0002t0001g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1120+667C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474911 | ||||||
chr19:8474935
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0084 | 2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1120+691G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8474935 | ||||||
chr19:8475015
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1120+771C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475015 | ||||||
chr19:8475275
|
GC | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(94): Show | 106 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.1120+1034delC | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8475275 | |||||
chr19:8475321
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1120+1077A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475321 | ||||||
chr19:8475347
|
G | A | 1 | a0001c0005t0001g0269 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1120+1103G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475347 | ||||||
chr19:8475376
|
T | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1120+1132T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475376 | ||||||
chr19:8475511
|
C | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0084 | 2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1120+1267C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475511 | ||||||
chr19:8475515
|
C | A | 12 | a0001c0001t0001g0019a0001c0001t0001g0177a0001c0001t0001g0274others(9): Show | 13 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1120+1271C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475515 | ||||||
chr19:8475540
|
T | C | 3 | a0001c0001t0001g0103a0001c0001t0001g0128a0001c0001t0001g0156 | 3 | HG00639.hp2 HG00673.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1120+1296T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475540 | ||||||
chr19:8475555
|
G | A | 7 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(4): Show | 8 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1120+1311G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475555 | ||||||
chr19:8475569
|
A | G | 1 | a0001c0002t0001g0327 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1120+1325A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475569 | ||||||
chr19:8475577
|
A | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0084 | 2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1120+1333A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475577 | ||||||
chr19:8475662
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1120+1418C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475662 | ||||||
chr19:8475905
|
CT | C | 18 | a0001c0001t0001g0056a0001c0001t0001g0077a0001c0001t0001g0080others(15): Show | 18 | HG01928.hp2 HG02080.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1120+1685delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8475905 | |||||
chr19:8475905
|
CTT | C | 163 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(160): Show | 180 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1120+1684_1120+168 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8475905 | |||||
chr19:8475905
|
CTTT | C | 38 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(35): Show | 42 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.1120+1683_1120+168 others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8475905 | |||||
chr19:8475905
|
CTTTT | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(67): Show | 77 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1120+1682_1120+168 others(8): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8475905 | |||||
chr19:8475909
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1120+1665T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475909 | ||||||
chr19:8475910
|
T | C | 10 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1120+1666T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475910 | ||||||
chr19:8475911
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1120+1667T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475911 | ||||||
chr19:8475931
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1120+1687A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8475931 | ||||||
chr19:8475955
|
T | TTGAGTTG others(6): Show |
2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1120+1716_1120+172 others(17): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8475955 | |||||
chr19:8476063
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1120+1819C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476063 | ||||||
chr19:8476198
|
C | T | 1 | a0001c0002t0001g0305 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1120+1954C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476198 | ||||||
chr19:8476219
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1120+1975C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476219 | ||||||
chr19:8476249
|
C | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0084 | 2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1120+2005C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476249 | ||||||
chr19:8476379
|
C | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1120+2135C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476379 | ||||||
chr19:8476434
|
G | C | 1 | a0001c0012t0001g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1120+2190G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476434 | ||||||
chr19:8476523
|
G | A | 3 | a0001c0005t0001g0267a0001c0005t0001g0268a0001c0005t0001g0269 | 3 | HG02559.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1120+2279G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476523 | ||||||
chr19:8476566
|
T | TAA | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1120+2334_1120+233 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8476566 | |||||
chr19:8476576
|
AAAAG | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(76): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1120+2334_1120+233 others(8): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8476576 | |||||
chr19:8476577
|
AAAG | A | 107 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0011others(104): Show | 118 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1120+2335_1120+233 others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8476577 | |||||
chr19:8476578
|
AAG | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(83): Show | 94 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.1120+2340_1120+234 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8476578 | |||||
chr19:8476579
|
AG | A | 4 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0165others(1): Show | 4 | NA18984.hp2 NA18998.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120+2336delG | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476579 | ||||||
chr19:8476867
|
C | T | 5 | a0001c0001t0001g0006a0001c0009t0001g0025a0001c0009t0001g0026others(2): Show | 6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1120+2623C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476867 | ||||||
chr19:8476906
|
G | T | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1120+2662G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8476906 | ||||||
chr19:8477049
|
A | G | 2 | a0001c0003t0001g0124a0001c0003t0001g0141 | 2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1120+2805A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477049 | ||||||
chr19:8477121
|
A | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1120+2877A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477121 | ||||||
chr19:8477213
|
C | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(9): Show | 13 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1120+2969C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477213 | ||||||
chr19:8477295
|
G | A | 1 | a0001c0002t0001g0306 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1120+3051G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477295 | ||||||
chr19:8477456
|
A | G | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(263): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1120+3212A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477456 | ||||||
chr19:8477537
|
A | C | 4 | a0001c0002t0001g0292a0001c0002t0001g0293a0001c0002t0001g0329others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+3293A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477537 | ||||||
chr19:8477562
|
G | T | 2 | a0001c0009t0001g0025a0001c0009t0001g0026 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1120+3318G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477562 | ||||||
chr19:8477660
|
CAAAA | C | 7 | a0001c0002t0001g0292a0001c0002t0001g0293a0001c0002t0001g0316others(4): Show | 7 | HG01934.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1120+3446_1120+344 others(8): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477660 | |||||
chr19:8477660
|
CAAAAA | C | 10 | a0001c0002t0001g0310a0001c0002t0001g0311a0001c0002t0001g0313others(7): Show | 10 | HG02559.hp2 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1120+3445_1120+344 others(9): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477660 | |||||
chr19:8477660
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0006a0001c0002t0001g0315 | 3 | HG02135.hp2 HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1120+3438_1120+344 others(16): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477660 | |||||
chr19:8477660
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0009t0001g0025a0001c0009t0001g0026 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1120+3437_1120+344 others(17): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477660 | |||||
chr19:8477660
|
CAAAAAAA others(7): Show |
C | 18 | a0001c0001t0001g0019a0001c0001t0001g0129a0001c0001t0001g0153others(15): Show | 19 | HG00323.hp1 HG01109.hp2 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.1120+3436_1120+344 others(18): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477660 | |||||
chr19:8477660
|
CAAAAAAA others(8): Show |
C | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(194): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1120+3435_1120+344 others(19): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477660 | |||||
chr19:8477660
|
CAAAAAAA others(9): Show |
C | 71 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(68): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1120+3434_1120+344 others(20): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477660 | |||||
chr19:8477660
|
CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0001g0042a0001c0004t0001g0290 | 2 | HG02647.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1120+3433_1120+344 others(21): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477660 | |||||
chr19:8477673
|
AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0001g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1120+3434_1120+346 others(33): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8477673 | |||||
chr19:8477733
|
G | A | 8 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0170others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1120+3489G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477733 | ||||||
chr19:8477790
|
C | T | 6 | a0001c0001t0001g0078a0001c0001t0001g0170a0001c0001t0001g0172others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1120+3546C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477790 | ||||||
chr19:8477853
|
C | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1120+3609C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477853 | ||||||
chr19:8477949
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1120+3705A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8477949 | ||||||
chr19:8478077
|
C | T | 1 | a0001c0001t0001g0254 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1120+3833C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478077 | ||||||
chr19:8478155
|
G | T | 1 | a0001c0009t0001g0026 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1120+3911G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478155 | ||||||
chr19:8478609
|
A | G | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1120+4365A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478609 | ||||||
chr19:8478722
|
A | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1121-4436A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478722 | ||||||
chr19:8478776
|
G | C | 1 | a0004c0013t0001g0062 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1121-4382G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478776 | ||||||
chr19:8478789
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0084 | 2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1121-4369G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478789 | ||||||
chr19:8478829
|
C | T | 15 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(12): Show | 15 | HG01168.hp2 HG01934.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1121-4329C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478829 | ||||||
chr19:8478950
|
T | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1121-4208T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478950 | ||||||
chr19:8478955
|
C | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1121-4203C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478955 | ||||||
chr19:8478965
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0126 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1121-4193G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8478965 | ||||||
chr19:8479016
|
G | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121-4142G>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479016 | ||||||
chr19:8479022
|
A | AT | 5 | a0001c0004t0001g0290a0001c0004t0001g0291a0001c0004t0001g0294others(2): Show | 5 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121-4130dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479022 | |||||
chr19:8479037
|
G | A | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(172): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1121-4121G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479037 | ||||||
chr19:8479078
|
C | CT | 19 | a0001c0001t0001g0039a0001c0001t0001g0073a0001c0001t0001g0078others(16): Show | 19 | HG01169.hp2 HG02080.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1121-4056dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479078 | |||||
chr19:8479078
|
C | CTT | 56 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(53): Show | 64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1121-4057_1121-405 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479078 | |||||
chr19:8479078
|
C | CTTT | 29 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0031others(26): Show | 31 | HG00423.hp1 HG00423.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1121-4058_1121-405 others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479078 | |||||
chr19:8479078
|
C | CTTTT | 7 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0001t0001g0188others(4): Show | 7 | HG01175.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1121-4059_1121-405 others(8): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479078 | |||||
chr19:8479078
|
CT | C | 6 | a0001c0001t0001g0095a0001c0001t0001g0164a0001c0002t0001g0301others(3): Show | 6 | HG02135.hp1 HG03041.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121-4056delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479078 | |||||
chr19:8479078
|
CTTTTTT | C | 6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG02280.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121-4061_1121-405 others(10): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479078 | |||||
chr19:8479078
|
CTTTTTTT others(3): Show |
C | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1121-4065_1121-405 others(14): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479078 | |||||
chr19:8479096
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1121-4062T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479096 | ||||||
chr19:8479096
|
T | TTTC | 74 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(71): Show | 82 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.1121-4060_1121-405 others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479096 | |||||
chr19:8479102
|
T | C | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1121-4056T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479102 | ||||||
chr19:8479142
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1121-4016A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479142 | ||||||
chr19:8479168
|
C | T | 5 | a0001c0004t0001g0290a0001c0004t0001g0291a0001c0004t0001g0294others(2): Show | 5 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121-3990C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479168 | ||||||
chr19:8479178
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1121-3980C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479178 | ||||||
chr19:8479205
|
A | C | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(304): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1121-3953A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479205 | ||||||
chr19:8479521
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0084 | 2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1121-3637C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479521 | ||||||
chr19:8479646
|
G | A | 5 | a0001c0001t0001g0006a0001c0009t0001g0025a0001c0009t0001g0026others(2): Show | 6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121-3512G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479646 | ||||||
chr19:8479671
|
T | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(172): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1121-3487T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479671 | ||||||
chr19:8479686
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0084 | 2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1121-3472C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479686 | ||||||
chr19:8479719
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1121-3439T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479719 | ||||||
chr19:8479743
|
C | G | 2 | a0001c0009t0001g0025a0001c0009t0001g0026 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1121-3415C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479743 | ||||||
chr19:8479755
|
TA | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0070others(14): Show | 19 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1121-3386delA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479755 | |||||
chr19:8479770
|
AAAT | A | 9 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(6): Show | 9 | HG01975.hp1 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1121-3387_1121-338 others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479770 | ||||||
chr19:8479771
|
A | AT | 8 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0043others(5): Show | 8 | HG01169.hp2 HG01928.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1121-3387_1121-338 others(5): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479771 | ||||||
chr19:8479771
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1121-3387A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479771 | ||||||
chr19:8479771
|
AAT | A | 12 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0092others(9): Show | 12 | HG01981.hp1 HG02723.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.1121-3386_1121-338 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479771 | ||||||
chr19:8479771
|
AATT | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(178): Show | 199 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1121-3386_1121-338 others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479771 | ||||||
chr19:8479772
|
A | AAT | 17 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(14): Show | 17 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.1121-3386_1121-338 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479772 | ||||||
chr19:8479772
|
A | AT | 9 | a0001c0001t0001g0034a0001c0001t0001g0055a0001c0002t0001g0292others(6): Show | 9 | HG00741.hp2 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1121-3366dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479772 | |||||
chr19:8479772
|
A | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(49): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.1121-3386A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479772 | ||||||
chr19:8479772
|
ATT | A | 8 | a0001c0001t0001g0080a0001c0001t0001g0121a0001c0001t0001g0122others(5): Show | 8 | HG00438.hp2 HG01943.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1121-3367_1121-336 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8479772 | |||||
chr19:8479811
|
A | G | 123 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(120): Show | 133 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1121-3347A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479811 | ||||||
chr19:8479935
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(88): Show | 99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1121-3223C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8479935 | ||||||
chr19:8480132
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1121-3026C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480132 | ||||||
chr19:8480232
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1121-2926C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480232 | ||||||
chr19:8480343
|
C | CA | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(252): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1121-2798dupA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8480343 | |||||
chr19:8480343
|
C | CAA | 7 | a0001c0001t0001g0006a0001c0001t0001g0066a0001c0001t0001g0083others(4): Show | 8 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1121-2799_1121-279 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8480343 | |||||
chr19:8480344
|
A | C | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1121-2814A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480344 | ||||||
chr19:8480518
|
T | G | 2 | a0001c0001t0001g0254a0001c0003t0001g0258 | 2 | HG00673.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1121-2640T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480518 | ||||||
chr19:8480527
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0145 | 2 | HG02040.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1121-2631C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480527 | ||||||
chr19:8480576
|
T | C | 1 | a0005c0011t0001g0307 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1121-2582T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480576 | ||||||
chr19:8480627
|
C | T | 19 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(16): Show | 19 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.1121-2531C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480627 | ||||||
chr19:8480875
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1121-2283C>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480875 | ||||||
chr19:8480965
|
A | G | 5 | a0001c0001t0001g0006a0001c0009t0001g0025a0001c0009t0001g0026others(2): Show | 6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121-2193A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8480965 | ||||||
chr19:8481114
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1121-2044C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481114 | ||||||
chr19:8481133
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1121-2025T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481133 | ||||||
chr19:8481230
|
G | A | 1 | a0001c0003t0001g0158 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1121-1928G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481230 | ||||||
chr19:8481241
|
T | C | 19 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(16): Show | 19 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.1121-1917T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481241 | ||||||
chr19:8481254
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(71): Show | 81 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1121-1904C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481254 | ||||||
chr19:8481380
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1121-1778G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481380 | ||||||
chr19:8481390
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121-1768C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481390 | ||||||
chr19:8481397
|
C | T | 5 | a0001c0003t0001g0157a0001c0003t0001g0158a0001c0003t0001g0159others(2): Show | 5 | HG01081.hp1 HG01243.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1121-1761C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481397 | ||||||
chr19:8481400
|
C | T | 1 | a0001c0002t0001g0293 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1121-1758C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481400 | ||||||
chr19:8481410
|
A | G | 3 | a0001c0001t0001g0006a0001c0009t0001g0025a0001c0009t0001g0026 | 4 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1121-1748A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481410 | ||||||
chr19:8481423
|
G | C | 1 | a0001c0001t0001g0054 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1121-1735G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481423 | ||||||
chr19:8481500
|
GC | G | 103 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(100): Show | 113 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1121-1656delC | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8481500 | |||||
chr19:8481516
|
C | G | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1121-1642C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481516 | ||||||
chr19:8481587
|
G | A | 3 | a0001c0001t0001g0006a0001c0009t0001g0025a0001c0009t0001g0026 | 4 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1121-1571G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8481587 | ||||||
chr19:8481943
|
TTTG | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1121-1200_1121-119 others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8481943 | |||||
chr19:8481967
|
C | CT | 6 | a0001c0002t0001g0022a0001c0002t0001g0297a0001c0002t0001g0298others(3): Show | 7 | HG02109.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1121-1170dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8481967 | |||||
chr19:8481967
|
CT | C | 70 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(67): Show | 78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.1121-1170delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8481967 | |||||
chr19:8481967
|
CTT | C | 139 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(136): Show | 150 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1121-1171_1121-117 others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8481967 | |||||
chr19:8481967
|
CTTT | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(86): Show | 97 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1121-1172_1121-117 others(7): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8481967 | |||||
chr19:8482036
|
G | A | 102 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(99): Show | 112 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1121-1122G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482036 | ||||||
chr19:8482041
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1121-1117C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482041 | ||||||
chr19:8482068
|
G | C | 1 | a0001c0003t0001g0140 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1121-1090G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482068 | ||||||
chr19:8482129
|
T | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0132a0001c0001t0001g0259others(1): Show | 6 | NA18961.hp2 NA18963.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121-1029T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482129 | ||||||
chr19:8482138
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1121-1020A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482138 | ||||||
chr19:8482165
|
A | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1121-993A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482165 | ||||||
chr19:8482217
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1121-941A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482217 | ||||||
chr19:8482255
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1121-903G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482255 | ||||||
chr19:8482296
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1121-862C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482296 | ||||||
chr19:8482309
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1121-849G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482309 | ||||||
chr19:8482353
|
C | T | 1 | a0001c0001t0001g0254 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1121-805C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482353 | ||||||
chr19:8482377
|
A | G | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1121-781A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482377 | ||||||
chr19:8482573
|
A | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1121-585A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482573 | ||||||
chr19:8482689
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1121-469T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482689 | ||||||
chr19:8482906
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0094others(9): Show | 15 | HG02071.hp1 HG02135.hp1 NA18747.hp1 others(12): Show |
intron_variant | MODIFIER | c.1121-252G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8482906 | ||||||
chr19:8483036
|
AC | A | 5 | a0001c0004t0001g0290a0001c0004t0001g0291a0001c0004t0001g0294others(2): Show | 5 | HG02486.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121-118delC | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr19 | 8483036 | |||||
chr19:8483135
|
T | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1121-23T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 12/15 | chr19 | 8483135 | ||||||
chr19:8483238
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1174+27G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483238 | ||||||
chr19:8483251
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1174+40A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483251 | ||||||
chr19:8483291
|
A | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(162): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1174+80A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483291 | ||||||
chr19:8483295
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1174+84C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483295 | ||||||
chr19:8483565
|
A | G | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1174+354A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483565 | ||||||
chr19:8483613
|
A | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1174+402A>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483613 | ||||||
chr19:8483618
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1174+407T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483618 | ||||||
chr19:8483657
|
A | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0072 | 2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1174+446A>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483657 | ||||||
chr19:8483705
|
G | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(88): Show | 99 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1174+494G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483705 | ||||||
chr19:8483845
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1174+634G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483845 | ||||||
chr19:8483854
|
T | C | 54 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(51): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.1174+643T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483854 | ||||||
chr19:8483870
|
A | G | 1 | a0001c0015t0001g0319 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1174+659A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483870 | ||||||
chr19:8483991
|
C | T | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1174+780C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8483991 | ||||||
chr19:8484011
|
G | A | 1 | a0001c0005t0001g0268 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1174+800G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484011 | ||||||
chr19:8484173
|
C | CT | 12 | a0001c0001t0001g0107a0001c0001t0001g0128a0001c0001t0001g0151others(9): Show | 12 | HG02080.hp1 HG02109.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1174+981dupT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr19 | 8484173 | |||||
chr19:8484173
|
CT | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(168): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1174+981delT | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr19 | 8484173 | |||||
chr19:8484173
|
CTT | C | 8 | a0001c0001t0001g0039a0001c0001t0001g0199a0001c0001t0001g0221others(5): Show | 8 | HG01169.hp2 HG02071.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1174+980_1174+981d others(4): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr19 | 8484173 | |||||
chr19:8484173
|
CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0001g0006a0001c0009t0001g0025a0001c0009t0001g0026others(2): Show | 6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174+972_1174+981d others(12): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr19 | 8484173 | |||||
chr19:8484177
|
T | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(8): Show | 12 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174+966T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484177 | ||||||
chr19:8484193
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1174+982G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484193 | ||||||
chr19:8484200
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1174+989G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484200 | ||||||
chr19:8484240
|
G | A | 6 | a0001c0001t0001g0076a0001c0001t0001g0143a0001c0001t0001g0146others(3): Show | 6 | HG02080.hp1 NA18971.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174+1029G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484240 | ||||||
chr19:8484326
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1174+1115G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484326 | ||||||
chr19:8484333
|
T | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1174+1122T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484333 | ||||||
chr19:8484377
|
A | G | 1 | a0001c0012t0001g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1174+1166A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484377 | ||||||
chr19:8484396
|
C | T | 7 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0276others(4): Show | 8 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+1185C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484396 | ||||||
chr19:8484441
|
G | A | 1 | a0001c0014t0001g0024 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1175-1162G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484441 | ||||||
chr19:8484533
|
T | C | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1175-1070T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484533 | ||||||
chr19:8484576
|
T | A | 16 | a0001c0002t0001g0312a0001c0002t0001g0313a0001c0002t0001g0314others(13): Show | 16 | HG01168.hp2 HG01934.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.1175-1027T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484576 | ||||||
chr19:8484635
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1175-968G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484635 | ||||||
chr19:8484684
|
T | A | 1 | a0001c0001t0001g0055 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1175-919T>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484684 | ||||||
chr19:8484762
|
C | T | 9 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0088others(6): Show | 9 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1175-841C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484762 | ||||||
chr19:8484774
|
G | A | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1175-829G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8484774 | ||||||
chr19:8485003
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1175-600G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485003 | ||||||
chr19:8485065
|
G | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0085a0001c0009t0001g0025others(3): Show | 7 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1175-538G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485065 | ||||||
chr19:8485172
|
C | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0276a0001c0001t0001g0277others(7): Show | 11 | HG00323.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1175-431C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485172 | ||||||
chr19:8485201
|
T | C | 1 | a0001c0001t0001g0013 | 2 | HG00099.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1175-402T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485201 | ||||||
chr19:8485223
|
G | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1175-380G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485223 | ||||||
chr19:8485224
|
G | C | 1 | a0001c0001t0001g0232 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1175-379G>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485224 | ||||||
chr19:8485386
|
A | G | 2 | a0001c0001t0001g0206a0001c0001t0001g0209 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1175-217A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485386 | ||||||
chr19:8485417
|
C | T | 1 | a0001c0002t0001g0326 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1175-186C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485417 | ||||||
chr19:8485489
|
T | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1175-114T>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 13/15 | chr19 | 8485489 | ||||||
chr19:8486468
|
T | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1977+63T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486468 | ||||||
chr19:8486625
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1977+220C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486625 | ||||||
chr19:8486626
|
G | A | 1 | a0001c0004t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1977+221G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486626 | ||||||
chr19:8486649
|
CTGAT | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(279): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1977+247_1977+250d others(6): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr19 | 8486649 | |||||
chr19:8486726
|
C | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1978-298C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486726 | ||||||
chr19:8486755
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1978-269T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486755 | ||||||
chr19:8486802
|
C | T | 1 | a0001c0004t0001g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1978-222C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486802 | ||||||
chr19:8486824
|
C | G | 1 | a0001c0001t0001g0051 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1978-200C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486824 | ||||||
chr19:8486846
|
C | T | 1 | a0001c0004t0001g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1978-178C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486846 | ||||||
chr19:8486968
|
A | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.1978-56A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 14/15 | chr19 | 8486968 | ||||||
chr19:8487119
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2029+44T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487119 | ||||||
chr19:8487132
|
C | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2029+57C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487132 | ||||||
chr19:8487152
|
C | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2029+77C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487152 | ||||||
chr19:8487283
|
C | T | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.2029+208C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487283 | ||||||
chr19:8487327
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0262 | 2 | NA18961.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.2029+252C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487327 | ||||||
chr19:8487329
|
C | G | 5 | a0001c0001t0001g0006a0001c0009t0001g0025a0001c0009t0001g0026others(2): Show | 6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2029+254C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487329 | ||||||
chr19:8487389
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(89): Show | 100 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2029+314A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487389 | ||||||
chr19:8487418
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2029+343C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487418 | ||||||
chr19:8487569
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2029+494C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487569 | ||||||
chr19:8487704
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2029+629C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487704 | ||||||
chr19:8487755
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2029+680T>C | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487755 | ||||||
chr19:8487887
|
C | G | 25 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0086others(22): Show | 27 | HG00423.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.2030-804C>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487887 | ||||||
chr19:8487916
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0149 | 2 | HG02523.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.2030-775C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487916 | ||||||
chr19:8487981
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2030-710A>G | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487981 | ||||||
chr19:8487995
|
C | T | 5 | a0001c0001t0001g0006a0001c0009t0001g0025a0001c0009t0001g0026others(2): Show | 6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2030-696C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8487995 | ||||||
chr19:8488039
|
G | A | 1 | a0001c0012t0001g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2030-652G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8488039 | ||||||
chr19:8488058
|
CA | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.2030-631delA | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr19 | 8488058 | |||||
chr19:8488071
|
GTCT | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02723.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2030-615_2030-613d others(5): Show |
HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr19 | 8488071 | |||||
chr19:8488245
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2030-446C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8488245 | ||||||
chr19:8488438
|
C | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(279): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2030-253C>T | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8488438 | ||||||
chr19:8488516
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(87): Show | 98 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2030-175G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8488516 | ||||||
chr19:8488557
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2030-134G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8488557 | ||||||
chr19:8488573
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0054others(2): Show | 6 | HG00733.hp1 HG00741.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.2030-118G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8488573 | ||||||
chr19:8488586
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0274 | 3 | HG01891.hp2 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2030-105G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8488586 | ||||||
chr19:8488610
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2030-81G>A | HNRNPM | ENSG00000099783.13 | transcript | ENST00000325495.9 | protein_coding | 15/15 | chr19 | 8488610 |