geneid | 58517 |
---|---|
ensemblid | ENSG00000119707.14 |
hgncid | 23244 |
symbol | RBM25 |
name | RNA binding motif protein 25 |
refseq_nuc | NM_021239.3 |
refseq_prot | NP_067062.1 |
ensembl_nuc | ENST00000261973.12 |
ensembl_prot | ENSP00000261973.7 |
mane_status | MANE Select |
chr | chr14 |
start | 73058534 |
end | 73123899 |
strand | + |
ver | v1.2 |
region | chr14:73058534-73123899 |
region5000 | chr14:73053534-73128899 |
regionname0 | RBM25_chr14_73058534_73123899 |
regionname5000 | RBM25_chr14_73053534_73128899 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 843 | 388 | 90 | 76 | 172 | 10 | 38 | 128 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2532 | 343 | 86 | 66 | 143 | 10 | 36 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
c0002 | 0/0 | 2532 | 43 | 3 | 9 | 29 | 0 | 2 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
c0003 | 0/0 | 2532 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
c0004 | 0/0 | 2532 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4282 | 151 | 29 | 18 | 90 | 2 | 12 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0002 | 0/1 | 4282 | 59 | 5 | 19 | 24 | 4 | 6 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0003 | 0/0 | 4282 | 34 | 2 | 6 | 26 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0004 | 0/0 | 4282 | 28 | 2 | 13 | 5 | 1 | 7 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0005 | 0/0 | 4283 | 18 | 11 | 5 | 1 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0006 | 0/0 | 4281 | 16 | 2 | 1 | 10 | 0 | 3 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0007 | 0/0 | 4282 | 10 | 9 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0008 | 0/0 | 4283 | 8 | 0 | 2 | 2 | 2 | 2 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0009 | 0/0 | 4282 | 6 | 1 | 3 | 0 | 0 | 2 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0010 | 0/0 | 4282 | 6 | 6 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0011 | 0/0 | 4281 | 5 | 5 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0012 | 0/0 | 4282 | 5 | 0 | 3 | 0 | 0 | 2 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0013 | 0/0 | 4282 | 5 | 4 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0014 | 0/0 | 4282 | 3 | 0 | 0 | 3 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0015 | 0/0 | 4282 | 3 | 3 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0016 | 0/0 | 4283 | 3 | 0 | 0 | 3 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0017 | 0/0 | 4282 | 2 | 0 | 0 | 2 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0018 | 0/0 | 4282 | 2 | 2 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0019 | 0/0 | 4283 | 2 | 2 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0020 | 0/0 | 4282 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0021 | 0/0 | 4282 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0022 | 0/0 | 4282 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0023 | 0/0 | 4282 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0024 | 0/0 | 4282 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0025 | 0/0 | 4281 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0026 | 0/0 | 4282 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0027 | 0/0 | 4283 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0028 | 0/0 | 4281 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0029 | 0/0 | 4282 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0030 | 1/0 | 4282 | 1 | 0 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0031 | 0/0 | 4282 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0032 | 0/0 | 4282 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0033 | 0/0 | 4283 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0034 | 0/0 | 4283 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0035 | 0/0 | 4283 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0036 | 0/0 | 4282 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0037 | 0/0 | 4283 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0038 | 0/0 | 4283 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0039 | 0/0 | 4282 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0040 | 0/0 | 4282 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
t0041 | 0/0 | 4282 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0002 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0004 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0232 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0379 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2532 | 343 | 86 | 66 | 143 | 10 | 36 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0002 | 0/0 | 2532 | 43 | 3 | 9 | 29 | 0 | 2 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0003 | 0/0 | 2532 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0004 | 0/0 | 2532 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6813 | 150 | 29 | 17 | 90 | 2 | 12 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0002 | 0/1 | 6813 | 59 | 5 | 19 | 24 | 4 | 6 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0004 | 0/0 | 6813 | 28 | 2 | 13 | 5 | 1 | 7 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0005 | 0/0 | 6814 | 18 | 11 | 5 | 1 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0006 | 0/0 | 6812 | 16 | 2 | 1 | 10 | 0 | 3 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0007 | 0/0 | 6813 | 10 | 9 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0008 | 0/0 | 6814 | 8 | 0 | 2 | 2 | 2 | 2 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0010 | 0/0 | 6813 | 6 | 6 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0011 | 0/0 | 6812 | 5 | 5 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0012 | 0/0 | 6813 | 5 | 0 | 3 | 0 | 0 | 2 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0013 | 0/0 | 6813 | 5 | 4 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0014 | 0/0 | 6813 | 3 | 0 | 0 | 3 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0015 | 0/0 | 6813 | 2 | 2 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0016 | 0/0 | 6814 | 3 | 0 | 0 | 3 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0018 | 0/0 | 6813 | 2 | 2 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0019 | 0/0 | 6814 | 2 | 2 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0020 | 0/0 | 6813 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0021 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0022 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0023 | 0/0 | 6813 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0024 | 0/0 | 6813 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0025 | 0/0 | 6812 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0026 | 0/0 | 6813 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0027 | 0/0 | 6814 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0028 | 0/0 | 6812 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0029 | 0/0 | 6813 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0030 | 1/0 | 6813 | 1 | 0 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0031 | 0/0 | 6813 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0032 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0034 | 0/0 | 6814 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0035 | 0/0 | 6814 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0036 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0037 | 0/0 | 6814 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0038 | 0/0 | 6814 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0039 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0040 | 0/0 | 6813 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0001t0041 | 0/0 | 6813 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0002t0003 | 0/0 | 6813 | 34 | 2 | 6 | 26 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0002t0009 | 0/0 | 6813 | 6 | 1 | 3 | 0 | 0 | 2 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0002t0017 | 0/0 | 6813 | 2 | 0 | 0 | 2 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0002t0033 | 0/0 | 6814 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0003t0001 | 0/0 | 6813 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
a0001c0004t0015 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | copy fasta | chr14 | 73053534 | 73128899 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0004 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0379 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0002g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0002 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0004g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0005g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0006g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0006g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0006g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0007g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0007g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0007g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0007g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0008g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0008g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0008g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0008g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0008g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0008g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0008g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0008g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0010g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0010g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0010g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0010g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0010g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0011g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0012g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0012g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0012g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0012g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0012g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0013g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0013g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0013g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0013g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0013g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0014g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0014g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0014g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0015g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0015g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0016g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0016g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0016g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0018g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0018g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0019g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0019g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0020g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0021g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0022g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0023g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0024g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0025g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0026g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0027g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0028g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0029g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0030g0232 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0031g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0032g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0034g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0035g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0036g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0037g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0038g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0039g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0040g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0001t0041g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0003g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0009g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0009g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0009g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0009g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0009g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0009g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0017g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0017g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0002t0033g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0003t0001g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
a0001c0004t0015g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0111 | EUR | GBR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0292 | EUR | GBR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00140 | hp1 | a0001 | c0001 | t0024 | g0334 | EUR | GBR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | GBR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00323 | hp1 | a0001 | c0001 | t0008 | g0012 | EUR | FIN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0087 | EUR | FIN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00408 | hp2 | a0001 | c0001 | t0006 | g0041 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00423 | hp1 | a0001 | c0002 | t0003 | g0256 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0306 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00544 | hp2 | a0001 | c0001 | t0006 | g0039 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00558 | hp2 | a0001 | c0001 | t0016 | g0088 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0315 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0375 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00735 | hp1 | a0001 | c0002 | t0009 | g0250 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00738 | hp2 | a0001 | c0002 | t0009 | g0280 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0297 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01069 | hp2 | a0001 | c0002 | t0003 | g0276 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0318 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0357 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01071 | hp1 | a0001 | c0002 | t0003 | g0273 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0316 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01074 | hp1 | a0001 | c0002 | t0003 | g0258 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01074 | hp2 | a0001 | c0001 | t0023 | g0045 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0300 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0037 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01099 | hp2 | a0001 | c0002 | t0003 | g0259 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0380 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01167 | hp2 | a0001 | c0001 | t0012 | g0015 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01168 | hp2 | a0001 | c0001 | t0008 | g0010 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01169 | hp2 | a0001 | c0001 | t0012 | g0013 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01175 | hp2 | a0001 | c0001 | t0040 | g0134 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01243 | hp1 | a0001 | c0001 | t0007 | g0290 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01256 | hp2 | a0001 | c0001 | t0005 | g0201 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01257 | hp1 | a0001 | c0001 | t0012 | g0014 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01261 | hp1 | a0001 | c0002 | t0003 | g0277 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01261 | hp2 | a0001 | c0001 | t0008 | g0009 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0376 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01358 | hp2 | a0001 | c0002 | t0009 | g0283 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0317 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0353 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01496 | hp2 | a0001 | c0001 | t0013 | g0056 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | IBS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0379 | EUR | IBS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01884 | hp2 | a0001 | c0001 | t0013 | g0058 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01891 | hp2 | a0001 | c0001 | t0010 | g0240 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01928 | hp1 | a0001 | c0001 | t0005 | g0202 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0308 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0200 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0303 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0314 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01975 | hp1 | a0001 | c0001 | t0025 | g0034 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0377 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0203 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0302 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02027 | hp1 | a0001 | c0002 | t0003 | g0260 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0304 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02055 | hp1 | a0001 | c0002 | t0009 | g0281 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02055 | hp2 | a0001 | c0001 | t0007 | g0244 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02056 | hp2 | a0001 | c0001 | t0006 | g0027 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02074 | hp1 | a0001 | c0001 | t0028 | g0351 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0305 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02135 | hp1 | a0001 | c0001 | t0016 | g0091 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02135 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02145 | hp1 | a0001 | c0001 | t0010 | g0238 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0036 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02148 | hp1 | a0001 | c0002 | t0003 | g0249 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02148 | hp2 | a0001 | c0001 | t0041 | g0086 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0367 | EAS | CDX | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02165 | hp1 | a0001 | c0002 | t0003 | g0272 | EAS | CDX | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | CDX | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0294 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02257 | hp2 | a0001 | c0001 | t0036 | g0231 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0213 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02293 | hp2 | a0001 | c0001 | t0004 | g0319 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0127 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0288 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02523 | hp2 | a0001 | c0002 | t0003 | g0261 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0228 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0347 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02615 | hp1 | a0001 | c0001 | t0027 | g0219 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02615 | hp2 | a0001 | c0001 | t0007 | g0287 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02622 | hp1 | a0001 | c0002 | t0003 | g0274 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02622 | hp2 | a0001 | c0001 | t0018 | g0369 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02630 | hp2 | a0001 | c0001 | t0007 | g0285 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02683 | hp1 | a0001 | c0001 | t0034 | g0063 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0352 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02698 | hp2 | a0001 | c0001 | t0031 | g0062 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02717 | hp1 | a0001 | c0001 | t0021 | g0286 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0289 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02723 | hp2 | a0001 | c0001 | t0019 | g0312 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02735 | hp1 | a0001 | c0001 | t0008 | g0011 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02735 | hp2 | a0001 | c0001 | t0012 | g0016 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02738 | hp1 | a0001 | c0001 | t0006 | g0040 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02809 | hp1 | a0001 | c0001 | t0011 | g0048 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02818 | hp1 | a0001 | c0001 | t0038 | g0220 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02818 | hp2 | a0001 | c0001 | t0039 | g0018 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0212 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0215 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02922 | hp1 | a0001 | c0001 | t0015 | g0021 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0245 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02976 | hp2 | a0001 | c0001 | t0018 | g0368 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03017 | hp2 | a0001 | c0002 | t0009 | g0284 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0246 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0361 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0373 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0216 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0362 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0221 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03209 | hp1 | a0001 | c0001 | t0010 | g0003 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03209 | hp2 | a0001 | c0001 | t0013 | g0053 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03225 | hp1 | a0001 | c0001 | t0010 | g0003 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03225 | hp2 | a0001 | c0002 | t0003 | g0248 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03453 | hp1 | a0001 | c0004 | t0015 | g0019 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03453 | hp2 | a0001 | c0001 | t0019 | g0313 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03486 | hp1 | a0001 | c0001 | t0010 | g0239 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0356 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03492 | hp1 | a0001 | c0001 | t0005 | g0340 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03540 | hp1 | a0001 | c0001 | t0015 | g0020 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03579 | hp1 | a0001 | c0001 | t0010 | g0241 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0307 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0309 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0358 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03704 | hp1 | a0001 | c0001 | t0006 | g0030 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0293 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0310 | SAS | BEB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03831 | hp2 | a0001 | c0001 | t0008 | g0007 | SAS | BEB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03942 | hp1 | a0001 | c0001 | t0006 | g0029 | SAS | BEB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0298 | SAS | BEB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG04115 | hp1 | a0001 | c0001 | t0035 | g0311 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0331 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG04184 | hp2 | a0001 | c0001 | t0012 | g0017 | SAS | BEB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0378 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0299 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0296 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG04228 | hp1 | a0001 | c0002 | t0009 | g0264 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0381 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0320 | AFR | YRI | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18522 | hp2 | a0001 | c0001 | t0013 | g0057 | AFR | YRI | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18612 | hp2 | a0001 | c0002 | t0003 | g0270 | EAS | CHB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | CHB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18747 | hp2 | a0001 | c0001 | t0006 | g0033 | EAS | CHB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0229 | AFR | YRI | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18906 | hp2 | a0001 | c0001 | t0011 | g0049 | AFR | YRI | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18941 | hp1 | a0001 | c0001 | t0020 | g0370 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18941 | hp2 | a0001 | c0002 | t0017 | g0251 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18942 | hp2 | a0001 | c0002 | t0003 | g0263 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18944 | hp1 | a0001 | c0001 | t0014 | g0188 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18944 | hp2 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18947 | hp1 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18947 | hp2 | a0001 | c0002 | t0003 | g0247 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18948 | hp1 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18950 | hp2 | a0001 | c0002 | t0017 | g0257 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18952 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18953 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18959 | hp1 | a0001 | c0002 | t0003 | g0265 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18960 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18964 | hp1 | a0001 | c0002 | t0003 | g0266 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18965 | hp1 | a0001 | c0001 | t0006 | g0031 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18975 | hp2 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18980 | hp1 | a0001 | c0002 | t0003 | g0268 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18984 | hp1 | a0001 | c0002 | t0003 | g0255 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18985 | hp2 | a0001 | c0002 | t0003 | g0262 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18986 | hp2 | a0001 | c0002 | t0003 | g0267 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18991 | hp1 | a0001 | c0001 | t0037 | g0198 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18992 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18993 | hp1 | a0001 | c0001 | t0014 | g0122 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18994 | hp1 | a0001 | c0002 | t0033 | g0254 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18997 | hp2 | a0001 | c0001 | t0026 | g0042 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18998 | hp1 | a0001 | c0002 | t0003 | g0278 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18999 | hp2 | a0001 | c0001 | t0029 | g0354 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19003 | hp2 | a0001 | c0001 | t0016 | g0067 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19009 | hp1 | a0001 | c0001 | t0014 | g0196 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19030 | hp1 | a0001 | c0001 | t0011 | g0050 | AFR | LWK | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19030 | hp2 | a0001 | c0001 | t0022 | g0043 | AFR | LWK | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19056 | hp1 | a0001 | c0002 | t0003 | g0252 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19063 | hp1 | a0001 | c0002 | t0003 | g0271 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19063 | hp2 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19064 | hp2 | a0001 | c0002 | t0003 | g0253 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19065 | hp1 | a0001 | c0001 | t0008 | g0008 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0374 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19067 | hp2 | a0001 | c0002 | t0003 | g0282 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19070 | hp1 | a0001 | c0002 | t0003 | g0269 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0301 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19084 | hp2 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19085 | hp2 | a0001 | c0002 | t0003 | g0275 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19091 | hp1 | a0001 | c0002 | t0003 | g0371 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0372 | AFR | YRI | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0242 | AFR | YRI | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | ASW | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ASW | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0073 | EUR | TSI | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA20805 | hp2 | a0001 | c0001 | t0008 | g0005 | EUR | TSI | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0214 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02486 | hp1 | a0001 | c0001 | t0011 | g0046 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02486 | hp2 | a0001 | c0001 | t0007 | g0291 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0204 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0230 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG03471 | hp2 | a0001 | c0001 | t0011 | g0047 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | USA | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | USA | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18955 | hp1 | a0001 | c0002 | t0003 | g0279 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | USA | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA20300 | hp2 | a0001 | c0001 | t0013 | g0024 | AFR | USA | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
NA21309 | hp2 | a0001 | c0001 | t0032 | g0025 | AFR | LWK | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0004 | REF | REF | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0030 | g0232 | REF | REF | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73077497
|
C | T | 1 | a0001c0004 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.285C>T | p.Ser95Ser | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/19 | 472/6813 | 285/2532 | 95/843 | chr14 | 73077497 | ||
chr14:73088047
|
A | G | 1 | a0001c0003 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.429A>G | p.Ala143Ala | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/19 | 616/6813 | 429/2532 | 143/843 | chr14 | 73088047 | ||
chr14:73114303
|
A | G | 1 | a0001c0002 | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
synonymous_variant | LOW | c.2409A>G | p.Ser803Ser | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/19 | 2596/6813 | 2409/2532 | 803/843 | chr14 | 73114303 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73058557
|
A | T | 5 | a0001c0001t0002a0001c0001t0010a0001c0001t0013others(2): Show | 74 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(71): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-164A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/19 | chr14 | 73058557 | ||||||
chr14:73058578
|
T | C | 1 | a0001c0001t0020 | 1 | NA18941.hp1 | 5_prime_UTR_variant | MODIFIER | c.-143T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/19 | 13064 | chr14 | 73058578 | |||||
chr14:73119824
|
T | C | 2 | a0001c0001t0007a0001c0001t0021 | 11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*19T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 19 | chr14 | 73119824 | |||||
chr14:73120371
|
AT | A | 1 | a0001c0001t0011 | 5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*569delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 569 | INFO_REALIGN_3_PRIME | chr14 | 73120371 | ||||
chr14:73120405
|
A | G | 1 | a0001c0001t0019 | 2 | HG02723.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*600A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 600 | chr14 | 73120405 | |||||
chr14:73120620
|
C | T | 1 | a0001c0001t0019 | 2 | HG02723.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*815C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 815 | chr14 | 73120620 | |||||
chr14:73120708
|
T | C | 3 | a0001c0001t0011a0001c0001t0022a0001c0001t0023 | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*903T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 903 | chr14 | 73120708 | |||||
chr14:73120968
|
C | T | 1 | a0001c0001t0010 | 6 | HG01891.hp2 HG02145.hp1 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1163C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1163 | chr14 | 73120968 | |||||
chr14:73121210
|
T | A | 1 | a0001c0001t0022 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1405T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1405 | chr14 | 73121210 | |||||
chr14:73121447
|
A | G | 1 | a0001c0001t0040 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1642A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1642 | chr14 | 73121447 | |||||
chr14:73121498
|
A | G | 1 | a0001c0001t0041 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1693A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1693 | chr14 | 73121498 | |||||
chr14:73121520
|
A | G | 1 | a0001c0001t0039 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1715A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1715 | chr14 | 73121520 | |||||
chr14:73121596
|
G | C | 1 | a0001c0001t0024 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1791G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1791 | chr14 | 73121596 | |||||
chr14:73121623
|
C | G | 1 | a0001c0001t0022 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1818C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1818 | chr14 | 73121623 | |||||
chr14:73121627
|
G | C | 3 | a0001c0001t0011a0001c0001t0022a0001c0001t0023 | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1822G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1822 | chr14 | 73121627 | |||||
chr14:73121635
|
T | C | 1 | a0001c0001t0008 | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1830T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1830 | chr14 | 73121635 | |||||
chr14:73121660
|
G | T | 1 | a0001c0001t0038 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1855G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1855 | chr14 | 73121660 | |||||
chr14:73121663
|
C | T | 2 | a0001c0001t0011a0001c0001t0023 | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1858C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1858 | chr14 | 73121663 | |||||
chr14:73121683
|
G | A | 7 | a0001c0001t0006a0001c0001t0008a0001c0001t0011others(4): Show | 33 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1878G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1878 | chr14 | 73121683 | |||||
chr14:73121696
|
T | G | 1 | a0001c0001t0008 | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1891T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1891 | chr14 | 73121696 | |||||
chr14:73121830
|
T | C | 1 | a0001c0001t0027 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2025T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2025 | chr14 | 73121830 | |||||
chr14:73121939
|
A | G | 3 | a0001c0001t0015a0001c0001t0039a0001c0004t0015 | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2134A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2134 | chr14 | 73121939 | |||||
chr14:73122202
|
A | G | 2 | a0001c0001t0014a0001c0001t0037 | 4 | NA18944.hp1 NA18991.hp1 NA18993.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2397A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2397 | chr14 | 73122202 | |||||
chr14:73122265
|
G | A | 1 | a0001c0001t0008 | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2460G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2460 | chr14 | 73122265 | |||||
chr14:73122276
|
G | T | 1 | a0001c0001t0036 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2471G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2471 | chr14 | 73122276 | |||||
chr14:73122279
|
G | GT | 10 | a0001c0001t0005a0001c0001t0008a0001c0001t0016others(7): Show | 37 | HG00323.hp1 HG00558.hp2 HG01168.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2487dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2488 | INFO_REALIGN_3_PRIME | chr14 | 73122279 | ||||
chr14:73122279
|
GT | G | 3 | a0001c0001t0006a0001c0001t0025a0001c0001t0028 | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2487delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2487 | INFO_REALIGN_3_PRIME | chr14 | 73122279 | ||||
chr14:73122293
|
G | C | 2 | a0001c0001t0011a0001c0001t0023 | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2488G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2488 | chr14 | 73122293 | |||||
chr14:73122315
|
G | A | 1 | a0001c0001t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2510G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2510 | chr14 | 73122315 | |||||
chr14:73122317
|
C | T | 1 | a0001c0001t0021 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2512C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2512 | chr14 | 73122317 | |||||
chr14:73122480
|
T | C | 8 | a0001c0001t0006a0001c0001t0008a0001c0001t0011others(5): Show | 38 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2675T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2675 | chr14 | 73122480 | |||||
chr14:73122556
|
G | A | 1 | a0001c0001t0025 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2751G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2751 | chr14 | 73122556 | |||||
chr14:73122581
|
G | A | 1 | a0001c0001t0029 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2776G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2776 | chr14 | 73122581 | |||||
chr14:73122589
|
C | G | 1 | a0001c0001t0032 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2784C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2784 | chr14 | 73122589 | |||||
chr14:73122789
|
C | T | 2 | a0001c0001t0004a0001c0001t0035 | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2984C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2984 | chr14 | 73122789 | |||||
chr14:73122910
|
A | G | 3 | a0001c0001t0031a0001c0001t0034a0001c0002t0009 | 8 | HG00735.hp1 HG00738.hp2 HG01358.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3105A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3105 | chr14 | 73122910 | |||||
chr14:73122976
|
C | T | 1 | a0001c0001t0010 | 6 | HG01891.hp2 HG02145.hp1 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3171C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3171 | chr14 | 73122976 | |||||
chr14:73122981
|
C | A | 2 | a0001c0001t0011a0001c0001t0023 | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3176C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3176 | chr14 | 73122981 | |||||
chr14:73123076
|
A | G | 1 | a0001c0001t0018 | 2 | HG02622.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3271A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3271 | chr14 | 73123076 | |||||
chr14:73123188
|
C | G | 19 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(16): Show | 122 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*3383C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3383 | chr14 | 73123188 | |||||
chr14:73123258
|
A | G | 1 | a0001c0001t0012 | 5 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3453A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3453 | chr14 | 73123258 | |||||
chr14:73123370
|
T | C | 2 | a0001c0001t0004a0001c0001t0035 | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3565T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3565 | chr14 | 73123370 | |||||
chr14:73123502
|
G | A | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(39): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
3_prime_UTR_variant | MODIFIER | c.*3697G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3697 | chr14 | 73123502 | |||||
chr14:73123604
|
C | A | 1 | a0001c0002t0017 | 2 | NA18941.hp2 NA18950.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3799C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3799 | chr14 | 73123604 | |||||
chr14:73123838
|
G | A | 2 | a0001c0001t0011a0001c0001t0023 | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4033G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 4033 | chr14 | 73123838 | |||||
chr14:73123840
|
T | C | 3 | a0001c0001t0006a0001c0001t0025a0001c0001t0026 | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4035T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 4035 | chr14 | 73123840 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73058764
|
G | A | 13 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007others(10): Show | 13 | HG00323.hp1 HG01167.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-16+59G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73058764 | ||||||
chr14:73058767
|
G | A | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+62G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73058767 | ||||||
chr14:73058842
|
G | A | 1 | a0001c0001t0002g0022 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-16+137G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73058842 | ||||||
chr14:73058843
|
A | G | 1 | a0001c0001t0002g0022 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-16+138A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73058843 | ||||||
chr14:73058858
|
G | A | 1 | a0001c0001t0008g0005 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-16+153G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73058858 | ||||||
chr14:73058966
|
T | A | 1 | a0001c0001t0002g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-16+261T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73058966 | ||||||
chr14:73058968
|
C | T | 3 | a0001c0001t0002g0379a0001c0001t0002g0380a0001c0001t0002g0381 | 3 | HG01106.hp1 HG01516.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-16+263C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73058968 | ||||||
chr14:73059002
|
G | C | 1 | a0001c0001t0002g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-16+297G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059002 | ||||||
chr14:73059251
|
C | T | 1 | a0001c0001t0001g0378 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-16+546C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059251 | ||||||
chr14:73059378
|
C | G | 1 | a0001c0003t0001g0377 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-16+673C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059378 | ||||||
chr14:73059416
|
C | A | 1 | a0001c0001t0013g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-16+711C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059416 | ||||||
chr14:73059440
|
C | A | 34 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(31): Show | 34 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.-16+735C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059440 | ||||||
chr14:73059452
|
A | G | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+747A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059452 | ||||||
chr14:73059496
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-16+791G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059496 | ||||||
chr14:73059599
|
C | T | 2 | a0001c0001t0001g0375a0001c0001t0001g0376 | 2 | HG00639.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-16+894C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059599 | ||||||
chr14:73059771
|
A | G | 1 | a0001c0001t0001g0374 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-16+1066A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059771 | ||||||
chr14:73059824
|
T | C | 9 | a0001c0001t0002g0052a0001c0001t0002g0054a0001c0001t0002g0055others(6): Show | 9 | HG01496.hp2 HG01884.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16+1119T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059824 | ||||||
chr14:73059881
|
T | C | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+1176T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059881 | ||||||
chr14:73059905
|
G | A | 58 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0060others(55): Show | 58 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-16+1200G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059905 | ||||||
chr14:73060084
|
G | C | 20 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(17): Show | 20 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+1379G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73060084 | ||||||
chr14:73060133
|
GGTTCAAG others(5084): Show |
G | 2 | a0001c0001t0008g0011a0001c0001t0008g0012 | 2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-16+1436_-15-6396d others(2): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73060133 | |||||
chr14:73060205
|
A | G | 2 | a0001c0001t0001g0372a0001c0001t0001g0373 | 2 | HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-16+1500A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73060205 | ||||||
chr14:73060259
|
G | A | 1 | a0001c0001t0001g0374 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-16+1554G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73060259 | ||||||
chr14:73060424
|
G | T | 1 | a0001c0002t0003g0371 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-16+1719G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73060424 | ||||||
chr14:73060545
|
A | G | 55 | a0001c0001t0001g0051a0001c0001t0001g0321a0001c0001t0001g0322others(52): Show | 56 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-16+1840A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73060545 | ||||||
chr14:73060595
|
A | G | 1 | a0001c0001t0020g0370 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-16+1890A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73060595 | ||||||
chr14:73060967
|
A | G | 1 | a0001c0001t0007g0320 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-16+2262A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73060967 | ||||||
chr14:73060985
|
C | CTT | 29 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(26): Show | 31 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-16+2281_-16+2282i others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73060985 | |||||
chr14:73061071
|
T | C | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+2366T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061071 | ||||||
chr14:73061092
|
C | T | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+2387C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061092 | ||||||
chr14:73061162
|
A | T | 1 | a0001c0001t0006g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-16+2457A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061162 | ||||||
chr14:73061245
|
A | G | 6 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(3): Show | 6 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+2540A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061245 | ||||||
chr14:73061421
|
A | G | 3 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0112 | 3 | HG00099.hp1 HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-16+2716A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061421 | ||||||
chr14:73061481
|
C | T | 123 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(120): Show | 128 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.-16+2776C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061481 | ||||||
chr14:73061528
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-16+2823G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061528 | ||||||
chr14:73061715
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-16+3010C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061715 | ||||||
chr14:73061772
|
T | C | 1 | a0001c0001t0002g0060 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-16+3067T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061772 | ||||||
chr14:73061930
|
C | T | 4 | a0001c0001t0001g0364a0001c0001t0001g0365a0001c0001t0001g0366others(1): Show | 4 | HG02155.hp2 NA18954.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+3225C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061930 | ||||||
chr14:73061937
|
G | A | 95 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(92): Show | 95 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.-16+3232G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061937 | ||||||
chr14:73061956
|
G | T | 1 | a0001c0001t0001g0372 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-16+3251G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061956 | ||||||
chr14:73062064
|
G | A | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+3359G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062064 | ||||||
chr14:73062077
|
G | C | 1 | a0001c0001t0006g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-16+3372G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062077 | ||||||
chr14:73062386
|
A | G | 58 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0060others(55): Show | 58 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-16+3681A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062386 | ||||||
chr14:73062442
|
G | A | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0012g0015 | 3 | HG01167.hp2 HG01169.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.-16+3737G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062442 | ||||||
chr14:73062557
|
G | A | 1 | a0001c0001t0032g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-16+3852G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062557 | ||||||
chr14:73062628
|
A | G | 1 | a0001c0001t0005g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-16+3923A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062628 | ||||||
chr14:73062654
|
G | C | 26 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(23): Show | 28 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-16+3949G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062654 | ||||||
chr14:73062690
|
A | G | 1 | a0001c0001t0001g0373 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-16+3985A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062690 | ||||||
chr14:73062859
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-16+4154C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062859 | ||||||
chr14:73062867
|
C | G | 1 | a0001c0001t0001g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-16+4162C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062867 | ||||||
chr14:73063085
|
A | G | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+4380A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063085 | ||||||
chr14:73063087
|
G | T | 2 | a0001c0001t0007g0290a0001c0001t0007g0291 | 2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-16+4382G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063087 | ||||||
chr14:73063222
|
TC | T | 10 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(7): Show | 10 | NA18946.hp1 NA18953.hp1 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.-16+4518delC | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063222 | ||||||
chr14:73063235
|
C | T | 4 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(1): Show | 4 | HG02647.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+4530C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063235 | ||||||
chr14:73063275
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-16+4570G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063275 | ||||||
chr14:73063321
|
T | C | 1 | a0001c0001t0023g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-16+4616T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063321 | ||||||
chr14:73063450
|
G | A | 37 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(34): Show | 37 | HG00408.hp2 HG00544.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.-16+4745G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063450 | ||||||
chr14:73063487
|
T | C | 4 | a0001c0001t0002g0061a0001c0001t0002g0064a0001c0001t0031g0062others(1): Show | 4 | HG02683.hp1 HG02698.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+4782T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063487 | ||||||
chr14:73063672
|
C | T | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+4967C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063672 | ||||||
chr14:73063871
|
T | C | 20 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(17): Show | 20 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+5166T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063871 | ||||||
chr14:73063873
|
G | T | 1 | a0001c0001t0002g0109 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-16+5168G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063873 | ||||||
chr14:73063895
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-16+5190C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063895 | ||||||
chr14:73063970
|
T | C | 149 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(146): Show | 154 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.-16+5265T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063970 | ||||||
chr14:73064548
|
C | T | 2 | a0001c0001t0008g0009a0001c0001t0008g0010 | 2 | HG01168.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-16+5843C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73064548 | ||||||
chr14:73064676
|
A | T | 1 | a0001c0001t0002g0107 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-16+5971A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73064676 | ||||||
chr14:73064700
|
G | A | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+5995G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73064700 | ||||||
chr14:73064752
|
T | C | 3 | a0001c0001t0007g0244a0001c0001t0007g0245a0001c0001t0007g0246 | 3 | HG02055.hp2 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-16+6047T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73064752 | ||||||
chr14:73064916
|
A | G | 4 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(1): Show | 4 | HG01256.hp2 HG01928.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+6211A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73064916 | ||||||
chr14:73064954
|
CT | C | 8 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0011g0046others(5): Show | 8 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16+6264delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73064954 | |||||
chr14:73064980
|
T | G | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.-16+6275T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73064980 | ||||||
chr14:73065025
|
A | G | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-16+6320A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065025 | ||||||
chr14:73065045
|
G | T | 19 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(16): Show | 19 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-16+6340G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065045 | ||||||
chr14:73065091
|
C | G | 95 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(92): Show | 95 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.-16+6386C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065091 | ||||||
chr14:73065118
|
TTTTGTTT others(1): Show |
T | 4 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(1): Show | 4 | HG02647.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+6429_-16+6436d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73065118 | |||||
chr14:73065270
|
A | G | 64 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0140others(61): Show | 64 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.-15-6357A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065270 | ||||||
chr14:73065316
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-15-6311C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065316 | ||||||
chr14:73065429
|
A | AT | 10 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0005g0230others(7): Show | 10 | HG00642.hp1 HG00735.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15-6184dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73065429 | |||||
chr14:73065569
|
C | T | 11 | a0001c0001t0007g0244a0001c0001t0007g0245a0001c0001t0007g0246others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15-6058C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065569 | ||||||
chr14:73065603
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-15-6024A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065603 | ||||||
chr14:73065752
|
A | G | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-5875A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065752 | ||||||
chr14:73065856
|
A | AGAGTTTT others(326): Show |
3 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362 | 3 | HG02976.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-15-5757_-15-5756i others(335): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73065856 | |||||
chr14:73065856
|
A | AGAGTTTT others(327): Show |
1 | a0001c0001t0001g0363 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-15-5757_-15-5756i others(336): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73065856 | |||||
chr14:73065947
|
T | C | 1 | a0001c0001t0002g0108 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-15-5680T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065947 | ||||||
chr14:73065962
|
T | C | 1 | a0001c0002t0003g0247 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-15-5665T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065962 | ||||||
chr14:73065968
|
A | G | 72 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0052others(69): Show | 73 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.-15-5659A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065968 | ||||||
chr14:73066180
|
C | T | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-5447C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066180 | ||||||
chr14:73066195
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0373 | 2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-15-5432G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066195 | ||||||
chr14:73066244
|
T | C | 1 | a0001c0001t0023g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-15-5383T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066244 | ||||||
chr14:73066260
|
T | C | 1 | a0001c0001t0023g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-15-5367T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066260 | ||||||
chr14:73066413
|
A | G | 20 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(17): Show | 20 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15-5214A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066413 | ||||||
chr14:73066504
|
G | A | 1 | a0001c0002t0003g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-15-5123G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066504 | ||||||
chr14:73066508
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-15-5119G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066508 | ||||||
chr14:73066576
|
G | A | 1 | a0001c0002t0003g0249 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-15-5051G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066576 | ||||||
chr14:73066637
|
A | G | 2 | a0001c0001t0019g0312a0001c0001t0019g0313 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-15-4990A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066637 | ||||||
chr14:73066646
|
CA | C | 220 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(217): Show | 223 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.-15-4962delA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73066646 | |||||
chr14:73066646
|
CAA | C | 99 | a0001c0001t0001g0137a0001c0001t0001g0237a0001c0001t0001g0321others(96): Show | 102 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.-15-4963_-15-4962d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73066646 | |||||
chr14:73066646
|
CAAA | C | 22 | a0001c0001t0004g0319a0001c0001t0006g0027a0001c0001t0006g0028others(19): Show | 22 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.-15-4964_-15-4962d others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73066646 | |||||
chr14:73066646
|
CAAAA | C | 7 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(4): Show | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15-4965_-15-4962d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73066646 | |||||
chr14:73066757
|
G | A | 4 | a0001c0001t0001g0113a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG00609.hp1 NA18980.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-4870G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066757 | ||||||
chr14:73066951
|
A | G | 1 | a0001c0002t0009g0284 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-15-4676A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066951 | ||||||
chr14:73066994
|
T | C | 20 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(17): Show | 20 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15-4633T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066994 | ||||||
chr14:73067066
|
A | AG | 5 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(2): Show | 5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-4561_-15-4560i others(3): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067066 | ||||||
chr14:73067067
|
A | AT | 25 | a0001c0001t0001g0114a0001c0001t0001g0192a0001c0001t0001g0193others(22): Show | 26 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.-15-4540dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73067067 | |||||
chr14:73067067
|
A | ATT | 54 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0060others(51): Show | 54 | HG00323.hp2 HG00558.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.-15-4541_-15-4540d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73067067 | |||||
chr14:73067067
|
A | ATTT | 6 | a0001c0001t0002g0068a0001c0001t0002g0102a0001c0001t0002g0103others(3): Show | 6 | HG01069.hp1 HG01167.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-4542_-15-4540d others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73067067 | |||||
chr14:73067067
|
A | T | 5 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(2): Show | 5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-4560A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067067 | ||||||
chr14:73067068
|
T | G | 1 | a0001c0001t0023g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-15-4559T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067068 | ||||||
chr14:73067072
|
T | A | 1 | a0001c0001t0001g0142 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-15-4555T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067072 | ||||||
chr14:73067090
|
T | C | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-4537T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067090 | ||||||
chr14:73067150
|
A | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0136a0001c0001t0001g0378 | 3 | HG03017.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-15-4477A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067150 | ||||||
chr14:73067172
|
C | T | 9 | a0001c0001t0002g0379a0001c0001t0002g0380a0001c0001t0002g0381others(6): Show | 9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15-4455C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067172 | ||||||
chr14:73067604
|
A | AT | 36 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0236others(33): Show | 37 | HG00323.hp1 HG00408.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15-4006dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73067604 | |||||
chr14:73067604
|
AT | A | 6 | a0001c0001t0001g0143a0001c0001t0002g0070a0001c0001t0002g0071others(3): Show | 6 | HG02165.hp2 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-4006delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73067604 | |||||
chr14:73067621
|
T | G | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-15-4006T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067621 | ||||||
chr14:73067690
|
G | A | 1 | a0001c0001t0032g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-15-3937G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067690 | ||||||
chr14:73067758
|
C | T | 2 | a0001c0001t0001g0355a0001c0001t0029g0354 | 2 | NA18999.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-15-3869C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067758 | ||||||
chr14:73067770
|
A | AT | 6 | a0001c0001t0001g0191a0001c0001t0001g0353a0001c0001t0002g0099others(3): Show | 6 | HG00609.hp2 HG00735.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-3843dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73067770 | |||||
chr14:73067812
|
C | T | 1 | a0001c0002t0003g0278 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-15-3815C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067812 | ||||||
chr14:73067860
|
A | G | 2 | a0001c0002t0003g0249a0001c0002t0003g0277 | 2 | HG01261.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-15-3767A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067860 | ||||||
chr14:73067949
|
A | G | 1 | a0001c0001t0019g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-15-3678A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067949 | ||||||
chr14:73068025
|
G | A | 1 | a0001c0001t0013g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-15-3602G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068025 | ||||||
chr14:73068047
|
C | T | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02258.hp1 HG02258.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-3580C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068047 | ||||||
chr14:73068176
|
T | C | 6 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-3451T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068176 | ||||||
chr14:73068182
|
T | A | 39 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(36): Show | 39 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.-15-3445T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068182 | ||||||
chr14:73068387
|
A | AT | 224 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(221): Show | 227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-15-3222dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73068387 | |||||
chr14:73068387
|
A | ATT | 29 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0218others(26): Show | 29 | HG00408.hp2 HG01081.hp2 HG01975.hp1 others(26): Show |
intron_variant | MODIFIER | c.-15-3223_-15-3222d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73068387 | |||||
chr14:73068387
|
A | ATTT | 9 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0190others(6): Show | 9 | HG00544.hp2 HG02738.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15-3224_-15-3222d others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73068387 | |||||
chr14:73068573
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-15-3054A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068573 | ||||||
chr14:73068670
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-15-2957G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068670 | ||||||
chr14:73068681
|
T | C | 1 | a0001c0001t0004g0295 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-15-2946T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068681 | ||||||
chr14:73068692
|
A | G | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-2935A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068692 | ||||||
chr14:73068825
|
C | T | 27 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(24): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.-15-2802C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068825 | ||||||
chr14:73069085
|
G | T | 1 | a0001c0001t0001g0227 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-15-2542G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069085 | ||||||
chr14:73069104
|
A | G | 13 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007others(10): Show | 13 | HG00323.hp1 HG01167.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15-2523A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069104 | ||||||
chr14:73069146
|
C | A | 17 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(14): Show | 17 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.-15-2481C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069146 | ||||||
chr14:73069264
|
C | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-15-2363C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069264 | ||||||
chr14:73069269
|
T | G | 11 | a0001c0001t0007g0244a0001c0001t0007g0245a0001c0001t0007g0246others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15-2358T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069269 | ||||||
chr14:73069354
|
T | C | 1 | a0001c0001t0004g0296 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-15-2273T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069354 | ||||||
chr14:73069417
|
C | T | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | HG01884.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-15-2210C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069417 | ||||||
chr14:73069632
|
C | T | 20 | a0001c0001t0001g0114a0001c0001t0001g0143a0001c0001t0001g0174others(17): Show | 20 | HG01123.hp2 HG01358.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15-1995C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069632 | ||||||
chr14:73069714
|
A | G | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-1913A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069714 | ||||||
chr14:73069746
|
T | TA | 8 | a0001c0001t0001g0205a0001c0001t0001g0349a0001c0001t0001g0350others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-1848dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAA | 6 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(3): Show | 6 | HG02451.hp2 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-1850_-15-1848d others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAA | 21 | a0001c0001t0001g0348a0001c0001t0007g0320a0001c0001t0011g0046others(18): Show | 21 | HG01069.hp2 HG01071.hp1 HG02165.hp1 others(18): Show |
intron_variant | MODIFIER | c.-15-1853_-15-1848d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA | 16 | a0001c0001t0001g0139a0001c0001t0001g0235a0001c0001t0001g0236others(13): Show | 16 | HG00735.hp2 HG01884.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15-1854_-15-1848d others(9): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA others(1): Show |
16 | a0001c0001t0001g0051a0001c0001t0001g0328a0001c0001t0001g0329others(13): Show | 19 | HG01261.hp1 HG01346.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.-15-1855_-15-1848d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA others(2): Show |
20 | a0001c0001t0001g0222a0001c0001t0001g0225a0001c0001t0001g0327others(17): Show | 20 | HG00639.hp2 HG00735.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15-1856_-15-1848d others(11): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA others(3): Show |
26 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0141others(23): Show | 26 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.-15-1857_-15-1848d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA others(4): Show |
33 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0142others(30): Show | 33 | HG00140.hp2 HG00544.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.-15-1858_-15-1848d others(13): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA others(5): Show |
20 | a0001c0001t0001g0116a0001c0001t0001g0126a0001c0001t0001g0157others(17): Show | 20 | HG00408.hp1 HG01070.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15-1859_-15-1848d others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA others(6): Show |
11 | a0001c0001t0001g0125a0001c0001t0001g0174a0001c0001t0001g0227others(8): Show | 12 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(9): Show |
intron_variant | MODIFIER | c.-15-1860_-15-1848d others(15): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA others(7): Show |
8 | a0001c0001t0001g0117a0001c0001t0001g0136a0001c0001t0001g0194others(5): Show | 8 | HG02818.hp2 HG03017.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-1861_-15-1848d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA others(8): Show |
7 | a0001c0001t0001g0124a0001c0001t0001g0153a0001c0001t0001g0154others(4): Show | 7 | HG01256.hp2 NA18942.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-1862_-15-1848d others(17): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA others(9): Show |
4 | a0001c0001t0001g0123a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02056.hp2 HG04204.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-1863_-15-1848d others(18): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA others(10): Show |
4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0356others(1): Show | 4 | HG02080.hp2 HG03491.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-1864_-15-1848d others(19): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA others(11): Show |
2 | a0001c0001t0001g0148a0001c0001t0014g0122 | 2 | NA18993.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-15-1865_-15-1848d others(20): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA others(12): Show |
6 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0186others(3): Show | 6 | HG02602.hp1 NA18941.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-1866_-15-1848d others(21): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA others(13): Show |
2 | a0001c0001t0001g0137a0001c0001t0001g0333 | 2 | NA18963.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-15-1867_-15-1848d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA others(14): Show |
2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02071.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-15-1868_-15-1848d others(23): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA others(15): Show |
3 | a0001c0001t0001g0138a0001c0001t0001g0185a0001c0001t0001g0332 | 3 | HG00642.hp1 NA18939.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-15-1869_-15-1848d others(24): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
T | TAAAAAAA others(25): Show |
1 | a0001c0001t0001g0119 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-15-1879_-15-1848d others(34): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
TAA | T | 7 | a0001c0001t0001g0133a0001c0001t0001g0210a0001c0001t0001g0233others(4): Show | 7 | HG00733.hp2 HG02132.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15-1849_-15-1848d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
TAAA | T | 19 | a0001c0001t0001g0211a0001c0001t0002g0022a0001c0001t0002g0065others(16): Show | 20 | HG01081.hp2 HG01106.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15-1850_-15-1848d others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
TAAAA | T | 56 | a0001c0001t0001g0115a0001c0001t0001g0199a0001c0001t0002g0023others(53): Show | 56 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-15-1851_-15-1848d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
TAAAAAAA others(2): Show |
T | 25 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(22): Show | 27 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15-1856_-15-1848d others(11): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
TAAAAAAA others(3): Show |
T | 8 | a0001c0001t0001g0184a0001c0001t0001g0367a0001c0001t0008g0005others(5): Show | 8 | HG02155.hp2 HG02735.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-1857_-15-1848d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
TAAAAAAA others(4): Show |
T | 3 | a0001c0001t0005g0203a0001c0001t0008g0012a0001c0001t0032g0025 | 3 | HG00323.hp1 HG02004.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-15-1858_-15-1848d others(13): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
TAAAAAAA others(7): Show |
T | 2 | a0001c0001t0005g0242a0001c0002t0009g0281 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-15-1861_-15-1848d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069746
|
TAAAAAAA others(8): Show |
T | 15 | a0001c0001t0001g0135a0001c0001t0001g0189a0001c0001t0001g0217others(12): Show | 15 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-15-1862_-15-1848d others(17): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | |||||
chr14:73069769
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0023g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-15-1857_-15-1846d others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069769 | ||||||
chr14:73069817
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-15-1810A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069817 | ||||||
chr14:73069818
|
T | A | 5 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(2): Show | 5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-1809T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069818 | ||||||
chr14:73069829
|
C | CT | 14 | a0001c0001t0001g0159a0001c0001t0001g0168a0001c0001t0001g0169others(11): Show | 14 | HG00408.hp1 HG01074.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-15-1782dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069829 | |||||
chr14:73069829
|
CT | C | 74 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0001g0350others(71): Show | 75 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-15-1782delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069829 | |||||
chr14:73069917
|
A | G | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-1710A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069917 | ||||||
chr14:73069940
|
G | A | 29 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(26): Show | 31 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-15-1687G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069940 | ||||||
chr14:73069974
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-15-1653C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069974 | ||||||
chr14:73070190
|
G | GGC | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-1434_-15-1433d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73070190 | |||||
chr14:73070220
|
T | G | 35 | a0001c0001t0001g0372a0001c0001t0002g0077a0001c0001t0002g0078others(32): Show | 37 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15-1407T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73070220 | ||||||
chr14:73070253
|
C | T | 1 | a0001c0001t0006g0032 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-15-1374C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73070253 | ||||||
chr14:73070341
|
G | A | 39 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(36): Show | 39 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.-15-1286G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73070341 | ||||||
chr14:73070442
|
TA | T | 379 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(376): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.-15-1174delA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73070442 | |||||
chr14:73070528
|
C | G | 1 | a0001c0001t0001g0156 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-15-1099C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73070528 | ||||||
chr14:73070677
|
G | A | 1 | a0001c0001t0002g0079 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-15-950G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73070677 | ||||||
chr14:73070916
|
C | T | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-711C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73070916 | ||||||
chr14:73070929
|
G | A | 1 | a0001c0001t0004g0292 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-15-698G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73070929 | ||||||
chr14:73070945
|
C | CA | 120 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(117): Show | 121 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.-15-668dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73070945 | |||||
chr14:73070945
|
C | CAA | 35 | a0001c0001t0001g0116a0001c0001t0001g0126a0001c0001t0001g0185others(32): Show | 35 | HG00609.hp1 HG00733.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.-15-669_-15-668dup others(2): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73070945 | |||||
chr14:73070980
|
G | T | 27 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(24): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.-15-647G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73070980 | ||||||
chr14:73071007
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-15-620C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071007 | ||||||
chr14:73071166
|
C | T | 1 | a0001c0001t0014g0196 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-15-461C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071166 | ||||||
chr14:73071199
|
G | A | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.-15-428G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071199 | ||||||
chr14:73071240
|
C | CA | 51 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0142others(48): Show | 54 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.-15-366dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73071240 | |||||
chr14:73071240
|
C | CAA | 7 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0002t0003g0248others(4): Show | 7 | HG00735.hp1 HG02027.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15-367_-15-366dup others(2): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73071240 | |||||
chr14:73071240
|
CA | C | 137 | a0001c0001t0001g0051a0001c0001t0001g0114a0001c0001t0001g0227others(134): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-15-366delA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73071240 | |||||
chr14:73071240
|
CAA | C | 33 | a0001c0001t0001g0348a0001c0001t0002g0096a0001c0001t0006g0026others(30): Show | 33 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.-15-367_-15-366del others(2): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73071240 | |||||
chr14:73071263
|
C | G | 11 | a0001c0001t0007g0244a0001c0001t0007g0245a0001c0001t0007g0246others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15-364C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071263 | ||||||
chr14:73071369
|
T | A | 1 | a0001c0001t0004g0308 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-15-258T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071369 | ||||||
chr14:73071380
|
C | T | 3 | a0001c0001t0001g0344a0001c0001t0001g0346a0001c0001t0001g0347 | 3 | HG02129.hp2 HG02280.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-15-247C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071380 | ||||||
chr14:73071384
|
A | G | 1 | a0001c0001t0039g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-15-243A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071384 | ||||||
chr14:73071400
|
G | A | 1 | a0001c0001t0004g0319 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-15-227G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071400 | ||||||
chr14:73071447
|
T | G | 11 | a0001c0001t0007g0244a0001c0001t0007g0245a0001c0001t0007g0246others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15-180T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071447 | ||||||
chr14:73071775
|
G | A | 2 | a0001c0001t0006g0027a0001c0001t0006g0038 | 2 | HG02056.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.106+28G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73071775 | ||||||
chr14:73071825
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.106+78A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73071825 | ||||||
chr14:73072031
|
G | A | 8 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007others(5): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+284G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072031 | ||||||
chr14:73072042
|
C | A | 1 | a0001c0001t0007g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.106+295C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072042 | ||||||
chr14:73072114
|
C | T | 1 | a0001c0001t0032g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.106+367C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072114 | ||||||
chr14:73072286
|
T | A | 1 | a0001c0001t0018g0368 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.106+539T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072286 | ||||||
chr14:73072323
|
C | CA | 8 | a0001c0001t0005g0147a0001c0001t0011g0046a0001c0001t0011g0047others(5): Show | 8 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.106+586dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 73072323 | |||||
chr14:73072507
|
T | C | 1 | a0001c0001t0032g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.106+760T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072507 | ||||||
chr14:73072586
|
A | T | 1 | a0001c0001t0001g0331 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.106+839A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072586 | ||||||
chr14:73072618
|
A | AATCC | 27 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(24): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.106+873_106+876dup others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 73072618 | |||||
chr14:73072721
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.106+974G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072721 | ||||||
chr14:73072723
|
G | A | 11 | a0001c0001t0007g0244a0001c0001t0007g0245a0001c0001t0007g0246others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+976G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072723 | ||||||
chr14:73072725
|
G | T | 3 | a0001c0002t0003g0248a0001c0002t0003g0258a0001c0002t0003g0259 | 3 | HG01074.hp1 HG01099.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.106+978G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072725 | ||||||
chr14:73072865
|
G | A | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+1118G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072865 | ||||||
chr14:73073193
|
T | G | 1 | a0001c0001t0001g0142 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.106+1446T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073193 | ||||||
chr14:73073404
|
C | G | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+1657C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073404 | ||||||
chr14:73073430
|
G | A | 29 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(26): Show | 31 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+1683G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073430 | ||||||
chr14:73073432
|
A | G | 96 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(93): Show | 96 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.106+1685A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073432 | ||||||
chr14:73073487
|
A | C | 1 | a0001c0001t0001g0183 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.106+1740A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073487 | ||||||
chr14:73073509
|
A | G | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+1762A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073509 | ||||||
chr14:73073514
|
G | A | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.106+1767G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073514 | ||||||
chr14:73073576
|
T | C | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.106+1829T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073576 | ||||||
chr14:73073669
|
C | T | 1 | a0001c0001t0007g0287 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.106+1922C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073669 | ||||||
chr14:73073762
|
A | G | 1 | a0001c0002t0003g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.106+2015A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073762 | ||||||
chr14:73073876
|
G | A | 2 | a0001c0001t0018g0368a0001c0001t0018g0369 | 2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.106+2129G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073876 | ||||||
chr14:73073922
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.106+2175G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073922 | ||||||
chr14:73073985
|
A | G | 1 | a0001c0002t0003g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.106+2238A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073985 | ||||||
chr14:73073990
|
G | A | 39 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(36): Show | 39 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.106+2243G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073990 | ||||||
chr14:73074048
|
G | A | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.107-2271G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074048 | ||||||
chr14:73074203
|
T | C | 1 | a0001c0001t0001g0336 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.107-2116T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074203 | ||||||
chr14:73074228
|
A | G | 168 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(165): Show | 169 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.107-2091A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074228 | ||||||
chr14:73074271
|
G | T | 1 | a0001c0001t0021g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.107-2048G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074271 | ||||||
chr14:73074342
|
A | C | 379 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(376): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.107-1977A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074342 | ||||||
chr14:73074358
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.107-1961T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074358 | ||||||
chr14:73074359
|
A | G | 3 | a0001c0001t0004g0298a0001c0001t0004g0309a0001c0001t0004g0310 | 3 | HG03688.hp1 HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.107-1960A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074359 | ||||||
chr14:73074449
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.107-1870T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074449 | ||||||
chr14:73074493
|
G | A | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.107-1826G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074493 | ||||||
chr14:73074661
|
C | T | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-1658C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074661 | ||||||
chr14:73074702
|
A | AT | 40 | a0001c0001t0002g0077a0001c0001t0002g0078a0001c0001t0004g0002others(37): Show | 42 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.107-1606dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 73074702 | |||||
chr14:73074750
|
C | G | 1 | a0001c0001t0004g0296 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.107-1569C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074750 | ||||||
chr14:73074750
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.107-1569C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074750 | ||||||
chr14:73074780
|
A | AC | 11 | a0001c0001t0007g0244a0001c0001t0007g0245a0001c0001t0007g0246others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.107-1538dupC | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 73074780 | |||||
chr14:73074835
|
A | G | 50 | a0001c0001t0001g0051a0001c0001t0001g0321a0001c0001t0001g0322others(47): Show | 51 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.107-1484A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074835 | ||||||
chr14:73074903
|
G | C | 1 | a0001c0001t0002g0064 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.107-1416G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074903 | ||||||
chr14:73074943
|
A | G | 18 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(15): Show | 18 | HG00733.hp2 HG01106.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.107-1376A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074943 | ||||||
chr14:73074971
|
C | T | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.107-1348C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074971 | ||||||
chr14:73074991
|
CT | C | 21 | a0001c0001t0001g0156a0001c0001t0001g0205a0001c0001t0001g0206others(18): Show | 21 | HG00733.hp1 HG00733.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.107-1313delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 73074991 | |||||
chr14:73075212
|
A | T | 7 | a0001c0002t0003g0001a0001c0002t0003g0255a0001c0002t0003g0256others(4): Show | 10 | HG00423.hp1 HG02135.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.107-1107A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075212 | ||||||
chr14:73075277
|
G | C | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-1042G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075277 | ||||||
chr14:73075306
|
G | A | 46 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(43): Show | 47 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.107-1013G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075306 | ||||||
chr14:73075393
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107-926A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075393 | ||||||
chr14:73075437
|
G | A | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.107-882G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075437 | ||||||
chr14:73075439
|
G | A | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-880G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075439 | ||||||
chr14:73075477
|
C | T | 39 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(36): Show | 39 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.107-842C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075477 | ||||||
chr14:73075485
|
C | T | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-834C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075485 | ||||||
chr14:73075582
|
A | G | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.107-737A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075582 | ||||||
chr14:73075655
|
A | C | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | HG02258.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.107-664A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075655 | ||||||
chr14:73075774
|
T | C | 27 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(24): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.107-545T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075774 | ||||||
chr14:73075854
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.107-465C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075854 | ||||||
chr14:73075926
|
G | A | 6 | a0001c0001t0001g0144a0001c0001t0001g0157a0001c0001t0001g0162others(3): Show | 6 | HG00140.hp2 HG01496.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-393G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075926 | ||||||
chr14:73075942
|
A | G | 13 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007others(10): Show | 13 | HG00323.hp1 HG01167.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.107-377A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075942 | ||||||
chr14:73076083
|
G | C | 1 | a0001c0001t0002g0080 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.107-236G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73076083 | ||||||
chr14:73076140
|
A | G | 2 | a0001c0001t0007g0290a0001c0001t0007g0291 | 2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.107-179A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73076140 | ||||||
chr14:73076282
|
C | T | 1 | a0001c0001t0001g0343 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.107-37C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73076282 | ||||||
chr14:73076402
|
T | C | 1 | a0001c0001t0002g0108 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.156+34T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | chr14 | 73076402 | ||||||
chr14:73076609
|
A | C | 278 | a0001c0001t0001g0051a0001c0001t0001g0205a0001c0001t0001g0206others(275): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.156+241A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | chr14 | 73076609 | ||||||
chr14:73076653
|
G | A | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.156+285G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | chr14 | 73076653 | ||||||
chr14:73076661
|
T | C | 2 | a0001c0001t0002g0004a0001c0001t0002g0357 | 3 | HG01070.hp2 HG01192.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.156+293T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | chr14 | 73076661 | ||||||
chr14:73076718
|
TAAAAG | T | 50 | a0001c0001t0001g0051a0001c0001t0001g0321a0001c0001t0001g0322others(47): Show | 51 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.156+353_156+357del others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr14 | 73076718 | |||||
chr14:73076851
|
G | A | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.156+483G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | chr14 | 73076851 | ||||||
chr14:73076856
|
G | T | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.156+488G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | chr14 | 73076856 | ||||||
chr14:73076909
|
G | A | 1 | a0001c0001t0011g0048 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.157-460G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | chr14 | 73076909 | ||||||
chr14:73077075
|
C | T | 28 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(25): Show | 30 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.157-294C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | chr14 | 73077075 | ||||||
chr14:73077888
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.324+352A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73077888 | ||||||
chr14:73077904
|
G | A | 117 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(114): Show | 122 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.324+368G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73077904 | ||||||
chr14:73077910
|
C | A | 377 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(374): Show | 384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.324+374C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73077910 | ||||||
chr14:73077934
|
G | A | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.324+398G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73077934 | ||||||
chr14:73078000
|
C | CA | 11 | a0001c0001t0007g0244a0001c0001t0007g0245a0001c0001t0007g0246others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.324+470dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73078000 | |||||
chr14:73078022
|
G | A | 1 | a0001c0001t0004g0310 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.324+486G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078022 | ||||||
chr14:73078186
|
T | C | 7 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(4): Show | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+650T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078186 | ||||||
chr14:73078273
|
A | T | 1 | a0001c0001t0008g0008 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.324+737A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078273 | ||||||
chr14:73078336
|
TAAAA | T | 7 | a0001c0001t0007g0244a0001c0001t0007g0245a0001c0001t0007g0246others(4): Show | 7 | HG02055.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+806_324+809del others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73078336 | |||||
chr14:73078346
|
G | A | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.324+810G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078346 | ||||||
chr14:73078365
|
G | A | 1 | a0001c0001t0006g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.324+829G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078365 | ||||||
chr14:73078419
|
A | G | 1 | a0001c0001t0001g0352 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.324+883A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078419 | ||||||
chr14:73078486
|
C | CA | 4 | a0001c0002t0003g0253a0001c0002t0003g0266a0001c0002t0003g0267others(1): Show | 4 | NA18964.hp1 NA18980.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+957dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73078486 | |||||
chr14:73078510
|
A | G | 1 | a0001c0001t0004g0296 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.324+974A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078510 | ||||||
chr14:73078629
|
A | T | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.324+1093A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078629 | ||||||
chr14:73078800
|
C | T | 8 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007others(5): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+1264C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078800 | ||||||
chr14:73078956
|
G | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | HG02258.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.324+1420G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078956 | ||||||
chr14:73079054
|
ACTTTTTT others(1151): Show |
A | 2 | a0001c0001t0008g0009a0001c0001t0008g0010 | 2 | HG01168.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.324+1527_324+2684d others(2): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73079054 | |||||
chr14:73079056
|
TTTTTTTA others(1150): Show |
T | 6 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007others(3): Show | 6 | HG00323.hp1 HG02735.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+1527_324+2683d others(2): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73079056 | |||||
chr14:73079094
|
G | A | 2 | a0001c0001t0006g0028a0001c0001t0026g0042 | 2 | NA18948.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.324+1558G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73079094 | ||||||
chr14:73079126
|
T | G | 1 | a0001c0001t0001g0222 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.324+1590T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73079126 | ||||||
chr14:73079156
|
C | T | 1 | a0001c0001t0005g0201 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.324+1620C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73079156 | ||||||
chr14:73079284
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.324+1748G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73079284 | ||||||
chr14:73079292
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.324+1756C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73079292 | ||||||
chr14:73079316
|
G | A | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.324+1780G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73079316 | ||||||
chr14:73079327
|
G | A | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.324+1791G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73079327 | ||||||
chr14:73079851
|
C | T | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.324+2315C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73079851 | ||||||
chr14:73080036
|
T | C | 100 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(97): Show | 100 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.324+2500T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080036 | ||||||
chr14:73080104
|
G | A | 3 | a0001c0001t0004g0298a0001c0001t0004g0309a0001c0001t0004g0310 | 3 | HG03688.hp1 HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.324+2568G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080104 | ||||||
chr14:73080155
|
A | G | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.324+2619A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080155 | ||||||
chr14:73080213
|
C | CT | 79 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0121others(76): Show | 79 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.324+2705dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | |||||
chr14:73080213
|
C | CTT | 16 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0146others(13): Show | 16 | HG00609.hp2 HG01123.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.324+2704_324+2705d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | |||||
chr14:73080213
|
C | CTTTT | 24 | a0001c0001t0001g0226a0001c0001t0007g0291a0001c0001t0021g0286others(21): Show | 27 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.324+2702_324+2705d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | |||||
chr14:73080213
|
C | CTTTTT | 27 | a0001c0001t0001g0227a0001c0001t0001g0360a0001c0001t0001g0361others(24): Show | 27 | HG00423.hp1 HG00735.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.324+2701_324+2705d others(7): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | |||||
chr14:73080213
|
C | CTTTTTT | 9 | a0001c0001t0001g0205a0001c0001t0001g0210a0001c0001t0001g0211others(6): Show | 9 | HG00733.hp2 HG01106.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.324+2700_324+2705d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | |||||
chr14:73080213
|
C | CTTTTTTT | 8 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(5): Show | 8 | HG02559.hp1 HG02717.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+2699_324+2705d others(9): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | |||||
chr14:73080213
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0363 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.324+2696_324+2705d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | |||||
chr14:73080213
|
CT | C | 26 | a0001c0001t0001g0322a0001c0001t0001g0336a0001c0001t0001g0372others(23): Show | 26 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.324+2705delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | |||||
chr14:73080213
|
CTT | C | 24 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(21): Show | 26 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.324+2704_324+2705d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | |||||
chr14:73080213
|
CTTTTT | C | 8 | a0001c0001t0001g0217a0001c0001t0005g0204a0001c0001t0005g0213others(5): Show | 8 | HG01074.hp2 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+2701_324+2705d others(7): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | |||||
chr14:73080213
|
CTTTTTT | C | 6 | a0001c0001t0005g0212a0001c0001t0011g0046a0001c0001t0011g0047others(3): Show | 6 | HG02486.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+2700_324+2705d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | |||||
chr14:73080246
|
T | C | 8 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007others(5): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+2710T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080246 | ||||||
chr14:73080251
|
T | C | 2 | a0001c0001t0001g0339a0001c0001t0028g0351 | 2 | HG02074.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.324+2715T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080251 | ||||||
chr14:73080254
|
T | C | 8 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007others(5): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+2718T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080254 | ||||||
chr14:73080369
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.324+2833G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080369 | ||||||
chr14:73080545
|
A | G | 2 | a0001c0001t0002g0052a0001c0001t0002g0059 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.325-2949A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080545 | ||||||
chr14:73080547
|
T | C | 1 | a0001c0001t0027g0219 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.325-2947T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080547 | ||||||
chr14:73080823
|
CT | C | 59 | a0001c0001t0001g0051a0001c0001t0001g0321a0001c0001t0001g0322others(56): Show | 60 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.325-2656delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080823 | |||||
chr14:73080837
|
TTA | T | 11 | a0001c0001t0001g0206a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG02258.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.325-2655_325-2654d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080837 | |||||
chr14:73080838
|
TA | T | 7 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(4): Show | 7 | HG00733.hp2 HG01106.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.325-2655delA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080838 | ||||||
chr14:73080865
|
T | C | 100 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(97): Show | 100 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.325-2629T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080865 | ||||||
chr14:73080886
|
G | A | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-2608G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080886 | ||||||
chr14:73080903
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.325-2591C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080903 | ||||||
chr14:73080905
|
A | G | 3 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0093 | 3 | NA18943.hp2 NA18963.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.325-2589A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080905 | ||||||
chr14:73080910
|
G | A | 1 | a0001c0001t0004g0300 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.325-2584G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080910 | ||||||
chr14:73080959
|
G | A | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.325-2535G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080959 | ||||||
chr14:73080965
|
T | C | 1 | a0001c0001t0032g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.325-2529T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080965 | ||||||
chr14:73081170
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.325-2324C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73081170 | ||||||
chr14:73081225
|
C | CAG | 43 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(40): Show | 43 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.325-2269_325-2268i others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73081225 | ||||||
chr14:73081239
|
G | C | 2 | a0001c0001t0006g0036a0001c0001t0006g0037 | 2 | HG01081.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.325-2255G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73081239 | ||||||
chr14:73081286
|
C | T | 9 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(6): Show | 9 | HG01074.hp2 HG02486.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.325-2208C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73081286 | ||||||
chr14:73081474
|
T | G | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-2020T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73081474 | ||||||
chr14:73081501
|
AT | A | 107 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(104): Show | 107 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.325-1986delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73081501 | |||||
chr14:73081688
|
C | CT | 3 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035 | 3 | NA18947.hp1 NA18965.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.325-1801dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73081688 | |||||
chr14:73081694
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.325-1800A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73081694 | ||||||
chr14:73081732
|
G | A | 26 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(23): Show | 26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.325-1762G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73081732 | ||||||
chr14:73081857
|
A | G | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-1637A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73081857 | ||||||
chr14:73082316
|
C | G | 39 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(36): Show | 39 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.325-1178C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082316 | ||||||
chr14:73082352
|
C | T | 8 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007others(5): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.325-1142C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082352 | ||||||
chr14:73082353
|
A | G | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-1141A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082353 | ||||||
chr14:73082424
|
T | C | 1 | a0001c0001t0032g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.325-1070T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082424 | ||||||
chr14:73082447
|
A | C | 39 | a0001c0002t0003g0247a0001c0002t0003g0248a0001c0002t0003g0249others(36): Show | 39 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.325-1047A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082447 | ||||||
chr14:73082449
|
G | A | 1 | a0001c0001t0013g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.325-1045G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082449 | ||||||
chr14:73082500
|
A | T | 1 | a0001c0001t0001g0133 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.325-994A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082500 | ||||||
chr14:73082889
|
G | A | 26 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(23): Show | 26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.325-605G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082889 | ||||||
chr14:73082899
|
A | T | 1 | a0001c0002t0003g0260 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.325-595A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082899 | ||||||
chr14:73082907
|
T | A | 3 | a0001c0001t0005g0204a0001c0001t0005g0213a0001c0001t0005g0214 | 3 | HG02109.hp1 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.325-587T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082907 | ||||||
chr14:73082907
|
T | TA | 35 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0002g0066others(32): Show | 35 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.325-574dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73082907 | |||||
chr14:73082907
|
TA | T | 31 | a0001c0001t0001g0163a0001c0001t0001g0172a0001c0001t0004g0002others(28): Show | 33 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.325-574delA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73082907 | |||||
chr14:73082941
|
G | A | 1 | a0001c0001t0006g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.325-553G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082941 | ||||||
chr14:73082943
|
G | A | 6 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(3): Show | 6 | HG01243.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-551G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082943 | ||||||
chr14:73083135
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.325-359A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73083135 | ||||||
chr14:73083269
|
TGCAAATG others(89): Show |
T | 1 | a0001c0001t0001g0151 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.325-217_325-122del others(96): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73083269 | |||||
chr14:73083343
|
T | G | 3 | a0001c0001t0002g0061a0001c0001t0031g0062a0001c0001t0034g0063 | 3 | HG02683.hp1 HG02698.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.325-151T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73083343 | ||||||
chr14:73083384
|
T | G | 11 | a0001c0001t0007g0244a0001c0001t0007g0245a0001c0001t0007g0246others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-110T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73083384 | ||||||
chr14:73083412
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.325-82A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73083412 | ||||||
chr14:73083415
|
A | T | 1 | a0001c0001t0006g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.325-79A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73083415 | ||||||
chr14:73083560
|
TTTTTTTC others(36): Show |
T | 1 | a0001c0001t0014g0196 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.382+12_382+54delTT others(41): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73083560 | |||||
chr14:73083692
|
A | G | 8 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007others(5): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.382+141A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73083692 | ||||||
chr14:73083732
|
GAGATC | G | 5 | a0001c0001t0010g0003a0001c0001t0010g0238a0001c0001t0010g0239others(2): Show | 6 | HG01891.hp2 HG02145.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+185_382+189del others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73083732 | |||||
chr14:73083803
|
G | T | 2 | a0001c0001t0018g0368a0001c0001t0018g0369 | 2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.382+252G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73083803 | ||||||
chr14:73083821
|
T | C | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.382+270T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73083821 | ||||||
chr14:73083842
|
A | C | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+291A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73083842 | ||||||
chr14:73083898
|
C | CT | 15 | a0001c0001t0001g0152a0001c0001t0001g0182a0001c0001t0001g0329others(12): Show | 15 | HG00741.hp1 HG00741.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.382+364dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73083898 | |||||
chr14:73083898
|
CT | C | 7 | a0001c0001t0001g0051a0001c0001t0001g0160a0001c0001t0001g0345others(4): Show | 7 | HG02015.hp2 HG02109.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.382+364delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73083898 | |||||
chr14:73084019
|
T | C | 55 | a0001c0001t0001g0051a0001c0001t0001g0321a0001c0001t0001g0322others(52): Show | 56 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.382+468T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084019 | ||||||
chr14:73084028
|
G | T | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+477G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084028 | ||||||
chr14:73084059
|
G | A | 30 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0249others(27): Show | 33 | HG00423.hp1 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.382+508G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084059 | ||||||
chr14:73084087
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.382+536G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084087 | ||||||
chr14:73084178
|
A | G | 5 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(2): Show | 5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.382+627A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084178 | ||||||
chr14:73084185
|
A | G | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.382+634A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084185 | ||||||
chr14:73084201
|
A | G | 2 | a0001c0001t0006g0036a0001c0001t0006g0037 | 2 | HG01081.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.382+650A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084201 | ||||||
chr14:73084201
|
A | T | 2 | a0001c0001t0004g0305a0001c0001t0004g0306 | 2 | HG00544.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.382+650A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084201 | ||||||
chr14:73084410
|
T | A | 1 | a0001c0001t0001g0235 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.382+859T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084410 | ||||||
chr14:73084537
|
G | GTTTGT | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.382+999_382+1003du others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73084537 | |||||
chr14:73084650
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.382+1099T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084650 | ||||||
chr14:73084718
|
A | G | 14 | a0001c0001t0001g0217a0001c0001t0005g0204a0001c0001t0005g0212others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.382+1167A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084718 | ||||||
chr14:73084767
|
C | G | 34 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(31): Show | 34 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.382+1216C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084767 | ||||||
chr14:73084811
|
A | C | 2 | a0001c0001t0018g0368a0001c0001t0018g0369 | 2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.382+1260A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084811 | ||||||
chr14:73084853
|
A | AT | 29 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(26): Show | 31 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.382+1313dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73084853 | |||||
chr14:73085055
|
T | C | 1 | a0001c0001t0001g0372 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.382+1504T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085055 | ||||||
chr14:73085064
|
G | C | 1 | a0001c0001t0001g0359 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.382+1513G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085064 | ||||||
chr14:73085065
|
C | A | 1 | a0001c0001t0001g0372 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.382+1514C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085065 | ||||||
chr14:73085075
|
G | A | 29 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(26): Show | 31 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.382+1524G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085075 | ||||||
chr14:73085099
|
A | G | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.382+1548A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085099 | ||||||
chr14:73085109
|
C | G | 2 | a0001c0001t0006g0027a0001c0001t0006g0038 | 2 | HG02056.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.382+1558C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085109 | ||||||
chr14:73085122
|
G | T | 1 | a0001c0002t0009g0264 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.382+1571G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085122 | ||||||
chr14:73085213
|
TTCACCGT others(5): Show |
T | 2 | a0001c0001t0019g0312a0001c0001t0019g0313 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.382+1663_382+1674d others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085213 | ||||||
chr14:73085295
|
A | G | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1744A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085295 | ||||||
chr14:73085306
|
C | G | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1755C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085306 | ||||||
chr14:73085309
|
G | A | 46 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(43): Show | 49 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.382+1758G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085309 | ||||||
chr14:73085316
|
CTCATCAG others(136): Show |
C | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1766_382+1908d others(2): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085316 | ||||||
chr14:73085325
|
A | G | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+1774A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085325 | ||||||
chr14:73085418
|
G | A | 1 | a0001c0001t0010g0241 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.382+1867G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085418 | ||||||
chr14:73085460
|
G | A | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1909G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085460 | ||||||
chr14:73085466
|
G | T | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1915G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085466 | ||||||
chr14:73085468
|
GTT | G | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1921_382+1922d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73085468 | |||||
chr14:73085475
|
G | A | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1924G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085475 | ||||||
chr14:73085483
|
T | C | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1932T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085483 | ||||||
chr14:73085484
|
G | T | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+1933G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085484 | ||||||
chr14:73085490
|
A | G | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1939A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085490 | ||||||
chr14:73085496
|
G | A | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1945G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085496 | ||||||
chr14:73085500
|
G | A | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1949G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085500 | ||||||
chr14:73085504
|
G | C | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1953G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085504 | ||||||
chr14:73085508
|
C | G | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1957C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085508 | ||||||
chr14:73085512
|
T | A | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1961T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085512 | ||||||
chr14:73085513
|
C | T | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1962C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085513 | ||||||
chr14:73085514
|
A | G | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1963A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085514 | ||||||
chr14:73085519
|
G | A | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1968G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085519 | ||||||
chr14:73085527
|
C | T | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1976C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085527 | ||||||
chr14:73085531
|
G | A | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1980G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085531 | ||||||
chr14:73085547
|
T | C | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1996T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085547 | ||||||
chr14:73085548
|
G | A | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1997G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085548 | ||||||
chr14:73085549
|
G | A | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1998G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085549 | ||||||
chr14:73085555
|
T | C | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+2004T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085555 | ||||||
chr14:73085673
|
G | A | 1 | a0001c0001t0006g0041 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.382+2122G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085673 | ||||||
chr14:73085690
|
G | A | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+2139G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085690 | ||||||
chr14:73085793
|
G | T | 34 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(31): Show | 34 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.383-2208G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085793 | ||||||
chr14:73085815
|
C | G | 5 | a0001c0001t0005g0221a0001c0001t0005g0228a0001c0001t0005g0229others(2): Show | 5 | HG02572.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.383-2186C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085815 | ||||||
chr14:73085861
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.383-2140G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085861 | ||||||
chr14:73085882
|
T | C | 5 | a0001c0001t0001g0217a0001c0001t0005g0212a0001c0001t0005g0215others(2): Show | 5 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-2119T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085882 | ||||||
chr14:73086070
|
T | C | 1 | a0001c0001t0015g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.383-1931T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086070 | ||||||
chr14:73086180
|
G | A | 2 | a0001c0001t0008g0011a0001c0001t0008g0012 | 2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.383-1821G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086180 | ||||||
chr14:73086352
|
C | T | 1 | a0001c0001t0039g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.383-1649C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086352 | ||||||
chr14:73086360
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0167 | 2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.383-1641C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086360 | ||||||
chr14:73086435
|
T | TA | 7 | a0001c0001t0001g0178a0001c0001t0001g0331a0001c0001t0002g0093others(4): Show | 7 | HG02055.hp2 HG02145.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.383-1551dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73086435 | |||||
chr14:73086435
|
TA | T | 11 | a0001c0001t0001g0182a0001c0001t0001g0372a0001c0001t0002g0065others(8): Show | 11 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-1551delA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73086435 | |||||
chr14:73086446
|
A | C | 12 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0002g0052others(9): Show | 12 | HG01496.hp2 HG01884.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.383-1555A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086446 | ||||||
chr14:73086458
|
G | A | 4 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(1): Show | 4 | HG01256.hp2 HG01928.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1543G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086458 | ||||||
chr14:73086561
|
T | C | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-1440T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086561 | ||||||
chr14:73086563
|
T | C | 26 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(23): Show | 26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.383-1438T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086563 | ||||||
chr14:73086731
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.383-1270G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086731 | ||||||
chr14:73086866
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.383-1135A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086866 | ||||||
chr14:73087048
|
A | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0036g0231 | 3 | HG02257.hp2 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.383-953A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087048 | ||||||
chr14:73087058
|
G | T | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-943G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087058 | ||||||
chr14:73087061
|
A | AATGTTAT | 380 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(377): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.383-940_383-939ins others(7): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087061 | ||||||
chr14:73087062
|
T | A | 380 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(377): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.383-939T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087062 | ||||||
chr14:73087081
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.383-920A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087081 | ||||||
chr14:73087108
|
T | C | 2 | a0001c0001t0006g0033a0001c0001t0006g0041 | 2 | HG00408.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.383-893T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087108 | ||||||
chr14:73087191
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.383-810T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087191 | ||||||
chr14:73087237
|
A | C | 31 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(28): Show | 31 | HG00558.hp1 HG00642.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.383-764A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087237 | ||||||
chr14:73087256
|
G | A | 1 | a0001c0001t0001g0376 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.383-745G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087256 | ||||||
chr14:73087333
|
GTTCT | G | 72 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(69): Show | 77 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.383-662_383-659del others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73087333 | |||||
chr14:73087396
|
C | CT | 23 | a0001c0001t0001g0348a0001c0001t0001g0372a0001c0001t0002g0073others(20): Show | 24 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.383-588dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73087396 | |||||
chr14:73087396
|
C | CTT | 18 | a0001c0001t0006g0027a0001c0001t0006g0028a0001c0001t0006g0029others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.383-589_383-588dup others(2): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73087396 | |||||
chr14:73087541
|
G | A | 1 | a0001c0001t0008g0009 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.383-460G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087541 | ||||||
chr14:73087544
|
C | T | 2 | a0001c0001t0018g0368a0001c0001t0018g0369 | 2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.383-457C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087544 | ||||||
chr14:73087552
|
C | T | 4 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(1): Show | 4 | HG02647.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-449C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087552 | ||||||
chr14:73087588
|
G | C | 1 | a0001c0002t0003g0270 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.383-413G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087588 | ||||||
chr14:73087617
|
G | C | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.383-384G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087617 | ||||||
chr14:73087631
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0002g0072 | 2 | HG01192.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.383-370G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087631 | ||||||
chr14:73087656
|
A | G | 1 | a0001c0002t0009g0281 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.383-345A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087656 | ||||||
chr14:73087686
|
C | T | 1 | a0001c0001t0016g0091 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.383-315C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087686 | ||||||
chr14:73087730
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.383-271T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087730 | ||||||
chr14:73087943
|
AT | A | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-50delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73087943 | |||||
chr14:73088176
|
G | A | 1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.543+15G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73088176 | ||||||
chr14:73088182
|
T | C | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.543+21T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73088182 | ||||||
chr14:73088361
|
T | A | 11 | a0001c0001t0007g0244a0001c0001t0007g0245a0001c0001t0007g0246others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+200T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73088361 | ||||||
chr14:73088463
|
G | A | 14 | a0001c0001t0001g0217a0001c0001t0005g0204a0001c0001t0005g0212others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.543+302G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73088463 | ||||||
chr14:73088620
|
A | T | 1 | a0001c0001t0002g0099 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.543+459A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73088620 | ||||||
chr14:73088717
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.543+556C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73088717 | ||||||
chr14:73088944
|
C | T | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+783C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73088944 | ||||||
chr14:73089063
|
C | A | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.543+902C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089063 | ||||||
chr14:73089205
|
A | C | 1 | a0001c0001t0001g0116 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.543+1044A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089205 | ||||||
chr14:73089295
|
C | A | 1 | a0001c0001t0005g0230 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.543+1134C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089295 | ||||||
chr14:73089304
|
C | G | 1 | a0001c0001t0004g0309 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.543+1143C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089304 | ||||||
chr14:73089387
|
C | T | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+1226C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089387 | ||||||
chr14:73089394
|
G | A | 1 | a0001c0001t0001g0359 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.543+1233G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089394 | ||||||
chr14:73089665
|
T | TTTTGTTT others(1): Show |
110 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0217others(107): Show | 115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.543+1517_543+1524d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73089665 | |||||
chr14:73089665
|
T | TTTTGTTT others(5): Show |
29 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(26): Show | 29 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.543+1513_543+1524d others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73089665 | |||||
chr14:73089665
|
T | TTTTGTTT others(9): Show |
3 | a0001c0001t0011g0047a0001c0001t0022g0043a0001c0001t0023g0045 | 3 | HG01074.hp2 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.543+1509_543+1524d others(18): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73089665 | |||||
chr14:73089665
|
T | TTTTGTTT others(13): Show |
1 | a0001c0001t0011g0048 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.543+1505_543+1524d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73089665 | |||||
chr14:73089665
|
T | TTTTGTTT others(17): Show |
3 | a0001c0001t0011g0046a0001c0001t0011g0049a0001c0001t0011g0050 | 3 | HG02486.hp1 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.543+1524_543+1525i others(26): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73089665 | |||||
chr14:73089708
|
C | T | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.543+1547C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089708 | ||||||
chr14:73089894
|
T | C | 7 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(4): Show | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+1733T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089894 | ||||||
chr14:73089964
|
C | G | 4 | a0001c0001t0013g0053a0001c0001t0013g0056a0001c0001t0013g0057others(1): Show | 4 | HG01496.hp2 HG01884.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+1803C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089964 | ||||||
chr14:73090057
|
C | G | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | HG01884.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.543+1896C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090057 | ||||||
chr14:73090075
|
C | T | 1 | a0001c0001t0001g0372 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.543+1914C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090075 | ||||||
chr14:73090133
|
C | T | 1 | a0001c0001t0007g0244 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.543+1972C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090133 | ||||||
chr14:73090216
|
A | G | 1 | a0001c0001t0002g0064 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.543+2055A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090216 | ||||||
chr14:73090294
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.543+2133A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090294 | ||||||
chr14:73090298
|
A | C | 1 | a0001c0001t0037g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.543+2137A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090298 | ||||||
chr14:73090330
|
C | T | 2 | a0001c0001t0008g0011a0001c0001t0008g0012 | 2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.543+2169C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090330 | ||||||
chr14:73090360
|
A | G | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+2199A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090360 | ||||||
chr14:73090465
|
G | A | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | HG01884.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.543+2304G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090465 | ||||||
chr14:73090677
|
C | T | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.543+2516C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090677 | ||||||
chr14:73090726
|
A | T | 1 | a0001c0001t0002g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.543+2565A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090726 | ||||||
chr14:73090741
|
G | A | 1 | a0001c0002t0003g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.543+2580G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090741 | ||||||
chr14:73090841
|
G | C | 56 | a0001c0001t0001g0051a0001c0001t0001g0321a0001c0001t0001g0322others(53): Show | 57 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.543+2680G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090841 | ||||||
chr14:73090864
|
A | G | 8 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007others(5): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.543+2703A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090864 | ||||||
chr14:73090888
|
ATTATATT others(4): Show |
A | 1 | a0001c0001t0001g0372 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.543+2741_543+2751d others(13): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73090888 | |||||
chr14:73090958
|
A | G | 16 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0029others(13): Show | 16 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.543+2797A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090958 | ||||||
chr14:73091089
|
C | T | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.543+2928C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73091089 | ||||||
chr14:73091281
|
G | A | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG01243.hp2 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+3120G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73091281 | ||||||
chr14:73091320
|
A | G | 1 | a0001c0001t0001g0372 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.543+3159A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73091320 | ||||||
chr14:73091352
|
C | T | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+3191C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73091352 | ||||||
chr14:73091418
|
T | C | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.543+3257T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73091418 | ||||||
chr14:73091424
|
G | A | 1 | a0001c0001t0005g0127 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.543+3263G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73091424 | ||||||
chr14:73091709
|
T | TA | 57 | a0001c0001t0001g0051a0001c0001t0001g0321a0001c0001t0001g0322others(54): Show | 58 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.543+3558dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73091709 | |||||
chr14:73091734
|
G | A | 1 | a0001c0001t0006g0039 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.543+3573G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73091734 | ||||||
chr14:73091877
|
C | CA | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+3725dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73091877 | |||||
chr14:73091934
|
A | AATG | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+3774_543+3775i others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73091934 | |||||
chr14:73091937
|
A | G | 14 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(11): Show | 14 | HG00733.hp2 HG01106.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.543+3776A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73091937 | ||||||
chr14:73092128
|
A | T | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.543+3967A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73092128 | ||||||
chr14:73092267
|
G | A | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+4106G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73092267 | ||||||
chr14:73092578
|
CT | C | 21 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(18): Show | 21 | HG00408.hp2 HG00544.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.544-4324delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73092578 | |||||
chr14:73092591
|
T | A | 2 | a0001c0001t0001g0339a0001c0001t0028g0351 | 2 | HG02074.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.544-4324T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73092591 | ||||||
chr14:73092610
|
A | C | 26 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(23): Show | 26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.544-4305A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73092610 | ||||||
chr14:73092638
|
A | G | 1 | a0001c0001t0032g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.544-4277A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73092638 | ||||||
chr14:73092648
|
G | A | 14 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(11): Show | 14 | HG00733.hp2 HG01106.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.544-4267G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73092648 | ||||||
chr14:73092858
|
T | C | 248 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(245): Show | 253 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.544-4057T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73092858 | ||||||
chr14:73092904
|
A | G | 1 | a0001c0002t0009g0281 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.544-4011A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73092904 | ||||||
chr14:73093152
|
A | T | 1 | a0001c0001t0001g0333 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.544-3763A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093152 | ||||||
chr14:73093545
|
C | T | 2 | a0001c0001t0018g0368a0001c0001t0018g0369 | 2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.544-3370C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093545 | ||||||
chr14:73093546
|
G | A | 27 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(24): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.544-3369G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093546 | ||||||
chr14:73093592
|
C | T | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.544-3323C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093592 | ||||||
chr14:73093732
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.544-3183C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093732 | ||||||
chr14:73093797
|
G | A | 27 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(24): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.544-3118G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093797 | ||||||
chr14:73093823
|
A | T | 5 | a0001c0001t0010g0003a0001c0001t0010g0238a0001c0001t0010g0239others(2): Show | 6 | HG01891.hp2 HG02145.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-3092A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093823 | ||||||
chr14:73093827
|
G | GA | 8 | a0001c0001t0001g0142a0001c0001t0001g0148a0001c0001t0001g0151others(5): Show | 8 | HG00609.hp1 HG00609.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-3081dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73093827 | |||||
chr14:73093852
|
G | A | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.544-3063G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093852 | ||||||
chr14:73093943
|
G | GT | 11 | a0001c0001t0001g0372a0001c0001t0004g0297a0001c0001t0004g0298others(8): Show | 11 | HG00741.hp2 HG01081.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-2968dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73093943 | |||||
chr14:73093948
|
G | GT | 16 | a0001c0001t0001g0157a0001c0001t0001g0165a0001c0001t0002g0099others(13): Show | 16 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.544-2949dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73093948 | |||||
chr14:73093948
|
G | GTT | 55 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(52): Show | 55 | HG00408.hp2 HG00544.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.544-2950_544-2949d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73093948 | |||||
chr14:73093948
|
G | T | 30 | a0001c0001t0001g0372a0001c0001t0004g0002a0001c0001t0004g0292others(27): Show | 32 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.544-2967G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093948 | ||||||
chr14:73093965
|
T | G | 1 | a0001c0001t0001g0374 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.544-2950T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093965 | ||||||
chr14:73093973
|
A | T | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.544-2942A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093973 | ||||||
chr14:73094045
|
G | A | 6 | a0001c0001t0001g0333a0001c0001t0011g0046a0001c0001t0011g0047others(3): Show | 6 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-2870G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094045 | ||||||
chr14:73094053
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.544-2862G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094053 | ||||||
chr14:73094101
|
G | A | 6 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(3): Show | 6 | HG01243.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-2814G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094101 | ||||||
chr14:73094181
|
C | A | 1 | a0001c0001t0005g0200 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.544-2734C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094181 | ||||||
chr14:73094204
|
C | T | 2 | a0001c0001t0019g0312a0001c0001t0019g0313 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.544-2711C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094204 | ||||||
chr14:73094295
|
TAGC | T | 5 | a0001c0001t0010g0003a0001c0001t0010g0238a0001c0001t0010g0239others(2): Show | 6 | HG01891.hp2 HG02145.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-2618_544-2616d others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73094295 | |||||
chr14:73094540
|
C | T | 2 | a0001c0001t0019g0312a0001c0001t0019g0313 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.544-2375C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094540 | ||||||
chr14:73094567
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.544-2348C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094567 | ||||||
chr14:73094616
|
A | G | 2 | a0001c0001t0004g0305a0001c0001t0004g0306 | 2 | HG00544.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.544-2299A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094616 | ||||||
chr14:73094621
|
C | T | 26 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(23): Show | 26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.544-2294C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094621 | ||||||
chr14:73094696
|
T | G | 1 | a0001c0002t0009g0284 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.544-2219T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094696 | ||||||
chr14:73094774
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0136 | 2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.544-2141C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094774 | ||||||
chr14:73094810
|
G | GGTGTGTG others(7): Show |
1 | a0001c0002t0003g0265 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.544-2086_544-2073d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73094810 | |||||
chr14:73094810
|
GGT | G | 117 | a0001c0001t0001g0051a0001c0001t0001g0150a0001c0001t0001g0153others(114): Show | 120 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.544-2074_544-2073d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73094810 | |||||
chr14:73094810
|
GGTGT | G | 204 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(201): Show | 206 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.544-2076_544-2073d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73094810 | |||||
chr14:73094810
|
GGTGTGTG others(1): Show |
G | 28 | a0001c0001t0001g0129a0001c0001t0004g0002a0001c0001t0004g0292others(25): Show | 30 | HG00099.hp2 HG00639.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.544-2080_544-2073d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73094810 | |||||
chr14:73094823
|
GTGTGTGT others(13): Show |
G | 8 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007others(5): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-2074_544-2055d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73094823 | |||||
chr14:73094833
|
G | C | 5 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(2): Show | 5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.544-2082G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094833 | ||||||
chr14:73094841
|
G | C | 1 | a0001c0001t0023g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.544-2074G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094841 | ||||||
chr14:73094843
|
C | G | 1 | a0001c0001t0023g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.544-2072C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094843 | ||||||
chr14:73095132
|
C | T | 2 | a0001c0001t0001g0349a0001c0001t0001g0350 | 2 | NA18991.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.544-1783C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095132 | ||||||
chr14:73095268
|
G | T | 1 | a0001c0001t0001g0331 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.544-1647G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095268 | ||||||
chr14:73095281
|
C | T | 5 | a0001c0001t0010g0003a0001c0001t0010g0238a0001c0001t0010g0239others(2): Show | 6 | HG01891.hp2 HG02145.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-1634C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095281 | ||||||
chr14:73095337
|
C | G | 380 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(377): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.544-1578C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095337 | ||||||
chr14:73095338
|
G | GC | 380 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(377): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.544-1577_544-1576i others(3): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095338 | ||||||
chr14:73095401
|
G | A | 1 | a0001c0001t0005g0202 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.544-1514G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095401 | ||||||
chr14:73095449
|
C | T | 1 | a0001c0001t0001g0330 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.544-1466C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095449 | ||||||
chr14:73095474
|
C | T | 26 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(23): Show | 26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.544-1441C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095474 | ||||||
chr14:73095482
|
T | C | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.544-1433T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095482 | ||||||
chr14:73095510
|
G | T | 1 | a0001c0001t0001g0141 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.544-1405G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095510 | ||||||
chr14:73095536
|
G | T | 1 | a0001c0001t0019g0312 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.544-1379G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095536 | ||||||
chr14:73095606
|
C | CA | 111 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(108): Show | 111 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.544-1296dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73095606 | |||||
chr14:73095667
|
C | T | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-1248C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095667 | ||||||
chr14:73095792
|
A | G | 26 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(23): Show | 26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.544-1123A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095792 | ||||||
chr14:73095945
|
C | T | 1 | a0001c0001t0002g0071 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.544-970C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095945 | ||||||
chr14:73096021
|
A | G | 1 | a0001c0001t0005g0204 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.544-894A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73096021 | ||||||
chr14:73096269
|
G | A | 1 | a0001c0002t0003g0278 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.544-646G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73096269 | ||||||
chr14:73096466
|
TTTTG | T | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-437_544-434del others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73096466 | |||||
chr14:73096536
|
A | G | 1 | a0001c0001t0023g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.544-379A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73096536 | ||||||
chr14:73096572
|
A | G | 6 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(3): Show | 6 | HG01884.hp1 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-343A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73096572 | ||||||
chr14:73096645
|
G | A | 1 | a0001c0002t0003g0271 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.544-270G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73096645 | ||||||
chr14:73096710
|
G | A | 1 | a0001c0001t0002g0065 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.544-205G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73096710 | ||||||
chr14:73096724
|
A | G | 2 | a0001c0001t0006g0036a0001c0001t0006g0037 | 2 | HG01081.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.544-191A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73096724 | ||||||
chr14:73096908
|
G | A | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | splice_region_variant&intron_variant | LOW | c.544-7G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73096908 | ||||||
chr14:73097131
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.729+31T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097131 | ||||||
chr14:73097134
|
C | T | 4 | a0001c0001t0004g0002a0001c0001t0004g0302a0001c0001t0004g0303others(1): Show | 6 | HG01168.hp1 HG01169.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.729+34C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097134 | ||||||
chr14:73097135
|
G | A | 1 | a0001c0001t0013g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.729+35G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097135 | ||||||
chr14:73097184
|
C | CTTTTTTC others(3): Show |
26 | a0001c0001t0001g0113a0001c0001t0001g0123a0001c0001t0001g0135others(23): Show | 27 | HG00642.hp1 HG01123.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.729+86_729+95dupTT others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097184 | |||||
chr14:73097191
|
C | CTTTTTTT others(4): Show |
10 | a0001c0001t0001g0139a0001c0001t0001g0189a0001c0001t0002g0052others(7): Show | 10 | HG00735.hp2 HG01175.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.729+95_729+96insTT others(9): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097191 | |||||
chr14:73097191
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0013g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.729+95_729+96insTT others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097191 | |||||
chr14:73097191
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0167 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.729+95_729+96insTT others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097191 | |||||
chr14:73097191
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0161 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.729+95_729+96insTT others(13): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097191 | |||||
chr14:73097192
|
T | TTTTTTTT others(2): Show |
132 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(129): Show | 135 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.729+95_729+96insTT others(7): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097192 | |||||
chr14:73097192
|
T | TTTTTTTT others(3): Show |
1 | a0001c0002t0003g0267 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.729+95_729+96insTT others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097192 | |||||
chr14:73097193
|
T | TTTTTTTT others(1): Show |
118 | a0001c0001t0001g0051a0001c0001t0001g0121a0001c0001t0001g0144others(115): Show | 121 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.729+95_729+96insTT others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097193 | |||||
chr14:73097193
|
TTTC | T | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.729+96_729+98delCT others(1): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097193 | |||||
chr14:73097194
|
T | TTTTTTTC | 8 | a0001c0001t0001g0156a0001c0001t0001g0376a0001c0001t0005g0340others(5): Show | 8 | HG00323.hp1 HG01346.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.729+95_729+96insTT others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097194 | |||||
chr14:73097196
|
C | T | 304 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(301): Show | 311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.729+96C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097196 | ||||||
chr14:73097201
|
T | C | 2 | a0001c0001t0002g0023a0001c0001t0023g0045 | 2 | HG00733.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.729+101T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097201 | ||||||
chr14:73097203
|
T | C | 1 | a0001c0001t0004g0293 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.729+103T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097203 | ||||||
chr14:73097204
|
T | C | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.729+104T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097204 | ||||||
chr14:73097232
|
A | C | 1 | a0001c0001t0036g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.729+132A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097232 | ||||||
chr14:73097233
|
C | G | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.729+133C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097233 | ||||||
chr14:73097239
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.729+139C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097239 | ||||||
chr14:73097358
|
G | A | 2 | a0001c0002t0003g0273a0001c0002t0003g0276 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.729+258G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097358 | ||||||
chr14:73097518
|
A | G | 1 | a0001c0001t0023g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.729+418A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097518 | ||||||
chr14:73097537
|
G | C | 1 | a0001c0002t0003g0261 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.729+437G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097537 | ||||||
chr14:73097615
|
A | G | 2 | a0001c0001t0006g0028a0001c0001t0026g0042 | 2 | NA18948.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.729+515A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097615 | ||||||
chr14:73097656
|
A | G | 1 | a0001c0001t0004g0300 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.729+556A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097656 | ||||||
chr14:73097667
|
G | T | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.729+567G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097667 | ||||||
chr14:73097835
|
T | G | 1 | a0001c0002t0003g0263 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.729+735T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097835 | ||||||
chr14:73097903
|
G | T | 1 | a0001c0001t0025g0034 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.729+803G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097903 | ||||||
chr14:73097933
|
A | G | 1 | a0001c0001t0039g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.729+833A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097933 | ||||||
chr14:73097977
|
G | T | 10 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0294others(7): Show | 12 | HG00099.hp2 HG00741.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.729+877G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097977 | ||||||
chr14:73098220
|
C | A | 1 | a0001c0001t0010g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.729+1120C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098220 | ||||||
chr14:73098420
|
C | A | 1 | a0001c0001t0007g0246 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.730-960C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098420 | ||||||
chr14:73098443
|
T | G | 8 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007others(5): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.730-937T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098443 | ||||||
chr14:73098531
|
A | G | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.730-849A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098531 | ||||||
chr14:73098556
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0167 | 2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.730-824T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098556 | ||||||
chr14:73098654
|
C | G | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.730-726C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098654 | ||||||
chr14:73098707
|
G | A | 2 | a0001c0001t0008g0011a0001c0001t0008g0012 | 2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.730-673G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098707 | ||||||
chr14:73098726
|
C | T | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-654C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098726 | ||||||
chr14:73098746
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.730-634C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098746 | ||||||
chr14:73098825
|
A | G | 1 | a0001c0001t0004g0295 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.730-555A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098825 | ||||||
chr14:73098877
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.730-503C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098877 | ||||||
chr14:73098892
|
C | T | 1 | a0001c0002t0009g0250 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.730-488C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098892 | ||||||
chr14:73099278
|
A | G | 2 | a0001c0001t0019g0312a0001c0001t0019g0313 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.730-102A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73099278 | ||||||
chr14:73099291
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.730-89C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73099291 | ||||||
chr14:73099299
|
A | T | 2 | a0001c0001t0002g0052a0001c0001t0002g0059 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.730-81A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73099299 | ||||||
chr14:73099332
|
G | A | 2 | a0001c0001t0002g0102a0001c0001t0002g0103 | 2 | HG01069.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.730-48G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73099332 | ||||||
chr14:73099552
|
A | G | 1 | a0001c0001t0004g0297 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.784-115A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 8/18 | chr14 | 73099552 | ||||||
chr14:73099623
|
A | G | 3 | a0001c0001t0002g0066a0001c0001t0002g0072a0001c0001t0002g0100 | 3 | HG01123.hp1 HG01192.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.784-44A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 8/18 | chr14 | 73099623 | ||||||
chr14:73099962
|
A | G | 2 | a0001c0001t0006g0027a0001c0001t0006g0038 | 2 | HG02056.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.867+212A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73099962 | ||||||
chr14:73100212
|
G | A | 14 | a0001c0001t0001g0217a0001c0001t0005g0204a0001c0001t0005g0212others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.867+462G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73100212 | ||||||
chr14:73100512
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.867+762A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73100512 | ||||||
chr14:73100578
|
A | G | 1 | a0001c0001t0013g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.867+828A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73100578 | ||||||
chr14:73100593
|
C | T | 1 | a0001c0001t0023g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.867+843C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73100593 | ||||||
chr14:73101041
|
A | C | 8 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007others(5): Show | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.867+1291A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73101041 | ||||||
chr14:73101133
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.867+1383A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73101133 | ||||||
chr14:73101474
|
G | GTA | 322 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(319): Show | 329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.868-1716_868-1715d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 73101474 | |||||
chr14:73101506
|
A | ATG | 7 | a0001c0001t0001g0372a0001c0001t0004g0299a0001c0001t0007g0287others(4): Show | 8 | HG01891.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.868-1680_868-1679d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 73101506 | |||||
chr14:73101506
|
ATG | A | 26 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(23): Show | 26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.868-1680_868-1679d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 73101506 | |||||
chr14:73101512
|
G | A | 2 | a0001c0001t0022g0043a0001c0001t0023g0045 | 2 | HG01074.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.868-1680G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73101512 | ||||||
chr14:73101512
|
G | GTA | 38 | a0001c0001t0001g0121a0001c0001t0002g0054a0001c0001t0002g0055others(35): Show | 40 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.868-1660_868-1659d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 73101512 | |||||
chr14:73101512
|
GTA | G | 40 | a0001c0001t0002g0079a0001c0002t0003g0001a0001c0002t0003g0247others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.868-1660_868-1659d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 73101512 | |||||
chr14:73101514
|
A | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG00558.hp2 NA18980.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.868-1678A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73101514 | ||||||
chr14:73101516
|
A | G | 1 | a0001c0002t0003g0253 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.868-1676A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73101516 | ||||||
chr14:73101549
|
C | T | 7 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(4): Show | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.868-1643C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73101549 | ||||||
chr14:73101826
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.868-1366A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73101826 | ||||||
chr14:73101961
|
G | A | 1 | a0001c0001t0023g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.868-1231G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73101961 | ||||||
chr14:73102257
|
T | C | 14 | a0001c0001t0001g0217a0001c0001t0005g0204a0001c0001t0005g0212others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.868-935T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102257 | ||||||
chr14:73102535
|
T | G | 2 | a0001c0001t0010g0003a0001c0001t0010g0241 | 3 | HG03209.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.868-657T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102535 | ||||||
chr14:73102632
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.868-560T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102632 | ||||||
chr14:73102635
|
C | T | 27 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(24): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.868-557C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102635 | ||||||
chr14:73102655
|
C | T | 1 | a0001c0001t0006g0039 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.868-537C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102655 | ||||||
chr14:73102767
|
A | G | 39 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(36): Show | 42 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.868-425A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102767 | ||||||
chr14:73102876
|
A | C | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.868-316A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102876 | ||||||
chr14:73102885
|
C | T | 2 | a0001c0001t0019g0312a0001c0001t0019g0313 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.868-307C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102885 | ||||||
chr14:73102959
|
T | G | 2 | a0001c0001t0002g0068a0001c0001t0002g0104 | 2 | NA18948.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.868-233T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102959 | ||||||
chr14:73103058
|
T | G | 1 | a0001c0001t0001g0345 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.868-134T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73103058 | ||||||
chr14:73103174
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.868-18G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73103174 | ||||||
chr14:73103781
|
T | G | 7 | a0001c0001t0002g0022a0001c0001t0002g0068a0001c0001t0002g0081others(4): Show | 7 | HG02015.hp1 HG02071.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1154+303T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103781 | ||||||
chr14:73103840
|
C | T | 1 | a0001c0001t0004g0299 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1154+362C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103840 | ||||||
chr14:73103890
|
TCTGTCTG others(24): Show |
T | 1 | a0001c0001t0001g0378 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1154+413_1154+443d others(33): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103890 | ||||||
chr14:73103897
|
GTCTGTCT others(13): Show |
G | 1 | a0001c0001t0006g0039 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1154+423_1154+442d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103897 | |||||
chr14:73103905
|
G | C | 2 | a0001c0001t0018g0368a0001c0001t0018g0369 | 2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1154+427G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103905 | ||||||
chr14:73103905
|
G | GTC | 8 | a0001c0001t0002g0022a0001c0001t0002g0060a0001c0001t0002g0074others(5): Show | 8 | HG01346.hp2 HG02135.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.1154+470_1154+471d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | |||||
chr14:73103905
|
G | GTCTC | 4 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0076others(1): Show | 4 | HG01192.hp2 HG01978.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154+468_1154+471d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | |||||
chr14:73103905
|
G | GTCTCTC | 4 | a0001c0001t0002g0075a0001c0001t0002g0101a0001c0001t0002g0381others(1): Show | 4 | HG01934.hp1 HG02148.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154+466_1154+471d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | |||||
chr14:73103905
|
GTC | G | 10 | a0001c0001t0002g0093a0001c0001t0004g0295a0001c0001t0004g0301others(7): Show | 10 | HG01361.hp2 HG01928.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.1154+470_1154+471d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | |||||
chr14:73103905
|
GTCTC | G | 10 | a0001c0001t0002g0108a0001c0001t0004g0292a0001c0001t0004g0293others(7): Show | 10 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.1154+468_1154+471d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | |||||
chr14:73103905
|
GTCTCTC | G | 4 | a0001c0001t0004g0298a0001c0001t0004g0309a0001c0002t0003g0247others(1): Show | 4 | HG03688.hp1 HG03942.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154+466_1154+471d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | |||||
chr14:73103905
|
GTCTCTCT others(1): Show |
G | 7 | a0001c0001t0006g0026a0001c0001t0006g0031a0001c0001t0006g0032others(4): Show | 7 | HG00735.hp1 HG03579.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.1154+464_1154+471d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | |||||
chr14:73103905
|
GTCTCTCT others(3): Show |
G | 10 | a0001c0001t0006g0027a0001c0001t0006g0029a0001c0001t0006g0038others(7): Show | 11 | HG01975.hp1 HG02056.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.1154+462_1154+471d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | |||||
chr14:73103905
|
GTCTCTCT others(5): Show |
G | 17 | a0001c0001t0001g0331a0001c0001t0001g0352a0001c0001t0001g0372others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.1154+460_1154+471d others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | |||||
chr14:73103905
|
GTCTCTCT others(7): Show |
G | 20 | a0001c0001t0006g0028a0001c0001t0006g0036a0001c0001t0006g0037others(17): Show | 23 | HG00423.hp1 HG00738.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1154+458_1154+471d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | |||||
chr14:73103905
|
GTCTCTCT others(9): Show |
G | 2 | a0001c0001t0007g0290a0001c0002t0003g0277 | 2 | HG01243.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1154+456_1154+471d others(18): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | |||||
chr14:73103905
|
GTCTCTCT others(13): Show |
G | 1 | a0001c0001t0010g0238 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1154+452_1154+471d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | |||||
chr14:73103909
|
C | G | 15 | a0001c0001t0001g0131a0001c0001t0001g0223a0001c0001t0001g0224others(12): Show | 15 | HG01358.hp2 HG01952.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1154+431C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103909 | ||||||
chr14:73103913
|
C | G | 1 | a0001c0001t0004g0304 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1154+435C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103913 | ||||||
chr14:73103923
|
C | G | 2 | a0001c0002t0009g0280a0001c0002t0009g0281 | 2 | HG00738.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1154+445C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103923 | ||||||
chr14:73103925
|
C | G | 1 | a0001c0001t0007g0290 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1154+447C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103925 | ||||||
chr14:73103926
|
TCTCTCTC others(25): Show |
T | 1 | a0001c0001t0001g0341 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1154+450_1154+481d others(34): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103926 | |||||
chr14:73103928
|
TCTCTCTC others(23): Show |
T | 2 | a0001c0001t0001g0332a0001c0001t0001g0342 | 2 | NA18939.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1154+452_1154+481d others(32): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103928 | |||||
chr14:73103930
|
TCTCTCTC others(15): Show |
T | 3 | a0001c0001t0007g0288a0001c0001t0007g0289a0001c0001t0023g0045 | 3 | HG01074.hp2 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1154+454_1154+475d others(24): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103930 | |||||
chr14:73103930
|
TCTCTCTC others(19): Show |
T | 5 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0343others(2): Show | 5 | HG02083.hp2 HG02630.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154+454_1154+479d others(28): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103930 | |||||
chr14:73103930
|
TCTCTCTC others(23): Show |
T | 9 | a0001c0001t0008g0005a0001c0001t0008g0007a0001c0001t0008g0009others(6): Show | 9 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1154+454_1154+483d others(32): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103930 | |||||
chr14:73103930
|
TCTCTCTC others(27): Show |
T | 3 | a0001c0001t0015g0020a0001c0001t0039g0018a0001c0004t0015g0019 | 3 | HG02818.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1154+454_1154+487d others(36): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103930 | |||||
chr14:73103932
|
TCTCTCTC others(11): Show |
T | 5 | a0001c0001t0001g0359a0001c0001t0007g0291a0001c0001t0026g0042others(2): Show | 5 | HG00642.hp2 HG01358.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154+456_1154+473d others(20): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103932 | |||||
chr14:73103932
|
TCTCTCTC others(13): Show |
T | 1 | a0001c0001t0019g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1154+456_1154+475d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103932 | |||||
chr14:73103932
|
TCTCTCTC others(15): Show |
T | 2 | a0001c0001t0005g0230a0001c0001t0019g0312 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1154+456_1154+477d others(24): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103932 | |||||
chr14:73103932
|
TCTCTCTC others(17): Show |
T | 16 | a0001c0001t0001g0051a0001c0001t0001g0217a0001c0001t0001g0233others(13): Show | 16 | HG00323.hp1 HG00639.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1154+456_1154+479d others(26): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103932 | |||||
chr14:73103932
|
TCTCTCTC others(19): Show |
T | 34 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(31): Show | 35 | HG00140.hp1 HG00423.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.1154+456_1154+481d others(28): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103932 | |||||
chr14:73103932
|
TCTCTCTC others(21): Show |
T | 3 | a0001c0001t0001g0355a0001c0001t0008g0006a0001c0001t0008g0008 | 3 | NA18944.hp2 NA19009.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1154+456_1154+483d others(30): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103932 | |||||
chr14:73103932
|
TCTCTCTC others(27): Show |
T | 1 | a0001c0001t0015g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1154+456_1154+489d others(36): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103932 | |||||
chr14:73103934
|
TCTCTCTC others(11): Show |
T | 3 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0049 | 3 | HG02486.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1154+458_1154+475d others(20): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103934 | |||||
chr14:73103934
|
TCTCTCTC others(13): Show |
T | 4 | a0001c0001t0002g0052a0001c0001t0002g0059a0001c0001t0007g0246others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154+458_1154+477d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103934 | |||||
chr14:73103934
|
TCTCTCTC others(15): Show |
T | 18 | a0001c0001t0001g0185a0001c0001t0001g0206a0001c0001t0001g0207others(15): Show | 18 | HG00733.hp2 HG01106.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1154+458_1154+479d others(24): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103934 | |||||
chr14:73103934
|
TCTCTCTC others(17): Show |
T | 11 | a0001c0001t0001g0124a0001c0001t0001g0225a0001c0001t0001g0226others(8): Show | 11 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1154+458_1154+481d others(26): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103934 | |||||
chr14:73103934
|
TCTCTCTC others(19): Show |
T | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0029g0354 | 3 | HG03098.hp1 HG06807.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1154+458_1154+483d others(28): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103934 | |||||
chr14:73103934
|
TCTCTCTC others(21): Show |
T | 1 | a0001c0001t0001g0373 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1154+458_1154+485d others(30): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103934 | |||||
chr14:73103936
|
TCTCTCTC others(7): Show |
T | 2 | a0001c0001t0006g0033a0001c0001t0006g0041 | 2 | HG00408.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1154+460_1154+473d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103936 | |||||
chr14:73103936
|
TCTCTCTC others(11): Show |
T | 8 | a0001c0001t0001g0172a0001c0001t0001g0208a0001c0001t0005g0201others(5): Show | 8 | HG01256.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1154+460_1154+477d others(20): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103936 | |||||
chr14:73103936
|
TCTCTCTC others(13): Show |
T | 11 | a0001c0001t0001g0120a0001c0001t0001g0141a0001c0001t0001g0187others(8): Show | 11 | HG01243.hp2 HG02602.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1154+460_1154+479d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103936 | |||||
chr14:73103936
|
TCTCTCTC others(15): Show |
T | 2 | a0001c0001t0001g0121a0001c0001t0001g0363 | 2 | HG02647.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1154+460_1154+481d others(24): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103936 | |||||
chr14:73103938
|
T | A | 2 | a0001c0001t0006g0040a0001c0002t0003g0265 | 2 | HG02738.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1154+460T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103938 | ||||||
chr14:73103938
|
TCTCTCTC others(7): Show |
T | 2 | a0001c0001t0001g0199a0001c0001t0005g0200 | 2 | HG00609.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1154+462_1154+475d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103938 | |||||
chr14:73103938
|
TCTCTCTC others(9): Show |
T | 12 | a0001c0001t0001g0113a0001c0001t0001g0140a0001c0001t0001g0151others(9): Show | 12 | HG00609.hp2 HG01496.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1154+462_1154+477d others(18): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103938 | |||||
chr14:73103938
|
TCTCTCTC others(11): Show |
T | 51 | a0001c0001t0001g0114a0001c0001t0001g0125a0001c0001t0001g0128others(48): Show | 51 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1154+462_1154+479d others(20): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103938 | |||||
chr14:73103938
|
TCTCTCTC others(13): Show |
T | 12 | a0001c0001t0001g0119a0001c0001t0001g0123a0001c0001t0001g0129others(9): Show | 12 | HG00642.hp1 HG00673.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1154+462_1154+481d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103938 | |||||
chr14:73103940
|
T | A | 2 | a0001c0001t0006g0040a0001c0002t0003g0265 | 2 | HG02738.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1154+462T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103940 | ||||||
chr14:73103940
|
TCTCTCTC others(7): Show |
T | 2 | a0001c0001t0001g0126a0001c0001t0001g0137 | 2 | HG02056.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1154+464_1154+477d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103940 | |||||
chr14:73103940
|
TCTCTCTC others(11): Show |
T | 3 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0131 | 3 | HG01952.hp1 HG03710.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1154+464_1154+481d others(20): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103940 | |||||
chr14:73103940
|
TCTCTCTC others(13): Show |
T | 2 | a0001c0001t0001g0116a0001c0001t0001g0118 | 2 | HG04184.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1154+464_1154+483d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103940 | |||||
chr14:73103942
|
T | A | 5 | a0001c0001t0006g0040a0001c0001t0010g0241a0001c0002t0003g0247others(2): Show | 5 | HG02738.hp1 HG03579.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154+464T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103942 | ||||||
chr14:73103942
|
TCTCTCTC others(7): Show |
T | 1 | a0001c0001t0004g0302 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1154+466_1154+479d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103942 | |||||
chr14:73103944
|
T | A | 18 | a0001c0001t0004g0296a0001c0001t0004g0299a0001c0001t0004g0306others(15): Show | 19 | HG00544.hp1 HG01361.hp2 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.1154+466T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103944 | ||||||
chr14:73103944
|
TCTCTCA | T | 3 | a0001c0001t0002g0064a0001c0001t0002g0079a0001c0001t0002g0379 | 3 | HG01516.hp2 HG03704.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.1154+468_1154+473d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103944 | |||||
chr14:73103944
|
TCTCTCAC others(1): Show |
T | 3 | a0001c0001t0002g0081a0001c0001t0004g0002a0001c0001t0004g0303 | 5 | HG01168.hp1 HG01169.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154+468_1154+475d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103944 | |||||
chr14:73103946
|
T | A | 51 | a0001c0001t0001g0331a0001c0001t0004g0296a0001c0001t0004g0297others(48): Show | 52 | HG00544.hp1 HG00544.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1154+468T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103946 | ||||||
chr14:73103948
|
T | A | 76 | a0001c0001t0001g0331a0001c0001t0001g0352a0001c0001t0002g0073others(73): Show | 80 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1154+470T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103948 | ||||||
chr14:73103948
|
T | TCTCA | 4 | a0001c0001t0002g0072a0001c0001t0002g0082a0001c0001t0002g0106others(1): Show | 4 | HG02071.hp1 NA18973.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154+471_1154+472i others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103948 | |||||
chr14:73103948
|
T | TCTCACAC others(3): Show |
1 | a0001c0001t0002g0111 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1154+471_1154+472i others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103948 | |||||
chr14:73103948
|
T | TCTCTCTC others(3): Show |
2 | a0001c0001t0002g0092a0001c0001t0002g0102 | 2 | HG01167.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1154+471_1154+472i others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103948 | |||||
chr14:73103948
|
T | TCTCTCTC others(5): Show |
1 | a0001c0001t0002g0103 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1154+471_1154+472i others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103948 | |||||
chr14:73103948
|
T | TCTCTCTC others(3): Show |
2 | a0001c0001t0002g0077a0001c0001t0034g0063 | 2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1154+471_1154+472i others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103948 | |||||
chr14:73103948
|
T | TCTCTCTC others(5): Show |
2 | a0001c0001t0002g0110a0001c0001t0002g0112 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1154+471_1154+472i others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103948 | |||||
chr14:73103948
|
T | TCTCTCTC others(7): Show |
1 | a0001c0001t0002g0078 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1154+471_1154+472i others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103948 | |||||
chr14:73103948
|
T | TCTCTCTC others(13): Show |
1 | a0001c0001t0002g0087 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1154+471_1154+472i others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103948 | |||||
chr14:73103950
|
A | T | 17 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0065others(14): Show | 17 | HG00733.hp1 HG01123.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1154+472A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103950 | ||||||
chr14:73103952
|
A | T | 4 | a0001c0001t0002g0022a0001c0001t0002g0071a0001c0001t0002g0074others(1): Show | 4 | NA18963.hp2 NA18990.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154+474A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103952 | ||||||
chr14:73103982
|
A | T | 2 | a0001c0001t0001g0331a0001c0001t0001g0352 | 2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1154+504A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103982 | ||||||
chr14:73103984
|
A | T | 3 | a0001c0001t0001g0331a0001c0001t0001g0352a0001c0001t0010g0241 | 3 | HG02698.hp1 HG03579.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1154+506A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103984 | ||||||
chr14:73103986
|
A | T | 9 | a0001c0001t0001g0331a0001c0001t0001g0352a0001c0001t0006g0040others(6): Show | 10 | HG01891.hp2 HG02145.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1154+508A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103986 | ||||||
chr14:73103988
|
A | T | 23 | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0001t0001g0156others(20): Show | 24 | HG01074.hp2 HG01361.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.1154+510A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103988 | ||||||
chr14:73103988
|
ACACACAC others(3): Show |
A | 1 | a0001c0001t0002g0380 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1154+512_1154+521d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103988 | |||||
chr14:73103990
|
A | T | 111 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0125others(108): Show | 112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1154+512A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103990 | ||||||
chr14:73103992
|
A | T | 224 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(221): Show | 227 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.1154+514A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103992 | ||||||
chr14:73103992
|
ACACT | A | 3 | a0001c0001t0002g0097a0001c0001t0002g0105a0001c0001t0002g0107 | 3 | HG02080.hp1 NA18951.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1154+516_1154+519d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103992 | |||||
chr14:73103994
|
A | T | 318 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(315): Show | 325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.1154+516A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103994 | ||||||
chr14:73103994
|
ACT | A | 3 | a0001c0001t0002g0090a0001c0001t0002g0096a0001c0001t0002g0098 | 3 | NA18975.hp1 NA18988.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1154+538_1154+539d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103994 | |||||
chr14:73103996
|
T | A | 27 | a0001c0001t0002g0022a0001c0001t0002g0064a0001c0001t0002g0065others(24): Show | 27 | HG00558.hp2 HG01123.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.1154+518T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103996 | ||||||
chr14:73103998
|
T | A | 2 | a0001c0001t0002g0064a0001c0001t0002g0381 | 2 | HG03704.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1154+520T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103998 | ||||||
chr14:73104109
|
C | G | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154+631C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104109 | ||||||
chr14:73104309
|
C | CTCCTAGT others(12): Show |
1 | a0001c0001t0002g0106 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1154+833_1154+851d others(21): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73104309 | |||||
chr14:73104311
|
C | T | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | HG01884.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1154+833C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104311 | ||||||
chr14:73104403
|
C | G | 1 | a0001c0001t0005g0204 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1154+925C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104403 | ||||||
chr14:73104422
|
G | T | 1 | a0001c0001t0001g0119 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1154+944G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104422 | ||||||
chr14:73104439
|
G | T | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1154+961G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104439 | ||||||
chr14:73104441
|
T | G | 2 | a0001c0001t0019g0312a0001c0001t0019g0313 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1154+963T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104441 | ||||||
chr14:73104511
|
A | G | 2 | a0001c0001t0012g0013a0001c0001t0012g0015 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1154+1033A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104511 | ||||||
chr14:73104698
|
C | T | 38 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(35): Show | 38 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.1155-1161C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104698 | ||||||
chr14:73104763
|
A | G | 1 | a0001c0002t0003g0249 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1155-1096A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104763 | ||||||
chr14:73104967
|
G | A | 7 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(4): Show | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1155-892G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104967 | ||||||
chr14:73105038
|
T | TAC | 7 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0372others(4): Show | 7 | HG02055.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1155-795_1155-794d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105038
|
T | TACAC | 33 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0249others(30): Show | 36 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.1155-797_1155-794d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105038
|
T | TACACAC | 8 | a0001c0001t0001g0218a0001c0001t0001g0223a0001c0001t0005g0242others(5): Show | 8 | HG02074.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1155-799_1155-794d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105038
|
T | TACACACA others(1): Show |
26 | a0001c0001t0001g0205a0001c0001t0001g0208a0001c0001t0001g0209others(23): Show | 28 | HG00099.hp2 HG00733.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1155-801_1155-794d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105038
|
T | TACACACA others(3): Show |
14 | a0001c0001t0001g0051a0001c0001t0001g0222a0001c0001t0001g0360others(11): Show | 14 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1155-803_1155-794d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105038
|
T | TACACACA others(5): Show |
9 | a0001c0001t0001g0217a0001c0001t0001g0337a0001c0001t0001g0363others(6): Show | 9 | HG01074.hp2 HG01891.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1155-805_1155-794d others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105038
|
T | TACACACA others(7): Show |
23 | a0001c0001t0001g0237a0001c0001t0001g0349a0001c0001t0001g0352others(20): Show | 23 | HG00733.hp1 HG01884.hp1 HG02148.hp2 others(20): Show |
intron_variant | MODIFIER | c.1155-807_1155-794d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105038
|
T | TACACACA others(9): Show |
57 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0333others(54): Show | 58 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1155-809_1155-794d others(18): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105038
|
T | TACACACA others(11): Show |
22 | a0001c0001t0001g0329a0001c0001t0001g0332a0001c0001t0001g0355others(19): Show | 23 | HG00323.hp2 HG01106.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.1155-811_1155-794d others(20): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105038
|
T | TACACACA others(13): Show |
27 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(24): Show | 27 | HG00558.hp2 HG01891.hp2 HG02132.hp1 others(24): Show |
intron_variant | MODIFIER | c.1155-813_1155-794d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105038
|
T | TACACACA others(15): Show |
19 | a0001c0001t0002g0054a0001c0001t0002g0099a0001c0001t0002g0379others(16): Show | 19 | HG01167.hp2 HG01169.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.1155-815_1155-794d others(24): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105038
|
T | TACACACA others(17): Show |
6 | a0001c0001t0004g0306a0001c0001t0004g0314a0001c0001t0008g0011others(3): Show | 6 | HG00544.hp1 HG01257.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1155-817_1155-794d others(26): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105038
|
T | TACACACA others(19): Show |
8 | a0001c0001t0001g0336a0001c0001t0004g0315a0001c0001t0004g0316others(5): Show | 8 | HG00323.hp1 HG00639.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.1155-819_1155-794d others(28): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105038
|
T | TACACACA others(25): Show |
2 | a0001c0001t0008g0009a0001c0001t0008g0010 | 2 | HG01168.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1155-794_1155-793i others(34): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105038
|
TAC | T | 22 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0001g0243others(19): Show | 22 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.1155-795_1155-794d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105038
|
TACAC | T | 93 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(90): Show | 93 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1155-797_1155-794d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105038
|
TACACAC | T | 4 | a0001c0001t0001g0124a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02717.hp2 HG06807.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1155-799_1155-794d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | |||||
chr14:73105066
|
G | C | 10 | a0001c0001t0001g0344a0001c0001t0001g0346a0001c0001t0001g0347others(7): Show | 10 | HG01074.hp2 HG02129.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1155-793G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73105066 | ||||||
chr14:73105126
|
C | CT | 60 | a0001c0001t0001g0051a0001c0001t0001g0225a0001c0001t0001g0233others(57): Show | 61 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1155-715dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105126 | |||||
chr14:73105126
|
C | CTT | 35 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0210others(32): Show | 35 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.1155-716_1155-715d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105126 | |||||
chr14:73105126
|
C | CTTTTTTT others(1): Show |
23 | a0001c0001t0006g0026a0001c0001t0006g0029a0001c0001t0006g0030others(20): Show | 23 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.1155-722_1155-715d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105126 | |||||
chr14:73105126
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0006g0027 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1155-724_1155-715d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105126 | |||||
chr14:73105126
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0011g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1155-725_1155-715d others(13): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105126 | |||||
chr14:73105126
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0011g0046a0001c0001t0011g0048a0001c0001t0011g0049others(1): Show | 4 | HG02486.hp1 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1155-726_1155-715d others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105126 | |||||
chr14:73105126
|
CT | C | 97 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(94): Show | 97 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.1155-715delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105126 | |||||
chr14:73105126
|
CTT | C | 73 | a0001c0001t0001g0378a0001c0001t0004g0002a0001c0001t0004g0292others(70): Show | 78 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1155-716_1155-715d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105126 | |||||
chr14:73105151
|
G | A | 1 | a0001c0001t0001g0356 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1155-708G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73105151 | ||||||
chr14:73105239
|
G | C | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1155-620G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73105239 | ||||||
chr14:73105429
|
A | G | 1 | a0001c0001t0007g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1155-430A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73105429 | ||||||
chr14:73105458
|
C | A | 1 | a0001c0001t0004g0293 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1155-401C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73105458 | ||||||
chr14:73105519
|
T | G | 1 | a0001c0001t0032g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1155-340T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73105519 | ||||||
chr14:73105707
|
T | C | 2 | a0001c0001t0001g0349a0001c0001t0001g0350 | 2 | NA18991.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1155-152T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73105707 | ||||||
chr14:73105720
|
A | C | 2 | a0001c0001t0001g0349a0001c0001t0001g0350 | 2 | NA18991.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1155-139A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73105720 | ||||||
chr14:73106099
|
C | T | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1377+18C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 11/18 | chr14 | 73106099 | ||||||
chr14:73106117
|
G | A | 47 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(44): Show | 48 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1377+36G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 11/18 | chr14 | 73106117 | ||||||
chr14:73106471
|
A | G | 1 | a0001c0001t0001g0372 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1467+186A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73106471 | ||||||
chr14:73106632
|
C | T | 14 | a0001c0001t0001g0217a0001c0001t0005g0204a0001c0001t0005g0212others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1467+347C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73106632 | ||||||
chr14:73106654
|
A | G | 2 | a0001c0001t0001g0349a0001c0001t0001g0350 | 2 | NA18991.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1467+369A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73106654 | ||||||
chr14:73106732
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1467+447C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73106732 | ||||||
chr14:73106824
|
C | T | 5 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0012g0015others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1467+539C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73106824 | ||||||
chr14:73106840
|
C | CT | 10 | a0001c0001t0008g0007a0001c0001t0008g0009a0001c0001t0008g0010others(7): Show | 11 | HG01168.hp2 HG01261.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1467+570dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr14 | 73106840 | |||||
chr14:73106840
|
CT | C | 78 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(75): Show | 79 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1467+570delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr14 | 73106840 | |||||
chr14:73106848
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0167 | 2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1467+563T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73106848 | ||||||
chr14:73106873
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1467+588C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73106873 | ||||||
chr14:73107151
|
G | A | 1 | a0001c0001t0001g0373 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1468-675G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73107151 | ||||||
chr14:73107195
|
G | A | 1 | a0001c0001t0002g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1468-631G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73107195 | ||||||
chr14:73107311
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1468-515T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73107311 | ||||||
chr14:73107379
|
CT | C | 18 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(15): Show | 18 | HG00733.hp2 HG01106.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1468-439delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr14 | 73107379 | |||||
chr14:73107601
|
T | C | 1 | a0001c0001t0002g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1468-225T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73107601 | ||||||
chr14:73107704
|
A | G | 7 | a0001c0001t0007g0244a0001c0001t0007g0245a0001c0001t0007g0246others(4): Show | 7 | HG02055.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1468-122A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73107704 | ||||||
chr14:73108056
|
G | A | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1541+157G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108056 | ||||||
chr14:73108059
|
G | T | 5 | a0001c0002t0009g0250a0001c0002t0009g0264a0001c0002t0009g0280others(2): Show | 5 | HG00735.hp1 HG00738.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1541+160G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108059 | ||||||
chr14:73108082
|
G | A | 1 | a0001c0001t0008g0012 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1541+183G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108082 | ||||||
chr14:73108302
|
A | G | 1 | a0001c0002t0003g0271 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1541+403A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108302 | ||||||
chr14:73108324
|
A | G | 2 | a0001c0002t0003g0247a0001c0002t0003g0262 | 2 | NA18947.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1541+425A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108324 | ||||||
chr14:73108335
|
C | T | 1 | a0001c0001t0004g0292 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1541+436C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108335 | ||||||
chr14:73108538
|
A | G | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1541+639A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108538 | ||||||
chr14:73108585
|
T | A | 1 | a0001c0001t0002g0108 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1541+686T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108585 | ||||||
chr14:73108755
|
C | T | 7 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(4): Show | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1542-587C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108755 | ||||||
chr14:73108977
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1542-365C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108977 | ||||||
chr14:73109015
|
C | G | 11 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007others(8): Show | 11 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1542-327C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73109015 | ||||||
chr14:73109106
|
T | C | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1542-236T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73109106 | ||||||
chr14:73109134
|
A | G | 1 | a0001c0001t0002g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1542-208A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73109134 | ||||||
chr14:73109190
|
C | G | 1 | a0001c0001t0001g0372 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1542-152C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73109190 | ||||||
chr14:73109210
|
A | G | 11 | a0001c0001t0007g0244a0001c0001t0007g0245a0001c0001t0007g0246others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1542-132A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73109210 | ||||||
chr14:73109315
|
G | T | 14 | a0001c0001t0002g0052a0001c0001t0002g0054a0001c0001t0002g0055others(11): Show | 15 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-27G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73109315 | ||||||
chr14:73109559
|
C | T | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1692+67C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109559 | ||||||
chr14:73109576
|
G | A | 1 | a0001c0001t0008g0005 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1692+84G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109576 | ||||||
chr14:73109609
|
C | T | 1 | a0001c0002t0003g0262 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1692+117C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109609 | ||||||
chr14:73109649
|
C | T | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1692+157C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109649 | ||||||
chr14:73109650
|
G | T | 1 | a0001c0003t0001g0377 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1692+158G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109650 | ||||||
chr14:73109693
|
C | T | 40 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1692+201C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109693 | ||||||
chr14:73109742
|
G | A | 1 | a0001c0001t0001g0372 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1692+250G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109742 | ||||||
chr14:73109834
|
C | G | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1692+342C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109834 | ||||||
chr14:73109915
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1692+423C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109915 | ||||||
chr14:73109995
|
G | A | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1692+503G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109995 | ||||||
chr14:73110025
|
C | T | 1 | a0001c0001t0001g0363 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1692+533C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73110025 | ||||||
chr14:73110053
|
T | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0036g0231 | 3 | HG02257.hp2 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1692+561T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73110053 | ||||||
chr14:73110184
|
C | CT | 19 | a0001c0001t0001g0205a0001c0001t0001g0208a0001c0001t0001g0209others(16): Show | 19 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1693-635dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr14 | 73110184 | |||||
chr14:73110282
|
G | A | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1693-549G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73110282 | ||||||
chr14:73110304
|
G | C | 308 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(305): Show | 314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1693-527G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73110304 | ||||||
chr14:73110317
|
A | G | 11 | a0001c0001t0007g0244a0001c0001t0007g0245a0001c0001t0007g0246others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1693-514A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73110317 | ||||||
chr14:73110346
|
C | G | 73 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(70): Show | 78 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1693-485C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73110346 | ||||||
chr14:73110574
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1693-257G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73110574 | ||||||
chr14:73110652
|
C | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0036g0231 | 3 | HG02257.hp2 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1693-179C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73110652 | ||||||
chr14:73111165
|
C | T | 1 | a0001c0001t0008g0009 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2017+10C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 15/18 | chr14 | 73111165 | ||||||
chr14:73111433
|
G | GAAGTATA others(4): Show |
1 | a0001c0001t0026g0042 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2018-94_2018-84dup others(11): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr14 | 73111433 | |||||
chr14:73111852
|
G | C | 1 | a0001c0001t0001g0372 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2292+50G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 16/18 | chr14 | 73111852 | ||||||
chr14:73112129
|
A | G | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2293-23A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 16/18 | chr14 | 73112129 | ||||||
chr14:73112413
|
G | GT | 314 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(311): Show | 321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.2391+172dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr14 | 73112413 | |||||
chr14:73112413
|
G | GTT | 8 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(5): Show | 8 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2391+171_2391+172d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr14 | 73112413 | |||||
chr14:73112546
|
A | G | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2391+296A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73112546 | ||||||
chr14:73112568
|
CT | C | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2391+319delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73112568 | ||||||
chr14:73112673
|
C | G | 139 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(136): Show | 139 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.2391+423C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73112673 | ||||||
chr14:73112826
|
C | T | 1 | a0001c0001t0001g0372 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2391+576C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73112826 | ||||||
chr14:73113037
|
G | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0123 | 2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2391+787G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113037 | ||||||
chr14:73113106
|
A | G | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2391+856A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113106 | ||||||
chr14:73113140
|
A | C | 6 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(3): Show | 6 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2391+890A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113140 | ||||||
chr14:73113250
|
T | C | 26 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(23): Show | 26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.2391+1000T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113250 | ||||||
chr14:73113368
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2392-918G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113368 | ||||||
chr14:73113431
|
C | G | 5 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(2): Show | 5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2392-855C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113431 | ||||||
chr14:73113507
|
A | G | 1 | a0001c0001t0002g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2392-779A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113507 | ||||||
chr14:73113517
|
C | T | 1 | a0001c0001t0004g0301 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2392-769C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113517 | ||||||
chr14:73113549
|
C | G | 34 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(31): Show | 34 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.2392-737C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113549 | ||||||
chr14:73113663
|
G | A | 1 | a0001c0001t0032g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2392-623G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113663 | ||||||
chr14:73113942
|
T | A | 2 | a0001c0001t0018g0368a0001c0001t0018g0369 | 2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2392-344T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113942 | ||||||
chr14:73113986
|
C | T | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2392-300C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113986 | ||||||
chr14:73113999
|
G | A | 1 | a0001c0001t0022g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2392-287G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113999 | ||||||
chr14:73114057
|
G | A | 2 | a0001c0001t0019g0312a0001c0001t0019g0313 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2392-229G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73114057 | ||||||
chr14:73114078
|
G | GTCAATTA others(23): Show |
3 | a0001c0001t0015g0020a0001c0001t0039g0018a0001c0004t0015g0019 | 3 | HG02818.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2392-208_2392-207i others(32): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73114078 | ||||||
chr14:73114080
|
C | A | 3 | a0001c0001t0015g0020a0001c0001t0039g0018a0001c0004t0015g0019 | 3 | HG02818.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2392-206C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73114080 | ||||||
chr14:73114081
|
T | A | 3 | a0001c0001t0015g0020a0001c0001t0039g0018a0001c0004t0015g0019 | 3 | HG02818.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2392-205T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73114081 | ||||||
chr14:73114083
|
C | T | 3 | a0001c0001t0015g0020a0001c0001t0039g0018a0001c0004t0015g0019 | 3 | HG02818.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2392-203C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73114083 | ||||||
chr14:73114120
|
C | G | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | HG01884.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2392-166C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73114120 | ||||||
chr14:73114366
|
T | C | 56 | a0001c0001t0001g0051a0001c0001t0001g0321a0001c0001t0001g0322others(53): Show | 57 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2439+33T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73114366 | ||||||
chr14:73114557
|
T | C | 10 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0294others(7): Show | 12 | HG00099.hp2 HG00741.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2439+224T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73114557 | ||||||
chr14:73114584
|
C | T | 29 | a0001c0001t0004g0002a0001c0001t0004g0292a0001c0001t0004g0293others(26): Show | 31 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2439+251C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73114584 | ||||||
chr14:73114666
|
C | T | 1 | a0001c0002t0003g0277 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2439+333C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73114666 | ||||||
chr14:73114762
|
C | T | 1 | a0001c0001t0007g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2439+429C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73114762 | ||||||
chr14:73114795
|
T | C | 1 | a0001c0001t0004g0319 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2439+462T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73114795 | ||||||
chr14:73114993
|
C | G | 39 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(36): Show | 42 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.2439+660C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73114993 | ||||||
chr14:73115028
|
G | A | 307 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(304): Show | 313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.2439+695G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115028 | ||||||
chr14:73115153
|
C | CGT | 22 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0162others(19): Show | 22 | HG00140.hp2 HG00408.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.2439+855_2439+856d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | |||||
chr14:73115153
|
C | CGTGT | 71 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(68): Show | 71 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.2439+853_2439+856d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | |||||
chr14:73115153
|
C | CGTGTGT | 30 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(27): Show | 30 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2439+851_2439+856d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | |||||
chr14:73115153
|
C | CGTGTGTG others(1): Show |
25 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0128others(22): Show | 25 | HG00558.hp1 HG00673.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2439+849_2439+856d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | |||||
chr14:73115153
|
C | CGTGTGTG others(3): Show |
3 | a0001c0001t0001g0149a0001c0001t0005g0204a0001c0001t0005g0228 | 3 | HG02559.hp2 HG02572.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2439+847_2439+856d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | |||||
chr14:73115153
|
CGT | C | 56 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0001t0001g0335others(53): Show | 58 | HG00140.hp1 HG00423.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.2439+855_2439+856d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | |||||
chr14:73115153
|
CGTGT | C | 47 | a0001c0001t0001g0051a0001c0001t0001g0345a0001c0001t0001g0361others(44): Show | 49 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.2439+853_2439+856d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | |||||
chr14:73115153
|
CGTGTGT | C | 6 | a0001c0001t0001g0360a0001c0001t0004g0293a0001c0001t0007g0288others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2439+851_2439+856d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | |||||
chr14:73115153
|
CGTGTGTG others(1): Show |
C | 8 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(5): Show | 8 | HG01074.hp2 HG02165.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2439+849_2439+856d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | |||||
chr14:73115153
|
CGTGTGTG others(3): Show |
C | 2 | a0001c0001t0001g0374a0001c0001t0016g0088 | 2 | HG00558.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2439+847_2439+856d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | |||||
chr14:73115153
|
CGTGTGTG others(5): Show |
C | 1 | a0001c0002t0003g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2439+845_2439+856d others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | |||||
chr14:73115191
|
T | G | 1 | a0001c0001t0004g0297 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2439+858T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115191 | ||||||
chr14:73115276
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2439+943G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115276 | ||||||
chr14:73115318
|
C | G | 4 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0005g0127others(1): Show | 4 | HG01943.hp2 HG01975.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.2439+985C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115318 | ||||||
chr14:73115401
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2439+1068C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115401 | ||||||
chr14:73115425
|
A | G | 9 | a0001c0001t0002g0052a0001c0001t0002g0054a0001c0001t0002g0055others(6): Show | 9 | HG01496.hp2 HG01884.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2439+1092A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115425 | ||||||
chr14:73115593
|
C | T | 39 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(36): Show | 42 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.2439+1260C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115593 | ||||||
chr14:73115644
|
CTG | C | 5 | a0001c0001t0001g0144a0001c0001t0001g0157a0001c0001t0001g0162others(2): Show | 5 | HG00140.hp2 HG01496.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2439+1314_2439+131 others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115644 | |||||
chr14:73115726
|
G | A | 39 | a0001c0002t0003g0001a0001c0002t0003g0247a0001c0002t0003g0248others(36): Show | 42 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.2439+1393G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115726 | ||||||
chr14:73115906
|
T | C | 7 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(4): Show | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2439+1573T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115906 | ||||||
chr14:73116070
|
T | C | 4 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(1): Show | 4 | HG02647.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2439+1737T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73116070 | ||||||
chr14:73116072
|
G | GT | 7 | a0001c0001t0001g0145a0001c0001t0001g0184a0001c0001t0001g0225others(4): Show | 7 | HG01361.hp2 HG02897.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.2439+1750dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73116072 | |||||
chr14:73116167
|
G | A | 1 | a0001c0002t0003g0268 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2439+1834G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73116167 | ||||||
chr14:73116590
|
G | C | 14 | a0001c0001t0001g0217a0001c0001t0005g0204a0001c0001t0005g0212others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2439+2257G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73116590 | ||||||
chr14:73116800
|
G | A | 1 | a0001c0001t0032g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2439+2467G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73116800 | ||||||
chr14:73117041
|
G | A | 2 | a0001c0001t0019g0312a0001c0001t0019g0313 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2440-2672G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117041 | ||||||
chr14:73117196
|
T | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0182 | 2 | NA18939.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.2440-2517T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117196 | ||||||
chr14:73117205
|
CTTTTCTT others(3): Show |
C | 1 | a0001c0001t0007g0246 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2440-2503_2440-249 others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117205 | |||||
chr14:73117205
|
CTTTTCTT others(6): Show |
C | 2 | a0001c0001t0026g0042a0001c0001t0037g0198 | 2 | NA18991.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.2440-2503_2440-249 others(17): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117205 | |||||
chr14:73117210
|
C | A | 3 | a0001c0001t0007g0288a0001c0001t0007g0291a0001c0001t0007g0320 | 3 | HG02451.hp2 HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2440-2503C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117210 | ||||||
chr14:73117210
|
C | CT | 7 | a0001c0001t0002g0061a0001c0001t0002g0068a0001c0001t0002g0077others(4): Show | 7 | HG02698.hp2 HG02738.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.2440-2469dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
C | CTT | 13 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0002g0082others(10): Show | 13 | HG01175.hp1 HG01256.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.2440-2470_2440-246 others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
C | CTTT | 10 | a0001c0001t0002g0065a0001c0001t0002g0072a0001c0001t0002g0095others(7): Show | 10 | HG00741.hp1 HG01123.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.2440-2471_2440-246 others(7): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
C | CTTTT | 6 | a0001c0001t0001g0223a0001c0001t0002g0023a0001c0001t0002g0064others(3): Show | 6 | HG00733.hp1 HG01106.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.2440-2472_2440-246 others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
C | CTTTTTTT others(2): Show |
4 | a0001c0001t0001g0208a0001c0001t0004g0002a0001c0001t0004g0296others(1): Show | 6 | HG01168.hp1 HG01169.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2440-2477_2440-246 others(13): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0001g0217a0001c0001t0004g0295a0001c0001t0004g0305others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.2440-2478_2440-246 others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0004g0299a0001c0001t0004g0306 | 2 | HG00544.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2440-2479_2440-246 others(15): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0004g0301 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2440-2482_2440-246 others(18): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0004g0302 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2440-2483_2440-246 others(19): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0005g0221 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2440-2484_2440-246 others(20): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0004g0297 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2440-2485_2440-246 others(21): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0004g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2440-2488_2440-246 others(24): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
C | CTTTTTTT others(16): Show |
2 | a0001c0001t0004g0304a0001c0001t0035g0311 | 2 | HG02040.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2440-2491_2440-246 others(27): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0004g0300 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2440-2495_2440-246 others(31): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
C | T | 4 | a0001c0001t0007g0244a0001c0001t0007g0245a0001c0001t0007g0285others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2440-2503C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117210 | ||||||
chr14:73117210
|
CT | C | 15 | a0001c0001t0001g0237a0001c0001t0002g0069a0001c0001t0002g0070others(12): Show | 15 | HG00323.hp2 HG00558.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.2440-2469delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
CTTTT | C | 7 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0011g0046others(4): Show | 7 | HG02486.hp1 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2440-2472_2440-246 others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
CTTTTTT | C | 13 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0131others(10): Show | 14 | HG01891.hp2 HG01952.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.2440-2474_2440-246 others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
CTTTTTTT | C | 34 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(31): Show | 34 | HG00140.hp2 HG00558.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.2440-2475_2440-246 others(11): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
CTTTTTTT others(1): Show |
C | 57 | a0001c0001t0001g0114a0001c0001t0001g0124a0001c0001t0001g0129others(54): Show | 57 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.2440-2476_2440-246 others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
CTTTTTTT others(2): Show |
C | 9 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0157others(6): Show | 9 | HG01074.hp2 HG02258.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2440-2477_2440-246 others(13): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0060others(1): Show | 4 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2440-2478_2440-246 others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0051a0001c0001t0001g0359 | 2 | HG00642.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.2440-2479_2440-246 others(15): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
CTTTTTTT others(5): Show |
C | 56 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(53): Show | 57 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2440-2480_2440-246 others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
CTTTTTTT others(6): Show |
C | 37 | a0001c0001t0001g0324a0001c0001t0001g0352a0001c0001t0002g0054others(34): Show | 37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.2440-2481_2440-246 others(17): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
CTTTTTTT others(7): Show |
C | 40 | a0001c0001t0002g0052a0001c0001t0002g0059a0001c0001t0006g0037others(37): Show | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.2440-2482_2440-246 others(18): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0032g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2440-2483_2440-246 others(19): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117210
|
CTTTTTTT others(13): Show |
C | 3 | a0001c0001t0001g0113a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | NA18980.hp2 NA19011.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2440-2488_2440-246 others(24): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | |||||
chr14:73117211
|
T | A | 2 | a0001c0001t0007g0290a0001c0001t0021g0286 | 2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2440-2502T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117211 | ||||||
chr14:73117212
|
T | A | 1 | a0001c0001t0007g0289 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2440-2501T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117212 | ||||||
chr14:73117215
|
T | C | 1 | a0001c0001t0002g0070 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2440-2498T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117215 | ||||||
chr14:73117220
|
T | A | 1 | a0001c0001t0007g0246 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2440-2493T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117220 | ||||||
chr14:73117220
|
T | C | 5 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(2): Show | 5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2440-2493T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117220 | ||||||
chr14:73117224
|
T | C | 1 | a0001c0001t0026g0042 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2440-2489T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117224 | ||||||
chr14:73117225
|
T | C | 1 | a0001c0001t0023g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2440-2488T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117225 | ||||||
chr14:73117336
|
A | G | 1 | a0001c0001t0002g0107 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2440-2377A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117336 | ||||||
chr14:73117385
|
G | A | 5 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(2): Show | 5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2440-2328G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117385 | ||||||
chr14:73117441
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0123 | 2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2440-2272G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117441 | ||||||
chr14:73117572
|
G | C | 7 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(4): Show | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2440-2141G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117572 | ||||||
chr14:73117649
|
G | A | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | HG01884.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2440-2064G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117649 | ||||||
chr14:73117777
|
T | A | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440-1936T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117777 | ||||||
chr14:73117814
|
A | T | 1 | a0001c0001t0001g0218 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2440-1899A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117814 | ||||||
chr14:73117881
|
C | T | 33 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(30): Show | 33 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.2440-1832C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117881 | ||||||
chr14:73117988
|
A | G | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2440-1725A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117988 | ||||||
chr14:73118313
|
TA | T | 7 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0190others(4): Show | 7 | NA18944.hp1 NA18971.hp2 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.2440-1395delA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73118313 | |||||
chr14:73118407
|
G | A | 4 | a0001c0002t0003g0261a0001c0002t0003g0271a0001c0002t0003g0272others(1): Show | 4 | HG02165.hp1 HG02523.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440-1306G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118407 | ||||||
chr14:73118477
|
CA | C | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG01243.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2440-1235delA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118477 | ||||||
chr14:73118478
|
A | G | 302 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(299): Show | 308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.2440-1235A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118478 | ||||||
chr14:73118479
|
G | GA | 7 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(4): Show | 7 | HG02486.hp1 HG02683.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2440-1219dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73118479 | |||||
chr14:73118480
|
A | G | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG01243.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2440-1233A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118480 | ||||||
chr14:73118589
|
T | C | 6 | a0001c0001t0011g0046a0001c0001t0011g0047a0001c0001t0011g0048others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2440-1124T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118589 | ||||||
chr14:73118599
|
G | A | 1 | a0001c0002t0003g0253 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2440-1114G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118599 | ||||||
chr14:73118709
|
T | G | 4 | a0001c0001t0015g0020a0001c0001t0015g0021a0001c0001t0039g0018others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440-1004T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118709 | ||||||
chr14:73118775
|
T | TTA | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2440-936_2440-935d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73118775 | |||||
chr14:73118868
|
A | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0167 | 2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.2440-845A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118868 | ||||||
chr14:73118894
|
G | A | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | HG01884.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2440-819G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118894 | ||||||
chr14:73118966
|
G | A | 1 | a0001c0001t0023g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2440-747G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118966 | ||||||
chr14:73119165
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2440-548C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119165 | ||||||
chr14:73119180
|
G | A | 37 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(34): Show | 37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.2440-533G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119180 | ||||||
chr14:73119270
|
T | G | 1 | a0001c0001t0018g0368 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2440-443T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119270 | ||||||
chr14:73119333
|
C | T | 1 | a0001c0002t0003g0269 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2440-380C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119333 | ||||||
chr14:73119334
|
G | A | 1 | a0001c0001t0001g0372 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2440-379G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119334 | ||||||
chr14:73119355
|
T | A | 2 | a0001c0001t0002g0052a0001c0001t0002g0059 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2440-358T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119355 | ||||||
chr14:73119368
|
T | C | 322 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0114others(319): Show | 329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.2440-345T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119368 | ||||||
chr14:73119432
|
G | A | 168 | a0001c0001t0001g0051a0001c0001t0001g0321a0001c0001t0001g0322others(165): Show | 174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.2440-281G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119432 | ||||||
chr14:73119442
|
T | A | 18 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2440-271T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119442 | ||||||
chr14:73119507
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2440-206C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119507 | ||||||
chr14:73119565
|
A | G | 2 | a0001c0001t0018g0368a0001c0001t0018g0369 | 2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2440-148A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119565 | ||||||
chr14:73119626
|
G | GA | 5 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0012g0015others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2440-82dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73119626 |