geneid | 57731 |
---|---|
ensemblid | ENSG00000160460.17 |
hgncid | 14896 |
symbol | SPTBN4 |
name | spectrin beta, non-erythrocytic 4 |
refseq_nuc | NM_020971.3 |
refseq_prot | NP_066022.2 |
ensembl_nuc | ENST00000598249.6 |
ensembl_prot | ENSP00000469242.1 |
mane_status | MANE Select |
chr | chr19 |
start | 40467001 |
end | 40576464 |
strand | + |
ver | v1.2 |
region | chr19:40467001-40576464 |
region5000 | chr19:40462001-40581464 |
regionname0 | SPTBN4_chr19_40467001_40576464 |
regionname5000 | SPTBN4_chr19_40462001_40581464 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 2564 | 114 | 24 | 22 | 47 | 7 | 12 | 33 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002 | 0/0 | 2564 | 39 | 17 | 7 | 5 | 4 | 6 | 4 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0003 | 0/0 | 2564 | 24 | 6 | 9 | 4 | 0 | 5 | 3 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0004 | 0/0 | 2564 | 21 | 12 | 4 | 0 | 1 | 4 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0005 | 0/0 | 2564 | 11 | 8 | 1 | 0 | 0 | 2 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0006 | 0/0 | 2564 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0007 | 0/0 | 2564 | 3 | 0 | 1 | 0 | 1 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0008 | 0/0 | 2564 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0009 | 0/0 | 2564 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0010 | 0/0 | 2564 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0011 | 0/0 | 2564 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0012 | 0/0 | 2564 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0013 | 0/0 | 2564 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0014 | 0/0 | 2564 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0015 | 0/0 | 2564 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0016 | 0/0 | 2564 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0017 | 0/0 | 2564 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0018 | 0/0 | 2564 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0019 | 0/0 | 2564 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0020 | 0/0 | 2564 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0021 | 0/0 | 2564 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0022 | 0/0 | 2564 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0023 | 0/0 | 2564 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 7695 | 66 | 2 | 17 | 33 | 3 | 9 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0002 | 0/0 | 7695 | 19 | 9 | 1 | 6 | 1 | 2 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0003 | 0/0 | 7695 | 17 | 6 | 2 | 3 | 3 | 3 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0004 | 0/0 | 7695 | 11 | 4 | 2 | 2 | 0 | 3 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0005 | 0/0 | 7695 | 11 | 0 | 8 | 0 | 0 | 3 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0006 | 0/0 | 7695 | 11 | 6 | 1 | 4 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0007 | 0/0 | 7695 | 10 | 2 | 4 | 0 | 1 | 3 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0008 | 0/0 | 7695 | 10 | 6 | 1 | 2 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0009 | 0/0 | 7695 | 8 | 6 | 0 | 0 | 0 | 2 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0010 | 0/0 | 7695 | 8 | 5 | 1 | 0 | 1 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0011 | 0/0 | 7695 | 4 | 4 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0012 | 0/0 | 7695 | 4 | 0 | 1 | 3 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0013 | 0/0 | 7695 | 3 | 3 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0014 | 0/0 | 7695 | 3 | 3 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0015 | 0/0 | 7695 | 3 | 3 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0016 | 0/0 | 7695 | 2 | 2 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0017 | 0/0 | 7695 | 2 | 0 | 0 | 2 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0018 | 0/0 | 7695 | 2 | 0 | 0 | 0 | 0 | 2 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0019 | 0/0 | 7695 | 2 | 0 | 2 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0020 | 0/0 | 7695 | 2 | 1 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0021 | 0/0 | 7695 | 2 | 1 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0022 | 0/0 | 7695 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0023 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0024 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0025 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0026 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0027 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0028 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0029 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0030 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0031 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0032 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0033 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0034 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0035 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0036 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0037 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0038 | 0/0 | 7695 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0039 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0040 | 0/0 | 7695 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0041 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0042 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0043 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0044 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0045 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0046 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0047 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0048 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0049 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0050 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0051 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0052 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0053 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0054 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
c0055 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1216 | 219 | 73 | 46 | 56 | 12 | 30 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
t0002 | 0/0 | 1216 | 5 | 0 | 2 | 0 | 2 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
t0003 | 0/0 | 1216 | 2 | 2 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
t0004 | 0/0 | 1216 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
t0005 | 0/0 | 1216 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
t0006 | 0/0 | 1216 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
t0007 | 0/0 | 1216 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
t0008 | 0/0 | 1216 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
t0009 | 0/0 | 1216 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
t0010 | 0/0 | 1216 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
t0011 | 0/0 | 1216 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 7695 | 66 | 2 | 17 | 33 | 3 | 9 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0002 | 0/0 | 7695 | 19 | 9 | 1 | 6 | 1 | 2 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0008 | 0/0 | 7695 | 10 | 6 | 1 | 2 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0010 | 0/0 | 7695 | 8 | 5 | 1 | 0 | 1 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0012 | 0/0 | 7695 | 4 | 0 | 1 | 3 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0017 | 0/0 | 7695 | 2 | 0 | 0 | 2 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0033 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0038 | 0/0 | 7695 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0041 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0048 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0054 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002c0003 | 0/0 | 7695 | 17 | 6 | 2 | 3 | 3 | 3 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002c0004 | 0/0 | 7695 | 11 | 4 | 2 | 2 | 0 | 3 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002c0015 | 0/0 | 7695 | 3 | 3 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002c0019 | 0/0 | 7695 | 2 | 0 | 2 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002c0020 | 0/0 | 7695 | 2 | 1 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002c0021 | 0/0 | 7695 | 2 | 1 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002c0034 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002c0045 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0003c0005 | 0/0 | 7695 | 11 | 0 | 8 | 0 | 0 | 3 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0003c0006 | 0/0 | 7695 | 11 | 6 | 1 | 4 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0003c0018 | 0/0 | 7695 | 2 | 0 | 0 | 0 | 0 | 2 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0004c0007 | 0/0 | 7695 | 10 | 2 | 4 | 0 | 1 | 3 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0004c0011 | 0/0 | 7695 | 4 | 4 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0004c0014 | 0/0 | 7695 | 3 | 3 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0004c0016 | 0/0 | 7695 | 2 | 2 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0004c0025 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0004c0027 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0005c0009 | 0/0 | 7695 | 8 | 6 | 0 | 0 | 0 | 2 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0005c0023 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0005c0026 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0005c0029 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0006c0043 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0006c0044 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0006c0053 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0007c0039 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0007c0047 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0007c0049 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0008c0013 | 0/0 | 7695 | 3 | 3 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0009c0024 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0009c0030 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0010c0055 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0011c0042 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0012c0050 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0013c0037 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0014c0040 | 0/0 | 7695 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0015c0035 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0016c0046 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0017c0036 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0018c0052 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0019c0051 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0020c0028 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0021c0031 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0022c0032 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0023c0022 | 0/0 | 7695 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 8910 | 65 | 2 | 17 | 32 | 3 | 9 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0001t0006 | 0/0 | 8910 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0002t0001 | 0/0 | 8910 | 15 | 7 | 1 | 6 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0002t0002 | 0/0 | 8910 | 2 | 0 | 0 | 0 | 1 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0002t0003 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0002t0005 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0008t0001 | 0/0 | 8910 | 10 | 6 | 1 | 2 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0010t0001 | 0/0 | 8910 | 7 | 4 | 1 | 0 | 1 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0010t0008 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0012t0001 | 0/0 | 8910 | 4 | 0 | 1 | 3 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0017t0001 | 0/0 | 8910 | 2 | 0 | 0 | 2 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0033t0001 | 0/0 | 8910 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0038t0001 | 0/0 | 8910 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0041t0001 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0048t0002 | 0/0 | 8910 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0001c0054t0001 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002c0003t0001 | 0/0 | 8910 | 17 | 6 | 2 | 3 | 3 | 3 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002c0004t0001 | 0/0 | 8910 | 11 | 4 | 2 | 2 | 0 | 3 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002c0015t0001 | 0/0 | 8910 | 3 | 3 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002c0019t0001 | 0/0 | 8910 | 2 | 0 | 2 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002c0020t0001 | 0/0 | 8910 | 2 | 1 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002c0021t0001 | 0/0 | 8910 | 2 | 1 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002c0034t0001 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0002c0045t0001 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0003c0005t0001 | 0/0 | 8910 | 8 | 0 | 6 | 0 | 0 | 2 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0003c0005t0002 | 0/0 | 8910 | 2 | 0 | 2 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0003c0005t0011 | 0/0 | 8910 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0003c0006t0001 | 0/0 | 8910 | 10 | 6 | 1 | 3 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0003c0006t0004 | 0/0 | 8910 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0003c0018t0001 | 0/0 | 8910 | 2 | 0 | 0 | 0 | 0 | 2 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0004c0007t0001 | 0/0 | 8910 | 8 | 0 | 4 | 0 | 1 | 3 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0004c0007t0003 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0004c0007t0010 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0004c0011t0001 | 0/0 | 8910 | 4 | 4 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0004c0014t0001 | 0/0 | 8910 | 3 | 3 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0004c0016t0001 | 0/0 | 8910 | 2 | 2 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0004c0025t0001 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0004c0027t0001 | 0/0 | 8910 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0005c0009t0001 | 0/0 | 8910 | 7 | 5 | 0 | 0 | 0 | 2 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0005c0009t0009 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0005c0023t0001 | 0/0 | 8910 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0005c0026t0001 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0005c0029t0001 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0006c0043t0001 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0006c0044t0001 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0006c0053t0001 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0007c0039t0001 | 0/0 | 8910 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0007c0047t0001 | 0/0 | 8910 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0007c0049t0001 | 0/0 | 8910 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0008c0013t0001 | 0/0 | 8910 | 3 | 3 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0009c0024t0001 | 0/0 | 8910 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0009c0030t0007 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0010c0055t0001 | 0/0 | 8910 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0011c0042t0001 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0012c0050t0001 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0013c0037t0001 | 0/0 | 8910 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0014c0040t0001 | 0/0 | 8910 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0015c0035t0001 | 0/0 | 8910 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0016c0046t0001 | 0/0 | 8910 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0017c0036t0001 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0018c0052t0001 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0019c0051t0001 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0020c0028t0001 | 0/0 | 8910 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0021c0031t0001 | 0/0 | 8910 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0022c0032t0001 | 0/0 | 8910 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
a0023c0022t0001 | 0/0 | 8910 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | copy fasta | chr19 | 40462001 | 40581464 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0001t0006g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0002t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0008t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0008t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0008t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0008t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0008t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0008t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0008t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0008t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0008t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0008t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0010t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0010t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0010t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0010t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0010t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0010t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0010t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0010t0008g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0012t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0012t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0012t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0012t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0017t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0017t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0033t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0038t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0041t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0048t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0001c0054t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0004t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0004t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0004t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0004t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0004t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0004t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0015t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0015t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0015t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0019t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0019t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0020t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0020t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0021t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0021t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0034t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0002c0045t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0005t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0005t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0005t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0005t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0005t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0005t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0005t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0005t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0005t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0005t0011g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0006t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0006t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0006t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0006t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0006t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0006t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0006t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0006t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0006t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0006t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0006t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0018t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0003c0018t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0007t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0007t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0007t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0007t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0007t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0007t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0007t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0007t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0007t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0007t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0011t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0011t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0011t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0011t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0014t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0014t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0014t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0016t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0016t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0025t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0004c0027t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0005c0009t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0005c0009t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0005c0009t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0005c0009t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0005c0009t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0005c0009t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0005c0009t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0005c0009t0009g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0005c0023t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0005c0026t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0005c0029t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0006c0043t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0006c0044t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0006c0053t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0007c0039t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0007c0047t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0007c0049t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0008c0013t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0008c0013t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0008c0013t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0009c0024t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0009c0030t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0010c0055t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0011c0042t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0012c0050t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0013c0037t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0014c0040t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0015c0035t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0016c0046t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0017c0036t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0018c0052t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0019c0051t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0020c0028t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0021c0031t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0022c0032t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
a0023c0022t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0009 | c0024 | t0001 | g0176 | EUR | GBR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG00099 | hp2 | a0001 | c0048 | t0002 | g0206 | EUR | GBR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG00140 | hp1 | a0002 | c0020 | t0001 | g0157 | EUR | GBR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG00140 | hp2 | a0004 | c0007 | t0001 | g0187 | EUR | GBR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG00280 | hp1 | a0001 | c0010 | t0001 | g0054 | EUR | FIN | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG00280 | hp2 | a0001 | c0008 | t0001 | g0117 | EUR | FIN | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG00642 | hp1 | a0004 | c0007 | t0001 | g0140 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG00738 | hp1 | a0004 | c0007 | t0001 | g0139 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG00738 | hp2 | a0004 | c0007 | t0001 | g0186 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG00741 | hp2 | a0022 | c0032 | t0001 | g0006 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01070 | hp1 | a0010 | c0055 | t0001 | g0020 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01070 | hp2 | a0003 | c0005 | t0001 | g0211 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01071 | hp1 | a0003 | c0005 | t0001 | g0210 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01071 | hp2 | a0001 | c0033 | t0001 | g0112 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01074 | hp1 | a0005 | c0023 | t0001 | g0191 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01081 | hp1 | a0002 | c0003 | t0001 | g0101 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01081 | hp2 | a0002 | c0004 | t0001 | g0069 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01099 | hp1 | a0002 | c0004 | t0001 | g0104 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01099 | hp2 | a0004 | c0007 | t0001 | g0004 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01106 | hp1 | a0002 | c0003 | t0001 | g0165 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01106 | hp2 | a0015 | c0035 | t0001 | g0106 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01109 | hp2 | a0003 | c0006 | t0001 | g0166 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01168 | hp2 | a0003 | c0005 | t0002 | g0208 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01169 | hp1 | a0003 | c0005 | t0002 | g0207 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01169 | hp2 | a0001 | c0012 | t0001 | g0039 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01175 | hp2 | a0003 | c0005 | t0001 | g0050 | AMR | PUR | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01255 | hp1 | a0003 | c0005 | t0001 | g0059 | AMR | CLM | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01257 | hp1 | a0003 | c0005 | t0001 | g0015 | AMR | CLM | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01257 | hp2 | a0001 | c0008 | t0001 | g0160 | AMR | CLM | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01261 | hp1 | a0002 | c0019 | t0001 | g0043 | AMR | CLM | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01358 | hp2 | a0002 | c0019 | t0001 | g0162 | AMR | CLM | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0228 | AMR | CLM | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01516 | hp1 | a0007 | c0039 | t0001 | g0118 | EUR | IBS | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01517 | hp1 | a0002 | c0003 | t0001 | g0016 | EUR | IBS | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01884 | hp1 | a0003 | c0006 | t0001 | g0213 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01891 | hp1 | a0005 | c0009 | t0001 | g0148 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01891 | hp2 | a0004 | c0007 | t0003 | g0002 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01928 | hp2 | a0003 | c0005 | t0001 | g0129 | AMR | PEL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01934 | hp1 | a0007 | c0047 | t0001 | g0209 | AMR | PEL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01978 | hp2 | a0002 | c0021 | t0001 | g0010 | AMR | PEL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02027 | hp2 | a0003 | c0006 | t0001 | g0035 | EAS | KHV | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02055 | hp1 | a0021 | c0031 | t0001 | g0057 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02055 | hp2 | a0001 | c0010 | t0001 | g0149 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02056 | hp1 | a0014 | c0040 | t0001 | g0218 | EAS | KHV | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | KHV | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | KHV | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02132 | hp2 | a0002 | c0003 | t0001 | g0034 | EAS | KHV | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02135 | hp1 | a0023 | c0022 | t0001 | g0012 | EAS | KHV | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02145 | hp1 | a0002 | c0003 | t0001 | g0197 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02145 | hp2 | a0003 | c0006 | t0001 | g0227 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02257 | hp1 | a0001 | c0054 | t0001 | g0090 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02257 | hp2 | a0001 | c0008 | t0001 | g0155 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02258 | hp1 | a0004 | c0007 | t0010 | g0136 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02258 | hp2 | a0002 | c0004 | t0001 | g0029 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02280 | hp1 | a0004 | c0014 | t0001 | g0058 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02280 | hp2 | a0002 | c0045 | t0001 | g0088 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02451 | hp1 | a0004 | c0016 | t0001 | g0003 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02451 | hp2 | a0005 | c0009 | t0009 | g0190 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02572 | hp1 | a0001 | c0008 | t0001 | g0061 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02572 | hp2 | a0006 | c0043 | t0001 | g0126 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02602 | hp2 | a0002 | c0003 | t0001 | g0073 | SAS | PJL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02615 | hp1 | a0004 | c0025 | t0001 | g0056 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02615 | hp2 | a0003 | c0006 | t0001 | g0132 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02630 | hp1 | a0019 | c0051 | t0001 | g0220 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02630 | hp2 | a0005 | c0009 | t0001 | g0007 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02647 | hp1 | a0005 | c0029 | t0001 | g0141 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02647 | hp2 | a0005 | c0009 | t0001 | g0008 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02717 | hp1 | a0017 | c0036 | t0001 | g0111 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02717 | hp2 | a0002 | c0021 | t0001 | g0219 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02723 | hp1 | a0005 | c0009 | t0001 | g0189 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02723 | hp2 | a0012 | c0050 | t0001 | g0023 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02738 | hp1 | a0007 | c0049 | t0001 | g0185 | SAS | PJL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02809 | hp1 | a0003 | c0006 | t0001 | g0215 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02809 | hp2 | a0002 | c0004 | t0001 | g0200 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0163 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02895 | hp1 | a0001 | c0008 | t0001 | g0060 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02895 | hp2 | a0001 | c0010 | t0001 | g0093 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02897 | hp1 | a0003 | c0006 | t0001 | g0216 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02897 | hp2 | a0001 | c0008 | t0001 | g0153 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02922 | hp1 | a0004 | c0011 | t0001 | g0172 | AFR | ESN | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02922 | hp2 | a0008 | c0013 | t0001 | g0145 | AFR | ESN | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02965 | hp1 | a0002 | c0003 | t0001 | g0121 | AFR | ESN | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02965 | hp2 | a0002 | c0015 | t0001 | g0089 | AFR | ESN | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02976 | hp1 | a0006 | c0053 | t0001 | g0094 | AFR | ESN | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02976 | hp2 | a0006 | c0044 | t0001 | g0167 | AFR | ESN | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03041 | hp1 | a0004 | c0014 | t0001 | g0146 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03041 | hp2 | a0002 | c0004 | t0001 | g0224 | AFR | GWD | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03098 | hp1 | a0001 | c0010 | t0001 | g0070 | AFR | MSL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03098 | hp2 | a0008 | c0013 | t0001 | g0147 | AFR | MSL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03139 | hp1 | a0002 | c0015 | t0001 | g0179 | AFR | ESN | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | ESN | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03209 | hp1 | a0001 | c0002 | t0005 | g0193 | AFR | MSL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03209 | hp2 | a0004 | c0014 | t0001 | g0055 | AFR | MSL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03225 | hp1 | a0002 | c0003 | t0001 | g0182 | AFR | MSL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03225 | hp2 | a0002 | c0034 | t0001 | g0154 | AFR | MSL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03239 | hp2 | a0002 | c0003 | t0001 | g0232 | SAS | PJL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03453 | hp1 | a0004 | c0011 | t0001 | g0138 | AFR | MSL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0194 | AFR | MSL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03486 | hp1 | a0002 | c0015 | t0001 | g0135 | AFR | MSL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03486 | hp2 | a0001 | c0008 | t0001 | g0151 | AFR | MSL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03491 | hp1 | a0004 | c0007 | t0001 | g0192 | SAS | PJL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03491 | hp2 | a0002 | c0004 | t0001 | g0222 | SAS | PJL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03516 | hp1 | a0003 | c0006 | t0001 | g0214 | AFR | ESN | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03516 | hp2 | a0008 | c0013 | t0001 | g0143 | AFR | ESN | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03579 | hp1 | a0004 | c0011 | t0001 | g0137 | AFR | MSL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03579 | hp2 | a0002 | c0003 | t0001 | g0221 | AFR | MSL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03669 | hp1 | a0003 | c0005 | t0001 | g0051 | SAS | PJL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03704 | hp1 | a0005 | c0009 | t0001 | g0175 | SAS | PJL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03704 | hp2 | a0002 | c0004 | t0001 | g0168 | SAS | PJL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03831 | hp1 | a0003 | c0005 | t0011 | g0052 | SAS | BEB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03831 | hp2 | a0002 | c0004 | t0001 | g0025 | SAS | BEB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0183 | SAS | BEB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03927 | hp2 | a0002 | c0003 | t0001 | g0127 | SAS | BEB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03942 | hp1 | a0003 | c0018 | t0001 | g0030 | SAS | BEB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03942 | hp2 | a0013 | c0037 | t0001 | g0079 | SAS | BEB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG04115 | hp1 | a0005 | c0009 | t0001 | g0144 | SAS | STU | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG04184 | hp1 | a0001 | c0010 | t0001 | g0098 | SAS | BEB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG04184 | hp2 | a0003 | c0018 | t0001 | g0234 | SAS | BEB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG04199 | hp1 | a0003 | c0005 | t0001 | g0011 | SAS | STU | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0076 | SAS | STU | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG04204 | hp1 | a0004 | c0007 | t0001 | g0188 | SAS | STU | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | STU | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG04228 | hp1 | a0020 | c0028 | t0001 | g0174 | SAS | STU | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG04228 | hp2 | a0004 | c0027 | t0001 | g0170 | SAS | STU | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18906 | hp1 | a0004 | c0016 | t0001 | g0177 | AFR | YRI | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0178 | AFR | YRI | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18946 | hp1 | a0002 | c0003 | t0001 | g0026 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18948 | hp2 | a0001 | c0012 | t0001 | g0123 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18967 | hp2 | a0001 | c0017 | t0001 | g0124 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18970 | hp1 | a0001 | c0001 | t0006 | g0233 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18970 | hp2 | a0003 | c0006 | t0004 | g0080 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18979 | hp2 | a0001 | c0012 | t0001 | g0068 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18983 | hp1 | a0003 | c0006 | t0001 | g0212 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18984 | hp1 | a0002 | c0004 | t0001 | g0095 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18999 | hp1 | a0001 | c0017 | t0001 | g0078 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA18999 | hp2 | a0001 | c0008 | t0001 | g0046 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19010 | hp1 | a0001 | c0008 | t0001 | g0077 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19043 | hp1 | a0004 | c0011 | t0001 | g0142 | AFR | LWK | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19043 | hp2 | a0001 | c0010 | t0001 | g0230 | AFR | LWK | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19054 | hp2 | a0002 | c0003 | t0001 | g0181 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19081 | hp1 | a0001 | c0038 | t0001 | g0105 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19085 | hp1 | a0001 | c0012 | t0001 | g0226 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19085 | hp2 | a0002 | c0004 | t0001 | g0096 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19088 | hp1 | a0003 | c0006 | t0001 | g0084 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA20129 | hp1 | a0001 | c0008 | t0001 | g0062 | AFR | ASW | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ASW | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0196 | EUR | TSI | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA20752 | hp2 | a0002 | c0003 | t0001 | g0063 | EUR | TSI | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA20805 | hp1 | a0002 | c0003 | t0001 | g0158 | EUR | TSI | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | TSI | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | GIH | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA20905 | hp2 | a0004 | c0007 | t0001 | g0173 | SAS | GIH | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01123 | hp1 | a0016 | c0046 | t0001 | g0164 | AMR | CLM | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG01123 | hp2 | a0001 | c0010 | t0001 | g0100 | AMR | CLM | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02109 | hp1 | a0001 | c0041 | t0001 | g0024 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02486 | hp1 | a0018 | c0052 | t0001 | g0122 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02486 | hp2 | a0009 | c0030 | t0007 | g0171 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02559 | hp1 | a0005 | c0026 | t0001 | g0005 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG02559 | hp2 | a0002 | c0020 | t0001 | g0229 | AFR | ACB | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03471 | hp1 | a0011 | c0042 | t0001 | g0223 | AFR | MSL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG03471 | hp2 | a0002 | c0004 | t0001 | g0042 | AFR | MSL | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG06807 | hp1 | a0002 | c0003 | t0001 | g0099 | AFR | USA | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
HG06807 | hp2 | a0005 | c0009 | t0001 | g0001 | AFR | USA | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | USA | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA20300 | hp2 | a0001 | c0010 | t0008 | g0075 | AFR | USA | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA21309 | hp1 | a0002 | c0003 | t0001 | g0198 | AFR | LWK | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | LWK | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0131 | REF | REF | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0085 | REF | REF | SPTBN4_chr19_40462001_40581464 | SPTBN4 | chr19 | 40462001 | 40581464 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:40472685
|
G | A | 1 | a0023 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.64G>A | p.Ala22Thr | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/36 | 384/8910 | 64/7695 | 22/2564 | chr19 | 40472685 | ||
chr19:40472733
|
G | A | 7 | a0004a0005a0008others(4): Show | 40 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(37): Show |
missense_variant | MODERATE | c.112G>A | p.Ala38Thr | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/36 | 432/8910 | 112/7695 | 38/2564 | chr19 | 40472733 | ||
chr19:40472737
|
C | T | 1 | a0022 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.116C>T | p.Ala39Val | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/36 | 436/8910 | 116/7695 | 39/2564 | chr19 | 40472737 | ||
chr19:40472742
|
A | G | 1 | a0010 | 1 | HG01070.hp1 | missense_variant | MODERATE | c.121A>G | p.Thr41Ala | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/36 | 441/8910 | 121/7695 | 41/2564 | chr19 | 40472742 | ||
chr19:40497584
|
C | T | 1 | a0021 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.764C>T | p.Ala255Val | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/36 | 1084/8910 | 764/7695 | 255/2564 | chr19 | 40497584 | ||
chr19:40502164
|
G | A | 1 | a0020 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.934G>A | p.Glu312Lys | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 9/36 | 1254/8910 | 934/7695 | 312/2564 | chr19 | 40502164 | ||
chr19:40506326
|
G | A | 1 | a0019 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.1756G>A | p.Ala586Thr | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/36 | 2076/8910 | 1756/7695 | 586/2564 | chr19 | 40506326 | ||
chr19:40513004
|
G | A | 3 | a0006a0008a0011 | 7 | HG02572.hp2 HG02922.hp2 HG02976.hp1 others(4): Show |
missense_variant | MODERATE | c.2215G>A | p.Val739Met | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/36 | 2535/8910 | 2215/7695 | 739/2564 | chr19 | 40513004 | ||
chr19:40519544
|
C | A | 1 | a0023 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.3047C>A | p.Ala1016Asp | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/36 | 3367/8910 | 3047/7695 | 1016/2564 | chr19 | 40519544 | ||
chr19:40519879
|
C | G | 1 | a0018 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.3382C>G | p.Leu1128Val | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/36 | 3702/8910 | 3382/7695 | 1128/2564 | chr19 | 40519879 | ||
chr19:40532667
|
G | A | 12 | a0002a0003a0005others(9): Show | 84 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(81): Show |
missense_variant | MODERATE | c.3991G>A | p.Gly1331Ser | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 19/36 | 4311/8910 | 3991/7695 | 1331/2564 | chr19 | 40532667 | ||
chr19:40560162
|
C | T | 1 | a0014 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.5674C>T | p.Arg1892Trp | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/36 | 5994/8910 | 5674/7695 | 1892/2564 | chr19 | 40560162 | ||
chr19:40566210
|
T | C | 1 | a0015 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.6187T>C | p.Trp2063Arg | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/36 | 6507/8910 | 6187/7695 | 2063/2564 | chr19 | 40566210 | ||
chr19:40567957
|
C | T | 4 | a0003a0009a0015others(1): Show | 28 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
missense_variant | MODERATE | c.6631C>T | p.Pro2211Ser | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/36 | 6951/8910 | 6631/7695 | 2211/2564 | chr19 | 40567957 | ||
chr19:40568180
|
G | C | 1 | a0012 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.6854G>C | p.Arg2285Pro | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/36 | 7174/8910 | 6854/7695 | 2285/2564 | chr19 | 40568180 | ||
chr19:40568256
|
G | A | 1 | a0007 | 3 | HG01516.hp1 HG01934.hp1 HG02738.hp1 |
missense_variant | MODERATE | c.6930G>A | p.Met2310Ile | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/36 | 7250/8910 | 6930/7695 | 2310/2564 | chr19 | 40568256 | ||
chr19:40569722
|
C | T | 1 | a0017 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.7022C>T | p.Ala2341Val | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/36 | 7342/8910 | 7022/7695 | 2341/2564 | chr19 | 40569722 | ||
chr19:40570649
|
C | G | 1 | a0013 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.7240C>G | p.Pro2414Ala | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 33/36 | 7560/8910 | 7240/7695 | 2414/2564 | chr19 | 40570649 | ||
chr19:40572090
|
C | G | 1 | a0008 | 3 | HG02922.hp2 HG03098.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.7391C>G | p.Ala2464Gly | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 34/36 | 7711/8910 | 7391/7695 | 2464/2564 | chr19 | 40572090 | ||
chr19:40572136
|
G | C | 2 | a0011a0016 | 2 | HG01123.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.7437G>C | p.Lys2479Asn | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 34/36 | 7757/8910 | 7437/7695 | 2479/2564 | chr19 | 40572136 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:40487788
|
G | A | 1 | a0001c0033 | 1 | HG01071.hp2 | synonymous_variant | LOW | c.261G>A | p.Val87Val | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/36 | 581/8910 | 261/7695 | 87/2564 | chr19 | 40487788 | ||
chr19:40502142
|
A | G | 29 | a0001c0002a0001c0008a0001c0041others(26): Show | 98 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(95): Show |
synonymous_variant | LOW | c.912A>G | p.Val304Val | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 9/36 | 1232/8910 | 912/7695 | 304/2564 | chr19 | 40502142 | ||
chr19:40502271
|
A | G | 1 | a0001c0012 | 4 | HG01169.hp2 NA18948.hp2 NA18979.hp2 others(1): Show |
synonymous_variant | LOW | c.1041A>G | p.Gln347Gln | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 9/36 | 1361/8910 | 1041/7695 | 347/2564 | chr19 | 40502271 | ||
chr19:40503910
|
C | T | 1 | a0004c0027 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.1443C>T | p.Tyr481Tyr | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/36 | 1763/8910 | 1443/7695 | 481/2564 | chr19 | 40503910 | ||
chr19:40504075
|
C | T | 2 | a0002c0019a0005c0026 | 3 | HG01261.hp1 HG01358.hp2 HG02559.hp1 |
synonymous_variant | LOW | c.1608C>T | p.Ala536Ala | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/36 | 1928/8910 | 1608/7695 | 536/2564 | chr19 | 40504075 | ||
chr19:40506247
|
G | A | 1 | a0001c0017 | 2 | NA18967.hp2 NA18999.hp1 |
synonymous_variant | LOW | c.1677G>A | p.Leu559Leu | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/36 | 1997/8910 | 1677/7695 | 559/2564 | chr19 | 40506247 | ||
chr19:40506283
|
C | T | 12 | a0001c0008a0001c0054a0002c0003others(9): Show | 56 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(53): Show |
synonymous_variant | LOW | c.1713C>T | p.Asp571Asp | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/36 | 2033/8910 | 1713/7695 | 571/2564 | chr19 | 40506283 | ||
chr19:40512925
|
A | G | 21 | a0001c0002a0001c0010a0001c0048others(18): Show | 56 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(53): Show |
synonymous_variant | LOW | c.2136A>G | p.Arg712Arg | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/36 | 2456/8910 | 2136/7695 | 712/2564 | chr19 | 40512925 | ||
chr19:40515398
|
C | T | 1 | a0012c0050 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.2853C>T | p.Gly951Gly | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/36 | 3173/8910 | 2853/7695 | 951/2564 | chr19 | 40515398 | ||
chr19:40519899
|
G | A | 1 | a0002c0045 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.3402G>A | p.Ala1134Ala | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/36 | 3722/8910 | 3402/7695 | 1134/2564 | chr19 | 40519899 | ||
chr19:40556184
|
C | T | 1 | a0004c0025 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.5185C>T | p.Leu1729Leu | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 25/36 | 5505/8910 | 5185/7695 | 1729/2564 | chr19 | 40556184 | ||
chr19:40557154
|
G | A | 2 | a0002c0015a0002c0045 | 4 | HG02280.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
synonymous_variant | LOW | c.5421G>A | p.Glu1807Glu | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/36 | 5741/8910 | 5421/7695 | 1807/2564 | chr19 | 40557154 | ||
chr19:40557259
|
C | T | 1 | a0006c0044 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.5526C>T | p.Asp1842Asp | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/36 | 5846/8910 | 5526/7695 | 1842/2564 | chr19 | 40557259 | ||
chr19:40566194
|
G | A | 1 | a0002c0034 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.6171G>A | p.Ala2057Ala | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/36 | 6491/8910 | 6171/7695 | 2057/2564 | chr19 | 40566194 | ||
chr19:40567803
|
C | T | 2 | a0007c0039a0007c0049 | 2 | HG01516.hp1 HG02738.hp1 |
synonymous_variant | LOW | c.6477C>T | p.Pro2159Pro | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/36 | 6797/8910 | 6477/7695 | 2159/2564 | chr19 | 40567803 | ||
chr19:40570618
|
C | T | 1 | a0001c0038 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.7209C>T | p.Ala2403Ala | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 33/36 | 7529/8910 | 7209/7695 | 2403/2564 | chr19 | 40570618 | ||
chr19:40572106
|
C | T | 1 | a0001c0048 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.7407C>T | p.His2469His | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 34/36 | 7727/8910 | 7407/7695 | 2469/2564 | chr19 | 40572106 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:40467043
|
C | A | 3 | a0001c0002t0002a0001c0048t0002a0003c0005t0002 | 5 | HG00099.hp2 HG01168.hp2 HG01169.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-278C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/36 | 5579 | chr19 | 40467043 | |||||
chr19:40467200
|
G | A | 1 | a0003c0006t0004 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-121G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/36 | 5422 | chr19 | 40467200 | |||||
chr19:40467206
|
C | G | 1 | a0003c0005t0011 | 1 | HG03831.hp1 | 5_prime_UTR_variant | MODIFIER | c.-115C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/36 | 5416 | chr19 | 40467206 | |||||
chr19:40575792
|
C | T | 2 | a0001c0002t0003a0004c0007t0003 | 2 | HG01891.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*223C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 36/36 | 223 | chr19 | 40575792 | |||||
chr19:40575794
|
A | C | 1 | a0004c0007t0010 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*225A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 36/36 | 225 | chr19 | 40575794 | |||||
chr19:40575845
|
G | C | 1 | a0001c0002t0005 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*276G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 36/36 | 276 | chr19 | 40575845 | |||||
chr19:40576061
|
A | T | 1 | a0005c0009t0009 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*492A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 36/36 | 492 | chr19 | 40576061 | |||||
chr19:40576103
|
G | A | 1 | a0001c0001t0006 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*534G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 36/36 | 534 | chr19 | 40576103 | |||||
chr19:40576334
|
G | C | 1 | a0009c0030t0007 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*765G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 36/36 | 765 | chr19 | 40576334 | |||||
chr19:40576389
|
G | T | 1 | a0001c0010t0008 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*820G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 36/36 | 820 | chr19 | 40576389 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:40467317
|
G | A | 8 | a0004c0007t0001g0004a0004c0007t0003g0002a0004c0016t0001g0003others(5): Show | 8 | HG00741.hp2 HG01099.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-16+12G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40467317 | ||||||
chr19:40467449
|
C | T | 8 | a0004c0007t0001g0004a0004c0007t0003g0002a0004c0016t0001g0003others(5): Show | 8 | HG00741.hp2 HG01099.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-16+144C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40467449 | ||||||
chr19:40467455
|
C | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 13 | HG01070.hp1 HG01109.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-16+150C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40467455 | ||||||
chr19:40467623
|
C | CG | 51 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0027others(48): Show | 51 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.-16+331dupG | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr19 | 40467623 | |||||
chr19:40467623
|
CG | C | 29 | a0001c0001t0001g0021a0001c0001t0001g0169a0001c0001t0001g0180others(26): Show | 29 | HG00099.hp1 HG00140.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.-16+331delG | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr19 | 40467623 | |||||
chr19:40467623
|
CGG | C | 48 | a0001c0001t0001g0195a0001c0001t0001g0199a0001c0001t0001g0201others(45): Show | 48 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.-16+330_-16+331del others(2): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr19 | 40467623 | |||||
chr19:40467625
|
G | C | 1 | a0001c0002t0001g0022 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-16+320G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40467625 | ||||||
chr19:40467626
|
G | C | 2 | a0001c0041t0001g0024a0012c0050t0001g0023 | 2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-16+321G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40467626 | ||||||
chr19:40467629
|
G | T | 1 | a0003c0018t0001g0234 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-16+324G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40467629 | ||||||
chr19:40467634
|
G | C | 1 | a0002c0004t0001g0025 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-16+329G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40467634 | ||||||
chr19:40467654
|
C | G | 27 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(24): Show | 27 | HG00140.hp1 HG01074.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.-16+349C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40467654 | ||||||
chr19:40467663
|
C | T | 3 | a0004c0007t0001g0186a0004c0007t0001g0187a0004c0007t0001g0188 | 3 | HG00140.hp2 HG00738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-16+358C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40467663 | ||||||
chr19:40467687
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-16+382C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40467687 | ||||||
chr19:40467776
|
C | T | 54 | a0001c0001t0001g0180a0001c0001t0001g0184a0001c0001t0001g0195others(51): Show | 54 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.-16+471C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40467776 | ||||||
chr19:40468080
|
C | CT | 92 | a0001c0001t0001g0180a0001c0001t0001g0184a0001c0001t0001g0195others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.-16+789dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr19 | 40468080 | |||||
chr19:40468080
|
C | CTT | 27 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(24): Show | 27 | HG00140.hp1 HG01074.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.-16+788_-16+789dup others(2): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr19 | 40468080 | |||||
chr19:40468117
|
A | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18974.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-16+812A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40468117 | ||||||
chr19:40468138
|
C | T | 5 | a0004c0014t0001g0058a0004c0014t0001g0146a0005c0009t0001g0148others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+833C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40468138 | ||||||
chr19:40468146
|
T | C | 122 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-16+841T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40468146 | ||||||
chr19:40468147
|
G | A | 1 | a0001c0002t0001g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-16+842G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40468147 | ||||||
chr19:40468457
|
A | G | 5 | a0004c0014t0001g0058a0004c0014t0001g0146a0005c0009t0001g0148others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+1152A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40468457 | ||||||
chr19:40468600
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-16+1295G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40468600 | ||||||
chr19:40468670
|
G | A | 1 | a0001c0002t0002g0196 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-16+1365G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40468670 | ||||||
chr19:40469014
|
G | A | 1 | a0001c0010t0001g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-16+1709G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40469014 | ||||||
chr19:40469100
|
G | GA | 53 | a0001c0001t0001g0180a0001c0001t0001g0184a0001c0001t0001g0195others(50): Show | 53 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.-16+1807dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr19 | 40469100 | |||||
chr19:40469260
|
CT | C | 5 | a0004c0014t0001g0058a0004c0014t0001g0146a0005c0009t0001g0148others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+1965delT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr19 | 40469260 | |||||
chr19:40469314
|
G | A | 1 | a0004c0027t0001g0170 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-16+2009G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40469314 | ||||||
chr19:40469346
|
C | G | 5 | a0004c0014t0001g0058a0004c0014t0001g0146a0005c0009t0001g0148others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+2041C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40469346 | ||||||
chr19:40469436
|
T | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0014 | 2 | HG01109.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-16+2131T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40469436 | ||||||
chr19:40469575
|
A | G | 68 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(65): Show | 68 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.-16+2270A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40469575 | ||||||
chr19:40469938
|
C | G | 1 | a0002c0004t0001g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-16+2633C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40469938 | ||||||
chr19:40469942
|
C | T | 1 | a0001c0001t0006g0233 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-16+2637C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40469942 | ||||||
chr19:40470002
|
A | T | 2 | a0001c0001t0001g0053a0001c0010t0001g0054 | 2 | HG00280.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.-15-2605A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470002 | ||||||
chr19:40470037
|
C | T | 1 | a0002c0003t0001g0232 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-15-2570C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470037 | ||||||
chr19:40470246
|
G | A | 2 | a0001c0002t0001g0071a0002c0003t0001g0026 | 2 | NA18946.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-15-2361G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470246 | ||||||
chr19:40470256
|
C | T | 1 | a0003c0005t0011g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-15-2351C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470256 | ||||||
chr19:40470294
|
C | T | 4 | a0001c0002t0001g0022a0001c0010t0001g0149a0001c0041t0001g0024others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-2313C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470294 | ||||||
chr19:40470295
|
G | A | 8 | a0004c0007t0001g0004a0004c0007t0003g0002a0004c0016t0001g0003others(5): Show | 8 | HG00741.hp2 HG01099.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-2312G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470295 | ||||||
chr19:40470307
|
TTTTTTTA others(1489): Show |
T | 1 | a0001c0002t0001g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-15-2298_-15-803de others(1): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr19 | 40470307 | |||||
chr19:40470350
|
A | G | 1 | a0004c0007t0003g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-15-2257A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470350 | ||||||
chr19:40470469
|
G | A | 5 | a0004c0014t0001g0058a0004c0014t0001g0146a0005c0009t0001g0148others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-2138G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470469 | ||||||
chr19:40470549
|
T | C | 131 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0064others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.-15-2058T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470549 | ||||||
chr19:40470605
|
C | T | 1 | a0003c0006t0001g0132 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-15-2002C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470605 | ||||||
chr19:40470673
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG00741.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-15-1934C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470673 | ||||||
chr19:40470682
|
G | T | 1 | a0004c0027t0001g0170 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-15-1925G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470682 | ||||||
chr19:40470686
|
G | C | 5 | a0004c0014t0001g0058a0004c0014t0001g0146a0005c0009t0001g0148others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-1921G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470686 | ||||||
chr19:40470719
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-15-1888G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470719 | ||||||
chr19:40470786
|
C | T | 4 | a0001c0001t0001g0128a0003c0005t0001g0050a0003c0005t0001g0051others(1): Show | 4 | HG01175.hp2 HG01255.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-1821C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470786 | ||||||
chr19:40470819
|
G | T | 56 | a0001c0001t0001g0180a0001c0001t0001g0184a0001c0001t0001g0195others(53): Show | 56 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.-15-1788G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470819 | ||||||
chr19:40470883
|
G | A | 2 | a0001c0002t0005g0193a0002c0015t0001g0179 | 2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-15-1724G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40470883 | ||||||
chr19:40470955
|
C | CT | 41 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0074others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.-15-1640dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr19 | 40470955 | |||||
chr19:40470955
|
CT | C | 8 | a0004c0007t0001g0004a0004c0007t0003g0002a0004c0016t0001g0003others(5): Show | 8 | HG00741.hp2 HG01099.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-1640delT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr19 | 40470955 | |||||
chr19:40471134
|
A | G | 8 | a0004c0007t0001g0004a0004c0007t0003g0002a0004c0016t0001g0003others(5): Show | 8 | HG00741.hp2 HG01099.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-1473A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40471134 | ||||||
chr19:40471163
|
T | A | 2 | a0005c0009t0001g0007a0005c0009t0001g0008 | 2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-15-1444T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40471163 | ||||||
chr19:40471236
|
C | T | 1 | a0001c0002t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-15-1371C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40471236 | ||||||
chr19:40471328
|
C | T | 4 | a0001c0001t0001g0161a0002c0003t0001g0165a0002c0004t0001g0069others(1): Show | 4 | HG01074.hp2 HG01081.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-1279C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40471328 | ||||||
chr19:40471435
|
A | G | 1 | a0001c0010t0001g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-15-1172A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40471435 | ||||||
chr19:40471507
|
C | A | 2 | a0004c0007t0010g0136a0009c0030t0007g0171 | 2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-15-1100C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40471507 | ||||||
chr19:40471604
|
G | A | 1 | a0001c0010t0008g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-15-1003G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40471604 | ||||||
chr19:40471680
|
T | C | 37 | a0001c0002t0003g0163a0004c0007t0001g0004a0004c0007t0001g0139others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15-927T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40471680 | ||||||
chr19:40471749
|
T | C | 4 | a0001c0002t0001g0194a0002c0003t0001g0197a0002c0003t0001g0198others(1): Show | 4 | HG02145.hp1 HG02976.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-858T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40471749 | ||||||
chr19:40471870
|
C | G | 1 | a0002c0003t0001g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-15-737C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40471870 | ||||||
chr19:40471905
|
A | AT | 36 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0028others(33): Show | 36 | HG00140.hp1 HG01074.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.-15-680dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr19 | 40471905 | |||||
chr19:40471905
|
A | ATT | 5 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0008t0001g0160others(2): Show | 5 | HG01257.hp2 HG02135.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-681_-15-680dup others(2): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr19 | 40471905 | |||||
chr19:40471905
|
AT | A | 9 | a0001c0001t0001g0184a0001c0002t0001g0022a0001c0002t0001g0076others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15-680delT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr19 | 40471905 | |||||
chr19:40471905
|
ATT | A | 50 | a0001c0001t0001g0180a0001c0001t0001g0195a0001c0001t0001g0199others(47): Show | 50 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.-15-681_-15-680del others(2): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr19 | 40471905 | |||||
chr19:40471905
|
ATTTTT | A | 6 | a0004c0014t0001g0058a0004c0014t0001g0146a0004c0016t0001g0177others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-684_-15-680del others(5): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr19 | 40471905 | |||||
chr19:40471905
|
ATTTTTT | A | 33 | a0004c0007t0001g0004a0004c0007t0001g0139a0004c0007t0001g0140others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.-15-685_-15-680del others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr19 | 40471905 | |||||
chr19:40471911
|
T | C | 6 | a0004c0014t0001g0058a0004c0014t0001g0146a0004c0016t0001g0177others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-696T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40471911 | ||||||
chr19:40471912
|
T | C | 33 | a0004c0007t0001g0004a0004c0007t0001g0139a0004c0007t0001g0140others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.-15-695T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40471912 | ||||||
chr19:40471913
|
T | C | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-15-694T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40471913 | ||||||
chr19:40472013
|
C | T | 6 | a0004c0007t0001g0173a0004c0027t0001g0170a0005c0009t0001g0144others(3): Show | 6 | HG00099.hp1 HG03704.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-594C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40472013 | ||||||
chr19:40472036
|
G | A | 5 | a0004c0014t0001g0058a0004c0014t0001g0146a0005c0009t0001g0148others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-571G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40472036 | ||||||
chr19:40472152
|
G | A | 8 | a0004c0007t0001g0004a0004c0007t0003g0002a0004c0016t0001g0003others(5): Show | 8 | HG00741.hp2 HG01099.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-455G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40472152 | ||||||
chr19:40472176
|
T | C | 5 | a0004c0014t0001g0058a0004c0014t0001g0146a0005c0009t0001g0148others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-431T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40472176 | ||||||
chr19:40472193
|
G | A | 1 | a0001c0008t0001g0077 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-15-414G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40472193 | ||||||
chr19:40472287
|
C | T | 35 | a0004c0007t0001g0004a0004c0007t0001g0139a0004c0007t0001g0140others(32): Show | 35 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-15-320C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40472287 | ||||||
chr19:40472288
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-15-319G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40472288 | ||||||
chr19:40472342
|
G | C | 2 | a0005c0009t0001g0189a0005c0009t0009g0190 | 2 | HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-15-265G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40472342 | ||||||
chr19:40472436
|
C | T | 3 | a0001c0002t0001g0178a0001c0002t0005g0193a0002c0015t0001g0179 | 3 | HG03139.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-15-171C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40472436 | ||||||
chr19:40472546
|
G | A | 53 | a0001c0001t0001g0180a0001c0001t0001g0184a0001c0001t0001g0195others(50): Show | 53 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.-15-61G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 1/35 | chr19 | 40472546 | ||||||
chr19:40472853
|
C | T | 40 | a0004c0007t0001g0004a0004c0007t0001g0139a0004c0007t0001g0140others(37): Show | 40 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.169+63C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40472853 | ||||||
chr19:40472854
|
C | T | 1 | a0001c0012t0001g0068 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.169+64C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40472854 | ||||||
chr19:40472878
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0019 | 2 | HG01175.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.169+88A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40472878 | ||||||
chr19:40472962
|
C | A | 40 | a0004c0007t0001g0004a0004c0007t0001g0139a0004c0007t0001g0140others(37): Show | 40 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.169+172C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40472962 | ||||||
chr19:40473058
|
A | T | 2 | a0004c0007t0010g0136a0009c0030t0007g0171 | 2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.169+268A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40473058 | ||||||
chr19:40473103
|
G | T | 1 | a0002c0004t0001g0029 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.169+313G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40473103 | ||||||
chr19:40473167
|
C | T | 31 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(28): Show | 31 | HG00140.hp1 HG01074.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.169+377C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40473167 | ||||||
chr19:40473280
|
T | C | 66 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.169+490T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40473280 | ||||||
chr19:40473354
|
G | GT | 20 | a0001c0001t0001g0047a0001c0001t0001g0074a0001c0001t0001g0125others(17): Show | 20 | HG01496.hp1 HG01516.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.169+584dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40473354 | |||||
chr19:40473354
|
G | GTTT | 23 | a0004c0007t0001g0139a0004c0007t0001g0140a0004c0007t0001g0173others(20): Show | 23 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.169+582_169+584dup others(3): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40473354 | |||||
chr19:40473354
|
G | GTTTT | 10 | a0004c0007t0001g0004a0004c0007t0001g0188a0004c0011t0001g0142others(7): Show | 10 | HG01099.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+581_169+584dup others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40473354 | |||||
chr19:40473354
|
G | GTTTTT | 6 | a0004c0007t0003g0002a0005c0009t0001g0001a0005c0009t0001g0148others(3): Show | 6 | HG00741.hp2 HG01891.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.169+580_169+584dup others(5): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40473354 | |||||
chr19:40473354
|
G | GTTTTTT | 20 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0152others(17): Show | 20 | HG00140.hp1 HG01074.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.169+579_169+584dup others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40473354 | |||||
chr19:40473398
|
C | T | 3 | a0001c0001t0001g0047a0001c0008t0001g0077a0001c0012t0001g0123 | 3 | NA18948.hp2 NA18979.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.169+608C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40473398 | ||||||
chr19:40473416
|
G | A | 50 | a0001c0001t0001g0180a0001c0001t0001g0184a0001c0001t0001g0195others(47): Show | 50 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.169+626G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40473416 | ||||||
chr19:40473421
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.169+631G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40473421 | ||||||
chr19:40473435
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.169+645G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40473435 | ||||||
chr19:40473444
|
A | C | 66 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.169+654A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40473444 | ||||||
chr19:40473725
|
C | A | 2 | a0001c0017t0001g0078a0001c0017t0001g0124 | 2 | NA18967.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.169+935C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40473725 | ||||||
chr19:40473907
|
A | G | 1 | a0002c0003t0001g0121 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.169+1117A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40473907 | ||||||
chr19:40473985
|
T | A | 36 | a0001c0002t0003g0163a0004c0007t0001g0004a0004c0007t0001g0139others(33): Show | 36 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.169+1195T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40473985 | ||||||
chr19:40473991
|
T | TA | 26 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(23): Show | 26 | HG00621.hp1 HG00621.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.169+1212dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40473991 | |||||
chr19:40473997
|
A | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0120 | 2 | HG01978.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.169+1207A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40473997 | ||||||
chr19:40474151
|
C | CA | 9 | a0001c0001t0001g0184a0001c0002t0001g0083a0001c0002t0002g0183others(6): Show | 9 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.169+1389dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40474151 | |||||
chr19:40474151
|
CA | C | 125 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(122): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.169+1389delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40474151 | |||||
chr19:40474151
|
CAA | C | 24 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(21): Show | 24 | HG00140.hp1 HG01074.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.169+1388_169+1389d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40474151 | |||||
chr19:40474321
|
CAA | C | 28 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.169+1532_169+1533d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40474321 | ||||||
chr19:40474432
|
A | AT | 5 | a0001c0001t0001g0119a0001c0001t0001g0184a0001c0017t0001g0124others(2): Show | 5 | HG02738.hp1 HG02738.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+1658dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40474432 | |||||
chr19:40474621
|
G | C | 65 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(62): Show | 65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.169+1831G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40474621 | ||||||
chr19:40474634
|
G | A | 8 | a0001c0008t0001g0060a0001c0008t0001g0061a0001c0008t0001g0062others(5): Show | 8 | HG01257.hp2 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.169+1844G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40474634 | ||||||
chr19:40474671
|
G | A | 57 | a0001c0001t0001g0180a0001c0001t0001g0184a0001c0001t0001g0195others(54): Show | 57 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.169+1881G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40474671 | ||||||
chr19:40474686
|
G | A | 5 | a0004c0014t0001g0058a0004c0014t0001g0146a0005c0009t0001g0148others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+1896G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40474686 | ||||||
chr19:40474817
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.169+2027G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40474817 | ||||||
chr19:40474818
|
G | T | 5 | a0004c0014t0001g0058a0004c0014t0001g0146a0005c0009t0001g0148others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+2028G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40474818 | ||||||
chr19:40474947
|
C | G | 64 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.169+2157C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40474947 | ||||||
chr19:40475291
|
A | G | 26 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(23): Show | 26 | HG00140.hp1 HG01074.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+2501A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40475291 | ||||||
chr19:40475455
|
C | CTTTA | 26 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(23): Show | 26 | HG00140.hp1 HG01074.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+2685_169+2688d others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40475455 | |||||
chr19:40475565
|
A | G | 4 | a0001c0002t0001g0022a0001c0010t0001g0149a0001c0041t0001g0024others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+2775A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40475565 | ||||||
chr19:40475962
|
C | T | 49 | a0001c0001t0001g0180a0001c0001t0001g0184a0001c0001t0001g0195others(46): Show | 49 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.169+3172C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40475962 | ||||||
chr19:40476243
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.169+3453G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40476243 | ||||||
chr19:40476345
|
C | CA | 34 | a0001c0002t0003g0163a0001c0012t0001g0039a0004c0007t0001g0004others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.169+3573dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40476345 | |||||
chr19:40476345
|
CA | C | 65 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0074others(62): Show | 65 | HG00099.hp2 HG00280.hp2 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.169+3573delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40476345 | |||||
chr19:40476362
|
A | G | 29 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 29 | HG00140.hp1 HG01074.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.169+3572A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40476362 | ||||||
chr19:40476468
|
A | G | 66 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.169+3678A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40476468 | ||||||
chr19:40476627
|
G | A | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.169+3837G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40476627 | ||||||
chr19:40476687
|
A | C | 4 | a0001c0002t0001g0022a0001c0010t0001g0149a0001c0041t0001g0024others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+3897A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40476687 | ||||||
chr19:40476691
|
CATTCTCC others(1244): Show |
C | 1 | a0008c0013t0001g0143 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.169+3922_169+5172d others(2): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40476691 | |||||
chr19:40476808
|
T | C | 67 | a0001c0001t0001g0027a0001c0001t0001g0064a0001c0001t0001g0065others(64): Show | 67 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.169+4018T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40476808 | ||||||
chr19:40476883
|
G | A | 56 | a0001c0001t0001g0180a0001c0001t0001g0184a0001c0001t0001g0195others(53): Show | 56 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.169+4093G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40476883 | ||||||
chr19:40476959
|
C | T | 65 | a0001c0001t0001g0027a0001c0001t0001g0064a0001c0001t0001g0065others(62): Show | 65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.169+4169C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40476959 | ||||||
chr19:40477025
|
T | TTTA | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0002t0001g0022others(4): Show | 7 | HG00642.hp2 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+4258_169+4260d others(5): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40477025 | |||||
chr19:40477025
|
T | TTTATTA | 21 | a0004c0007t0001g0139a0004c0007t0001g0140a0004c0007t0001g0173others(18): Show | 21 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.169+4255_169+4260d others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40477025 | |||||
chr19:40477025
|
T | TTTATTAT others(2): Show |
3 | a0004c0007t0001g0192a0004c0007t0010g0136a0009c0030t0007g0171 | 3 | HG02258.hp1 HG02486.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.169+4252_169+4260d others(11): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40477025 | |||||
chr19:40477127
|
A | G | 56 | a0001c0001t0001g0180a0001c0001t0001g0184a0001c0001t0001g0195others(53): Show | 56 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.169+4337A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40477127 | ||||||
chr19:40477338
|
T | C | 2 | a0005c0009t0001g0007a0005c0009t0001g0008 | 2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.169+4548T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40477338 | ||||||
chr19:40477415
|
T | C | 2 | a0005c0009t0001g0007a0005c0009t0001g0008 | 2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.169+4625T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40477415 | ||||||
chr19:40477668
|
G | A | 5 | a0004c0014t0001g0058a0004c0014t0001g0146a0005c0009t0001g0148others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+4878G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40477668 | ||||||
chr19:40477753
|
T | C | 1 | a0002c0003t0001g0063 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.169+4963T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40477753 | ||||||
chr19:40477860
|
C | T | 5 | a0004c0014t0001g0058a0004c0014t0001g0146a0005c0009t0001g0148others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+5070C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40477860 | ||||||
chr19:40478321
|
T | TA | 6 | a0001c0002t0001g0178a0001c0002t0003g0163a0001c0002t0005g0193others(3): Show | 6 | HG01123.hp1 HG01891.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.169+5543dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40478321 | |||||
chr19:40478513
|
C | T | 1 | a0004c0011t0001g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.169+5723C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40478513 | ||||||
chr19:40478535
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.169+5745A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40478535 | ||||||
chr19:40478567
|
A | T | 7 | a0004c0007t0001g0139a0004c0007t0001g0140a0004c0014t0001g0058others(4): Show | 7 | HG00642.hp1 HG00738.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+5777A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40478567 | ||||||
chr19:40478826
|
C | T | 3 | a0001c0002t0001g0178a0001c0002t0005g0193a0002c0015t0001g0179 | 3 | HG03139.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.169+6036C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40478826 | ||||||
chr19:40478997
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.169+6207G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40478997 | ||||||
chr19:40479086
|
C | G | 8 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(5): Show | 8 | HG01255.hp1 HG02074.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+6296C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40479086 | ||||||
chr19:40479096
|
T | G | 78 | a0001c0001t0001g0031a0001c0001t0001g0064a0001c0001t0001g0114others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.169+6306T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40479096 | ||||||
chr19:40479396
|
G | A | 1 | a0002c0019t0001g0162 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.169+6606G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40479396 | ||||||
chr19:40479441
|
T | G | 1 | a0001c0001t0001g0152 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.169+6651T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40479441 | ||||||
chr19:40479447
|
C | T | 1 | a0002c0003t0001g0121 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.169+6657C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40479447 | ||||||
chr19:40479529
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0005g0193a0001c0010t0001g0230others(1): Show | 4 | HG03139.hp1 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+6739A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40479529 | ||||||
chr19:40479558
|
C | T | 26 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0002t0001g0022others(23): Show | 26 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+6768C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40479558 | ||||||
chr19:40479633
|
C | T | 1 | a0004c0011t0001g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.169+6843C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40479633 | ||||||
chr19:40479675
|
C | CAT | 37 | a0001c0001t0001g0021a0001c0001t0001g0048a0001c0001t0001g0053others(34): Show | 37 | HG00280.hp1 HG00280.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.169+6912_169+6913d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40479675 | |||||
chr19:40479675
|
C | CATAT | 15 | a0001c0001t0001g0047a0001c0002t0002g0183a0001c0008t0001g0077others(12): Show | 15 | HG01070.hp1 HG01884.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.169+6910_169+6913d others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40479675 | |||||
chr19:40479675
|
C | CATATAT | 14 | a0001c0001t0001g0092a0001c0001t0001g0156a0001c0001t0001g0184others(11): Show | 14 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.169+6908_169+6913d others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40479675 | |||||
chr19:40479675
|
C | CATATATA others(1): Show |
11 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0161others(8): Show | 11 | HG00741.hp2 HG01074.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.169+6906_169+6913d others(10): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40479675 | |||||
chr19:40479675
|
C | CATATATA others(3): Show |
15 | a0001c0001t0001g0065a0001c0001t0001g0114a0001c0001t0001g0203others(12): Show | 15 | HG02040.hp2 HG02071.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.169+6904_169+6913d others(12): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40479675 | |||||
chr19:40479675
|
C | CATATATA others(5): Show |
6 | a0001c0001t0001g0180a0001c0001t0001g0225a0001c0002t0001g0228others(3): Show | 6 | HG01257.hp2 HG01496.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+6902_169+6913d others(14): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40479675 | |||||
chr19:40479675
|
C | CATATATA others(7): Show |
10 | a0001c0008t0001g0061a0001c0008t0001g0062a0001c0008t0001g0155others(7): Show | 10 | HG01978.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.169+6900_169+6913d others(16): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40479675 | |||||
chr19:40479675
|
C | CATATATA others(9): Show |
6 | a0001c0001t0001g0028a0001c0001t0001g0201a0001c0008t0001g0060others(3): Show | 6 | HG01358.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.169+6898_169+6913d others(18): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40479675 | |||||
chr19:40479675
|
C | CATATATA others(11): Show |
3 | a0001c0001t0001g0009a0001c0001t0001g0014a0004c0014t0001g0055 | 3 | HG01109.hp1 HG01168.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.169+6896_169+6913d others(20): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40479675 | |||||
chr19:40479675
|
C | CATATATA others(13): Show |
1 | a0003c0018t0001g0030 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.169+6894_169+6913d others(22): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40479675 | |||||
chr19:40479675
|
CAT | C | 24 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0045others(21): Show | 24 | HG01071.hp2 HG01106.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.169+6912_169+6913d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40479675 | |||||
chr19:40479675
|
CATAT | C | 14 | a0001c0001t0001g0130a0001c0001t0001g0131a0002c0003t0001g0182others(11): Show | 14 | HG00642.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.169+6910_169+6913d others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40479675 | |||||
chr19:40479675
|
CATATAT | C | 7 | a0004c0014t0001g0058a0004c0014t0001g0146a0005c0009t0001g0148others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.169+6908_169+6913d others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40479675 | |||||
chr19:40479675
|
CATATATA others(1): Show |
C | 6 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0002t0001g0159others(3): Show | 6 | HG01255.hp1 HG02135.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.169+6906_169+6913d others(10): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40479675 | |||||
chr19:40479702
|
A | ATATATAT others(5): Show |
1 | a0004c0011t0001g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.169+6913_169+6914i others(14): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40479702 | |||||
chr19:40479704
|
T | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0091a0003c0005t0001g0051 | 3 | HG01346.hp1 HG01346.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.169+6914T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40479704 | ||||||
chr19:40479851
|
G | A | 1 | a0005c0009t0001g0001 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.169+7061G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40479851 | ||||||
chr19:40479884
|
T | G | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0002t0001g0159others(18): Show | 21 | HG00099.hp1 HG01255.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.169+7094T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40479884 | ||||||
chr19:40479938
|
C | CA | 12 | a0001c0001t0001g0130a0001c0001t0001g0131a0002c0003t0001g0182others(9): Show | 12 | HG00741.hp1 HG01099.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.169+7160dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40479938 | |||||
chr19:40479989
|
C | T | 22 | a0001c0001t0001g0028a0001c0001t0001g0092a0001c0001t0001g0114others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.169+7199C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40479989 | ||||||
chr19:40480120
|
G | A | 2 | a0002c0003t0001g0197a0002c0003t0001g0198 | 2 | HG02145.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.169+7330G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40480120 | ||||||
chr19:40480144
|
G | A | 1 | a0001c0010t0001g0100 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.169+7354G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40480144 | ||||||
chr19:40480251
|
C | CA | 80 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(77): Show |
intron_variant | MODIFIER | c.170-7427dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40480251 | |||||
chr19:40480251
|
CA | C | 16 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0108others(13): Show | 16 | HG01884.hp1 HG02145.hp2 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.170-7427delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40480251 | |||||
chr19:40480396
|
C | G | 55 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp2 HG00741.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.170-7301C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40480396 | ||||||
chr19:40480421
|
AAAAC | A | 55 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp2 HG00741.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.170-7266_170-7263d others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40480421 | |||||
chr19:40480463
|
G | A | 4 | a0001c0002t0001g0178a0001c0002t0005g0193a0001c0010t0001g0230others(1): Show | 4 | HG03139.hp1 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-7234G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40480463 | ||||||
chr19:40480566
|
A | T | 4 | a0001c0002t0001g0022a0001c0010t0001g0070a0001c0010t0001g0149others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-7131A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40480566 | ||||||
chr19:40480623
|
G | C | 1 | a0004c0011t0001g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.170-7074G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40480623 | ||||||
chr19:40480657
|
G | T | 101 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(98): Show |
intron_variant | MODIFIER | c.170-7040G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40480657 | ||||||
chr19:40480759
|
G | A | 1 | a0004c0011t0001g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.170-6938G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40480759 | ||||||
chr19:40480787
|
G | A | 6 | a0004c0007t0001g0173a0004c0007t0001g0192a0005c0009t0001g0144others(3): Show | 6 | HG00099.hp1 HG03491.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-6910G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40480787 | ||||||
chr19:40480825
|
G | A | 3 | a0001c0002t0001g0194a0002c0003t0001g0197a0002c0003t0001g0198 | 3 | HG02145.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.170-6872G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40480825 | ||||||
chr19:40481092
|
T | C | 41 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(38): Show | 41 | HG00099.hp2 HG00741.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.170-6605T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40481092 | ||||||
chr19:40481162
|
G | A | 4 | a0001c0002t0001g0022a0001c0010t0001g0070a0001c0010t0001g0149others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-6535G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40481162 | ||||||
chr19:40481193
|
G | A | 1 | a0004c0011t0001g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.170-6504G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40481193 | ||||||
chr19:40481423
|
T | C | 2 | a0002c0004t0001g0029a0004c0016t0001g0003 | 2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.170-6274T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40481423 | ||||||
chr19:40481439
|
A | G | 125 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(122): Show |
intron_variant | MODIFIER | c.170-6258A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40481439 | ||||||
chr19:40481442
|
G | A | 3 | a0002c0004t0001g0029a0002c0015t0001g0135a0004c0016t0001g0003 | 3 | HG02258.hp2 HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.170-6255G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40481442 | ||||||
chr19:40481731
|
C | T | 17 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0008t0001g0046others(14): Show | 17 | HG01884.hp1 HG02135.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-5966C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40481731 | ||||||
chr19:40481849
|
G | T | 1 | a0004c0011t0001g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.170-5848G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40481849 | ||||||
chr19:40481888
|
T | C | 1 | a0002c0004t0001g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.170-5809T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40481888 | ||||||
chr19:40481891
|
A | G | 17 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0008t0001g0046others(14): Show | 17 | HG01884.hp1 HG02135.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-5806A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40481891 | ||||||
chr19:40481937
|
C | CT | 22 | a0001c0001t0001g0028a0001c0001t0001g0092a0001c0001t0001g0114others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.170-5748dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40481937 | |||||
chr19:40482217
|
G | A | 15 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0002t0001g0159others(12): Show | 15 | HG01255.hp1 HG01891.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.170-5480G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40482217 | ||||||
chr19:40482258
|
A | G | 22 | a0001c0001t0001g0028a0001c0001t0001g0092a0001c0001t0001g0114others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.170-5439A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40482258 | ||||||
chr19:40482551
|
T | C | 1 | a0002c0003t0001g0165 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.170-5146T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40482551 | ||||||
chr19:40482759
|
C | A | 12 | a0001c0001t0001g0130a0001c0001t0001g0131a0002c0003t0001g0182others(9): Show | 12 | HG00741.hp1 HG01099.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.170-4938C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40482759 | ||||||
chr19:40482817
|
C | T | 1 | a0004c0011t0001g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.170-4880C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40482817 | ||||||
chr19:40482854
|
G | C | 1 | a0002c0003t0001g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.170-4843G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40482854 | ||||||
chr19:40482858
|
G | C | 4 | a0001c0002t0001g0022a0001c0010t0001g0070a0001c0010t0001g0149others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-4839G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40482858 | ||||||
chr19:40483068
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.170-4629C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40483068 | ||||||
chr19:40483126
|
C | T | 18 | a0001c0001t0001g0028a0001c0001t0001g0092a0001c0001t0001g0114others(15): Show | 18 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.170-4571C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40483126 | ||||||
chr19:40483139
|
T | C | 7 | a0001c0002t0001g0022a0001c0010t0001g0070a0001c0010t0001g0149others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-4558T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40483139 | ||||||
chr19:40483146
|
C | T | 2 | a0004c0007t0001g0139a0004c0007t0001g0140 | 2 | HG00642.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.170-4551C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40483146 | ||||||
chr19:40483153
|
G | A | 1 | a0003c0018t0001g0030 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.170-4544G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40483153 | ||||||
chr19:40483441
|
T | TA | 15 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0008t0001g0046others(12): Show | 15 | HG01884.hp1 HG02135.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.170-4256_170-4255i others(3): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40483441 | ||||||
chr19:40483442
|
T | A | 15 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0008t0001g0046others(12): Show | 15 | HG01884.hp1 HG02135.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.170-4255T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40483442 | ||||||
chr19:40483553
|
T | A | 1 | a0004c0011t0001g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.170-4144T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40483553 | ||||||
chr19:40483955
|
ATCGCAAA others(5): Show |
A | 19 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0002t0003g0163others(16): Show | 19 | HG01123.hp1 HG01884.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.170-3731_170-3720d others(14): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40483955 | |||||
chr19:40484081
|
C | A | 1 | a0002c0015t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.170-3616C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40484081 | ||||||
chr19:40484081
|
C | T | 3 | a0001c0002t0001g0178a0001c0002t0005g0193a0001c0010t0001g0230 | 3 | HG03209.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.170-3616C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40484081 | ||||||
chr19:40484091
|
G | A | 4 | a0001c0002t0001g0178a0001c0002t0005g0193a0001c0010t0001g0230others(1): Show | 4 | HG03139.hp1 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-3606G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40484091 | ||||||
chr19:40484269
|
G | A | 21 | a0001c0001t0001g0028a0001c0001t0001g0092a0001c0001t0001g0114others(18): Show | 21 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.170-3428G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40484269 | ||||||
chr19:40484337
|
A | T | 1 | a0001c0010t0001g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.170-3360A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40484337 | ||||||
chr19:40484430
|
G | A | 3 | a0001c0002t0001g0022a0001c0010t0001g0149a0001c0041t0001g0024 | 3 | HG02055.hp2 HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.170-3267G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40484430 | ||||||
chr19:40484518
|
T | G | 1 | a0002c0004t0001g0224 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.170-3179T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40484518 | ||||||
chr19:40484556
|
T | C | 6 | a0002c0003t0001g0182a0002c0003t0001g0221a0004c0011t0001g0138others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-3141T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40484556 | ||||||
chr19:40484677
|
T | C | 4 | a0001c0002t0001g0022a0001c0010t0001g0149a0001c0041t0001g0024others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-3020T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40484677 | ||||||
chr19:40484702
|
T | C | 46 | a0001c0001t0001g0028a0001c0001t0001g0067a0001c0001t0001g0156others(43): Show | 46 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.170-2995T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40484702 | ||||||
chr19:40484739
|
A | G | 1 | a0019c0051t0001g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.170-2958A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40484739 | ||||||
chr19:40484755
|
A | G | 2 | a0001c0010t0001g0230a0019c0051t0001g0220 | 2 | HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.170-2942A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40484755 | ||||||
chr19:40484774
|
T | TA | 6 | a0001c0001t0001g0217a0004c0007t0001g0173a0004c0007t0001g0192others(3): Show | 6 | HG03491.hp1 HG03704.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-2915dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40484774 | |||||
chr19:40484775
|
A | T | 3 | a0001c0010t0001g0230a0004c0007t0010g0136a0005c0009t0001g0001 | 3 | HG02258.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.170-2922A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40484775 | ||||||
chr19:40484946
|
ACAAAAAC | A | 81 | a0001c0001t0001g0065a0001c0001t0001g0156a0001c0001t0001g0161others(78): Show | 81 | HG00099.hp2 HG01074.hp2 HG01169.hp1 others(78): Show |
intron_variant | MODIFIER | c.170-2744_170-2738d others(9): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40484946 | |||||
chr19:40484953
|
C | A | 1 | a0002c0004t0001g0025 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.170-2744C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40484953 | ||||||
chr19:40485005
|
G | A | 1 | a0002c0004t0001g0222 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.170-2692G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40485005 | ||||||
chr19:40485087
|
C | T | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.170-2610C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40485087 | ||||||
chr19:40485092
|
C | G | 1 | a0001c0008t0001g0077 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.170-2605C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40485092 | ||||||
chr19:40485231
|
C | T | 14 | a0001c0001t0001g0028a0001c0001t0001g0092a0001c0001t0001g0114others(11): Show | 14 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.170-2466C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40485231 | ||||||
chr19:40485361
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.170-2336G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40485361 | ||||||
chr19:40485366
|
C | G | 2 | a0001c0002t0003g0163a0016c0046t0001g0164 | 2 | HG01123.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.170-2331C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40485366 | ||||||
chr19:40485656
|
T | G | 2 | a0001c0002t0003g0163a0016c0046t0001g0164 | 2 | HG01123.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.170-2041T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40485656 | ||||||
chr19:40485805
|
CA | C | 43 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(40): Show | 43 | HG00099.hp2 HG01074.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.170-1882delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40485805 | |||||
chr19:40485856
|
G | A | 43 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(40): Show | 43 | HG00099.hp2 HG01074.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.170-1841G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40485856 | ||||||
chr19:40485978
|
T | TA | 52 | a0001c0001t0001g0028a0001c0001t0001g0067a0001c0001t0001g0092others(49): Show | 52 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.170-1704dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40485978 | |||||
chr19:40485978
|
T | TAA | 14 | a0001c0002t0003g0163a0001c0010t0008g0075a0004c0007t0001g0173others(11): Show | 14 | HG01123.hp1 HG02572.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.170-1705_170-1704d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40485978 | |||||
chr19:40486061
|
G | C | 19 | a0001c0001t0001g0156a0001c0002t0001g0178a0001c0002t0005g0193others(16): Show | 19 | HG01109.hp2 HG01884.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.170-1636G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40486061 | ||||||
chr19:40486130
|
C | T | 1 | a0005c0009t0001g0008 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.170-1567C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40486130 | ||||||
chr19:40486208
|
C | G | 15 | a0001c0001t0001g0092a0001c0001t0001g0114a0001c0001t0001g0180others(12): Show | 15 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.170-1489C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40486208 | ||||||
chr19:40486371
|
C | CT | 13 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0097others(10): Show | 13 | HG01169.hp1 HG01175.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.170-1310dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40486371 | |||||
chr19:40486467
|
C | T | 233 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.170-1230C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40486467 | ||||||
chr19:40486605
|
T | G | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.170-1092T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40486605 | ||||||
chr19:40486913
|
G | T | 2 | a0008c0013t0001g0145a0008c0013t0001g0147 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.170-784G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40486913 | ||||||
chr19:40487009
|
T | A | 9 | a0001c0002t0003g0163a0001c0010t0001g0093a0002c0003t0001g0182others(6): Show | 9 | HG01123.hp1 HG02055.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.170-688T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40487009 | ||||||
chr19:40487012
|
G | GA | 9 | a0001c0002t0003g0163a0001c0010t0001g0093a0002c0003t0001g0182others(6): Show | 9 | HG01123.hp1 HG02055.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.170-684dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40487012 | |||||
chr19:40487021
|
T | TGACTGCT others(7): Show |
2 | a0001c0002t0003g0163a0016c0046t0001g0164 | 2 | HG01123.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.170-671_170-658dup others(14): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40487021 | |||||
chr19:40487039
|
T | TGCTGAGG | 7 | a0001c0010t0001g0093a0002c0003t0001g0182a0002c0003t0001g0221others(4): Show | 7 | HG02055.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-658_170-657ins others(7): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40487039 | ||||||
chr19:40487041
|
T | TGGA | 7 | a0001c0010t0001g0093a0002c0003t0001g0182a0002c0003t0001g0221others(4): Show | 7 | HG02055.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-656_170-655ins others(3): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40487041 | ||||||
chr19:40487044
|
T | C | 7 | a0001c0010t0001g0093a0002c0003t0001g0182a0002c0003t0001g0221others(4): Show | 7 | HG02055.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-653T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40487044 | ||||||
chr19:40487090
|
G | A | 1 | a0012c0050t0001g0023 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.170-607G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40487090 | ||||||
chr19:40487182
|
A | G | 1 | a0001c0010t0008g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.170-515A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40487182 | ||||||
chr19:40487346
|
CTCT | C | 18 | a0001c0001t0001g0156a0001c0002t0001g0178a0001c0002t0005g0193others(15): Show | 18 | HG01109.hp2 HG01884.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.170-349_170-347del others(3): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40487346 | |||||
chr19:40487348
|
C | CT | 19 | a0001c0001t0001g0092a0001c0001t0001g0113a0001c0001t0001g0114others(16): Show | 19 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.170-334dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr19 | 40487348 | |||||
chr19:40487427
|
G | C | 101 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(98): Show | 101 | HG00099.hp2 HG00741.hp2 HG01070.hp2 others(98): Show |
intron_variant | MODIFIER | c.170-270G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40487427 | ||||||
chr19:40487509
|
C | T | 10 | a0001c0001t0001g0225a0001c0010t0001g0230a0004c0007t0001g0173others(7): Show | 10 | HG02630.hp1 HG02630.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.170-188C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40487509 | ||||||
chr19:40487535
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.170-162G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 2/35 | chr19 | 40487535 | ||||||
chr19:40487949
|
C | T | 3 | a0001c0002t0001g0022a0001c0010t0001g0149a0001c0041t0001g0024 | 3 | HG02055.hp2 HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.321+101C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40487949 | ||||||
chr19:40488127
|
G | A | 1 | a0001c0010t0008g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.321+279G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40488127 | ||||||
chr19:40488237
|
A | G | 15 | a0001c0001t0001g0092a0001c0001t0001g0114a0001c0001t0001g0180others(12): Show | 15 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.321+389A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40488237 | ||||||
chr19:40488553
|
A | G | 10 | a0001c0002t0003g0163a0001c0010t0001g0093a0001c0010t0008g0075others(7): Show | 10 | HG01123.hp1 HG02055.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.321+705A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40488553 | ||||||
chr19:40488599
|
C | T | 9 | a0001c0002t0003g0163a0001c0010t0001g0093a0002c0003t0001g0182others(6): Show | 9 | HG01123.hp1 HG02055.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.321+751C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40488599 | ||||||
chr19:40488625
|
C | T | 43 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(40): Show | 43 | HG00099.hp2 HG01074.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.321+777C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40488625 | ||||||
chr19:40488650
|
A | G | 5 | a0003c0006t0001g0213a0003c0006t0001g0214a0003c0006t0001g0215others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+802A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40488650 | ||||||
chr19:40488826
|
A | AT | 4 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0152others(1): Show | 4 | HG00642.hp1 HG00642.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.321+985dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr19 | 40488826 | |||||
chr19:40488863
|
A | G | 3 | a0001c0002t0001g0022a0001c0010t0001g0149a0001c0041t0001g0024 | 3 | HG02055.hp2 HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.321+1015A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40488863 | ||||||
chr19:40488889
|
C | T | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.321+1041C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40488889 | ||||||
chr19:40489028
|
T | A | 1 | a0001c0002t0002g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.322-1047T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40489028 | ||||||
chr19:40489173
|
G | C | 1 | a0001c0001t0001g0092 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.322-902G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40489173 | ||||||
chr19:40489228
|
A | AAAAAAGA others(3): Show |
9 | a0001c0001t0001g0156a0001c0008t0001g0046a0001c0008t0001g0077others(6): Show | 9 | HG02040.hp1 HG02135.hp1 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.322-844_322-843ins others(10): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr19 | 40489228 | |||||
chr19:40489228
|
A | AAAAAGAA others(2): Show |
56 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(53): Show | 56 | HG00099.hp2 HG01074.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.322-844_322-843ins others(9): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr19 | 40489228 | |||||
chr19:40489228
|
A | AAAAGAAA others(1): Show |
29 | a0001c0001t0001g0092a0001c0001t0001g0180a0001c0001t0001g0184others(26): Show | 29 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.322-843_322-836dup others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr19 | 40489228 | |||||
chr19:40489228
|
A | AAAAGAAA others(5): Show |
1 | a0001c0001t0001g0114 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.322-836_322-835ins others(12): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr19 | 40489228 | |||||
chr19:40489228
|
A | AAGAAAGA others(3): Show |
1 | a0001c0010t0008g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.322-846_322-845ins others(10): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr19 | 40489228 | |||||
chr19:40489228
|
A | G | 5 | a0001c0001t0001g0225a0001c0010t0001g0230a0004c0011t0001g0138others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-847A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40489228 | ||||||
chr19:40489239
|
A | AG | 4 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0152others(1): Show | 4 | HG00642.hp1 HG00642.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-836_322-835ins others(1): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40489239 | ||||||
chr19:40489239
|
A | G | 1 | a0001c0010t0008g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.322-836A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40489239 | ||||||
chr19:40489369
|
GA | G | 8 | a0001c0001t0001g0028a0001c0001t0001g0067a0003c0005t0001g0059others(5): Show | 8 | HG01255.hp1 HG01358.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.322-705delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40489369 | ||||||
chr19:40489382
|
C | CA | 72 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(69): Show | 72 | HG00099.hp2 HG00741.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.322-693_322-692ins others(1): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40489382 | ||||||
chr19:40489703
|
G | A | 1 | a0004c0007t0001g0192 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.322-372G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40489703 | ||||||
chr19:40489780
|
T | TA | 48 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(45): Show | 48 | HG00099.hp2 HG01074.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.322-295_322-294ins others(1): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40489780 | ||||||
chr19:40489780
|
T | TG | 7 | a0001c0010t0001g0093a0002c0003t0001g0182a0002c0003t0001g0221others(4): Show | 7 | HG02055.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-290dupG | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr19 | 40489780 | |||||
chr19:40489864
|
T | A | 7 | a0001c0010t0001g0093a0002c0003t0001g0182a0002c0003t0001g0221others(4): Show | 7 | HG02055.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-211T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40489864 | ||||||
chr19:40490047
|
C | T | 1 | a0001c0001t0001g0048 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.322-28C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 3/35 | chr19 | 40490047 | ||||||
chr19:40490572
|
A | G | 7 | a0001c0010t0001g0093a0002c0003t0001g0182a0002c0003t0001g0221others(4): Show | 7 | HG02055.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.495+324A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40490572 | ||||||
chr19:40490584
|
C | G | 89 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(86): Show | 89 | HG00099.hp2 HG00741.hp2 HG01074.hp2 others(86): Show |
intron_variant | MODIFIER | c.495+336C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40490584 | ||||||
chr19:40490606
|
C | T | 2 | a0001c0002t0002g0183a0001c0048t0002g0206 | 2 | HG00099.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.495+358C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40490606 | ||||||
chr19:40490656
|
C | T | 2 | a0001c0002t0003g0163a0016c0046t0001g0164 | 2 | HG01123.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.495+408C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40490656 | ||||||
chr19:40490750
|
G | A | 19 | a0001c0001t0001g0156a0001c0002t0001g0178a0001c0002t0005g0193others(16): Show | 19 | HG01109.hp2 HG01884.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.495+502G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40490750 | ||||||
chr19:40490832
|
A | C | 10 | a0001c0002t0003g0163a0001c0010t0001g0093a0001c0010t0008g0075others(7): Show | 10 | HG01123.hp1 HG02055.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.495+584A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40490832 | ||||||
chr19:40490913
|
A | G | 7 | a0001c0010t0001g0093a0002c0003t0001g0182a0002c0003t0001g0221others(4): Show | 7 | HG02055.hp1 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.495+665A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40490913 | ||||||
chr19:40490985
|
T | C | 3 | a0001c0002t0001g0022a0001c0010t0001g0149a0001c0041t0001g0024 | 3 | HG02055.hp2 HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.495+737T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40490985 | ||||||
chr19:40491020
|
C | A | 2 | a0004c0007t0010g0136a0005c0029t0001g0141 | 2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.495+772C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40491020 | ||||||
chr19:40491081
|
A | G | 3 | a0001c0010t0001g0054a0001c0010t0001g0098a0002c0019t0001g0043 | 3 | HG00280.hp1 HG01261.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.495+833A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40491081 | ||||||
chr19:40491152
|
C | T | 9 | a0001c0002t0003g0163a0001c0010t0001g0093a0002c0003t0001g0182others(6): Show | 9 | HG01123.hp1 HG02055.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.495+904C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40491152 | ||||||
chr19:40491218
|
C | A | 1 | a0004c0007t0001g0004 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.495+970C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40491218 | ||||||
chr19:40491309
|
C | T | 19 | a0001c0001t0001g0156a0001c0002t0001g0178a0001c0002t0005g0193others(16): Show | 19 | HG01109.hp2 HG01884.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.495+1061C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40491309 | ||||||
chr19:40491333
|
T | C | 1 | a0001c0008t0001g0160 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.495+1085T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40491333 | ||||||
chr19:40491533
|
G | A | 53 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(50): Show | 53 | HG00099.hp2 HG01074.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.495+1285G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40491533 | ||||||
chr19:40491540
|
G | A | 3 | a0001c0002t0001g0022a0001c0010t0001g0149a0001c0041t0001g0024 | 3 | HG02055.hp2 HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.495+1292G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40491540 | ||||||
chr19:40491575
|
C | G | 1 | a0001c0033t0001g0112 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.495+1327C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40491575 | ||||||
chr19:40491713
|
C | CA | 38 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0032others(35): Show | 38 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.496-1225dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr19 | 40491713 | |||||
chr19:40491713
|
C | CAAA | 12 | a0001c0001t0001g0114a0001c0001t0001g0180a0001c0001t0001g0184others(9): Show | 12 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.496-1227_496-1225d others(5): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr19 | 40491713 | |||||
chr19:40491713
|
C | CAAAA | 10 | a0001c0001t0001g0092a0001c0010t0001g0070a0001c0010t0001g0093others(7): Show | 10 | HG02055.hp1 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.496-1228_496-1225d others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr19 | 40491713 | |||||
chr19:40491713
|
C | CAAAAA | 18 | a0001c0001t0001g0203a0001c0002t0001g0022a0001c0002t0005g0193others(15): Show | 18 | HG01109.hp2 HG01257.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.496-1229_496-1225d others(7): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr19 | 40491713 | |||||
chr19:40491713
|
C | CAAAAAA | 33 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(30): Show | 33 | HG00099.hp2 HG01074.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.496-1230_496-1225d others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr19 | 40491713 | |||||
chr19:40491713
|
C | CAAAAAAA | 11 | a0001c0001t0001g0065a0001c0002t0001g0202a0001c0008t0001g0046others(8): Show | 11 | HG01978.hp2 HG02071.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.496-1231_496-1225d others(9): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr19 | 40491713 | |||||
chr19:40491713
|
C | CAAAAAAA others(4): Show |
1 | a0001c0010t0008g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.496-1235_496-1225d others(13): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr19 | 40491713 | |||||
chr19:40491713
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0225a0001c0010t0001g0230a0004c0011t0001g0142 | 3 | HG02886.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.496-1236_496-1225d others(14): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr19 | 40491713 | |||||
chr19:40491713
|
C | CAAAAAAA others(6): Show |
1 | a0019c0051t0001g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.496-1237_496-1225d others(15): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr19 | 40491713 | |||||
chr19:40491713
|
CA | C | 5 | a0004c0007t0001g0173a0004c0007t0001g0192a0005c0009t0001g0144others(2): Show | 5 | HG03491.hp1 HG03704.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.496-1225delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr19 | 40491713 | |||||
chr19:40491788
|
T | TGAGG | 43 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(40): Show | 43 | HG00099.hp2 HG01074.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.496-1174_496-1171d others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr19 | 40491788 | |||||
chr19:40491809
|
G | A | 4 | a0001c0001t0001g0225a0001c0010t0001g0230a0004c0011t0001g0142others(1): Show | 4 | HG02630.hp1 HG02886.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.496-1154G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40491809 | ||||||
chr19:40491962
|
C | T | 14 | a0001c0001t0001g0092a0001c0001t0001g0114a0001c0001t0001g0180others(11): Show | 14 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.496-1001C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40491962 | ||||||
chr19:40492029
|
AC | A | 9 | a0001c0002t0003g0163a0001c0010t0001g0093a0002c0003t0001g0182others(6): Show | 9 | HG01123.hp1 HG02055.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.496-933delC | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40492029 | ||||||
chr19:40492030
|
C | A | 3 | a0001c0010t0008g0075a0002c0004t0001g0029a0005c0009t0001g0001 | 3 | HG02258.hp2 HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.496-933C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40492030 | ||||||
chr19:40492031
|
A | C | 2 | a0002c0004t0001g0029a0005c0009t0001g0001 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.496-932A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40492031 | ||||||
chr19:40492040
|
AC | A | 10 | a0001c0002t0003g0163a0001c0010t0001g0093a0001c0010t0008g0075others(7): Show | 10 | HG01123.hp1 HG02055.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.496-922delC | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40492040 | ||||||
chr19:40492041
|
C | CA | 51 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(48): Show | 51 | HG00099.hp2 HG01074.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.496-911dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr19 | 40492041 | |||||
chr19:40492046
|
A | C | 1 | a0005c0023t0001g0191 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.496-917A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40492046 | ||||||
chr19:40492047
|
A | C | 10 | a0001c0002t0003g0163a0001c0010t0001g0093a0001c0010t0008g0075others(7): Show | 10 | HG01123.hp1 HG02055.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.496-916A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40492047 | ||||||
chr19:40492080
|
T | C | 1 | a0005c0023t0001g0191 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.496-883T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40492080 | ||||||
chr19:40492205
|
G | A | 9 | a0001c0001t0001g0027a0001c0001t0001g0074a0002c0003t0001g0063others(6): Show | 9 | HG00099.hp1 HG01081.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.496-758G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40492205 | ||||||
chr19:40492352
|
T | C | 2 | a0001c0002t0003g0163a0016c0046t0001g0164 | 2 | HG01123.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.496-611T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40492352 | ||||||
chr19:40492464
|
G | A | 1 | a0003c0005t0001g0015 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.496-499G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40492464 | ||||||
chr19:40492583
|
C | G | 1 | a0005c0009t0001g0001 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.496-380C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 4/35 | chr19 | 40492583 | ||||||
chr19:40493170
|
C | T | 1 | a0001c0010t0008g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.587+116C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 5/35 | chr19 | 40493170 | ||||||
chr19:40493352
|
G | C | 2 | a0002c0004t0001g0029a0005c0009t0001g0001 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.587+298G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 5/35 | chr19 | 40493352 | ||||||
chr19:40493407
|
C | T | 1 | a0003c0005t0011g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.587+353C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 5/35 | chr19 | 40493407 | ||||||
chr19:40493486
|
T | C | 107 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(104): Show | 107 | HG00099.hp2 HG00741.hp2 HG01070.hp2 others(104): Show |
intron_variant | MODIFIER | c.587+432T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 5/35 | chr19 | 40493486 | ||||||
chr19:40493529
|
G | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0082 | 2 | HG02056.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.587+475G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 5/35 | chr19 | 40493529 | ||||||
chr19:40493899
|
G | A | 3 | a0001c0010t0008g0075a0002c0004t0001g0029a0005c0009t0001g0001 | 3 | HG02258.hp2 HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.587+845G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 5/35 | chr19 | 40493899 | ||||||
chr19:40494097
|
G | GT | 42 | a0001c0001t0001g0092a0001c0001t0001g0114a0001c0001t0001g0156others(39): Show | 42 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.588-799dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 5/35 | INFO_REALIGN_3_PRIME | chr19 | 40494097 | |||||
chr19:40494205
|
T | G | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.588-692T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 5/35 | chr19 | 40494205 | ||||||
chr19:40494303
|
C | T | 25 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0092others(22): Show | 25 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.588-594C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 5/35 | chr19 | 40494303 | ||||||
chr19:40494514
|
C | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0082 | 2 | HG02056.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.588-383C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 5/35 | chr19 | 40494514 | ||||||
chr19:40494533
|
A | G | 3 | a0006c0043t0001g0126a0006c0044t0001g0167a0008c0013t0001g0143 | 3 | HG02572.hp2 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.588-364A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 5/35 | chr19 | 40494533 | ||||||
chr19:40494550
|
G | C | 13 | a0001c0010t0001g0093a0002c0003t0001g0182a0002c0003t0001g0221others(10): Show | 13 | HG02055.hp1 HG02135.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.588-347G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 5/35 | chr19 | 40494550 | ||||||
chr19:40494550
|
GTATC | G | 41 | a0001c0001t0001g0028a0001c0001t0001g0044a0001c0001t0001g0092others(38): Show | 41 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.588-333_588-330del others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 5/35 | INFO_REALIGN_3_PRIME | chr19 | 40494550 | |||||
chr19:40494629
|
AATCT | A | 24 | a0001c0001t0001g0028a0001c0002t0001g0037a0001c0002t0001g0083others(21): Show | 24 | HG01109.hp2 HG01257.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.588-260_588-257del others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 5/35 | INFO_REALIGN_3_PRIME | chr19 | 40494629 | |||||
chr19:40494791
|
T | G | 1 | a0006c0053t0001g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.588-106T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 5/35 | chr19 | 40494791 | ||||||
chr19:40494810
|
A | G | 9 | a0001c0008t0001g0060a0001c0008t0001g0061a0001c0008t0001g0062others(6): Show | 9 | HG01257.hp2 HG02257.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.588-87A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 5/35 | chr19 | 40494810 | ||||||
chr19:40495174
|
C | T | 3 | a0003c0006t0001g0084a0003c0006t0001g0212a0003c0006t0004g0080 | 3 | NA18970.hp2 NA18983.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.668+197C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40495174 | ||||||
chr19:40495194
|
A | G | 10 | a0001c0001t0001g0128a0003c0005t0001g0050a0003c0005t0001g0051others(7): Show | 10 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.668+217A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40495194 | ||||||
chr19:40495200
|
T | C | 2 | a0004c0014t0001g0058a0004c0014t0001g0146 | 2 | HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.668+223T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40495200 | ||||||
chr19:40495366
|
G | A | 1 | a0004c0007t0001g0173 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.668+389G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40495366 | ||||||
chr19:40495596
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.668+619C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40495596 | ||||||
chr19:40495597
|
G | A | 2 | a0001c0002t0001g0086a0001c0002t0005g0193 | 2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.668+620G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40495597 | ||||||
chr19:40495847
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.668+870G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40495847 | ||||||
chr19:40495941
|
C | T | 1 | a0004c0007t0003g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.668+964C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40495941 | ||||||
chr19:40496014
|
G | T | 33 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(30): Show | 33 | HG00099.hp2 HG01123.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.668+1037G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40496014 | ||||||
chr19:40496301
|
C | T | 1 | a0012c0050t0001g0023 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.669-1188C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40496301 | ||||||
chr19:40496402
|
G | A | 2 | a0001c0001t0001g0225a0001c0010t0001g0149 | 2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.669-1087G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40496402 | ||||||
chr19:40496427
|
G | A | 1 | a0001c0010t0001g0054 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.669-1062G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40496427 | ||||||
chr19:40496445
|
C | T | 2 | a0002c0004t0001g0095a0002c0004t0001g0096 | 2 | NA18984.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.669-1044C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40496445 | ||||||
chr19:40496446
|
G | A | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.669-1043G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40496446 | ||||||
chr19:40496533
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.669-956C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40496533 | ||||||
chr19:40496544
|
A | G | 34 | a0001c0002t0001g0231a0001c0008t0001g0060a0001c0008t0001g0061others(31): Show | 34 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.669-945A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40496544 | ||||||
chr19:40496650
|
A | G | 1 | a0001c0041t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.669-839A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40496650 | ||||||
chr19:40496902
|
G | A | 1 | a0001c0002t0001g0202 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.669-587G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40496902 | ||||||
chr19:40497059
|
C | T | 3 | a0003c0006t0001g0084a0003c0006t0001g0212a0003c0006t0004g0080 | 3 | NA18970.hp2 NA18983.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.669-430C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40497059 | ||||||
chr19:40497069
|
T | A | 41 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.669-420T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40497069 | ||||||
chr19:40497072
|
C | CA | 9 | a0001c0001t0001g0033a0001c0001t0001g0082a0001c0001t0001g0113others(6): Show | 9 | HG00621.hp2 HG01081.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.669-394dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr19 | 40497072 | |||||
chr19:40497072
|
CA | C | 43 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(40): Show |
intron_variant | MODIFIER | c.669-394delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr19 | 40497072 | |||||
chr19:40497086
|
A | T | 40 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0028others(37): Show | 40 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.669-403A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40497086 | ||||||
chr19:40497153
|
A | G | 13 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0097others(10): Show | 13 | HG00280.hp1 HG01099.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.669-336A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40497153 | ||||||
chr19:40497232
|
C | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0097others(7): Show | 10 | HG00280.hp1 HG01099.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.669-257C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40497232 | ||||||
chr19:40497272
|
C | A | 1 | a0001c0001t0001g0225 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.669-217C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40497272 | ||||||
chr19:40497286
|
C | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0028others(36): Show | 39 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.669-203C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40497286 | ||||||
chr19:40497308
|
C | T | 1 | a0001c0010t0001g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.669-181C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40497308 | ||||||
chr19:40497322
|
T | A | 1 | a0020c0028t0001g0174 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.669-167T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 6/35 | chr19 | 40497322 | ||||||
chr19:40497672
|
C | T | 1 | a0001c0041t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.784+68C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40497672 | ||||||
chr19:40497791
|
C | T | 1 | a0001c0041t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.784+187C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40497791 | ||||||
chr19:40497955
|
C | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0045a0001c0001t0001g0091others(2): Show | 5 | HG01071.hp2 HG01346.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+351C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40497955 | ||||||
chr19:40498002
|
G | A | 1 | a0001c0041t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.784+398G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498002 | ||||||
chr19:40498011
|
A | G | 1 | a0001c0041t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.784+407A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498011 | ||||||
chr19:40498086
|
A | C | 165 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.784+482A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498086 | ||||||
chr19:40498147
|
G | C | 41 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.784+543G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498147 | ||||||
chr19:40498151
|
C | T | 1 | a0005c0009t0001g0175 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.784+547C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498151 | ||||||
chr19:40498168
|
T | C | 56 | a0001c0001t0001g0201a0001c0002t0001g0086a0001c0002t0001g0231others(53): Show | 56 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.784+564T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498168 | ||||||
chr19:40498229
|
A | G | 165 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.784+625A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498229 | ||||||
chr19:40498343
|
G | A | 1 | a0001c0041t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.784+739G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498343 | ||||||
chr19:40498345
|
G | A | 6 | a0006c0043t0001g0126a0006c0044t0001g0167a0008c0013t0001g0143others(3): Show | 6 | HG02572.hp2 HG02922.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.784+741G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498345 | ||||||
chr19:40498373
|
T | TTTTA | 72 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0033others(69): Show | 72 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.784+813_784+816dup others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40498373 | |||||
chr19:40498373
|
T | TTTTATTT others(1): Show |
12 | a0001c0001t0001g0114a0001c0001t0001g0203a0001c0008t0001g0046others(9): Show | 12 | HG02040.hp2 HG02630.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.784+809_784+816dup others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40498373 | |||||
chr19:40498373
|
TTTTA | T | 7 | a0001c0002t0001g0159a0001c0002t0001g0205a0001c0010t0001g0230others(4): Show | 7 | HG02559.hp2 HG04199.hp1 HG04228.hp2 others(4): Show |
intron_variant | MODIFIER | c.784+813_784+816del others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40498373 | |||||
chr19:40498373
|
TTTTATTT others(1): Show |
T | 34 | a0001c0001t0001g0225a0001c0002t0001g0017a0001c0002t0001g0022others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.784+809_784+816del others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40498373 | |||||
chr19:40498373
|
TTTTATTT others(5): Show |
T | 4 | a0001c0002t0005g0193a0002c0019t0001g0043a0002c0019t0001g0162others(1): Show | 4 | HG01261.hp1 HG01358.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.784+805_784+816del others(12): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40498373 | |||||
chr19:40498373
|
TTTTATTT others(17): Show |
T | 1 | a0012c0050t0001g0023 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.784+793_784+816del others(24): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40498373 | |||||
chr19:40498417
|
A | T | 1 | a0002c0004t0001g0029 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.784+813A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498417 | ||||||
chr19:40498421
|
T | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0195others(1): Show | 4 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.784+817T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498421 | ||||||
chr19:40498554
|
C | T | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.784+950C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498554 | ||||||
chr19:40498626
|
C | G | 1 | a0002c0019t0001g0043 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.784+1022C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498626 | ||||||
chr19:40498826
|
C | G | 2 | a0002c0004t0001g0095a0002c0004t0001g0096 | 2 | NA18984.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.784+1222C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498826 | ||||||
chr19:40498846
|
T | C | 165 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.784+1242T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498846 | ||||||
chr19:40498891
|
G | A | 3 | a0003c0006t0001g0084a0003c0006t0001g0212a0003c0006t0004g0080 | 3 | NA18970.hp2 NA18983.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.784+1287G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498891 | ||||||
chr19:40498991
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.784+1387C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40498991 | ||||||
chr19:40499068
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.784+1464C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40499068 | ||||||
chr19:40499138
|
C | T | 2 | a0002c0003t0001g0121a0005c0009t0001g0008 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.784+1534C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40499138 | ||||||
chr19:40499149
|
T | C | 43 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.784+1545T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40499149 | ||||||
chr19:40499195
|
A | AT | 61 | a0001c0001t0001g0201a0001c0001t0001g0225a0001c0002t0001g0086others(58): Show | 61 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.784+1606dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40499195 | |||||
chr19:40499195
|
A | ATTT | 40 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0032others(37): Show | 40 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.784+1604_784+1606d others(5): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40499195 | |||||
chr19:40499259
|
C | G | 99 | a0001c0001t0001g0201a0001c0002t0001g0017a0001c0002t0001g0022others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.784+1655C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40499259 | ||||||
chr19:40499563
|
A | AT | 5 | a0001c0001t0001g0110a0001c0001t0001g0115a0001c0017t0001g0124others(2): Show | 5 | HG00642.hp2 HG01928.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.784+1972dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40499563 | |||||
chr19:40499593
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.784+1989C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40499593 | ||||||
chr19:40499641
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.784+2037C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40499641 | ||||||
chr19:40499695
|
C | T | 1 | a0001c0041t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.784+2091C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40499695 | ||||||
chr19:40499723
|
T | C | 3 | a0003c0006t0001g0084a0003c0006t0001g0212a0003c0006t0004g0080 | 3 | NA18970.hp2 NA18983.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.784+2119T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40499723 | ||||||
chr19:40500076
|
C | CTAAAAAA others(55): Show |
1 | a0012c0050t0001g0023 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.785-1843_785-1842i others(64): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40500076 | |||||
chr19:40500081
|
A | AAAAAAAA others(58): Show |
1 | a0001c0002t0002g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.785-1839_785-1838i others(67): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40500081 | |||||
chr19:40500081
|
A | AAAAAAAA others(57): Show |
12 | a0001c0002t0001g0071a0001c0002t0001g0178a0001c0002t0001g0194others(9): Show | 12 | HG01496.hp1 HG02071.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.785-1839_785-1838i others(66): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40500081 | |||||
chr19:40500081
|
A | AAAAAAAA others(56): Show |
43 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.785-1839_785-1838i others(65): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40500081 | |||||
chr19:40500081
|
A | AAAAAAAA others(55): Show |
40 | a0001c0002t0001g0086a0001c0002t0001g0231a0001c0002t0005g0193others(37): Show | 40 | HG00280.hp2 HG01081.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.785-1839_785-1838i others(64): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40500081 | |||||
chr19:40500081
|
A | AAAAAAAA others(52): Show |
1 | a0001c0041t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.785-1839_785-1838i others(61): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40500081 | |||||
chr19:40500081
|
A | C | 1 | a0012c0050t0001g0023 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.785-1840A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40500081 | ||||||
chr19:40500191
|
A | C | 1 | a0002c0004t0001g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.785-1730A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40500191 | ||||||
chr19:40500277
|
C | G | 1 | a0001c0041t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.785-1644C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40500277 | ||||||
chr19:40500460
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.785-1461A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40500460 | ||||||
chr19:40500511
|
A | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0103a0001c0001t0001g0110others(2): Show | 5 | HG00642.hp2 HG01928.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.785-1410A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40500511 | ||||||
chr19:40500519
|
G | A | 41 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0028others(38): Show | 41 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.785-1402G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40500519 | ||||||
chr19:40500568
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.785-1353C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40500568 | ||||||
chr19:40500569
|
C | T | 1 | a0005c0029t0001g0141 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.785-1352C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40500569 | ||||||
chr19:40500678
|
A | T | 1 | a0001c0001t0001g0048 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.785-1243A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40500678 | ||||||
chr19:40500712
|
T | C | 41 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.785-1209T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40500712 | ||||||
chr19:40500868
|
AGAAAG | A | 6 | a0006c0043t0001g0126a0006c0044t0001g0167a0008c0013t0001g0143others(3): Show | 6 | HG02572.hp2 HG02922.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.785-1033_785-1029d others(7): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40500868 | |||||
chr19:40501042
|
A | C | 1 | a0008c0013t0001g0143 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.785-879A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40501042 | ||||||
chr19:40501170
|
C | T | 2 | a0001c0002t0001g0086a0001c0002t0005g0193 | 2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.785-751C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40501170 | ||||||
chr19:40501203
|
A | G | 164 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.785-718A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40501203 | ||||||
chr19:40501241
|
G | GA | 45 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0028others(42): Show | 45 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.785-668dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40501241 | |||||
chr19:40501622
|
C | T | 1 | a0005c0009t0009g0190 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.785-299C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40501622 | ||||||
chr19:40501665
|
T | C | 1 | a0001c0002t0001g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.785-256T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | chr19 | 40501665 | ||||||
chr19:40501890
|
GTC | G | 55 | a0001c0002t0001g0086a0001c0002t0001g0231a0001c0002t0005g0193others(52): Show | 55 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.785-29_785-28delCT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr19 | 40501890 | |||||
chr19:40502598
|
A | C | 2 | a0001c0001t0001g0225a0001c0010t0001g0149 | 2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1203+91A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 10/35 | chr19 | 40502598 | ||||||
chr19:40502962
|
T | G | 1 | a0001c0041t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1362+29T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 11/35 | chr19 | 40502962 | ||||||
chr19:40502970
|
C | T | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1362+37C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 11/35 | chr19 | 40502970 | ||||||
chr19:40503040
|
GA | G | 24 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0097others(21): Show | 24 | HG00280.hp1 HG01099.hp1 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.1362+108delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 11/35 | chr19 | 40503040 | ||||||
chr19:40503146
|
G | A | 2 | a0001c0001t0001g0217a0004c0007t0001g0186 | 2 | HG00738.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1362+213G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 11/35 | chr19 | 40503146 | ||||||
chr19:40503228
|
A | G | 1 | a0001c0054t0001g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1362+295A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 11/35 | chr19 | 40503228 | ||||||
chr19:40503234
|
T | G | 6 | a0006c0043t0001g0126a0006c0044t0001g0167a0008c0013t0001g0143others(3): Show | 6 | HG02572.hp2 HG02922.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1362+301T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 11/35 | chr19 | 40503234 | ||||||
chr19:40503338
|
G | A | 4 | a0001c0001t0001g0064a0004c0007t0001g0173a0004c0007t0001g0188others(1): Show | 4 | HG01516.hp1 HG02602.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1362+405G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 11/35 | chr19 | 40503338 | ||||||
chr19:40503650
|
G | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1363-180G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 11/35 | chr19 | 40503650 | ||||||
chr19:40504137
|
C | CG | 35 | a0001c0001t0001g0074a0001c0002t0001g0017a0001c0002t0001g0178others(32): Show | 35 | HG00280.hp1 HG01099.hp1 HG01106.hp1 others(32): Show |
splice_region_variant&intron_variant | LOW | c.1665+7dupG | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40504137 | |||||
chr19:40504137
|
C | CT | 2 | a0001c0001t0001g0184a0004c0007t0001g0140 | 2 | HG00642.hp1 HG02738.hp2 |
splice_region_variant&intron_variant | LOW | c.1665+5_1665+6insT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40504137 | ||||||
chr19:40504138
|
G | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0028others(36): Show | 39 | HG00099.hp1 HG00621.hp1 HG00738.hp1 others(36): Show |
splice_region_variant&intron_variant | LOW | c.1665+6G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40504138 | ||||||
chr19:40504140
|
C | G | 164 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
splice_region_variant&intron_variant | LOW | c.1665+8C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40504140 | ||||||
chr19:40504421
|
C | A | 1 | a0012c0050t0001g0023 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1665+289C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40504421 | ||||||
chr19:40504537
|
C | T | 30 | a0001c0008t0001g0060a0001c0008t0001g0061a0001c0008t0001g0062others(27): Show | 30 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1665+405C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40504537 | ||||||
chr19:40504585
|
C | T | 6 | a0006c0043t0001g0126a0006c0044t0001g0167a0008c0013t0001g0143others(3): Show | 6 | HG02572.hp2 HG02922.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1665+453C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40504585 | ||||||
chr19:40504625
|
C | T | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1665+493C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40504625 | ||||||
chr19:40504668
|
C | CA | 46 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(43): Show | 46 | HG00099.hp1 HG00280.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.1665+547dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40504668 | |||||
chr19:40504668
|
C | CAA | 8 | a0001c0001t0001g0049a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG00741.hp1 HG01074.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1665+546_1665+547d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40504668 | |||||
chr19:40504680
|
C | A | 1 | a0004c0007t0010g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1665+548C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40504680 | ||||||
chr19:40504752
|
G | A | 1 | a0004c0007t0003g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1665+620G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40504752 | ||||||
chr19:40504851
|
C | CA | 39 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.1665+728dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40504851 | |||||
chr19:40504934
|
T | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0217others(2): Show | 5 | HG00738.hp2 HG01081.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1665+802T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40504934 | ||||||
chr19:40505042
|
A | AAG | 42 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0028others(39): Show | 42 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1665+926_1665+927d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505042 | |||||
chr19:40505086
|
C | T | 2 | a0002c0004t0001g0042a0002c0004t0001g0200 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1665+954C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40505086 | ||||||
chr19:40505094
|
A | G | 1 | a0001c0002t0002g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1665+962A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40505094 | ||||||
chr19:40505221
|
C | CA | 5 | a0001c0002t0001g0086a0001c0002t0002g0183a0001c0002t0005g0193others(2): Show | 5 | HG01884.hp2 HG03098.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1666-995dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505221 | |||||
chr19:40505221
|
CA | C | 110 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0028others(107): Show | 110 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1666-995delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505221 | |||||
chr19:40505221
|
CAA | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0097others(8): Show | 11 | HG00280.hp1 HG01099.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1666-996_1666-995d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505221 | |||||
chr19:40505275
|
C | T | 37 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(34): Show | 37 | HG00099.hp2 HG00140.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.1666-961C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40505275 | ||||||
chr19:40505354
|
A | G | 164 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1666-882A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40505354 | ||||||
chr19:40505382
|
C | CA | 31 | a0001c0001t0001g0113a0001c0002t0001g0037a0001c0008t0001g0077others(28): Show | 31 | HG01081.hp1 HG01884.hp1 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.1666-832dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505382 | |||||
chr19:40505382
|
C | CAA | 34 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0071others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.1666-833_1666-832d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505382 | |||||
chr19:40505382
|
C | CAAAA | 38 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0028others(35): Show | 38 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1666-835_1666-832d others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505382 | |||||
chr19:40505382
|
CA | C | 8 | a0001c0001t0001g0053a0001c0001t0001g0114a0001c0001t0001g0134others(5): Show | 8 | HG01099.hp1 HG01891.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.1666-832delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505382 | |||||
chr19:40505402
|
A | G | 1 | a0012c0050t0001g0023 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1666-834A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40505402 | ||||||
chr19:40505643
|
C | G | 37 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(34): Show | 37 | HG00099.hp2 HG00140.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.1666-593C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40505643 | ||||||
chr19:40505700
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1666-536G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40505700 | ||||||
chr19:40505700
|
G | GAGGA | 35 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0087others(32): Show | 35 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1666-485_1666-482d others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505700 | |||||
chr19:40505700
|
G | GAGGAAGG others(1): Show |
23 | a0001c0001t0001g0107a0001c0002t0001g0076a0001c0002t0001g0228others(20): Show | 23 | HG00099.hp2 HG00280.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1666-489_1666-482d others(10): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505700 | |||||
chr19:40505700
|
G | GAGGAAGG others(5): Show |
19 | a0001c0001t0001g0038a0001c0002t0001g0037a0001c0008t0001g0155others(16): Show | 19 | HG01081.hp1 HG01261.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1666-493_1666-482d others(14): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505700 | |||||
chr19:40505700
|
G | GAGGAAGG others(9): Show |
8 | a0001c0002t0002g0183a0001c0008t0001g0046a0001c0010t0001g0093others(5): Show | 8 | HG01106.hp1 HG02145.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1666-497_1666-482d others(18): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505700 | |||||
chr19:40505700
|
G | GAGGAAGG others(13): Show |
2 | a0001c0008t0001g0077a0001c0008t0001g0151 | 2 | HG03486.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1666-501_1666-482d others(22): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505700 | |||||
chr19:40505700
|
G | GAGGAAGG others(17): Show |
1 | a0003c0006t0001g0035 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1666-505_1666-482d others(26): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505700 | |||||
chr19:40505700
|
GAGGA | G | 57 | a0001c0001t0001g0021a0001c0001t0001g0028a0001c0001t0001g0032others(54): Show | 57 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1666-485_1666-482d others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505700 | |||||
chr19:40505700
|
GAGGAAGG others(1): Show |
G | 8 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0204others(5): Show | 8 | HG01175.hp1 HG01255.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1666-489_1666-482d others(10): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505700 | |||||
chr19:40505700
|
GAGGAAGG others(5): Show |
G | 2 | a0004c0007t0010g0136a0012c0050t0001g0023 | 2 | HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1666-493_1666-482d others(14): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505700 | |||||
chr19:40505700
|
GAGGAAGG others(9): Show |
G | 1 | a0001c0041t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1666-497_1666-482d others(18): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr19 | 40505700 | |||||
chr19:40505755
|
A | G | 3 | a0002c0003t0001g0182a0002c0003t0001g0221a0005c0009t0001g0007 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1666-481A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40505755 | ||||||
chr19:40505758
|
G | GGAAGAA | 3 | a0002c0003t0001g0182a0002c0003t0001g0221a0005c0009t0001g0007 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1666-478_1666-477i others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40505758 | ||||||
chr19:40506190
|
C | T | 5 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0040others(2): Show | 5 | HG00621.hp2 HG02027.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.1666-46C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 12/35 | chr19 | 40506190 | ||||||
chr19:40506519
|
A | G | 1 | a0002c0034t0001g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1816+133A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40506519 | ||||||
chr19:40506794
|
A | G | 56 | a0001c0008t0001g0046a0001c0008t0001g0060a0001c0008t0001g0061others(53): Show | 56 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.1816+408A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40506794 | ||||||
chr19:40507307
|
C | A | 2 | a0002c0004t0001g0104a0002c0020t0001g0157 | 2 | HG00140.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1816+921C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40507307 | ||||||
chr19:40507308
|
C | T | 1 | a0009c0030t0007g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1816+922C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40507308 | ||||||
chr19:40507334
|
A | T | 125 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0097others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.1816+948A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40507334 | ||||||
chr19:40507541
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1816+1155A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40507541 | ||||||
chr19:40507662
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1816+1276G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40507662 | ||||||
chr19:40507691
|
C | T | 1 | a0004c0007t0010g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1816+1305C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40507691 | ||||||
chr19:40507692
|
G | A | 1 | a0003c0006t0001g0084 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1816+1306G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40507692 | ||||||
chr19:40508201
|
G | C | 41 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0028others(38): Show | 41 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1816+1815G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40508201 | ||||||
chr19:40508203
|
C | T | 1 | a0004c0007t0001g0004 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1816+1817C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40508203 | ||||||
chr19:40508412
|
C | T | 7 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0097others(4): Show | 7 | HG00280.hp1 HG01123.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1816+2026C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40508412 | ||||||
chr19:40508850
|
G | T | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1816+2464G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40508850 | ||||||
chr19:40508913
|
C | T | 35 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(32): Show | 35 | HG00099.hp2 HG00741.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.1816+2527C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40508913 | ||||||
chr19:40509015
|
T | C | 59 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0097others(56): Show | 59 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.1816+2629T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40509015 | ||||||
chr19:40509017
|
G | A | 7 | a0006c0043t0001g0126a0006c0044t0001g0167a0006c0053t0001g0094others(4): Show | 7 | HG02572.hp2 HG02922.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1816+2631G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40509017 | ||||||
chr19:40509085
|
C | CT | 31 | a0001c0001t0001g0009a0001c0001t0001g0038a0001c0002t0005g0193others(28): Show | 31 | HG01109.hp1 HG01109.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.1816+2718dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr19 | 40509085 | |||||
chr19:40509085
|
C | CTT | 8 | a0001c0010t0008g0075a0006c0044t0001g0167a0006c0053t0001g0094others(5): Show | 8 | HG02723.hp2 HG02922.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1816+2717_1816+271 others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr19 | 40509085 | |||||
chr19:40509085
|
CT | C | 52 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0097others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1816+2718delT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr19 | 40509085 | |||||
chr19:40509294
|
A | G | 75 | a0001c0002t0001g0086a0001c0002t0005g0193a0001c0008t0001g0046others(72): Show | 75 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.1816+2908A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40509294 | ||||||
chr19:40509315
|
G | A | 48 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0097others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.1816+2929G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40509315 | ||||||
chr19:40509408
|
GC | G | 2 | a0001c0002t0001g0083a0004c0014t0001g0055 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1816+3023delC | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40509408 | ||||||
chr19:40509500
|
T | C | 11 | a0001c0002t0001g0086a0001c0002t0005g0193a0001c0010t0008g0075others(8): Show | 11 | HG01884.hp2 HG02572.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1817-3106T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40509500 | ||||||
chr19:40509536
|
C | T | 1 | a0001c0041t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1817-3070C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40509536 | ||||||
chr19:40509795
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1817-2811G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40509795 | ||||||
chr19:40509797
|
A | C | 11 | a0001c0002t0001g0086a0001c0002t0005g0193a0001c0010t0008g0075others(8): Show | 11 | HG01884.hp2 HG02572.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1817-2809A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40509797 | ||||||
chr19:40510058
|
C | T | 75 | a0001c0002t0001g0086a0001c0002t0005g0193a0001c0008t0001g0046others(72): Show | 75 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.1817-2548C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40510058 | ||||||
chr19:40510098
|
G | A | 18 | a0001c0008t0001g0046a0001c0008t0001g0077a0002c0003t0001g0127others(15): Show | 18 | HG01884.hp1 HG02027.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1817-2508G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40510098 | ||||||
chr19:40510468
|
C | T | 1 | a0003c0006t0001g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1817-2138C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40510468 | ||||||
chr19:40510577
|
A | G | 1 | a0001c0041t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1817-2029A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40510577 | ||||||
chr19:40510582
|
T | C | 48 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0097others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.1817-2024T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40510582 | ||||||
chr19:40510647
|
G | C | 1 | a0002c0015t0001g0135 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1817-1959G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40510647 | ||||||
chr19:40510665
|
C | T | 99 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1817-1941C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40510665 | ||||||
chr19:40510784
|
G | C | 1 | a0001c0010t0008g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1817-1822G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40510784 | ||||||
chr19:40510922
|
C | T | 2 | a0001c0002t0001g0086a0001c0002t0005g0193 | 2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1817-1684C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40510922 | ||||||
chr19:40511028
|
A | C | 65 | a0001c0008t0001g0046a0001c0008t0001g0060a0001c0008t0001g0061others(62): Show | 65 | HG00140.hp1 HG00280.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.1817-1578A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40511028 | ||||||
chr19:40511165
|
G | T | 7 | a0006c0043t0001g0126a0006c0044t0001g0167a0006c0053t0001g0094others(4): Show | 7 | HG02572.hp2 HG02922.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1817-1441G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40511165 | ||||||
chr19:40511202
|
G | A | 11 | a0001c0002t0001g0086a0001c0002t0005g0193a0001c0010t0008g0075others(8): Show | 11 | HG01884.hp2 HG02572.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1817-1404G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40511202 | ||||||
chr19:40511230
|
C | T | 1 | a0002c0003t0001g0232 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1817-1376C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40511230 | ||||||
chr19:40511249
|
CA | C | 120 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1817-1348delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr19 | 40511249 | |||||
chr19:40511274
|
G | A | 18 | a0001c0008t0001g0046a0001c0008t0001g0077a0002c0003t0001g0127others(15): Show | 18 | HG01884.hp1 HG02027.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1817-1332G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40511274 | ||||||
chr19:40511325
|
A | G | 122 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0097others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1817-1281A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40511325 | ||||||
chr19:40511563
|
G | A | 43 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(40): Show | 43 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1817-1043G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40511563 | ||||||
chr19:40511577
|
A | T | 64 | a0001c0008t0001g0046a0001c0008t0001g0060a0001c0008t0001g0061others(61): Show | 64 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.1817-1029A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40511577 | ||||||
chr19:40511845
|
C | T | 18 | a0001c0008t0001g0046a0001c0008t0001g0077a0002c0003t0001g0127others(15): Show | 18 | HG01884.hp1 HG02027.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1817-761C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40511845 | ||||||
chr19:40511907
|
G | T | 120 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1817-699G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40511907 | ||||||
chr19:40511955
|
C | T | 4 | a0001c0010t0001g0054a0001c0010t0001g0070a0001c0010t0001g0098others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1817-651C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40511955 | ||||||
chr19:40512009
|
A | G | 1 | a0001c0010t0008g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1817-597A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40512009 | ||||||
chr19:40512079
|
C | T | 6 | a0001c0010t0001g0093a0004c0011t0001g0137a0004c0011t0001g0138others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1817-527C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 13/35 | chr19 | 40512079 | ||||||
chr19:40513688
|
T | C | 1 | a0001c0002t0001g0083 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2765+134T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | chr19 | 40513688 | ||||||
chr19:40513704
|
C | T | 1 | a0009c0030t0007g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2765+150C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | chr19 | 40513704 | ||||||
chr19:40513736
|
A | G | 10 | a0001c0010t0001g0054a0001c0010t0001g0070a0001c0010t0001g0093others(7): Show | 10 | HG00280.hp1 HG01123.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2765+182A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | chr19 | 40513736 | ||||||
chr19:40513812
|
C | T | 37 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(34): Show | 37 | HG00099.hp1 HG00621.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.2765+258C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | chr19 | 40513812 | ||||||
chr19:40513898
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2765+344C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | chr19 | 40513898 | ||||||
chr19:40513903
|
T | G | 1 | a0001c0001t0001g0225 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2765+349T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | chr19 | 40513903 | ||||||
chr19:40513904
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2765+350A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | chr19 | 40513904 | ||||||
chr19:40513905
|
T | C | 43 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(40): Show | 43 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.2765+351T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | chr19 | 40513905 | ||||||
chr19:40513971
|
G | A | 37 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(34): Show | 37 | HG00099.hp1 HG00621.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.2765+417G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | chr19 | 40513971 | ||||||
chr19:40513984
|
C | T | 1 | a0003c0005t0001g0015 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2765+430C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | chr19 | 40513984 | ||||||
chr19:40514158
|
G | C | 164 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.2765+604G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | chr19 | 40514158 | ||||||
chr19:40514640
|
C | T | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2766-671C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | chr19 | 40514640 | ||||||
chr19:40514740
|
A | T | 1 | a0001c0001t0006g0233 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2766-571A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | chr19 | 40514740 | ||||||
chr19:40514947
|
A | G | 1 | a0001c0010t0001g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2766-364A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | chr19 | 40514947 | ||||||
chr19:40515094
|
G | T | 1 | a0001c0002t0001g0076 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2766-217G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | chr19 | 40515094 | ||||||
chr19:40515097
|
T | G | 2 | a0002c0004t0001g0104a0005c0023t0001g0191 | 2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.2766-214T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | chr19 | 40515097 | ||||||
chr19:40515182
|
GAGA | G | 52 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.2766-126_2766-124d others(5): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr19 | 40515182 | |||||
chr19:40515630
|
C | A | 7 | a0006c0043t0001g0126a0006c0044t0001g0167a0006c0053t0001g0094others(4): Show | 7 | HG02572.hp2 HG02922.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2903+182C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40515630 | ||||||
chr19:40515746
|
G | A | 2 | a0001c0002t0001g0086a0001c0002t0005g0193 | 2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2903+298G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40515746 | ||||||
chr19:40515867
|
TGC | T | 2 | a0001c0008t0001g0060a0001c0008t0001g0153 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2903+424_2903+425d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr19 | 40515867 | |||||
chr19:40515870
|
G | GCA | 17 | a0001c0001t0001g0119a0001c0041t0001g0024a0002c0003t0001g0063others(14): Show | 17 | HG00140.hp1 HG01074.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.2903+423_2903+424i others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr19 | 40515870 | |||||
chr19:40515872
|
G | A | 92 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.2903+424G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40515872 | ||||||
chr19:40515872
|
G | GCA | 16 | a0001c0001t0001g0047a0001c0008t0001g0046a0001c0008t0001g0077others(13): Show | 16 | HG01884.hp1 HG02027.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.2903+451_2903+452d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr19 | 40515872 | |||||
chr19:40515872
|
GCA | G | 48 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0071others(45): Show | 48 | HG00099.hp2 HG00741.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.2903+451_2903+452d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr19 | 40515872 | |||||
chr19:40515872
|
GCACA | G | 3 | a0001c0002t0001g0086a0001c0002t0005g0193a0001c0010t0008g0075 | 3 | HG01884.hp2 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2903+449_2903+452d others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr19 | 40515872 | |||||
chr19:40515876
|
A | G | 7 | a0006c0043t0001g0126a0006c0044t0001g0167a0006c0053t0001g0094others(4): Show | 7 | HG02572.hp2 HG02922.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2903+428A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40515876 | ||||||
chr19:40515914
|
C | CACACACA others(7): Show |
1 | a0001c0041t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2903+480_2903+493d others(16): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr19 | 40515914 | |||||
chr19:40515922
|
T | TATATATA others(7): Show |
3 | a0004c0007t0003g0002a0004c0016t0001g0003a0005c0009t0001g0148 | 3 | HG01891.hp1 HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2903+487_2903+488i others(16): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr19 | 40515922 | |||||
chr19:40515928
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0019 | 2 | HG01175.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2903+480T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40515928 | ||||||
chr19:40515930
|
CACACATA others(13): Show |
C | 18 | a0001c0001t0001g0044a0001c0001t0001g0053a0001c0001t0001g0064others(15): Show | 18 | HG00741.hp2 HG01074.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.2903+548_2903+567d others(22): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr19 | 40515930 | |||||
chr19:40515934
|
CATATAT | C | 60 | a0001c0008t0001g0046a0001c0008t0001g0060a0001c0008t0001g0061others(57): Show | 60 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.2903+488_2903+493d others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr19 | 40515934 | |||||
chr19:40515937
|
ATATACG | A | 55 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(52): Show | 55 | HG00099.hp2 HG00280.hp1 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.2903+494_2903+499d others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr19 | 40515937 | |||||
chr19:40515943
|
G | A | 60 | a0001c0008t0001g0046a0001c0008t0001g0060a0001c0008t0001g0061others(57): Show | 60 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.2903+495G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40515943 | ||||||
chr19:40515950
|
T | C | 115 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2903+502T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40515950 | ||||||
chr19:40515982
|
C | T | 1 | a0002c0020t0001g0157 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2903+534C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40515982 | ||||||
chr19:40516022
|
C | T | 173 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0021others(170): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.2903+574C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40516022 | ||||||
chr19:40516023
|
G | GTATATAT others(17): Show |
4 | a0001c0001t0001g0064a0004c0007t0001g0173a0004c0007t0001g0188others(1): Show | 4 | HG01516.hp1 HG02602.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.2903+588_2903+611d others(26): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr19 | 40516023 | |||||
chr19:40516070
|
G | GTA | 46 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(43): Show | 46 | HG00099.hp2 HG00741.hp2 HG01123.hp1 others(43): Show |
intron_variant | MODIFIER | c.2903+633_2903+634d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr19 | 40516070 | |||||
chr19:40516070
|
G | GTATA | 10 | a0001c0010t0001g0054a0001c0010t0001g0070a0001c0010t0001g0093others(7): Show | 10 | HG00280.hp1 HG01123.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2903+631_2903+634d others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr19 | 40516070 | |||||
chr19:40516175
|
T | C | 35 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(32): Show | 35 | HG00099.hp2 HG00741.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.2903+727T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40516175 | ||||||
chr19:40516237
|
CA | C | 81 | a0001c0001t0001g0150a0001c0001t0001g0161a0001c0002t0001g0017others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.2903+808delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr19 | 40516237 | |||||
chr19:40516237
|
CAA | C | 33 | a0001c0002t0001g0086a0001c0002t0005g0193a0001c0008t0001g0046others(30): Show | 33 | HG01074.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.2903+807_2903+808d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr19 | 40516237 | |||||
chr19:40516237
|
CAAA | C | 7 | a0006c0043t0001g0126a0006c0044t0001g0167a0006c0053t0001g0094others(4): Show | 7 | HG02572.hp2 HG02922.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2903+806_2903+808d others(5): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr19 | 40516237 | |||||
chr19:40516478
|
A | C | 4 | a0001c0010t0001g0054a0001c0010t0001g0070a0001c0010t0001g0098others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2903+1030A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40516478 | ||||||
chr19:40516541
|
C | T | 1 | a0004c0007t0010g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2903+1093C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40516541 | ||||||
chr19:40516553
|
G | A | 7 | a0006c0043t0001g0126a0006c0044t0001g0167a0006c0053t0001g0094others(4): Show | 7 | HG02572.hp2 HG02922.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2903+1105G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40516553 | ||||||
chr19:40516749
|
G | A | 3 | a0003c0006t0001g0084a0003c0006t0001g0212a0003c0006t0004g0080 | 3 | NA18970.hp2 NA18983.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2903+1301G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40516749 | ||||||
chr19:40516917
|
G | T | 14 | a0001c0002t0001g0017a0001c0002t0001g0071a0001c0002t0001g0076others(11): Show | 14 | HG00099.hp2 HG01496.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.2903+1469G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40516917 | ||||||
chr19:40516918
|
C | T | 1 | a0002c0003t0001g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2903+1470C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40516918 | ||||||
chr19:40517077
|
C | G | 1 | a0013c0037t0001g0079 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2903+1629C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40517077 | ||||||
chr19:40517604
|
C | T | 120 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.2904-1797C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40517604 | ||||||
chr19:40517605
|
G | A | 2 | a0003c0005t0002g0207a0003c0005t0002g0208 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2904-1796G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40517605 | ||||||
chr19:40517694
|
A | G | 120 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.2904-1707A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40517694 | ||||||
chr19:40517711
|
C | T | 5 | a0002c0004t0001g0029a0002c0004t0001g0042a0002c0004t0001g0200others(2): Show | 5 | HG02258.hp2 HG02809.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2904-1690C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40517711 | ||||||
chr19:40517861
|
C | A | 1 | a0004c0011t0001g0138 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2904-1540C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40517861 | ||||||
chr19:40518178
|
C | T | 2 | a0004c0011t0001g0142a0021c0031t0001g0057 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2904-1223C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40518178 | ||||||
chr19:40518211
|
C | T | 1 | a0002c0021t0001g0010 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2904-1190C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40518211 | ||||||
chr19:40518622
|
C | T | 1 | a0004c0007t0010g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2904-779C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40518622 | ||||||
chr19:40518756
|
A | G | 42 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(39): Show | 42 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.2904-645A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40518756 | ||||||
chr19:40518871
|
C | T | 56 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(53): Show | 56 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.2904-530C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40518871 | ||||||
chr19:40518915
|
A | T | 1 | a0002c0003t0001g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2904-486A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40518915 | ||||||
chr19:40519315
|
G | T | 10 | a0001c0010t0001g0054a0001c0010t0001g0070a0001c0010t0001g0093others(7): Show | 10 | HG00280.hp1 HG01123.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2904-86G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40519315 | ||||||
chr19:40519336
|
G | A | 120 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.2904-65G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 15/35 | chr19 | 40519336 | ||||||
chr19:40520171
|
A | G | 3 | a0001c0002t0001g0086a0001c0002t0005g0193a0001c0010t0008g0075 | 3 | HG01884.hp2 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3654+20A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40520171 | ||||||
chr19:40520233
|
G | A | 7 | a0006c0043t0001g0126a0006c0044t0001g0167a0006c0053t0001g0094others(4): Show | 7 | HG02572.hp2 HG02922.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.3654+82G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40520233 | ||||||
chr19:40520262
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3654+111G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40520262 | ||||||
chr19:40520811
|
G | A | 1 | a0012c0050t0001g0023 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3654+660G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40520811 | ||||||
chr19:40520897
|
T | C | 1 | a0005c0009t0001g0175 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3654+746T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40520897 | ||||||
chr19:40520928
|
C | CT | 15 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0049others(12): Show | 15 | HG00621.hp1 HG02602.hp2 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.3654+789dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr19 | 40520928 | |||||
chr19:40521070
|
G | A | 6 | a0001c0010t0001g0093a0004c0011t0001g0137a0004c0011t0001g0138others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3654+919G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40521070 | ||||||
chr19:40521072
|
G | A | 55 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(52): Show | 55 | HG00099.hp2 HG00280.hp1 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.3654+921G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40521072 | ||||||
chr19:40521165
|
C | T | 5 | a0002c0003t0001g0063a0002c0003t0001g0232a0005c0009t0001g0144others(2): Show | 5 | HG03239.hp2 HG03704.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.3654+1014C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40521165 | ||||||
chr19:40521296
|
G | A | 36 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(33): Show | 36 | HG00099.hp2 HG00741.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.3654+1145G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40521296 | ||||||
chr19:40521329
|
C | T | 1 | a0001c0002t0001g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3654+1178C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40521329 | ||||||
chr19:40521350
|
CTATTGTT others(14): Show |
C | 1 | a0004c0027t0001g0170 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3654+1203_3654+122 others(25): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr19 | 40521350 | |||||
chr19:40521448
|
G | A | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3654+1297G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40521448 | ||||||
chr19:40521636
|
C | G | 1 | a0005c0009t0001g0001 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3654+1485C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40521636 | ||||||
chr19:40521725
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3654+1574C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40521725 | ||||||
chr19:40521746
|
A | G | 1 | a0001c0041t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3654+1595A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40521746 | ||||||
chr19:40521924
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3655-1513C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40521924 | ||||||
chr19:40522087
|
C | T | 1 | a0013c0037t0001g0079 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3655-1350C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40522087 | ||||||
chr19:40522093
|
C | G | 1 | a0001c0010t0001g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3655-1344C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40522093 | ||||||
chr19:40522275
|
G | A | 1 | a0002c0003t0001g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3655-1162G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40522275 | ||||||
chr19:40522348
|
A | AT | 6 | a0001c0001t0001g0009a0001c0001t0001g0038a0001c0041t0001g0024others(3): Show | 6 | HG01109.hp1 HG01255.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.3655-1069dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr19 | 40522348 | |||||
chr19:40522348
|
A | ATT | 14 | a0001c0002t0001g0086a0001c0002t0005g0193a0001c0010t0001g0054others(11): Show | 14 | HG00280.hp1 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.3655-1070_3655-106 others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr19 | 40522348 | |||||
chr19:40522348
|
AT | A | 58 | a0001c0001t0001g0150a0001c0008t0001g0046a0001c0008t0001g0060others(55): Show | 58 | HG00140.hp1 HG00280.hp2 HG01074.hp1 others(55): Show |
intron_variant | MODIFIER | c.3655-1069delT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr19 | 40522348 | |||||
chr19:40522348
|
ATT | A | 6 | a0002c0003t0001g0034a0003c0006t0001g0216a0003c0018t0001g0030others(3): Show | 6 | HG01070.hp1 HG02132.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3655-1070_3655-106 others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr19 | 40522348 | |||||
chr19:40522348
|
ATTT | A | 36 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(33): Show | 36 | HG00099.hp2 HG00741.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.3655-1071_3655-106 others(7): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr19 | 40522348 | |||||
chr19:40522604
|
G | A | 1 | a0002c0003t0001g0063 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3655-833G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40522604 | ||||||
chr19:40522825
|
C | T | 5 | a0006c0043t0001g0126a0006c0044t0001g0167a0008c0013t0001g0143others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3655-612C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40522825 | ||||||
chr19:40523000
|
G | A | 6 | a0001c0010t0001g0093a0004c0011t0001g0137a0004c0011t0001g0138others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3655-437G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40523000 | ||||||
chr19:40523194
|
T | C | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3655-243T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40523194 | ||||||
chr19:40523356
|
G | A | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3655-81G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40523356 | ||||||
chr19:40523404
|
G | C | 2 | a0004c0011t0001g0142a0021c0031t0001g0057 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3655-33G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 16/35 | chr19 | 40523404 | ||||||
chr19:40523850
|
C | A | 2 | a0003c0005t0001g0210a0003c0005t0001g0211 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.3857+211C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40523850 | ||||||
chr19:40523913
|
C | T | 75 | a0001c0008t0001g0046a0001c0008t0001g0060a0001c0008t0001g0061others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.3857+274C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40523913 | ||||||
chr19:40524021
|
T | G | 1 | a0002c0020t0001g0229 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3857+382T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40524021 | ||||||
chr19:40524039
|
A | G | 58 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.3857+400A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40524039 | ||||||
chr19:40524068
|
C | T | 1 | a0012c0050t0001g0023 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3857+429C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40524068 | ||||||
chr19:40524588
|
C | T | 1 | a0003c0018t0001g0030 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3857+949C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40524588 | ||||||
chr19:40525320
|
C | CT | 28 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0033others(25): Show | 28 | HG00621.hp2 HG01169.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.3857+1700dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr19 | 40525320 | |||||
chr19:40525320
|
CT | C | 49 | a0001c0002t0001g0017a0001c0002t0001g0022a0001c0002t0001g0037others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG01123.hp1 others(46): Show |
intron_variant | MODIFIER | c.3857+1700delT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr19 | 40525320 | |||||
chr19:40525320
|
CTT | C | 32 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(29): Show | 32 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.3857+1699_3857+170 others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr19 | 40525320 | |||||
chr19:40525488
|
G | A | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3857+1849G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40525488 | ||||||
chr19:40525667
|
G | A | 1 | a0001c0041t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3857+2028G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40525667 | ||||||
chr19:40525675
|
T | C | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3857+2036T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40525675 | ||||||
chr19:40525716
|
C | T | 39 | a0001c0008t0001g0060a0001c0008t0001g0061a0001c0008t0001g0062others(36): Show | 39 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.3857+2077C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40525716 | ||||||
chr19:40525885
|
T | A | 168 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.3857+2246T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40525885 | ||||||
chr19:40526167
|
C | CT | 83 | a0001c0001t0001g0033a0001c0001t0001g0066a0001c0002t0001g0071others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.3857+2551dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr19 | 40526167 | |||||
chr19:40526167
|
CT | C | 29 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(26): Show | 29 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.3857+2551delT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr19 | 40526167 | |||||
chr19:40526198
|
A | T | 28 | a0001c0008t0001g0046a0002c0003t0001g0127a0003c0005t0001g0011others(25): Show | 28 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.3857+2559A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40526198 | ||||||
chr19:40526492
|
C | T | 74 | a0001c0008t0001g0046a0001c0008t0001g0060a0001c0008t0001g0061others(71): Show | 74 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.3858-2549C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40526492 | ||||||
chr19:40526562
|
A | G | 105 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.3858-2479A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40526562 | ||||||
chr19:40526647
|
C | T | 6 | a0001c0010t0001g0093a0004c0011t0001g0137a0004c0011t0001g0138others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3858-2394C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40526647 | ||||||
chr19:40526879
|
G | A | 13 | a0002c0003t0001g0063a0002c0003t0001g0197a0002c0003t0001g0198others(10): Show | 13 | HG00140.hp1 HG01074.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.3858-2162G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40526879 | ||||||
chr19:40527122
|
C | G | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3858-1919C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40527122 | ||||||
chr19:40527202
|
C | T | 38 | a0001c0001t0001g0201a0001c0002t0001g0017a0001c0002t0001g0022others(35): Show | 38 | HG00099.hp2 HG00741.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.3858-1839C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40527202 | ||||||
chr19:40527268
|
C | G | 5 | a0006c0043t0001g0126a0006c0044t0001g0167a0008c0013t0001g0143others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3858-1773C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40527268 | ||||||
chr19:40527392
|
T | C | 2 | a0002c0003t0001g0121a0005c0009t0001g0008 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3858-1649T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40527392 | ||||||
chr19:40527408
|
A | G | 1 | a0003c0006t0001g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3858-1633A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40527408 | ||||||
chr19:40527408
|
A | T | 38 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(35): Show | 38 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.3858-1633A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40527408 | ||||||
chr19:40527477
|
T | C | 34 | a0001c0001t0001g0201a0001c0002t0001g0017a0001c0002t0001g0022others(31): Show | 34 | HG00099.hp2 HG01123.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.3858-1564T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40527477 | ||||||
chr19:40527813
|
T | C | 5 | a0006c0043t0001g0126a0006c0044t0001g0167a0008c0013t0001g0143others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3858-1228T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40527813 | ||||||
chr19:40527980
|
T | TG | 17 | a0001c0001t0001g0064a0001c0002t0001g0086a0001c0002t0005g0193others(14): Show | 17 | HG01123.hp2 HG01257.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.3858-1055dupG | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr19 | 40527980 | |||||
chr19:40528055
|
C | CA | 47 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(44): Show | 47 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.3858-965dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr19 | 40528055 | |||||
chr19:40528055
|
CA | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0008t0001g0060others(2): Show | 5 | HG01109.hp1 HG01168.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3858-965delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr19 | 40528055 | |||||
chr19:40528076
|
AG | A | 4 | a0002c0015t0001g0089a0002c0015t0001g0135a0002c0015t0001g0179others(1): Show | 4 | HG02280.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3858-963delG | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr19 | 40528076 | |||||
chr19:40528077
|
G | A | 76 | a0002c0003t0001g0016a0002c0003t0001g0026a0002c0003t0001g0034others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.3858-964G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40528077 | ||||||
chr19:40528117
|
A | G | 1 | a0001c0002t0001g0037 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3858-924A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40528117 | ||||||
chr19:40528458
|
C | T | 5 | a0001c0001t0001g0064a0001c0002t0001g0086a0001c0002t0005g0193others(2): Show | 5 | HG01884.hp2 HG02602.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.3858-583C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40528458 | ||||||
chr19:40528479
|
G | A | 32 | a0001c0001t0001g0201a0001c0002t0001g0017a0001c0002t0001g0022others(29): Show | 32 | HG00099.hp2 HG01496.hp1 HG01516.hp1 others(29): Show |
intron_variant | MODIFIER | c.3858-562G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40528479 | ||||||
chr19:40528817
|
C | T | 29 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(26): Show | 29 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.3858-224C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40528817 | ||||||
chr19:40528828
|
C | T | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3858-213C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40528828 | ||||||
chr19:40529005
|
G | A | 84 | a0002c0003t0001g0016a0002c0003t0001g0026a0002c0003t0001g0034others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.3858-36G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 17/35 | chr19 | 40529005 | ||||||
chr19:40529414
|
C | T | 17 | a0001c0001t0001g0064a0001c0002t0001g0086a0001c0002t0005g0193others(14): Show | 17 | HG01123.hp2 HG01257.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.3948+283C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40529414 | ||||||
chr19:40529426
|
A | C | 2 | a0001c0041t0001g0024a0012c0050t0001g0023 | 2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3948+295A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40529426 | ||||||
chr19:40529467
|
G | A | 26 | a0002c0003t0001g0127a0003c0005t0001g0011a0003c0005t0001g0015others(23): Show | 26 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.3948+336G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40529467 | ||||||
chr19:40529742
|
G | T | 28 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(25): Show | 28 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.3948+611G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40529742 | ||||||
chr19:40529782
|
C | A | 112 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.3948+651C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40529782 | ||||||
chr19:40530059
|
C | T | 28 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(25): Show | 28 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.3948+928C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40530059 | ||||||
chr19:40530214
|
C | T | 2 | a0001c0041t0001g0024a0012c0050t0001g0023 | 2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3948+1083C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40530214 | ||||||
chr19:40530281
|
C | G | 17 | a0001c0001t0001g0064a0001c0002t0001g0086a0001c0002t0005g0193others(14): Show | 17 | HG01123.hp2 HG01257.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.3948+1150C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40530281 | ||||||
chr19:40530406
|
C | T | 11 | a0001c0008t0001g0060a0001c0008t0001g0061a0001c0008t0001g0062others(8): Show | 11 | HG01123.hp2 HG01257.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3948+1275C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40530406 | ||||||
chr19:40530471
|
G | C | 2 | a0001c0002t0001g0083a0004c0014t0001g0055 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3948+1340G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40530471 | ||||||
chr19:40530584
|
G | A | 84 | a0002c0003t0001g0016a0002c0003t0001g0026a0002c0003t0001g0034others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.3948+1453G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40530584 | ||||||
chr19:40530674
|
T | C | 232 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.3948+1543T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40530674 | ||||||
chr19:40530773
|
C | A | 1 | a0002c0015t0001g0135 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3948+1642C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40530773 | ||||||
chr19:40530807
|
C | T | 2 | a0001c0017t0001g0078a0001c0017t0001g0124 | 2 | NA18967.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.3948+1676C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40530807 | ||||||
chr19:40530814
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3948+1683G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40530814 | ||||||
chr19:40530896
|
C | T | 1 | a0001c0002t0001g0083 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3949-1729C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40530896 | ||||||
chr19:40531367
|
G | C | 17 | a0001c0001t0001g0064a0001c0002t0001g0086a0001c0002t0005g0193others(14): Show | 17 | HG01123.hp2 HG01257.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.3949-1258G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40531367 | ||||||
chr19:40531442
|
G | A | 1 | a0009c0030t0007g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3949-1183G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40531442 | ||||||
chr19:40531461
|
T | A | 7 | a0001c0010t0001g0093a0004c0007t0003g0002a0004c0011t0001g0137others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.3949-1164T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40531461 | ||||||
chr19:40531464
|
G | GT | 37 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0018others(34): Show | 37 | HG00099.hp2 HG00642.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.3949-1126dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr19 | 40531464 | |||||
chr19:40531464
|
G | GTT | 28 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0038others(25): Show | 28 | HG00738.hp2 HG01071.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.3949-1127_3949-112 others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr19 | 40531464 | |||||
chr19:40531464
|
G | GTTT | 5 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0006g0233others(2): Show | 5 | HG00280.hp1 HG01978.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.3949-1128_3949-112 others(7): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr19 | 40531464 | |||||
chr19:40531464
|
GT | G | 13 | a0001c0001t0001g0064a0001c0001t0001g0113a0001c0002t0001g0086others(10): Show | 13 | HG01884.hp2 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.3949-1126delT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr19 | 40531464 | |||||
chr19:40531464
|
GTT | G | 5 | a0001c0002t0005g0193a0001c0008t0001g0046a0001c0008t0001g0153others(2): Show | 5 | HG00741.hp2 HG02486.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3949-1127_3949-112 others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr19 | 40531464 | |||||
chr19:40531464
|
GTTTT | G | 20 | a0002c0003t0001g0127a0002c0003t0001g0181a0002c0003t0001g0182others(17): Show | 20 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.3949-1129_3949-112 others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr19 | 40531464 | |||||
chr19:40531464
|
GTTTTT | G | 51 | a0002c0003t0001g0016a0002c0003t0001g0026a0002c0003t0001g0034others(48): Show | 51 | HG00099.hp1 HG01070.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.3949-1130_3949-112 others(9): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr19 | 40531464 | |||||
chr19:40531464
|
GTTTTTT | G | 5 | a0002c0004t0001g0095a0002c0015t0001g0089a0002c0015t0001g0135others(2): Show | 5 | HG02280.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3949-1131_3949-112 others(10): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr19 | 40531464 | |||||
chr19:40531464
|
GTTTTTTT others(4): Show |
G | 4 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0067others(1): Show | 4 | HG01358.hp1 NA18967.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.3949-1136_3949-112 others(15): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr19 | 40531464 | |||||
chr19:40531464
|
GTTTTTTT others(5): Show |
G | 24 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(21): Show | 24 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.3949-1137_3949-112 others(16): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr19 | 40531464 | |||||
chr19:40531464
|
GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0001g0092 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3949-1138_3949-112 others(17): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr19 | 40531464 | |||||
chr19:40531464
|
GTTTTTTT others(8): Show |
G | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3949-1140_3949-112 others(19): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr19 | 40531464 | |||||
chr19:40531464
|
GTTTTTTT others(9): Show |
G | 2 | a0011c0042t0001g0223a0016c0046t0001g0164 | 2 | HG01123.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3949-1141_3949-112 others(20): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr19 | 40531464 | |||||
chr19:40531464
|
GTTTTTTT others(11): Show |
G | 2 | a0001c0002t0001g0083a0004c0014t0001g0055 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3949-1143_3949-112 others(22): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr19 | 40531464 | |||||
chr19:40531464
|
GTTTTTTT others(12): Show |
G | 7 | a0001c0010t0001g0093a0004c0007t0003g0002a0004c0011t0001g0137others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.3949-1144_3949-112 others(23): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr19 | 40531464 | |||||
chr19:40531467
|
T | TG | 2 | a0001c0002t0001g0037a0001c0002t0001g0178 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3949-1158_3949-115 others(5): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40531467 | ||||||
chr19:40531477
|
T | G | 4 | a0002c0015t0001g0089a0002c0015t0001g0135a0002c0015t0001g0179others(1): Show | 4 | HG02280.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3949-1148T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40531477 | ||||||
chr19:40531485
|
T | G | 1 | a0003c0006t0001g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3949-1140T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40531485 | ||||||
chr19:40531502
|
A | T | 1 | a0001c0001t0001g0047 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3949-1123A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40531502 | ||||||
chr19:40531669
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3949-956G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40531669 | ||||||
chr19:40531684
|
C | T | 3 | a0002c0003t0001g0182a0002c0003t0001g0221a0005c0009t0001g0007 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3949-941C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40531684 | ||||||
chr19:40531967
|
C | T | 170 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.3949-658C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40531967 | ||||||
chr19:40532174
|
T | C | 29 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(26): Show | 29 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.3949-451T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40532174 | ||||||
chr19:40532274
|
T | G | 1 | a0022c0032t0001g0006 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3949-351T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40532274 | ||||||
chr19:40532288
|
TG | T | 162 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.3949-329delG | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr19 | 40532288 | |||||
chr19:40532451
|
C | A | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3949-174C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 18/35 | chr19 | 40532451 | ||||||
chr19:40532876
|
C | A | 1 | a0002c0003t0001g0063 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4095+105C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 19/35 | chr19 | 40532876 | ||||||
chr19:40533068
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4095+297A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 19/35 | chr19 | 40533068 | ||||||
chr19:40533472
|
C | T | 1 | a0014c0040t0001g0218 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4096-608C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 19/35 | chr19 | 40533472 | ||||||
chr19:40533701
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4096-379C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 19/35 | chr19 | 40533701 | ||||||
chr19:40533871
|
T | C | 2 | a0001c0041t0001g0024a0012c0050t0001g0023 | 2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.4096-209T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 19/35 | chr19 | 40533871 | ||||||
chr19:40533973
|
C | G | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4096-107C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 19/35 | chr19 | 40533973 | ||||||
chr19:40534027
|
C | G | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4096-53C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 19/35 | chr19 | 40534027 | ||||||
chr19:40534427
|
G | A | 83 | a0002c0003t0001g0016a0002c0003t0001g0026a0002c0003t0001g0034others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.4359+84G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40534427 | ||||||
chr19:40534492
|
C | T | 27 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(24): Show | 27 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.4359+149C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40534492 | ||||||
chr19:40534649
|
C | T | 1 | a0005c0009t0001g0001 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4359+306C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40534649 | ||||||
chr19:40534897
|
C | T | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4359+554C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40534897 | ||||||
chr19:40535027
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4359+684T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40535027 | ||||||
chr19:40535200
|
C | T | 84 | a0002c0003t0001g0016a0002c0003t0001g0026a0002c0003t0001g0034others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.4359+857C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40535200 | ||||||
chr19:40535258
|
A | G | 26 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(23): Show | 26 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.4359+915A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40535258 | ||||||
chr19:40535263
|
G | T | 8 | a0001c0008t0001g0060a0001c0008t0001g0061a0001c0008t0001g0062others(5): Show | 8 | HG01257.hp2 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.4359+920G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40535263 | ||||||
chr19:40535318
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4359+975A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40535318 | ||||||
chr19:40535560
|
CA | C | 69 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(66): Show | 69 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.4359+1232delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40535560 | |||||
chr19:40535708
|
G | A | 1 | a0001c0002t0001g0022 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4359+1365G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40535708 | ||||||
chr19:40535782
|
A | C | 1 | a0001c0010t0001g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4359+1439A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40535782 | ||||||
chr19:40535917
|
A | G | 1 | a0002c0034t0001g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4359+1574A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40535917 | ||||||
chr19:40536052
|
A | G | 1 | a0001c0002t0001g0071 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.4359+1709A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40536052 | ||||||
chr19:40536097
|
A | G | 84 | a0002c0003t0001g0016a0002c0003t0001g0026a0002c0003t0001g0034others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.4359+1754A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40536097 | ||||||
chr19:40536153
|
G | A | 28 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(25): Show | 28 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.4359+1810G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40536153 | ||||||
chr19:40536221
|
C | G | 1 | a0002c0034t0001g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4359+1878C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40536221 | ||||||
chr19:40536290
|
T | C | 11 | a0001c0008t0001g0060a0001c0008t0001g0061a0001c0008t0001g0062others(8): Show | 11 | HG01123.hp2 HG01257.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.4359+1947T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40536290 | ||||||
chr19:40536446
|
A | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0097 | 3 | HG01516.hp2 HG01517.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.4359+2103A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40536446 | ||||||
chr19:40536849
|
A | G | 90 | a0001c0001t0001g0072a0001c0002t0001g0083a0001c0010t0001g0070others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.4359+2506A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40536849 | ||||||
chr19:40536895
|
C | T | 44 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(41): Show | 44 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.4359+2552C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40536895 | ||||||
chr19:40536909
|
G | A | 10 | a0001c0010t0001g0093a0002c0004t0001g0029a0002c0004t0001g0224others(7): Show | 10 | HG01123.hp1 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.4359+2566G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40536909 | ||||||
chr19:40537144
|
G | A | 86 | a0001c0001t0001g0072a0001c0010t0001g0070a0001c0010t0001g0093others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.4359+2801G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40537144 | ||||||
chr19:40537421
|
A | G | 3 | a0002c0003t0001g0182a0002c0003t0001g0221a0005c0009t0001g0007 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4359+3078A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40537421 | ||||||
chr19:40537504
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4359+3161G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40537504 | ||||||
chr19:40537569
|
T | G | 1 | a0004c0014t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4359+3226T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40537569 | ||||||
chr19:40537726
|
CCTCCCTG others(46): Show |
C | 1 | a0004c0007t0003g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4359+3389_4359+344 others(57): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40537726 | |||||
chr19:40537861
|
G | A | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4359+3518G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40537861 | ||||||
chr19:40538114
|
C | T | 3 | a0006c0043t0001g0126a0006c0044t0001g0167a0008c0013t0001g0143 | 3 | HG02572.hp2 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4359+3771C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40538114 | ||||||
chr19:40538126
|
C | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0217a0001c0008t0001g0117others(2): Show | 5 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.4359+3783C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40538126 | ||||||
chr19:40538191
|
CCAACCTG others(2): Show |
C | 84 | a0001c0001t0001g0072a0001c0010t0001g0070a0001c0010t0001g0093others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.4359+3853_4359+386 others(13): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40538191 | |||||
chr19:40538347
|
CCT | C | 229 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.4359+4006_4359+400 others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40538347 | |||||
chr19:40538390
|
C | CA | 8 | a0001c0010t0001g0149a0001c0010t0001g0230a0002c0003t0001g0073others(5): Show | 8 | HG02055.hp2 HG02572.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.4359+4062dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40538390 | |||||
chr19:40538410
|
A | G | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4359+4067A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40538410 | ||||||
chr19:40538537
|
G | A | 2 | a0001c0054t0001g0090a0006c0053t0001g0094 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4359+4194G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40538537 | ||||||
chr19:40538722
|
G | C | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4359+4379G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40538722 | ||||||
chr19:40538732
|
C | T | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4359+4389C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40538732 | ||||||
chr19:40538758
|
T | C | 43 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(40): Show | 43 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.4359+4415T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40538758 | ||||||
chr19:40538866
|
A | G | 3 | a0008c0013t0001g0143a0008c0013t0001g0145a0008c0013t0001g0147 | 3 | HG02922.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4359+4523A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40538866 | ||||||
chr19:40539110
|
C | T | 225 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.4359+4767C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40539110 | ||||||
chr19:40539269
|
C | T | 1 | a0017c0036t0001g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4359+4926C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40539269 | ||||||
chr19:40539591
|
C | G | 1 | a0001c0001t0001g0044 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.4359+5248C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40539591 | ||||||
chr19:40539668
|
C | T | 26 | a0003c0005t0001g0011a0003c0005t0001g0015a0003c0005t0001g0050others(23): Show | 26 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.4359+5325C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40539668 | ||||||
chr19:40539669
|
G | A | 2 | a0001c0001t0001g0225a0018c0052t0001g0122 | 2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.4359+5326G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40539669 | ||||||
chr19:40539769
|
C | T | 1 | a0001c0002t0001g0022 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4359+5426C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40539769 | ||||||
chr19:40539827
|
C | T | 44 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(41): Show | 44 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.4359+5484C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40539827 | ||||||
chr19:40539865
|
A | T | 84 | a0001c0001t0001g0072a0001c0010t0001g0070a0001c0010t0001g0093others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.4359+5522A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40539865 | ||||||
chr19:40539925
|
C | G | 2 | a0001c0010t0001g0149a0001c0010t0001g0230 | 2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4359+5582C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40539925 | ||||||
chr19:40539930
|
A | AT | 85 | a0001c0001t0001g0072a0001c0001t0001g0225a0001c0010t0001g0070others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.4359+5600dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40539930 | |||||
chr19:40540159
|
T | G | 2 | a0001c0010t0001g0149a0001c0010t0001g0230 | 2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4359+5816T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40540159 | ||||||
chr19:40540323
|
T | C | 1 | a0001c0001t0001g0041 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.4359+5980T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40540323 | ||||||
chr19:40540348
|
G | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(36): Show | 39 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.4359+6005G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40540348 | ||||||
chr19:40540354
|
G | T | 2 | a0001c0001t0001g0064a0004c0007t0001g0188 | 2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.4359+6011G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40540354 | ||||||
chr19:40540404
|
T | G | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4359+6061T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40540404 | ||||||
chr19:40540641
|
G | A | 43 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0008t0001g0046others(40): Show | 43 | HG00140.hp1 HG01070.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.4359+6298G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40540641 | ||||||
chr19:40540720
|
G | C | 3 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023 | 3 | HG02109.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.4359+6377G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40540720 | ||||||
chr19:40540806
|
C | A | 38 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(35): Show | 38 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4359+6463C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40540806 | ||||||
chr19:40540814
|
C | CA | 16 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0065others(13): Show | 16 | HG00140.hp2 HG01071.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.4359+6497dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40540814 | |||||
chr19:40540814
|
CAAA | C | 8 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0041others(5): Show | 8 | HG00621.hp1 HG01496.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.4359+6495_4359+649 others(7): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40540814 | |||||
chr19:40540814
|
CAAAA | C | 43 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(40): Show | 43 | HG00741.hp1 HG01074.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.4359+6494_4359+649 others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40540814 | |||||
chr19:40540814
|
CAAAAA | C | 70 | a0001c0001t0001g0064a0001c0002t0003g0163a0001c0008t0001g0046others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.4359+6493_4359+649 others(9): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40540814 | |||||
chr19:40540814
|
CAAAAAA | C | 15 | a0001c0010t0001g0070a0002c0003t0001g0099a0002c0003t0001g0182others(12): Show | 15 | HG01123.hp1 HG01168.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.4359+6492_4359+649 others(10): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40540814 | |||||
chr19:40540837
|
A | G | 1 | a0003c0006t0001g0216 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.4359+6494A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40540837 | ||||||
chr19:40540900
|
C | G | 1 | a0001c0002t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4359+6557C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40540900 | ||||||
chr19:40540968
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0107 | 2 | NA19077.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.4359+6625C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40540968 | ||||||
chr19:40541038
|
C | T | 1 | a0002c0003t0001g0099 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4359+6695C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40541038 | ||||||
chr19:40541046
|
G | T | 1 | a0002c0003t0001g0197 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4359+6703G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40541046 | ||||||
chr19:40541333
|
T | C | 1 | a0002c0004t0001g0025 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4359+6990T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40541333 | ||||||
chr19:40541390
|
C | T | 1 | a0001c0010t0001g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4359+7047C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40541390 | ||||||
chr19:40541454
|
G | T | 43 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(40): Show | 43 | HG00140.hp1 HG01070.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.4359+7111G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40541454 | ||||||
chr19:40541575
|
G | T | 88 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.4359+7232G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40541575 | ||||||
chr19:40541627
|
G | A | 135 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(132): Show | 135 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.4359+7284G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40541627 | ||||||
chr19:40541642
|
G | A | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4359+7299G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40541642 | ||||||
chr19:40541777
|
C | T | 1 | a0002c0034t0001g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4360-7412C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40541777 | ||||||
chr19:40541864
|
C | A | 89 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.4360-7325C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40541864 | ||||||
chr19:40541864
|
C | G | 49 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(46): Show | 49 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.4360-7325C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40541864 | ||||||
chr19:40541887
|
C | T | 3 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023 | 3 | HG02109.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.4360-7302C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40541887 | ||||||
chr19:40541919
|
T | G | 89 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.4360-7270T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40541919 | ||||||
chr19:40541995
|
C | T | 2 | a0004c0014t0001g0055a0004c0016t0001g0003 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4360-7194C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40541995 | ||||||
chr19:40542014
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4360-7175C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40542014 | ||||||
chr19:40542148
|
C | G | 1 | a0001c0002t0003g0163 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4360-7041C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40542148 | ||||||
chr19:40542271
|
C | T | 4 | a0003c0005t0001g0050a0003c0005t0001g0051a0003c0005t0001g0059others(1): Show | 4 | HG01175.hp2 HG01255.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.4360-6918C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40542271 | ||||||
chr19:40542342
|
C | G | 2 | a0004c0014t0001g0055a0004c0016t0001g0003 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4360-6847C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40542342 | ||||||
chr19:40542682
|
T | G | 45 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(42): Show | 45 | HG00140.hp1 HG01070.hp1 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.4360-6507T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40542682 | ||||||
chr19:40542759
|
G | C | 1 | a0004c0027t0001g0170 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4360-6430G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40542759 | ||||||
chr19:40542800
|
TTTTTTTT others(7): Show |
T | 1 | a0004c0007t0003g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4360-6375_4360-636 others(18): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40542800 | |||||
chr19:40542872
|
G | A | 43 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(40): Show | 43 | HG00140.hp1 HG01070.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.4360-6317G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40542872 | ||||||
chr19:40543221
|
G | C | 1 | a0002c0003t0001g0034 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4360-5968G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40543221 | ||||||
chr19:40543280
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0028others(1): Show | 4 | HG00280.hp1 HG01109.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.4360-5909C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40543280 | ||||||
chr19:40543382
|
C | T | 4 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4360-5807C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40543382 | ||||||
chr19:40543835
|
A | C | 6 | a0003c0006t0001g0132a0003c0006t0001g0213a0003c0006t0001g0214others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.4360-5354A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40543835 | ||||||
chr19:40544006
|
C | G | 92 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(89): Show |
intron_variant | MODIFIER | c.4360-5183C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40544006 | ||||||
chr19:40544127
|
CT | C | 61 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0038others(58): Show | 61 | HG00099.hp1 HG00741.hp2 HG01070.hp2 others(58): Show |
intron_variant | MODIFIER | c.4360-5044delT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40544127 | |||||
chr19:40544127
|
CTT | C | 83 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0032others(80): Show | 83 | HG00140.hp1 HG00621.hp1 HG00741.hp1 others(80): Show |
intron_variant | MODIFIER | c.4360-5045_4360-504 others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40544127 | |||||
chr19:40544136
|
T | C | 1 | a0002c0004t0001g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4360-5053T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40544136 | ||||||
chr19:40544204
|
G | A | 89 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.4360-4985G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40544204 | ||||||
chr19:40544223
|
AC | A | 3 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023 | 3 | HG02109.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.4360-4964delC | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40544223 | |||||
chr19:40544344
|
A | G | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4360-4845A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40544344 | ||||||
chr19:40544372
|
G | A | 92 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(89): Show |
intron_variant | MODIFIER | c.4360-4817G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40544372 | ||||||
chr19:40544389
|
G | A | 1 | a0001c0002t0001g0116 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4360-4800G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40544389 | ||||||
chr19:40544440
|
C | CT | 60 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0027others(57): Show | 60 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.4360-4725dupT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40544440 | |||||
chr19:40544440
|
C | CTT | 15 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0049others(12): Show | 15 | HG01175.hp1 HG01358.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.4360-4726_4360-472 others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40544440 | |||||
chr19:40544440
|
C | CTTT | 48 | a0001c0001t0001g0072a0001c0008t0001g0046a0001c0041t0001g0024others(45): Show | 48 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.4360-4727_4360-472 others(7): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40544440 | |||||
chr19:40544440
|
C | CTTTT | 36 | a0001c0001t0001g0064a0001c0010t0001g0070a0001c0010t0001g0093others(33): Show | 36 | HG01071.hp1 HG01106.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.4360-4728_4360-472 others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40544440 | |||||
chr19:40544440
|
C | CTTTTT | 6 | a0002c0004t0001g0029a0003c0005t0001g0211a0004c0011t0001g0138others(3): Show | 6 | HG01070.hp2 HG01123.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.4360-4729_4360-472 others(9): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40544440 | |||||
chr19:40544509
|
A | G | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4360-4680A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40544509 | ||||||
chr19:40544695
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4360-4494C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40544695 | ||||||
chr19:40544729
|
G | A | 3 | a0004c0014t0001g0055a0004c0016t0001g0003a0013c0037t0001g0079 | 3 | HG02451.hp1 HG03209.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.4360-4460G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40544729 | ||||||
chr19:40544867
|
G | T | 89 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.4360-4322G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40544867 | ||||||
chr19:40545083
|
T | A | 89 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.4360-4106T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40545083 | ||||||
chr19:40545083
|
T | G | 4 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4360-4106T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40545083 | ||||||
chr19:40545241
|
G | A | 92 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(89): Show |
intron_variant | MODIFIER | c.4360-3948G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40545241 | ||||||
chr19:40545374
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4360-3815G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40545374 | ||||||
chr19:40545415
|
A | G | 39 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(36): Show | 39 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.4360-3774A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40545415 | ||||||
chr19:40545421
|
C | G | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4360-3768C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40545421 | ||||||
chr19:40545549
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4360-3640C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40545549 | ||||||
chr19:40545752
|
T | G | 2 | a0004c0014t0001g0055a0004c0016t0001g0003 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4360-3437T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40545752 | ||||||
chr19:40545903
|
C | T | 5 | a0001c0041t0001g0024a0004c0007t0010g0136a0004c0014t0001g0055others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.4360-3286C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40545903 | ||||||
chr19:40545919
|
T | C | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4360-3270T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40545919 | ||||||
chr19:40546003
|
T | C | 3 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023 | 3 | HG02109.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.4360-3186T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40546003 | ||||||
chr19:40546011
|
T | C | 1 | a0004c0014t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4360-3178T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40546011 | ||||||
chr19:40546049
|
C | CA | 6 | a0002c0021t0001g0010a0003c0005t0001g0050a0004c0014t0001g0055others(3): Show | 6 | HG01175.hp2 HG01978.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.4360-3120dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40546049 | |||||
chr19:40546049
|
CA | C | 115 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(112): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.4360-3120delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40546049 | |||||
chr19:40546049
|
CAA | C | 6 | a0001c0001t0001g0033a0001c0001t0001g0119a0001c0008t0001g0155others(3): Show | 6 | HG00621.hp2 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.4360-3121_4360-312 others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40546049 | |||||
chr19:40546082
|
G | A | 89 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.4360-3107G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40546082 | ||||||
chr19:40546097
|
T | C | 2 | a0004c0014t0001g0055a0004c0016t0001g0003 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4360-3092T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40546097 | ||||||
chr19:40546124
|
C | T | 1 | a0001c0002t0003g0163 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4360-3065C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40546124 | ||||||
chr19:40546213
|
G | A | 2 | a0002c0003t0001g0121a0005c0009t0001g0008 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.4360-2976G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40546213 | ||||||
chr19:40546225
|
CA | C | 45 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(42): Show | 45 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.4360-2948delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40546225 | |||||
chr19:40546442
|
G | A | 3 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023 | 3 | HG02109.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.4360-2747G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40546442 | ||||||
chr19:40546457
|
A | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0107 | 2 | NA19077.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.4360-2732A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40546457 | ||||||
chr19:40546463
|
G | T | 1 | a0005c0009t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4360-2726G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40546463 | ||||||
chr19:40546635
|
G | A | 1 | a0002c0003t0001g0158 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4360-2554G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40546635 | ||||||
chr19:40546693
|
T | C | 1 | a0001c0002t0001g0116 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4360-2496T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40546693 | ||||||
chr19:40546751
|
A | G | 5 | a0001c0041t0001g0024a0004c0007t0010g0136a0004c0014t0001g0055others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.4360-2438A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40546751 | ||||||
chr19:40547034
|
AT | A | 92 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(89): Show |
intron_variant | MODIFIER | c.4360-2148delT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40547034 | |||||
chr19:40547041
|
T | A | 2 | a0002c0003t0001g0121a0005c0009t0001g0008 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.4360-2148T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40547041 | ||||||
chr19:40547077
|
T | C | 139 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(136): Show |
intron_variant | MODIFIER | c.4360-2112T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40547077 | ||||||
chr19:40547212
|
A | G | 2 | a0011c0042t0001g0223a0016c0046t0001g0164 | 2 | HG01123.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4360-1977A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40547212 | ||||||
chr19:40547599
|
C | T | 1 | a0001c0010t0001g0100 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4360-1590C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40547599 | ||||||
chr19:40547805
|
T | C | 3 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023 | 3 | HG02109.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.4360-1384T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40547805 | ||||||
chr19:40547870
|
A | G | 3 | a0008c0013t0001g0143a0008c0013t0001g0145a0008c0013t0001g0147 | 3 | HG02922.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4360-1319A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40547870 | ||||||
chr19:40547897
|
A | C | 1 | a0017c0036t0001g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4360-1292A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40547897 | ||||||
chr19:40548125
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4360-1064C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40548125 | ||||||
chr19:40548352
|
A | G | 89 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.4360-837A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40548352 | ||||||
chr19:40548572
|
G | A | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4360-617G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40548572 | ||||||
chr19:40548584
|
A | G | 38 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(35): Show | 38 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4360-605A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40548584 | ||||||
chr19:40548620
|
C | T | 2 | a0003c0005t0001g0011a0003c0005t0011g0052 | 2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.4360-569C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40548620 | ||||||
chr19:40548654
|
G | A | 5 | a0001c0002t0001g0017a0001c0002t0001g0071a0001c0002t0001g0116others(2): Show | 5 | HG02083.hp2 NA18946.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.4360-535G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40548654 | ||||||
chr19:40548714
|
C | CA | 13 | a0001c0001t0001g0150a0001c0002t0001g0037a0001c0002t0001g0231others(10): Show | 13 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.4360-462dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr19 | 40548714 | |||||
chr19:40548974
|
G | A | 1 | a0005c0009t0001g0175 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4360-215G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40548974 | ||||||
chr19:40549092
|
C | T | 1 | a0001c0012t0001g0226 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4360-97C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 20/35 | chr19 | 40549092 | ||||||
chr19:40549784
|
T | C | 2 | a0004c0014t0001g0055a0004c0016t0001g0003 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4584+371T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 21/35 | chr19 | 40549784 | ||||||
chr19:40549804
|
C | A | 2 | a0002c0003t0001g0121a0005c0009t0001g0008 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.4584+391C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 21/35 | chr19 | 40549804 | ||||||
chr19:40550069
|
G | A | 1 | a0002c0003t0001g0101 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4585-169G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 21/35 | chr19 | 40550069 | ||||||
chr19:40550083
|
G | GA | 15 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0041others(12): Show | 15 | HG01071.hp2 HG01109.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.4585-143dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr19 | 40550083 | |||||
chr19:40550188
|
G | T | 1 | a0002c0015t0001g0135 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4585-50G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 21/35 | chr19 | 40550188 | ||||||
chr19:40550215
|
C | T | 1 | a0002c0034t0001g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4585-23C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 21/35 | chr19 | 40550215 | ||||||
chr19:40550504
|
AT | A | 44 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(41): Show | 44 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.4674+193delT | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr19 | 40550504 | |||||
chr19:40550504
|
ATT | A | 94 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(91): Show |
intron_variant | MODIFIER | c.4674+192_4674+193d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr19 | 40550504 | |||||
chr19:40550698
|
C | CG | 11 | a0001c0008t0001g0060a0001c0008t0001g0061a0001c0008t0001g0062others(8): Show | 11 | HG01123.hp2 HG01257.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.4674+377dupG | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr19 | 40550698 | |||||
chr19:40550725
|
G | T | 1 | a0004c0011t0001g0138 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4674+398G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40550725 | ||||||
chr19:40550752
|
C | T | 38 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(35): Show | 38 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4674+425C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40550752 | ||||||
chr19:40550799
|
G | A | 2 | a0004c0014t0001g0055a0004c0016t0001g0003 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4674+472G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40550799 | ||||||
chr19:40550886
|
G | A | 97 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(94): Show |
intron_variant | MODIFIER | c.4674+559G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40550886 | ||||||
chr19:40550910
|
A | G | 1 | a0004c0014t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4674+583A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40550910 | ||||||
chr19:40551045
|
C | T | 1 | a0004c0011t0001g0137 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4674+718C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40551045 | ||||||
chr19:40551212
|
A | G | 3 | a0008c0013t0001g0143a0008c0013t0001g0145a0008c0013t0001g0147 | 3 | HG02922.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4674+885A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40551212 | ||||||
chr19:40551237
|
C | T | 2 | a0001c0002t0001g0228a0001c0002t0002g0196 | 2 | HG01496.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.4674+910C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40551237 | ||||||
chr19:40551384
|
ATC | A | 35 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(32): Show | 35 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.4674+1072_4674+107 others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr19 | 40551384 | |||||
chr19:40551399
|
T | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0199 | 2 | HG02738.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.4674+1072T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40551399 | ||||||
chr19:40551399
|
T | TCA | 5 | a0001c0001t0001g0048a0001c0041t0001g0024a0004c0007t0010g0136others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.4674+1092_4674+109 others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr19 | 40551399 | |||||
chr19:40551399
|
T | TCACA | 2 | a0004c0014t0001g0055a0004c0016t0001g0003 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4674+1090_4674+109 others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr19 | 40551399 | |||||
chr19:40551399
|
TCA | T | 14 | a0001c0001t0001g0217a0001c0001t0001g0225a0002c0003t0001g0016others(11): Show | 14 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.4674+1092_4674+109 others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr19 | 40551399 | |||||
chr19:40551399
|
TCACA | T | 83 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0002t0003g0163others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.4674+1090_4674+109 others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr19 | 40551399 | |||||
chr19:40551401
|
A | T | 5 | a0001c0001t0001g0036a0001c0001t0001g0103a0001c0001t0001g0110others(2): Show | 5 | HG00642.hp2 HG01928.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.4674+1074A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40551401 | ||||||
chr19:40551469
|
G | T | 1 | a0002c0003t0001g0034 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4674+1142G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40551469 | ||||||
chr19:40551537
|
T | TA | 3 | a0003c0005t0001g0050a0003c0005t0001g0051a0003c0005t0001g0129 | 3 | HG01175.hp2 HG01928.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.4674+1216dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr19 | 40551537 | |||||
chr19:40551886
|
T | C | 4 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4674+1559T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40551886 | ||||||
chr19:40551993
|
C | CA | 11 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0067others(8): Show | 11 | HG01168.hp1 HG02451.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.4674+1682dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr19 | 40551993 | |||||
chr19:40552040
|
G | A | 2 | a0002c0003t0001g0121a0005c0009t0001g0008 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.4674+1713G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40552040 | ||||||
chr19:40552283
|
G | A | 4 | a0002c0015t0001g0089a0002c0015t0001g0135a0002c0015t0001g0179others(1): Show | 4 | HG02280.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4675-1864G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40552283 | ||||||
chr19:40552455
|
C | CA | 7 | a0001c0001t0001g0027a0001c0001t0001g0041a0001c0001t0001g0065others(4): Show | 7 | HG01169.hp2 HG01517.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.4675-1673dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr19 | 40552455 | |||||
chr19:40552455
|
CA | C | 93 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0047others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.4675-1673delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr19 | 40552455 | |||||
chr19:40552512
|
C | T | 91 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.4675-1635C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40552512 | ||||||
chr19:40552517
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0074 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.4675-1630T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40552517 | ||||||
chr19:40552569
|
A | G | 100 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(97): Show |
intron_variant | MODIFIER | c.4675-1578A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40552569 | ||||||
chr19:40552587
|
C | T | 1 | a0003c0018t0001g0234 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4675-1560C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40552587 | ||||||
chr19:40552693
|
A | T | 38 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(35): Show | 38 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.4675-1454A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40552693 | ||||||
chr19:40552741
|
G | A | 2 | a0002c0020t0001g0229a0002c0021t0001g0219 | 2 | HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4675-1406G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40552741 | ||||||
chr19:40552744
|
G | A | 1 | a0007c0049t0001g0185 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4675-1403G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40552744 | ||||||
chr19:40552771
|
G | T | 141 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(138): Show | 141 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.4675-1376G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40552771 | ||||||
chr19:40552896
|
C | A | 140 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(137): Show |
intron_variant | MODIFIER | c.4675-1251C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40552896 | ||||||
chr19:40553015
|
T | C | 3 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023 | 3 | HG02109.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.4675-1132T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40553015 | ||||||
chr19:40553279
|
A | G | 91 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.4675-868A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40553279 | ||||||
chr19:40553284
|
A | G | 233 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.4675-863A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40553284 | ||||||
chr19:40553478
|
G | A | 97 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(94): Show |
intron_variant | MODIFIER | c.4675-669G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40553478 | ||||||
chr19:40553488
|
G | C | 2 | a0004c0014t0001g0055a0004c0016t0001g0003 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4675-659G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40553488 | ||||||
chr19:40553498
|
A | C | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4675-649A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40553498 | ||||||
chr19:40553593
|
G | A | 1 | a0001c0002t0001g0116 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4675-554G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 22/35 | chr19 | 40553593 | ||||||
chr19:40554710
|
A | G | 38 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(35): Show | 38 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.5084+64A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554710 | ||||||
chr19:40554821
|
G | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+175G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554821 | ||||||
chr19:40554823
|
A | G | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+177A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554823 | ||||||
chr19:40554825
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+179G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554825 | ||||||
chr19:40554853
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+207G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554853 | ||||||
chr19:40554854
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+208G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554854 | ||||||
chr19:40554855
|
A | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+209A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554855 | ||||||
chr19:40554859
|
G | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+213G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554859 | ||||||
chr19:40554861
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+215G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554861 | ||||||
chr19:40554862
|
T | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+216T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554862 | ||||||
chr19:40554863
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+217G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554863 | ||||||
chr19:40554869
|
G | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+223G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554869 | ||||||
chr19:40554871
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+225G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554871 | ||||||
chr19:40554872
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+226G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554872 | ||||||
chr19:40554873
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+227G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554873 | ||||||
chr19:40554874
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+228G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554874 | ||||||
chr19:40554875
|
A | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+229A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554875 | ||||||
chr19:40554879
|
T | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+233T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554879 | ||||||
chr19:40554880
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+234G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554880 | ||||||
chr19:40554881
|
T | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+235T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554881 | ||||||
chr19:40554883
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+237G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554883 | ||||||
chr19:40554884
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+238G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554884 | ||||||
chr19:40554885
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+239G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554885 | ||||||
chr19:40554886
|
G | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+240G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554886 | ||||||
chr19:40554887
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+241G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554887 | ||||||
chr19:40554889
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+243G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554889 | ||||||
chr19:40554891
|
A | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+245A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554891 | ||||||
chr19:40554893
|
A | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+247A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554893 | ||||||
chr19:40554894
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+248G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554894 | ||||||
chr19:40554896
|
G | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+250G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554896 | ||||||
chr19:40554898
|
A | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+252A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554898 | ||||||
chr19:40554899
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+253G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554899 | ||||||
chr19:40554900
|
G | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+254G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554900 | ||||||
chr19:40554902
|
G | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+256G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554902 | ||||||
chr19:40554903
|
A | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+257A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554903 | ||||||
chr19:40554905
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+259G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554905 | ||||||
chr19:40554906
|
T | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+260T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554906 | ||||||
chr19:40554907
|
C | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+261C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554907 | ||||||
chr19:40554912
|
A | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+266A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554912 | ||||||
chr19:40554913
|
C | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+267C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554913 | ||||||
chr19:40554915
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+269G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554915 | ||||||
chr19:40554916
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+270G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554916 | ||||||
chr19:40554917
|
G | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+271G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554917 | ||||||
chr19:40554918
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+272G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554918 | ||||||
chr19:40554921
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+275G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554921 | ||||||
chr19:40554922
|
A | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+276A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554922 | ||||||
chr19:40554923
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+277G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554923 | ||||||
chr19:40554926
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+280G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554926 | ||||||
chr19:40554928
|
A | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+282A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554928 | ||||||
chr19:40554937
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+291G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554937 | ||||||
chr19:40554938
|
G | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+292G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554938 | ||||||
chr19:40554939
|
A | G | 3 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023 | 3 | HG02109.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.5084+293A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554939 | ||||||
chr19:40554974
|
G | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+328G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554974 | ||||||
chr19:40554990
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+344G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554990 | ||||||
chr19:40554996
|
A | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+350A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554996 | ||||||
chr19:40554997
|
T | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+351T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554997 | ||||||
chr19:40554999
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+353G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40554999 | ||||||
chr19:40555000
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+354G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555000 | ||||||
chr19:40555003
|
A | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+357A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555003 | ||||||
chr19:40555005
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+359G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555005 | ||||||
chr19:40555006
|
G | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+360G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555006 | ||||||
chr19:40555007
|
C | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+361C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555007 | ||||||
chr19:40555008
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+362G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555008 | ||||||
chr19:40555009
|
G | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+363G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555009 | ||||||
chr19:40555011
|
G | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+365G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555011 | ||||||
chr19:40555012
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+366G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555012 | ||||||
chr19:40555013
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+367G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555013 | ||||||
chr19:40555014
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+368G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555014 | ||||||
chr19:40555017
|
G | A | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+371G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555017 | ||||||
chr19:40555018
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+372G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555018 | ||||||
chr19:40555020
|
G | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+374G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555020 | ||||||
chr19:40555025
|
C | CTCAAAAT others(6): Show |
1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+379_5084+380i others(15): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555025 | ||||||
chr19:40555050
|
T | C | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+404T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555050 | ||||||
chr19:40555061
|
G | T | 1 | a0007c0039t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5084+415G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555061 | ||||||
chr19:40555319
|
C | G | 91 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.5084+673C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555319 | ||||||
chr19:40555385
|
G | A | 3 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023 | 3 | HG02109.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.5085-699G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555385 | ||||||
chr19:40555414
|
C | A | 91 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.5085-670C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555414 | ||||||
chr19:40555447
|
C | T | 1 | a0009c0030t0007g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5085-637C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555447 | ||||||
chr19:40555489
|
CA | C | 87 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0199others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.5085-576delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr19 | 40555489 | |||||
chr19:40555489
|
CAA | C | 40 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0032others(37): Show | 40 | HG00621.hp1 HG00741.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.5085-577_5085-576d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr19 | 40555489 | |||||
chr19:40555571
|
G | A | 1 | a0001c0010t0008g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5085-513G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555571 | ||||||
chr19:40555577
|
G | A | 95 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(92): Show |
intron_variant | MODIFIER | c.5085-507G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555577 | ||||||
chr19:40555590
|
C | A | 1 | a0001c0001t0001g0040 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.5085-494C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555590 | ||||||
chr19:40555841
|
T | C | 3 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023 | 3 | HG02109.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.5085-243T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | chr19 | 40555841 | ||||||
chr19:40555917
|
C | CA | 91 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.5085-158dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr19 | 40555917 | |||||
chr19:40556321
|
G | T | 3 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023 | 3 | HG02109.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.5289+33G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 25/35 | chr19 | 40556321 | ||||||
chr19:40556573
|
A | T | 1 | a0001c0002t0001g0083 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5289+285A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 25/35 | chr19 | 40556573 | ||||||
chr19:40556584
|
T | TATG | 91 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.5289+317_5289+319d others(5): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 25/35 | INFO_REALIGN_3_PRIME | chr19 | 40556584 | |||||
chr19:40556752
|
C | T | 91 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.5290-271C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 25/35 | chr19 | 40556752 | ||||||
chr19:40556996
|
A | AC | 41 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0031others(38): Show | 41 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.5290-16dupC | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 25/35 | INFO_REALIGN_3_PRIME | chr19 | 40556996 | |||||
chr19:40556996
|
A | ACC | 15 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0040others(12): Show | 15 | HG00621.hp1 HG00741.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.5290-17_5290-16dup others(2): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 25/35 | INFO_REALIGN_3_PRIME | chr19 | 40556996 | |||||
chr19:40556996
|
A | ACCC | 16 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0067others(13): Show | 16 | HG01074.hp2 HG01099.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.5290-18_5290-16dup others(3): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 25/35 | INFO_REALIGN_3_PRIME | chr19 | 40556996 | |||||
chr19:40556996
|
AC | A | 18 | a0001c0001t0001g0201a0001c0008t0001g0046a0001c0041t0001g0024others(15): Show | 18 | HG00140.hp1 HG01517.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.5290-16delC | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 25/35 | INFO_REALIGN_3_PRIME | chr19 | 40556996 | |||||
chr19:40557007
|
C | G | 3 | a0003c0006t0001g0084a0003c0006t0001g0212a0003c0006t0004g0080 | 3 | NA18970.hp2 NA18983.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.5290-16C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 25/35 | chr19 | 40557007 | ||||||
chr19:40557456
|
C | A | 3 | a0008c0013t0001g0143a0008c0013t0001g0145a0008c0013t0001g0147 | 3 | HG02922.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.5670+53C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40557456 | ||||||
chr19:40557465
|
G | C | 1 | a0004c0007t0003g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5670+62G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40557465 | ||||||
chr19:40557521
|
C | T | 94 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(91): Show |
intron_variant | MODIFIER | c.5670+118C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40557521 | ||||||
chr19:40557609
|
A | G | 3 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023 | 3 | HG02109.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.5670+206A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40557609 | ||||||
chr19:40557708
|
A | G | 3 | a0008c0013t0001g0143a0008c0013t0001g0145a0008c0013t0001g0147 | 3 | HG02922.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.5670+305A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40557708 | ||||||
chr19:40557774
|
C | T | 3 | a0008c0013t0001g0143a0008c0013t0001g0145a0008c0013t0001g0147 | 3 | HG02922.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.5670+371C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40557774 | ||||||
chr19:40557875
|
G | A | 91 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.5670+472G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40557875 | ||||||
chr19:40557918
|
C | CA | 23 | a0001c0001t0001g0027a0001c0001t0001g0053a0001c0001t0001g0067others(20): Show | 23 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.5670+537dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr19 | 40557918 | |||||
chr19:40557918
|
CA | C | 7 | a0001c0001t0001g0114a0001c0001t0001g0204a0001c0041t0001g0024others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.5670+537delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr19 | 40557918 | |||||
chr19:40558068
|
C | T | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5670+665C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40558068 | ||||||
chr19:40558097
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0082a0001c0001t0001g0180 | 3 | HG02056.hp2 HG02083.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.5670+694C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40558097 | ||||||
chr19:40558468
|
T | C | 1 | a0004c0027t0001g0170 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5670+1065T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40558468 | ||||||
chr19:40558620
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.5670+1217A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40558620 | ||||||
chr19:40558734
|
A | G | 87 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.5670+1331A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40558734 | ||||||
chr19:40558911
|
A | AATT | 114 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0028others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.5671-1212_5671-121 others(7): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr19 | 40558911 | |||||
chr19:40558911
|
A | AATTATT | 47 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0031others(44): Show | 47 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.5671-1215_5671-121 others(10): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr19 | 40558911 | |||||
chr19:40558911
|
A | AATTATTA others(5): Show |
1 | a0002c0021t0001g0219 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5671-1221_5671-121 others(16): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr19 | 40558911 | |||||
chr19:40558911
|
AATT | A | 11 | a0001c0008t0001g0061a0001c0008t0001g0062a0001c0008t0001g0151others(8): Show | 11 | HG01257.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.5671-1212_5671-121 others(7): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr19 | 40558911 | |||||
chr19:40558911
|
AATTATTA others(5): Show |
A | 1 | a0001c0001t0001g0128 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5671-1221_5671-121 others(16): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr19 | 40558911 | |||||
chr19:40558947
|
T | TATGATGA others(8): Show |
1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5671-1208_5671-120 others(19): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr19 | 40558947 | |||||
chr19:40558993
|
C | T | 3 | a0002c0003t0001g0182a0002c0003t0001g0221a0005c0009t0001g0007 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.5671-1166C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40558993 | ||||||
chr19:40559035
|
A | G | 141 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(138): Show | 141 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.5671-1124A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40559035 | ||||||
chr19:40559283
|
A | G | 1 | a0016c0046t0001g0164 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.5671-876A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40559283 | ||||||
chr19:40559313
|
G | A | 2 | a0011c0042t0001g0223a0016c0046t0001g0164 | 2 | HG01123.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.5671-846G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40559313 | ||||||
chr19:40559459
|
G | A | 1 | a0004c0014t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5671-700G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40559459 | ||||||
chr19:40559522
|
C | T | 1 | a0004c0007t0001g0187 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.5671-637C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40559522 | ||||||
chr19:40559676
|
A | G | 2 | a0004c0014t0001g0055a0004c0016t0001g0003 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5671-483A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 26/35 | chr19 | 40559676 | ||||||
chr19:40560744
|
A | C | 2 | a0001c0002t0002g0183a0001c0048t0002g0206 | 2 | HG00099.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.5915+341A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40560744 | ||||||
chr19:40560794
|
A | T | 1 | a0002c0021t0001g0219 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5915+391A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40560794 | ||||||
chr19:40560889
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.5915+486G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40560889 | ||||||
chr19:40560921
|
GAT | G | 38 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(35): Show | 38 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.5915+520_5915+521d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr19 | 40560921 | |||||
chr19:40560922
|
A | G | 2 | a0004c0014t0001g0055a0004c0016t0001g0003 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5915+519A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40560922 | ||||||
chr19:40560970
|
C | T | 13 | a0001c0010t0001g0093a0002c0003t0001g0182a0002c0003t0001g0221others(10): Show | 13 | HG01123.hp1 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.5915+567C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40560970 | ||||||
chr19:40561164
|
C | A | 16 | a0001c0001t0001g0072a0002c0003t0001g0063a0002c0003t0001g0073others(13): Show | 16 | HG00140.hp1 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.5915+761C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40561164 | ||||||
chr19:40561245
|
TC | T | 2 | a0002c0003t0001g0121a0005c0009t0001g0008 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.5915+843delC | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40561245 | ||||||
chr19:40561293
|
A | G | 92 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(89): Show |
intron_variant | MODIFIER | c.5915+890A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40561293 | ||||||
chr19:40561377
|
T | G | 89 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(86): Show |
intron_variant | MODIFIER | c.5915+974T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40561377 | ||||||
chr19:40561531
|
T | C | 39 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(36): Show | 39 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.5915+1128T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40561531 | ||||||
chr19:40561676
|
G | A | 2 | a0004c0014t0001g0055a0004c0016t0001g0003 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5915+1273G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40561676 | ||||||
chr19:40561686
|
G | A | 2 | a0004c0014t0001g0055a0004c0016t0001g0003 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5915+1283G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40561686 | ||||||
chr19:40561803
|
C | T | 1 | a0001c0010t0008g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5915+1400C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40561803 | ||||||
chr19:40561822
|
CA | C | 5 | a0001c0001t0001g0115a0001c0001t0001g0128a0004c0007t0001g0139others(2): Show | 5 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.5915+1433delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr19 | 40561822 | |||||
chr19:40562127
|
G | GGCACTGG others(14): Show |
1 | a0001c0001t0001g0091 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.5915+1725_5915+174 others(25): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr19 | 40562127 | |||||
chr19:40562265
|
T | C | 139 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(136): Show |
intron_variant | MODIFIER | c.5915+1862T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40562265 | ||||||
chr19:40562353
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5915+1950A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40562353 | ||||||
chr19:40562359
|
G | A | 1 | a0001c0002t0001g0202 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.5915+1956G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40562359 | ||||||
chr19:40562516
|
C | T | 2 | a0004c0014t0001g0055a0004c0016t0001g0003 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5915+2113C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40562516 | ||||||
chr19:40562529
|
C | CA | 40 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(37): Show | 40 | HG00099.hp2 HG00621.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.5915+2149dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr19 | 40562529 | |||||
chr19:40562529
|
C | CAA | 18 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0049others(15): Show | 18 | HG00621.hp1 HG00741.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.5915+2148_5915+214 others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr19 | 40562529 | |||||
chr19:40562529
|
CA | C | 77 | a0001c0001t0001g0072a0001c0001t0001g0217a0001c0008t0001g0046others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.5915+2149delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr19 | 40562529 | |||||
chr19:40562529
|
CAA | C | 5 | a0002c0003t0001g0121a0005c0009t0001g0008a0008c0013t0001g0145others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.5915+2148_5915+214 others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr19 | 40562529 | |||||
chr19:40562549
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.5915+2146A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40562549 | ||||||
chr19:40562633
|
G | A | 1 | a0001c0002t0001g0071 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.5915+2230G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40562633 | ||||||
chr19:40562810
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5915+2407G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40562810 | ||||||
chr19:40562834
|
C | CA | 6 | a0001c0001t0001g0114a0008c0013t0001g0143a0008c0013t0001g0145others(3): Show | 6 | HG02056.hp1 HG02486.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.5915+2444dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr19 | 40562834 | |||||
chr19:40562909
|
C | T | 1 | a0004c0007t0003g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5915+2506C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40562909 | ||||||
chr19:40562969
|
G | A | 2 | a0002c0020t0001g0229a0002c0021t0001g0219 | 2 | HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.5916-2454G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40562969 | ||||||
chr19:40563061
|
T | C | 89 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(86): Show |
intron_variant | MODIFIER | c.5916-2362T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40563061 | ||||||
chr19:40563559
|
C | T | 38 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(35): Show | 38 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.5916-1864C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40563559 | ||||||
chr19:40563608
|
G | A | 3 | a0002c0003t0001g0016a0002c0003t0001g0158a0010c0055t0001g0020 | 3 | HG01070.hp1 HG01517.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.5916-1815G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40563608 | ||||||
chr19:40563624
|
G | A | 28 | a0003c0005t0001g0011a0003c0005t0001g0015a0003c0005t0001g0050others(25): Show | 28 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.5916-1799G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40563624 | ||||||
chr19:40563745
|
A | G | 3 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023 | 3 | HG02109.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.5916-1678A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40563745 | ||||||
chr19:40563823
|
C | A | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5916-1600C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40563823 | ||||||
chr19:40564090
|
C | G | 89 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(86): Show |
intron_variant | MODIFIER | c.5916-1333C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40564090 | ||||||
chr19:40564289
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.5916-1134A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40564289 | ||||||
chr19:40564834
|
T | TA | 6 | a0002c0003t0001g0121a0002c0020t0001g0157a0005c0009t0001g0008others(3): Show | 6 | HG00140.hp1 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.5916-575dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr19 | 40564834 | |||||
chr19:40564834
|
TA | T | 5 | a0001c0001t0001g0114a0002c0034t0001g0154a0004c0014t0001g0055others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.5916-575delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr19 | 40564834 | |||||
chr19:40564842
|
A | C | 39 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(36): Show | 39 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.5916-581A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40564842 | ||||||
chr19:40565014
|
C | CA | 3 | a0008c0013t0001g0143a0008c0013t0001g0145a0008c0013t0001g0147 | 3 | HG02922.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.5916-408dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr19 | 40565014 | |||||
chr19:40565049
|
G | A | 1 | a0001c0012t0001g0068 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.5916-374G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40565049 | ||||||
chr19:40565189
|
C | T | 3 | a0002c0003t0001g0182a0002c0003t0001g0221a0005c0009t0001g0007 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.5916-234C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40565189 | ||||||
chr19:40565242
|
G | A | 2 | a0004c0014t0001g0055a0004c0016t0001g0003 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5916-181G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | chr19 | 40565242 | ||||||
chr19:40565271
|
A | AAAAAG | 21 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0040others(18): Show | 21 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.5916-128_5916-124d others(7): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr19 | 40565271 | |||||
chr19:40565271
|
A | AAAAAGAA others(3): Show |
1 | a0001c0001t0001g0152 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.5916-133_5916-124d others(12): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr19 | 40565271 | |||||
chr19:40565271
|
AAAAAG | A | 23 | a0001c0001t0001g0072a0001c0001t0001g0203a0002c0003t0001g0063others(20): Show | 23 | HG00140.hp1 HG01074.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.5916-128_5916-124d others(7): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr19 | 40565271 | |||||
chr19:40565271
|
AAAAAGAA others(3): Show |
A | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5916-133_5916-124d others(12): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr19 | 40565271 | |||||
chr19:40565795
|
C | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(36): Show | 39 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.6139+50C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 29/35 | chr19 | 40565795 | ||||||
chr19:40565968
|
A | C | 1 | a0001c0002t0001g0159 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.6140-195A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 29/35 | chr19 | 40565968 | ||||||
chr19:40566100
|
G | C | 1 | a0001c0001t0001g0199 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.6140-63G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 29/35 | chr19 | 40566100 | ||||||
chr19:40566143
|
C | T | 1 | a0001c0012t0001g0068 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.6140-20C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 29/35 | chr19 | 40566143 | ||||||
chr19:40566459
|
C | T | 1 | a0004c0007t0003g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6336+100C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | chr19 | 40566459 | ||||||
chr19:40566844
|
A | C | 39 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(36): Show | 39 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.6336+485A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | chr19 | 40566844 | ||||||
chr19:40566938
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.6336+579C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | chr19 | 40566938 | ||||||
chr19:40566983
|
AC | A | 9 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0067others(6): Show | 9 | HG00741.hp2 HG02738.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.6336+625delC | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | chr19 | 40566983 | ||||||
chr19:40566984
|
C | A | 126 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.6336+625C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | chr19 | 40566984 | ||||||
chr19:40566987
|
C | A | 39 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(36): Show | 39 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.6336+628C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | chr19 | 40566987 | ||||||
chr19:40567111
|
G | A | 1 | a0001c0002t0001g0116 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.6337-552G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | chr19 | 40567111 | ||||||
chr19:40567190
|
G | A | 1 | a0002c0003t0001g0158 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.6337-473G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | chr19 | 40567190 | ||||||
chr19:40567266
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.6337-397T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | chr19 | 40567266 | ||||||
chr19:40567298
|
A | AAAAT | 60 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0021others(57): Show | 60 | HG00140.hp1 HG01070.hp1 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.6337-321_6337-318d others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr19 | 40567298 | |||||
chr19:40567298
|
A | AAAATAAA others(1): Show |
3 | a0007c0047t0001g0209a0012c0050t0001g0023a0019c0051t0001g0220 | 3 | HG01934.hp1 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.6337-325_6337-318d others(10): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr19 | 40567298 | |||||
chr19:40567298
|
A | AAAATAAA others(5): Show |
1 | a0001c0002t0001g0022 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6337-329_6337-318d others(14): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr19 | 40567298 | |||||
chr19:40567298
|
AAAAT | A | 74 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(71): Show | 74 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.6337-321_6337-318d others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr19 | 40567298 | |||||
chr19:40567298
|
AAAATAAA others(5): Show |
A | 2 | a0001c0001t0001g0195a0008c0013t0001g0143 | 2 | HG03516.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.6337-329_6337-318d others(14): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr19 | 40567298 | |||||
chr19:40567298
|
AAAATAAA others(9): Show |
A | 2 | a0008c0013t0001g0145a0008c0013t0001g0147 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.6337-333_6337-318d others(18): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr19 | 40567298 | |||||
chr19:40567348
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6337-315C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | chr19 | 40567348 | ||||||
chr19:40567410
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.6337-253G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | chr19 | 40567410 | ||||||
chr19:40567448
|
C | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(36): Show | 39 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.6337-215C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | chr19 | 40567448 | ||||||
chr19:40567477
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(5): Show | 8 | HG01175.hp1 HG01255.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.6337-186C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | chr19 | 40567477 | ||||||
chr19:40567516
|
C | T | 3 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023 | 3 | HG02109.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.6337-147C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | chr19 | 40567516 | ||||||
chr19:40567626
|
C | T | 2 | a0004c0014t0001g0055a0004c0016t0001g0003 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.6337-37C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 30/35 | chr19 | 40567626 | ||||||
chr19:40568350
|
G | T | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6956+68G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/35 | chr19 | 40568350 | ||||||
chr19:40568384
|
C | A | 1 | a0004c0011t0001g0138 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6956+102C>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/35 | chr19 | 40568384 | ||||||
chr19:40568534
|
C | G | 1 | a0005c0009t0001g0175 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.6956+252C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/35 | chr19 | 40568534 | ||||||
chr19:40568748
|
G | C | 3 | a0002c0004t0001g0025a0002c0004t0001g0168a0002c0004t0001g0222 | 3 | HG03491.hp2 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.6956+466G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/35 | chr19 | 40568748 | ||||||
chr19:40568956
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.6956+674G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/35 | chr19 | 40568956 | ||||||
chr19:40569032
|
G | C | 136 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.6957-625G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/35 | chr19 | 40569032 | ||||||
chr19:40569374
|
G | T | 1 | a0001c0002t0001g0205 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.6957-283G>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/35 | chr19 | 40569374 | ||||||
chr19:40569426
|
C | CA | 27 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(24): Show | 27 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.6957-212dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr19 | 40569426 | |||||
chr19:40569426
|
C | CAA | 7 | a0001c0001t0001g0067a0001c0001t0001g0092a0001c0001t0001g0119others(4): Show | 7 | HG02257.hp1 HG02976.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.6957-213_6957-212d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr19 | 40569426 | |||||
chr19:40569426
|
CA | C | 94 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(91): Show |
intron_variant | MODIFIER | c.6957-212delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr19 | 40569426 | |||||
chr19:40569426
|
CAAAAAA | C | 13 | a0001c0002t0001g0086a0001c0002t0005g0193a0001c0008t0001g0060others(10): Show | 13 | HG01123.hp2 HG01257.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.6957-217_6957-212d others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr19 | 40569426 | |||||
chr19:40569514
|
G | A | 4 | a0001c0041t0001g0024a0004c0007t0010g0136a0012c0050t0001g0023others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.6957-143G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/35 | chr19 | 40569514 | ||||||
chr19:40569583
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.6957-74C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 31/35 | chr19 | 40569583 | ||||||
chr19:40569756
|
G | C | 134 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(131): Show | 134 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.7026+30G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | chr19 | 40569756 | ||||||
chr19:40569779
|
G | A | 1 | a0001c0002t0001g0228 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.7026+53G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | chr19 | 40569779 | ||||||
chr19:40569936
|
C | CCA | 15 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0066others(12): Show | 15 | HG01074.hp1 HG01109.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.7026+247_7026+248d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569936 | |||||
chr19:40569936
|
C | CCACA | 19 | a0001c0001t0001g0021a0001c0012t0001g0039a0001c0033t0001g0112others(16): Show | 19 | HG01071.hp2 HG01081.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.7026+245_7026+248d others(6): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569936 | |||||
chr19:40569936
|
C | CCACACA | 29 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0008t0001g0046others(26): Show | 29 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.7026+243_7026+248d others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569936 | |||||
chr19:40569936
|
C | CCACACAC others(1): Show |
20 | a0002c0003t0001g0026a0002c0004t0001g0095a0002c0004t0001g0096others(17): Show | 20 | HG00099.hp1 HG00738.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.7026+241_7026+248d others(10): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569936 | |||||
chr19:40569936
|
C | CCACACAC others(3): Show |
5 | a0002c0003t0001g0016a0002c0020t0001g0229a0002c0021t0001g0010others(2): Show | 5 | HG01517.hp1 HG01891.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.7026+239_7026+248d others(12): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569936 | |||||
chr19:40569936
|
C | CCACACAC others(5): Show |
7 | a0001c0001t0001g0217a0002c0003t0001g0034a0002c0003t0001g0158others(4): Show | 7 | HG00741.hp2 HG02132.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.7026+237_7026+248d others(14): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569936 | |||||
chr19:40569936
|
CCA | C | 6 | a0001c0001t0001g0087a0001c0001t0001g0169a0002c0020t0001g0157others(3): Show | 6 | HG00140.hp1 HG02922.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.7026+247_7026+248d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569936 | |||||
chr19:40569936
|
CCACACA | C | 6 | a0001c0001t0001g0027a0001c0001t0001g0053a0001c0001t0001g0074others(3): Show | 6 | HG01516.hp2 HG01517.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.7026+243_7026+248d others(8): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569936 | |||||
chr19:40569936
|
CCACACAC others(1): Show |
C | 78 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0031others(75): Show | 78 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.7026+241_7026+248d others(10): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569936 | |||||
chr19:40569936
|
CCACACAC others(3): Show |
C | 2 | a0001c0001t0001g0225a0006c0044t0001g0167 | 2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.7026+239_7026+248d others(12): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569936 | |||||
chr19:40569936
|
CCACACAC others(5): Show |
C | 1 | a0006c0053t0001g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.7026+237_7026+248d others(14): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569936 | |||||
chr19:40569955
|
CACACACA others(13): Show |
C | 1 | a0001c0010t0008g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.7026+243_7026+262d others(22): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569955 | |||||
chr19:40569961
|
C | CACACACA others(23): Show |
1 | a0005c0009t0001g0148 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.7026+248_7026+249i others(32): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569961 | |||||
chr19:40569961
|
C | CACACACA others(15): Show |
2 | a0002c0003t0001g0197a0002c0003t0001g0198 | 2 | HG02145.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.7026+248_7026+249i others(24): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569961 | |||||
chr19:40569963
|
CACACACA others(5): Show |
C | 2 | a0001c0010t0001g0093a0004c0025t0001g0056 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7026+249_7026+260d others(14): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569963 | |||||
chr19:40569969
|
CACACAGA others(13): Show |
C | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7026+249_7026+268d others(22): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569969 | |||||
chr19:40569975
|
G | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0120 | 2 | HG01978.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.7026+249G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | chr19 | 40569975 | ||||||
chr19:40569979
|
C | G | 1 | a0001c0001t0001g0045 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.7026+253C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | chr19 | 40569979 | ||||||
chr19:40569989
|
G | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0120 | 2 | HG01978.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.7026+263G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | chr19 | 40569989 | ||||||
chr19:40569989
|
GAC | G | 5 | a0001c0002t0001g0022a0001c0002t0001g0194a0001c0054t0001g0090others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.7026+275_7026+276d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40569989 | |||||
chr19:40569993
|
C | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0120a0018c0052t0001g0122 | 3 | HG01978.hp1 HG01993.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.7026+267C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | chr19 | 40569993 | ||||||
chr19:40570019
|
T | TAC | 13 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0008t0001g0060others(10): Show | 13 | HG00621.hp1 HG01123.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.7026+301_7026+302d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr19 | 40570019 | |||||
chr19:40570029
|
G | C | 39 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(36): Show | 39 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.7026+303G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | chr19 | 40570029 | ||||||
chr19:40570084
|
T | C | 134 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(131): Show | 134 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.7027-352T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | chr19 | 40570084 | ||||||
chr19:40570147
|
T | C | 134 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(131): Show | 134 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.7027-289T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | chr19 | 40570147 | ||||||
chr19:40570424
|
C | T | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7027-12C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 32/35 | chr19 | 40570424 | ||||||
chr19:40570843
|
C | G | 188 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.7319+115C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 33/35 | chr19 | 40570843 | ||||||
chr19:40570865
|
T | TG | 6 | a0001c0041t0001g0024a0004c0007t0010g0136a0004c0014t0001g0058others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.7319+143dupG | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr19 | 40570865 | |||||
chr19:40571061
|
C | T | 1 | a0018c0052t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7319+333C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 33/35 | chr19 | 40571061 | ||||||
chr19:40571110
|
C | T | 2 | a0004c0014t0001g0055a0004c0016t0001g0003 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.7319+382C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 33/35 | chr19 | 40571110 | ||||||
chr19:40571257
|
T | C | 1 | a0001c0002t0005g0193 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.7319+529T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 33/35 | chr19 | 40571257 | ||||||
chr19:40571595
|
T | C | 139 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(136): Show |
intron_variant | MODIFIER | c.7320-424T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 33/35 | chr19 | 40571595 | ||||||
chr19:40571613
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG02074.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.7320-406C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 33/35 | chr19 | 40571613 | ||||||
chr19:40571821
|
A | T | 2 | a0001c0010t0001g0149a0001c0010t0001g0230 | 2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.7320-198A>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 33/35 | chr19 | 40571821 | ||||||
chr19:40571985
|
C | T | 87 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0217others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.7320-34C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 33/35 | chr19 | 40571985 | ||||||
chr19:40571986
|
G | A | 1 | a0014c0040t0001g0218 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.7320-33G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 33/35 | chr19 | 40571986 | ||||||
chr19:40572011
|
C | T | 1 | a0011c0042t0001g0223 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.7320-8C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 33/35 | chr19 | 40572011 | ||||||
chr19:40572205
|
A | G | 1 | a0001c0002t0001g0116 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.7493+13A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 34/35 | chr19 | 40572205 | ||||||
chr19:40572288
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0082a0001c0001t0001g0180 | 3 | HG02056.hp2 HG02083.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.7494-50G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 34/35 | chr19 | 40572288 | ||||||
chr19:40572314
|
G | C | 133 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0027others(130): Show | 133 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.7494-24G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 34/35 | chr19 | 40572314 | ||||||
chr19:40572684
|
C | T | 3 | a0008c0013t0001g0143a0008c0013t0001g0145a0008c0013t0001g0147 | 3 | HG02922.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.7536+304C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40572684 | ||||||
chr19:40572685
|
G | A | 15 | a0001c0001t0001g0072a0002c0003t0001g0063a0002c0003t0001g0073others(12): Show | 15 | HG00140.hp1 HG01074.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.7536+305G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40572685 | ||||||
chr19:40572782
|
A | C | 1 | a0002c0020t0001g0229 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7536+402A>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40572782 | ||||||
chr19:40572787
|
C | T | 1 | a0002c0003t0001g0016 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.7536+407C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40572787 | ||||||
chr19:40573303
|
T | G | 1 | a0004c0016t0001g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7536+923T>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40573303 | ||||||
chr19:40573559
|
A | G | 2 | a0002c0003t0001g0121a0005c0009t0001g0008 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.7536+1179A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40573559 | ||||||
chr19:40573781
|
T | C | 16 | a0001c0010t0001g0149a0001c0010t0001g0230a0001c0041t0001g0024others(13): Show | 16 | HG01123.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.7536+1401T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40573781 | ||||||
chr19:40573970
|
C | T | 1 | a0005c0026t0001g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.7537-1441C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40573970 | ||||||
chr19:40574115
|
CAAACA | C | 77 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0027others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.7537-1267_7537-126 others(9): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr19 | 40574115 | |||||
chr19:40574167
|
C | G | 1 | a0020c0028t0001g0174 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.7537-1244C>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40574167 | ||||||
chr19:40574408
|
C | T | 62 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0027others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.7537-1003C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40574408 | ||||||
chr19:40574422
|
C | T | 62 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0027others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.7537-989C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40574422 | ||||||
chr19:40574767
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0091others(1): Show | 4 | HG00140.hp2 HG01109.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.7537-644C>T | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40574767 | ||||||
chr19:40574823
|
T | C | 1 | a0001c0001t0006g0233 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.7537-588T>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40574823 | ||||||
chr19:40574879
|
G | A | 2 | a0003c0005t0002g0207a0003c0005t0002g0208 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.7537-532G>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40574879 | ||||||
chr19:40574908
|
A | G | 115 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.7537-503A>G | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40574908 | ||||||
chr19:40574910
|
G | C | 1 | a0001c0002t0005g0193 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.7537-501G>C | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40574910 | ||||||
chr19:40575014
|
C | CA | 47 | a0001c0001t0001g0064a0001c0001t0001g0217a0001c0008t0001g0046others(44): Show | 47 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.7537-379dupA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr19 | 40575014 | |||||
chr19:40575014
|
C | CAA | 9 | a0001c0001t0001g0225a0002c0004t0001g0104a0004c0014t0001g0055others(6): Show | 9 | HG01099.hp1 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.7537-380_7537-379d others(4): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr19 | 40575014 | |||||
chr19:40575014
|
CA | C | 5 | a0001c0001t0001g0114a0001c0002t0005g0193a0001c0008t0001g0151others(2): Show | 5 | HG03209.hp1 HG03486.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.7537-379delA | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr19 | 40575014 | |||||
chr19:40575149
|
ATAT | A | 3 | a0003c0006t0001g0084a0003c0006t0001g0212a0003c0006t0004g0080 | 3 | NA18970.hp2 NA18983.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.7537-255_7537-253d others(5): Show |
SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr19 | 40575149 | |||||
chr19:40575389
|
T | A | 6 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0130others(3): Show | 6 | HG00741.hp1 HG01074.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.7537-22T>A | SPTBN4 | ENSG00000160460.17 | transcript | ENST00000598249.6 | protein_coding | 35/35 | chr19 | 40575389 |